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 2 32673862 32673862 + Splice_Site SNP G G T TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr2:32673862G>T c.e22-1 BLCA 2 32613998 32613998 + Missense_Mutation SNP C C G TCGA-ZF-A9R9-01A-11D-A38G-08 TCGA-ZF-A9R9-10A-01D-A38J-08 g.chr2:32613998C>G c.826C>G c.(826-828)Cgt>Ggt p.R276G BLCA 2 32617216 32617216 + Missense_Mutation SNP C C G TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr2:32617216C>G c.949C>G c.(949-951)Cag>Gag p.Q317E BLCA 2 32620589 32620589 + Missense_Mutation SNP C C G TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr2:32620589C>G c.962C>G c.(961-963)tCt>tGt p.S321C BLCA 2 32626345 32626345 + Silent SNP T T C TCGA-E5-A2PC-01A-11D-A202-08 TCGA-E5-A2PC-10B-01D-A202-08 g.chr2:32626345T>C c.1149T>C c.(1147-1149)gaT>gaC p.D383D BLCA 2 32626450 32626450 + Missense_Mutation SNP G G A TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr2:32626450G>A c.1254G>A c.(1252-1254)atG>atA p.M418I BLCA 2 32626592 32626592 + Missense_Mutation SNP C C T TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr2:32626592C>T c.1319C>T c.(1318-1320)tCa>tTa p.S440L BLCA 2 32626615 32626615 + Missense_Mutation SNP G G A TCGA-G2-A2EF-01A-12D-A18F-08 TCGA-G2-A2EF-10A-01D-A18F-08 g.chr2:32626615G>A c.1342G>A c.(1342-1344)Gat>Aat p.D448N BLCA 2 32626655 32626655 + Missense_Mutation SNP C C G TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr2:32626655C>G c.1382C>G c.(1381-1383)tCt>tGt p.S461C BLCA 2 32626664 32626664 + Missense_Mutation SNP C C T TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr2:32626664C>T c.1391C>T c.(1390-1392)tCa>tTa p.S464L BLCA 2 32631587 32631587 + Missense_Mutation SNP C C T TCGA-XF-A9T6-01A-11D-A42E-08 TCGA-XF-A9T6-10A-01D-A42H-08 g.chr2:32631587C>T c.1439C>T c.(1438-1440)tCa>tTa p.S480L BLCA 2 32639854 32639854 + Missense_Mutation SNP G G A TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr2:32639854G>A c.1495G>A c.(1495-1497)Gaa>Aaa p.E499K BLCA 2 32640101 32640101 + Missense_Mutation SNP C C T TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr2:32640101C>T c.1742C>T c.(1741-1743)tCa>tTa p.S581L BLCA 2 32640253 32640253 + Missense_Mutation SNP C C T TCGA-ZF-A9RL-01A-11D-A38G-08 TCGA-ZF-A9RL-10A-01D-A38J-08 g.chr2:32640253C>T c.1894C>T c.(1894-1896)Ctt>Ttt p.L632F BLCA 2 32640519 32640519 + Silent SNP G G A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr2:32640519G>A c.2160G>A c.(2158-2160)ttG>ttA p.L720L BLCA 2 32640622 32640622 + Missense_Mutation SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr2:32640622G>A c.2263G>A c.(2263-2265)Gaa>Aaa p.E755K BLCA 2 32640936 32640936 + Silent SNP C C G TCGA-GD-A3OS-01A-12D-A21Z-08 TCGA-GD-A3OS-10A-01D-A21Z-08 g.chr2:32640936C>G c.2577C>G c.(2575-2577)ctC>ctG p.L859L BLCA 2 32640936 32640936 + Silent SNP C C G TCGA-ZF-A9RG-01A-21D-A42E-08 TCGA-ZF-A9RG-10A-01D-A42H-08 g.chr2:32640936C>G c.2577C>G c.(2575-2577)ctC>ctG p.L859L BLCA 2 32656088 32656088 + Missense_Mutation SNP C C G TCGA-ZF-A9R2-01A-11D-A391-08 TCGA-ZF-A9R2-10A-01D-A394-08 g.chr2:32656088C>G c.3178C>G c.(3178-3180)Caa>Gaa p.Q1060E BLCA 2 32664625 32664625 + Silent SNP G G A TCGA-2F-A9KT-01A-11D-A38G-08 TCGA-2F-A9KT-10A-01D-A38J-08 g.chr2:32664625G>A c.3681G>A c.(3679-3681)gtG>gtA p.V1227V BLCA 2 32666516 32666516 + Silent SNP A A G TCGA-4Z-AA86-01A-11D-A391-08 TCGA-4Z-AA86-10A-01D-A394-08 g.chr2:32666516A>G c.3930A>G c.(3928-3930)tcA>tcG p.S1310S BLCA 2 32668572 32668572 + Missense_Mutation SNP G G T TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr2:32668572G>T c.4252G>T c.(4252-4254)Gac>Tac p.D1418Y BLCA 2 32670646 32670646 + Missense_Mutation SNP G G A TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr2:32670646G>A c.4394G>A c.(4393-4395)gGa>gAa p.G1465E BLCA 2 32673877 32673877 + Missense_Mutation SNP G G A TCGA-DK-A1A7-01A-11D-A13W-08 TCGA-DK-A1A7-10A-01D-A13W-08 g.chr2:32673877G>A c.4499G>A c.(4498-4500)aGc>aAc p.S1500N BLCA 2 32673888 32673888 + Missense_Mutation SNP G G A TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr2:32673888G>A c.4510G>A c.(4510-4512)Gat>Aat p.D1504N BLCA 2 32678919 32678919 + Silent SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr2:32678919C>T c.4662C>T c.(4660-4662)ttC>ttT p.F1554F BLCA 2 32678953 32678953 + Missense_Mutation SNP C C G TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr2:32678953C>G c.4696C>G c.(4696-4698)Ctg>Gtg p.L1566V BLCA 2 32689742 32689742 + Missense_Mutation SNP C C T TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr2:32689742C>T c.5107C>T c.(5107-5109)Ctt>Ttt p.L1703F BLCA 2 32689802 32689802 + Missense_Mutation SNP G G A TCGA-K4-A6FZ-01A-11D-A31L-08 TCGA-K4-A6FZ-10A-01D-A31J-08 g.chr2:32689802G>A c.5167G>A c.(5167-5169)Gaa>Aaa p.E1723K BLCA 2 32692602 32692602 + Missense_Mutation SNP G G T TCGA-E7-A7DU-01A-11D-A32B-08 TCGA-E7-A7DU-10A-01D-A329-08 g.chr2:32692602G>T c.5366G>T c.(5365-5367)aGa>aTa p.R1789I BLCA 2 32692639 32692639 + Silent SNP G G A TCGA-E7-A7DU-01A-11D-A32B-08 TCGA-E7-A7DU-10A-01D-A329-08 g.chr2:32692639G>A c.5403G>A c.(5401-5403)ttG>ttA p.L1801L BLCA 2 32692643 32692643 + Missense_Mutation SNP G G A TCGA-E7-A7DU-01A-11D-A32B-08 TCGA-E7-A7DU-10A-01D-A329-08 g.chr2:32692643G>A c.5407G>A c.(5407-5409)Gat>Aat p.D1803N BLCA 2 32692709 32692709 + Missense_Mutation SNP G G C TCGA-E7-A7DU-01A-11D-A32B-08 TCGA-E7-A7DU-10A-01D-A329-08 g.chr2:32692709G>C c.5473G>C c.(5473-5475)Gag>Cag p.E1825Q BLCA 2 32694656 32694656 + Silent SNP A A G TCGA-BL-A13I-01A-11D-A13W-08 TCGA-BL-A13I-11A-11D-A13W-08 g.chr2:32694656A>G c.6321A>G c.(6319-6321)gaA>gaG p.E2107E BLCA 2 32703843 32703843 + Missense_Mutation SNP G G C TCGA-XF-A9SY-01A-21D-A42E-08 TCGA-XF-A9SY-10A-01D-A42H-08 g.chr2:32703843G>C c.7209G>C c.(7207-7209)tgG>tgC p.W2403C BLCA 2 32703874 32703874 + Missense_Mutation SNP G G C TCGA-YF-AA3L-01A-11D-A38G-08 TCGA-YF-AA3L-10A-01D-A38J-08 g.chr2:32703874G>C c.7240G>C c.(7240-7242)Gat>Cat p.D2414H BLCA 2 32706501 32706501 + Missense_Mutation SNP C C G TCGA-DK-AA74-01A-11D-A391-08 TCGA-DK-AA74-10A-01D-A394-08 g.chr2:32706501C>G c.7522C>G c.(7522-7524)Ctt>Gtt p.L2508V BLCA 2 32712726 32712726 + Missense_Mutation SNP C C T TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chr2:32712726C>T c.7826C>T c.(7825-7827)cCc>cTc p.P2609L BLCA 2 32715215 32715215 + Missense_Mutation SNP A A C TCGA-FJ-A3ZE-01A-11D-A23M-08 TCGA-FJ-A3ZE-10A-01D-A23K-08 g.chr2:32715215A>C c.8203A>C c.(8203-8205)Aat>Cat p.N2735H BLCA 2 32716552 32716552 + Missense_Mutation SNP C C G TCGA-BT-A20N-01A-11D-A14W-08 TCGA-BT-A20N-11A-11D-A14W-08 g.chr2:32716552C>G c.8267C>G c.(8266-8268)cCa>cGa p.P2756R BLCA 2 32716581 32716581 + Missense_Mutation SNP C C G TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr2:32716581C>G c.8296C>G c.(8296-8298)Ctt>Gtt p.L2766V BLCA 2 32724726 32724726 + Missense_Mutation SNP G G A TCGA-ZF-AA4X-01A-11D-A38G-08 TCGA-ZF-AA4X-10A-01D-A38J-08 g.chr2:32724726G>A c.8581G>A c.(8581-8583)Gaa>Aaa p.E2861K BLCA 2 32724730 32724730 + Missense_Mutation SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr2:32724730C>T c.8585C>T c.(8584-8586)tCg>tTg p.S2862L BLCA 2 32724793 32724793 + Missense_Mutation SNP C C T TCGA-4Z-AA7Q-01A-11D-A391-08 TCGA-4Z-AA7Q-10A-01D-A394-08 g.chr2:32724793C>T c.8648C>T c.(8647-8649)tCa>tTa p.S2883L BLCA 2 32726904 32726904 + Missense_Mutation SNP G G C TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr2:32726904G>C c.9156G>C c.(9154-9156)atG>atC p.M3052I BLCA 2 32730212 32730212 + Missense_Mutation SNP C C T TCGA-ZF-AA5N-01A-11D-A42E-08 TCGA-ZF-AA5N-10A-01D-A42H-08 g.chr2:32730212C>T c.9640C>T c.(9640-9642)Ctt>Ttt p.L3214F BLCA 2 32733070 32733070 + Missense_Mutation SNP G G A TCGA-K4-A6MB-01A-11D-A31L-08 TCGA-K4-A6MB-10A-01D-A31J-08 g.chr2:32733070G>A c.9724G>A c.(9724-9726)Gaa>Aaa p.E3242K BLCA 2 32733132 32733132 + Silent SNP C C T TCGA-E5-A4TZ-01A-11D-A31L-08 TCGA-E5-A4TZ-10B-01D-A31J-08 g.chr2:32733132C>T c.9786C>T c.(9784-9786)ctC>ctT p.L3262L BLCA 2 32734865 32734865 + Missense_Mutation SNP G G C TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr2:32734865G>C c.10041G>C c.(10039-10041)atG>atC p.M3347I BLCA 2 32738069 32738069 + Missense_Mutation SNP G G T TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr2:32738069G>T c.10416G>T c.(10414-10416)atG>atT p.M3472I BLCA 2 32738106 32738106 + Missense_Mutation SNP G G A TCGA-DK-A2I6-01A-12D-A18F-08 TCGA-DK-A2I6-10A-01D-A18F-08 g.chr2:32738106G>A c.10453G>A c.(10453-10455)Ggt>Agt p.G3485S BLCA 2 32738107 32738107 + Missense_Mutation SNP G G T TCGA-DK-A2I6-01A-12D-A18F-08 TCGA-DK-A2I6-10A-01D-A18F-08 g.chr2:32738107G>T c.10454G>T c.(10453-10455)gGt>gTt p.G3485V BLCA 2 32738130 32738130 + Missense_Mutation SNP C C A TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr2:32738130C>A c.10477C>A c.(10477-10479)Cat>Aat p.H3493N BLCA 2 32738163 32738163 + Missense_Mutation SNP A A G TCGA-DK-AA6R-01A-11D-A42E-08 TCGA-DK-AA6R-10A-01D-A42H-08 g.chr2:32738163A>G c.10510A>G c.(10510-10512)Agt>Ggt p.S3504G BLCA 2 32740283 32740283 + Missense_Mutation SNP G G A TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr2:32740283G>A c.10795G>A c.(10795-10797)Gca>Aca p.A3599T BLCA 2 32740370 32740370 + Missense_Mutation SNP G G C TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr2:32740370G>C c.10882G>C c.(10882-10884)Gac>Cac p.D3628H BLCA 2 32740564 32740577 + Frame_Shift_Del DEL AGTTGGCAATAGCC AGTTGGCAATAGCC - TCGA-4Z-AA84-01A-11D-A391-08 TCGA-4Z-AA84-10A-01D-A394-08 g.chr2:32740564_32740577delAGTTGGCAATAGCC c.11076_11089delAGTTGGCAATAGCC c.(11074-11091)gaagttggcaatagccatfs p.VGNSH3693fs BLCA 2 32740707 32740707 + Missense_Mutation SNP C C T TCGA-XF-A9SP-01A-11D-A391-08 TCGA-XF-A9SP-10A-01D-A394-08 g.chr2:32740707C>T c.11219C>T c.(11218-11220)tCa>tTa p.S3740L BLCA 2 32740790 32740790 + Missense_Mutation SNP C C G TCGA-K4-A3WS-01A-11D-A22Z-08 TCGA-K4-A3WS-10A-01D-A22Z-08 g.chr2:32740790C>G c.11302C>G c.(11302-11304)Cta>Gta p.L3768V BLCA 2 32743450 32743450 + Nonsense_Mutation SNP C C T TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr2:32743450C>T c.11479C>T c.(11479-11481)Cag>Tag p.Q3827* BLCA 2 32743962 32743962 + Missense_Mutation SNP C C T TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr2:32743962C>T c.11572C>T c.(11572-11574)Ctt>Ttt p.L3858F BLCA 2 32743965 32743965 + Missense_Mutation SNP C C T TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr2:32743965C>T c.11575C>T c.(11575-11577)Cat>Tat p.H3859Y BLCA 2 32743998 32743998 + Missense_Mutation SNP C C G TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr2:32743998C>G c.11608C>G c.(11608-11610)Ctt>Gtt p.L3870V BLCA 2 32750012 32750012 + Missense_Mutation SNP A A C TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr2:32750012A>C c.11681A>C c.(11680-11682)aAa>aCa p.K3894T BLCA 2 32754759 32754759 + Missense_Mutation SNP A A G TCGA-K4-A6FZ-01A-11D-A31L-08 TCGA-K4-A6FZ-10A-01D-A31J-08 g.chr2:32754759A>G c.11962A>G c.(11962-11964)Act>Gct p.T3988A BLCA 2 32768338 32768338 + Missense_Mutation SNP C C G TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr2:32768338C>G c.12322C>G c.(12322-12324)Cag>Gag p.Q4108E BLCA 2 32768541 32768541 + Silent SNP G G A TCGA-XF-A9SL-01A-11D-A391-08 TCGA-XF-A9SL-10A-01D-A394-08 g.chr2:32768541G>A c.12525G>A c.(12523-12525)ctG>ctA p.L4175L BLCA 2 32770731 32770731 + Missense_Mutation SNP C C T TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr2:32770731C>T c.12614C>T c.(12613-12615)tCa>tTa p.S4205L BLCA 2 32770833 32770833 + Missense_Mutation SNP T T C TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr2:32770833T>C c.12716T>C c.(12715-12717)tTg>tCg p.L4239S BLCA 2 32800276 32800276 + Missense_Mutation SNP C C T TCGA-4Z-AA7Y-01A-11D-A391-08 TCGA-4Z-AA7Y-10A-01D-A394-08 g.chr2:32800276C>T c.13198C>T c.(13198-13200)Cgg>Tgg p.R4400W BLCA 2 32800360 32800360 + Missense_Mutation SNP G G C TCGA-4Z-AA86-01A-11D-A391-08 TCGA-4Z-AA86-10A-01D-A394-08 g.chr2:32800360G>C c.13282G>C c.(13282-13284)Gaa>Caa p.E4428Q BLCA 2 32819082 32819082 + Missense_Mutation SNP G G C TCGA-E7-A7PW-01A-11D-A34U-08 TCGA-E7-A7PW-10A-01D-A34X-08 g.chr2:32819082G>C c.13456G>C c.(13456-13458)Gag>Cag p.E4486Q BLCA 2 32822962 32822962 + Missense_Mutation SNP C C T TCGA-YF-AA3M-01A-11D-A42E-08 TCGA-YF-AA3M-10D-01D-A42H-08 g.chr2:32822962C>T c.13757C>T c.(13756-13758)tCa>tTa p.S4586L BLCA 2 32822980 32822980 + Missense_Mutation SNP C C T TCGA-FD-A6TD-01A-51D-A339-08 TCGA-FD-A6TD-10A-21D-A339-08 g.chr2:32822980C>T c.13775C>T c.(13774-13776)tCt>tTt p.S4592F BLCA 2 32822983 32822983 + Missense_Mutation SNP C C T TCGA-FD-A6TD-01A-51D-A339-08 TCGA-FD-A6TD-10A-21D-A339-08 g.chr2:32822983C>T c.13778C>T c.(13777-13779)tCa>tTa p.S4593L BLCA 2 32824809 32824809 + Missense_Mutation SNP C C G TCGA-YF-AA3M-01A-11D-A42E-08 TCGA-YF-AA3M-10D-01D-A42H-08 g.chr2:32824809C>G c.13834C>G c.(13834-13836)Cta>Gta p.L4612V BLCA 2 32824875 32824875 + Missense_Mutation SNP C C G TCGA-FD-A6TD-01A-51D-A339-08 TCGA-FD-A6TD-10A-21D-A339-08 g.chr2:32824875C>G c.13900C>G c.(13900-13902)Caa>Gaa p.Q4634E BLCA 2 32828145 32828145 + Missense_Mutation SNP T T A TCGA-UY-A8OB-01A-12D-A42E-08 TCGA-UY-A8OB-11A-12D-A42H-08 g.chr2:32828145T>A c.14065T>A c.(14065-14067)Ttg>Atg p.L4689M BLCA 2 32832544 32832544 + Missense_Mutation SNP T T G TCGA-XF-A9T3-01A-11D-A42E-08 TCGA-XF-A9T3-10A-01D-A42H-08 g.chr2:32832544T>G c.14093T>G c.(14092-14094)cTt>cGt p.L4698R BLCA 2 32832589 32832589 + Missense_Mutation SNP G G T TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr2:32832589G>T c.14138G>T c.(14137-14139)cGg>cTg p.R4713L BLCA 2 32832589 32832589 + Missense_Mutation SNP G G T TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr2:32832589G>T c.14138G>T c.(14137-14139)cGg>cTg p.R4713L BLCA 2 32832645 32832645 + Nonsense_Mutation SNP C C T TCGA-BT-A3PJ-01A-21D-A21Z-08 TCGA-BT-A3PJ-10A-01D-A21Z-08 g.chr2:32832645C>T c.14194C>T c.(14194-14196)Cga>Tga p.R4732* BLCA 2 32832677 32832677 + Silent SNP A A G TCGA-FD-A5BZ-01A-11D-A289-08 TCGA-FD-A5BZ-10A-01D-A289-08 g.chr2:32832677A>G c.14226A>G c.(14224-14226)gaA>gaG p.E4742E BLCA 2 32842861 32842861 + Missense_Mutation SNP G G A TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr2:32842861G>A c.14464G>A c.(14464-14466)Gac>Aac p.D4822N BLCA 2 32842873 32842873 + Nonsense_Mutation SNP G G T TCGA-FD-A5BT-01A-11D-A26M-08 TCGA-FD-A5BT-10A-01D-A26K-08 g.chr2:32842873G>T c.14476G>T c.(14476-14478)Gag>Tag p.E4826* BRCA 2 32602710 32602710 + Missense_Mutation SNP T T C TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr2:32602710T>C c.380T>C c.(379-381)aTa>aCa p.I127T BRCA 2 32631603 32631603 + Silent SNP T T C TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr2:32631603T>C c.1455T>C c.(1453-1455)caT>caC p.H485H BRCA 2 32640645 32640645 + Silent SNP A A G TCGA-B6-A0IJ-01A-11W-A050-09 TCGA-B6-A0IJ-10A-01W-A055-09 g.chr2:32640645A>G c.2286A>G c.(2284-2286)caA>caG p.Q762Q BRCA 2 32640653 32640653 + Missense_Mutation SNP C C A TCGA-A8-A07R-01A-21W-A050-09 TCGA-A8-A07R-10B-01D-A047-09 g.chr2:32640653C>A c.2294C>A c.(2293-2295)gCc>gAc p.A765D BRCA 2 32640667 32640669 + In_Frame_Del DEL AAT AAT - TCGA-BH-A1FJ-01A-11D-A13L-09 TCGA-BH-A1FJ-11B-42D-A188-09 g.chr2:32640667_32640669delAAT c.2308_2310delAAT c.(2308-2310)aatdel p.N770del BRCA 2 32654312 32654312 + Missense_Mutation SNP T T C TCGA-AR-A256-01A-11D-A167-09 TCGA-AR-A256-10A-01D-A167-09 g.chr2:32654312T>C c.2971T>C c.(2971-2973)Tct>Cct p.S991P BRCA 2 32656007 32656007 + Missense_Mutation SNP A A G TCGA-AR-A24H-01A-11D-A167-09 TCGA-AR-A24H-10A-01D-A167-09 g.chr2:32656007A>G c.3097A>G c.(3097-3099)Act>Gct p.T1033A BRCA 2 32673930 32673930 + Frame_Shift_Del DEL A A - TCGA-BH-A0EE-01A-11W-A050-09 TCGA-BH-A0EE-10A-01W-A055-09 g.chr2:32673930delA c.4552delA c.(4552-4554)aaafs p.K1518fs BRCA 2 32688310 32688310 + Missense_Mutation SNP C C T TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr2:32688310C>T c.4802C>T c.(4801-4803)aCa>aTa p.T1601I BRCA 2 32694469 32694469 + Missense_Mutation SNP C C T TCGA-AR-A2LE-01A-11D-A17W-09 TCGA-AR-A2LE-10A-01D-A17W-09 g.chr2:32694469C>T c.6134C>T c.(6133-6135)tCt>tTt p.S2045F BRCA 2 32698261 32698261 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr2:32698261G>T c.6674G>T c.(6673-6675)aGa>aTa p.R2225I BRCA 2 32702619 32702619 + Missense_Mutation SNP T T A TCGA-AO-A0J5-01A-11W-A050-09 TCGA-AO-A0J5-10A-01W-A055-09 g.chr2:32702619T>A c.7036T>A c.(7036-7038)Tgt>Agt p.C2346S BRCA 2 32718729 32718729 + Silent SNP T T A TCGA-PE-A5DD-01A-12D-A27P-09 TCGA-PE-A5DD-10A-01D-A27P-09 g.chr2:32718729T>A c.8463T>A c.(8461-8463)acT>acA p.T2821T BRCA 2 32738164 32738164 + Missense_Mutation SNP G G A TCGA-A2-A0D0-01A-11W-A019-09 TCGA-A2-A0D0-10A-01W-A021-09 g.chr2:32738164G>A c.10511G>A c.(10510-10512)aGt>aAt p.S3504N BRCA 2 32740628 32740628 + Missense_Mutation SNP G G A TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr2:32740628G>A c.11140G>A c.(11140-11142)Gca>Aca p.A3714T BRCA 2 32743984 32743984 + Missense_Mutation SNP C C T TCGA-D8-A1JL-01A-11D-A13L-09 TCGA-D8-A1JL-10A-01D-A188-09 g.chr2:32743984C>T c.11594C>T c.(11593-11595)aCa>aTa p.T3865I BRCA 2 32768600 32768600 + Missense_Mutation SNP G G T TCGA-AR-A2LE-01A-11D-A17W-09 TCGA-AR-A2LE-10A-01D-A17W-09 g.chr2:32768600G>T c.12584G>T c.(12583-12585)gGa>gTa p.G4195V BRCA 2 32770731 32770731 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr2:32770731C>T c.12614C>T c.(12613-12615)tCa>tTa p.S4205L BRCA 2 32770872 32770872 + Missense_Mutation SNP C C T TCGA-AR-A0TX-01A-11D-A099-09 TCGA-AR-A0TX-10A-01D-A099-09 g.chr2:32770872C>T c.12755C>T c.(12754-12756)tCt>tTt p.S4252F BRCA 2 32774504 32774504 + Missense_Mutation SNP C C T TCGA-E2-A574-01A-11D-A29N-09 TCGA-E2-A574-10A-01D-A29N-09 g.chr2:32774504C>T c.13100C>T c.(13099-13101)tCc>tTc p.S4367F BRCA 2 32800342 32800342 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr2:32800342G>A c.13264G>A c.(13264-13266)Gag>Aag p.E4422K BRCA 2 32822992 32822992 + Missense_Mutation SNP G G T TCGA-A7-A13F-01A-11D-A12Q-09 TCGA-A7-A13F-10A-01D-A12Q-09 g.chr2:32822992G>T c.13787G>T c.(13786-13788)aGt>aTt p.S4596I BRCA 2 32824821 32824821 + Missense_Mutation SNP C C A TCGA-A8-A097-01A-11W-A050-09 TCGA-A8-A097-10A-01D-A047-09 g.chr2:32824821C>A c.13846C>A c.(13846-13848)Cca>Aca p.P4616T BRCA 2 32824940 32824940 + Silent SNP C C T TCGA-C8-A1HE-01A-11D-A188-09 TCGA-C8-A1HE-10A-01D-A13O-09 g.chr2:32824940C>T c.13965C>T c.(13963-13965)ttC>ttT p.F4655F BRCA 2 32832625 32832625 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr2:32832625G>A c.14174G>A c.(14173-14175)cGa>cAa p.R4725Q BRCA 2 32836514 32836514 + Splice_Site SNP G G T TCGA-A8-A081-01A-11W-A019-09 TCGA-A8-A081-10A-01W-A021-09 g.chr2:32836514G>T c.e73-1 BRCA 2 32836564 32836564 + Missense_Mutation SNP G G A TCGA-AN-A0XW-01A-11D-A10G-09 TCGA-AN-A0XW-10A-01D-A10G-09 g.chr2:32836564G>A c.14309G>A c.(14308-14310)tGt>tAt p.C4770Y CESC 2 32605237 32605237 + Missense_Mutation SNP C C T TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr2:32605237C>T c.524C>T c.(523-525)tCa>tTa p.S175L CESC 2 32605301 32605301 + Silent SNP C C G TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr2:32605301C>G c.588C>G c.(586-588)ctC>ctG p.L196L CESC 2 32640932 32640932 + Missense_Mutation SNP C C T TCGA-C5-A7CL-01A-11D-A32I-09 TCGA-C5-A7CL-10A-01D-A32I-09 g.chr2:32640932C>T c.2573C>T c.(2572-2574)tCg>tTg p.S858L CESC 2 32666475 32666475 + Missense_Mutation SNP C C G TCGA-C5-A1MP-01A-11D-A14W-08 TCGA-C5-A1MP-10A-01D-A14W-08 g.chr2:32666475C>G c.3889C>G c.(3889-3891)Caa>Gaa p.Q1297E CESC 2 32678919 32678919 + Silent SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr2:32678919C>T c.4662C>T c.(4660-4662)ttC>ttT p.F1554F CESC 2 32693008 32693008 + Missense_Mutation SNP G G A TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr2:32693008G>A c.5609G>A c.(5608-5610)aGa>aAa p.R1870K CESC 2 32694554 32694554 + Missense_Mutation SNP G G T TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr2:32694554G>T c.6219G>T c.(6217-6219)aaG>aaT p.K2073N CESC 2 32716581 32716581 + Missense_Mutation SNP C C T TCGA-C5-A2LZ-01A-11D-A20U-09 TCGA-C5-A2LZ-10B-01D-A20U-09 g.chr2:32716581C>T c.8296C>T c.(8296-8298)Ctt>Ttt p.L2766F CESC 2 32740651 32740651 + Missense_Mutation SNP C C G TCGA-C5-A7CG-01A-11D-A32I-09 TCGA-C5-A7CG-10A-01D-A32I-09 g.chr2:32740651C>G c.11163C>G c.(11161-11163)caC>caG p.H3721Q CESC 2 32743990 32743990 + Missense_Mutation SNP C C T TCGA-EK-A2RA-01A-11D-A18J-09 TCGA-EK-A2RA-10A-01D-A18J-09 g.chr2:32743990C>T c.11600C>T c.(11599-11601)tCa>tTa p.S3867L CESC 2 32772925 32772925 + Silent SNP G G T TCGA-Q1-A73P-01A-11D-A32I-09 TCGA-Q1-A73P-10B-01D-A32I-09 g.chr2:32772925G>T c.12819G>T c.(12817-12819)gtG>gtT p.V4273V CHOL 2 32613960 32613960 + Missense_Mutation SNP T T C TCGA-ZH-A8Y1-01A-11D-A417-09 TCGA-ZH-A8Y1-10A-01D-A41A-09 g.chr2:32613960T>C c.788T>C c.(787-789)tTa>tCa p.L263S CHOL 2 32631613 32631613 + Missense_Mutation SNP G G T TCGA-W5-AA2U-01A-11D-A417-09 TCGA-W5-AA2U-10A-01D-A41A-09 g.chr2:32631613G>T c.1465G>T c.(1465-1467)Gat>Tat p.D489Y CHOL 2 32667184 32667184 + Silent SNP T T C TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr2:32667184T>C c.3996T>C c.(3994-3996)gtT>gtC p.V1332V CHOL 2 32678936 32678936 + Missense_Mutation SNP T T G TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr2:32678936T>G c.4679T>G c.(4678-4680)cTt>cGt p.L1560R CHOL 2 32724972 32724972 + Missense_Mutation SNP A A G TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr2:32724972A>G c.8827A>G c.(8827-8829)Aga>Gga p.R2943G CHOL 2 32725169 32725169 + Missense_Mutation SNP G G T TCGA-YR-A95A-01A-12D-A417-09 TCGA-YR-A95A-10A-01D-A41A-09 g.chr2:32725169G>T c.9024G>T c.(9022-9024)atG>atT p.M3008I CHOL 2 32774511 32774511 + Silent SNP C C T TCGA-ZH-A8Y8-01A-51D-A417-09 TCGA-ZH-A8Y8-10A-01D-A41A-09 g.chr2:32774511C>T c.13107C>T c.(13105-13107)ctC>ctT p.L4369L COAD 2 32605222 32605222 + Splice_Site SNP C C G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr2:32605222C>G c.509C>G c.(508-510)gCa>gGa p.A170G COAD 2 32605255 32605255 + Missense_Mutation SNP T T C TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr2:32605255T>C c.542T>C c.(541-543)gTa>gCa p.V181A COAD 2 32605312 32605313 + Frame_Shift_Ins INS - - A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr2:32605312_32605313insA c.599_600insA c.(598-603)ttaaaafs p.LK200fs COAD 2 32605320 32605320 + Missense_Mutation SNP A A C TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr2:32605320A>C c.607A>C c.(607-609)Aca>Cca p.T203P COAD 2 32605322 32605322 + Silent SNP A A T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr2:32605322A>T c.609A>T c.(607-609)acA>acT p.T203T COAD 2 32626307 32626307 + Missense_Mutation SNP A A G TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr2:32626307A>G c.1111A>G c.(1111-1113)Act>Gct p.T371A COAD 2 32626447 32626448 + Frame_Shift_Ins INS - - A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr2:32626447_32626448insA c.1251_1252insA c.(1252-1254)atgfs p.M418fs COAD 2 32640419 32640419 + Missense_Mutation SNP A A G TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr2:32640419A>G c.2060A>G c.(2059-2061)tAc>tGc p.Y687C COAD 2 32640420 32640420 + Silent SNP C C T TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chr2:32640420C>T c.2061C>T c.(2059-2061)taC>taT p.Y687Y COAD 2 32640462 32640462 + Silent SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr2:32640462G>A c.2103G>A c.(2101-2103)ccG>ccA p.P701P COAD 2 32640529 32640529 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr2:32640529A>C c.2170A>C c.(2170-2172)Aag>Cag p.K724Q COAD 2 32640719 32640719 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr2:32640719A>C c.2360A>C c.(2359-2361)aAt>aCt p.N787T COAD 2 32641017 32641017 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr2:32641017G>T c.2658G>T c.(2656-2658)aaG>aaT p.K886N COAD 2 32654308 32654308 + Silent SNP A A G TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr2:32654308A>G c.2967A>G c.(2965-2967)gaA>gaG p.E989E COAD 2 32658781 32658781 + Silent SNP C C T TCGA-AA-3930-01A-01W-0995-10 TCGA-AA-3930-10A-01W-0995-10 g.chr2:32658781C>T c.3318C>T c.(3316-3318)ttC>ttT p.F1106F COAD 2 32658810 32658810 + Missense_Mutation SNP A A C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32658810A>C c.3347A>C c.(3346-3348)aAt>aCt p.N1116T COAD 2 32661226 32661226 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr2:32661226C>T c.3605C>T c.(3604-3606)aCg>aTg p.T1202M COAD 2 32666440 32666440 + Missense_Mutation SNP G G A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr2:32666440G>A c.3854G>A c.(3853-3855)cGt>cAt p.R1285H COAD 2 32667199 32667199 + Frame_Shift_Del DEL A A - TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr2:32667199delA c.4011delA c.(4009-4011)agafs p.R1337fs COAD 2 32667239 32667239 + Missense_Mutation SNP C C A TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr2:32667239C>A c.4051C>A c.(4051-4053)Ctt>Att p.L1351I COAD 2 32667499 32667499 + Frame_Shift_Del DEL C C - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr2:32667499delC c.4214delC c.(4213-4215)gccfs p.A1405fs COAD 2 32673990 32673990 + Missense_Mutation SNP C C A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr2:32673990C>A c.4612C>A c.(4612-4614)Ctt>Att p.L1538I COAD 2 32688326 32688326 + Silent SNP G G A TCGA-CM-6170-01A-11D-1650-10 TCGA-CM-6170-10A-01D-1650-10 g.chr2:32688326G>A c.4818G>A c.(4816-4818)tcG>tcA p.S1606S COAD 2 32688351 32688351 + Missense_Mutation SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr2:32688351G>A c.4843G>A c.(4843-4845)Gta>Ata p.V1615I COAD 2 32688377 32688377 + Silent SNP A A G TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr2:32688377A>G c.4869A>G c.(4867-4869)gcA>gcG p.A1623A COAD 2 32689661 32689661 + Missense_Mutation SNP G G A TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr2:32689661G>A c.5026G>A c.(5026-5028)Gtg>Atg p.V1676M COAD 2 32689781 32689781 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32689781G>A c.5146G>A c.(5146-5148)Gtt>Att p.V1716I COAD 2 32689791 32689791 + Missense_Mutation SNP T T C TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr2:32689791T>C c.5156T>C c.(5155-5157)gTg>gCg p.V1719A COAD 2 32689838 32689838 + Frame_Shift_Del DEL C C - TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr2:32689838delC c.5203delC c.(5203-5205)cccfs p.P1736fs COAD 2 32692602 32692602 + Missense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32692602G>T c.5366G>T c.(5365-5367)aGa>aTa p.R1789I COAD 2 32693058 32693058 + Missense_Mutation SNP T T C TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr2:32693058T>C c.5659T>C c.(5659-5661)Tgg>Cgg p.W1887R COAD 2 32694521 32694521 + Silent SNP C C G TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr2:32694521C>G c.6186C>G c.(6184-6186)ctC>ctG p.L2062L COAD 2 32695268 32695268 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr2:32695268G>T c.6380G>T c.(6379-6381)aGa>aTa p.R2127I COAD 2 32696194 32696194 + Splice_Site SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr2:32696194T>G c.e32+2 COAD 2 32702482 32702482 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr2:32702482G>A c.6899G>A c.(6898-6900)cGt>cAt p.R2300H COAD 2 32703729 32703729 + Silent SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32703729G>A c.7095G>A c.(7093-7095)acG>acA p.T2365T COAD 2 32703801 32703801 + Silent SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr2:32703801A>G c.7167A>G c.(7165-7167)ggA>ggG p.G2389G COAD 2 32707542 32707542 + Missense_Mutation SNP A A T TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr2:32707542A>T c.7588A>T c.(7588-7590)Acc>Tcc p.T2530S COAD 2 32710802 32710802 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr2:32710802G>A c.7789G>A c.(7789-7791)Gca>Aca p.A2597T COAD 2 32724803 32724803 + Silent SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr2:32724803C>T c.8658C>T c.(8656-8658)tcC>tcT p.S2886S COAD 2 32724879 32724879 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32724879G>A c.8734G>A c.(8734-8736)Gaa>Aaa p.E2912K COAD 2 32725167 32725167 + Missense_Mutation SNP A A G TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr2:32725167A>G c.9022A>G c.(9022-9024)Atg>Gtg p.M3008V COAD 2 32725168 32725168 + Missense_Mutation SNP T T C TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr2:32725168T>C c.9023T>C c.(9022-9024)aTg>aCg p.M3008T COAD 2 32725168 32725168 + Missense_Mutation SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr2:32725168T>C c.9023T>C c.(9022-9024)aTg>aCg p.M3008T COAD 2 32726904 32726904 + Missense_Mutation SNP G G T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr2:32726904G>T c.9156G>T c.(9154-9156)atG>atT p.M3052I COAD 2 32733144 32733144 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr2:32733144A>C c.9798A>C c.(9796-9798)aaA>aaC p.K3266N COAD 2 32733149 32733149 + Missense_Mutation SNP A A G TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr2:32733149A>G c.9803A>G c.(9802-9804)cAg>cGg p.Q3268R COAD 2 32740194 32740194 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr2:32740194C>A c.10706C>A c.(10705-10707)cCt>cAt p.P3569H COAD 2 32740213 32740213 + Silent SNP T T C TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr2:32740213T>C c.10725T>C c.(10723-10725)caT>caC p.H3575H COAD 2 32740238 32740238 + Frame_Shift_Del DEL A A - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr2:32740238delA c.10750delA c.(10750-10752)aaafs p.K3585fs COAD 2 32740574 32740574 + Missense_Mutation SNP A A G TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr2:32740574A>G c.11086A>G c.(11086-11088)Agc>Ggc p.S3696G COAD 2 32743444 32743444 + Missense_Mutation SNP T T C TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr2:32743444T>C c.11473T>C c.(11473-11475)Ttt>Ctt p.F3825L COAD 2 32750663 32750663 + Missense_Mutation SNP C C A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr2:32750663C>A c.11888C>A c.(11887-11889)cCa>cAa p.P3963Q COAD 2 32754748 32754748 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr2:32754748C>T c.11951C>T c.(11950-11952)gCc>gTc p.A3984V COAD 2 32754832 32754832 + Missense_Mutation SNP T T C TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr2:32754832T>C c.12035T>C c.(12034-12036)gTt>gCt p.V4012A COAD 2 32754865 32754865 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr2:32754865C>A c.12068C>A c.(12067-12069)tCt>tAt p.S4023Y COAD 2 32756604 32756604 + Nonsense_Mutation SNP G G T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr2:32756604G>T c.12277G>T c.(12277-12279)Gaa>Taa p.E4093* COAD 2 32770876 32770876 + Silent SNP T T C TCGA-CM-5863-01A-21D-1835-10 TCGA-CM-5863-10A-01D-1835-10 g.chr2:32770876T>C c.12759T>C c.(12757-12759)gcT>gcC p.A4253A COAD 2 32800226 32800226 + Missense_Mutation SNP T T C TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr2:32800226T>C c.13148T>C c.(13147-13149)cTg>cCg p.L4383P COAD 2 32800258 32800258 + Missense_Mutation SNP G G T TCGA-F4-6808-01A-11D-1835-10 TCGA-F4-6808-10A-01D-1835-10 g.chr2:32800258G>T c.13180G>T c.(13180-13182)Gca>Tca p.A4394S COAD 2 32800267 32800267 + Missense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr2:32800267G>A c.13189G>A c.(13189-13191)Gaa>Aaa p.E4397K COAD 2 32800304 32800304 + Missense_Mutation SNP T T C TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr2:32800304T>C c.13226T>C c.(13225-13227)gTg>gCg p.V4409A COAD 2 32800401 32800401 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr2:32800401G>T c.13323G>T c.(13321-13323)aaG>aaT p.K4441N COAD 2 32800427 32800427 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr2:32800427G>A c.13349G>A c.(13348-13350)cGt>cAt p.R4450H COAD 2 32820106 32820106 + Nonsense_Mutation SNP A A T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr2:32820106A>T c.13507A>T c.(13507-13509)Aaa>Taa p.K4503* COAD 2 32820108 32820108 + Silent SNP A A G TCGA-A6-6649-01A-11D-1771-10 TCGA-A6-6649-10A-01D-1771-10 g.chr2:32820108A>G c.13509A>G c.(13507-13509)aaA>aaG p.K4503K COAD 2 32820108 32820108 + Silent SNP A A G TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr2:32820108A>G c.13509A>G c.(13507-13509)aaA>aaG p.K4503K COAD 2 32820108 32820108 + Silent SNP A A G TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr2:32820108A>G c.13509A>G c.(13507-13509)aaA>aaG p.K4503K COAD 2 32820108 32820108 + Silent SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr2:32820108A>G c.13509A>G c.(13507-13509)aaA>aaG p.K4503K COAD 2 32820108 32820108 + Silent SNP A A G TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr2:32820108A>G c.13509A>G c.(13507-13509)aaA>aaG p.K4503K COAD 2 32824826 32824826 + Silent SNP G G T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr2:32824826G>T c.13851G>T c.(13849-13851)gcG>gcT p.A4617A COAD 2 32832625 32832625 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr2:32832625G>A c.14174G>A c.(14173-14175)cGa>cAa p.R4725Q COAD 2 32842945 32842945 + Nonsense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr2:32842945G>T c.14548G>T c.(14548-14550)Gaa>Taa p.E4850* COAD 2 32842945 32842945 + Nonsense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr2:32842945G>T c.14548G>T c.(14548-14550)Gaa>Taa p.E4850* COAD 2 32842945 32842945 + Nonsense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32842945G>T c.14548G>T c.(14548-14550)Gaa>Taa p.E4850* COADREAD 2 32605222 32605222 + Splice_Site SNP C C G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr2:32605222C>G c.509C>G c.(508-510)gCa>gGa p.A170G COADREAD 2 32605255 32605255 + Missense_Mutation SNP T T C TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr2:32605255T>C c.542T>C c.(541-543)gTa>gCa p.V181A COADREAD 2 32605312 32605313 + Frame_Shift_Ins INS - - A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr2:32605312_32605313insA c.599_600insA c.(598-603)ttaaaafs p.LK200fs COADREAD 2 32605320 32605320 + Missense_Mutation SNP A A C TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr2:32605320A>C c.607A>C c.(607-609)Aca>Cca p.T203P COADREAD 2 32605322 32605322 + Silent SNP A A T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr2:32605322A>T c.609A>T c.(607-609)acA>acT p.T203T COADREAD 2 32626307 32626307 + Missense_Mutation SNP A A G TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr2:32626307A>G c.1111A>G c.(1111-1113)Act>Gct p.T371A COADREAD 2 32626447 32626448 + Frame_Shift_Ins INS - - A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr2:32626447_32626448insA c.1251_1252insA c.(1252-1254)atgfs p.M418fs COADREAD 2 32640364 32640364 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr2:32640364G>T c.2005G>T c.(2005-2007)Gaa>Taa p.E669* COADREAD 2 32640419 32640419 + Missense_Mutation SNP A A G TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr2:32640419A>G c.2060A>G c.(2059-2061)tAc>tGc p.Y687C COADREAD 2 32640420 32640420 + Silent SNP C C T TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chr2:32640420C>T c.2061C>T c.(2059-2061)taC>taT p.Y687Y COADREAD 2 32640462 32640462 + Silent SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr2:32640462G>A c.2103G>A c.(2101-2103)ccG>ccA p.P701P COADREAD 2 32640529 32640529 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr2:32640529A>C c.2170A>C c.(2170-2172)Aag>Cag p.K724Q COADREAD 2 32640719 32640719 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr2:32640719A>C c.2360A>C c.(2359-2361)aAt>aCt p.N787T COADREAD 2 32641017 32641017 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr2:32641017G>T c.2658G>T c.(2656-2658)aaG>aaT p.K886N COADREAD 2 32654233 32654233 + Silent SNP C C T TCGA-AF-2693-01A-02D-1733-10 TCGA-AF-2693-10A-01D-1733-10 g.chr2:32654233C>T c.2892C>T c.(2890-2892)ctC>ctT p.L964L COADREAD 2 32654308 32654308 + Silent SNP A A G TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr2:32654308A>G c.2967A>G c.(2965-2967)gaA>gaG p.E989E COADREAD 2 32658781 32658781 + Silent SNP C C T TCGA-AA-3930-01A-01W-0995-10 TCGA-AA-3930-10A-01W-0995-10 g.chr2:32658781C>T c.3318C>T c.(3316-3318)ttC>ttT p.F1106F COADREAD 2 32658810 32658810 + Missense_Mutation SNP A A C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32658810A>C c.3347A>C c.(3346-3348)aAt>aCt p.N1116T COADREAD 2 32661226 32661226 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr2:32661226C>T c.3605C>T c.(3604-3606)aCg>aTg p.T1202M COADREAD 2 32666440 32666440 + Missense_Mutation SNP G G A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr2:32666440G>A c.3854G>A c.(3853-3855)cGt>cAt p.R1285H COADREAD 2 32667199 32667199 + Frame_Shift_Del DEL A A - TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr2:32667199delA c.4011delA c.(4009-4011)agafs p.R1337fs COADREAD 2 32667239 32667239 + Missense_Mutation SNP C C A TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr2:32667239C>A c.4051C>A c.(4051-4053)Ctt>Att p.L1351I COADREAD 2 32667430 32667430 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr2:32667430G>A c.4145G>A c.(4144-4146)cGa>cAa p.R1382Q COADREAD 2 32667499 32667499 + Frame_Shift_Del DEL C C - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr2:32667499delC c.4214delC c.(4213-4215)gccfs p.A1405fs COADREAD 2 32673990 32673990 + Missense_Mutation SNP C C A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr2:32673990C>A c.4612C>A c.(4612-4614)Ctt>Att p.L1538I COADREAD 2 32688326 32688326 + Silent SNP G G A TCGA-CM-6170-01A-11D-1650-10 TCGA-CM-6170-10A-01D-1650-10 g.chr2:32688326G>A c.4818G>A c.(4816-4818)tcG>tcA p.S1606S COADREAD 2 32688351 32688351 + Missense_Mutation SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr2:32688351G>A c.4843G>A c.(4843-4845)Gta>Ata p.V1615I COADREAD 2 32688377 32688377 + Silent SNP A A G TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr2:32688377A>G c.4869A>G c.(4867-4869)gcA>gcG p.A1623A COADREAD 2 32689661 32689661 + Missense_Mutation SNP G G A TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr2:32689661G>A c.5026G>A c.(5026-5028)Gtg>Atg p.V1676M COADREAD 2 32689781 32689781 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32689781G>A c.5146G>A c.(5146-5148)Gtt>Att p.V1716I COADREAD 2 32689791 32689791 + Missense_Mutation SNP T T C TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr2:32689791T>C c.5156T>C c.(5155-5157)gTg>gCg p.V1719A COADREAD 2 32689838 32689838 + Frame_Shift_Del DEL C C - TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr2:32689838delC c.5203delC c.(5203-5205)cccfs p.P1736fs COADREAD 2 32692602 32692602 + Missense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32692602G>T c.5366G>T c.(5365-5367)aGa>aTa p.R1789I COADREAD 2 32693058 32693058 + Missense_Mutation SNP T T C TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr2:32693058T>C c.5659T>C c.(5659-5661)Tgg>Cgg p.W1887R COADREAD 2 32694521 32694521 + Silent SNP C C G TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr2:32694521C>G c.6186C>G c.(6184-6186)ctC>ctG p.L2062L COADREAD 2 32695268 32695268 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr2:32695268G>T c.6380G>T c.(6379-6381)aGa>aTa p.R2127I COADREAD 2 32696194 32696194 + Splice_Site SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr2:32696194T>G c.e32+2 COADREAD 2 32702482 32702482 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr2:32702482G>A c.6899G>A c.(6898-6900)cGt>cAt p.R2300H COADREAD 2 32702499 32702499 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr2:32702499G>T c.6916G>T c.(6916-6918)Gaa>Taa p.E2306* COADREAD 2 32703729 32703729 + Silent SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32703729G>A c.7095G>A c.(7093-7095)acG>acA p.T2365T COADREAD 2 32703801 32703801 + Silent SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr2:32703801A>G c.7167A>G c.(7165-7167)ggA>ggG p.G2389G COADREAD 2 32707542 32707542 + Missense_Mutation SNP A A T TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr2:32707542A>T c.7588A>T c.(7588-7590)Acc>Tcc p.T2530S COADREAD 2 32710802 32710802 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr2:32710802G>A c.7789G>A c.(7789-7791)Gca>Aca p.A2597T COADREAD 2 32724803 32724803 + Silent SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr2:32724803C>T c.8658C>T c.(8656-8658)tcC>tcT p.S2886S COADREAD 2 32724879 32724879 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32724879G>A c.8734G>A c.(8734-8736)Gaa>Aaa p.E2912K COADREAD 2 32725167 32725167 + Missense_Mutation SNP A A G TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr2:32725167A>G c.9022A>G c.(9022-9024)Atg>Gtg p.M3008V COADREAD 2 32725168 32725168 + Missense_Mutation SNP T T C TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr2:32725168T>C c.9023T>C c.(9022-9024)aTg>aCg p.M3008T COADREAD 2 32725168 32725168 + Missense_Mutation SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr2:32725168T>C c.9023T>C c.(9022-9024)aTg>aCg p.M3008T COADREAD 2 32726811 32726811 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr2:32726811A>C c.9063A>C c.(9061-9063)gaA>gaC p.E3021D COADREAD 2 32726904 32726904 + Missense_Mutation SNP G G T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr2:32726904G>T c.9156G>T c.(9154-9156)atG>atT p.M3052I COADREAD 2 32733144 32733144 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr2:32733144A>C c.9798A>C c.(9796-9798)aaA>aaC p.K3266N COADREAD 2 32733149 32733149 + Missense_Mutation SNP A A G TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr2:32733149A>G c.9803A>G c.(9802-9804)cAg>cGg p.Q3268R COADREAD 2 32733313 32733313 + Missense_Mutation SNP G G A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr2:32733313G>A c.9967G>A c.(9967-9969)Gta>Ata p.V3323I COADREAD 2 32740194 32740194 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr2:32740194C>A c.10706C>A c.(10705-10707)cCt>cAt p.P3569H COADREAD 2 32740213 32740213 + Silent SNP T T C TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr2:32740213T>C c.10725T>C c.(10723-10725)caT>caC p.H3575H COADREAD 2 32740238 32740238 + Frame_Shift_Del DEL A A - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr2:32740238delA c.10750delA c.(10750-10752)aaafs p.K3585fs COADREAD 2 32740574 32740574 + Missense_Mutation SNP A A G TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr2:32740574A>G c.11086A>G c.(11086-11088)Agc>Ggc p.S3696G COADREAD 2 32743444 32743444 + Missense_Mutation SNP T T C TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr2:32743444T>C c.11473T>C c.(11473-11475)Ttt>Ctt p.F3825L COADREAD 2 32750029 32750029 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr2:32750029G>T c.11698G>T c.(11698-11700)Gaa>Taa p.E3900* COADREAD 2 32750663 32750663 + Missense_Mutation SNP C C A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr2:32750663C>A c.11888C>A c.(11887-11889)cCa>cAa p.P3963Q COADREAD 2 32754748 32754748 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr2:32754748C>T c.11951C>T c.(11950-11952)gCc>gTc p.A3984V COADREAD 2 32754832 32754832 + Missense_Mutation SNP T T C TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr2:32754832T>C c.12035T>C c.(12034-12036)gTt>gCt p.V4012A COADREAD 2 32754865 32754865 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr2:32754865C>A c.12068C>A c.(12067-12069)tCt>tAt p.S4023Y COADREAD 2 32756604 32756604 + Nonsense_Mutation SNP G G T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr2:32756604G>T c.12277G>T c.(12277-12279)Gaa>Taa p.E4093* COADREAD 2 32770876 32770876 + Silent SNP T T C TCGA-CM-5863-01A-21D-1835-10 TCGA-CM-5863-10A-01D-1835-10 g.chr2:32770876T>C c.12759T>C c.(12757-12759)gcT>gcC p.A4253A COADREAD 2 32770897 32770897 + Silent SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr2:32770897A>G c.12780A>G c.(12778-12780)cgA>cgG p.R4260R COADREAD 2 32800226 32800226 + Missense_Mutation SNP T T C TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr2:32800226T>C c.13148T>C c.(13147-13149)cTg>cCg p.L4383P COADREAD 2 32800258 32800258 + Missense_Mutation SNP G G T TCGA-F4-6808-01A-11D-1835-10 TCGA-F4-6808-10A-01D-1835-10 g.chr2:32800258G>T c.13180G>T c.(13180-13182)Gca>Tca p.A4394S COADREAD 2 32800267 32800267 + Missense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr2:32800267G>A c.13189G>A c.(13189-13191)Gaa>Aaa p.E4397K COADREAD 2 32800304 32800304 + Missense_Mutation SNP T T C TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr2:32800304T>C c.13226T>C c.(13225-13227)gTg>gCg p.V4409A COADREAD 2 32800401 32800401 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr2:32800401G>T c.13323G>T c.(13321-13323)aaG>aaT p.K4441N COADREAD 2 32800427 32800427 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr2:32800427G>A c.13349G>A c.(13348-13350)cGt>cAt p.R4450H COADREAD 2 32819112 32819112 + Missense_Mutation SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr2:32819112C>T c.13486C>T c.(13486-13488)Cgg>Tgg p.R4496W COADREAD 2 32820106 32820106 + Missense_Mutation SNP A A G TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr2:32820106A>G c.13507A>G c.(13507-13509)Aaa>Gaa p.K4503E COADREAD 2 32820106 32820106 + Nonsense_Mutation SNP A A T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr2:32820106A>T c.13507A>T c.(13507-13509)Aaa>Taa p.K4503* COADREAD 2 32820108 32820108 + Silent SNP A A G TCGA-A6-6649-01A-11D-1771-10 TCGA-A6-6649-10A-01D-1771-10 g.chr2:32820108A>G c.13509A>G c.(13507-13509)aaA>aaG p.K4503K COADREAD 2 32820108 32820108 + Silent SNP A A G TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr2:32820108A>G c.13509A>G c.(13507-13509)aaA>aaG p.K4503K COADREAD 2 32820108 32820108 + Silent SNP A A G TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr2:32820108A>G c.13509A>G c.(13507-13509)aaA>aaG p.K4503K COADREAD 2 32820108 32820108 + Silent SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr2:32820108A>G c.13509A>G c.(13507-13509)aaA>aaG p.K4503K COADREAD 2 32820108 32820108 + Silent SNP A A G TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr2:32820108A>G c.13509A>G c.(13507-13509)aaA>aaG p.K4503K COADREAD 2 32824826 32824826 + Silent SNP G G T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr2:32824826G>T c.13851G>T c.(13849-13851)gcG>gcT p.A4617A COADREAD 2 32832625 32832625 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr2:32832625G>A c.14174G>A c.(14173-14175)cGa>cAa p.R4725Q COADREAD 2 32842945 32842945 + Nonsense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr2:32842945G>T c.14548G>T c.(14548-14550)Gaa>Taa p.E4850* COADREAD 2 32842945 32842945 + Nonsense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr2:32842945G>T c.14548G>T c.(14548-14550)Gaa>Taa p.E4850* COADREAD 2 32842945 32842945 + Nonsense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr2:32842945G>T c.14548G>T c.(14548-14550)Gaa>Taa p.E4850* DLBC 2 32673884 32673884 + Silent SNP A A G TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr2:32673884A>G c.4506A>G c.(4504-4506)ccA>ccG p.P1502P DLBC 2 32724813 32724813 + Nonsense_Mutation SNP C C T TCGA-FA-8693-01A-11D-2397-10 TCGA-FA-8693-10A-01D-2397-10 g.chr2:32724813C>T c.8668C>T c.(8668-8670)Cga>Tga p.R2890* DLBC 2 32773075 32773075 + Silent SNP T T C TCGA-GS-A9TQ-01A-11D-A382-10 TCGA-GS-A9TQ-10A-01D-A385-10 g.chr2:32773075T>C c.12969T>C c.(12967-12969)ctT>ctC p.L4323L DLBC 2 32774473 32774473 + Missense_Mutation SNP C C T TCGA-GR-7351-01A-11D-2210-10 TCGA-GR-7351-10A-01D-2210-10 g.chr2:32774473C>T c.13069C>T c.(13069-13071)Cct>Tct p.P4357S ESCA 2 32626374 32626374 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr2:32626374C>T c.1178C>T c.(1177-1179)tCg>tTg p.S393L ESCA 2 32640137 32640137 + Missense_Mutation SNP G G A TCGA-JY-A93D-01A-11D-A387-09 TCGA-JY-A93D-10A-01D-A38A-09 g.chr2:32640137G>A c.1778G>A c.(1777-1779)gGt>gAt p.G593D ESCA 2 32640225 32640225 + Silent SNP G G T TCGA-RE-A7BO-01A-11D-A33E-09 TCGA-RE-A7BO-10A-01D-A33H-09 g.chr2:32640225G>T c.1866G>T c.(1864-1866)ctG>ctT p.L622L ESCA 2 32640482 32640482 + Missense_Mutation SNP C C T TCGA-2H-A9GQ-01A-11D-A37C-09 TCGA-2H-A9GQ-11A-11D-A37F-09 g.chr2:32640482C>T c.2123C>T c.(2122-2124)tCt>tTt p.S708F ESCA 2 32661251 32661251 + Splice_Site SNP A A T TCGA-VR-A8Q7-01A-11D-A37C-09 TCGA-VR-A8Q7-10A-01D-A37F-09 g.chr2:32661251A>T c.3630A>T c.(3628-3630)aaA>aaT p.K1210N ESCA 2 32689617 32689617 + Missense_Mutation SNP C C T TCGA-Z6-A8JD-01A-11D-A36J-09 TCGA-Z6-A8JD-10A-01D-A36M-09 g.chr2:32689617C>T c.4982C>T c.(4981-4983)gCa>gTa p.A1661V ESCA 2 32693120 32693120 + Missense_Mutation SNP G G C TCGA-2H-A9GG-01A-11D-A37C-09 TCGA-2H-A9GG-11A-11D-A37F-09 g.chr2:32693120G>C c.5721G>C c.(5719-5721)caG>caC p.Q1907H ESCA 2 32693541 32693541 + Silent SNP G G A TCGA-JY-A6F8-01A-11D-A33E-09 TCGA-JY-A6F8-10A-01D-A33H-09 g.chr2:32693541G>A c.5817G>A c.(5815-5817)ttG>ttA p.L1939L ESCA 2 32693623 32693623 + Missense_Mutation SNP G G C TCGA-Q9-A6FU-01A-11D-A31U-09 TCGA-Q9-A6FU-10A-01D-A31U-09 g.chr2:32693623G>C c.5899G>C c.(5899-5901)Gac>Cac p.D1967H ESCA 2 32695336 32695336 + Nonsense_Mutation SNP C C T TCGA-2H-A9GO-01A-11D-A37C-09 TCGA-2H-A9GO-11A-11D-A37F-09 g.chr2:32695336C>T c.6448C>T c.(6448-6450)Cag>Tag p.Q2150* ESCA 2 32735596 32735596 + Missense_Mutation SNP T T C TCGA-L5-A4OM-01A-11D-A27G-09 TCGA-L5-A4OM-11A-11D-A27G-09 g.chr2:32735596T>C c.10241T>C c.(10240-10242)tTg>tCg p.L3414S ESCA 2 32740345 32740345 + Silent SNP T T C TCGA-2H-A9GF-01A-11D-A37C-09 TCGA-2H-A9GF-11A-11D-A37F-09 g.chr2:32740345T>C c.10857T>C c.(10855-10857)tcT>tcC p.S3619S ESCA 2 32740485 32740485 + Missense_Mutation SNP G G A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr2:32740485G>A c.10997G>A c.(10996-10998)cGc>cAc p.R3666H ESCA 2 32754752 32754752 + Missense_Mutation SNP G G T TCGA-KH-A6WC-01A-11D-A33E-09 TCGA-KH-A6WC-10B-01D-A33H-09 g.chr2:32754752G>T c.11955G>T c.(11953-11955)caG>caT p.Q3985H ESCA 2 32819095 32819095 + Missense_Mutation SNP C C T TCGA-LN-A8HZ-01A-11D-A36J-09 TCGA-LN-A8HZ-10A-01D-A36M-09 g.chr2:32819095C>T c.13469C>T c.(13468-13470)gCa>gTa p.A4490V GBM 2 32695356 32695356 + Missense_Mutation SNP T T A TCGA-06-0749-01A-01W-0348-08 TCGA-06-0749-10A-01W-0348-08 g.chr2:32695356T>A c.6468T>A c.(6466-6468)caT>caA p.H2156Q GBM 2 32710744 32710744 + Silent SNP G G A TCGA-19-1790-01B-01D-1353-08 TCGA-19-1790-10B-01D-1353-08 g.chr2:32710744G>A c.7731G>A c.(7729-7731)caG>caA p.Q2577Q GBM 2 32727897 32727897 + Missense_Mutation SNP A A T TCGA-16-1048-01B-01D-1353-08 TCGA-16-1048-10A-01D-1353-08 g.chr2:32727897A>T c.9243A>T c.(9241-9243)ttA>ttT p.L3081F GBM 2 32740406 32740406 + Missense_Mutation SNP G G A TCGA-06-0142-01A-01D-1490-08 TCGA-06-0142-10A-01D-1490-08 g.chr2:32740406G>A c.10918G>A c.(10918-10920)Gct>Act p.A3640T GBM 2 32774411 32774411 + Missense_Mutation SNP G G A TCGA-16-0861-01A-01W-0424-08 TCGA-16-0861-10A-01W-0424-08 g.chr2:32774411G>A c.13007G>A c.(13006-13008)aGt>aAt p.S4336N GBMLGG 2 32613827 32613827 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:32613827G>T c.655G>T c.(655-657)Gtt>Ttt p.V219F GBMLGG 2 32688447 32688447 + Nonsense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:32688447C>T c.4939C>T c.(4939-4941)Cag>Tag p.Q1647* GBMLGG 2 32695356 32695356 + Missense_Mutation SNP T T A TCGA-06-0749-01A-01W-0348-08 TCGA-06-0749-10A-01W-0348-08 g.chr2:32695356T>A c.6468T>A c.(6466-6468)caT>caA p.H2156Q GBMLGG 2 32702460 32702460 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:32702460C>T c.6877C>T c.(6877-6879)Cgt>Tgt p.R2293C GBMLGG 2 32706407 32706407 + Frame_Shift_Del DEL T T - TCGA-HT-7608-01A-11D-2086-08 TCGA-HT-7608-10A-01D-2086-08 g.chr2:32706407delT c.7428delT c.(7426-7428)tctfs p.S2476fs GBMLGG 2 32710744 32710744 + Silent SNP G G A TCGA-19-1790-01B-01D-1353-08 TCGA-19-1790-10B-01D-1353-08 g.chr2:32710744G>A c.7731G>A c.(7729-7731)caG>caA p.Q2577Q GBMLGG 2 32724735 32724735 + Missense_Mutation SNP A A T TCGA-DB-A64O-01A-11D-A29Q-08 TCGA-DB-A64O-10A-01D-A29Q-08 g.chr2:32724735A>T c.8590A>T c.(8590-8592)Aca>Tca p.T2864S GBMLGG 2 32727897 32727897 + Missense_Mutation SNP A A T TCGA-16-1048-01B-01D-1353-08 TCGA-16-1048-10A-01D-1353-08 g.chr2:32727897A>T c.9243A>T c.(9241-9243)ttA>ttT p.L3081F GBMLGG 2 32735686 32735686 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:32735686C>A c.10331C>A c.(10330-10332)cCt>cAt p.P3444H GBMLGG 2 32740275 32740275 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:32740275C>T c.10787C>T c.(10786-10788)tCt>tTt p.S3596F GBMLGG 2 32740406 32740406 + Missense_Mutation SNP G G A TCGA-06-0142-01A-01D-1490-08 TCGA-06-0142-10A-01D-1490-08 g.chr2:32740406G>A c.10918G>A c.(10918-10920)Gct>Act p.A3640T GBMLGG 2 32774411 32774411 + Missense_Mutation SNP G G A TCGA-16-0861-01A-01W-0424-08 TCGA-16-0861-10A-01W-0424-08 g.chr2:32774411G>A c.13007G>A c.(13006-13008)aGt>aAt p.S4336N GBMLGG 2 32819095 32819095 + Missense_Mutation SNP C C T TCGA-HW-8320-01A-11D-2395-08 TCGA-HW-8320-10A-01D-2396-08 g.chr2:32819095C>T c.13469C>T c.(13468-13470)gCa>gTa p.A4490V HNSC 2 32605289 32605289 + Silent SNP C C T TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr2:32605289C>T c.576C>T c.(574-576)ttC>ttT p.F192F HNSC 2 32613839 32613839 + Missense_Mutation SNP C C T TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chr2:32613839C>T c.667C>T c.(667-669)Ctt>Ttt p.L223F HNSC 2 32626362 32626362 + Missense_Mutation SNP C C G TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr2:32626362C>G c.1166C>G c.(1165-1167)tCt>tGt p.S389C HNSC 2 32640703 32640703 + Missense_Mutation SNP G G T TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr2:32640703G>T c.2344G>T c.(2344-2346)Ggt>Tgt p.G782C HNSC 2 32640716 32640716 + Nonsense_Mutation SNP C C A TCGA-F7-A50J-01A-21D-A28R-08 TCGA-F7-A50J-10A-01D-A28U-08 g.chr2:32640716C>A c.2357C>A c.(2356-2358)tCa>tAa p.S786* HNSC 2 32640742 32640742 + Missense_Mutation SNP A A C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr2:32640742A>C c.2383A>C c.(2383-2385)Aat>Cat p.N795H HNSC 2 32641134 32641153 + Frame_Shift_Del DEL AGTGGAGCCTCCCAAAAAGG AGTGGAGCCTCCCAAAAAGG - TCGA-BA-5558-01A-01D-1512-08 TCGA-BA-5558-10A-01D-1512-08 g.chr2:32641134_32641153delAGTGGAGCCTCCCAAAAAGG c.2775_2794delAGTGGAGCCTCCCAAAAAGG c.(2773-2796)aaagtggagcctcccaaaaaggagfs p.VEPPKKE926fs HNSC 2 32664671 32664671 + Missense_Mutation SNP G G T TCGA-CN-4729-01A-01D-1434-08 TCGA-CN-4729-10A-01D-1434-08 g.chr2:32664671G>T c.3727G>T c.(3727-3729)Gta>Tta p.V1243L HNSC 2 32667175 32667175 + Silent SNP G G A TCGA-CV-7099-01A-41D-2012-08 TCGA-CV-7099-10A-01D-2013-08 g.chr2:32667175G>A c.3987G>A c.(3985-3987)gaG>gaA p.E1329E HNSC 2 32667279 32667279 + Missense_Mutation SNP C C T TCGA-CR-7371-01A-11D-2012-08 TCGA-CR-7371-10A-01D-2013-08 g.chr2:32667279C>T c.4091C>T c.(4090-4092)tCa>tTa p.S1364L HNSC 2 32688441 32688441 + Nonsense_Mutation SNP C C T TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr2:32688441C>T c.4933C>T c.(4933-4935)Cag>Tag p.Q1645* HNSC 2 32689676 32689676 + Missense_Mutation SNP G G A TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr2:32689676G>A c.5041G>A c.(5041-5043)Gtg>Atg p.V1681M HNSC 2 32689715 32689715 + Missense_Mutation SNP A A T TCGA-T2-A6WZ-01A-21D-A34J-08 TCGA-T2-A6WZ-10B-01D-A34M-08 g.chr2:32689715A>T c.5080A>T c.(5080-5082)Att>Ttt p.I1694F HNSC 2 32692772 32692772 + Missense_Mutation SNP G G A TCGA-P3-A6T5-01A-11D-A34J-08 TCGA-P3-A6T5-10A-01D-A34M-08 g.chr2:32692772G>A c.5536G>A c.(5536-5538)Gac>Aac p.D1846N HNSC 2 32701366 32701366 + Missense_Mutation SNP A A G TCGA-CN-4730-01A-01D-1434-08 TCGA-CN-4730-10A-01D-1434-08 g.chr2:32701366A>G c.6806A>G c.(6805-6807)tAt>tGt p.Y2269C HNSC 2 32715162 32715162 + Missense_Mutation SNP G G A TCGA-H7-A6C4-01A-11D-A30E-08 TCGA-H7-A6C4-10A-01D-A30H-08 g.chr2:32715162G>A c.8150G>A c.(8149-8151)cGg>cAg p.R2717Q HNSC 2 32724766 32724766 + Nonsense_Mutation SNP C C G TCGA-CV-7095-01A-21D-2012-08 TCGA-CV-7095-10A-01D-2013-08 g.chr2:32724766C>G c.8621C>G c.(8620-8622)tCa>tGa p.S2874* HNSC 2 32726872 32726872 + Missense_Mutation SNP A A G TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chr2:32726872A>G c.9124A>G c.(9124-9126)Acc>Gcc p.T3042A HNSC 2 32728184 32728184 + Missense_Mutation SNP C C T TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chr2:32728184C>T c.9380C>T c.(9379-9381)tCa>tTa p.S3127L HNSC 2 32728276 32728276 + Missense_Mutation SNP G G A TCGA-CV-6935-01A-11D-1912-08 TCGA-CV-6935-10A-01D-1912-08 g.chr2:32728276G>A c.9472G>A c.(9472-9474)Gaa>Aaa p.E3158K HNSC 2 32730182 32730182 + Nonsense_Mutation SNP G G T TCGA-CN-4738-01A-02D-1512-08 TCGA-CN-4738-10A-01D-1512-08 g.chr2:32730182G>T c.9610G>T c.(9610-9612)Gag>Tag p.E3204* HNSC 2 32733227 32733227 + Nonsense_Mutation SNP C C G TCGA-DQ-5625-01A-01D-1870-08 TCGA-DQ-5625-10A-01D-1870-08 g.chr2:32733227C>G c.9881C>G c.(9880-9882)tCa>tGa p.S3294* HNSC 2 32735635 32735635 + Missense_Mutation SNP C C A TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chr2:32735635C>A c.10280C>A c.(10279-10281)tCt>tAt p.S3427Y HNSC 2 32738125 32738127 + In_Frame_Del DEL CTT CTT - TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr2:32738125_32738127delCTT c.10472_10474delCTT c.(10471-10476)ccttct>cct p.S3492del HNSC 2 32750671 32750671 + Missense_Mutation SNP C C T TCGA-MT-A67F-01A-11D-A30E-08 TCGA-MT-A67F-10A-01D-A30H-08 g.chr2:32750671C>T c.11896C>T c.(11896-11898)Cac>Tac p.H3966Y HNSC 2 32750697 32750697 + Splice_Site SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr2:32750697T>C c.e59+2 HNSC 2 32768426 32768426 + Missense_Mutation SNP C C T TCGA-P3-A5QA-01A-11D-A28R-08 TCGA-P3-A5QA-10A-01D-A28U-08 g.chr2:32768426C>T c.12410C>T c.(12409-12411)gCg>gTg p.A4137V HNSC 2 32770763 32770763 + Missense_Mutation SNP G G T TCGA-CN-5356-01A-01D-1434-08 TCGA-CN-5356-10A-01D-1434-08 g.chr2:32770763G>T c.12646G>T c.(12646-12648)Gtc>Ttc p.V4216F HNSC 2 32773002 32773002 + Missense_Mutation SNP C C T TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chr2:32773002C>T c.12896C>T c.(12895-12897)tCt>tTt p.S4299F HNSC 2 32822887 32822887 + Missense_Mutation SNP C C T TCGA-RS-A6TO-01A-32D-A34J-08 TCGA-RS-A6TO-10A-01D-A34M-08 g.chr2:32822887C>T c.13682C>T c.(13681-13683)tCt>tTt p.S4561F HNSC 2 32824950 32824950 + Missense_Mutation SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr2:32824950C>T c.13975C>T c.(13975-13977)Ctt>Ttt p.L4659F HNSC 2 32832521 32832521 + Splice_Site SNP G G T TCGA-BA-A6DA-01A-31D-A31L-08 TCGA-BA-A6DA-10A-01D-A31J-08 g.chr2:32832521G>T c.e72-1 KICH 2 32617105 32617105 + Splice_Site SNP A A G TCGA-KM-8477-01A-11D-2310-10 TCGA-KM-8477-10A-01D-2311-10 g.chr2:32617105A>G c.e5-1 KICH 2 32641045 32641045 + Missense_Mutation SNP G G A TCGA-KN-8434-01A-11D-2310-10 TCGA-KN-8434-11A-01D-2311-10 g.chr2:32641045G>A c.2686G>A c.(2686-2688)Gac>Aac p.D896N KICH 2 32694461 32694461 + Splice_Site SNP A A G TCGA-KM-8440-01A-11D-2310-10 TCGA-KM-8440-10A-01D-2311-10 g.chr2:32694461A>G c.e30-1 KICH 2 32713733 32713733 + Missense_Mutation SNP A A G TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr2:32713733A>G c.8047A>G c.(8047-8049)Ata>Gta p.I2683V KICH 2 32718631 32718631 + Missense_Mutation SNP A A G TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr2:32718631A>G c.8365A>G c.(8365-8367)Atg>Gtg p.M2789V KIPAN 2 32605236 32605236 + Missense_Mutation SNP T T C TCGA-CZ-5465-01A-01D-1806-10 TCGA-CZ-5465-11A-01D-1501-10 g.chr2:32605236T>C c.523T>C c.(523-525)Tca>Cca p.S175P KIPAN 2 32617105 32617105 + Splice_Site SNP A A G TCGA-KM-8477-01A-11D-2310-10 TCGA-KM-8477-10A-01D-2311-10 g.chr2:32617105A>G c.e5-1 KIPAN 2 32626579 32626579 + Nonsense_Mutation SNP C C T TCGA-HE-7130-01A-11D-1961-08 TCGA-HE-7130-10A-01D-1962-08 g.chr2:32626579C>T c.1306C>T c.(1306-1308)Cag>Tag p.Q436* KIPAN 2 32631577 32631577 + Missense_Mutation SNP C C A TCGA-2Z-A9J5-01A-21D-A382-10 TCGA-2Z-A9J5-10A-01D-A385-10 g.chr2:32631577C>A c.1429C>A c.(1429-1431)Ctg>Atg p.L477M KIPAN 2 32631593 32631593 + Missense_Mutation SNP G G A TCGA-B0-5110-01A-01D-1421-08 TCGA-B0-5110-11A-01D-1421-08 g.chr2:32631593G>A c.1445G>A c.(1444-1446)aGt>aAt p.S482N KIPAN 2 32640306 32640306 + Missense_Mutation SNP G G T TCGA-SX-A7SL-01A-11D-A34Z-10 TCGA-SX-A7SL-10A-01D-A34Z-10 g.chr2:32640306G>T c.1947G>T c.(1945-1947)atG>atT p.M649I KIPAN 2 32640716 32640716 + Nonsense_Mutation SNP C C A TCGA-B0-5092-01A-01D-1421-08 TCGA-B0-5092-11A-01D-1421-08 g.chr2:32640716C>A c.2357C>A c.(2356-2358)tCa>tAa p.S786* KIPAN 2 32640925 32640925 + Missense_Mutation SNP A A G TCGA-B8-5163-01A-01D-1421-08 TCGA-B8-5163-10A-01D-1421-08 g.chr2:32640925A>G c.2566A>G c.(2566-2568)Att>Gtt p.I856V KIPAN 2 32641045 32641045 + Missense_Mutation SNP G G A TCGA-KN-8434-01A-11D-2310-10 TCGA-KN-8434-11A-01D-2311-10 g.chr2:32641045G>A c.2686G>A c.(2686-2688)Gac>Aac p.D896N KIPAN 2 32656054 32656054 + Missense_Mutation SNP A A C TCGA-BQ-5881-01A-11D-1589-08 TCGA-BQ-5881-11A-01D-1589-08 g.chr2:32656054A>C c.3144A>C c.(3142-3144)gaA>gaC p.E1048D KIPAN 2 32664671 32664671 + Missense_Mutation SNP G G T TCGA-A3-3331-01A-01W-0886-08 TCGA-A3-3331-11A-01W-0886-08 g.chr2:32664671G>T c.3727G>T c.(3727-3729)Gta>Tta p.V1243L KIPAN 2 32667276 32667276 + Missense_Mutation SNP A A C TCGA-EV-5902-01A-11D-1589-08 TCGA-EV-5902-10A-01D-1589-08 g.chr2:32667276A>C c.4088A>C c.(4087-4089)cAt>cCt p.H1363P KIPAN 2 32673959 32673959 + Silent SNP C C A TCGA-B0-5104-01A-01D-1421-08 TCGA-B0-5104-11A-01D-1421-08 g.chr2:32673959C>A c.4581C>A c.(4579-4581)gtC>gtA p.V1527V KIPAN 2 32689778 32689778 + Missense_Mutation SNP G G T TCGA-BP-5169-01A-01D-1429-08 TCGA-BP-5169-11A-01D-1429-08 g.chr2:32689778G>T c.5143G>T c.(5143-5145)Gca>Tca p.A1715S KIPAN 2 32692693 32692693 + Missense_Mutation SNP T T G TCGA-CJ-4893-01A-01D-1373-10 TCGA-CJ-4893-11A-01D-1373-10 g.chr2:32692693T>G c.5457T>G c.(5455-5457)atT>atG p.I1819M KIPAN 2 32693017 32693017 + Missense_Mutation SNP T T G TCGA-BP-4977-01A-01D-1462-08 TCGA-BP-4977-11A-01D-1462-08 g.chr2:32693017T>G c.5618T>G c.(5617-5619)aTc>aGc p.I1873S KIPAN 2 32693677 32693677 + Missense_Mutation SNP A A T TCGA-CZ-5451-01A-01D-1501-10 TCGA-CZ-5451-11A-01D-1501-10 g.chr2:32693677A>T c.5953A>T c.(5953-5955)Aat>Tat p.N1985Y KIPAN 2 32694461 32694461 + Splice_Site SNP A A G TCGA-KM-8440-01A-11D-2310-10 TCGA-KM-8440-10A-01D-2311-10 g.chr2:32694461A>G c.e30-1 KIPAN 2 32702603 32702603 + Silent SNP C C A TCGA-Y8-A8RZ-01A-11D-A36X-10 TCGA-Y8-A8RZ-10A-01D-A370-10 g.chr2:32702603C>A c.7020C>A c.(7018-7020)ctC>ctA p.L2340L KIPAN 2 32713733 32713733 + Missense_Mutation SNP A A G TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr2:32713733A>G c.8047A>G c.(8047-8049)Ata>Gta p.I2683V KIPAN 2 32718631 32718631 + Missense_Mutation SNP A A G TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr2:32718631A>G c.8365A>G c.(8365-8367)Atg>Gtg p.M2789V KIPAN 2 32740159 32740160 + Frame_Shift_Ins INS - - TC TCGA-WN-AB4C-01A-11D-A42J-10 TCGA-WN-AB4C-10A-01D-A42M-10 g.chr2:32740159_32740160insTC c.10671_10672insTC c.(10672-10674)tctfs p.S3558fs KIPAN 2 32740321 32740321 + Silent SNP T T C TCGA-2Z-A9JS-01A-21D-A42J-10 TCGA-2Z-A9JS-10A-01D-A42M-10 g.chr2:32740321T>C c.10833T>C c.(10831-10833)gcT>gcC p.A3611A KIPAN 2 32754825 32754825 + Missense_Mutation SNP T T C TCGA-IA-A83W-01A-11D-A34Z-10 TCGA-IA-A83W-11A-11D-A34Z-10 g.chr2:32754825T>C c.12028T>C c.(12028-12030)Tca>Cca p.S4010P KIPAN 2 32824826 32824826 + Silent SNP G G T TCGA-UZ-A9PU-01A-11D-A42J-10 TCGA-UZ-A9PU-10A-01D-A42M-10 g.chr2:32824826G>T c.13851G>T c.(13849-13851)gcG>gcT p.A4617A KIRC 2 32605236 32605236 + Missense_Mutation SNP T T C TCGA-CZ-5465-01A-01D-1806-10 TCGA-CZ-5465-11A-01D-1501-10 g.chr2:32605236T>C c.523T>C c.(523-525)Tca>Cca p.S175P KIRC 2 32631593 32631593 + Missense_Mutation SNP G G A TCGA-B0-5110-01A-01D-1421-08 TCGA-B0-5110-11A-01D-1421-08 g.chr2:32631593G>A c.1445G>A c.(1444-1446)aGt>aAt p.S482N KIRC 2 32640716 32640716 + Nonsense_Mutation SNP C C A TCGA-B0-5092-01A-01D-1421-08 TCGA-B0-5092-11A-01D-1421-08 g.chr2:32640716C>A c.2357C>A c.(2356-2358)tCa>tAa p.S786* KIRC 2 32640925 32640925 + Missense_Mutation SNP A A G TCGA-B8-5163-01A-01D-1421-08 TCGA-B8-5163-10A-01D-1421-08 g.chr2:32640925A>G c.2566A>G c.(2566-2568)Att>Gtt p.I856V KIRC 2 32664671 32664671 + Missense_Mutation SNP G G T TCGA-A3-3331-01A-01W-0886-08 TCGA-A3-3331-11A-01W-0886-08 g.chr2:32664671G>T c.3727G>T c.(3727-3729)Gta>Tta p.V1243L KIRC 2 32673959 32673959 + Silent SNP C C A TCGA-B0-5104-01A-01D-1421-08 TCGA-B0-5104-11A-01D-1421-08 g.chr2:32673959C>A c.4581C>A c.(4579-4581)gtC>gtA p.V1527V KIRC 2 32689778 32689778 + Missense_Mutation SNP G G T TCGA-BP-5169-01A-01D-1429-08 TCGA-BP-5169-11A-01D-1429-08 g.chr2:32689778G>T c.5143G>T c.(5143-5145)Gca>Tca p.A1715S KIRC 2 32692693 32692693 + Missense_Mutation SNP T T G TCGA-CJ-4893-01A-01D-1373-10 TCGA-CJ-4893-11A-01D-1373-10 g.chr2:32692693T>G c.5457T>G c.(5455-5457)atT>atG p.I1819M KIRC 2 32693017 32693017 + Missense_Mutation SNP T T G TCGA-BP-4977-01A-01D-1462-08 TCGA-BP-4977-11A-01D-1462-08 g.chr2:32693017T>G c.5618T>G c.(5617-5619)aTc>aGc p.I1873S KIRC 2 32693677 32693677 + Missense_Mutation SNP A A T TCGA-CZ-5451-01A-01D-1501-10 TCGA-CZ-5451-11A-01D-1501-10 g.chr2:32693677A>T c.5953A>T c.(5953-5955)Aat>Tat p.N1985Y KIRP 2 32626579 32626579 + Nonsense_Mutation SNP C C T TCGA-HE-7130-01A-11D-1961-08 TCGA-HE-7130-10A-01D-1962-08 g.chr2:32626579C>T c.1306C>T c.(1306-1308)Cag>Tag p.Q436* KIRP 2 32631577 32631577 + Missense_Mutation SNP C C A TCGA-2Z-A9J5-01A-21D-A382-10 TCGA-2Z-A9J5-10A-01D-A385-10 g.chr2:32631577C>A c.1429C>A c.(1429-1431)Ctg>Atg p.L477M KIRP 2 32640306 32640306 + Missense_Mutation SNP G G T TCGA-SX-A7SL-01A-11D-A34Z-10 TCGA-SX-A7SL-10A-01D-A34Z-10 g.chr2:32640306G>T c.1947G>T c.(1945-1947)atG>atT p.M649I KIRP 2 32656054 32656054 + Missense_Mutation SNP A A C TCGA-BQ-5881-01A-11D-1589-08 TCGA-BQ-5881-11A-01D-1589-08 g.chr2:32656054A>C c.3144A>C c.(3142-3144)gaA>gaC p.E1048D KIRP 2 32667276 32667276 + Missense_Mutation SNP A A C TCGA-EV-5902-01A-11D-1589-08 TCGA-EV-5902-10A-01D-1589-08 g.chr2:32667276A>C c.4088A>C c.(4087-4089)cAt>cCt p.H1363P KIRP 2 32702603 32702603 + Silent SNP C C A TCGA-Y8-A8RZ-01A-11D-A36X-10 TCGA-Y8-A8RZ-10A-01D-A370-10 g.chr2:32702603C>A c.7020C>A c.(7018-7020)ctC>ctA p.L2340L KIRP 2 32740159 32740160 + Frame_Shift_Ins INS - - TC TCGA-WN-AB4C-01A-11D-A42J-10 TCGA-WN-AB4C-10A-01D-A42M-10 g.chr2:32740159_32740160insTC c.10671_10672insTC c.(10672-10674)tctfs p.S3558fs KIRP 2 32740321 32740321 + Silent SNP T T C TCGA-2Z-A9JS-01A-21D-A42J-10 TCGA-2Z-A9JS-10A-01D-A42M-10 g.chr2:32740321T>C c.10833T>C c.(10831-10833)gcT>gcC p.A3611A KIRP 2 32754825 32754825 + Missense_Mutation SNP T T C TCGA-IA-A83W-01A-11D-A34Z-10 TCGA-IA-A83W-11A-11D-A34Z-10 g.chr2:32754825T>C c.12028T>C c.(12028-12030)Tca>Cca p.S4010P KIRP 2 32824826 32824826 + Silent SNP G G T TCGA-UZ-A9PU-01A-11D-A42J-10 TCGA-UZ-A9PU-10A-01D-A42M-10 g.chr2:32824826G>T c.13851G>T c.(13849-13851)gcG>gcT p.A4617A LGG 2 32613827 32613827 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:32613827G>T c.655G>T c.(655-657)Gtt>Ttt p.V219F LGG 2 32688447 32688447 + Nonsense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:32688447C>T c.4939C>T c.(4939-4941)Cag>Tag p.Q1647* LGG 2 32702460 32702460 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:32702460C>T c.6877C>T c.(6877-6879)Cgt>Tgt p.R2293C LGG 2 32706407 32706407 + Frame_Shift_Del DEL T T - TCGA-HT-7608-01A-11D-2086-08 TCGA-HT-7608-10A-01D-2086-08 g.chr2:32706407delT c.7428delT c.(7426-7428)tctfs p.S2476fs LGG 2 32724735 32724735 + Missense_Mutation SNP A A T TCGA-DB-A64O-01A-11D-A29Q-08 TCGA-DB-A64O-10A-01D-A29Q-08 g.chr2:32724735A>T c.8590A>T c.(8590-8592)Aca>Tca p.T2864S LGG 2 32735686 32735686 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:32735686C>A c.10331C>A c.(10330-10332)cCt>cAt p.P3444H LGG 2 32740275 32740275 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:32740275C>T c.10787C>T c.(10786-10788)tCt>tTt p.S3596F LGG 2 32819095 32819095 + Missense_Mutation SNP C C T TCGA-HW-8320-01A-11D-2395-08 TCGA-HW-8320-10A-01D-2396-08 g.chr2:32819095C>T c.13469C>T c.(13468-13470)gCa>gTa p.A4490V LIHC 2 32602706 32602706 + Missense_Mutation SNP G G T TCGA-DD-A1EK-01A-11D-A20W-10 TCGA-DD-A1EK-10A-01D-A20W-10 g.chr2:32602706G>T c.376G>T c.(376-378)Gtt>Ttt p.V126F LIHC 2 32613893 32613893 + Frame_Shift_Del DEL A A - TCGA-BD-A3EP-01A-11D-A22F-10 TCGA-BD-A3EP-11A-12D-A22F-10 g.chr2:32613893delA c.721delA c.(721-723)aaafs p.K241fs LIHC 2 32640007 32640007 + Nonsense_Mutation SNP G G T TCGA-CC-A3MC-01A-11D-A22F-10 TCGA-CC-A3MC-10A-01D-A22F-10 g.chr2:32640007G>T c.1648G>T c.(1648-1650)Gaa>Taa p.E550* LIHC 2 32640568 32640568 + Missense_Mutation SNP A A G TCGA-DD-A3A1-01A-11D-A20W-10 TCGA-DD-A3A1-11A-11D-A20W-10 g.chr2:32640568A>G c.2209A>G c.(2209-2211)Act>Gct p.T737A LIHC 2 32641025 32641025 + Missense_Mutation SNP T T C TCGA-ED-A7PY-01A-11D-A33Q-10 TCGA-ED-A7PY-10A-01D-A33Q-10 g.chr2:32641025T>C c.2666T>C c.(2665-2667)tTt>tCt p.F889S LIHC 2 32654298 32654298 + Missense_Mutation SNP A A C TCGA-G3-A3CK-01A-11D-A20W-10 TCGA-G3-A3CK-10A-01D-A20W-10 g.chr2:32654298A>C c.2957A>C c.(2956-2958)aAa>aCa p.K986T LIHC 2 32660588 32660588 + Missense_Mutation SNP A A G TCGA-G3-A3CG-01A-11D-A20W-10 TCGA-G3-A3CG-10A-01D-A20W-10 g.chr2:32660588A>G c.3434A>G c.(3433-3435)aAt>aGt p.N1145S LIHC 2 32661167 32661167 + Silent SNP A A T TCGA-DD-AAC8-01A-11D-A40R-10 TCGA-DD-AAC8-10A-01D-A40U-10 g.chr2:32661167A>T c.3546A>T c.(3544-3546)ctA>ctT p.L1182L LIHC 2 32678911 32678911 + Missense_Mutation SNP G G T TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr2:32678911G>T c.4654G>T c.(4654-4656)Ggt>Tgt p.G1552C LIHC 2 32689764 32689764 + Missense_Mutation SNP C C G TCGA-XR-A8TG-01A-11D-A35Z-10 TCGA-XR-A8TG-10A-01D-A35Z-10 g.chr2:32689764C>G c.5129C>G c.(5128-5130)aCt>aGt p.T1710S LIHC 2 32692803 32692803 + Missense_Mutation SNP T T C TCGA-DD-A1EC-01A-21D-A12Z-10 TCGA-DD-A1EC-11A-11D-A12Z-10 g.chr2:32692803T>C c.5567T>C c.(5566-5568)aTg>aCg p.M1856T LIHC 2 32695253 32695253 + Missense_Mutation SNP C C G TCGA-DD-AACF-01A-11D-A40R-10 TCGA-DD-AACF-10A-01D-A40U-10 g.chr2:32695253C>G c.6365C>G c.(6364-6366)tCc>tGc p.S2122C LIHC 2 32696085 32696085 + Missense_Mutation SNP T T C TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr2:32696085T>C c.6485T>C c.(6484-6486)gTa>gCa p.V2162A LIHC 2 32696135 32696135 + Silent SNP C C T TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr2:32696135C>T c.6535C>T c.(6535-6537)Ctg>Ttg p.L2179L LIHC 2 32703821 32703821 + Missense_Mutation SNP A A G TCGA-G3-AAV7-01A-11D-A382-10 TCGA-G3-AAV7-10A-01D-A385-10 g.chr2:32703821A>G c.7187A>G c.(7186-7188)gAt>gGt p.D2396G LIHC 2 32706429 32706429 + Missense_Mutation SNP G G C TCGA-RC-A6M4-01A-11D-A32G-10 TCGA-RC-A6M4-10A-01D-A32G-10 g.chr2:32706429G>C c.7450G>C c.(7450-7452)Gac>Cac p.D2484H LIHC 2 32724628 32724628 + Missense_Mutation SNP C C T TCGA-CC-A9FU-01A-11D-A36X-10 TCGA-CC-A9FU-10A-01D-A370-10 g.chr2:32724628C>T c.8483C>T c.(8482-8484)aCa>aTa p.T2828I LIHC 2 32724674 32724675 + Silent DNP TC TC AT TCGA-EP-A2KC-01A-11D-A20W-10 TCGA-EP-A2KC-10A-01D-A20W-10 g.chr2:32724674_32724675TC>AT c.8529_8530TC>AT c.(8527-8532)acTCtg>acATtg p.2843_2844TL>TL LIHC 2 32724675 32724675 + Silent SNP C C T TCGA-DD-AACJ-01A-11D-A40R-10 TCGA-DD-AACJ-10A-01D-A40U-10 g.chr2:32724675C>T c.8530C>T c.(8530-8532)Ctg>Ttg p.L2844L LIHC 2 32726807 32726807 + Missense_Mutation SNP A A C TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr2:32726807A>C c.9059A>C c.(9058-9060)cAt>cCt p.H3020P LIHC 2 32733177 32733177 + Silent SNP T T C TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr2:32733177T>C c.9831T>C c.(9829-9831)gcT>gcC p.A3277A LIHC 2 32750591 32750591 + Missense_Mutation SNP G G A TCGA-5R-AAAM-01A-12D-A40R-10 TCGA-5R-AAAM-10A-01D-A40U-10 g.chr2:32750591G>A c.11816G>A c.(11815-11817)aGg>aAg p.R3939K LIHC 2 32750644 32750644 + Missense_Mutation SNP A A C TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr2:32750644A>C c.11869A>C c.(11869-11871)Aac>Cac p.N3957H LIHC 2 32768519 32768519 + Missense_Mutation SNP C C T TCGA-RC-A6M5-01A-11D-A32G-10 TCGA-RC-A6M5-10A-01D-A32G-10 g.chr2:32768519C>T c.12503C>T c.(12502-12504)cCg>cTg p.P4168L LIHC 2 32774378 32774378 + Splice_Site SNP A A G TCGA-DD-AACE-01A-11D-A40R-10 TCGA-DD-AACE-10A-01D-A40U-10 g.chr2:32774378A>G c.e65-1 LIHC 2 32822997 32822997 + Missense_Mutation SNP T T G TCGA-2Y-A9HB-01A-11D-A38X-10 TCGA-2Y-A9HB-10A-01D-A38X-10 g.chr2:32822997T>G c.13792T>G c.(13792-13794)Ttt>Gtt p.F4598V LIHC 2 32842852 32842852 + Missense_Mutation SNP C C A TCGA-T1-A6J8-01A-11D-A32G-10 TCGA-T1-A6J8-10A-01D-A32G-10 g.chr2:32842852C>A c.14455C>A c.(14455-14457)Cct>Act p.P4819T LUAD 2 32602748 32602748 + Missense_Mutation SNP C C T TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chr2:32602748C>T c.418C>T c.(418-420)Ctt>Ttt p.L140F LUAD 2 32613848 32613848 + Missense_Mutation SNP C C T TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr2:32613848C>T c.676C>T c.(676-678)Cat>Tat p.H226Y LUAD 2 32613998 32613998 + Missense_Mutation SNP C C T TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr2:32613998C>T c.826C>T c.(826-828)Cgt>Tgt p.R276C LUAD 2 32626377 32626377 + Missense_Mutation SNP G G A TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr2:32626377G>A c.1181G>A c.(1180-1182)gGg>gAg p.G394E LUAD 2 32639984 32639984 + Missense_Mutation SNP C C T TCGA-86-8281-01A-11D-2284-08 TCGA-86-8281-10A-01D-2284-08 g.chr2:32639984C>T c.1625C>T c.(1624-1626)cCt>cTt p.P542L LUAD 2 32640172 32640172 + Missense_Mutation SNP C C G TCGA-55-A493-01A-11D-A24D-08 TCGA-55-A493-10A-01D-A24F-08 g.chr2:32640172C>G c.1813C>G c.(1813-1815)Caa>Gaa p.Q605E LUAD 2 32640261 32640261 + Missense_Mutation SNP C C G TCGA-55-7815-01A-11D-2167-08 TCGA-55-7815-10A-01D-2167-08 g.chr2:32640261C>G c.1902C>G c.(1900-1902)agC>agG p.S634R LUAD 2 32640306 32640306 + Missense_Mutation SNP G G A TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr2:32640306G>A c.1947G>A c.(1945-1947)atG>atA p.M649I LUAD 2 32640490 32640490 + Frame_Shift_Del DEL C C - TCGA-91-6829-01A-21D-1855-08 TCGA-91-6829-11A-01D-1855-08 g.chr2:32640490delC c.2131delC c.(2131-2133)cccfs p.P711fs LUAD 2 32640656 32640656 + Missense_Mutation SNP T T G TCGA-L9-A443-01A-12D-A24D-08 TCGA-L9-A443-10A-01D-A24F-08 g.chr2:32640656T>G c.2297T>G c.(2296-2298)tTg>tGg p.L766W LUAD 2 32640813 32640813 + Missense_Mutation SNP G G T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr2:32640813G>T c.2454G>T c.(2452-2454)agG>agT p.R818S LUAD 2 32640830 32640830 + Missense_Mutation SNP A A G TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr2:32640830A>G c.2471A>G c.(2470-2472)tAt>tGt p.Y824C LUAD 2 32658718 32658719 + Frame_Shift_Ins INS - - T TCGA-05-5423-01A-01D-1625-08 TCGA-05-5423-10A-01D-1625-08 g.chr2:32658718_32658719insT c.3255_3256insT c.(3256-3258)tggfs p.W1086fs LUAD 2 32658763 32658763 + Missense_Mutation SNP G G T TCGA-17-Z001-01A-01W-0746-08 TCGA-17-Z001-11A-01W-0746-08 g.chr2:32658763G>T c.3300G>T c.(3298-3300)atG>atT p.M1100I LUAD 2 32658783 32658783 + Missense_Mutation SNP A A G TCGA-93-A4JN-01A-11D-A24P-08 TCGA-93-A4JN-10A-01D-A24P-08 g.chr2:32658783A>G c.3320A>G c.(3319-3321)aAa>aGa p.K1107R LUAD 2 32664699 32664699 + Missense_Mutation SNP A A C TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr2:32664699A>C c.3755A>C c.(3754-3756)cAg>cCg p.Q1252P LUAD 2 32664726 32664726 + Nonsense_Mutation SNP C C A TCGA-71-8520-01A-11D-2393-08 TCGA-71-8520-10A-01D-2393-08 g.chr2:32664726C>A c.3782C>A c.(3781-3783)tCa>tAa p.S1261* LUAD 2 32673862 32673862 + Splice_Site SNP G G T TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr2:32673862G>T c.e22-1 LUAD 2 32673888 32673888 + Missense_Mutation SNP G G T TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr2:32673888G>T c.4510G>T c.(4510-4512)Gat>Tat p.D1504Y LUAD 2 32673983 32673983 + Silent SNP A A C TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr2:32673983A>C c.4605A>C c.(4603-4605)tcA>tcC p.S1535S LUAD 2 32673994 32673994 + Missense_Mutation SNP C C T TCGA-17-Z033-01A-01W-0746-08 TCGA-17-Z033-11A-01W-0746-08 g.chr2:32673994C>T c.4616C>T c.(4615-4617)tCa>tTa p.S1539L LUAD 2 32678889 32678889 + Silent SNP C C T TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr2:32678889C>T c.4632C>T c.(4630-4632)gtC>gtT p.V1544V LUAD 2 32678942 32678950 + In_Frame_Del DEL AAGTTGAAC AAGTTGAAC - TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr2:32678942_32678950delAAGTTGAAC c.4685_4693delAAGTTGAAC c.(4684-4695)gaagttgaacct>gct p.1562_1565EVEP>A LUAD 2 32678999 32678999 + Missense_Mutation SNP G G C TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chr2:32678999G>C c.4742G>C c.(4741-4743)aGg>aCg p.R1581T LUAD 2 32688372 32688372 + Missense_Mutation SNP C C T TCGA-49-4505-01A-01D-1931-08 TCGA-49-4505-11A-01D-1265-08 g.chr2:32688372C>T c.4864C>T c.(4864-4866)Cat>Tat p.H1622Y LUAD 2 32689617 32689617 + Missense_Mutation SNP C C T TCGA-38-4632-01A-01D-1753-08 TCGA-38-4632-11A-01D-1753-08 g.chr2:32689617C>T c.4982C>T c.(4981-4983)gCa>gTa p.A1661V LUAD 2 32693083 32693083 + Missense_Mutation SNP A A T TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr2:32693083A>T c.5684A>T c.(5683-5685)cAt>cTt p.H1895L LUAD 2 32693563 32693563 + Missense_Mutation SNP C C G TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr2:32693563C>G c.5839C>G c.(5839-5841)Cta>Gta p.L1947V LUAD 2 32694488 32694488 + Missense_Mutation SNP G G T TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr2:32694488G>T c.6153G>T c.(6151-6153)caG>caT p.Q2051H LUAD 2 32694557 32694557 + Missense_Mutation SNP A A G TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr2:32694557A>G c.6222A>G c.(6220-6222)atA>atG p.I2074M LUAD 2 32710768 32710768 + Missense_Mutation SNP G G T TCGA-86-8672-01A-21D-2393-08 TCGA-86-8672-10A-01D-2393-08 g.chr2:32710768G>T c.7755G>T c.(7753-7755)atG>atT p.M2585I LUAD 2 32715142 32715142 + Missense_Mutation SNP G G C TCGA-38-4630-01A-01D-1265-08 TCGA-38-4630-11A-01D-1265-08 g.chr2:32715142G>C c.8130G>C c.(8128-8130)tgG>tgC p.W2710C LUAD 2 32715149 32715149 + Missense_Mutation SNP A A T TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr2:32715149A>T c.8137A>T c.(8137-8139)Aat>Tat p.N2713Y LUAD 2 32715201 32715201 + Missense_Mutation SNP C C G TCGA-69-A59K-01A-11D-A25L-08 TCGA-69-A59K-10A-01D-A25L-08 g.chr2:32715201C>G c.8189C>G c.(8188-8190)aCa>aGa p.T2730R LUAD 2 32718708 32718708 + Missense_Mutation SNP G G T TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chr2:32718708G>T c.8442G>T c.(8440-8442)aaG>aaT p.K2814N LUAD 2 32724693 32724693 + Missense_Mutation SNP G G A TCGA-17-Z049-01A-01W-0746-08 TCGA-17-Z049-11A-01W-0747-08 g.chr2:32724693G>A c.8548G>A c.(8548-8550)Gtc>Atc p.V2850I LUAD 2 32724733 32724733 + Missense_Mutation SNP T T C TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr2:32724733T>C c.8588T>C c.(8587-8589)gTt>gCt p.V2863A LUAD 2 32724814 32724814 + Missense_Mutation SNP G G T TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chr2:32724814G>T c.8669G>T c.(8668-8670)cGa>cTa p.R2890L LUAD 2 32726951 32726951 + Missense_Mutation SNP G G T TCGA-38-4632-01A-01D-1753-08 TCGA-38-4632-11A-01D-1753-08 g.chr2:32726951G>T c.9203G>T c.(9202-9204)aGa>aTa p.R3068I LUAD 2 32727861 32727861 + Splice_Site SNP G G T TCGA-78-8660-01A-11D-2393-08 TCGA-78-8660-10A-01D-2393-08 g.chr2:32727861G>T c.e48-1 LUAD 2 32730165 32730165 + Missense_Mutation SNP C C T TCGA-17-Z016-01A-01W-0746-08 TCGA-17-Z016-11A-01W-0746-08 g.chr2:32730165C>T c.9593C>T c.(9592-9594)tCc>tTc p.S3198F LUAD 2 32730166 32730166 + Silent SNP C C T TCGA-17-Z016-01A-01W-0746-08 TCGA-17-Z016-11A-01W-0746-08 g.chr2:32730166C>T c.9594C>T c.(9592-9594)tcC>tcT p.S3198S LUAD 2 32735027 32735027 + Silent SNP G G C TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr2:32735027G>C c.10203G>C c.(10201-10203)ctG>ctC p.L3401L LUAD 2 32735679 32735679 + Missense_Mutation SNP C C G TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chr2:32735679C>G c.10324C>G c.(10324-10326)Cag>Gag p.Q3442E LUAD 2 32738056 32738056 + Missense_Mutation SNP G G T TCGA-86-7714-01A-12D-2167-08 TCGA-86-7714-10A-01D-2167-08 g.chr2:32738056G>T c.10403G>T c.(10402-10404)aGa>aTa p.R3468I LUAD 2 32740150 32740150 + Silent SNP A A G TCGA-55-A492-01A-11D-A24D-08 TCGA-55-A492-10A-01D-A24F-08 g.chr2:32740150A>G c.10662A>G c.(10660-10662)ccA>ccG p.P3554P LUAD 2 32740258 32740258 + Silent SNP A A T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr2:32740258A>T c.10770A>T c.(10768-10770)tcA>tcT p.S3590S LUAD 2 32740674 32740674 + Missense_Mutation SNP A A G TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chr2:32740674A>G c.11186A>G c.(11185-11187)cAt>cGt p.H3729R LUAD 2 32768471 32768471 + Missense_Mutation SNP C C G TCGA-38-4632-01A-01D-1753-08 TCGA-38-4632-11A-01D-1753-08 g.chr2:32768471C>G c.12455C>G c.(12454-12456)cCc>cGc p.P4152R LUAD 2 32768555 32768555 + Missense_Mutation SNP A A T TCGA-38-4632-01A-01D-1753-08 TCGA-38-4632-11A-01D-1753-08 g.chr2:32768555A>T c.12539A>T c.(12538-12540)cAt>cTt p.H4180L LUAD 2 32772983 32772983 + Missense_Mutation SNP A A C TCGA-44-6144-01A-11D-1753-08 TCGA-44-6144-10A-01D-1753-08 g.chr2:32772983A>C c.12877A>C c.(12877-12879)Act>Cct p.T4293P LUAD 2 32774389 32774389 + Missense_Mutation SNP A A T TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr2:32774389A>T c.12985A>T c.(12985-12987)Agt>Tgt p.S4329C LUAD 2 32774406 32774406 + Silent SNP C C T TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr2:32774406C>T c.13002C>T c.(13000-13002)gtC>gtT p.V4334V LUAD 2 32774454 32774454 + Silent SNP G G T TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr2:32774454G>T c.13050G>T c.(13048-13050)ggG>ggT p.G4350G LUAD 2 32800426 32800426 + Missense_Mutation SNP C C T TCGA-78-7154-01A-11D-2036-08 TCGA-78-7154-10A-01D-2036-08 g.chr2:32800426C>T c.13348C>T c.(13348-13350)Cgt>Tgt p.R4450C LUAD 2 32820195 32820195 + Missense_Mutation SNP G G T TCGA-55-7910-01A-11D-2167-08 TCGA-55-7910-11A-01D-2167-08 g.chr2:32820195G>T c.13596G>T c.(13594-13596)atG>atT p.M4532I LUAD 2 32832633 32832633 + Missense_Mutation SNP G G A TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr2:32832633G>A c.14182G>A c.(14182-14184)Gat>Aat p.D4728N LUAD 2 32836581 32836581 + Missense_Mutation SNP G G T TCGA-38-7271-01A-11D-2036-08 TCGA-38-7271-11A-01D-2036-08 g.chr2:32836581G>T c.14326G>T c.(14326-14328)Gat>Tat p.D4776Y LUAD 2 32836633 32836633 + Missense_Mutation SNP A A G TCGA-64-5775-01A-01D-1625-08 TCGA-64-5775-10A-01D-1625-08 g.chr2:32836633A>G c.14378A>G c.(14377-14379)cAt>cGt p.H4793R LUSC 2 32664696 32664696 + Missense_Mutation SNP A A T TCGA-34-5239-01A-21D-1817-08 TCGA-34-5239-10A-01D-1817-08 g.chr2:32664696A>T c.3752A>T c.(3751-3753)cAc>cTc p.H1251L LUSC 2 32667235 32667235 + Missense_Mutation SNP G G C TCGA-60-2723-01A-01D-1522-08 TCGA-60-2723-11A-01D-1522-08 g.chr2:32667235G>C c.4047G>C c.(4045-4047)caG>caC p.Q1349H LUSC 2 32673984 32673984 + Missense_Mutation SNP G G T TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr2:32673984G>T c.4606G>T c.(4606-4608)Gat>Tat p.D1536Y LUSC 2 32692709 32692709 + Missense_Mutation SNP G G C TCGA-66-2754-01A-01D-0983-08 TCGA-66-2754-11A-01D-0983-08 g.chr2:32692709G>C c.5473G>C c.(5473-5475)Gag>Cag p.E1825Q LUSC 2 32703790 32703790 + Missense_Mutation SNP C C G TCGA-43-6770-01A-11D-1817-08 TCGA-43-6770-11A-01D-1817-08 g.chr2:32703790C>G c.7156C>G c.(7156-7158)Ctt>Gtt p.L2386V LUSC 2 32703827 32703827 + Missense_Mutation SNP C C A TCGA-66-2758-01A-02D-1522-08 TCGA-66-2758-11A-01D-1522-08 g.chr2:32703827C>A c.7193C>A c.(7192-7194)tCt>tAt p.S2398Y LUSC 2 32712731 32712731 + Nonsense_Mutation SNP G G T TCGA-18-3406-01A-01D-0983-08 TCGA-18-3406-11A-01D-0983-08 g.chr2:32712731G>T c.7831G>T c.(7831-7833)Gga>Tga p.G2611* LUSC 2 32725073 32725073 + Silent SNP G G A TCGA-85-6560-01A-11D-1817-08 TCGA-85-6560-10A-01D-1817-08 g.chr2:32725073G>A c.8928G>A c.(8926-8928)tcG>tcA p.S2976S LUSC 2 32726824 32726824 + Missense_Mutation SNP G G T TCGA-46-3767-01A-01D-0983-08 TCGA-46-3767-10A-01D-0983-08 g.chr2:32726824G>T c.9076G>T c.(9076-9078)Ggg>Tgg p.G3026W LUSC 2 32730095 32730095 + Missense_Mutation SNP A A T TCGA-60-2724-01A-01D-1522-08 TCGA-60-2724-11A-01D-1522-08 g.chr2:32730095A>T c.9523A>T c.(9523-9525)Act>Tct p.T3175S LUSC 2 32734914 32734914 + Missense_Mutation SNP G G T TCGA-34-5928-01A-11D-1817-08 TCGA-34-5928-10A-01D-1817-08 g.chr2:32734914G>T c.10090G>T c.(10090-10092)Gcc>Tcc p.A3364S LUSC 2 32738083 32738083 + Missense_Mutation SNP C C T TCGA-37-3789-01A-01D-0983-08 TCGA-37-3789-10A-01D-0983-08 g.chr2:32738083C>T c.10430C>T c.(10429-10431)cCt>cTt p.P3477L LUSC 2 32738147 32738147 + Silent SNP A A G TCGA-34-5240-01A-01D-1441-08 TCGA-34-5240-10A-01D-1441-08 g.chr2:32738147A>G c.10494A>G c.(10492-10494)gcA>gcG p.A3498A LUSC 2 32740349 32740349 + Missense_Mutation SNP G G C TCGA-37-3789-01A-01D-0983-08 TCGA-37-3789-10A-01D-0983-08 g.chr2:32740349G>C c.10861G>C c.(10861-10863)Gaa>Caa p.E3621Q LUSC 2 32740388 32740388 + Missense_Mutation SNP C C G TCGA-18-3419-01A-01D-0983-08 TCGA-18-3419-11A-01D-0983-08 g.chr2:32740388C>G c.10900C>G c.(10900-10902)Ctt>Gtt p.L3634V LUSC 2 32740406 32740406 + Missense_Mutation SNP G G T TCGA-43-6771-01A-11D-1817-08 TCGA-43-6771-11A-01D-1817-08 g.chr2:32740406G>T c.10918G>T c.(10918-10920)Gct>Tct p.A3640S LUSC 2 32750596 32750596 + Missense_Mutation SNP A A T TCGA-43-6771-01A-11D-1817-08 TCGA-43-6771-11A-01D-1817-08 g.chr2:32750596A>T c.11821A>T c.(11821-11823)Agg>Tgg p.R3941W LUSC 2 32750665 32750665 + Missense_Mutation SNP G G T TCGA-66-2756-01A-01D-1522-08 TCGA-66-2756-11A-01D-1522-08 g.chr2:32750665G>T c.11890G>T c.(11890-11892)Gtg>Ttg p.V3964L LUSC 2 32750675 32750675 + Missense_Mutation SNP T T C TCGA-37-5819-01A-01D-1632-08 TCGA-37-5819-10A-01D-1632-08 g.chr2:32750675T>C c.11900T>C c.(11899-11901)cTg>cCg p.L3967P LUSC 2 32754743 32754743 + Silent SNP A A G TCGA-66-2770-01A-01D-1522-08 TCGA-66-2770-11A-01D-1522-08 g.chr2:32754743A>G c.11946A>G c.(11944-11946)acA>acG p.T3982T LUSC 2 32768395 32768395 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr2:32768395G>A c.12379G>A c.(12379-12381)Gag>Aag p.E4127K LUSC 2 32773032 32773032 + Missense_Mutation SNP C C T TCGA-18-3407-01A-01D-0983-08 TCGA-18-3407-11A-01D-0983-08 g.chr2:32773032C>T c.12926C>T c.(12925-12927)gCc>gTc p.A4309V LUSC 2 32773076 32773076 + Silent SNP C C T TCGA-33-4538-01A-01D-1267-08 TCGA-33-4538-11A-01D-1267-08 g.chr2:32773076C>T c.12970C>T c.(12970-12972)Ctg>Ttg p.L4324L LUSC 2 32774431 32774431 + Missense_Mutation SNP C C G TCGA-37-3789-01A-01D-0983-08 TCGA-37-3789-10A-01D-0983-08 g.chr2:32774431C>G c.13027C>G c.(13027-13029)Cag>Gag p.Q4343E LUSC 2 32774500 32774500 + Missense_Mutation SNP C C G TCGA-21-1070-01A-01D-1521-08 TCGA-21-1070-11A-01D-1521-08 g.chr2:32774500C>G c.13096C>G c.(13096-13098)Cag>Gag p.Q4366E LUSC 2 32774511 32774511 + Silent SNP C C G TCGA-66-2795-01A-02D-0983-08 TCGA-66-2795-11A-01D-0983-08 g.chr2:32774511C>G c.13107C>G c.(13105-13107)ctC>ctG p.L4369L LUSC 2 32820187 32820187 + Missense_Mutation SNP G G T TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr2:32820187G>T c.13588G>T c.(13588-13590)Gct>Tct p.A4530S LUSC 2 32820204 32820204 + Silent SNP A A G TCGA-21-5787-01A-01D-1632-08 TCGA-21-5787-10A-01D-1632-08 g.chr2:32820204A>G c.13605A>G c.(13603-13605)ttA>ttG p.L4535L LUSC 2 32823032 32823032 + Missense_Mutation SNP G G C TCGA-60-2720-01A-01D-1522-08 TCGA-60-2720-11A-01D-1522-08 g.chr2:32823032G>C c.13827G>C c.(13825-13827)atG>atC p.M4609I LUSC 2 32832614 32832614 + Silent SNP A A T TCGA-18-3406-01A-01D-0983-08 TCGA-18-3406-11A-01D-0983-08 g.chr2:32832614A>T c.14163A>T c.(14161-14163)acA>acT p.T4721T LUSC 2 32832622 32832622 + Missense_Mutation SNP C C T TCGA-21-1077-01A-01D-1521-08 TCGA-21-1077-11A-01D-1521-08 g.chr2:32832622C>T c.14171C>T c.(14170-14172)tCt>tTt p.S4724F LUSC 2 32836642 32836642 + Missense_Mutation SNP C C G TCGA-33-4582-01A-01D-1441-08 TCGA-33-4582-11A-01D-1441-08 g.chr2:32836642C>G c.14387C>G c.(14386-14388)gCt>gGt p.A4796G LUSC 2 32842813 32842813 + Missense_Mutation SNP G G A TCGA-43-6647-01A-11D-1817-08 TCGA-43-6647-11A-01D-1817-08 g.chr2:32842813G>A c.14416G>A c.(14416-14418)Gaa>Aaa p.E4806K OV 2 32617172 32617172 + Missense_Mutation SNP G G C TCGA-13-0883-01A-02W-0420-08 TCGA-13-0883-10A-01D-0399-08 g.chr2:32617172G>C c.905G>C c.(904-906)aGg>aCg p.R302T OV 2 32640332 32640332 + Missense_Mutation SNP A A T TCGA-09-1670-01A-01W-0633-09 TCGA-09-1670-10A-01W-0633-09 g.chr2:32640332A>T c.1973A>T c.(1972-1974)cAt>cTt p.H658L OV 2 32660642 32660642 + Missense_Mutation SNP A A C TCGA-42-2589-01A-01D-1526-09 TCGA-42-2589-10A-01D-1526-09 g.chr2:32660642A>C c.3488A>C c.(3487-3489)gAg>gCg p.E1163A OV 2 32690187 32690187 + Missense_Mutation SNP C C G TCGA-23-1031-01A-01W-0486-08 TCGA-23-1031-10A-01W-0486-08 g.chr2:32690187C>G c.5311C>G c.(5311-5313)Caa>Gaa p.Q1771E OV 2 32693060 32693060 + Nonsense_Mutation SNP G G A TCGA-25-1324-01A-01W-0490-10 TCGA-25-1324-10A-01W-0490-10 g.chr2:32693060G>A c.5661G>A c.(5659-5661)tgG>tgA p.W1887* OV 2 32770875 32770875 + Missense_Mutation SNP C C T TCGA-24-2030-01A-01W-0722-08 TCGA-24-2030-10A-01W-0722-08 g.chr2:32770875C>T c.12758C>T c.(12757-12759)gCt>gTt p.A4253V OV 2 32828095 32828095 + Missense_Mutation SNP C C T TCGA-25-1318-01A-01W-0490-10 TCGA-25-1318-10A-01W-0490-10 g.chr2:32828095C>T c.14015C>T c.(14014-14016)aCg>aTg p.T4672M PAAD 2 32582309 32582309 + Missense_Mutation SNP G G A TCGA-3A-A9IH-01A-12D-A397-08 TCGA-3A-A9IH-10A-01D-A39A-08 g.chr2:32582309G>A c.80G>A c.(79-81)cGg>cAg p.R27Q PAAD 2 32613902 32613902 + Missense_Mutation SNP C C A TCGA-YB-A89D-01A-12D-A36O-08 TCGA-YB-A89D-10A-01D-A367-08 g.chr2:32613902C>A c.730C>A c.(730-732)Caa>Aaa p.Q244K PAAD 2 32673919 32673919 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr2:32673919G>T c.4541G>T c.(4540-4542)gGc>gTc p.G1514V PAAD 2 32673997 32673997 + Splice_Site SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr2:32673997G>A c.e22+1 PAAD 2 32702455 32702455 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr2:32702455G>A c.6872G>A c.(6871-6873)cGt>cAt p.R2291H PAAD 2 32706462 32706462 + Missense_Mutation SNP G G A TCGA-IB-AAUW-01A-12D-A38G-08 TCGA-IB-AAUW-10A-01D-A38J-08 g.chr2:32706462G>A c.7483G>A c.(7483-7485)Gac>Aac p.D2495N PAAD 2 32734896 32734896 + Missense_Mutation SNP C C G TCGA-3A-A9IL-01A-11D-A38G-08 TCGA-3A-A9IL-10A-01D-A38J-08 g.chr2:32734896C>G c.10072C>G c.(10072-10074)Ctg>Gtg p.L3358V PAAD 2 32740700 32740700 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr2:32740700G>A c.11212G>A c.(11212-11214)Gca>Aca p.A3738T PAAD 2 32774494 32774494 + Missense_Mutation SNP C C T TCGA-2J-AABK-01A-31D-A40W-08 TCGA-2J-AABK-10A-01D-A40W-08 g.chr2:32774494C>T c.13090C>T c.(13090-13092)Ctc>Ttc p.L4364F PAAD 2 32774524 32774524 + Missense_Mutation SNP T T C TCGA-IB-AAUQ-01A-22D-A40W-08 TCGA-IB-AAUQ-10A-01D-A40W-08 g.chr2:32774524T>C c.13120T>C c.(13120-13122)Tca>Cca p.S4374P PCPG 2 32693033 32693033 + Nonsense_Mutation SNP C C G TCGA-RW-A8AZ-01A-11D-A35D-08 TCGA-RW-A8AZ-10A-01D-A35B-08 g.chr2:32693033C>G c.5634C>G c.(5632-5634)taC>taG p.Y1878* PCPG 2 32819095 32819095 + Missense_Mutation SNP C C T TCGA-RW-A68A-01A-11D-A35D-08 TCGA-RW-A68A-11A-21D-A35B-08 g.chr2:32819095C>T c.13469C>T c.(13468-13470)gCa>gTa p.A4490V PRAD 2 32667453 32667453 + Missense_Mutation SNP C C T TCGA-J9-A52C-01A-11D-A26M-08 TCGA-J9-A52C-10A-01D-A26K-08 g.chr2:32667453C>T c.4168C>T c.(4168-4170)Cgt>Tgt p.R1390C PRAD 2 32712725 32712725 + Missense_Mutation SNP C C A TCGA-HC-7210-01A-11D-2114-08 TCGA-HC-7210-10A-01D-2115-08 g.chr2:32712725C>A c.7825C>A c.(7825-7827)Ccc>Acc p.P2609T PRAD 2 32728305 32728305 + Splice_Site SNP T T C TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr2:32728305T>C c.e49+2 PRAD 2 32740210 32740210 + Missense_Mutation SNP T T A TCGA-ZG-A8QZ-01A-11D-A377-08 TCGA-ZG-A8QZ-10A-01D-A37A-08 g.chr2:32740210T>A c.10722T>A c.(10720-10722)caT>caA p.H3574Q PRAD 2 32756565 32756565 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr2:32756565C>T c.12238C>T c.(12238-12240)Ctg>Ttg p.L4080L PRAD 2 32824954 32824954 + Missense_Mutation SNP A A C TCGA-CH-5767-01A-11D-1786-08 TCGA-CH-5767-11B-01D-1786-08 g.chr2:32824954A>C c.13979A>C c.(13978-13980)tAt>tCt p.Y4660S READ 2 32640364 32640364 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr2:32640364G>T c.2005G>T c.(2005-2007)Gaa>Taa p.E669* READ 2 32654233 32654233 + Silent SNP C C T TCGA-AF-2693-01A-02D-1733-10 TCGA-AF-2693-10A-01D-1733-10 g.chr2:32654233C>T c.2892C>T c.(2890-2892)ctC>ctT p.L964L READ 2 32667430 32667430 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr2:32667430G>A c.4145G>A c.(4144-4146)cGa>cAa p.R1382Q READ 2 32702499 32702499 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr2:32702499G>T c.6916G>T c.(6916-6918)Gaa>Taa p.E2306* READ 2 32726811 32726811 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr2:32726811A>C c.9063A>C c.(9061-9063)gaA>gaC p.E3021D READ 2 32733313 32733313 + Missense_Mutation SNP G G A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr2:32733313G>A c.9967G>A c.(9967-9969)Gta>Ata p.V3323I READ 2 32750029 32750029 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr2:32750029G>T c.11698G>T c.(11698-11700)Gaa>Taa p.E3900* READ 2 32770897 32770897 + Silent SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr2:32770897A>G c.12780A>G c.(12778-12780)cgA>cgG p.R4260R READ 2 32819112 32819112 + Missense_Mutation SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr2:32819112C>T c.13486C>T c.(13486-13488)Cgg>Tgg p.R4496W READ 2 32820106 32820106 + Missense_Mutation SNP A A G TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr2:32820106A>G c.13507A>G c.(13507-13509)Aaa>Gaa p.K4503E SARC 2 32605333 32605333 + Missense_Mutation SNP C C T TCGA-FX-A3RE-01A-11D-A228-09 TCGA-FX-A3RE-10A-01D-A22A-09 g.chr2:32605333C>T c.620C>T c.(619-621)aCt>aTt p.T207I SARC 2 32728303 32728303 + Splice_Site SNP G G T TCGA-SG-A849-01A-11D-A351-09 TCGA-SG-A849-10A-01D-A351-09 g.chr2:32728303G>T c.9499G>T c.(9499-9501)Ggt>Tgt p.G3167C SARC 2 32774387 32774387 + Missense_Mutation SNP C C T TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr2:32774387C>T c.12983C>T c.(12982-12984)gCc>gTc p.A4328V SARC 2 32774388 32774388 + Silent SNP C C T TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr2:32774388C>T c.12984C>T c.(12982-12984)gcC>gcT p.A4328A SKCM 2 32605261 32605261 + Missense_Mutation SNP T T A TCGA-FW-A3TV-06A-11D-A23B-08 TCGA-FW-A3TV-10A-01D-A23B-08 g.chr2:32605261T>A c.548T>A c.(547-549)aTt>aAt p.I183N SKCM 2 32626358 32626358 + Missense_Mutation SNP A A G TCGA-EE-A2A0-06A-11D-A196-08 TCGA-EE-A2A0-10A-01D-A198-08 g.chr2:32626358A>G c.1162A>G c.(1162-1164)Ata>Gta p.I388V SKCM 2 32640055 32640055 + Missense_Mutation SNP T T A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr2:32640055T>A c.1696T>A c.(1696-1698)Tgt>Agt p.C566S SKCM 2 32640219 32640219 + Silent SNP T T G TCGA-GN-A267-06A-21D-A196-08 TCGA-GN-A267-10A-01D-A198-08 g.chr2:32640219T>G c.1860T>G c.(1858-1860)tcT>tcG p.S620S SKCM 2 32640294 32640294 + Silent SNP C C T TCGA-D3-A3MV-06A-11D-A21A-08 TCGA-D3-A3MV-10A-01D-A21A-08 g.chr2:32640294C>T c.1935C>T c.(1933-1935)atC>atT p.I645I SKCM 2 32654243 32654243 + Missense_Mutation SNP G G A TCGA-D3-A2JN-06A-11D-A196-08 TCGA-D3-A2JN-10A-01D-A198-08 g.chr2:32654243G>A c.2902G>A c.(2902-2904)Gga>Aga p.G968R SKCM 2 32655963 32655963 + Missense_Mutation SNP C C T TCGA-D3-A5GR-06A-11D-A27K-08 TCGA-D3-A5GR-10A-01D-A27N-08 g.chr2:32655963C>T c.3053C>T c.(3052-3054)aCc>aTc p.T1018I SKCM 2 32655964 32655964 + Silent SNP C C T TCGA-D3-A5GR-06A-11D-A27K-08 TCGA-D3-A5GR-10A-01D-A27N-08 g.chr2:32655964C>T c.3054C>T c.(3052-3054)acC>acT p.T1018T SKCM 2 32666457 32666457 + Missense_Mutation SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr2:32666457C>T c.3871C>T c.(3871-3873)Cgg>Tgg p.R1291W SKCM 2 32689700 32689700 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr2:32689700C>T c.5065C>T c.(5065-5067)Cat>Tat p.H1689Y SKCM 2 32689721 32689721 + Missense_Mutation SNP C C T TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr2:32689721C>T c.5086C>T c.(5086-5088)Ccc>Tcc p.P1696S SKCM 2 32706501 32706501 + Missense_Mutation SNP C C T TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr2:32706501C>T c.7522C>T c.(7522-7524)Ctt>Ttt p.L2508F SKCM 2 32710714 32710714 + Silent SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr2:32710714G>A c.7701G>A c.(7699-7701)ctG>ctA p.L2567L SKCM 2 32710715 32710715 + Missense_Mutation SNP G G T TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr2:32710715G>T c.7702G>T c.(7702-7704)Gat>Tat p.D2568Y SKCM 2 32710717 32710717 + Missense_Mutation SNP T T A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr2:32710717T>A c.7704T>A c.(7702-7704)gaT>gaA p.D2568E SKCM 2 32712786 32712786 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr2:32712786T>G c.7886T>G c.(7885-7887)cTt>cGt p.L2629R SKCM 2 32712801 32712801 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr2:32712801C>T c.7901C>T c.(7900-7902)tCa>tTa p.S2634L SKCM 2 32715118 32715118 + Silent SNP T T C TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr2:32715118T>C c.8106T>C c.(8104-8106)acT>acC p.T2702T SKCM 2 32724761 32724761 + Silent SNP T T C TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr2:32724761T>C c.8616T>C c.(8614-8616)acT>acC p.T2872T SKCM 2 32724764 32724764 + Silent SNP C C T TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr2:32724764C>T c.8619C>T c.(8617-8619)tgC>tgT p.C2873C SKCM 2 32724803 32724803 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr2:32724803C>T c.8658C>T c.(8656-8658)tcC>tcT p.S2886S SKCM 2 32724814 32724814 + Missense_Mutation SNP G G A TCGA-FS-A1ZE-06A-11D-A197-08 TCGA-FS-A1ZE-10A-01D-A199-08 g.chr2:32724814G>A c.8669G>A c.(8668-8670)cGa>cAa p.R2890Q SKCM 2 32724828 32724828 + Missense_Mutation SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr2:32724828G>A c.8683G>A c.(8683-8685)Gga>Aga p.G2895R SKCM 2 32724829 32724829 + Missense_Mutation SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr2:32724829G>A c.8684G>A c.(8683-8685)gGa>gAa p.G2895E SKCM 2 32724849 32724849 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr2:32724849C>T c.8704C>T c.(8704-8706)Cgt>Tgt p.R2902C SKCM 2 32724999 32724999 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr2:32724999G>A c.8854G>A c.(8854-8856)Gat>Aat p.D2952N SKCM 2 32726811 32726811 + Missense_Mutation SNP A A T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr2:32726811A>T c.9063A>T c.(9061-9063)gaA>gaT p.E3021D SKCM 2 32733298 32733298 + Missense_Mutation SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr2:32733298C>T c.9952C>T c.(9952-9954)Cca>Tca p.P3318S SKCM 2 32738066 32738066 + Silent SNP G G A TCGA-ER-A198-06A-11D-A196-08 TCGA-ER-A198-10A-01D-A198-08 g.chr2:32738066G>A c.10413G>A c.(10411-10413)agG>agA p.R3471R SKCM 2 32738123 32738123 + Silent SNP T T A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr2:32738123T>A c.10470T>A c.(10468-10470)tcT>tcA p.S3490S SKCM 2 32740464 32740464 + Missense_Mutation SNP T T A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr2:32740464T>A c.10976T>A c.(10975-10977)aTt>aAt p.I3659N SKCM 2 32740598 32740598 + Missense_Mutation SNP G G T TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chr2:32740598G>T c.11110G>T c.(11110-11112)Ggt>Tgt p.G3704C SKCM 2 32740645 32740645 + Missense_Mutation SNP G G T TCGA-EE-A3JE-06A-11D-A20D-08 TCGA-EE-A3JE-10A-01D-A20D-08 g.chr2:32740645G>T c.11157G>T c.(11155-11157)ttG>ttT p.L3719F SKCM 2 32743456 32743456 + Missense_Mutation SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr2:32743456C>T c.11485C>T c.(11485-11487)Cca>Tca p.P3829S SKCM 2 32750561 32750561 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr2:32750561C>T c.11786C>T c.(11785-11787)tCa>tTa p.S3929L SKCM 2 32754816 32754816 + Nonsense_Mutation SNP A A T TCGA-D3-A3MU-06A-11D-A21A-08 TCGA-D3-A3MU-10A-01D-A21A-08 g.chr2:32754816A>T c.12019A>T c.(12019-12021)Aaa>Taa p.K4007* SKCM 2 32768346 32768346 + Silent SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr2:32768346G>A c.12330G>A c.(12328-12330)aaG>aaA p.K4110K SKCM 2 32768572 32768572 + Nonsense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr2:32768572C>T c.12556C>T c.(12556-12558)Cga>Tga p.R4186* SKCM 2 32773047 32773047 + Missense_Mutation SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr2:32773047G>A c.12941G>A c.(12940-12942)aGg>aAg p.R4314K SKCM 2 32774474 32774474 + Missense_Mutation SNP C C T TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr2:32774474C>T c.13070C>T c.(13069-13071)cCt>cTt p.P4357L SKCM 2 32800257 32800257 + Silent SNP G G A TCGA-EE-A2GN-06A-11D-A196-08 TCGA-EE-A2GN-10A-01D-A198-08 g.chr2:32800257G>A c.13179G>A c.(13177-13179)cgG>cgA p.R4393R SKCM 2 32800289 32800289 + Missense_Mutation SNP C C T TCGA-ER-A1A1-06A-11D-A197-08 TCGA-ER-A1A1-10A-01D-A199-08 g.chr2:32800289C>T c.13211C>T c.(13210-13212)tCt>tTt p.S4404F SKCM 2 32824895 32824895 + Silent SNP C C T TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr2:32824895C>T c.13920C>T c.(13918-13920)ccC>ccT p.P4640P SKCM 2 32824896 32824896 + Missense_Mutation SNP C C T TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr2:32824896C>T c.13921C>T c.(13921-13923)Cct>Tct p.P4641S SKCM 2 32828074 32828074 + Splice_Site DEL T T - TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr2:32828074delT c.13994delT c.(13993-13995)gtt>gt p.V4665fs SKCM 2 32828126 32828126 + Missense_Mutation SNP T T G TCGA-DA-A1IA-06A-11D-A196-08 TCGA-DA-A1IA-10A-01D-A198-08 g.chr2:32828126T>G c.14046T>G c.(14044-14046)aaT>aaG p.N4682K SKCM 2 32828135 32828135 + Silent SNP C C A TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr2:32828135C>A c.14055C>A c.(14053-14055)acC>acA p.T4685T SKCM 2 32832604 32832604 + Missense_Mutation SNP C C T TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr2:32832604C>T c.14153C>T c.(14152-14154)cCc>cTc p.P4718L SKCM 2 32832604 32832604 + Missense_Mutation SNP C C T TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr2:32832604C>T c.14153C>T c.(14152-14154)cCc>cTc p.P4718L

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 2 32706417 32706417 single base substitution G C missense_variant D2480H 7438G>C BLCA-CN 2 32819095 32819095 single base substitution C T exon_variant BLCA-CN 2 32819095 32819095 single base substitution C T missense_variant A4490V 13469C>T BLCA-US 2 32617216 32617216 single base substitution C G missense_variant Q317E 949C>G BLCA-US 2 32617216 32617216 single base substitution C G splice_region_variant BLCA-US 2 32620589 32620589 single base substitution C G exon_variant BLCA-US 2 32620589 32620589 single base substitution C G missense_variant S321C 962C>G BLCA-US 2 32626345 32626345 single base substitution T C exon_variant BLCA-US 2 32626345 32626345 single base substitution T C synonymous_variant D383D 1149T>C BLCA-US 2 32626450 32626450 single base substitution G A exon_variant BLCA-US 2 32626450 32626450 single base substitution G A missense_variant M418I 1254G>A BLCA-US 2 32626615 32626615 single base substitution G A downstream_gene_variant BLCA-US 2 32626615 32626615 single base substitution G A missense_variant D448N 1342G>A BLCA-US 2 32640519 32640519 single base substitution G A synonymous_variant L720L 2160G>A BLCA-US 2 32640622 32640622 single base substitution G A missense_variant E755K 2263G>A BLCA-US 2 32640936 32640936 single base substitution C G synonymous_variant L859L 2577C>G BLCA-US 2 32668572 32668572 single base substitution G T downstream_gene_variant BLCA-US 2 32668572 32668572 single base substitution G T exon_variant BLCA-US 2 32668572 32668572 single base substitution G T missense_variant D1418Y 4252G>T BLCA-US 2 32670646 32670646 single base substitution G A downstream_gene_variant BLCA-US 2 32670646 32670646 single base substitution G A exon_variant BLCA-US 2 32670646 32670646 single base substitution G A missense_variant G1465E 4394G>A BLCA-US 2 32673877 32673877 single base substitution G A exon_variant BLCA-US 2 32673877 32673877 single base substitution G A missense_variant S1500N 4499G>A BLCA-US 2 32673888 32673888 single base substitution G A exon_variant BLCA-US 2 32673888 32673888 single base substitution G A missense_variant D1504N 4510G>A BLCA-US 2 32678919 32678919 single base substitution C T downstream_gene_variant BLCA-US 2 32678919 32678919 single base substitution C T synonymous_variant F1554F 4662C>T BLCA-US 2 32678953 32678953 single base substitution C G downstream_gene_variant BLCA-US 2 32678953 32678953 single base substitution C G missense_variant L1566V 4696C>G BLCA-US 2 32694656 32694656 single base substitution A G synonymous_variant E2107E 6321A>G BLCA-US 2 32694656 32694656 single base substitution A G upstream_gene_variant BLCA-US 2 32715215 32715215 single base substitution A C missense_variant N2735H 8203A>C BLCA-US 2 32716552 32716552 single base substitution C G missense_variant P2756R 8267C>G BLCA-US 2 32716581 32716581 single base substitution C G missense_variant L2766V 8296C>G BLCA-US 2 32738069 32738069 single base substitution G T exon_variant BLCA-US 2 32738069 32738069 single base substitution G T missense_variant M3472I 10416G>T BLCA-US 2 32738069 32738069 single base substitution G T upstream_gene_variant BLCA-US 2 32740283 32740283 single base substitution G A downstream_gene_variant BLCA-US 2 32740283 32740283 single base substitution G A missense_variant A3599T 10795G>A BLCA-US 2 32740283 32740283 single base substitution G A upstream_gene_variant BLCA-US 2 32740370 32740370 single base substitution G C downstream_gene_variant BLCA-US 2 32740370 32740370 single base substitution G C missense_variant D3628H 10882G>C BLCA-US 2 32740370 32740370 single base substitution G C upstream_gene_variant BLCA-US 2 32740790 32740790 single base substitution C G downstream_gene_variant BLCA-US 2 32740790 32740790 single base substitution C G missense_variant L3768V 11302C>G BLCA-US 2 32740790 32740790 single base substitution C G upstream_gene_variant BLCA-US 2 32743450 32743450 single base substitution C T exon_variant BLCA-US 2 32743450 32743450 single base substitution C T stop_gained Q3827* 11479C>T BLCA-US 2 32743962 32743962 single base substitution C T exon_variant BLCA-US 2 32743962 32743962 single base substitution C T missense_variant L3858F 11572C>T BLCA-US 2 32743965 32743965 single base substitution C T exon_variant BLCA-US 2 32743965 32743965 single base substitution C T missense_variant H3859Y 11575C>T BLCA-US 2 32743998 32743998 single base substitution C G exon_variant BLCA-US 2 32743998 32743998 single base substitution C G missense_variant L3870V 11608C>G BLCA-US 2 32770731 32770731 single base substitution C T exon_variant BLCA-US 2 32770731 32770731 single base substitution C T missense_variant S4205L 12614C>T BLCA-US 2 32832589 32832589 single base substitution G T exon_variant BLCA-US 2 32832589 32832589 single base substitution G T missense_variant R4713L 14138G>T BLCA-US 2 32832645 32832645 single base substitution C T exon_variant BLCA-US 2 32832645 32832645 single base substitution C T stop_gained R4732* 14194C>T BOCA-FR 2 32632188 32632188 single base substitution A G intron_variant BOCA-FR 2 32735705 32735705 single base substitution C T splice_region_variant BOCA-FR 2 32819026 32819026 single base substitution C T exon_variant BOCA-FR 2 32819026 32819026 single base substitution C T missense_variant S4467F 13400C>T BRCA-EU 2 32577739 32577739 single base substitution A G upstream_gene_variant BRCA-EU 2 32577930 32577930 single base substitution C T upstream_gene_variant BRCA-EU 2 32578142 32578142 single base substitution A T upstream_gene_variant BRCA-EU 2 32578646 32578646 single base substitution C T upstream_gene_variant BRCA-EU 2 32579259 32579259 single base substitution T G upstream_gene_variant BRCA-EU 2 32579417 32579417 single base substitution C T upstream_gene_variant BRCA-EU 2 32579496 32579496 single base substitution C T upstream_gene_variant BRCA-EU 2 32579646 32579646 single base substitution C A upstream_gene_variant BRCA-EU 2 32579718 32579718 single base substitution G A upstream_gene_variant BRCA-EU 2 32581875 32581875 single base substitution C T upstream_gene_variant BRCA-EU 2 32582254 32582254 single base substitution C A missense_variant P9T 25C>A BRCA-EU 2 32582726 32582726 single base substitution C T intron_variant BRCA-EU 2 32584788 32584788 single base substitution T A intron_variant BRCA-EU 2 32586436 32586436 single base substitution C G intron_variant BRCA-EU 2 32588236 32588236 deletion of <=200bp A - intron_variant BRCA-EU 2 32588378 32588386 deletion of <=200bp AGACTCTGT - intron_variant BRCA-EU 2 32590836 32590836 single base substitution A C intron_variant BRCA-EU 2 32591808 32591808 single base substitution T C intron_variant BRCA-EU 2 32594538 32594538 single base substitution C G intron_variant BRCA-EU 2 32594621 32594621 single base substitution G A intron_variant BRCA-EU 2 32594960 32594960 single base substitution G T intron_variant BRCA-EU 2 32596575 32596575 single base substitution T C intron_variant BRCA-EU 2 32598690 32598690 single base substitution C G intron_variant BRCA-EU 2 32599051 32599051 single base substitution G A intron_variant BRCA-EU 2 32600561 32600561 deletion of <=200bp A - intron_variant BRCA-EU 2 32603481 32603481 single base substitution A C intron_variant BRCA-EU 2 32603721 32603721 single base substitution C A intron_variant BRCA-EU 2 32606644 32606644 single base substitution C T intron_variant BRCA-EU 2 32607626 32607626 single base substitution G A intron_variant BRCA-EU 2 32608493 32608493 single base substitution T C intron_variant BRCA-EU 2 32608968 32608968 single base substitution C T intron_variant BRCA-EU 2 32608968 32608968 single base substitution C T upstream_gene_variant BRCA-EU 2 32611317 32611317 single base substitution C T intron_variant BRCA-EU 2 32611317 32611317 single base substitution C T upstream_gene_variant BRCA-EU 2 32616111 32616111 single base substitution C T intron_variant BRCA-EU 2 32616612 32616612 single base substitution G A intron_variant BRCA-EU 2 32617565 32617565 single base substitution C T intron_variant BRCA-EU 2 32617678 32617678 single base substitution T A intron_variant BRCA-EU 2 32617697 32617697 insertion of <=200bp - T intron_variant BRCA-EU 2 32618578 32618581 deletion of <=200bp TTTA - intron_variant BRCA-EU 2 32618800 32618800 single base substitution G A intron_variant BRCA-EU 2 32619426 32619426 single base substitution C T intron_variant BRCA-EU 2 32619812 32619812 single base substitution C T intron_variant BRCA-EU 2 32621483 32621483 single base substitution G A intron_variant BRCA-EU 2 32621971 32621971 insertion of <=200bp - T intron_variant BRCA-EU 2 32622489 32622489 single base substitution G C intron_variant BRCA-EU 2 32623608 32623608 single base substitution T A intron_variant BRCA-EU 2 32623974 32623974 single base substitution C G intron_variant BRCA-EU 2 32624101 32624128 deletion of <=200bp GTTTAAAAACAATGGTTCTTTAAGAAAC - intron_variant BRCA-EU 2 32624387 32624412 deletion of <=200bp CAAGTGATGCACCCATCTCAGCCTCC - intron_variant BRCA-EU 2 32625214 32625214 single base substitution G A intron_variant BRCA-EU 2 32626096 32626096 single base substitution T C intron_variant BRCA-EU 2 32626310 32626310 single base substitution C G exon_variant BRCA-EU 2 32626310 32626310 single base substitution C G missense_variant L372V 1114C>G BRCA-EU 2 32626560 32626560 single base substitution T C downstream_gene_variant BRCA-EU 2 32626560 32626560 single base substitution T C synonymous_variant Y429Y 1287T>C BRCA-EU 2 32626671 32626671 single base substitution A G downstream_gene_variant BRCA-EU 2 32626671 32626671 single base substitution A G missense_variant I466M 1398A>G BRCA-EU 2 32627692 32627692 single base substitution C T downstream_gene_variant BRCA-EU 2 32627692 32627692 single base substitution C T intron_variant BRCA-EU 2 32628449 32628449 single base substitution T C downstream_gene_variant BRCA-EU 2 32628449 32628449 single base substitution T C intron_variant BRCA-EU 2 32629639 32629639 single base substitution C G downstream_gene_variant BRCA-EU 2 32629639 32629639 single base substitution C G intron_variant BRCA-EU 2 32630711 32630711 single base substitution G A downstream_gene_variant BRCA-EU 2 32630711 32630711 single base substitution G A intron_variant BRCA-EU 2 32632572 32632572 single base substitution C A intron_variant BRCA-EU 2 32633331 32633331 single base substitution C T intron_variant BRCA-EU 2 32633429 32633429 single base substitution C T intron_variant BRCA-EU 2 32633577 32633577 deletion of <=200bp T - intron_variant BRCA-EU 2 32633723 32633723 single base substitution C T intron_variant BRCA-EU 2 32634219 32634219 deletion of <=200bp T - intron_variant BRCA-EU 2 32634219 32634219 insertion of <=200bp - T intron_variant BRCA-EU 2 32634802 32634802 single base substitution A T intron_variant BRCA-EU 2 32636356 32636356 single base substitution C G intron_variant BRCA-EU 2 32636503 32636503 single base substitution T A intron_variant BRCA-EU 2 32636958 32636958 single base substitution G A intron_variant BRCA-EU 2 32638538 32638538 single base substitution G A intron_variant BRCA-EU 2 32642463 32642463 single base substitution C T intron_variant BRCA-EU 2 32643317 32643317 single base substitution A T intron_variant BRCA-EU 2 32643359 32643359 single base substitution C G intron_variant BRCA-EU 2 32643738 32643738 single base substitution G A intron_variant BRCA-EU 2 32644877 32644877 single base substitution C G intron_variant BRCA-EU 2 32646123 32646123 single base substitution C G intron_variant BRCA-EU 2 32647548 32647548 single base substitution C T intron_variant BRCA-EU 2 32647950 32647950 single base substitution T G intron_variant BRCA-EU 2 32648662 32648662 single base substitution A T intron_variant BRCA-EU 2 32651529 32651529 single base substitution G A intron_variant BRCA-EU 2 32651893 32651893 single base substitution T C intron_variant BRCA-EU 2 32652076 32652076 single base substitution C T intron_variant BRCA-EU 2 32652937 32653008 deletion of <=200bp CTTTTGCCAGGTGGTTGTTGCTTTGTTTGTTTTGTGAAAACAAACAAACTGTTGAATCTGTGAAATCTGAAT - intron_variant BRCA-EU 2 32653060 32653060 single base substitution G T intron_variant BRCA-EU 2 32653331 32653331 single base substitution T C intron_variant BRCA-EU 2 32654116 32654116 single base substitution T A intron_variant BRCA-EU 2 32654116 32654116 single base substitution T A upstream_gene_variant BRCA-EU 2 32655073 32655073 single base substitution G C intron_variant BRCA-EU 2 32655073 32655073 single base substitution G C upstream_gene_variant BRCA-EU 2 32655300 32655300 deletion of <=200bp T - intron_variant BRCA-EU 2 32655300 32655300 deletion of <=200bp T - upstream_gene_variant BRCA-EU 2 32656527 32656527 single base substitution G A intron_variant BRCA-EU 2 32656527 32656527 single base substitution G A upstream_gene_variant BRCA-EU 2 32656952 32656952 single base substitution G C intron_variant BRCA-EU 2 32656952 32656952 single base substitution G C upstream_gene_variant BRCA-EU 2 32656962 32656962 single base substitution A G intron_variant BRCA-EU 2 32656962 32656962 single base substitution A G upstream_gene_variant BRCA-EU 2 32657776 32657776 single base substitution C T intron_variant BRCA-EU 2 32657776 32657776 single base substitution C T upstream_gene_variant BRCA-EU 2 32659842 32659842 single base substitution C G intron_variant BRCA-EU 2 32659842 32659842 single base substitution C G upstream_gene_variant BRCA-EU 2 32660410 32660410 single base substitution C T intron_variant BRCA-EU 2 32660410 32660410 single base substitution C T upstream_gene_variant BRCA-EU 2 32663354 32663354 single base substitution A T intron_variant BRCA-EU 2 32663826 32663826 single base substitution C T intron_variant BRCA-EU 2 32663826 32663826 single base substitution C T upstream_gene_variant BRCA-EU 2 32663920 32663920 single base substitution G A intron_variant BRCA-EU 2 32663920 32663920 single base substitution G A upstream_gene_variant BRCA-EU 2 32664210 32664210 single base substitution T C intron_variant BRCA-EU 2 32664210 32664210 single base substitution T C upstream_gene_variant BRCA-EU 2 32666617 32666617 single base substitution C G downstream_gene_variant BRCA-EU 2 32666617 32666617 single base substitution C G intron_variant BRCA-EU 2 32666617 32666617 single base substitution C G upstream_gene_variant BRCA-EU 2 32667064 32667064 single base substitution A G downstream_gene_variant BRCA-EU 2 32667064 32667064 single base substitution A G intron_variant BRCA-EU 2 32667064 32667064 single base substitution A G upstream_gene_variant BRCA-EU 2 32667908 32667908 deletion of <=200bp T - downstream_gene_variant BRCA-EU 2 32667908 32667908 deletion of <=200bp T - intron_variant BRCA-EU 2 32667908 32667908 deletion of <=200bp T - upstream_gene_variant BRCA-EU 2 32668334 32668334 single base substitution G C downstream_gene_variant BRCA-EU 2 32668334 32668334 single base substitution G C intron_variant BRCA-EU 2 32668334 32668334 single base substitution G C upstream_gene_variant BRCA-EU 2 32668898 32668898 single base substitution T A downstream_gene_variant BRCA-EU 2 32668898 32668898 single base substitution T A intron_variant BRCA-EU 2 32670840 32670840 single base substitution C G downstream_gene_variant BRCA-EU 2 32670840 32670840 single base substitution C G intron_variant BRCA-EU 2 32673555 32673555 deletion of <=200bp A - intron_variant BRCA-EU 2 32673656 32673656 single base substitution C G intron_variant BRCA-EU 2 32673714 32673714 single base substitution G A intron_variant BRCA-EU 2 32673962 32673962 single base substitution G A exon_variant BRCA-EU 2 32673962 32673962 single base substitution G A synonymous_variant Q1528Q 4584G>A BRCA-EU 2 32677837 32677837 single base substitution G A downstream_gene_variant BRCA-EU 2 32677837 32677837 single base substitution G A intron_variant BRCA-EU 2 32677918 32677918 single base substitution C T downstream_gene_variant BRCA-EU 2 32677918 32677918 single base substitution C T intron_variant BRCA-EU 2 32678466 32678466 single base substitution G A downstream_gene_variant BRCA-EU 2 32678466 32678466 single base substitution G A intron_variant BRCA-EU 2 32678673 32678673 single base substitution C G downstream_gene_variant BRCA-EU 2 32678673 32678673 single base substitution C G intron_variant BRCA-EU 2 32680536 32680536 single base substitution A G intron_variant BRCA-EU 2 32680690 32680690 single base substitution G A intron_variant BRCA-EU 2 32680981 32680981 single base substitution A T intron_variant BRCA-EU 2 32681267 32681267 single base substitution C T intron_variant BRCA-EU 2 32682407 32682407 single base substitution C T intron_variant BRCA-EU 2 32683506 32683506 single base substitution C G intron_variant BRCA-EU 2 32683620 32683620 single base substitution C T intron_variant BRCA-EU 2 32684010 32684010 single base substitution G A intron_variant BRCA-EU 2 32684437 32684437 single base substitution C G intron_variant BRCA-EU 2 32686956 32686956 single base substitution T G intron_variant BRCA-EU 2 32687137 32687137 deletion of <=200bp G - intron_variant BRCA-EU 2 32687300 32687300 single base substitution T C intron_variant BRCA-EU 2 32688762 32688762 single base substitution C G intron_variant BRCA-EU 2 32691315 32691315 single base substitution C G intron_variant BRCA-EU 2 32691693 32691693 deletion of <=200bp A - intron_variant BRCA-EU 2 32691802 32691802 single base substitution C G intron_variant BRCA-EU 2 32691876 32691876 deletion of <=200bp T - intron_variant BRCA-EU 2 32693014 32693014 single base substitution A G missense_variant K1872R 5615A>G BRCA-EU 2 32693189 32693189 single base substitution G C intron_variant BRCA-EU 2 32693189 32693189 single base substitution G C upstream_gene_variant BRCA-EU 2 32693597 32693597 single base substitution G A missense_variant R1958Q 5873G>A BRCA-EU 2 32693597 32693597 single base substitution G A upstream_gene_variant BRCA-EU 2 32693960 32693960 insertion of <=200bp - A intron_variant BRCA-EU 2 32693960 32693960 insertion of <=200bp - A upstream_gene_variant BRCA-EU 2 32696983 32696983 single base substitution G A intron_variant BRCA-EU 2 32696983 32696983 single base substitution G A upstream_gene_variant BRCA-EU 2 32697445 32697445 single base substitution G A intron_variant BRCA-EU 2 32697445 32697445 single base substitution G A upstream_gene_variant BRCA-EU 2 32698075 32698075 single base substitution C G exon_variant BRCA-EU 2 32698075 32698075 single base substitution C G intron_variant BRCA-EU 2 32698486 32698486 single base substitution G T intron_variant BRCA-EU 2 32698590 32698590 single base substitution C T intron_variant BRCA-EU 2 32700001 32700001 single base substitution G A intron_variant BRCA-EU 2 32701357 32701357 single base substitution G A downstream_gene_variant BRCA-EU 2 32701357 32701357 single base substitution G A missense_variant G2266E 6797G>A BRCA-EU 2 32701360 32701360 single base substitution C T downstream_gene_variant BRCA-EU 2 32701360 32701360 single base substitution C T missense_variant S2267L 6800C>T BRCA-EU 2 32701536 32701536 deletion of <=200bp T - downstream_gene_variant BRCA-EU 2 32701536 32701536 deletion of <=200bp T - intron_variant BRCA-EU 2 32702072 32702072 single base substitution T C downstream_gene_variant BRCA-EU 2 32702072 32702072 single base substitution T C intron_variant BRCA-EU 2 32702451 32702451 single base substitution A G downstream_gene_variant BRCA-EU 2 32702451 32702451 single base substitution A G missense_variant I2290V 6868A>G BRCA-EU 2 32702559 32702559 single base substitution G T downstream_gene_variant BRCA-EU 2 32702559 32702559 single base substitution G T stop_gained E2326* 6976G>T BRCA-EU 2 32702560 32702560 single base substitution A T downstream_gene_variant BRCA-EU 2 32702560 32702560 single base substitution A T missense_variant E2326V 6977A>T BRCA-EU 2 32702622 32702622 single base substitution C G downstream_gene_variant BRCA-EU 2 32702622 32702622 single base substitution C G missense_variant H2347D 7039C>G BRCA-EU 2 32703094 32703094 single base substitution G A downstream_gene_variant BRCA-EU 2 32703094 32703094 single base substitution G A intron_variant BRCA-EU 2 32703460 32703460 single base substitution T G downstream_gene_variant BRCA-EU 2 32703460 32703460 single base substitution T G intron_variant BRCA-EU 2 32704040 32704040 single base substitution A G downstream_gene_variant BRCA-EU 2 32704040 32704040 single base substitution A G intron_variant BRCA-EU 2 32706587 32706587 single base substitution C T intron_variant BRCA-EU 2 32706735 32706735 single base substitution G C intron_variant BRCA-EU 2 32706939 32706939 single base substitution G A intron_variant BRCA-EU 2 32707190 32707190 insertion of <=200bp - T intron_variant BRCA-EU 2 32707285 32707285 single base substitution A C intron_variant BRCA-EU 2 32707476 32707476 insertion of <=200bp - T intron_variant BRCA-EU 2 32708889 32708889 single base substitution C T intron_variant BRCA-EU 2 32709785 32709785 single base substitution T A intron_variant BRCA-EU 2 32709920 32709920 deletion of <=200bp T - intron_variant BRCA-EU 2 32710690 32710690 single base substitution C G intron_variant BRCA-EU 2 32712421 32712421 single base substitution C G intron_variant BRCA-EU 2 32713211 32713211 single base substitution C T intron_variant BRCA-EU 2 32713792 32713792 single base substitution T C intron_variant BRCA-EU 2 32714644 32714644 single base substitution C G intron_variant BRCA-EU 2 32715923 32715923 single base substitution C T intron_variant BRCA-EU 2 32716656 32716656 single base substitution A G intron_variant BRCA-EU 2 32716772 32716772 single base substitution T G intron_variant BRCA-EU 2 32717648 32717648 single base substitution C T intron_variant BRCA-EU 2 32718042 32718042 deletion of <=200bp T - intron_variant BRCA-EU 2 32718244 32718244 single base substitution G C intron_variant BRCA-EU 2 32718293 32718293 single base substitution C G intron_variant BRCA-EU 2 32718800 32718800 single base substitution T A intron_variant BRCA-EU 2 32718801 32718801 single base substitution C T intron_variant BRCA-EU 2 32719123 32719123 single base substitution G A intron_variant BRCA-EU 2 32719649 32719649 single base substitution G C intron_variant BRCA-EU 2 32721837 32721837 single base substitution G C intron_variant BRCA-EU 2 32722023 32722023 single base substitution C T intron_variant BRCA-EU 2 32722201 32722201 single base substitution A T intron_variant BRCA-EU 2 32722206 32722206 single base substitution A T intron_variant BRCA-EU 2 32722379 32722379 deletion of <=200bp T - intron_variant BRCA-EU 2 32723204 32723204 single base substitution C T intron_variant BRCA-EU 2 32723204 32723204 single base substitution C T upstream_gene_variant BRCA-EU 2 32724475 32724475 single base substitution C G intron_variant BRCA-EU 2 32724475 32724475 single base substitution C G upstream_gene_variant BRCA-EU 2 32724591 32724591 insertion of <=200bp - TC intron_variant BRCA-EU 2 32724591 32724591 insertion of <=200bp - TC upstream_gene_variant BRCA-EU 2 32724793 32724793 single base substitution C G stop_gained S2883* 8648C>G BRCA-EU 2 32724793 32724793 single base substitution C G upstream_gene_variant BRCA-EU 2 32725137 32725137 single base substitution C T synonymous_variant L2998L 8992C>T BRCA-EU 2 32725137 32725137 single base substitution C T upstream_gene_variant BRCA-EU 2 32725227 32725227 deletion of <=200bp T - intron_variant BRCA-EU 2 32725227 32725227 deletion of <=200bp T - upstream_gene_variant BRCA-EU 2 32725252 32725252 single base substitution C T intron_variant BRCA-EU 2 32725252 32725252 single base substitution C T upstream_gene_variant BRCA-EU 2 32725940 32725940 single base substitution A G intron_variant BRCA-EU 2 32725940 32725940 single base substitution A G upstream_gene_variant BRCA-EU 2 32726352 32726352 single base substitution C T intron_variant BRCA-EU 2 32726352 32726352 single base substitution C T upstream_gene_variant BRCA-EU 2 32726401 32726401 single base substitution G C intron_variant BRCA-EU 2 32726401 32726401 single base substitution G C upstream_gene_variant BRCA-EU 2 32727104 32727104 single base substitution A C intron_variant BRCA-EU 2 32727104 32727104 single base substitution A C upstream_gene_variant BRCA-EU 2 32727433 32727433 single base substitution G C intron_variant BRCA-EU 2 32727433 32727433 single base substitution G C upstream_gene_variant BRCA-EU 2 32728961 32728961 single base substitution G T intron_variant BRCA-EU 2 32730275 32730275 single base substitution G C exon_variant BRCA-EU 2 32730275 32730275 single base substitution G C splice_region_variant BRCA-EU 2 32730275 32730275 single base substitution G C upstream_gene_variant BRCA-EU 2 32732098 32732098 single base substitution C T downstream_gene_variant BRCA-EU 2 32732098 32732098 single base substitution C T intron_variant BRCA-EU 2 32732098 32732098 single base substitution C T upstream_gene_variant BRCA-EU 2 32732132 32732132 single base substitution G T downstream_gene_variant BRCA-EU 2 32732132 32732132 single base substitution G T intron_variant BRCA-EU 2 32732132 32732132 single base substitution G T upstream_gene_variant BRCA-EU 2 32734285 32734285 single base substitution C G downstream_gene_variant BRCA-EU 2 32734285 32734285 single base substitution C G intron_variant BRCA-EU 2 32734285 32734285 single base substitution C G upstream_gene_variant BRCA-EU 2 32736956 32736956 single base substitution G T intron_variant BRCA-EU 2 32736956 32736956 single base substitution G T upstream_gene_variant BRCA-EU 2 32737265 32737265 single base substitution G T intron_variant BRCA-EU 2 32737265 32737265 single base substitution G T upstream_gene_variant BRCA-EU 2 32739947 32739950 deletion of <=200bp AAAT - downstream_gene_variant BRCA-EU 2 32739947 32739950 deletion of <=200bp AAAT - intron_variant BRCA-EU 2 32739947 32739950 deletion of <=200bp AAAT - upstream_gene_variant BRCA-EU 2 32740225 32740225 single base substitution G T downstream_gene_variant BRCA-EU 2 32740225 32740225 single base substitution G T missense_variant M3579I 10737G>T BRCA-EU 2 32740225 32740225 single base substitution G T upstream_gene_variant BRCA-EU 2 32741274 32741274 single base substitution A G downstream_gene_variant BRCA-EU 2 32741274 32741274 single base substitution A G intron_variant BRCA-EU 2 32741845 32741845 single base substitution T G downstream_gene_variant BRCA-EU 2 32741845 32741845 single base substitution T G intron_variant BRCA-EU 2 32741856 32741856 single base substitution A C downstream_gene_variant BRCA-EU 2 32741856 32741856 single base substitution A C intron_variant BRCA-EU 2 32742272 32742272 single base substitution G T downstream_gene_variant BRCA-EU 2 32742272 32742272 single base substitution G T intron_variant BRCA-EU 2 32743661 32743661 insertion of <=200bp - TAGCC intron_variant BRCA-EU 2 32746104 32746104 single base substitution T G downstream_gene_variant BRCA-EU 2 32746104 32746104 single base substitution T G intron_variant BRCA-EU 2 32746104 32746104 single base substitution T G upstream_gene_variant BRCA-EU 2 32747065 32747065 insertion of <=200bp - T downstream_gene_variant BRCA-EU 2 32747065 32747065 insertion of <=200bp - T intron_variant BRCA-EU 2 32747065 32747065 insertion of <=200bp - T upstream_gene_variant BRCA-EU 2 32747248 32747248 single base substitution C T downstream_gene_variant BRCA-EU 2 32747248 32747248 single base substitution C T intron_variant BRCA-EU 2 32747248 32747248 single base substitution C T upstream_gene_variant BRCA-EU 2 32747958 32747958 single base substitution T C downstream_gene_variant BRCA-EU 2 32747958 32747958 single base substitution T C intron_variant BRCA-EU 2 32747958 32747958 single base substitution T C upstream_gene_variant BRCA-EU 2 32748211 32748211 single base substitution C G downstream_gene_variant BRCA-EU 2 32748211 32748211 single base substitution C G intron_variant BRCA-EU 2 32748211 32748211 single base substitution C G upstream_gene_variant BRCA-EU 2 32749135 32749135 single base substitution G T downstream_gene_variant BRCA-EU 2 32749135 32749135 single base substitution G T intron_variant BRCA-EU 2 32749135 32749135 single base substitution G T upstream_gene_variant BRCA-EU 2 32750194 32750194 single base substitution G C intron_variant BRCA-EU 2 32750671 32750671 single base substitution C A exon_variant BRCA-EU 2 32750671 32750671 single base substitution C A missense_variant H3966N 11896C>A BRCA-EU 2 32752273 32752273 single base substitution C T intron_variant BRCA-EU 2 32753756 32753756 single base substitution C T intron_variant BRCA-EU 2 32754807 32754807 single base substitution C G exon_variant BRCA-EU 2 32754807 32754807 single base substitution C G missense_variant L4004V 12010C>G BRCA-EU 2 32755782 32755782 single base substitution T A intron_variant BRCA-EU 2 32756156 32756156 single base substitution C T intron_variant BRCA-EU 2 32756642 32756642 single base substitution G A intron_variant BRCA-EU 2 32757874 32757874 single base substitution C G intron_variant BRCA-EU 2 32758998 32758998 single base substitution C G intron_variant BRCA-EU 2 32760150 32760150 single base substitution G A intron_variant BRCA-EU 2 32760288 32760288 single base substitution A G intron_variant BRCA-EU 2 32761215 32761215 single base substitution G A intron_variant BRCA-EU 2 32761436 32761436 single base substitution G T intron_variant BRCA-EU 2 32762036 32762036 single base substitution T C intron_variant BRCA-EU 2 32763247 32763247 single base substitution G C intron_variant BRCA-EU 2 32763926 32763926 single base substitution G T intron_variant BRCA-EU 2 32764488 32764488 single base substitution A G intron_variant BRCA-EU 2 32764785 32764785 single base substitution C T intron_variant BRCA-EU 2 32765504 32765504 single base substitution G A intron_variant BRCA-EU 2 32766403 32766403 single base substitution T C intron_variant BRCA-EU 2 32768426 32768426 single base substitution C G exon_variant BRCA-EU 2 32768426 32768426 single base substitution C G missense_variant A4137G 12410C>G BRCA-EU 2 32770120 32770120 deletion of <=200bp A - intron_variant BRCA-EU 2 32770120 32770120 insertion of <=200bp - A intron_variant BRCA-EU 2 32770201 32770202 deletion of <=200bp TC - intron_variant BRCA-EU 2 32771511 32771511 single base substitution G T intron_variant BRCA-EU 2 32773119 32773119 deletion of <=200bp T - intron_variant BRCA-EU 2 32777080 32777080 single base substitution G A intron_variant BRCA-EU 2 32777877 32777877 single base substitution G A intron_variant BRCA-EU 2 32778653 32778653 single base substitution C T intron_variant BRCA-EU 2 32780600 32780600 single base substitution G C intron_variant BRCA-EU 2 32781292 32781292 single base substitution C G intron_variant BRCA-EU 2 32785014 32785014 single base substitution C T intron_variant BRCA-EU 2 32786680 32786680 deletion of <=200bp T - intron_variant BRCA-EU 2 32787931 32787931 insertion of <=200bp - T intron_variant BRCA-EU 2 32788096 32788096 single base substitution G C intron_variant BRCA-EU 2 32791229 32791229 single base substitution A T intron_variant BRCA-EU 2 32791737 32791737 single base substitution G A intron_variant BRCA-EU 2 32793438 32793438 single base substitution T G intron_variant BRCA-EU 2 32793532 32793532 single base substitution C A intron_variant BRCA-EU 2 32794275 32794275 single base substitution T A intron_variant BRCA-EU 2 32794336 32794336 single base substitution G A intron_variant BRCA-EU 2 32795347 32795347 deletion of <=200bp T - intron_variant BRCA-EU 2 32795406 32795406 single base substitution G A intron_variant BRCA-EU 2 32795406 32795406 single base substitution G A upstream_gene_variant BRCA-EU 2 32796106 32796106 single base substitution G A intron_variant BRCA-EU 2 32796106 32796106 single base substitution G A upstream_gene_variant BRCA-EU 2 32799826 32799826 deletion of <=200bp T - intron_variant BRCA-EU 2 32799826 32799826 deletion of <=200bp T - upstream_gene_variant BRCA-EU 2 32800817 32800817 single base substitution G C intron_variant BRCA-EU 2 32802053 32802053 single base substitution G C intron_variant BRCA-EU 2 32802091 32802091 deletion of <=200bp C - intron_variant BRCA-EU 2 32802187 32802187 single base substitution C T intron_variant BRCA-EU 2 32802888 32802888 single base substitution C G intron_variant BRCA-EU 2 32805323 32805323 single base substitution C G intron_variant BRCA-EU 2 32806424 32806424 single base substitution T C intron_variant BRCA-EU 2 32806553 32806553 deletion of <=200bp T - intron_variant BRCA-EU 2 32807567 32807567 single base substitution A G intron_variant BRCA-EU 2 32808809 32808809 single base substitution T C intron_variant BRCA-EU 2 32810030 32810030 deletion of <=200bp A - intron_variant BRCA-EU 2 32811141 32811141 single base substitution G C intron_variant BRCA-EU 2 32812914 32812914 single base substitution G T intron_variant BRCA-EU 2 32812947 32812947 single base substitution G C intron_variant BRCA-EU 2 32814104 32814104 deletion of <=200bp T - intron_variant BRCA-EU 2 32815368 32815368 single base substitution C A intron_variant BRCA-EU 2 32816007 32816007 single base substitution C G exon_variant BRCA-EU 2 32816007 32816007 single base substitution C G intron_variant BRCA-EU 2 32816264 32816264 single base substitution T G intron_variant BRCA-EU 2 32817042 32817042 single base substitution C G intron_variant BRCA-EU 2 32818664 32818664 single base substitution A G intron_variant BRCA-EU 2 32818743 32818743 single base substitution A G intron_variant BRCA-EU 2 32819023 32819023 single base substitution C T exon_variant BRCA-EU 2 32819023 32819023 single base substitution C T missense_variant A4466V 13397C>T BRCA-EU 2 32819505 32819505 deletion of <=200bp C - downstream_gene_variant BRCA-EU 2 32819505 32819505 deletion of <=200bp C - intron_variant BRCA-EU 2 32820071 32820071 single base substitution T C downstream_gene_variant BRCA-EU 2 32820071 32820071 single base substitution T C intron_variant BRCA-EU 2 32820253 32820253 deletion of <=200bp T - downstream_gene_variant BRCA-EU 2 32820253 32820253 deletion of <=200bp T - intron_variant BRCA-EU 2 32820311 32820311 single base substitution C T downstream_gene_variant BRCA-EU 2 32820311 32820311 single base substitution C T intron_variant BRCA-EU 2 32821837 32821837 single base substitution C G downstream_gene_variant BRCA-EU 2 32821837 32821837 single base substitution C G intron_variant BRCA-EU 2 32822278 32822278 single base substitution G C downstream_gene_variant BRCA-EU 2 32822278 32822278 single base substitution G C intron_variant BRCA-EU 2 32822316 32822316 single base substitution C T downstream_gene_variant BRCA-EU 2 32822316 32822316 single base substitution C T intron_variant BRCA-EU 2 32825680 32825680 single base substitution T G intron_variant BRCA-EU 2 32825680 32825680 single base substitution T G upstream_gene_variant BRCA-EU 2 32826343 32826343 single base substitution T G intron_variant BRCA-EU 2 32826343 32826343 single base substitution T G upstream_gene_variant BRCA-EU 2 32826551 32826551 single base substitution G A intron_variant BRCA-EU 2 32826551 32826551 single base substitution G A upstream_gene_variant BRCA-EU 2 32828247 32828247 deletion of <=200bp A - intron_variant BRCA-EU 2 32828674 32828674 single base substitution C T intron_variant BRCA-EU 2 32829604 32829604 single base substitution G T intron_variant BRCA-EU 2 32830370 32830370 single base substitution T C intron_variant BRCA-EU 2 32832627 32832627 single base substitution G A exon_variant BRCA-EU 2 32832627 32832627 single base substitution G A missense_variant E4726K 14176G>A BRCA-EU 2 32835092 32835092 insertion of <=200bp - A intron_variant BRCA-EU 2 32835824 32835824 single base substitution C G intron_variant BRCA-EU 2 32836817 32836817 deletion of <=200bp T - downstream_gene_variant BRCA-EU 2 32836817 32836817 deletion of <=200bp T - intron_variant BRCA-EU 2 32838126 32838126 single base substitution C A downstream_gene_variant BRCA-EU 2 32838126 32838126 single base substitution C A intron_variant BRCA-EU 2 32838602 32838602 single base substitution C T downstream_gene_variant BRCA-EU 2 32838602 32838602 single base substitution C T intron_variant BRCA-EU 2 32839369 32839369 single base substitution C G downstream_gene_variant BRCA-EU 2 32839369 32839369 single base substitution C G intron_variant BRCA-EU 2 32839732 32839732 single base substitution T A downstream_gene_variant BRCA-EU 2 32839732 32839732 single base substitution T A intron_variant BRCA-EU 2 32840087 32840087 single base substitution T G downstream_gene_variant BRCA-EU 2 32840087 32840087 single base substitution T G intron_variant BRCA-EU 2 32840890 32840890 single base substitution C T downstream_gene_variant BRCA-EU 2 32840890 32840890 single base substitution C T intron_variant BRCA-EU 2 32841836 32841836 single base substitution T C intron_variant BRCA-EU 2 32842292 32842292 deletion of <=200bp C - intron_variant BRCA-EU 2 32845552 32845552 single base substitution G T downstream_gene_variant BRCA-EU 2 32845858 32845858 single base substitution C T downstream_gene_variant BRCA-EU 2 32846983 32846983 deletion of <=200bp A - downstream_gene_variant BRCA-EU 2 32846983 32846984 deletion of <=200bp AA - downstream_gene_variant BRCA-EU 2 32847886 32847905 deletion of <=200bp CTGCTATTTTTGTTATTGCC - downstream_gene_variant BRCA-EU 2 32847981 32847981 single base substitution T C downstream_gene_variant BRCA-EU 2 32848058 32848058 single base substitution A G downstream_gene_variant BRCA-EU 2 32848084 32848084 single base substitution A T downstream_gene_variant BRCA-FR 2 32578646 32578646 single base substitution C T upstream_gene_variant BRCA-FR 2 32607243 32607243 single base substitution A G intron_variant BRCA-FR 2 32617678 32617678 single base substitution T A intron_variant BRCA-FR 2 32626310 32626310 single base substitution C G exon_variant BRCA-FR 2 32626310 32626310 single base substitution C G missense_variant L372V 1114C>G BRCA-FR 2 32638278 32638278 single base substitution C T intron_variant BRCA-FR 2 32643738 32643738 single base substitution G A intron_variant BRCA-FR 2 32654116 32654116 single base substitution T A intron_variant BRCA-FR 2 32654116 32654116 single base substitution T A upstream_gene_variant BRCA-FR 2 32656962 32656962 single base substitution A G intron_variant BRCA-FR 2 32656962 32656962 single base substitution A G upstream_gene_variant BRCA-FR 2 32670840 32670840 single base substitution C G downstream_gene_variant BRCA-FR 2 32670840 32670840 single base substitution C G intron_variant BRCA-FR 2 32677918 32677918 single base substitution C T downstream_gene_variant BRCA-FR 2 32677918 32677918 single base substitution C T intron_variant BRCA-FR 2 32702559 32702559 single base substitution G T downstream_gene_variant BRCA-FR 2 32702559 32702559 single base substitution G T stop_gained E2326* 6976G>T BRCA-FR 2 32702560 32702560 single base substitution A T downstream_gene_variant BRCA-FR 2 32702560 32702560 single base substitution A T missense_variant E2326V 6977A>T BRCA-FR 2 32702622 32702622 single base substitution C G downstream_gene_variant BRCA-FR 2 32702622 32702622 single base substitution C G missense_variant H2347D 7039C>G BRCA-FR 2 32704040 32704040 single base substitution A G downstream_gene_variant BRCA-FR 2 32704040 32704040 single base substitution A G intron_variant BRCA-FR 2 32713211 32713211 single base substitution C T intron_variant BRCA-FR 2 32713792 32713792 single base substitution T C intron_variant BRCA-FR 2 32715923 32715923 single base substitution C T intron_variant BRCA-FR 2 32718244 32718244 single base substitution G C intron_variant BRCA-FR 2 32718293 32718293 single base substitution C G intron_variant BRCA-FR 2 32720343 32720343 single base substitution C G intron_variant BRCA-FR 2 32722023 32722023 single base substitution C T intron_variant BRCA-FR 2 32726309 32726309 single base substitution C A intron_variant BRCA-FR 2 32726309 32726309 single base substitution C A upstream_gene_variant BRCA-FR 2 32727104 32727104 single base substitution A C intron_variant BRCA-FR 2 32727104 32727104 single base substitution A C upstream_gene_variant BRCA-FR 2 32736956 32736956 single base substitution G T intron_variant BRCA-FR 2 32736956 32736956 single base substitution G T upstream_gene_variant BRCA-FR 2 32750194 32750194 single base substitution G C intron_variant BRCA-FR 2 32770578 32770578 single base substitution A T intron_variant BRCA-FR 2 32788096 32788096 single base substitution G C intron_variant BRCA-FR 2 32791229 32791229 single base substitution A T intron_variant BRCA-FR 2 32792698 32792698 single base substitution C T intron_variant BRCA-FR 2 32794275 32794275 single base substitution T A intron_variant BRCA-FR 2 32795484 32795484 single base substitution C G intron_variant BRCA-FR 2 32795484 32795484 single base substitution C G upstream_gene_variant BRCA-FR 2 32805323 32805323 single base substitution C G intron_variant BRCA-FR 2 32811141 32811141 single base substitution G C intron_variant BRCA-FR 2 32815368 32815368 single base substitution C A intron_variant BRCA-FR 2 32822278 32822278 single base substitution G C downstream_gene_variant BRCA-FR 2 32822278 32822278 single base substitution G C intron_variant BRCA-FR 2 32842613 32842613 single base substitution C T intron_variant BRCA-UK 2 32577930 32577930 single base substitution C T upstream_gene_variant BRCA-UK 2 32582795 32582795 single base substitution C T intron_variant BRCA-UK 2 32591808 32591808 single base substitution T C intron_variant BRCA-UK 2 32603721 32603721 single base substitution C A intron_variant BRCA-UK 2 32615953 32615953 single base substitution T C intron_variant BRCA-UK 2 32626671 32626671 single base substitution A G downstream_gene_variant BRCA-UK 2 32626671 32626671 single base substitution A G missense_variant I466M 1398A>G BRCA-UK 2 32640805 32640805 single base substitution G C missense_variant E816Q 2446G>C BRCA-UK 2 32641081 32641081 single base substitution C G missense_variant Q908E 2722C>G BRCA-UK 2 32651529 32651529 single base substitution G A intron_variant BRCA-UK 2 32667454 32667454 single base substitution G A downstream_gene_variant BRCA-UK 2 32667454 32667454 single base substitution G A missense_variant R1390H 4169G>A BRCA-UK 2 32667454 32667454 single base substitution G A upstream_gene_variant BRCA-UK 2 32680690 32680690 single base substitution G A intron_variant BRCA-UK 2 32684437 32684437 single base substitution C G intron_variant BRCA-UK 2 32686727 32686727 single base substitution G A intron_variant BRCA-UK 2 32690199 32690199 single base substitution C T missense_variant H1775Y 5323C>T BRCA-UK 2 32694762 32694762 single base substitution G C intron_variant BRCA-UK 2 32694762 32694762 single base substitution G C upstream_gene_variant BRCA-UK 2 32703818 32703818 single base substitution G T downstream_gene_variant BRCA-UK 2 32703818 32703818 single base substitution G T missense_variant G2395V 7184G>T BRCA-UK 2 32714644 32714644 single base substitution C G intron_variant BRCA-UK 2 32727433 32727433 single base substitution G C intron_variant BRCA-UK 2 32727433 32727433 single base substitution G C upstream_gene_variant BRCA-UK 2 32738608 32738608 single base substitution G A downstream_gene_variant BRCA-UK 2 32738608 32738608 single base substitution G A intron_variant BRCA-UK 2 32738608 32738608 single base substitution G A upstream_gene_variant BRCA-UK 2 32743990 32743990 single base substitution C T exon_variant BRCA-UK 2 32743990 32743990 single base substitution C T missense_variant S3867L 11600C>T BRCA-UK 2 32744484 32744484 single base substitution C T downstream_gene_variant BRCA-UK 2 32744484 32744484 single base substitution C T intron_variant BRCA-UK 2 32750374 32750374 single base substitution G A intron_variant BRCA-UK 2 32785606 32785606 single base substitution C G intron_variant BRCA-UK 2 32789163 32789163 single base substitution C A intron_variant BRCA-UK 2 32791737 32791737 single base substitution G A intron_variant BRCA-UK 2 32835092 32835092 insertion of <=200bp - A intron_variant BRCA-US 2 32602710 32602710 single base substitution T C missense_variant I127T 380T>C BRCA-US 2 32631603 32631603 single base substitution T C synonymous_variant H485H 1455T>C BRCA-US 2 32640645 32640645 single base substitution A G synonymous_variant Q762Q 2286A>G BRCA-US 2 32640653 32640653 single base substitution C A missense_variant A765D 2294C>A BRCA-US 2 32640667 32640669 deletion of <=200bp AAT - inframe_deletion N770 BRCA-US 2 32654312 32654312 single base substitution T C missense_variant S991P 2971T>C BRCA-US 2 32654312 32654312 single base substitution T C upstream_gene_variant BRCA-US 2 32656007 32656007 single base substitution A G missense_variant T1033A 3097A>G BRCA-US 2 32656007 32656007 single base substitution A G upstream_gene_variant BRCA-US 2 32673930 32673930 deletion of <=200bp A - exon_variant BRCA-US 2 32673930 32673930 deletion of <=200bp A - frameshift_variant K1518 BRCA-US 2 32688310 32688310 single base substitution C T missense_variant T1601I 4802C>T BRCA-US 2 32694469 32694469 single base substitution C T missense_variant S2045F 6134C>T BRCA-US 2 32694469 32694469 single base substitution C T upstream_gene_variant BRCA-US 2 32698261 32698261 single base substitution G T exon_variant BRCA-US 2 32698261 32698261 single base substitution G T missense_variant R2225I 6674G>T BRCA-US 2 32702619 32702619 single base substitution T A downstream_gene_variant BRCA-US 2 32702619 32702619 single base substitution T A missense_variant C2346S 7036T>A BRCA-US 2 32738164 32738164 single base substitution G A downstream_gene_variant BRCA-US 2 32738164 32738164 single base substitution G A missense_variant S3504N 10511G>A BRCA-US 2 32738164 32738164 single base substitution G A upstream_gene_variant BRCA-US 2 32738180 32738180 single base substitution A G downstream_gene_variant BRCA-US 2 32738180 32738180 single base substitution A G synonymous_variant V3509V 10527A>G BRCA-US 2 32738180 32738180 single base substitution A G upstream_gene_variant BRCA-US 2 32740628 32740628 single base substitution G A downstream_gene_variant BRCA-US 2 32740628 32740628 single base substitution G A missense_variant A3714T 11140G>A BRCA-US 2 32740628 32740628 single base substitution G A upstream_gene_variant BRCA-US 2 32743984 32743984 single base substitution C T exon_variant BRCA-US 2 32743984 32743984 single base substitution C T missense_variant T3865I 11594C>T BRCA-US 2 32768600 32768600 single base substitution G T exon_variant BRCA-US 2 32768600 32768600 single base substitution G T missense_variant G4195V 12584G>T BRCA-US 2 32770731 32770731 single base substitution C T exon_variant BRCA-US 2 32770731 32770731 single base substitution C T missense_variant S4205L 12614C>T BRCA-US 2 32770872 32770872 single base substitution C T exon_variant BRCA-US 2 32770872 32770872 single base substitution C T missense_variant S4252F 12755C>T BRCA-US 2 32774504 32774504 single base substitution C T exon_variant BRCA-US 2 32774504 32774504 single base substitution C T missense_variant S4367F 13100C>T BRCA-US 2 32800342 32800342 single base substitution G A exon_variant BRCA-US 2 32800342 32800342 single base substitution G A missense_variant E4422K 13264G>A BRCA-US 2 32800342 32800342 single base substitution G A upstream_gene_variant BRCA-US 2 32822992 32822992 single base substitution G T downstream_gene_variant BRCA-US 2 32822992 32822992 single base substitution G T exon_variant BRCA-US 2 32822992 32822992 single base substitution G T missense_variant S4596I 13787G>T BRCA-US 2 32822992 32822992 single base substitution G T upstream_gene_variant BRCA-US 2 32824821 32824821 single base substitution C A exon_variant BRCA-US 2 32824821 32824821 single base substitution C A missense_variant P4616T 13846C>A BRCA-US 2 32824821 32824821 single base substitution C A upstream_gene_variant BRCA-US 2 32824940 32824940 single base substitution C T exon_variant BRCA-US 2 32824940 32824940 single base substitution C T synonymous_variant F4655F 13965C>T BRCA-US 2 32824940 32824940 single base substitution C T upstream_gene_variant BRCA-US 2 32832625 32832625 single base substitution G A exon_variant BRCA-US 2 32832625 32832625 single base substitution G A missense_variant R4725Q 14174G>A BRCA-US 2 32836514 32836514 single base substitution G T splice_acceptor_variant BRCA-US 2 32836564 32836564 single base substitution G A exon_variant BRCA-US 2 32836564 32836564 single base substitution G A missense_variant C4770Y 14309G>A BTCA-JP 2 32582218 32582218 single base substitution C T 5_prime_UTR_variant BTCA-JP 2 32626511 32626511 single base substitution T C downstream_gene_variant BTCA-JP 2 32626511 32626511 single base substitution T C intron_variant BTCA-JP 2 32626676 32626676 single base substitution A T downstream_gene_variant BTCA-JP 2 32626676 32626676 single base substitution A T missense_variant K468I 1403A>T BTCA-JP 2 32640654 32640654 single base substitution C A synonymous_variant A765A 2295C>A BTCA-JP 2 32641122 32641122 single base substitution A C missense_variant E921D 2763A>C BTCA-JP 2 32656247 32656247 single base substitution A T intron_variant BTCA-JP 2 32656247 32656247 single base substitution A T upstream_gene_variant BTCA-JP 2 32656249 32656249 single base substitution C T intron_variant BTCA-JP 2 32656249 32656249 single base substitution C T upstream_gene_variant BTCA-JP 2 32660542 32660542 single base substitution A T intron_variant BTCA-JP 2 32660542 32660542 single base substitution A T upstream_gene_variant BTCA-JP 2 32660605 32660605 single base substitution G T intron_variant BTCA-JP 2 32660605 32660605 single base substitution G T missense_variant V1151F 3451G>T BTCA-JP 2 32660605 32660605 single base substitution G T upstream_gene_variant BTCA-JP 2 32667122 32667122 deletion of <=200bp T - downstream_gene_variant BTCA-JP 2 32667122 32667122 deletion of <=200bp T - intron_variant BTCA-JP 2 32667122 32667122 deletion of <=200bp T - upstream_gene_variant BTCA-JP 2 32689679 32689679 single base substitution G A missense_variant A1682T 5044G>A BTCA-JP 2 32693198 32693199 deletion of <=200bp TT - intron_variant BTCA-JP 2 32693198 32693199 deletion of <=200bp TT - upstream_gene_variant BTCA-JP 2 32707476 32707476 deletion of <=200bp T - intron_variant BTCA-JP 2 32707634 32707634 single base substitution C T synonymous_variant S2560S 7680C>T BTCA-JP 2 32728077 32728077 single base substitution T C intron_variant BTCA-JP 2 32818980 32818980 single base substitution A G splice_acceptor_variant BTCA-JP 2 32820253 32820253 deletion of <=200bp T - downstream_gene_variant BTCA-JP 2 32820253 32820253 deletion of <=200bp T - intron_variant BTCA-JP 2 32842877 32842877 single base substitution T C exon_variant BTCA-JP 2 32842877 32842877 single base substitution T C missense_variant V4827A 14480T>C BTCA-JP 2 32843055 32843055 single base substitution A G 3_prime_UTR_variant BTCA-JP 2 32843055 32843055 single base substitution A G exon_variant CESC-US 2 32605237 32605237 single base substitution C T missense_variant S175L 524C>T CESC-US 2 32605301 32605301 single base substitution C G synonymous_variant L196L 588C>G CESC-US 2 32640932 32640932 single base substitution C T missense_variant S858L 2573C>T CESC-US 2 32666475 32666475 single base substitution C G intron_variant CESC-US 2 32666475 32666475 single base substitution C G missense_variant Q1297E 3889C>G CESC-US 2 32666475 32666475 single base substitution C G missense_variant Q183E 547C>G CESC-US 2 32666475 32666475 single base substitution C G upstream_gene_variant CESC-US 2 32678919 32678919 single base substitution C T downstream_gene_variant CESC-US 2 32678919 32678919 single base substitution C T synonymous_variant F1554F 4662C>T CESC-US 2 32693008 32693008 single base substitution G A missense_variant R1870K 5609G>A CESC-US 2 32694554 32694554 single base substitution G T missense_variant K2073N 6219G>T CESC-US 2 32694554 32694554 single base substitution G T upstream_gene_variant CESC-US 2 32716581 32716581 single base substitution C T missense_variant L2766F 8296C>T CESC-US 2 32740651 32740651 single base substitution C G downstream_gene_variant CESC-US 2 32740651 32740651 single base substitution C G missense_variant H3721Q 11163C>G CESC-US 2 32740651 32740651 single base substitution C G upstream_gene_variant CESC-US 2 32743990 32743990 single base substitution C T exon_variant CESC-US 2 32743990 32743990 single base substitution C T missense_variant S3867L 11600C>T CESC-US 2 32757248 32757248 single base substitution G T intron_variant CESC-US 2 32772925 32772925 single base substitution G T exon_variant CESC-US 2 32772925 32772925 single base substitution G T synonymous_variant V4273V 12819G>T CLLE-ES 2 32580733 32580733 single base substitution A G upstream_gene_variant CLLE-ES 2 32583158 32583158 single base substitution C G intron_variant CLLE-ES 2 32605832 32605832 single base substitution C T intron_variant CLLE-ES 2 32615803 32615803 single base substitution A G intron_variant CLLE-ES 2 32619350 32619350 single base substitution A T intron_variant CLLE-ES 2 32622721 32622721 single base substitution C T intron_variant CLLE-ES 2 32639901 32639901 single base substitution A G synonymous_variant Q514Q 1542A>G CLLE-ES 2 32658175 32658175 deletion of <=200bp C - intron_variant CLLE-ES 2 32658175 32658175 deletion of <=200bp C - upstream_gene_variant CLLE-ES 2 32660378 32660378 single base substitution A T intron_variant CLLE-ES 2 32660378 32660378 single base substitution A T upstream_gene_variant CLLE-ES 2 32685243 32685243 single base substitution T A intron_variant CLLE-ES 2 32686530 32686530 single base substitution T G intron_variant CLLE-ES 2 32705538 32705538 single base substitution A G downstream_gene_variant CLLE-ES 2 32705538 32705538 single base substitution A G intron_variant CLLE-ES 2 32711421 32711421 single base substitution A G intron_variant CLLE-ES 2 32739251 32739251 single base substitution G A downstream_gene_variant CLLE-ES 2 32739251 32739251 single base substitution G A intron_variant CLLE-ES 2 32739251 32739251 single base substitution G A upstream_gene_variant CLLE-ES 2 32740548 32740548 single base substitution T G downstream_gene_variant CLLE-ES 2 32740548 32740548 single base substitution T G missense_variant L3687R 11060T>G CLLE-ES 2 32740548 32740548 single base substitution T G upstream_gene_variant CLLE-ES 2 32755228 32755228 single base substitution C T intron_variant CLLE-ES 2 32761530 32761530 single base substitution C T intron_variant CLLE-ES 2 32779007 32779007 single base substitution T C intron_variant CLLE-ES 2 32782715 32782715 single base substitution A G intron_variant CLLE-ES 2 32787674 32787674 single base substitution A T intron_variant CLLE-ES 2 32788930 32788930 single base substitution G T intron_variant CLLE-ES 2 32804892 32804892 single base substitution T C intron_variant CLLE-ES 2 32820718 32820718 single base substitution C A downstream_gene_variant CLLE-ES 2 32820718 32820718 single base substitution C A intron_variant CLLE-ES 2 32830470 32830470 single base substitution G A intron_variant CLLE-ES 2 32833233 32833233 single base substitution A T intron_variant COAD-US 2 32605255 32605255 single base substitution T C missense_variant V181A 542T>C COAD-US 2 32605312 32605312 insertion of <=200bp - A frameshift_variant L200Y? COAD-US 2 32605320 32605320 single base substitution A C missense_variant T203P 607A>C COAD-US 2 32605322 32605322 single base substitution A T synonymous_variant T203T 609A>T COAD-US 2 32626447 32626447 insertion of <=200bp - A exon_variant COAD-US 2 32626447 32626447 insertion of <=200bp - A frameshift_variant L417L? COAD-US 2 32640462 32640462 single base substitution G A synonymous_variant P701P 2103G>A COAD-US 2 32640529 32640529 single base substitution A C missense_variant K724Q 2170A>C COAD-US 2 32641017 32641017 single base substitution G T missense_variant K886N 2658G>T COAD-US 2 32661226 32661226 single base substitution C T exon_variant COAD-US 2 32661226 32661226 single base substitution C T missense_variant T1202M 3605C>T COAD-US 2 32661226 32661226 single base substitution C T missense_variant T88M 263C>T COAD-US 2 32667239 32667239 single base substitution C A 3_prime_UTR_variant COAD-US 2 32667239 32667239 single base substitution C A downstream_gene_variant COAD-US 2 32667239 32667239 single base substitution C A missense_variant L1351I 4051C>A COAD-US 2 32667239 32667239 single base substitution C A upstream_gene_variant COAD-US 2 32667499 32667499 deletion of <=200bp C - downstream_gene_variant COAD-US 2 32667499 32667499 deletion of <=200bp C - frameshift_variant A1405 COAD-US 2 32667499 32667499 deletion of <=200bp C - upstream_gene_variant COAD-US 2 32688326 32688326 single base substitution G A synonymous_variant S1606S 4818G>A COAD-US 2 32689661 32689661 single base substitution G A missense_variant V1676M 5026G>A COAD-US 2 32689838 32689838 deletion of <=200bp C - frameshift_variant P1735 COAD-US 2 32694521 32694521 single base substitution C G synonymous_variant L2062L 6186C>G COAD-US 2 32694521 32694521 single base substitution C G upstream_gene_variant COAD-US 2 32695268 32695268 single base substitution G T missense_variant R2127I 6380G>T COAD-US 2 32695268 32695268 single base substitution G T upstream_gene_variant COAD-US 2 32696194 32696194 single base substitution T G splice_donor_variant COAD-US 2 32696194 32696194 single base substitution T G upstream_gene_variant COAD-US 2 32702482 32702482 single base substitution G A downstream_gene_variant COAD-US 2 32702482 32702482 single base substitution G A missense_variant R2300H 6899G>A COAD-US 2 32703801 32703801 single base substitution A G downstream_gene_variant COAD-US 2 32703801 32703801 single base substitution A G synonymous_variant G2389G 7167A>G COAD-US 2 32704541 32704541 single base substitution G T downstream_gene_variant COAD-US 2 32704541 32704541 single base substitution G T missense_variant A2422S 7264G>T COAD-US 2 32704542 32704542 single base substitution C T downstream_gene_variant COAD-US 2 32704542 32704542 single base substitution C T missense_variant A2422V 7265C>T COAD-US 2 32707542 32707542 single base substitution A T missense_variant T2530S 7588A>T COAD-US 2 32724803 32724803 single base substitution C T synonymous_variant S2886S 8658C>T COAD-US 2 32724803 32724803 single base substitution C T upstream_gene_variant COAD-US 2 32726904 32726904 single base substitution G T missense_variant M3052I 9156G>T COAD-US 2 32726904 32726904 single base substitution G T upstream_gene_variant COAD-US 2 32733167 32733167 single base substitution T C downstream_gene_variant COAD-US 2 32733167 32733167 single base substitution T C missense_variant V3274A 9821T>C COAD-US 2 32733167 32733167 single base substitution T C upstream_gene_variant COAD-US 2 32740213 32740213 single base substitution T C downstream_gene_variant COAD-US 2 32740213 32740213 single base substitution T C synonymous_variant H3575H 10725T>C COAD-US 2 32740213 32740213 single base substitution T C upstream_gene_variant COAD-US 2 32740238 32740238 deletion of <=200bp A - downstream_gene_variant COAD-US 2 32740238 32740238 deletion of <=200bp A - frameshift_variant K3584 COAD-US 2 32740238 32740238 deletion of <=200bp A - upstream_gene_variant COAD-US 2 32740284 32740284 single base substitution C T downstream_gene_variant COAD-US 2 32740284 32740284 single base substitution C T missense_variant A3599V 10796C>T COAD-US 2 32740284 32740284 single base substitution C T upstream_gene_variant COAD-US 2 32740574 32740574 single base substitution A G downstream_gene_variant COAD-US 2 32740574 32740574 single base substitution A G missense_variant S3696G 11086A>G COAD-US 2 32740574 32740574 single base substitution A G upstream_gene_variant COAD-US 2 32754748 32754748 single base substitution C T exon_variant COAD-US 2 32754748 32754748 single base substitution C T missense_variant A3984V 11951C>T COAD-US 2 32754832 32754832 single base substitution T C exon_variant COAD-US 2 32754832 32754832 single base substitution T C missense_variant V4012A 12035T>C COAD-US 2 32754865 32754865 single base substitution C A exon_variant COAD-US 2 32754865 32754865 single base substitution C A missense_variant S4023Y 12068C>A COAD-US 2 32800258 32800258 single base substitution G T exon_variant COAD-US 2 32800258 32800258 single base substitution G T missense_variant A4394S 13180G>T COAD-US 2 32800258 32800258 single base substitution G T upstream_gene_variant COAD-US 2 32800267 32800267 single base substitution G A exon_variant COAD-US 2 32800267 32800267 single base substitution G A missense_variant E4397K 13189G>A COAD-US 2 32800267 32800267 single base substitution G A upstream_gene_variant COAD-US 2 32800427 32800427 single base substitution G A exon_variant COAD-US 2 32800427 32800427 single base substitution G A missense_variant R4450H 13349G>A COAD-US 2 32820101 32820101 deletion of <=200bp A - downstream_gene_variant COAD-US 2 32820101 32820101 deletion of <=200bp A - frameshift_variant E4501 COAD-US 2 32820101 32820101 deletion of <=200bp A - splice_region_variant COAD-US 2 32822957 32822957 single base substitution G A downstream_gene_variant COAD-US 2 32822957 32822957 single base substitution G A exon_variant COAD-US 2 32822957 32822957 single base substitution G A synonymous_variant T4584T 13752G>A COAD-US 2 32822957 32822957 single base substitution G A upstream_gene_variant COAD-US 2 32824826 32824826 single base substitution G T exon_variant COAD-US 2 32824826 32824826 single base substitution G T synonymous_variant A4617A 13851G>T COAD-US 2 32824826 32824826 single base substitution G T upstream_gene_variant COAD-US 2 32842945 32842945 single base substitution G T exon_variant COAD-US 2 32842945 32842945 single base substitution G T stop_gained E4850* 14548G>T COCA-CN 2 32582113 32582113 single base substitution C A 5_prime_UTR_variant COCA-CN 2 32582596 32582596 single base substitution G T intron_variant COCA-CN 2 32639968 32639968 single base substitution G T stop_gained E537* 1609G>T COCA-CN 2 32640386 32640386 single base substitution A G missense_variant E676G 2027A>G COCA-CN 2 32641105 32641105 single base substitution G T missense_variant D916Y 2746G>T COCA-CN 2 32661218 32661218 single base substitution A C exon_variant COCA-CN 2 32661218 32661218 single base substitution A C synonymous_variant G1199G 3597A>C COCA-CN 2 32661218 32661218 single base substitution A C synonymous_variant G85G 255A>C COCA-CN 2 32661310 32661310 single base substitution G A intron_variant COCA-CN 2 32662506 32662506 single base substitution C A intron_variant COCA-CN 2 32666457 32666457 single base substitution C T intron_variant COCA-CN 2 32666457 32666457 single base substitution C T missense_variant R1291W 3871C>T COCA-CN 2 32666457 32666457 single base substitution C T missense_variant R177W 529C>T COCA-CN 2 32666457 32666457 single base substitution C T upstream_gene_variant COCA-CN 2 32667454 32667454 single base substitution G A downstream_gene_variant COCA-CN 2 32667454 32667454 single base substitution G A missense_variant R1390H 4169G>A COCA-CN 2 32667454 32667454 single base substitution G A upstream_gene_variant COCA-CN 2 32668438 32668438 single base substitution G A downstream_gene_variant COCA-CN 2 32668438 32668438 single base substitution G A intron_variant COCA-CN 2 32668438 32668438 single base substitution G A upstream_gene_variant COCA-CN 2 32689713 32689713 single base substitution T C missense_variant V1693A 5078T>C COCA-CN 2 32689913 32689913 single base substitution T C intron_variant COCA-CN 2 32690236 32690236 single base substitution A C splice_region_variant COCA-CN 2 32690273 32690273 single base substitution G T intron_variant COCA-CN 2 32702455 32702455 single base substitution G A downstream_gene_variant COCA-CN 2 32702455 32702455 single base substitution G A missense_variant R2291H 6872G>A COCA-CN 2 32713706 32713706 single base substitution A T missense_variant T2674S 8020A>T COCA-CN 2 32715119 32715119 single base substitution A G missense_variant S2703G 8107A>G COCA-CN 2 32716518 32716518 single base substitution C T stop_gained Q2745* 8233C>T COCA-CN 2 32718637 32718637 single base substitution G T stop_gained E2791* 8371G>T COCA-CN 2 32724582 32724582 single base substitution C T intron_variant COCA-CN 2 32724582 32724582 single base substitution C T upstream_gene_variant COCA-CN 2 32724586 32724586 single base substitution T C intron_variant COCA-CN 2 32724586 32724586 single base substitution T C upstream_gene_variant COCA-CN 2 32724588 32724588 single base substitution C G intron_variant COCA-CN 2 32724588 32724588 single base substitution C G upstream_gene_variant COCA-CN 2 32729968 32729968 single base substitution G A intron_variant COCA-CN 2 32729968 32729968 single base substitution G A upstream_gene_variant COCA-CN 2 32730060 32730064 deletion of <=200bp TATCT - intron_variant COCA-CN 2 32730060 32730064 deletion of <=200bp TATCT - splice_region_variant COCA-CN 2 32730060 32730064 deletion of <=200bp TATCT - upstream_gene_variant COCA-CN 2 32733150 32733150 single base substitution G A downstream_gene_variant COCA-CN 2 32733150 32733150 single base substitution G A synonymous_variant Q3268Q 9804G>A COCA-CN 2 32733150 32733150 single base substitution G A upstream_gene_variant COCA-CN 2 32733336 32733336 single base substitution G T downstream_gene_variant COCA-CN 2 32733336 32733336 single base substitution G T intron_variant COCA-CN 2 32733336 32733336 single base substitution G T upstream_gene_variant COCA-CN 2 32741771 32741771 single base substitution T C downstream_gene_variant COCA-CN 2 32741771 32741771 single base substitution T C intron_variant COCA-CN 2 32743390 32743390 single base substitution T C exon_variant COCA-CN 2 32743390 32743390 single base substitution T C missense_variant F3807L 11419T>C COCA-CN 2 32770823 32770823 single base substitution C T exon_variant COCA-CN 2 32770823 32770823 single base substitution C T missense_variant R4236W 12706C>T COCA-CN 2 32819112 32819112 single base substitution C T exon_variant COCA-CN 2 32819112 32819112 single base substitution C T missense_variant R4496W 13486C>T COCA-CN 2 32820221 32820221 single base substitution A C downstream_gene_variant COCA-CN 2 32820221 32820221 single base substitution A C intron_variant COCA-CN 2 32832645 32832645 single base substitution C T exon_variant COCA-CN 2 32832645 32832645 single base substitution C T stop_gained R4732* 14194C>T COCA-CN 2 32842945 32842945 single base substitution G T exon_variant COCA-CN 2 32842945 32842945 single base substitution G T stop_gained E4850* 14548G>T EOPC-DE 2 32580696 32580696 single base substitution T A upstream_gene_variant EOPC-DE 2 32624512 32624512 single base substitution A G intron_variant EOPC-DE 2 32759238 32759238 single base substitution C T intron_variant ESAD-UK 2 32577851 32577851 single base substitution T G upstream_gene_variant ESAD-UK 2 32579954 32579954 single base substitution A C upstream_gene_variant ESAD-UK 2 32580048 32580048 single base substitution G A upstream_gene_variant ESAD-UK 2 32580838 32580838 single base substitution C G upstream_gene_variant ESAD-UK 2 32589275 32589275 single base substitution C T intron_variant ESAD-UK 2 32589695 32589695 single base substitution T C intron_variant ESAD-UK 2 32592556 32592556 single base substitution A G intron_variant ESAD-UK 2 32592629 32592629 single base substitution C T intron_variant ESAD-UK 2 32595908 32595908 single base substitution G A intron_variant ESAD-UK 2 32596077 32596077 single base substitution A G intron_variant ESAD-UK 2 32596595 32596595 single base substitution G A intron_variant ESAD-UK 2 32596918 32596918 single base substitution G A intron_variant ESAD-UK 2 32598336 32598336 single base substitution G A intron_variant ESAD-UK 2 32598964 32598964 single base substitution C G intron_variant ESAD-UK 2 32600569 32600569 single base substitution C A intron_variant ESAD-UK 2 32600763 32600763 single base substitution G A intron_variant ESAD-UK 2 32601914 32601914 insertion of <=200bp - TACA intron_variant ESAD-UK 2 32601916 32601918 deletion of <=200bp CTC - intron_variant ESAD-UK 2 32601919 32601919 single base substitution T A intron_variant ESAD-UK 2 32603767 32603767 single base substitution C T intron_variant ESAD-UK 2 32604577 32604577 insertion of <=200bp - T intron_variant ESAD-UK 2 32605411 32605411 single base substitution C T intron_variant ESAD-UK 2 32608547 32608547 single base substitution A G intron_variant ESAD-UK 2 32609319 32609319 single base substitution A G intron_variant ESAD-UK 2 32609319 32609319 single base substitution A G upstream_gene_variant ESAD-UK 2 32610217 32610217 deletion of <=200bp A - intron_variant ESAD-UK 2 32610217 32610217 deletion of <=200bp A - upstream_gene_variant ESAD-UK 2 32610959 32610959 single base substitution G A intron_variant ESAD-UK 2 32610959 32610959 single base substitution G A upstream_gene_variant ESAD-UK 2 32611516 32611516 single base substitution T C intron_variant ESAD-UK 2 32611516 32611516 single base substitution T C upstream_gene_variant ESAD-UK 2 32611518 32611518 single base substitution T C intron_variant ESAD-UK 2 32611518 32611518 single base substitution T C upstream_gene_variant ESAD-UK 2 32612967 32612967 single base substitution T C intron_variant ESAD-UK 2 32612967 32612967 single base substitution T C upstream_gene_variant ESAD-UK 2 32615050 32615050 single base substitution C G intron_variant ESAD-UK 2 32617277 32617279 deletion of <=200bp ATT - intron_variant ESAD-UK 2 32617586 32617586 single base substitution A G intron_variant ESAD-UK 2 32618233 32618233 single base substitution G A intron_variant ESAD-UK 2 32620235 32620235 single base substitution C T intron_variant ESAD-UK 2 32620613 32620613 single base substitution T C exon_variant ESAD-UK 2 32620613 32620613 single base substitution T C missense_variant F329S 986T>C ESAD-UK 2 32620747 32620747 single base substitution A T intron_variant ESAD-UK 2 32622751 32622751 single base substitution C T intron_variant ESAD-UK 2 32623608 32623608 single base substitution T A intron_variant ESAD-UK 2 32624107 32624107 single base substitution A C intron_variant ESAD-UK 2 32626281 32626281 single base substitution A C exon_variant ESAD-UK 2 32626281 32626281 single base substitution A C missense_variant H362P 1085A>C ESAD-UK 2 32628889 32628889 single base substitution G A downstream_gene_variant ESAD-UK 2 32628889 32628889 single base substitution G A intron_variant ESAD-UK 2 32632671 32632671 insertion of <=200bp - T intron_variant ESAD-UK 2 32634940 32634940 single base substitution G C intron_variant ESAD-UK 2 32637059 32637059 single base substitution G T intron_variant ESAD-UK 2 32637757 32637757 insertion of <=200bp - T intron_variant ESAD-UK 2 32637829 32637829 single base substitution C T intron_variant ESAD-UK 2 32638383 32638383 single base substitution G T intron_variant ESAD-UK 2 32638606 32638606 single base substitution C T intron_variant ESAD-UK 2 32641033 32641033 single base substitution G T stop_gained E892* 2674G>T ESAD-UK 2 32641069 32641069 single base substitution G C missense_variant V904L 2710G>C ESAD-UK 2 32641601 32641601 single base substitution C A intron_variant ESAD-UK 2 32642030 32642030 single base substitution A C intron_variant ESAD-UK 2 32643010 32643010 single base substitution G C intron_variant ESAD-UK 2 32643972 32643972 single base substitution C A intron_variant ESAD-UK 2 32644233 32644233 single base substitution G A intron_variant ESAD-UK 2 32644508 32644508 single base substitution A G intron_variant ESAD-UK 2 32645592 32645592 insertion of <=200bp - T intron_variant ESAD-UK 2 32647308 32647308 single base substitution C T intron_variant ESAD-UK 2 32648010 32648010 insertion of <=200bp - T intron_variant ESAD-UK 2 32649527 32649527 single base substitution T G intron_variant ESAD-UK 2 32650304 32650304 single base substitution C T intron_variant ESAD-UK 2 32652601 32652601 single base substitution G A intron_variant ESAD-UK 2 32654892 32654892 single base substitution C T intron_variant ESAD-UK 2 32654892 32654892 single base substitution C T upstream_gene_variant ESAD-UK 2 32657931 32657931 single base substitution T A intron_variant ESAD-UK 2 32657931 32657931 single base substitution T A upstream_gene_variant ESAD-UK 2 32658183 32658183 single base substitution C T intron_variant ESAD-UK 2 32658183 32658183 single base substitution C T upstream_gene_variant ESAD-UK 2 32660055 32660055 single base substitution G C intron_variant ESAD-UK 2 32660055 32660055 single base substitution G C upstream_gene_variant ESAD-UK 2 32660921 32660921 single base substitution C T intron_variant ESAD-UK 2 32660921 32660921 single base substitution C T upstream_gene_variant ESAD-UK 2 32666204 32666204 deletion of <=200bp T - intron_variant ESAD-UK 2 32666204 32666204 deletion of <=200bp T - upstream_gene_variant ESAD-UK 2 32667987 32667987 single base substitution C T downstream_gene_variant ESAD-UK 2 32667987 32667987 single base substitution C T intron_variant ESAD-UK 2 32667987 32667987 single base substitution C T upstream_gene_variant ESAD-UK 2 32668826 32668826 single base substitution G A downstream_gene_variant ESAD-UK 2 32668826 32668826 single base substitution G A intron_variant ESAD-UK 2 32669390 32669390 single base substitution C T downstream_gene_variant ESAD-UK 2 32669390 32669390 single base substitution C T intron_variant ESAD-UK 2 32669825 32669825 insertion of <=200bp - A downstream_gene_variant ESAD-UK 2 32669825 32669825 insertion of <=200bp - A intron_variant ESAD-UK 2 32670108 32670108 single base substitution G A downstream_gene_variant ESAD-UK 2 32670108 32670108 single base substitution G A intron_variant ESAD-UK 2 32670769 32670769 single base substitution C T downstream_gene_variant ESAD-UK 2 32670769 32670769 single base substitution C T intron_variant ESAD-UK 2 32673909 32673909 single base substitution G A exon_variant ESAD-UK 2 32673909 32673909 single base substitution G A missense_variant E1511K 4531G>A ESAD-UK 2 32675658 32675658 single base substitution T C downstream_gene_variant ESAD-UK 2 32675658 32675658 single base substitution T C intron_variant ESAD-UK 2 32676344 32676344 single base substitution C T downstream_gene_variant ESAD-UK 2 32676344 32676344 single base substitution C T intron_variant ESAD-UK 2 32676406 32676406 single base substitution T G downstream_gene_variant ESAD-UK 2 32676406 32676406 single base substitution T G intron_variant ESAD-UK 2 32679578 32679578 single base substitution G A intron_variant ESAD-UK 2 32679694 32679694 single base substitution G A intron_variant ESAD-UK 2 32681117 32681117 single base substitution T C intron_variant ESAD-UK 2 32682972 32682972 single base substitution C G intron_variant ESAD-UK 2 32684099 32684099 single base substitution G C intron_variant ESAD-UK 2 32685161 32685161 single base substitution G A intron_variant ESAD-UK 2 32685798 32685798 single base substitution T G intron_variant ESAD-UK 2 32687369 32687369 single base substitution A C intron_variant ESAD-UK 2 32687526 32687526 single base substitution G A intron_variant ESAD-UK 2 32692866 32692866 single base substitution A C intron_variant ESAD-UK 2 32693117 32693117 single base substitution C T synonymous_variant N1906N 5718C>T ESAD-UK 2 32693117 32693117 single base substitution C T upstream_gene_variant ESAD-UK 2 32693286 32693286 single base substitution G A intron_variant ESAD-UK 2 32693286 32693286 single base substitution G A upstream_gene_variant ESAD-UK 2 32694681 32694681 single base substitution A T missense_variant R2116W 6346A>T ESAD-UK 2 32694681 32694681 single base substitution A T upstream_gene_variant ESAD-UK 2 32695048 32695048 single base substitution T C intron_variant ESAD-UK 2 32695048 32695048 single base substitution T C upstream_gene_variant ESAD-UK 2 32697150 32697150 single base substitution G T intron_variant ESAD-UK 2 32697150 32697150 single base substitution G T upstream_gene_variant ESAD-UK 2 32698204 32698204 single base substitution A G exon_variant ESAD-UK 2 32698204 32698204 single base substitution A G missense_variant N2206S 6617A>G ESAD-UK 2 32699292 32699292 single base substitution C T intron_variant ESAD-UK 2 32700616 32700616 single base substitution T A intron_variant ESAD-UK 2 32700789 32700789 deletion of <=200bp T - intron_variant ESAD-UK 2 32702562 32702562 single base substitution C A downstream_gene_variant ESAD-UK 2 32702562 32702562 single base substitution C A missense_variant R2327S 6979C>A ESAD-UK 2 32702683 32702683 single base substitution T A downstream_gene_variant ESAD-UK 2 32702683 32702683 single base substitution T A intron_variant ESAD-UK 2 32702923 32702923 deletion of <=200bp T - downstream_gene_variant ESAD-UK 2 32702923 32702923 deletion of <=200bp T - intron_variant ESAD-UK 2 32705828 32705828 single base substitution G C downstream_gene_variant ESAD-UK 2 32705828 32705828 single base substitution G C intron_variant ESAD-UK 2 32706008 32706008 single base substitution G T downstream_gene_variant ESAD-UK 2 32706008 32706008 single base substitution G T intron_variant ESAD-UK 2 32706265 32706265 single base substitution G A downstream_gene_variant ESAD-UK 2 32706265 32706265 single base substitution G A intron_variant ESAD-UK 2 32708967 32708967 single base substitution G A intron_variant ESAD-UK 2 32709571 32709571 single base substitution T C intron_variant ESAD-UK 2 32710397 32710397 single base substitution T A intron_variant ESAD-UK 2 32710882 32710882 deletion of <=200bp T - intron_variant ESAD-UK 2 32710984 32710984 single base substitution G A intron_variant ESAD-UK 2 32713253 32713253 insertion of <=200bp - A intron_variant ESAD-UK 2 32714186 32714186 single base substitution G A intron_variant ESAD-UK 2 32714256 32714256 single base substitution G T intron_variant ESAD-UK 2 32714777 32714777 single base substitution C T intron_variant ESAD-UK 2 32715269 32715269 single base substitution C G intron_variant ESAD-UK 2 32716842 32716842 single base substitution C T intron_variant ESAD-UK 2 32716898 32716898 single base substitution A G intron_variant ESAD-UK 2 32717390 32717390 single base substitution C T intron_variant ESAD-UK 2 32720017 32720017 single base substitution G A intron_variant ESAD-UK 2 32723058 32723058 single base substitution C T intron_variant ESAD-UK 2 32723058 32723058 single base substitution C T upstream_gene_variant ESAD-UK 2 32723860 32723860 single base substitution C G intron_variant ESAD-UK 2 32723860 32723860 single base substitution C G upstream_gene_variant ESAD-UK 2 32727334 32727334 deletion of <=200bp T - intron_variant ESAD-UK 2 32727334 32727334 deletion of <=200bp T - upstream_gene_variant ESAD-UK 2 32728044 32728044 single base substitution T A intron_variant ESAD-UK 2 32729998 32729998 single base substitution A G intron_variant ESAD-UK 2 32729998 32729998 single base substitution A G upstream_gene_variant ESAD-UK 2 32730767 32730767 single base substitution T C downstream_gene_variant ESAD-UK 2 32730767 32730767 single base substitution T C intron_variant ESAD-UK 2 32730767 32730767 single base substitution T C upstream_gene_variant ESAD-UK 2 32730852 32730852 single base substitution A T downstream_gene_variant ESAD-UK 2 32730852 32730852 single base substitution A T intron_variant ESAD-UK 2 32730852 32730852 single base substitution A T upstream_gene_variant ESAD-UK 2 32731127 32731127 single base substitution G T downstream_gene_variant ESAD-UK 2 32731127 32731127 single base substitution G T intron_variant ESAD-UK 2 32731127 32731127 single base substitution G T upstream_gene_variant ESAD-UK 2 32731158 32731158 single base substitution T G downstream_gene_variant ESAD-UK 2 32731158 32731158 single base substitution T G intron_variant ESAD-UK 2 32731158 32731158 single base substitution T G upstream_gene_variant ESAD-UK 2 32732588 32732588 single base substitution G T downstream_gene_variant ESAD-UK 2 32732588 32732588 single base substitution G T intron_variant ESAD-UK 2 32732588 32732588 single base substitution G T upstream_gene_variant ESAD-UK 2 32736941 32736941 single base substitution A C intron_variant ESAD-UK 2 32736941 32736941 single base substitution A C upstream_gene_variant ESAD-UK 2 32737597 32737597 deletion of <=200bp A - intron_variant ESAD-UK 2 32737597 32737597 deletion of <=200bp A - upstream_gene_variant ESAD-UK 2 32739894 32739894 insertion of <=200bp - TA downstream_gene_variant ESAD-UK 2 32739894 32739894 insertion of <=200bp - TA intron_variant ESAD-UK 2 32739894 32739894 insertion of <=200bp - TA upstream_gene_variant ESAD-UK 2 32742291 32742291 single base substitution T G downstream_gene_variant ESAD-UK 2 32742291 32742291 single base substitution T G intron_variant ESAD-UK 2 32743117 32743117 single base substitution C A downstream_gene_variant ESAD-UK 2 32743117 32743117 single base substitution C A intron_variant ESAD-UK 2 32743246 32743246 single base substitution T G intron_variant ESAD-UK 2 32743458 32743458 single base substitution A T exon_variant ESAD-UK 2 32743458 32743458 single base substitution A T synonymous_variant P3829P 11487A>T ESAD-UK 2 32745183 32745183 single base substitution T A downstream_gene_variant ESAD-UK 2 32745183 32745183 single base substitution T A intron_variant ESAD-UK 2 32745183 32745183 single base substitution T A upstream_gene_variant ESAD-UK 2 32749674 32749674 single base substitution T C intron_variant ESAD-UK 2 32749674 32749674 single base substitution T C upstream_gene_variant ESAD-UK 2 32752433 32752433 single base substitution G T intron_variant ESAD-UK 2 32756338 32756338 single base substitution G T intron_variant ESAD-UK 2 32758943 32758943 single base substitution T C intron_variant ESAD-UK 2 32761275 32761275 single base substitution C T intron_variant ESAD-UK 2 32762048 32762048 single base substitution C G intron_variant ESAD-UK 2 32762578 32762578 single base substitution A G intron_variant ESAD-UK 2 32766818 32766818 single base substitution G C intron_variant ESAD-UK 2 32768170 32768170 single base substitution A T intron_variant ESAD-UK 2 32770158 32770158 single base substitution G A intron_variant ESAD-UK 2 32770657 32770657 single base substitution T C intron_variant ESAD-UK 2 32770658 32770658 single base substitution T A intron_variant ESAD-UK 2 32771327 32771327 single base substitution C T intron_variant ESAD-UK 2 32771516 32771516 single base substitution G A intron_variant ESAD-UK 2 32772707 32772707 single base substitution C T intron_variant ESAD-UK 2 32773850 32773850 deletion of <=200bp A - intron_variant ESAD-UK 2 32774250 32774250 single base substitution A G intron_variant ESAD-UK 2 32774254 32774254 single base substitution C A intron_variant ESAD-UK 2 32778338 32778338 single base substitution G A intron_variant ESAD-UK 2 32780128 32780128 single base substitution T C intron_variant ESAD-UK 2 32780328 32780328 single base substitution C G intron_variant ESAD-UK 2 32781486 32781486 single base substitution G A intron_variant ESAD-UK 2 32782335 32782335 single base substitution A G intron_variant ESAD-UK 2 32786444 32786444 single base substitution G C intron_variant ESAD-UK 2 32787529 32787529 single base substitution T G intron_variant ESAD-UK 2 32788496 32788496 single base substitution C G intron_variant ESAD-UK 2 32789016 32789016 single base substitution G A intron_variant ESAD-UK 2 32789429 32789429 single base substitution T G intron_variant ESAD-UK 2 32789486 32789486 single base substitution A T intron_variant ESAD-UK 2 32789805 32789805 single base substitution T C intron_variant ESAD-UK 2 32789916 32789916 single base substitution T C intron_variant ESAD-UK 2 32790286 32790286 single base substitution A T intron_variant ESAD-UK 2 32790729 32790729 single base substitution T A intron_variant ESAD-UK 2 32790927 32790927 single base substitution G A intron_variant ESAD-UK 2 32792436 32792436 single base substitution G A intron_variant ESAD-UK 2 32793633 32793633 single base substitution T G intron_variant ESAD-UK 2 32794276 32794276 single base substitution G C intron_variant ESAD-UK 2 32798383 32798383 single base substitution G A intron_variant ESAD-UK 2 32798383 32798383 single base substitution G A upstream_gene_variant ESAD-UK 2 32799030 32799030 single base substitution T A intron_variant ESAD-UK 2 32799030 32799030 single base substitution T A upstream_gene_variant ESAD-UK 2 32799464 32799464 single base substitution C T intron_variant ESAD-UK 2 32799464 32799464 single base substitution C T upstream_gene_variant ESAD-UK 2 32800126 32800126 single base substitution G A intron_variant ESAD-UK 2 32800126 32800126 single base substitution G A upstream_gene_variant ESAD-UK 2 32802102 32802102 single base substitution A G intron_variant ESAD-UK 2 32803068 32803068 single base substitution T G intron_variant ESAD-UK 2 32803693 32803693 single base substitution C G intron_variant ESAD-UK 2 32804017 32804017 single base substitution C T intron_variant ESAD-UK 2 32805315 32805315 single base substitution G A intron_variant ESAD-UK 2 32806553 32806553 deletion of <=200bp T - intron_variant ESAD-UK 2 32806651 32806651 single base substitution G A intron_variant ESAD-UK 2 32809169 32809169 single base substitution G C intron_variant ESAD-UK 2 32809623 32809623 deletion of <=200bp T - intron_variant ESAD-UK 2 32809947 32809947 single base substitution C G intron_variant ESAD-UK 2 32810231 32810231 single base substitution C T intron_variant ESAD-UK 2 32811447 32811447 single base substitution G T intron_variant ESAD-UK 2 32812165 32812165 deletion of <=200bp T - intron_variant ESAD-UK 2 32812395 32812395 single base substitution A G intron_variant ESAD-UK 2 32814104 32814104 deletion of <=200bp T - intron_variant ESAD-UK 2 32814164 32814164 single base substitution C T intron_variant ESAD-UK 2 32814573 32814583 deletion of <=200bp CTCCTACTTTG - intron_variant ESAD-UK 2 32816676 32816676 single base substitution A G intron_variant ESAD-UK 2 32817472 32817472 single base substitution T C intron_variant ESAD-UK 2 32817988 32817988 single base substitution T A intron_variant ESAD-UK 2 32818784 32818784 single base substitution T A intron_variant ESAD-UK 2 32822504 32822504 single base substitution C G downstream_gene_variant ESAD-UK 2 32822504 32822504 single base substitution C G intron_variant ESAD-UK 2 32823711 32823711 single base substitution A G downstream_gene_variant ESAD-UK 2 32823711 32823711 single base substitution A G intron_variant ESAD-UK 2 32823711 32823711 single base substitution A G upstream_gene_variant ESAD-UK 2 32824234 32824234 single base substitution A G downstream_gene_variant ESAD-UK 2 32824234 32824234 single base substitution A G intron_variant ESAD-UK 2 32824234 32824234 single base substitution A G upstream_gene_variant ESAD-UK 2 32824895 32824895 single base substitution C T exon_variant ESAD-UK 2 32824895 32824895 single base substitution C T synonymous_variant P4640P 13920C>T ESAD-UK 2 32824895 32824895 single base substitution C T upstream_gene_variant ESAD-UK 2 32828764 32828764 single base substitution C T intron_variant ESAD-UK 2 32828766 32828766 single base substitution G T intron_variant ESAD-UK 2 32830432 32830432 single base substitution T G intron_variant ESAD-UK 2 32830465 32830481 deletion of <=200bp AAAGAGTCCTTTTTTAT - intron_variant ESAD-UK 2 32831379 32831379 single base substitution G A intron_variant ESAD-UK 2 32831912 32831912 single base substitution A C intron_variant ESAD-UK 2 32832062 32832062 single base substitution G T intron_variant ESAD-UK 2 32832219 32832219 deletion of <=200bp T - intron_variant ESAD-UK 2 32833517 32833517 single base substitution C T intron_variant ESAD-UK 2 32834117 32834117 single base substitution T G intron_variant ESAD-UK 2 32839082 32839082 insertion of <=200bp - T downstream_gene_variant ESAD-UK 2 32839082 32839082 insertion of <=200bp - T intron_variant ESAD-UK 2 32839193 32839193 single base substitution T G downstream_gene_variant ESAD-UK 2 32839193 32839193 single base substitution T G intron_variant ESAD-UK 2 32839234 32839234 single base substitution G C downstream_gene_variant ESAD-UK 2 32839234 32839234 single base substitution G C intron_variant ESAD-UK 2 32840016 32840016 single base substitution A G downstream_gene_variant ESAD-UK 2 32840016 32840016 single base substitution A G intron_variant ESAD-UK 2 32840737 32840737 single base substitution G A downstream_gene_variant ESAD-UK 2 32840737 32840737 single base substitution G A intron_variant ESAD-UK 2 32841547 32841547 single base substitution C T downstream_gene_variant ESAD-UK 2 32841547 32841547 single base substitution C T intron_variant ESAD-UK 2 32842986 32842986 single base substitution G A 3_prime_UTR_variant ESAD-UK 2 32842986 32842986 single base substitution G A exon_variant ESAD-UK 2 32843295 32843295 single base substitution A T 3_prime_UTR_variant ESAD-UK 2 32843295 32843295 single base substitution A T exon_variant ESAD-UK 2 32843616 32843616 single base substitution T C 3_prime_UTR_variant ESAD-UK 2 32843616 32843616 single base substitution T C exon_variant ESAD-UK 2 32843626 32843626 single base substitution A G 3_prime_UTR_variant ESAD-UK 2 32843626 32843626 single base substitution A G exon_variant ESAD-UK 2 32844068 32844068 single base substitution C T downstream_gene_variant ESAD-UK 2 32846763 32846763 single base substitution G A downstream_gene_variant ESAD-UK 2 32846896 32846896 single base substitution A T downstream_gene_variant ESAD-UK 2 32846983 32846983 deletion of <=200bp A - downstream_gene_variant ESAD-UK 2 32847718 32847718 single base substitution C T downstream_gene_variant ESAD-UK 2 32848336 32848336 single base substitution C A downstream_gene_variant ESCA-CN 2 32626252 32626252 single base substitution C T exon_variant ESCA-CN 2 32626252 32626252 single base substitution C T synonymous_variant S352S 1056C>T ESCA-CN 2 32626412 32626412 single base substitution C T exon_variant ESCA-CN 2 32626412 32626412 single base substitution C T stop_gained R406* 1216C>T ESCA-CN 2 32640916 32640916 single base substitution C G missense_variant Q853E 2557C>G ESCA-CN 2 32666496 32666496 single base substitution C G intron_variant ESCA-CN 2 32666496 32666496 single base substitution C G missense_variant R1304G 3910C>G ESCA-CN 2 32666496 32666496 single base substitution C G missense_variant R190G 568C>G ESCA-CN 2 32666496 32666496 single base substitution C G upstream_gene_variant ESCA-CN 2 32667257 32667257 single base substitution T A 3_prime_UTR_variant ESCA-CN 2 32667257 32667257 single base substitution T A downstream_gene_variant ESCA-CN 2 32667257 32667257 single base substitution T A missense_variant C1357S 4069T>A ESCA-CN 2 32667257 32667257 single base substitution T A upstream_gene_variant ESCA-CN 2 32698243 32698243 single base substitution G T exon_variant ESCA-CN 2 32698243 32698243 single base substitution G T missense_variant G2219V 6656G>T ESCA-CN 2 32703847 32703847 single base substitution C T downstream_gene_variant ESCA-CN 2 32703847 32703847 single base substitution C T stop_gained Q2405* 7213C>T ESCA-CN 2 32706454 32706454 single base substitution T C missense_variant M2492T 7475T>C ESCA-CN 2 32728200 32728200 single base substitution T C exon_variant ESCA-CN 2 32728200 32728200 single base substitution T C synonymous_variant F3132F 9396T>C ESCA-CN 2 32756495 32756495 single base substitution A G exon_variant ESCA-CN 2 32756495 32756495 single base substitution A G missense_variant I4056M 12168A>G GBM-US 2 32695356 32695356 single base substitution T A missense_variant H2156Q 6468T>A GBM-US 2 32695356 32695356 single base substitution T A upstream_gene_variant GBM-US 2 32710744 32710744 single base substitution G A synonymous_variant Q2577Q 7731G>A GBM-US 2 32740406 32740406 single base substitution G A downstream_gene_variant GBM-US 2 32740406 32740406 single base substitution G A missense_variant A3640T 10918G>A GBM-US 2 32740406 32740406 single base substitution G A upstream_gene_variant GBM-US 2 32774411 32774411 single base substitution G A exon_variant GBM-US 2 32774411 32774411 single base substitution G A missense_variant S4336N 13007G>A KIRC-US 2 32605236 32605236 single base substitution T C missense_variant S175P 523T>C KIRC-US 2 32613998 32613998 single base substitution C T exon_variant KIRC-US 2 32613998 32613998 single base substitution C T missense_variant R276C 826C>T KIRC-US 2 32631593 32631593 single base substitution G A missense_variant S482N 1445G>A KIRC-US 2 32640716 32640716 single base substitution C A stop_gained S786* 2357C>A KIRC-US 2 32640925 32640925 single base substitution A G missense_variant I856V 2566A>G KIRC-US 2 32641040 32641040 single base substitution C T missense_variant T894M 2681C>T KIRC-US 2 32673959 32673959 single base substitution C A exon_variant KIRC-US 2 32673959 32673959 single base substitution C A synonymous_variant V1527V 4581C>A KIRC-US 2 32689778 32689778 single base substitution G T missense_variant A1715S 5143G>T KIRC-US 2 32692693 32692693 single base substitution T G missense_variant I1819M 5457T>G KIRC-US 2 32693017 32693017 single base substitution T G missense_variant I1873S 5618T>G KIRC-US 2 32693677 32693677 single base substitution A T missense_variant N1985Y 5953A>T KIRC-US 2 32693677 32693677 single base substitution A T upstream_gene_variant KIRP-US 2 32626579 32626579 single base substitution C T downstream_gene_variant KIRP-US 2 32626579 32626579 single base substitution C T stop_gained Q436* 1306C>T KIRP-US 2 32656054 32656054 single base substitution A C missense_variant E1048D 3144A>C KIRP-US 2 32656054 32656054 single base substitution A C upstream_gene_variant KIRP-US 2 32660618 32660618 deletion of <=200bp A - frameshift_variant E1155 KIRP-US 2 32660618 32660618 deletion of <=200bp A - intron_variant KIRP-US 2 32660618 32660618 deletion of <=200bp A - upstream_gene_variant KIRP-US 2 32667276 32667276 single base substitution A C 3_prime_UTR_variant KIRP-US 2 32667276 32667276 single base substitution A C downstream_gene_variant KIRP-US 2 32667276 32667276 single base substitution A C missense_variant H1363P 4088A>C KIRP-US 2 32667276 32667276 single base substitution A C upstream_gene_variant KIRP-US 2 32693046 32693046 single base substitution T C missense_variant Y1883H 5647T>C KIRP-US 2 32726845 32726845 single base substitution G A missense_variant G3033R 9097G>A KIRP-US 2 32726845 32726845 single base substitution G A upstream_gene_variant LAML-CN 2 32667451 32667451 single base substitution T G downstream_gene_variant LAML-CN 2 32667451 32667451 single base substitution T G missense_variant V1389G 4166T>G LAML-CN 2 32667451 32667451 single base substitution T G upstream_gene_variant LAML-CN 2 32822922 32822922 single base substitution G A downstream_gene_variant LAML-CN 2 32822922 32822922 single base substitution G A exon_variant LAML-CN 2 32822922 32822922 single base substitution G A missense_variant A4573T 13717G>A LAML-CN 2 32822922 32822922 single base substitution G A upstream_gene_variant LAML-KR 2 32591910 32591910 single base substitution T G intron_variant LAML-KR 2 32627063 32627063 single base substitution C T downstream_gene_variant LAML-KR 2 32627063 32627063 single base substitution C T intron_variant LAML-KR 2 32664807 32664807 single base substitution C T intron_variant LAML-KR 2 32664807 32664807 single base substitution C T upstream_gene_variant LAML-KR 2 32672350 32672350 single base substitution G A downstream_gene_variant LAML-KR 2 32672350 32672350 single base substitution G A intron_variant LAML-KR 2 32672406 32672406 single base substitution A G downstream_gene_variant LAML-KR 2 32672406 32672406 single base substitution A G intron_variant LAML-KR 2 32672440 32672440 single base substitution G A downstream_gene_variant LAML-KR 2 32672440 32672440 single base substitution G A intron_variant LAML-KR 2 32672568 32672568 single base substitution C T intron_variant LAML-KR 2 32701579 32701579 single base substitution A C downstream_gene_variant LAML-KR 2 32701579 32701579 single base substitution A C intron_variant LAML-KR 2 32795521 32795521 single base substitution G A intron_variant LAML-KR 2 32795521 32795521 single base substitution G A upstream_gene_variant LGG-US 2 32706407 32706407 deletion of <=200bp T - frameshift_variant S2476 LGG-US 2 32724735 32724735 single base substitution A T missense_variant T2864S 8590A>T LGG-US 2 32724735 32724735 single base substitution A T upstream_gene_variant LGG-US 2 32819095 32819095 single base substitution C T exon_variant LGG-US 2 32819095 32819095 single base substitution C T missense_variant A4490V 13469C>T LIAD-FR 2 32698255 32698255 single base substitution T C exon_variant LIAD-FR 2 32698255 32698255 single base substitution T C missense_variant L2223P 6668T>C LIAD-FR 2 32724727 32724727 single base substitution A G missense_variant E2861G 8582A>G LIAD-FR 2 32724727 32724727 single base substitution A G upstream_gene_variant LICA-CN 2 32626287 32626287 single base substitution A T exon_variant LICA-CN 2 32626287 32626287 single base substitution A T missense_variant Q364L 1091A>T LICA-CN 2 32656110 32656110 single base substitution A G missense_variant H1067R 3200A>G LICA-CN 2 32656110 32656110 single base substitution A G upstream_gene_variant LICA-CN 2 32678909 32678909 single base substitution A T downstream_gene_variant LICA-CN 2 32678909 32678909 single base substitution A T missense_variant E1551V 4652A>T LICA-CN 2 32689597 32689597 single base substitution G T missense_variant K1654N 4962G>T LICA-CN 2 32733050 32733050 single base substitution G C downstream_gene_variant LICA-CN 2 32733050 32733050 single base substitution G C missense_variant C3235S 9704G>C LICA-CN 2 32733050 32733050 single base substitution G C upstream_gene_variant LICA-CN 2 32754721 32754721 single base substitution A T exon_variant LICA-CN 2 32754721 32754721 single base substitution A T missense_variant Q3975L 11924A>T LICA-CN 2 32824929 32824929 single base substitution A T exon_variant LICA-CN 2 32824929 32824929 single base substitution A T missense_variant S4652C 13954A>T LICA-CN 2 32824929 32824929 single base substitution A T upstream_gene_variant LICA-FR 2 32578257 32578257 single base substitution T C upstream_gene_variant LICA-FR 2 32594497 32594497 deletion of <=200bp T - intron_variant LICA-FR 2 32613449 32613449 deletion of <=200bp A - intron_variant LICA-FR 2 32613449 32613449 deletion of <=200bp A - upstream_gene_variant LICA-FR 2 32623324 32623324 single base substitution A G intron_variant LICA-FR 2 32625405 32625405 deletion of <=200bp T - intron_variant LICA-FR 2 32626235 32626235 single base substitution G C exon_variant LICA-FR 2 32626235 32626235 single base substitution G C missense_variant E347Q 1039G>C LICA-FR 2 32640772 32640772 single base substitution G A missense_variant A805T 2413G>A LICA-FR 2 32641034 32641034 deletion of <=200bp A - frameshift_variant E892 LICA-FR 2 32660624 32660624 insertion of <=200bp - T frameshift_variant M1157I? LICA-FR 2 32660624 32660624 insertion of <=200bp - T intron_variant LICA-FR 2 32660624 32660624 insertion of <=200bp - T upstream_gene_variant LICA-FR 2 32672492 32672492 single base substitution C T intron_variant LICA-FR 2 32673454 32673454 single base substitution C T intron_variant LICA-FR 2 32688321 32688321 single base substitution G A missense_variant A1605T 4813G>A LICA-FR 2 32689892 32689892 single base substitution G A splice_donor_variant LICA-FR 2 32690304 32690304 single base substitution A T intron_variant LICA-FR 2 32693714 32693714 single base substitution C T missense_variant A1997V 5990C>T LICA-FR 2 32693714 32693714 single base substitution C T upstream_gene_variant LICA-FR 2 32701310 32701310 single base substitution G A exon_variant LICA-FR 2 32701310 32701310 single base substitution G A synonymous_variant K2250K 6750G>A LICA-FR 2 32702585 32702585 single base substitution A C downstream_gene_variant LICA-FR 2 32702585 32702585 single base substitution A C missense_variant K2334N 7002A>C LICA-FR 2 32712732 32712732 single base substitution G A missense_variant G2611E 7832G>A LICA-FR 2 32748883 32748883 single base substitution G A downstream_gene_variant LICA-FR 2 32748883 32748883 single base substitution G A intron_variant LICA-FR 2 32748883 32748883 single base substitution G A upstream_gene_variant LICA-FR 2 32750138 32750138 single base substitution A G intron_variant LICA-FR 2 32757202 32757202 insertion of <=200bp - GTGTGTGT intron_variant LICA-FR 2 32764017 32764017 single base substitution A T intron_variant LICA-FR 2 32764395 32764395 single base substitution G A intron_variant LICA-FR 2 32768589 32768589 single base substitution G A exon_variant LICA-FR 2 32768589 32768589 single base substitution G A synonymous_variant V4191V 12573G>A LICA-FR 2 32773652 32773652 single base substitution C T intron_variant LICA-FR 2 32777754 32777754 single base substitution C A intron_variant LICA-FR 2 32789598 32789598 single base substitution A G intron_variant LICA-FR 2 32800396 32800396 single base substitution A G exon_variant LICA-FR 2 32800396 32800396 single base substitution A G missense_variant M4440V 13318A>G LICA-FR 2 32813338 32813338 single base substitution G T intron_variant LICA-FR 2 32821536 32821536 deletion of <=200bp A - downstream_gene_variant LICA-FR 2 32821536 32821536 deletion of <=200bp A - intron_variant LICA-FR 2 32825811 32825811 single base substitution A G intron_variant LICA-FR 2 32825811 32825811 single base substitution A G upstream_gene_variant LICA-FR 2 32829172 32829172 single base substitution A G intron_variant LICA-FR 2 32836592 32836592 single base substitution G A exon_variant LICA-FR 2 32836592 32836592 single base substitution G A synonymous_variant Q4779Q 14337G>A LICA-FR 2 32836623 32836623 single base substitution A T exon_variant LICA-FR 2 32836623 32836623 single base substitution A T missense_variant M4790L 14368A>T LIHC-US 2 32602706 32602706 single base substitution G T missense_variant V126F 376G>T LIHC-US 2 32613893 32613893 deletion of <=200bp A - exon_variant LIHC-US 2 32613893 32613893 deletion of <=200bp A - frameshift_variant K241 LIHC-US 2 32626685 32626685 single base substitution G A downstream_gene_variant LIHC-US 2 32626685 32626685 single base substitution G A missense_variant G471E 1412G>A LIHC-US 2 32640007 32640007 single base substitution G T stop_gained E550* 1648G>T LIHC-US 2 32641025 32641025 single base substitution T C missense_variant F889S 2666T>C LIHC-US 2 32654298 32654298 single base substitution A C missense_variant K986T 2957A>C LIHC-US 2 32654298 32654298 single base substitution A C upstream_gene_variant LIHC-US 2 32678911 32678911 single base substitution G T downstream_gene_variant LIHC-US 2 32678911 32678911 single base substitution G T missense_variant G1552C 4654G>T LIHC-US 2 32692803 32692803 single base substitution T C missense_variant M1856T 5567T>C LIHC-US 2 32726807 32726807 single base substitution A C missense_variant H3020P 9059A>C LIHC-US 2 32726807 32726807 single base substitution A C upstream_gene_variant LIHC-US 2 32733177 32733177 single base substitution T C downstream_gene_variant LIHC-US 2 32733177 32733177 single base substitution T C synonymous_variant A3277A 9831T>C LIHC-US 2 32733177 32733177 single base substitution T C upstream_gene_variant LIHC-US 2 32750644 32750644 single base substitution A C exon_variant LIHC-US 2 32750644 32750644 single base substitution A C missense_variant N3957H 11869A>C LIHC-US 2 32773060 32773060 single base substitution A G exon_variant LIHC-US 2 32773060 32773060 single base substitution A G synonymous_variant E4318E 12954A>G LINC-JP 2 32593206 32593206 single base substitution A G intron_variant LINC-JP 2 32594758 32594758 single base substitution A T intron_variant LINC-JP 2 32603148 32603148 single base substitution A G intron_variant LINC-JP 2 32606700 32606700 single base substitution G A intron_variant LINC-JP 2 32613901 32613901 single base substitution T G exon_variant LINC-JP 2 32613901 32613901 single base substitution T G missense_variant N243K 729T>G LINC-JP 2 32614798 32614798 single base substitution C A intron_variant LINC-JP 2 32626366 32626366 single base substitution C T exon_variant LINC-JP 2 32626366 32626366 single base substitution C T synonymous_variant C390C 1170C>T LINC-JP 2 32628400 32628400 single base substitution G T downstream_gene_variant LINC-JP 2 32628400 32628400 single base substitution G T intron_variant LINC-JP 2 32631392 32631392 single base substitution A T downstream_gene_variant LINC-JP 2 32631392 32631392 single base substitution A T intron_variant LINC-JP 2 32637713 32637713 single base substitution T C intron_variant LINC-JP 2 32645337 32645337 single base substitution G T intron_variant LINC-JP 2 32645898 32645898 single base substitution A G intron_variant LINC-JP 2 32656195 32656195 single base substitution A G intron_variant LINC-JP 2 32656195 32656195 single base substitution A G upstream_gene_variant LINC-JP 2 32656219 32656219 single base substitution C T intron_variant LINC-JP 2 32656219 32656219 single base substitution C T upstream_gene_variant LINC-JP 2 32658721 32658721 single base substitution G A stop_gained W1086* 3258G>A LINC-JP 2 32658721 32658721 single base substitution G A stop_gained W2* 6G>A LINC-JP 2 32658721 32658721 single base substitution G A upstream_gene_variant LINC-JP 2 32659496 32659496 single base substitution A G intron_variant LINC-JP 2 32659496 32659496 single base substitution A G upstream_gene_variant LINC-JP 2 32660542 32660542 single base substitution A T intron_variant LINC-JP 2 32660542 32660542 single base substitution A T upstream_gene_variant LINC-JP 2 32662258 32662258 single base substitution A G intron_variant LINC-JP 2 32664600 32664600 single base substitution C T exon_variant LINC-JP 2 32664600 32664600 single base substitution C T missense_variant S105L 314C>T LINC-JP 2 32664600 32664600 single base substitution C T missense_variant S1219L 3656C>T LINC-JP 2 32664600 32664600 single base substitution C T upstream_gene_variant LINC-JP 2 32673919 32673919 single base substitution G T exon_variant LINC-JP 2 32673919 32673919 single base substitution G T missense_variant G1514V 4541G>T LINC-JP 2 32688343 32688343 single base substitution C A missense_variant A1612E 4835C>A LINC-JP 2 32692785 32692785 single base substitution C A missense_variant P1850H 5549C>A LINC-JP 2 32692994 32692994 single base substitution G T synonymous_variant G1865G 5595G>T LINC-JP 2 32694106 32694106 single base substitution G T intron_variant LINC-JP 2 32694106 32694106 single base substitution G T upstream_gene_variant LINC-JP 2 32697721 32697721 single base substitution A G intron_variant LINC-JP 2 32697721 32697721 single base substitution A G upstream_gene_variant LINC-JP 2 32702538 32702538 single base substitution C T downstream_gene_variant LINC-JP 2 32702538 32702538 single base substitution C T missense_variant L2319F 6955C>T LINC-JP 2 32703941 32703941 single base substitution A G downstream_gene_variant LINC-JP 2 32703941 32703941 single base substitution A G intron_variant LINC-JP 2 32709427 32709427 single base substitution T C intron_variant LINC-JP 2 32712685 32712685 single base substitution A G intron_variant LINC-JP 2 32714726 32714726 single base substitution G T intron_variant LINC-JP 2 32715049 32715049 single base substitution T G intron_variant LINC-JP 2 32718480 32718480 single base substitution C T intron_variant LINC-JP 2 32718880 32718880 single base substitution G A intron_variant LINC-JP 2 32724675 32724675 single base substitution C G missense_variant L2844V 8530C>G LINC-JP 2 32724675 32724675 single base substitution C G upstream_gene_variant LINC-JP 2 32732962 32732962 single base substitution A G downstream_gene_variant LINC-JP 2 32732962 32732962 single base substitution A G intron_variant LINC-JP 2 32732962 32732962 single base substitution A G upstream_gene_variant LINC-JP 2 32738027 32738027 single base substitution T G exon_variant LINC-JP 2 32738027 32738027 single base substitution T G missense_variant S3458R 10374T>G LINC-JP 2 32738027 32738027 single base substitution T G upstream_gene_variant LINC-JP 2 32740309 32740309 single base substitution A C downstream_gene_variant LINC-JP 2 32740309 32740309 single base substitution A C missense_variant E3607D 10821A>C LINC-JP 2 32740309 32740309 single base substitution A C upstream_gene_variant LINC-JP 2 32744993 32744993 single base substitution G T downstream_gene_variant LINC-JP 2 32744993 32744993 single base substitution G T intron_variant LINC-JP 2 32744993 32744993 single base substitution G T upstream_gene_variant LINC-JP 2 32749944 32749944 single base substitution T A exon_variant LINC-JP 2 32749944 32749944 single base substitution T A intron_variant LINC-JP 2 32750089 32750089 single base substitution A T intron_variant LINC-JP 2 32750089 32750089 single base substitution A T splice_region_variant LINC-JP 2 32763021 32763021 single base substitution G A intron_variant LINC-JP 2 32765013 32765013 single base substitution A C intron_variant LINC-JP 2 32766741 32766741 single base substitution G T intron_variant LINC-JP 2 32769846 32769846 single base substitution C A intron_variant LINC-JP 2 32772718 32772718 single base substitution A G intron_variant LINC-JP 2 32785935 32785935 deletion of <=200bp T - intron_variant LINC-JP 2 32787254 32787254 single base substitution A G intron_variant LINC-JP 2 32809435 32809435 single base substitution G A intron_variant LINC-JP 2 32809557 32809557 single base substitution G T intron_variant LINC-JP 2 32811919 32811919 single base substitution T C intron_variant LINC-JP 2 32819142 32819142 single base substitution C T exon_variant LINC-JP 2 32819142 32819142 single base substitution C T intron_variant LINC-JP 2 32820245 32820245 single base substitution A T downstream_gene_variant LINC-JP 2 32820245 32820245 single base substitution A T intron_variant LINC-JP 2 32822169 32822169 single base substitution C T downstream_gene_variant LINC-JP 2 32822169 32822169 single base substitution C T intron_variant LINC-JP 2 32836984 32836984 single base substitution C T downstream_gene_variant LINC-JP 2 32836984 32836984 single base substitution C T intron_variant LINC-JP 2 32839341 32839341 single base substitution G C downstream_gene_variant LINC-JP 2 32839341 32839341 single base substitution G C intron_variant LINC-JP 2 32839543 32839543 single base substitution A G downstream_gene_variant LINC-JP 2 32839543 32839543 single base substitution A G intron_variant LINC-JP 2 32841342 32841342 single base substitution T G downstream_gene_variant LINC-JP 2 32841342 32841342 single base substitution T G intron_variant LIRI-JP 2 32578524 32578524 single base substitution G C upstream_gene_variant LIRI-JP 2 32579450 32579450 single base substitution C A upstream_gene_variant LIRI-JP 2 32580556 32580556 single base substitution G A upstream_gene_variant LIRI-JP 2 32584957 32584957 single base substitution A G intron_variant LIRI-JP 2 32585124 32585124 single base substitution G C intron_variant LIRI-JP 2 32586258 32586258 single base substitution C T intron_variant LIRI-JP 2 32589026 32589026 single base substitution A G intron_variant LIRI-JP 2 32589874 32589874 single base substitution T C intron_variant LIRI-JP 2 32590134 32590134 single base substitution A T intron_variant LIRI-JP 2 32592203 32592203 single base substitution A G intron_variant LIRI-JP 2 32593581 32593581 single base substitution C G intron_variant LIRI-JP 2 32595447 32595447 single base substitution A C intron_variant LIRI-JP 2 32596998 32596998 single base substitution T A intron_variant LIRI-JP 2 32600233 32600233 single base substitution A G intron_variant LIRI-JP 2 32601889 32601889 single base substitution A G intron_variant LIRI-JP 2 32604724 32604724 single base substitution G A intron_variant LIRI-JP 2 32605410 32605410 single base substitution C A intron_variant LIRI-JP 2 32605709 32605709 single base substitution A G intron_variant LIRI-JP 2 32606762 32606762 single base substitution C T intron_variant LIRI-JP 2 32608703 32608703 single base substitution C A intron_variant LIRI-JP 2 32610685 32610685 single base substitution A G intron_variant LIRI-JP 2 32610685 32610685 single base substitution A G upstream_gene_variant LIRI-JP 2 32610988 32610988 single base substitution T C intron_variant LIRI-JP 2 32610988 32610988 single base substitution T C upstream_gene_variant LIRI-JP 2 32612320 32612320 single base substitution C T intron_variant LIRI-JP 2 32612320 32612320 single base substitution C T upstream_gene_variant LIRI-JP 2 32617026 32617026 single base substitution A G intron_variant LIRI-JP 2 32617687 32617687 single base substitution A G intron_variant LIRI-JP 2 32617814 32617814 single base substitution C T intron_variant LIRI-JP 2 32618697 32618697 single base substitution C T intron_variant LIRI-JP 2 32622509 32622509 single base substitution A C intron_variant LIRI-JP 2 32624472 32624472 single base substitution C T intron_variant LIRI-JP 2 32626285 32626285 single base substitution A G exon_variant LIRI-JP 2 32626285 32626285 single base substitution A G synonymous_variant T363T 1089A>G LIRI-JP 2 32627890 32627890 insertion of <=200bp - T downstream_gene_variant LIRI-JP 2 32627890 32627890 insertion of <=200bp - T intron_variant LIRI-JP 2 32630853 32630853 single base substitution T C downstream_gene_variant LIRI-JP 2 32630853 32630853 single base substitution T C intron_variant LIRI-JP 2 32633404 32633404 single base substitution C T intron_variant LIRI-JP 2 32635929 32635929 single base substitution C T intron_variant LIRI-JP 2 32636778 32636778 single base substitution T A intron_variant LIRI-JP 2 32637105 32637105 single base substitution A G intron_variant LIRI-JP 2 32640015 32640015 single base substitution A G synonymous_variant T552T 1656A>G LIRI-JP 2 32640235 32640235 single base substitution A G missense_variant T626A 1876A>G LIRI-JP 2 32640558 32640558 single base substitution A G missense_variant I733M 2199A>G LIRI-JP 2 32642532 32642532 single base substitution A G intron_variant LIRI-JP 2 32643037 32643037 single base substitution G A intron_variant LIRI-JP 2 32643174 32643174 single base substitution A G intron_variant LIRI-JP 2 32643730 32643730 single base substitution A G intron_variant LIRI-JP 2 32644388 32644388 single base substitution A G intron_variant LIRI-JP 2 32644571 32644571 single base substitution A C intron_variant LIRI-JP 2 32644822 32644822 single base substitution G A intron_variant LIRI-JP 2 32646253 32646253 single base substitution C T intron_variant LIRI-JP 2 32646828 32646828 single base substitution C T intron_variant LIRI-JP 2 32647703 32647703 single base substitution T G intron_variant LIRI-JP 2 32648078 32648078 single base substitution T G intron_variant LIRI-JP 2 32648840 32648840 single base substitution T C intron_variant LIRI-JP 2 32649663 32649663 single base substitution A G intron_variant LIRI-JP 2 32649718 32649718 single base substitution G T intron_variant LIRI-JP 2 32650191 32650191 single base substitution A G intron_variant LIRI-JP 2 32650627 32650627 single base substitution C A intron_variant LIRI-JP 2 32651706 32651706 single base substitution T C intron_variant LIRI-JP 2 32652974 32652977 deletion of <=200bp AAAC - intron_variant LIRI-JP 2 32654969 32654969 single base substitution A G intron_variant LIRI-JP 2 32654969 32654969 single base substitution A G upstream_gene_variant LIRI-JP 2 32655331 32655331 single base substitution A G intron_variant LIRI-JP 2 32655331 32655331 single base substitution A G upstream_gene_variant LIRI-JP 2 32657708 32657708 single base substitution G A intron_variant LIRI-JP 2 32657708 32657708 single base substitution G A upstream_gene_variant LIRI-JP 2 32659934 32659934 single base substitution A G intron_variant LIRI-JP 2 32659934 32659934 single base substitution A G upstream_gene_variant LIRI-JP 2 32661616 32661616 single base substitution T A intron_variant LIRI-JP 2 32661628 32661628 single base substitution C T intron_variant LIRI-JP 2 32662817 32662817 single base substitution A G intron_variant LIRI-JP 2 32664208 32664208 single base substitution T G intron_variant LIRI-JP 2 32664208 32664208 single base substitution T G upstream_gene_variant LIRI-JP 2 32664575 32664575 single base substitution G C splice_acceptor_variant LIRI-JP 2 32664575 32664575 single base substitution G C upstream_gene_variant LIRI-JP 2 32664858 32664858 single base substitution A G intron_variant LIRI-JP 2 32664858 32664858 single base substitution A G upstream_gene_variant LIRI-JP 2 32665628 32665628 single base substitution C T intron_variant LIRI-JP 2 32665628 32665628 single base substitution C T upstream_gene_variant LIRI-JP 2 32666222 32666222 single base substitution A C intron_variant LIRI-JP 2 32666222 32666222 single base substitution A C upstream_gene_variant LIRI-JP 2 32667309 32667309 deletion of <=200bp T - downstream_gene_variant LIRI-JP 2 32667309 32667309 deletion of <=200bp T - intron_variant LIRI-JP 2 32667309 32667309 deletion of <=200bp T - upstream_gene_variant LIRI-JP 2 32668063 32668063 single base substitution A G downstream_gene_variant LIRI-JP 2 32668063 32668063 single base substitution A G intron_variant LIRI-JP 2 32668063 32668063 single base substitution A G upstream_gene_variant LIRI-JP 2 32669433 32669433 single base substitution C T downstream_gene_variant LIRI-JP 2 32669433 32669433 single base substitution C T intron_variant LIRI-JP 2 32670249 32670249 single base substitution T C downstream_gene_variant LIRI-JP 2 32670249 32670249 single base substitution T C intron_variant LIRI-JP 2 32670598 32670598 single base substitution A G downstream_gene_variant LIRI-JP 2 32670598 32670598 single base substitution A G exon_variant LIRI-JP 2 32670598 32670598 single base substitution A G missense_variant Y1449C 4346A>G LIRI-JP 2 32674612 32674612 single base substitution A T downstream_gene_variant LIRI-JP 2 32674612 32674612 single base substitution A T intron_variant LIRI-JP 2 32674637 32674637 single base substitution G A downstream_gene_variant LIRI-JP 2 32674637 32674637 single base substitution G A intron_variant LIRI-JP 2 32675624 32675624 single base substitution A C downstream_gene_variant LIRI-JP 2 32675624 32675624 single base substitution A C intron_variant LIRI-JP 2 32675878 32675878 single base substitution A G downstream_gene_variant LIRI-JP 2 32675878 32675878 single base substitution A G intron_variant LIRI-JP 2 32677867 32677867 single base substitution A G downstream_gene_variant LIRI-JP 2 32677867 32677867 single base substitution A G intron_variant LIRI-JP 2 32678936 32678936 single base substitution T G downstream_gene_variant LIRI-JP 2 32678936 32678936 single base substitution T G missense_variant L1560R 4679T>G LIRI-JP 2 32680399 32680399 single base substitution G A intron_variant LIRI-JP 2 32681064 32681064 single base substitution C T intron_variant LIRI-JP 2 32681688 32681688 single base substitution G A intron_variant LIRI-JP 2 32683017 32683017 single base substitution T C intron_variant LIRI-JP 2 32683360 32683360 single base substitution T G intron_variant LIRI-JP 2 32686641 32686641 single base substitution C A intron_variant LIRI-JP 2 32687798 32687798 single base substitution T C intron_variant LIRI-JP 2 32687884 32687884 single base substitution C T intron_variant LIRI-JP 2 32689736 32689736 single base substitution A T missense_variant T1701S 5101A>T LIRI-JP 2 32691024 32691024 single base substitution A G intron_variant LIRI-JP 2 32691380 32691380 single base substitution A G intron_variant LIRI-JP 2 32691478 32691478 single base substitution A T intron_variant LIRI-JP 2 32692178 32692178 single base substitution C G intron_variant LIRI-JP 2 32692577 32692577 deletion of <=200bp C - intron_variant LIRI-JP 2 32693441 32693441 single base substitution A G intron_variant LIRI-JP 2 32693441 32693441 single base substitution A G upstream_gene_variant LIRI-JP 2 32694096 32694096 single base substitution A G intron_variant LIRI-JP 2 32694096 32694096 single base substitution A G upstream_gene_variant LIRI-JP 2 32696414 32696414 single base substitution A G intron_variant LIRI-JP 2 32696414 32696414 single base substitution A G upstream_gene_variant LIRI-JP 2 32697586 32697586 single base substitution G C intron_variant LIRI-JP 2 32697586 32697586 single base substitution G C upstream_gene_variant LIRI-JP 2 32698932 32698932 single base substitution C T intron_variant LIRI-JP 2 32699714 32699714 single base substitution T C intron_variant LIRI-JP 2 32701605 32701605 single base substitution G A downstream_gene_variant LIRI-JP 2 32701605 32701605 single base substitution G A intron_variant LIRI-JP 2 32701990 32701990 single base substitution A G downstream_gene_variant LIRI-JP 2 32701990 32701990 single base substitution A G intron_variant LIRI-JP 2 32702180 32702180 single base substitution A T downstream_gene_variant LIRI-JP 2 32702180 32702180 single base substitution A T intron_variant LIRI-JP 2 32702928 32702930 deletion of <=200bp TTA - downstream_gene_variant LIRI-JP 2 32702928 32702930 deletion of <=200bp TTA - intron_variant LIRI-JP 2 32704852 32704852 single base substitution T G downstream_gene_variant LIRI-JP 2 32704852 32704852 single base substitution T G intron_variant LIRI-JP 2 32709384 32709384 single base substitution C A intron_variant LIRI-JP 2 32710897 32710897 single base substitution A C intron_variant LIRI-JP 2 32711662 32711662 single base substitution T A intron_variant LIRI-JP 2 32712597 32712597 single base substitution C T intron_variant LIRI-JP 2 32713322 32713322 single base substitution A G intron_variant LIRI-JP 2 32713344 32713344 single base substitution A C intron_variant LIRI-JP 2 32713464 32713464 single base substitution T C intron_variant LIRI-JP 2 32713852 32713852 single base substitution A G intron_variant LIRI-JP 2 32717236 32717236 single base substitution C T intron_variant LIRI-JP 2 32718187 32718187 single base substitution G T intron_variant LIRI-JP 2 32718749 32718749 single base substitution A G intron_variant LIRI-JP 2 32720987 32720987 single base substitution C T intron_variant LIRI-JP 2 32721061 32721061 single base substitution C T intron_variant LIRI-JP 2 32721604 32721604 single base substitution C T intron_variant LIRI-JP 2 32721615 32721615 single base substitution A G intron_variant LIRI-JP 2 32722535 32722535 single base substitution A G intron_variant LIRI-JP 2 32723462 32723462 single base substitution A T intron_variant LIRI-JP 2 32723462 32723462 single base substitution A T upstream_gene_variant LIRI-JP 2 32724459 32724459 single base substitution A T intron_variant LIRI-JP 2 32724459 32724459 single base substitution A T upstream_gene_variant LIRI-JP 2 32727036 32727036 single base substitution A G intron_variant LIRI-JP 2 32727036 32727036 single base substitution A G upstream_gene_variant LIRI-JP 2 32727879 32727879 single base substitution C T synonymous_variant C3075C 9225C>T LIRI-JP 2 32727879 32727879 single base substitution C T upstream_gene_variant LIRI-JP 2 32731267 32731267 single base substitution C G downstream_gene_variant LIRI-JP 2 32731267 32731267 single base substitution C G intron_variant LIRI-JP 2 32731267 32731267 single base substitution C G upstream_gene_variant LIRI-JP 2 32731857 32731857 single base substitution A G downstream_gene_variant LIRI-JP 2 32731857 32731857 single base substitution A G intron_variant LIRI-JP 2 32731857 32731857 single base substitution A G upstream_gene_variant LIRI-JP 2 32731992 32731992 single base substitution G T downstream_gene_variant LIRI-JP 2 32731992 32731992 single base substitution G T intron_variant LIRI-JP 2 32731992 32731992 single base substitution G T upstream_gene_variant LIRI-JP 2 32732497 32732497 single base substitution T A downstream_gene_variant LIRI-JP 2 32732497 32732497 single base substitution T A intron_variant LIRI-JP 2 32732497 32732497 single base substitution T A upstream_gene_variant LIRI-JP 2 32733877 32733877 single base substitution C T downstream_gene_variant LIRI-JP 2 32733877 32733877 single base substitution C T intron_variant LIRI-JP 2 32733877 32733877 single base substitution C T upstream_gene_variant LIRI-JP 2 32734162 32734163 deletion of <=200bp TT - downstream_gene_variant LIRI-JP 2 32734162 32734163 deletion of <=200bp TT - intron_variant LIRI-JP 2 32734162 32734163 deletion of <=200bp TT - upstream_gene_variant LIRI-JP 2 32736144 32736144 single base substitution A T intron_variant LIRI-JP 2 32736144 32736144 single base substitution A T upstream_gene_variant LIRI-JP 2 32736589 32736589 single base substitution G T intron_variant LIRI-JP 2 32736589 32736589 single base substitution G T upstream_gene_variant LIRI-JP 2 32736632 32736632 single base substitution C T intron_variant LIRI-JP 2 32736632 32736632 single base substitution C T upstream_gene_variant LIRI-JP 2 32737033 32737033 single base substitution A T intron_variant LIRI-JP 2 32737033 32737033 single base substitution A T upstream_gene_variant LIRI-JP 2 32737144 32737144 single base substitution T C intron_variant LIRI-JP 2 32737144 32737144 single base substitution T C upstream_gene_variant LIRI-JP 2 32737317 32737317 single base substitution A T intron_variant LIRI-JP 2 32737317 32737317 single base substitution A T upstream_gene_variant LIRI-JP 2 32737582 32737582 single base substitution A G intron_variant LIRI-JP 2 32737582 32737582 single base substitution A G upstream_gene_variant LIRI-JP 2 32740558 32740558 single base substitution G T downstream_gene_variant LIRI-JP 2 32740558 32740558 single base substitution G T missense_variant L3690F 11070G>T LIRI-JP 2 32740558 32740558 single base substitution G T upstream_gene_variant LIRI-JP 2 32741830 32741830 single base substitution A C downstream_gene_variant LIRI-JP 2 32741830 32741830 single base substitution A C intron_variant LIRI-JP 2 32741932 32741932 single base substitution A G downstream_gene_variant LIRI-JP 2 32741932 32741932 single base substitution A G intron_variant LIRI-JP 2 32743279 32743279 single base substitution A G intron_variant LIRI-JP 2 32746040 32746040 single base substitution G A downstream_gene_variant LIRI-JP 2 32746040 32746040 single base substitution G A intron_variant LIRI-JP 2 32746040 32746040 single base substitution G A upstream_gene_variant LIRI-JP 2 32747632 32747632 single base substitution A T downstream_gene_variant LIRI-JP 2 32747632 32747632 single base substitution A T intron_variant LIRI-JP 2 32747632 32747632 single base substitution A T upstream_gene_variant LIRI-JP 2 32747782 32747782 single base substitution A G downstream_gene_variant LIRI-JP 2 32747782 32747782 single base substitution A G intron_variant LIRI-JP 2 32747782 32747782 single base substitution A G upstream_gene_variant LIRI-JP 2 32753106 32753106 single base substitution C T intron_variant LIRI-JP 2 32755301 32755301 single base substitution A G intron_variant LIRI-JP 2 32755740 32755741 deletion of <=200bp AT - intron_variant LIRI-JP 2 32756659 32756659 single base substitution T C intron_variant LIRI-JP 2 32759184 32759184 single base substitution T C intron_variant LIRI-JP 2 32759677 32759677 single base substitution A G intron_variant LIRI-JP 2 32760790 32760790 single base substitution G T intron_variant LIRI-JP 2 32763161 32763161 single base substitution G A intron_variant LIRI-JP 2 32764313 32764313 single base substitution A G intron_variant LIRI-JP 2 32764460 32764460 single base substitution T C intron_variant LIRI-JP 2 32766214 32766214 single base substitution A G intron_variant LIRI-JP 2 32766365 32766365 single base substitution T A intron_variant LIRI-JP 2 32766710 32766710 single base substitution G A intron_variant LIRI-JP 2 32766736 32766736 single base substitution A G intron_variant LIRI-JP 2 32767077 32767077 single base substitution T A intron_variant LIRI-JP 2 32769189 32769189 single base substitution G A intron_variant LIRI-JP 2 32770543 32770543 single base substitution A G intron_variant LIRI-JP 2 32772509 32772509 single base substitution A G intron_variant LIRI-JP 2 32772775 32772775 single base substitution A G intron_variant LIRI-JP 2 32774486 32774502 deletion of <=200bp TCGAGCTTCTCAGTCAG - exon_variant LIRI-JP 2 32774486 32774502 deletion of <=200bp TCGAGCTTCTCAGTCAG - frameshift_variant LELLSQ4361 LIRI-JP 2 32775462 32775462 single base substitution A C intron_variant LIRI-JP 2 32776969 32776969 single base substitution G A intron_variant LIRI-JP 2 32778844 32778844 single base substitution G T intron_variant LIRI-JP 2 32779882 32779882 single base substitution C A intron_variant LIRI-JP 2 32780479 32780479 single base substitution G A intron_variant LIRI-JP 2 32780556 32780556 single base substitution A G intron_variant LIRI-JP 2 32783758 32783758 single base substitution T C intron_variant LIRI-JP 2 32785272 32785272 single base substitution A G intron_variant LIRI-JP 2 32785600 32785600 single base substitution T C intron_variant LIRI-JP 2 32786972 32786972 single base substitution G T intron_variant LIRI-JP 2 32791177 32791177 single base substitution A G intron_variant LIRI-JP 2 32791985 32791985 single base substitution T A intron_variant LIRI-JP 2 32792304 32792304 single base substitution T A intron_variant LIRI-JP 2 32794523 32794523 single base substitution C T intron_variant LIRI-JP 2 32794570 32794570 single base substitution G T intron_variant LIRI-JP 2 32795338 32795338 single base substitution T C intron_variant LIRI-JP 2 32795619 32795619 single base substitution G T intron_variant LIRI-JP 2 32795619 32795619 single base substitution G T upstream_gene_variant LIRI-JP 2 32796241 32796241 single base substitution T G intron_variant LIRI-JP 2 32796241 32796241 single base substitution T G upstream_gene_variant LIRI-JP 2 32796288 32796288 single base substitution A G intron_variant LIRI-JP 2 32796288 32796288 single base substitution A G upstream_gene_variant LIRI-JP 2 32797237 32797237 single base substitution T C intron_variant LIRI-JP 2 32797237 32797237 single base substitution T C upstream_gene_variant LIRI-JP 2 32798660 32798660 single base substitution A G intron_variant LIRI-JP 2 32798660 32798660 single base substitution A G upstream_gene_variant LIRI-JP 2 32801381 32801381 single base substitution A C intron_variant LIRI-JP 2 32803943 32803943 single base substitution C T intron_variant LIRI-JP 2 32804825 32804825 single base substitution A G intron_variant LIRI-JP 2 32804869 32804869 single base substitution A G intron_variant LIRI-JP 2 32805549 32805549 single base substitution T A intron_variant LIRI-JP 2 32806009 32806009 single base substitution A G intron_variant LIRI-JP 2 32807128 32807128 single base substitution G A intron_variant LIRI-JP 2 32808676 32808676 single base substitution T C intron_variant LIRI-JP 2 32808824 32808824 single base substitution C T intron_variant LIRI-JP 2 32808920 32808920 single base substitution C G intron_variant LIRI-JP 2 32808988 32808988 single base substitution G A intron_variant LIRI-JP 2 32813467 32813467 single base substitution G A intron_variant LIRI-JP 2 32813964 32813964 single base substitution A G intron_variant LIRI-JP 2 32814678 32814678 single base substitution A G intron_variant LIRI-JP 2 32820317 32820317 single base substitution A G downstream_gene_variant LIRI-JP 2 32820317 32820317 single base substitution A G intron_variant LIRI-JP 2 32822188 32822188 single base substitution C T downstream_gene_variant LIRI-JP 2 32822188 32822188 single base substitution C T intron_variant LIRI-JP 2 32822374 32822374 single base substitution A C downstream_gene_variant LIRI-JP 2 32822374 32822374 single base substitution A C intron_variant LIRI-JP 2 32823362 32823362 single base substitution A G downstream_gene_variant LIRI-JP 2 32823362 32823362 single base substitution A G intron_variant LIRI-JP 2 32823362 32823362 single base substitution A G upstream_gene_variant LIRI-JP 2 32824580 32824580 single base substitution G T intron_variant LIRI-JP 2 32824580 32824580 single base substitution G T upstream_gene_variant LIRI-JP 2 32825817 32825817 single base substitution C G intron_variant LIRI-JP 2 32825817 32825817 single base substitution C G upstream_gene_variant LIRI-JP 2 32827020 32827020 single base substitution T G intron_variant LIRI-JP 2 32827020 32827020 single base substitution T G upstream_gene_variant LIRI-JP 2 32827184 32827184 single base substitution A G intron_variant LIRI-JP 2 32827184 32827184 single base substitution A G upstream_gene_variant LIRI-JP 2 32827949 32827949 single base substitution A G exon_variant LIRI-JP 2 32827949 32827949 single base substitution A G intron_variant LIRI-JP 2 32828182 32828182 single base substitution A G intron_variant LIRI-JP 2 32828459 32828459 single base substitution A T intron_variant LIRI-JP 2 32828948 32828948 single base substitution A G intron_variant LIRI-JP 2 32829360 32829360 single base substitution A G intron_variant LIRI-JP 2 32832315 32832315 single base substitution A C intron_variant LIRI-JP 2 32832680 32832680 single base substitution A T exon_variant LIRI-JP 2 32832680 32832680 single base substitution A T missense_variant Q4743H 14229A>T LIRI-JP 2 32833099 32833099 single base substitution A G intron_variant LIRI-JP 2 32833136 32833136 single base substitution G T intron_variant LIRI-JP 2 32833584 32833584 single base substitution C T intron_variant LIRI-JP 2 32833942 32833942 single base substitution C T intron_variant LIRI-JP 2 32834280 32834280 single base substitution G T intron_variant LIRI-JP 2 32834531 32834531 single base substitution A G intron_variant LIRI-JP 2 32837354 32837354 single base substitution G T downstream_gene_variant LIRI-JP 2 32837354 32837354 single base substitution G T intron_variant LIRI-JP 2 32838114 32838114 single base substitution C A downstream_gene_variant LIRI-JP 2 32838114 32838114 single base substitution C A intron_variant LIRI-JP 2 32840686 32840686 single base substitution T C downstream_gene_variant LIRI-JP 2 32840686 32840686 single base substitution T C intron_variant LIRI-JP 2 32841871 32841871 single base substitution T C intron_variant LIRI-JP 2 32843309 32843309 single base substitution A G 3_prime_UTR_variant LIRI-JP 2 32843309 32843309 single base substitution A G exon_variant LIRI-JP 2 32843644 32843644 single base substitution G A 3_prime_UTR_variant LIRI-JP 2 32843644 32843644 single base substitution G A exon_variant LIRI-JP 2 32847073 32847073 single base substitution T G downstream_gene_variant LIRI-JP 2 32847838 32847838 single base substitution A C downstream_gene_variant LUSC-KR 2 32577120 32577120 single base substitution G T upstream_gene_variant LUSC-KR 2 32578588 32578588 single base substitution G A upstream_gene_variant LUSC-KR 2 32579190 32579190 single base substitution G A upstream_gene_variant LUSC-KR 2 32587402 32587402 single base substitution G T intron_variant LUSC-KR 2 32588835 32588835 single base substitution A T intron_variant LUSC-KR 2 32593323 32593323 single base substitution C T intron_variant LUSC-KR 2 32593398 32593398 single base substitution G T intron_variant LUSC-KR 2 32597883 32597883 single base substitution G C intron_variant LUSC-KR 2 32598420 32598420 single base substitution A G intron_variant LUSC-KR 2 32599491 32599491 single base substitution G A intron_variant LUSC-KR 2 32606700 32606700 single base substitution G T intron_variant LUSC-KR 2 32616031 32616031 single base substitution C G intron_variant LUSC-KR 2 32617661 32617661 single base substitution A G intron_variant LUSC-KR 2 32619893 32619893 single base substitution G C intron_variant LUSC-KR 2 32621937 32621937 single base substitution G T intron_variant LUSC-KR 2 32633381 32633381 single base substitution G T intron_variant LUSC-KR 2 32634967 32634967 single base substitution C G intron_variant LUSC-KR 2 32641554 32641554 single base substitution A T intron_variant LUSC-KR 2 32643174 32643174 single base substitution A G intron_variant LUSC-KR 2 32643506 32643506 single base substitution A G intron_variant LUSC-KR 2 32646120 32646120 single base substitution C A intron_variant LUSC-KR 2 32646121 32646121 single base substitution C A intron_variant LUSC-KR 2 32646216 32646216 single base substitution C T intron_variant LUSC-KR 2 32647441 32647441 single base substitution T C intron_variant LUSC-KR 2 32648184 32648184 single base substitution G T intron_variant LUSC-KR 2 32657060 32657060 single base substitution A T intron_variant LUSC-KR 2 32657060 32657060 single base substitution A T upstream_gene_variant LUSC-KR 2 32658971 32658971 single base substitution C A intron_variant LUSC-KR 2 32658971 32658971 single base substitution C A upstream_gene_variant LUSC-KR 2 32659493 32659493 single base substitution G T intron_variant LUSC-KR 2 32659493 32659493 single base substitution G T upstream_gene_variant LUSC-KR 2 32661699 32661699 single base substitution G T intron_variant LUSC-KR 2 32666190 32666190 single base substitution T A intron_variant LUSC-KR 2 32666190 32666190 single base substitution T A upstream_gene_variant LUSC-KR 2 32669665 32669665 single base substitution C T downstream_gene_variant LUSC-KR 2 32669665 32669665 single base substitution C T intron_variant LUSC-KR 2 32672426 32672426 single base substitution T C downstream_gene_variant LUSC-KR 2 32672426 32672426 single base substitution T C intron_variant LUSC-KR 2 32672439 32672439 single base substitution C T downstream_gene_variant LUSC-KR 2 32672439 32672439 single base substitution C T intron_variant LUSC-KR 2 32672440 32672440 single base substitution G A downstream_gene_variant LUSC-KR 2 32672440 32672440 single base substitution G A intron_variant LUSC-KR 2 32677413 32677413 single base substitution G T downstream_gene_variant LUSC-KR 2 32677413 32677413 single base substitution G T intron_variant LUSC-KR 2 32678902 32678902 single base substitution G A downstream_gene_variant LUSC-KR 2 32678902 32678902 single base substitution G A missense_variant A1549T 4645G>A LUSC-KR 2 32681065 32681065 single base substitution G T intron_variant LUSC-KR 2 32686110 32686110 single base substitution C G intron_variant LUSC-KR 2 32686141 32686141 single base substitution C T intron_variant LUSC-KR 2 32686199 32686199 single base substitution C T intron_variant LUSC-KR 2 32690273 32690273 single base substitution G T intron_variant LUSC-KR 2 32690304 32690304 single base substitution A T intron_variant LUSC-KR 2 32692770 32692770 single base substitution A C missense_variant H1845P 5534A>C LUSC-KR 2 32692915 32692915 single base substitution C G intron_variant LUSC-KR 2 32695056 32695056 single base substitution A G intron_variant LUSC-KR 2 32695056 32695056 single base substitution A G upstream_gene_variant LUSC-KR 2 32697325 32697325 single base substitution C T intron_variant LUSC-KR 2 32697325 32697325 single base substitution C T upstream_gene_variant LUSC-KR 2 32713688 32713688 single base substitution A T missense_variant S2668C 8002A>T LUSC-KR 2 32717446 32717446 single base substitution G T intron_variant LUSC-KR 2 32718583 32718583 single base substitution C T intron_variant LUSC-KR 2 32720533 32720533 single base substitution G A intron_variant LUSC-KR 2 32723505 32723505 single base substitution G T intron_variant LUSC-KR 2 32723505 32723505 single base substitution G T upstream_gene_variant LUSC-KR 2 32726254 32726254 single base substitution A G intron_variant LUSC-KR 2 32726254 32726254 single base substitution A G upstream_gene_variant LUSC-KR 2 32729542 32729542 single base substitution G T intron_variant LUSC-KR 2 32737625 32737625 single base substitution A T intron_variant LUSC-KR 2 32737625 32737625 single base substitution A T upstream_gene_variant LUSC-KR 2 32743539 32743539 single base substitution T G intron_variant LUSC-KR 2 32743540 32743540 single base substitution C A intron_variant LUSC-KR 2 32744005 32744005 single base substitution G A exon_variant LUSC-KR 2 32744005 32744005 single base substitution G A missense_variant R3872K 11615G>A LUSC-KR 2 32745471 32745471 single base substitution G C downstream_gene_variant LUSC-KR 2 32745471 32745471 single base substitution G C intron_variant LUSC-KR 2 32745471 32745471 single base substitution G C upstream_gene_variant LUSC-KR 2 32746806 32746806 single base substitution C A downstream_gene_variant LUSC-KR 2 32746806 32746806 single base substitution C A intron_variant LUSC-KR 2 32746806 32746806 single base substitution C A upstream_gene_variant LUSC-KR 2 32750205 32750205 single base substitution A T intron_variant LUSC-KR 2 32759270 32759270 single base substitution G A intron_variant LUSC-KR 2 32759283 32759283 single base substitution A G intron_variant LUSC-KR 2 32769239 32769239 single base substitution A G intron_variant LUSC-KR 2 32775006 32775006 single base substitution A G intron_variant LUSC-KR 2 32776858 32776858 single base substitution C T intron_variant LUSC-KR 2 32777688 32777688 single base substitution C G intron_variant LUSC-KR 2 32778579 32778579 single base substitution C A intron_variant LUSC-KR 2 32778723 32778723 single base substitution G T intron_variant LUSC-KR 2 32782645 32782645 single base substitution G C intron_variant LUSC-KR 2 32784902 32784902 single base substitution G A intron_variant LUSC-KR 2 32786464 32786464 single base substitution G A intron_variant LUSC-KR 2 32789761 32789761 single base substitution A G intron_variant LUSC-KR 2 32794692 32794692 single base substitution A G intron_variant LUSC-KR 2 32794719 32794719 single base substitution A G intron_variant LUSC-KR 2 32797828 32797828 single base substitution G T intron_variant LUSC-KR 2 32797828 32797828 single base substitution G T upstream_gene_variant LUSC-KR 2 32800498 32800498 single base substitution G T intron_variant LUSC-KR 2 32804642 32804642 single base substitution G T intron_variant LUSC-KR 2 32807285 32807285 single base substitution A T intron_variant LUSC-KR 2 32808655 32808655 single base substitution G T intron_variant LUSC-KR 2 32813266 32813266 single base substitution C A intron_variant LUSC-KR 2 32816003 32816003 single base substitution A T exon_variant LUSC-KR 2 32816003 32816003 single base substitution A T intron_variant LUSC-KR 2 32817094 32817094 single base substitution C T intron_variant LUSC-KR 2 32817881 32817881 single base substitution C T intron_variant LUSC-KR 2 32820006 32820006 single base substitution A T downstream_gene_variant LUSC-KR 2 32820006 32820006 single base substitution A T intron_variant LUSC-KR 2 32822184 32822184 single base substitution G C downstream_gene_variant LUSC-KR 2 32822184 32822184 single base substitution G C intron_variant LUSC-KR 2 32828465 32828465 single base substitution G T intron_variant LUSC-KR 2 32838168 32838168 single base substitution T A downstream_gene_variant LUSC-KR 2 32838168 32838168 single base substitution T A intron_variant LUSC-KR 2 32841896 32841896 single base substitution G A intron_variant LUSC-US 2 32664696 32664696 single base substitution A T exon_variant LUSC-US 2 32664696 32664696 single base substitution A T missense_variant H1251L 3752A>T LUSC-US 2 32664696 32664696 single base substitution A T missense_variant H137L 410A>T LUSC-US 2 32664696 32664696 single base substitution A T upstream_gene_variant LUSC-US 2 32667235 32667235 single base substitution G C 3_prime_UTR_variant LUSC-US 2 32667235 32667235 single base substitution G C downstream_gene_variant LUSC-US 2 32667235 32667235 single base substitution G C missense_variant Q1349H 4047G>C LUSC-US 2 32667235 32667235 single base substitution G C upstream_gene_variant LUSC-US 2 32673984 32673984 single base substitution G T exon_variant LUSC-US 2 32673984 32673984 single base substitution G T missense_variant D1536Y 4606G>T LUSC-US 2 32692709 32692709 single base substitution G C missense_variant E1825Q 5473G>C LUSC-US 2 32703790 32703790 single base substitution C G downstream_gene_variant LUSC-US 2 32703790 32703790 single base substitution C G missense_variant L2386V 7156C>G LUSC-US 2 32703827 32703827 single base substitution C A downstream_gene_variant LUSC-US 2 32703827 32703827 single base substitution C A missense_variant S2398Y 7193C>A LUSC-US 2 32712731 32712731 single base substitution G T stop_gained G2611* 7831G>T LUSC-US 2 32725073 32725073 single base substitution G A synonymous_variant S2976S 8928G>A LUSC-US 2 32725073 32725073 single base substitution G A upstream_gene_variant LUSC-US 2 32726824 32726824 single base substitution G T missense_variant G3026W 9076G>T LUSC-US 2 32726824 32726824 single base substitution G T upstream_gene_variant LUSC-US 2 32730095 32730095 single base substitution A T exon_variant LUSC-US 2 32730095 32730095 single base substitution A T missense_variant T3175S 9523A>T LUSC-US 2 32730095 32730095 single base substitution A T upstream_gene_variant LUSC-US 2 32734914 32734914 single base substitution G T downstream_gene_variant LUSC-US 2 32734914 32734914 single base substitution G T exon_variant LUSC-US 2 32734914 32734914 single base substitution G T missense_variant A3364S 10090G>T LUSC-US 2 32738083 32738083 single base substitution C T exon_variant LUSC-US 2 32738083 32738083 single base substitution C T missense_variant P3477L 10430C>T LUSC-US 2 32738083 32738083 single base substitution C T upstream_gene_variant LUSC-US 2 32738147 32738147 single base substitution A G exon_variant LUSC-US 2 32738147 32738147 single base substitution A G synonymous_variant A3498A 10494A>G LUSC-US 2 32738147 32738147 single base substitution A G upstream_gene_variant LUSC-US 2 32740349 32740349 single base substitution G C downstream_gene_variant LUSC-US 2 32740349 32740349 single base substitution G C missense_variant E3621Q 10861G>C LUSC-US 2 32740349 32740349 single base substitution G C upstream_gene_variant LUSC-US 2 32740388 32740388 single base substitution C G downstream_gene_variant LUSC-US 2 32740388 32740388 single base substitution C G missense_variant L3634V 10900C>G LUSC-US 2 32740388 32740388 single base substitution C G upstream_gene_variant LUSC-US 2 32740406 32740406 single base substitution G T downstream_gene_variant LUSC-US 2 32740406 32740406 single base substitution G T missense_variant A3640S 10918G>T LUSC-US 2 32740406 32740406 single base substitution G T upstream_gene_variant LUSC-US 2 32750596 32750596 single base substitution A T exon_variant LUSC-US 2 32750596 32750596 single base substitution A T missense_variant R3941W 11821A>T LUSC-US 2 32750665 32750665 single base substitution G T exon_variant LUSC-US 2 32750665 32750665 single base substitution G T missense_variant V3964L 11890G>T LUSC-US 2 32750675 32750675 single base substitution T C exon_variant LUSC-US 2 32750675 32750675 single base substitution T C missense_variant L3967P 11900T>C LUSC-US 2 32754743 32754743 single base substitution A G exon_variant LUSC-US 2 32754743 32754743 single base substitution A G synonymous_variant T3982T 11946A>G LUSC-US 2 32768395 32768395 single base substitution G A exon_variant LUSC-US 2 32768395 32768395 single base substitution G A missense_variant E4127K 12379G>A LUSC-US 2 32773032 32773032 single base substitution C T exon_variant LUSC-US 2 32773032 32773032 single base substitution C T missense_variant A4309V 12926C>T LUSC-US 2 32773076 32773076 single base substitution C T exon_variant LUSC-US 2 32773076 32773076 single base substitution C T synonymous_variant L4324L 12970C>T LUSC-US 2 32774431 32774431 single base substitution C G exon_variant LUSC-US 2 32774431 32774431 single base substitution C G missense_variant Q4343E 13027C>G LUSC-US 2 32774500 32774500 single base substitution C G exon_variant LUSC-US 2 32774500 32774500 single base substitution C G missense_variant Q4366E 13096C>G LUSC-US 2 32774511 32774511 single base substitution C G exon_variant LUSC-US 2 32774511 32774511 single base substitution C G synonymous_variant L4369L 13107C>G LUSC-US 2 32820187 32820187 single base substitution G T downstream_gene_variant LUSC-US 2 32820187 32820187 single base substitution G T exon_variant LUSC-US 2 32820187 32820187 single base substitution G T missense_variant A4530S 13588G>T LUSC-US 2 32820204 32820204 single base substitution A G downstream_gene_variant LUSC-US 2 32820204 32820204 single base substitution A G exon_variant LUSC-US 2 32820204 32820204 single base substitution A G synonymous_variant L4535L 13605A>G LUSC-US 2 32823032 32823032 single base substitution G C downstream_gene_variant LUSC-US 2 32823032 32823032 single base substitution G C exon_variant LUSC-US 2 32823032 32823032 single base substitution G C missense_variant M4609I 13827G>C LUSC-US 2 32823032 32823032 single base substitution G C upstream_gene_variant LUSC-US 2 32832614 32832614 single base substitution A T exon_variant LUSC-US 2 32832614 32832614 single base substitution A T synonymous_variant T4721T 14163A>T LUSC-US 2 32832622 32832622 single base substitution C T exon_variant LUSC-US 2 32832622 32832622 single base substitution C T missense_variant S4724F 14171C>T LUSC-US 2 32836642 32836642 single base substitution C G exon_variant LUSC-US 2 32836642 32836642 single base substitution C G missense_variant A4796G 14387C>G LUSC-US 2 32842813 32842813 single base substitution G A exon_variant LUSC-US 2 32842813 32842813 single base substitution G A missense_variant E4806K 14416G>A MALY-DE 2 32585172 32585172 single base substitution G A intron_variant MALY-DE 2 32587739 32587739 single base substitution A T intron_variant MALY-DE 2 32595130 32595131 deletion of <=200bp AC - intron_variant MALY-DE 2 32599152 32599152 single base substitution A G intron_variant MALY-DE 2 32615955 32615955 single base substitution G T intron_variant MALY-DE 2 32617282 32617282 single base substitution C T intron_variant MALY-DE 2 32626362 32626362 single base substitution C T exon_variant MALY-DE 2 32626362 32626362 single base substitution C T missense_variant S389F 1166C>T MALY-DE 2 32627667 32627667 single base substitution C T downstream_gene_variant MALY-DE 2 32627667 32627667 single base substitution C T intron_variant MALY-DE 2 32629164 32629164 insertion of <=200bp - T downstream_gene_variant MALY-DE 2 32629164 32629164 insertion of <=200bp - T intron_variant MALY-DE 2 32630989 32630989 single base substitution C T downstream_gene_variant MALY-DE 2 32630989 32630989 single base substitution C T intron_variant MALY-DE 2 32634112 32634112 single base substitution T G intron_variant MALY-DE 2 32639605 32639605 single base substitution T G intron_variant MALY-DE 2 32640265 32640265 single base substitution A T stop_gained K636* 1906A>T MALY-DE 2 32640316 32640316 single base substitution A T missense_variant M653L 1957A>T MALY-DE 2 32652362 32652362 single base substitution T A intron_variant MALY-DE 2 32652808 32652809 deletion of <=200bp GT - intron_variant MALY-DE 2 32653057 32653057 single base substitution T G intron_variant MALY-DE 2 32657399 32657399 single base substitution C T intron_variant MALY-DE 2 32657399 32657399 single base substitution C T upstream_gene_variant MALY-DE 2 32660932 32660932 single base substitution T G intron_variant MALY-DE 2 32660932 32660932 single base substitution T G upstream_gene_variant MALY-DE 2 32671163 32671163 single base substitution A T downstream_gene_variant MALY-DE 2 32671163 32671163 single base substitution A T intron_variant MALY-DE 2 32678785 32678785 single base substitution T A downstream_gene_variant MALY-DE 2 32678785 32678785 single base substitution T A intron_variant MALY-DE 2 32679772 32679772 single base substitution T G intron_variant MALY-DE 2 32681800 32681800 single base substitution A C intron_variant MALY-DE 2 32684999 32684999 single base substitution A T intron_variant MALY-DE 2 32686861 32686861 single base substitution C T intron_variant MALY-DE 2 32693394 32693394 single base substitution T G intron_variant MALY-DE 2 32693394 32693394 single base substitution T G upstream_gene_variant MALY-DE 2 32696666 32696666 single base substitution A G intron_variant MALY-DE 2 32696666 32696666 single base substitution A G upstream_gene_variant MALY-DE 2 32699928 32699928 single base substitution A G intron_variant MALY-DE 2 32702627 32702627 deletion of <=200bp A - downstream_gene_variant MALY-DE 2 32702627 32702627 deletion of <=200bp A - frameshift_variant A2348 MALY-DE 2 32705854 32705854 single base substitution C T downstream_gene_variant MALY-DE 2 32705854 32705854 single base substitution C T intron_variant MALY-DE 2 32708089 32708089 single base substitution G C intron_variant MALY-DE 2 32708771 32708771 single base substitution A T intron_variant MALY-DE 2 32710032 32710032 single base substitution C T intron_variant MALY-DE 2 32716818 32716818 single base substitution C G intron_variant MALY-DE 2 32723053 32723053 single base substitution G T intron_variant MALY-DE 2 32723053 32723053 single base substitution G T upstream_gene_variant MALY-DE 2 32723564 32723564 single base substitution T C intron_variant MALY-DE 2 32723564 32723564 single base substitution T C upstream_gene_variant MALY-DE 2 32724567 32724568 deletion of <=200bp TC - intron_variant MALY-DE 2 32724567 32724568 deletion of <=200bp TC - upstream_gene_variant MALY-DE 2 32736541 32736541 single base substitution T G intron_variant MALY-DE 2 32736541 32736541 single base substitution T G upstream_gene_variant MALY-DE 2 32739155 32739155 single base substitution A G downstream_gene_variant MALY-DE 2 32739155 32739155 single base substitution A G intron_variant MALY-DE 2 32739155 32739155 single base substitution A G upstream_gene_variant MALY-DE 2 32739894 32739895 deletion of <=200bp TA - downstream_gene_variant MALY-DE 2 32739894 32739895 deletion of <=200bp TA - intron_variant MALY-DE 2 32739894 32739895 deletion of <=200bp TA - upstream_gene_variant MALY-DE 2 32740211 32740211 single base substitution C G downstream_gene_variant MALY-DE 2 32740211 32740211 single base substitution C G missense_variant H3575D 10723C>G MALY-DE 2 32740211 32740211 single base substitution C G upstream_gene_variant MALY-DE 2 32741271 32741271 single base substitution A G downstream_gene_variant MALY-DE 2 32741271 32741271 single base substitution A G intron_variant MALY-DE 2 32748393 32748393 single base substitution T G downstream_gene_variant MALY-DE 2 32748393 32748393 single base substitution T G intron_variant MALY-DE 2 32748393 32748393 single base substitution T G upstream_gene_variant MALY-DE 2 32763571 32763571 single base substitution A G intron_variant MALY-DE 2 32763912 32763912 single base substitution T G intron_variant MALY-DE 2 32776252 32776252 single base substitution T C intron_variant MALY-DE 2 32780534 32780534 single base substitution C T intron_variant MALY-DE 2 32783521 32783521 single base substitution C G intron_variant MALY-DE 2 32789867 32789867 single base substitution C T intron_variant MALY-DE 2 32801517 32801517 single base substitution T C intron_variant MALY-DE 2 32802141 32802141 single base substitution A G intron_variant MALY-DE 2 32807565 32807565 single base substitution T C intron_variant MALY-DE 2 32813283 32813283 single base substitution G A intron_variant MALY-DE 2 32826734 32826734 single base substitution G C intron_variant MALY-DE 2 32826734 32826734 single base substitution G C upstream_gene_variant MALY-DE 2 32832630 32832630 single base substitution T C exon_variant MALY-DE 2 32832630 32832630 single base substitution T C missense_variant Y4727H 14179T>C MALY-DE 2 32833088 32833088 single base substitution G T intron_variant MALY-DE 2 32847348 32847348 single base substitution T A downstream_gene_variant MELA-AU 2 32577146 32577146 single base substitution C T upstream_gene_variant MELA-AU 2 32577979 32577979 single base substitution C T upstream_gene_variant MELA-AU 2 32578472 32578472 single base substitution C T upstream_gene_variant MELA-AU 2 32578927 32578927 single base substitution G A upstream_gene_variant MELA-AU 2 32579224 32579225 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 2 32579305 32579305 single base substitution C T upstream_gene_variant MELA-AU 2 32579417 32579417 single base substitution C T upstream_gene_variant MELA-AU 2 32579458 32579458 single base substitution C T upstream_gene_variant MELA-AU 2 32579910 32579910 single base substitution T A upstream_gene_variant MELA-AU 2 32580372 32580372 single base substitution C T upstream_gene_variant MELA-AU 2 32582609 32582609 single base substitution C T intron_variant MELA-AU 2 32583529 32583529 single base substitution C T intron_variant MELA-AU 2 32583981 32583981 single base substitution C T intron_variant MELA-AU 2 32585038 32585038 single base substitution G A intron_variant MELA-AU 2 32585556 32585556 single base substitution C T intron_variant MELA-AU 2 32586992 32586992 single base substitution C T intron_variant MELA-AU 2 32587486 32587486 single base substitution C T intron_variant MELA-AU 2 32587582 32587582 single base substitution T C intron_variant MELA-AU 2 32587883 32587883 single base substitution C T intron_variant MELA-AU 2 32588430 32588430 single base substitution C T intron_variant MELA-AU 2 32589361 32589361 single base substitution T C intron_variant MELA-AU 2 32590561 32590561 single base substitution C T intron_variant MELA-AU 2 32591315 32591315 single base substitution C T intron_variant MELA-AU 2 32591316 32591316 single base substitution C T intron_variant MELA-AU 2 32591798 32591798 single base substitution C T intron_variant MELA-AU 2 32592643 32592644 multiple base substitution (>=2bp and <=200bp) AC TT intron_variant MELA-AU 2 32592807 32592808 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32592857 32592857 single base substitution C T intron_variant MELA-AU 2 32593545 32593545 single base substitution T C intron_variant MELA-AU 2 32594126 32594126 single base substitution G A intron_variant MELA-AU 2 32594134 32594134 single base substitution C T intron_variant MELA-AU 2 32594402 32594402 single base substitution C T intron_variant MELA-AU 2 32594753 32594753 single base substitution C T intron_variant MELA-AU 2 32596473 32596473 single base substitution C G intron_variant MELA-AU 2 32596970 32596970 single base substitution T C intron_variant MELA-AU 2 32597124 32597124 single base substitution C T intron_variant MELA-AU 2 32597371 32597371 single base substitution C T intron_variant MELA-AU 2 32597545 32597545 single base substitution C T intron_variant MELA-AU 2 32598750 32598750 single base substitution C T intron_variant MELA-AU 2 32599457 32599457 single base substitution C T intron_variant MELA-AU 2 32599759 32599759 deletion of <=200bp C - intron_variant MELA-AU 2 32599807 32599807 single base substitution T C intron_variant MELA-AU 2 32600340 32600340 single base substitution G A intron_variant MELA-AU 2 32600536 32600536 single base substitution C T intron_variant MELA-AU 2 32601496 32601496 single base substitution T A intron_variant MELA-AU 2 32602216 32602216 single base substitution C T intron_variant MELA-AU 2 32602217 32602218 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32603355 32603355 single base substitution C T intron_variant MELA-AU 2 32603471 32603471 single base substitution C T intron_variant MELA-AU 2 32603887 32603887 single base substitution C T intron_variant MELA-AU 2 32604362 32604362 single base substitution C T intron_variant MELA-AU 2 32604373 32604373 single base substitution G A intron_variant MELA-AU 2 32606202 32606202 single base substitution C T intron_variant MELA-AU 2 32606208 32606208 single base substitution C T intron_variant MELA-AU 2 32606504 32606504 single base substitution C T intron_variant MELA-AU 2 32606847 32606847 single base substitution C T intron_variant MELA-AU 2 32607304 32607304 single base substitution C T intron_variant MELA-AU 2 32608709 32608710 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32609002 32609002 single base substitution C T intron_variant MELA-AU 2 32609002 32609002 single base substitution C T upstream_gene_variant MELA-AU 2 32609178 32609178 single base substitution C T intron_variant MELA-AU 2 32609178 32609178 single base substitution C T upstream_gene_variant MELA-AU 2 32609648 32609649 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32609648 32609649 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 2 32610265 32610265 single base substitution C T intron_variant MELA-AU 2 32610265 32610265 single base substitution C T upstream_gene_variant MELA-AU 2 32610560 32610560 single base substitution C T intron_variant MELA-AU 2 32610560 32610560 single base substitution C T upstream_gene_variant MELA-AU 2 32611599 32611599 single base substitution C T intron_variant MELA-AU 2 32611599 32611599 single base substitution C T upstream_gene_variant MELA-AU 2 32611803 32611803 single base substitution C T intron_variant MELA-AU 2 32611803 32611803 single base substitution C T upstream_gene_variant MELA-AU 2 32611906 32611906 single base substitution T A intron_variant MELA-AU 2 32611906 32611906 single base substitution T A upstream_gene_variant MELA-AU 2 32611974 32611974 single base substitution C T intron_variant MELA-AU 2 32611974 32611974 single base substitution C T upstream_gene_variant MELA-AU 2 32612181 32612181 single base substitution C A intron_variant MELA-AU 2 32612181 32612181 single base substitution C A upstream_gene_variant MELA-AU 2 32612260 32612260 single base substitution A G intron_variant MELA-AU 2 32612260 32612260 single base substitution A G upstream_gene_variant MELA-AU 2 32612613 32612613 single base substitution A C intron_variant MELA-AU 2 32612613 32612613 single base substitution A C upstream_gene_variant MELA-AU 2 32613275 32613275 single base substitution C T intron_variant MELA-AU 2 32613275 32613275 single base substitution C T upstream_gene_variant MELA-AU 2 32613331 32613331 single base substitution C T intron_variant MELA-AU 2 32613331 32613331 single base substitution C T upstream_gene_variant MELA-AU 2 32613332 32613332 single base substitution C T intron_variant MELA-AU 2 32613332 32613332 single base substitution C T upstream_gene_variant MELA-AU 2 32614115 32614115 single base substitution C T intron_variant MELA-AU 2 32614405 32614405 single base substitution C T intron_variant MELA-AU 2 32614459 32614459 single base substitution G A intron_variant MELA-AU 2 32614687 32614688 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32614855 32614855 single base substitution C T intron_variant MELA-AU 2 32614874 32614874 single base substitution C T intron_variant MELA-AU 2 32615348 32615348 single base substitution C T intron_variant MELA-AU 2 32615582 32615582 single base substitution C T intron_variant MELA-AU 2 32616919 32616919 single base substitution C T intron_variant MELA-AU 2 32617579 32617579 single base substitution C T intron_variant MELA-AU 2 32619922 32619922 single base substitution T C intron_variant MELA-AU 2 32620142 32620142 single base substitution C T intron_variant MELA-AU 2 32620302 32620302 single base substitution C T intron_variant MELA-AU 2 32621720 32621720 single base substitution C T intron_variant MELA-AU 2 32621826 32621826 single base substitution C T intron_variant MELA-AU 2 32622672 32622672 single base substitution G A intron_variant MELA-AU 2 32622721 32622721 single base substitution C T intron_variant MELA-AU 2 32624890 32624890 single base substitution C T intron_variant MELA-AU 2 32625151 32625151 single base substitution G A intron_variant MELA-AU 2 32625441 32625441 single base substitution C T intron_variant MELA-AU 2 32625456 32625456 single base substitution G T intron_variant MELA-AU 2 32626210 32626210 single base substitution C T intron_variant MELA-AU 2 32626253 32626254 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 2 32626253 32626254 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P353L 1057CC>TT MELA-AU 2 32627043 32627043 single base substitution A G downstream_gene_variant MELA-AU 2 32627043 32627043 single base substitution A G intron_variant MELA-AU 2 32628137 32628137 single base substitution C T downstream_gene_variant MELA-AU 2 32628137 32628137 single base substitution C T intron_variant MELA-AU 2 32628218 32628218 single base substitution C T downstream_gene_variant MELA-AU 2 32628218 32628218 single base substitution C T intron_variant MELA-AU 2 32628418 32628418 single base substitution C T downstream_gene_variant MELA-AU 2 32628418 32628418 single base substitution C T intron_variant MELA-AU 2 32628562 32628562 single base substitution G A downstream_gene_variant MELA-AU 2 32628562 32628562 single base substitution G A intron_variant MELA-AU 2 32629533 32629533 single base substitution C T downstream_gene_variant MELA-AU 2 32629533 32629533 single base substitution C T intron_variant MELA-AU 2 32629571 32629571 single base substitution C T downstream_gene_variant MELA-AU 2 32629571 32629571 single base substitution C T intron_variant MELA-AU 2 32629741 32629741 single base substitution T A downstream_gene_variant MELA-AU 2 32629741 32629741 single base substitution T A intron_variant MELA-AU 2 32630177 32630177 single base substitution G A downstream_gene_variant MELA-AU 2 32630177 32630177 single base substitution G A intron_variant MELA-AU 2 32630885 32630885 single base substitution C T downstream_gene_variant MELA-AU 2 32630885 32630885 single base substitution C T intron_variant MELA-AU 2 32631207 32631207 single base substitution C T downstream_gene_variant MELA-AU 2 32631207 32631207 single base substitution C T intron_variant MELA-AU 2 32632196 32632196 single base substitution G A intron_variant MELA-AU 2 32632230 32632230 single base substitution T G intron_variant MELA-AU 2 32632855 32632855 single base substitution C T intron_variant MELA-AU 2 32633350 32633350 single base substitution C T intron_variant MELA-AU 2 32633604 32633604 single base substitution C T intron_variant MELA-AU 2 32633605 32633605 single base substitution C T intron_variant MELA-AU 2 32633922 32633922 single base substitution C T intron_variant MELA-AU 2 32634108 32634108 single base substitution C T intron_variant MELA-AU 2 32634318 32634318 single base substitution C T intron_variant MELA-AU 2 32635201 32635201 single base substitution C T intron_variant MELA-AU 2 32635933 32635933 single base substitution T G intron_variant MELA-AU 2 32636214 32636214 single base substitution C T intron_variant MELA-AU 2 32636225 32636225 single base substitution C T intron_variant MELA-AU 2 32638331 32638331 single base substitution C T intron_variant MELA-AU 2 32639053 32639053 single base substitution C T intron_variant MELA-AU 2 32639735 32639735 single base substitution A C intron_variant MELA-AU 2 32640055 32640055 single base substitution T A missense_variant C566S 1696T>A MELA-AU 2 32641450 32641450 single base substitution C A intron_variant MELA-AU 2 32642294 32642294 single base substitution T A intron_variant MELA-AU 2 32642703 32642703 single base substitution A C intron_variant MELA-AU 2 32643427 32643427 single base substitution C T intron_variant MELA-AU 2 32644122 32644122 single base substitution C T intron_variant MELA-AU 2 32644402 32644402 single base substitution A T intron_variant MELA-AU 2 32644736 32644736 single base substitution G A intron_variant MELA-AU 2 32644898 32644898 single base substitution G A intron_variant MELA-AU 2 32645203 32645204 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 2 32646129 32646129 single base substitution G A intron_variant MELA-AU 2 32646637 32646637 single base substitution C T intron_variant MELA-AU 2 32647919 32647919 single base substitution C T intron_variant MELA-AU 2 32648754 32648754 single base substitution C T intron_variant MELA-AU 2 32649118 32649118 single base substitution A T intron_variant MELA-AU 2 32649823 32649823 single base substitution C T intron_variant MELA-AU 2 32650687 32650687 single base substitution C T intron_variant MELA-AU 2 32650861 32650861 single base substitution C T intron_variant MELA-AU 2 32650941 32650941 single base substitution C T intron_variant MELA-AU 2 32651055 32651055 single base substitution C T intron_variant MELA-AU 2 32651167 32651167 single base substitution G A intron_variant MELA-AU 2 32651553 32651553 single base substitution C T intron_variant MELA-AU 2 32652397 32652397 single base substitution C T intron_variant MELA-AU 2 32652722 32652722 single base substitution C T intron_variant MELA-AU 2 32653282 32653282 single base substitution C T intron_variant MELA-AU 2 32654484 32654484 single base substitution T C intron_variant MELA-AU 2 32654484 32654484 single base substitution T C upstream_gene_variant MELA-AU 2 32654854 32654854 single base substitution C T intron_variant MELA-AU 2 32654854 32654854 single base substitution C T upstream_gene_variant MELA-AU 2 32654998 32654998 single base substitution A G intron_variant MELA-AU 2 32654998 32654998 single base substitution A G upstream_gene_variant MELA-AU 2 32655618 32655618 single base substitution T A intron_variant MELA-AU 2 32655618 32655618 single base substitution T A upstream_gene_variant MELA-AU 2 32657572 32657572 single base substitution C T intron_variant MELA-AU 2 32657572 32657572 single base substitution C T upstream_gene_variant MELA-AU 2 32658531 32658532 multiple base substitution (>=2bp and <=200bp) TC AT intron_variant MELA-AU 2 32658531 32658532 multiple base substitution (>=2bp and <=200bp) TC AT upstream_gene_variant MELA-AU 2 32658852 32658852 single base substitution C T missense_variant P1130L 3389C>T MELA-AU 2 32658852 32658852 single base substitution C T missense_variant P46L 137C>T MELA-AU 2 32658852 32658852 single base substitution C T upstream_gene_variant MELA-AU 2 32659357 32659357 deletion of <=200bp T - intron_variant MELA-AU 2 32659357 32659357 deletion of <=200bp T - upstream_gene_variant MELA-AU 2 32659466 32659466 single base substitution C T intron_variant MELA-AU 2 32659466 32659466 single base substitution C T upstream_gene_variant MELA-AU 2 32659521 32659521 single base substitution C T intron_variant MELA-AU 2 32659521 32659521 single base substitution C T upstream_gene_variant MELA-AU 2 32659576 32659576 single base substitution G A intron_variant MELA-AU 2 32659576 32659576 single base substitution G A upstream_gene_variant MELA-AU 2 32660389 32660389 single base substitution C T intron_variant MELA-AU 2 32660389 32660389 single base substitution C T upstream_gene_variant MELA-AU 2 32660679 32660679 single base substitution C T intron_variant MELA-AU 2 32660679 32660679 single base substitution C T upstream_gene_variant MELA-AU 2 32660731 32660731 single base substitution C T intron_variant MELA-AU 2 32660731 32660731 single base substitution C T upstream_gene_variant MELA-AU 2 32661363 32661363 single base substitution C T intron_variant MELA-AU 2 32661746 32661746 single base substitution C T intron_variant MELA-AU 2 32662794 32662794 single base substitution T C intron_variant MELA-AU 2 32663263 32663263 single base substitution C T intron_variant MELA-AU 2 32663266 32663266 single base substitution C T intron_variant MELA-AU 2 32664351 32664352 deletion of <=200bp AA - intron_variant MELA-AU 2 32664351 32664352 deletion of <=200bp AA - upstream_gene_variant MELA-AU 2 32664596 32664596 single base substitution C T exon_variant MELA-AU 2 32664596 32664596 single base substitution C T missense_variant R104C 310C>T MELA-AU 2 32664596 32664596 single base substitution C T missense_variant R1218C 3652C>T MELA-AU 2 32664596 32664596 single base substitution C T upstream_gene_variant MELA-AU 2 32664717 32664717 single base substitution C T exon_variant MELA-AU 2 32664717 32664717 single base substitution C T missense_variant S1258L 3773C>T MELA-AU 2 32664717 32664717 single base substitution C T missense_variant S144L 431C>T MELA-AU 2 32664717 32664717 single base substitution C T upstream_gene_variant MELA-AU 2 32665037 32665037 single base substitution C T intron_variant MELA-AU 2 32665037 32665037 single base substitution C T upstream_gene_variant MELA-AU 2 32665057 32665057 single base substitution C T intron_variant MELA-AU 2 32665057 32665057 single base substitution C T upstream_gene_variant MELA-AU 2 32665069 32665069 single base substitution C T intron_variant MELA-AU 2 32665069 32665069 single base substitution C T upstream_gene_variant MELA-AU 2 32665518 32665518 single base substitution C T intron_variant MELA-AU 2 32665518 32665518 single base substitution C T upstream_gene_variant MELA-AU 2 32665545 32665545 single base substitution T G intron_variant MELA-AU 2 32665545 32665545 single base substitution T G upstream_gene_variant MELA-AU 2 32666172 32666173 multiple base substitution (>=2bp and <=200bp) TT GG intron_variant MELA-AU 2 32666172 32666173 multiple base substitution (>=2bp and <=200bp) TT GG upstream_gene_variant MELA-AU 2 32666266 32666290 deletion of <=200bp TATCATTTTAACTTGAGATTTATAT - intron_variant MELA-AU 2 32666266 32666290 deletion of <=200bp TATCATTTTAACTTGAGATTTATAT - upstream_gene_variant MELA-AU 2 32666317 32666317 single base substitution C T intron_variant MELA-AU 2 32666317 32666317 single base substitution C T upstream_gene_variant MELA-AU 2 32666538 32666538 single base substitution C T downstream_gene_variant MELA-AU 2 32666538 32666538 single base substitution C T intron_variant MELA-AU 2 32666538 32666538 single base substitution C T splice_region_variant MELA-AU 2 32666538 32666538 single base substitution C T upstream_gene_variant MELA-AU 2 32666717 32666717 single base substitution C T downstream_gene_variant MELA-AU 2 32666717 32666717 single base substitution C T intron_variant MELA-AU 2 32666717 32666717 single base substitution C T upstream_gene_variant MELA-AU 2 32667980 32667980 single base substitution C T downstream_gene_variant MELA-AU 2 32667980 32667980 single base substitution C T intron_variant MELA-AU 2 32667980 32667980 single base substitution C T upstream_gene_variant MELA-AU 2 32668406 32668406 single base substitution T C downstream_gene_variant MELA-AU 2 32668406 32668406 single base substitution T C intron_variant MELA-AU 2 32668406 32668406 single base substitution T C upstream_gene_variant MELA-AU 2 32668453 32668453 single base substitution C T downstream_gene_variant MELA-AU 2 32668453 32668453 single base substitution C T intron_variant MELA-AU 2 32668453 32668453 single base substitution C T upstream_gene_variant MELA-AU 2 32668824 32668824 single base substitution C T downstream_gene_variant MELA-AU 2 32668824 32668824 single base substitution C T intron_variant MELA-AU 2 32670427 32670428 multiple base substitution (>=2bp and <=200bp) CC AT downstream_gene_variant MELA-AU 2 32670427 32670428 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 2 32670751 32670751 single base substitution C T downstream_gene_variant MELA-AU 2 32670751 32670751 single base substitution C T intron_variant MELA-AU 2 32670874 32670874 single base substitution C T downstream_gene_variant MELA-AU 2 32670874 32670874 single base substitution C T intron_variant MELA-AU 2 32672445 32672445 single base substitution G A downstream_gene_variant MELA-AU 2 32672445 32672445 single base substitution G A intron_variant MELA-AU 2 32672554 32672554 single base substitution C T intron_variant MELA-AU 2 32674109 32674109 single base substitution C T exon_variant MELA-AU 2 32674109 32674109 single base substitution C T intron_variant MELA-AU 2 32674468 32674468 single base substitution T A downstream_gene_variant MELA-AU 2 32674468 32674468 single base substitution T A intron_variant MELA-AU 2 32674479 32674479 single base substitution T G downstream_gene_variant MELA-AU 2 32674479 32674479 single base substitution T G intron_variant MELA-AU 2 32674632 32674632 single base substitution T C downstream_gene_variant MELA-AU 2 32674632 32674632 single base substitution T C intron_variant MELA-AU 2 32675175 32675175 single base substitution C T downstream_gene_variant MELA-AU 2 32675175 32675175 single base substitution C T intron_variant MELA-AU 2 32675372 32675372 single base substitution C T downstream_gene_variant MELA-AU 2 32675372 32675372 single base substitution C T intron_variant MELA-AU 2 32675725 32675725 single base substitution C T downstream_gene_variant MELA-AU 2 32675725 32675725 single base substitution C T intron_variant MELA-AU 2 32675902 32675902 single base substitution C T downstream_gene_variant MELA-AU 2 32675902 32675902 single base substitution C T intron_variant MELA-AU 2 32676503 32676503 single base substitution C T downstream_gene_variant MELA-AU 2 32676503 32676503 single base substitution C T intron_variant MELA-AU 2 32676540 32676540 single base substitution T G downstream_gene_variant MELA-AU 2 32676540 32676540 single base substitution T G intron_variant MELA-AU 2 32677721 32677721 single base substitution C A downstream_gene_variant MELA-AU 2 32677721 32677721 single base substitution C A intron_variant MELA-AU 2 32679206 32679206 single base substitution C T downstream_gene_variant MELA-AU 2 32679206 32679206 single base substitution C T intron_variant MELA-AU 2 32679721 32679721 single base substitution C T intron_variant MELA-AU 2 32679850 32679850 single base substitution C T intron_variant MELA-AU 2 32680821 32680821 single base substitution C T intron_variant MELA-AU 2 32681188 32681188 single base substitution C T intron_variant MELA-AU 2 32682161 32682161 single base substitution C T intron_variant MELA-AU 2 32682174 32682174 single base substitution C T intron_variant MELA-AU 2 32682526 32682526 single base substitution C T intron_variant MELA-AU 2 32682759 32682759 single base substitution C T intron_variant MELA-AU 2 32682813 32682813 single base substitution C G intron_variant MELA-AU 2 32683583 32683583 single base substitution C T intron_variant MELA-AU 2 32683982 32683982 single base substitution C T intron_variant MELA-AU 2 32683991 32683991 single base substitution C T intron_variant MELA-AU 2 32684176 32684176 single base substitution C T intron_variant MELA-AU 2 32684802 32684802 single base substitution C T intron_variant MELA-AU 2 32684891 32684891 single base substitution T C intron_variant MELA-AU 2 32684902 32684902 single base substitution G A intron_variant MELA-AU 2 32685107 32685107 single base substitution C T intron_variant MELA-AU 2 32685826 32685826 single base substitution C T intron_variant MELA-AU 2 32687524 32687524 single base substitution G A intron_variant MELA-AU 2 32687906 32687907 multiple base substitution (>=2bp and <=200bp) CC TA intron_variant MELA-AU 2 32687947 32687947 single base substitution C T intron_variant MELA-AU 2 32688475 32688475 single base substitution C T intron_variant MELA-AU 2 32688811 32688811 single base substitution C T intron_variant MELA-AU 2 32689067 32689067 single base substitution G A intron_variant MELA-AU 2 32691062 32691062 single base substitution G A intron_variant MELA-AU 2 32691269 32691269 single base substitution C T intron_variant MELA-AU 2 32691375 32691375 single base substitution A T intron_variant MELA-AU 2 32691387 32691387 single base substitution C T intron_variant MELA-AU 2 32691398 32691398 single base substitution G A intron_variant MELA-AU 2 32691708 32691708 single base substitution T C intron_variant MELA-AU 2 32692496 32692496 single base substitution C T intron_variant MELA-AU 2 32692789 32692789 single base substitution C T synonymous_variant P1851P 5553C>T MELA-AU 2 32692882 32692882 single base substitution A G intron_variant MELA-AU 2 32692963 32692963 single base substitution C T splice_region_variant MELA-AU 2 32694402 32694402 single base substitution T C intron_variant MELA-AU 2 32694402 32694402 single base substitution T C upstream_gene_variant MELA-AU 2 32695559 32695559 single base substitution C T intron_variant MELA-AU 2 32695559 32695559 single base substitution C T upstream_gene_variant MELA-AU 2 32695559 32695560 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32695559 32695560 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 2 32695868 32695868 single base substitution C A intron_variant MELA-AU 2 32695868 32695868 single base substitution C A upstream_gene_variant MELA-AU 2 32695886 32695886 single base substitution C T intron_variant MELA-AU 2 32695886 32695886 single base substitution C T upstream_gene_variant MELA-AU 2 32696913 32696913 single base substitution G T intron_variant MELA-AU 2 32696913 32696913 single base substitution G T upstream_gene_variant MELA-AU 2 32697802 32697802 single base substitution C T intron_variant MELA-AU 2 32697802 32697802 single base substitution C T upstream_gene_variant MELA-AU 2 32698429 32698429 single base substitution C T intron_variant MELA-AU 2 32698456 32698456 single base substitution C T intron_variant MELA-AU 2 32700155 32700155 single base substitution C T intron_variant MELA-AU 2 32700556 32700556 single base substitution C T intron_variant MELA-AU 2 32700871 32700871 single base substitution A G intron_variant MELA-AU 2 32701039 32701039 single base substitution G A intron_variant MELA-AU 2 32701631 32701631 single base substitution C T downstream_gene_variant MELA-AU 2 32701631 32701631 single base substitution C T intron_variant MELA-AU 2 32701935 32701935 single base substitution A T downstream_gene_variant MELA-AU 2 32701935 32701935 single base substitution A T intron_variant MELA-AU 2 32702391 32702391 single base substitution C T downstream_gene_variant MELA-AU 2 32702391 32702391 single base substitution C T intron_variant MELA-AU 2 32702454 32702454 single base substitution C T downstream_gene_variant MELA-AU 2 32702454 32702454 single base substitution C T missense_variant R2291C 6871C>T MELA-AU 2 32702465 32702465 single base substitution G A downstream_gene_variant MELA-AU 2 32702465 32702465 single base substitution G A synonymous_variant R2294R 6882G>A MELA-AU 2 32702853 32702853 single base substitution G A downstream_gene_variant MELA-AU 2 32702853 32702853 single base substitution G A intron_variant MELA-AU 2 32702971 32702971 single base substitution C T downstream_gene_variant MELA-AU 2 32702971 32702971 single base substitution C T intron_variant MELA-AU 2 32703431 32703431 single base substitution T A downstream_gene_variant MELA-AU 2 32703431 32703431 single base substitution T A intron_variant MELA-AU 2 32703469 32703469 single base substitution C T downstream_gene_variant MELA-AU 2 32703469 32703469 single base substitution C T intron_variant MELA-AU 2 32703962 32703962 single base substitution C T downstream_gene_variant MELA-AU 2 32703962 32703962 single base substitution C T intron_variant MELA-AU 2 32704124 32704124 single base substitution G A downstream_gene_variant MELA-AU 2 32704124 32704124 single base substitution G A intron_variant MELA-AU 2 32704519 32704519 single base substitution C T downstream_gene_variant MELA-AU 2 32704519 32704519 single base substitution C T intron_variant MELA-AU 2 32705053 32705053 single base substitution C T downstream_gene_variant MELA-AU 2 32705053 32705053 single base substitution C T intron_variant MELA-AU 2 32705748 32705748 single base substitution C T downstream_gene_variant MELA-AU 2 32705748 32705748 single base substitution C T intron_variant MELA-AU 2 32706351 32706351 single base substitution A G intron_variant MELA-AU 2 32706827 32706827 single base substitution C T intron_variant MELA-AU 2 32707112 32707112 single base substitution A T intron_variant MELA-AU 2 32707489 32707489 single base substitution C T splice_region_variant MELA-AU 2 32707643 32707643 single base substitution C T synonymous_variant V2563V 7689C>T MELA-AU 2 32707679 32707679 single base substitution A G intron_variant MELA-AU 2 32707687 32707687 single base substitution C T intron_variant MELA-AU 2 32708140 32708140 single base substitution C G intron_variant MELA-AU 2 32708533 32708533 single base substitution C T intron_variant MELA-AU 2 32708560 32708560 single base substitution C T intron_variant MELA-AU 2 32708982 32708983 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32709003 32709003 single base substitution C T intron_variant MELA-AU 2 32709383 32709383 single base substitution C T intron_variant MELA-AU 2 32709406 32709406 single base substitution G A intron_variant MELA-AU 2 32709503 32709503 single base substitution C T intron_variant MELA-AU 2 32710372 32710372 single base substitution C T intron_variant MELA-AU 2 32710637 32710637 single base substitution C T intron_variant MELA-AU 2 32711959 32711959 single base substitution C T intron_variant MELA-AU 2 32712008 32712008 single base substitution T A intron_variant MELA-AU 2 32712303 32712303 single base substitution C T intron_variant MELA-AU 2 32712390 32712391 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 2 32712517 32712517 single base substitution C T intron_variant MELA-AU 2 32713826 32713826 single base substitution T C intron_variant MELA-AU 2 32714335 32714335 single base substitution C T intron_variant MELA-AU 2 32715087 32715087 single base substitution C T intron_variant MELA-AU 2 32715656 32715656 single base substitution A G intron_variant MELA-AU 2 32715893 32715893 single base substitution T C intron_variant MELA-AU 2 32715964 32715964 single base substitution C T intron_variant MELA-AU 2 32716498 32716498 single base substitution C T missense_variant S2738F 8213C>T MELA-AU 2 32716678 32716678 single base substitution C T intron_variant MELA-AU 2 32716767 32716767 single base substitution T G intron_variant MELA-AU 2 32717095 32717095 single base substitution A T intron_variant MELA-AU 2 32717259 32717259 single base substitution C T intron_variant MELA-AU 2 32718461 32718461 single base substitution C T intron_variant MELA-AU 2 32719197 32719197 single base substitution T C intron_variant MELA-AU 2 32719380 32719380 single base substitution C T intron_variant MELA-AU 2 32719385 32719385 single base substitution C T intron_variant MELA-AU 2 32719391 32719391 single base substitution T C intron_variant MELA-AU 2 32719419 32719419 single base substitution C T intron_variant MELA-AU 2 32719580 32719580 single base substitution A C intron_variant MELA-AU 2 32719758 32719758 single base substitution C T intron_variant MELA-AU 2 32720289 32720289 single base substitution T A intron_variant MELA-AU 2 32720396 32720396 single base substitution C T intron_variant MELA-AU 2 32720762 32720762 single base substitution C T intron_variant MELA-AU 2 32721001 32721001 single base substitution T C intron_variant MELA-AU 2 32721226 32721226 single base substitution C T intron_variant MELA-AU 2 32721763 32721763 single base substitution C T intron_variant MELA-AU 2 32721809 32721809 single base substitution A T intron_variant MELA-AU 2 32722140 32722140 single base substitution C T intron_variant MELA-AU 2 32722654 32722654 single base substitution G T intron_variant MELA-AU 2 32722708 32722708 single base substitution G T intron_variant MELA-AU 2 32722981 32722981 single base substitution T A intron_variant MELA-AU 2 32722981 32722981 single base substitution T A upstream_gene_variant MELA-AU 2 32723590 32723590 single base substitution T A intron_variant MELA-AU 2 32723590 32723590 single base substitution T A upstream_gene_variant MELA-AU 2 32723906 32723906 single base substitution G A intron_variant MELA-AU 2 32723906 32723906 single base substitution G A upstream_gene_variant MELA-AU 2 32724217 32724217 single base substitution T C intron_variant MELA-AU 2 32724217 32724217 single base substitution T C upstream_gene_variant MELA-AU 2 32724287 32724287 single base substitution C T intron_variant MELA-AU 2 32724287 32724287 single base substitution C T upstream_gene_variant MELA-AU 2 32725576 32725576 single base substitution C T intron_variant MELA-AU 2 32725576 32725576 single base substitution C T upstream_gene_variant MELA-AU 2 32725929 32725929 single base substitution C T intron_variant MELA-AU 2 32725929 32725929 single base substitution C T upstream_gene_variant MELA-AU 2 32727123 32727124 multiple base substitution (>=2bp and <=200bp) CT TC intron_variant MELA-AU 2 32727123 32727124 multiple base substitution (>=2bp and <=200bp) CT TC upstream_gene_variant MELA-AU 2 32727406 32727406 single base substitution T A intron_variant MELA-AU 2 32727406 32727406 single base substitution T A upstream_gene_variant MELA-AU 2 32727662 32727662 single base substitution T G intron_variant MELA-AU 2 32727662 32727662 single base substitution T G upstream_gene_variant MELA-AU 2 32727691 32727691 single base substitution G T intron_variant MELA-AU 2 32727691 32727691 single base substitution G T upstream_gene_variant MELA-AU 2 32728782 32728782 single base substitution C T intron_variant MELA-AU 2 32728886 32728886 single base substitution C T intron_variant MELA-AU 2 32729318 32729318 single base substitution T A intron_variant MELA-AU 2 32729405 32729405 single base substitution T C intron_variant MELA-AU 2 32729756 32729756 single base substitution A C intron_variant MELA-AU 2 32729756 32729756 single base substitution A C upstream_gene_variant MELA-AU 2 32729819 32729819 single base substitution T A intron_variant MELA-AU 2 32729819 32729819 single base substitution T A upstream_gene_variant MELA-AU 2 32730257 32730257 single base substitution C T exon_variant MELA-AU 2 32730257 32730257 single base substitution C T missense_variant L3229F 9685C>T MELA-AU 2 32730257 32730257 single base substitution C T upstream_gene_variant MELA-AU 2 32730528 32730528 single base substitution C T downstream_gene_variant MELA-AU 2 32730528 32730528 single base substitution C T intron_variant MELA-AU 2 32730528 32730528 single base substitution C T upstream_gene_variant MELA-AU 2 32730740 32730740 single base substitution C T downstream_gene_variant MELA-AU 2 32730740 32730740 single base substitution C T intron_variant MELA-AU 2 32730740 32730740 single base substitution C T upstream_gene_variant MELA-AU 2 32730811 32730811 single base substitution A T downstream_gene_variant MELA-AU 2 32730811 32730811 single base substitution A T intron_variant MELA-AU 2 32730811 32730811 single base substitution A T upstream_gene_variant MELA-AU 2 32732184 32732184 single base substitution C T downstream_gene_variant MELA-AU 2 32732184 32732184 single base substitution C T intron_variant MELA-AU 2 32732184 32732184 single base substitution C T upstream_gene_variant MELA-AU 2 32732576 32732576 single base substitution C T downstream_gene_variant MELA-AU 2 32732576 32732576 single base substitution C T intron_variant MELA-AU 2 32732576 32732576 single base substitution C T upstream_gene_variant MELA-AU 2 32732807 32732807 single base substitution T G downstream_gene_variant MELA-AU 2 32732807 32732807 single base substitution T G intron_variant MELA-AU 2 32732807 32732807 single base substitution T G upstream_gene_variant MELA-AU 2 32733057 32733057 single base substitution C T downstream_gene_variant MELA-AU 2 32733057 32733057 single base substitution C T synonymous_variant S3237S 9711C>T MELA-AU 2 32733057 32733057 single base substitution C T upstream_gene_variant MELA-AU 2 32733196 32733196 single base substitution C T downstream_gene_variant MELA-AU 2 32733196 32733196 single base substitution C T missense_variant R3284C 9850C>T MELA-AU 2 32733196 32733196 single base substitution C T upstream_gene_variant MELA-AU 2 32734192 32734192 single base substitution G A downstream_gene_variant MELA-AU 2 32734192 32734192 single base substitution G A intron_variant MELA-AU 2 32734192 32734192 single base substitution G A upstream_gene_variant MELA-AU 2 32734480 32734481 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 2 32734480 32734481 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32734480 32734481 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 2 32735863 32735863 single base substitution C T intron_variant MELA-AU 2 32735863 32735863 single base substitution C T upstream_gene_variant MELA-AU 2 32736177 32736177 single base substitution C T intron_variant MELA-AU 2 32736177 32736177 single base substitution C T upstream_gene_variant MELA-AU 2 32736270 32736270 single base substitution T C intron_variant MELA-AU 2 32736270 32736270 single base substitution T C upstream_gene_variant MELA-AU 2 32737205 32737206 multiple base substitution (>=2bp and <=200bp) TC AT intron_variant MELA-AU 2 32737205 32737206 multiple base substitution (>=2bp and <=200bp) TC AT upstream_gene_variant MELA-AU 2 32739444 32739444 single base substitution C T downstream_gene_variant MELA-AU 2 32739444 32739444 single base substitution C T intron_variant MELA-AU 2 32739444 32739444 single base substitution C T upstream_gene_variant MELA-AU 2 32739557 32739557 single base substitution G A downstream_gene_variant MELA-AU 2 32739557 32739557 single base substitution G A intron_variant MELA-AU 2 32739557 32739557 single base substitution G A upstream_gene_variant MELA-AU 2 32739634 32739634 single base substitution C T downstream_gene_variant MELA-AU 2 32739634 32739634 single base substitution C T intron_variant MELA-AU 2 32739634 32739634 single base substitution C T upstream_gene_variant MELA-AU 2 32740054 32740054 single base substitution T C downstream_gene_variant MELA-AU 2 32740054 32740054 single base substitution T C splice_region_variant MELA-AU 2 32740054 32740054 single base substitution T C upstream_gene_variant MELA-AU 2 32740161 32740161 single base substitution C T downstream_gene_variant MELA-AU 2 32740161 32740161 single base substitution C T missense_variant S3558F 10673C>T MELA-AU 2 32740161 32740161 single base substitution C T upstream_gene_variant MELA-AU 2 32740464 32740464 single base substitution T A downstream_gene_variant MELA-AU 2 32740464 32740464 single base substitution T A missense_variant I3659N 10976T>A MELA-AU 2 32740464 32740464 single base substitution T A upstream_gene_variant MELA-AU 2 32742112 32742112 single base substitution G A downstream_gene_variant MELA-AU 2 32742112 32742112 single base substitution G A intron_variant MELA-AU 2 32742384 32742384 single base substitution G T downstream_gene_variant MELA-AU 2 32742384 32742384 single base substitution G T intron_variant MELA-AU 2 32742722 32742722 single base substitution C T downstream_gene_variant MELA-AU 2 32742722 32742722 single base substitution C T intron_variant MELA-AU 2 32742800 32742800 single base substitution C T downstream_gene_variant MELA-AU 2 32742800 32742800 single base substitution C T intron_variant MELA-AU 2 32742819 32742819 single base substitution T C downstream_gene_variant MELA-AU 2 32742819 32742819 single base substitution T C intron_variant MELA-AU 2 32743249 32743249 single base substitution C T intron_variant MELA-AU 2 32743456 32743456 single base substitution C T exon_variant MELA-AU 2 32743456 32743456 single base substitution C T missense_variant P3829S 11485C>T MELA-AU 2 32743760 32743760 single base substitution C T intron_variant MELA-AU 2 32744842 32744842 single base substitution C T downstream_gene_variant MELA-AU 2 32744842 32744842 single base substitution C T intron_variant MELA-AU 2 32744842 32744842 single base substitution C T upstream_gene_variant MELA-AU 2 32745465 32745465 single base substitution T G downstream_gene_variant MELA-AU 2 32745465 32745465 single base substitution T G intron_variant MELA-AU 2 32745465 32745465 single base substitution T G upstream_gene_variant MELA-AU 2 32746958 32746958 single base substitution C T downstream_gene_variant MELA-AU 2 32746958 32746958 single base substitution C T intron_variant MELA-AU 2 32746958 32746958 single base substitution C T upstream_gene_variant MELA-AU 2 32746984 32746984 single base substitution G A downstream_gene_variant MELA-AU 2 32746984 32746984 single base substitution G A intron_variant MELA-AU 2 32746984 32746984 single base substitution G A upstream_gene_variant MELA-AU 2 32747065 32747065 deletion of <=200bp T - downstream_gene_variant MELA-AU 2 32747065 32747065 deletion of <=200bp T - intron_variant MELA-AU 2 32747065 32747065 deletion of <=200bp T - upstream_gene_variant MELA-AU 2 32747130 32747130 single base substitution C T downstream_gene_variant MELA-AU 2 32747130 32747130 single base substitution C T intron_variant MELA-AU 2 32747130 32747130 single base substitution C T upstream_gene_variant MELA-AU 2 32747938 32747938 deletion of <=200bp T - downstream_gene_variant MELA-AU 2 32747938 32747938 deletion of <=200bp T - intron_variant MELA-AU 2 32747938 32747938 deletion of <=200bp T - upstream_gene_variant MELA-AU 2 32750498 32750498 single base substitution C G intron_variant MELA-AU 2 32750707 32750707 single base substitution C T intron_variant MELA-AU 2 32750828 32750828 single base substitution C T intron_variant MELA-AU 2 32752104 32752104 single base substitution C T intron_variant MELA-AU 2 32753153 32753153 single base substitution C T intron_variant MELA-AU 2 32753974 32753974 single base substitution C T intron_variant MELA-AU 2 32754692 32754692 single base substitution G A intron_variant MELA-AU 2 32754750 32754750 single base substitution C T exon_variant MELA-AU 2 32754750 32754750 single base substitution C T stop_gained Q3985* 11953C>T MELA-AU 2 32754783 32754783 single base substitution C T exon_variant MELA-AU 2 32754783 32754783 single base substitution C T missense_variant P3996S 11986C>T MELA-AU 2 32754941 32754941 single base substitution C T intron_variant MELA-AU 2 32755380 32755380 single base substitution T G intron_variant MELA-AU 2 32757070 32757070 single base substitution G A intron_variant MELA-AU 2 32757173 32757173 single base substitution A G intron_variant MELA-AU 2 32757175 32757176 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 2 32759923 32759923 single base substitution C T intron_variant MELA-AU 2 32761933 32761933 single base substitution C T intron_variant MELA-AU 2 32761992 32761992 single base substitution C T intron_variant MELA-AU 2 32762041 32762041 single base substitution C T intron_variant MELA-AU 2 32762649 32762649 single base substitution C T intron_variant MELA-AU 2 32762988 32762988 single base substitution C T intron_variant MELA-AU 2 32763929 32763929 single base substitution C T intron_variant MELA-AU 2 32763969 32763969 single base substitution C T intron_variant MELA-AU 2 32765492 32765492 single base substitution C T intron_variant MELA-AU 2 32765675 32765675 single base substitution C T intron_variant MELA-AU 2 32766882 32766882 single base substitution C T intron_variant MELA-AU 2 32767028 32767028 single base substitution C T intron_variant MELA-AU 2 32767560 32767560 single base substitution A C intron_variant MELA-AU 2 32767590 32767590 single base substitution C T intron_variant MELA-AU 2 32768092 32768092 single base substitution C T intron_variant MELA-AU 2 32768157 32768157 single base substitution G A intron_variant MELA-AU 2 32768204 32768204 single base substitution C T intron_variant MELA-AU 2 32768270 32768270 single base substitution A G intron_variant MELA-AU 2 32769728 32769728 single base substitution C T intron_variant MELA-AU 2 32769830 32769830 single base substitution C T intron_variant MELA-AU 2 32770526 32770526 single base substitution C T intron_variant MELA-AU 2 32771203 32771203 single base substitution C T intron_variant MELA-AU 2 32771204 32771204 single base substitution C T intron_variant MELA-AU 2 32771317 32771317 single base substitution C T intron_variant MELA-AU 2 32771814 32771829 deletion of <=200bp TCTAAGAGTAAATCTG - intron_variant MELA-AU 2 32771833 32771833 single base substitution A G intron_variant MELA-AU 2 32772343 32772343 single base substitution C T intron_variant MELA-AU 2 32772633 32772633 single base substitution C T intron_variant MELA-AU 2 32773047 32773047 single base substitution G A exon_variant MELA-AU 2 32773047 32773047 single base substitution G A missense_variant R4314K 12941G>A MELA-AU 2 32773160 32773160 single base substitution C T intron_variant MELA-AU 2 32773596 32773597 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32773793 32773793 single base substitution G A intron_variant MELA-AU 2 32774791 32774791 single base substitution T A intron_variant MELA-AU 2 32775252 32775252 single base substitution C T intron_variant MELA-AU 2 32776037 32776037 single base substitution C T intron_variant MELA-AU 2 32777622 32777622 single base substitution C T intron_variant MELA-AU 2 32777972 32777972 single base substitution C G intron_variant MELA-AU 2 32778319 32778319 single base substitution T C intron_variant MELA-AU 2 32778828 32778828 single base substitution T A intron_variant MELA-AU 2 32779302 32779302 single base substitution C T intron_variant MELA-AU 2 32779361 32779361 single base substitution C T intron_variant MELA-AU 2 32779904 32779904 single base substitution C T intron_variant MELA-AU 2 32780689 32780689 single base substitution C T intron_variant MELA-AU 2 32781770 32781770 single base substitution C T intron_variant MELA-AU 2 32782012 32782012 single base substitution C A intron_variant MELA-AU 2 32782014 32782014 single base substitution A G intron_variant MELA-AU 2 32782329 32782329 single base substitution T C intron_variant MELA-AU 2 32782350 32782350 single base substitution C T intron_variant MELA-AU 2 32782438 32782438 single base substitution G T intron_variant MELA-AU 2 32783812 32783812 single base substitution T A intron_variant MELA-AU 2 32786042 32786042 single base substitution G A intron_variant MELA-AU 2 32787207 32787207 single base substitution C T intron_variant MELA-AU 2 32787426 32787426 single base substitution C T intron_variant MELA-AU 2 32789059 32789059 single base substitution C T intron_variant MELA-AU 2 32789198 32789198 single base substitution C T intron_variant MELA-AU 2 32789357 32789357 single base substitution G A intron_variant MELA-AU 2 32789466 32789467 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 2 32789998 32789998 single base substitution G A intron_variant MELA-AU 2 32791138 32791138 single base substitution A T intron_variant MELA-AU 2 32791179 32791179 single base substitution A G intron_variant MELA-AU 2 32791808 32791808 single base substitution C T intron_variant MELA-AU 2 32792007 32792007 single base substitution C T intron_variant MELA-AU 2 32792291 32792292 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32792373 32792373 single base substitution C A intron_variant MELA-AU 2 32792378 32792378 single base substitution G A intron_variant MELA-AU 2 32792386 32792386 single base substitution C T intron_variant MELA-AU 2 32792582 32792582 single base substitution T A intron_variant MELA-AU 2 32793848 32793848 single base substitution T C intron_variant MELA-AU 2 32795100 32795100 single base substitution C T intron_variant MELA-AU 2 32795851 32795851 single base substitution C T intron_variant MELA-AU 2 32795851 32795851 single base substitution C T upstream_gene_variant MELA-AU 2 32796970 32796970 single base substitution C T intron_variant MELA-AU 2 32796970 32796970 single base substitution C T upstream_gene_variant MELA-AU 2 32797177 32797177 single base substitution C A intron_variant MELA-AU 2 32797177 32797177 single base substitution C A upstream_gene_variant MELA-AU 2 32798882 32798882 single base substitution T C intron_variant MELA-AU 2 32798882 32798882 single base substitution T C upstream_gene_variant MELA-AU 2 32799938 32799938 single base substitution C T intron_variant MELA-AU 2 32799938 32799938 single base substitution C T upstream_gene_variant MELA-AU 2 32800650 32800650 single base substitution T C intron_variant MELA-AU 2 32800958 32800959 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32801451 32801451 single base substitution C T intron_variant MELA-AU 2 32801510 32801510 single base substitution T C intron_variant MELA-AU 2 32802042 32802042 single base substitution T C intron_variant MELA-AU 2 32802606 32802606 single base substitution C T intron_variant MELA-AU 2 32803248 32803248 single base substitution C T intron_variant MELA-AU 2 32803961 32803961 single base substitution C T intron_variant MELA-AU 2 32804638 32804639 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 2 32805005 32805005 single base substitution A C intron_variant MELA-AU 2 32805867 32805867 single base substitution C T intron_variant MELA-AU 2 32806107 32806107 single base substitution C T intron_variant MELA-AU 2 32806124 32806124 single base substitution C T intron_variant MELA-AU 2 32807035 32807035 single base substitution T A intron_variant MELA-AU 2 32807074 32807074 single base substitution T C intron_variant MELA-AU 2 32807122 32807122 single base substitution C T intron_variant MELA-AU 2 32807335 32807335 single base substitution G A intron_variant MELA-AU 2 32808311 32808311 single base substitution C T intron_variant MELA-AU 2 32808594 32808594 single base substitution C T intron_variant MELA-AU 2 32808682 32808682 single base substitution G A intron_variant MELA-AU 2 32808741 32808741 single base substitution A G intron_variant MELA-AU 2 32808772 32808772 single base substitution C T intron_variant MELA-AU 2 32808809 32808809 single base substitution T G intron_variant MELA-AU 2 32808810 32808810 single base substitution C T intron_variant MELA-AU 2 32809272 32809272 single base substitution C T intron_variant MELA-AU 2 32810170 32810170 single base substitution C T intron_variant MELA-AU 2 32810688 32810688 single base substitution C T intron_variant MELA-AU 2 32811050 32811050 single base substitution A C intron_variant MELA-AU 2 32811598 32811598 single base substitution C T intron_variant MELA-AU 2 32812745 32812745 single base substitution C T intron_variant MELA-AU 2 32813377 32813377 single base substitution C T intron_variant MELA-AU 2 32813908 32813908 single base substitution C T intron_variant MELA-AU 2 32813949 32813949 single base substitution C T intron_variant MELA-AU 2 32814562 32814562 single base substitution C T intron_variant MELA-AU 2 32815248 32815248 single base substitution T A intron_variant MELA-AU 2 32815323 32815323 single base substitution G A intron_variant MELA-AU 2 32815404 32815404 single base substitution T C intron_variant MELA-AU 2 32816314 32816314 single base substitution C T intron_variant MELA-AU 2 32816655 32816655 single base substitution A G intron_variant MELA-AU 2 32817887 32817887 single base substitution C T intron_variant MELA-AU 2 32817905 32817906 multiple base substitution (>=2bp and <=200bp) AC TT intron_variant MELA-AU 2 32818649 32818649 single base substitution C T intron_variant MELA-AU 2 32818794 32818794 single base substitution C G intron_variant MELA-AU 2 32818949 32818949 single base substitution C T intron_variant MELA-AU 2 32819731 32819731 single base substitution C T downstream_gene_variant MELA-AU 2 32819731 32819731 single base substitution C T intron_variant MELA-AU 2 32819788 32819788 single base substitution T C downstream_gene_variant MELA-AU 2 32819788 32819788 single base substitution T C intron_variant MELA-AU 2 32819800 32819800 single base substitution C T downstream_gene_variant MELA-AU 2 32819800 32819800 single base substitution C T intron_variant MELA-AU 2 32819804 32819804 single base substitution T C downstream_gene_variant MELA-AU 2 32819804 32819804 single base substitution T C intron_variant MELA-AU 2 32819818 32819818 single base substitution C A downstream_gene_variant MELA-AU 2 32819818 32819818 single base substitution C A intron_variant MELA-AU 2 32820026 32820026 single base substitution A G downstream_gene_variant MELA-AU 2 32820026 32820026 single base substitution A G intron_variant MELA-AU 2 32820365 32820365 single base substitution C T downstream_gene_variant MELA-AU 2 32820365 32820365 single base substitution C T intron_variant MELA-AU 2 32821107 32821107 single base substitution C T downstream_gene_variant MELA-AU 2 32821107 32821107 single base substitution C T intron_variant MELA-AU 2 32821512 32821512 single base substitution G A downstream_gene_variant MELA-AU 2 32821512 32821512 single base substitution G A intron_variant MELA-AU 2 32821772 32821772 single base substitution C T downstream_gene_variant MELA-AU 2 32821772 32821772 single base substitution C T intron_variant MELA-AU 2 32822157 32822157 single base substitution C T downstream_gene_variant MELA-AU 2 32822157 32822157 single base substitution C T intron_variant MELA-AU 2 32822302 32822302 single base substitution C T downstream_gene_variant MELA-AU 2 32822302 32822302 single base substitution C T intron_variant MELA-AU 2 32822497 32822497 single base substitution C T downstream_gene_variant MELA-AU 2 32822497 32822497 single base substitution C T intron_variant MELA-AU 2 32822597 32822597 single base substitution C T downstream_gene_variant MELA-AU 2 32822597 32822597 single base substitution C T intron_variant MELA-AU 2 32822597 32822597 single base substitution C T upstream_gene_variant MELA-AU 2 32822836 32822836 single base substitution C T downstream_gene_variant MELA-AU 2 32822836 32822836 single base substitution C T exon_variant MELA-AU 2 32822836 32822836 single base substitution C T missense_variant S4544F 13631C>T MELA-AU 2 32822836 32822836 single base substitution C T upstream_gene_variant MELA-AU 2 32823417 32823417 single base substitution T G downstream_gene_variant MELA-AU 2 32823417 32823417 single base substitution T G intron_variant MELA-AU 2 32823417 32823417 single base substitution T G upstream_gene_variant MELA-AU 2 32823464 32823464 single base substitution C T downstream_gene_variant MELA-AU 2 32823464 32823464 single base substitution C T intron_variant MELA-AU 2 32823464 32823464 single base substitution C T upstream_gene_variant MELA-AU 2 32825302 32825302 single base substitution C T intron_variant MELA-AU 2 32825302 32825302 single base substitution C T upstream_gene_variant MELA-AU 2 32826740 32826740 single base substitution T A intron_variant MELA-AU 2 32826740 32826740 single base substitution T A upstream_gene_variant MELA-AU 2 32827533 32827533 single base substitution T G intron_variant MELA-AU 2 32827533 32827533 single base substitution T G upstream_gene_variant MELA-AU 2 32827940 32827940 single base substitution T A exon_variant MELA-AU 2 32827940 32827940 single base substitution T A intron_variant MELA-AU 2 32827953 32827953 single base substitution A C exon_variant MELA-AU 2 32827953 32827953 single base substitution A C intron_variant MELA-AU 2 32828398 32828398 single base substitution C T intron_variant MELA-AU 2 32829385 32829385 single base substitution C T intron_variant MELA-AU 2 32830506 32830506 single base substitution C T intron_variant MELA-AU 2 32831535 32831535 single base substitution C T intron_variant MELA-AU 2 32832236 32832236 single base substitution C T intron_variant MELA-AU 2 32833444 32833444 single base substitution C T intron_variant MELA-AU 2 32833454 32833454 single base substitution C T intron_variant MELA-AU 2 32833470 32833470 single base substitution C T intron_variant MELA-AU 2 32833790 32833790 single base substitution T C intron_variant MELA-AU 2 32834147 32834147 single base substitution C T intron_variant MELA-AU 2 32835122 32835122 single base substitution C T intron_variant MELA-AU 2 32835837 32835837 single base substitution C T intron_variant MELA-AU 2 32835874 32835874 single base substitution C T intron_variant MELA-AU 2 32836017 32836017 single base substitution G A intron_variant MELA-AU 2 32836303 32836303 single base substitution G A intron_variant MELA-AU 2 32836940 32836940 single base substitution C T downstream_gene_variant MELA-AU 2 32836940 32836940 single base substitution C T intron_variant MELA-AU 2 32836972 32836972 single base substitution C T downstream_gene_variant MELA-AU 2 32836972 32836972 single base substitution C T intron_variant MELA-AU 2 32837452 32837452 single base substitution G A downstream_gene_variant MELA-AU 2 32837452 32837452 single base substitution G A intron_variant MELA-AU 2 32837530 32837530 single base substitution C T downstream_gene_variant MELA-AU 2 32837530 32837530 single base substitution C T intron_variant MELA-AU 2 32838717 32838717 single base substitution C T downstream_gene_variant MELA-AU 2 32838717 32838717 single base substitution C T intron_variant MELA-AU 2 32838747 32838747 single base substitution C T downstream_gene_variant MELA-AU 2 32838747 32838747 single base substitution C T intron_variant MELA-AU 2 32839526 32839526 single base substitution G A downstream_gene_variant MELA-AU 2 32839526 32839526 single base substitution G A intron_variant MELA-AU 2 32839643 32839643 single base substitution C T downstream_gene_variant MELA-AU 2 32839643 32839643 single base substitution C T intron_variant MELA-AU 2 32839813 32839813 single base substitution C T downstream_gene_variant MELA-AU 2 32839813 32839813 single base substitution C T intron_variant MELA-AU 2 32840254 32840254 single base substitution C T downstream_gene_variant MELA-AU 2 32840254 32840254 single base substitution C T intron_variant MELA-AU 2 32840311 32840311 single base substitution G A downstream_gene_variant MELA-AU 2 32840311 32840311 single base substitution G A intron_variant MELA-AU 2 32841017 32841017 single base substitution C T downstream_gene_variant MELA-AU 2 32841017 32841017 single base substitution C T intron_variant MELA-AU 2 32841048 32841048 single base substitution C T downstream_gene_variant MELA-AU 2 32841048 32841048 single base substitution C T intron_variant MELA-AU 2 32842352 32842352 single base substitution C T intron_variant MELA-AU 2 32842606 32842606 single base substitution A G intron_variant MELA-AU 2 32842832 32842832 single base substitution C T exon_variant MELA-AU 2 32842832 32842832 single base substitution C T missense_variant P4812L 14435C>T MELA-AU 2 32843754 32843754 single base substitution C T 3_prime_UTR_variant MELA-AU 2 32843754 32843754 single base substitution C T exon_variant MELA-AU 2 32843759 32843759 single base substitution G T 3_prime_UTR_variant MELA-AU 2 32843759 32843759 single base substitution G T exon_variant MELA-AU 2 32844396 32844396 single base substitution C T downstream_gene_variant MELA-AU 2 32844635 32844635 single base substitution G A downstream_gene_variant MELA-AU 2 32845568 32845568 single base substitution T G downstream_gene_variant MELA-AU 2 32846220 32846221 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 2 32847225 32847225 single base substitution C T downstream_gene_variant MELA-AU 2 32847536 32847536 single base substitution C T downstream_gene_variant MELA-AU 2 32847679 32847679 single base substitution C T downstream_gene_variant MELA-AU 2 32847707 32847707 single base substitution C T downstream_gene_variant MELA-AU 2 32847934 32847934 single base substitution C T downstream_gene_variant MELA-AU 2 32848475 32848475 single base substitution A T downstream_gene_variant ORCA-IN 2 32605381 32605381 single base substitution C G intron_variant ORCA-IN 2 32606913 32606913 single base substitution C T intron_variant ORCA-IN 2 32621993 32621993 single base substitution G A intron_variant ORCA-IN 2 32626286 32626286 single base substitution C A exon_variant ORCA-IN 2 32626286 32626286 single base substitution C A missense_variant Q364K 1090C>A ORCA-IN 2 32651333 32651333 single base substitution C T intron_variant ORCA-IN 2 32679343 32679343 single base substitution G A intron_variant ORCA-IN 2 32686070 32686071 multiple base substitution (>=2bp and <=200bp) CT GC intron_variant ORCA-IN 2 32686135 32686135 single base substitution G C intron_variant ORCA-IN 2 32690725 32690725 single base substitution C G intron_variant ORCA-IN 2 32691210 32691210 single base substitution C G intron_variant ORCA-IN 2 32693147 32693147 single base substitution G C missense_variant M1916I 5748G>C ORCA-IN 2 32693147 32693147 single base substitution G C upstream_gene_variant ORCA-IN 2 32707988 32707988 deletion of <=200bp G - intron_variant ORCA-IN 2 32722868 32722868 single base substitution A T intron_variant ORCA-IN 2 32724843 32724843 single base substitution C G missense_variant L2900V 8698C>G ORCA-IN 2 32724843 32724843 single base substitution C G upstream_gene_variant ORCA-IN 2 32732500 32732500 single base substitution C T downstream_gene_variant ORCA-IN 2 32732500 32732500 single base substitution C T intron_variant ORCA-IN 2 32732500 32732500 single base substitution C T upstream_gene_variant ORCA-IN 2 32779415 32779415 single base substitution G T intron_variant ORCA-IN 2 32787231 32787231 single base substitution T A intron_variant ORCA-IN 2 32788376 32788376 single base substitution C T intron_variant ORCA-IN 2 32805021 32805021 deletion of <=200bp G - intron_variant ORCA-IN 2 32805295 32805295 single base substitution A G intron_variant ORCA-IN 2 32822932 32822932 single base substitution G A downstream_gene_variant ORCA-IN 2 32822932 32822932 single base substitution G A exon_variant ORCA-IN 2 32822932 32822932 single base substitution G A missense_variant R4576H 13727G>A ORCA-IN 2 32822932 32822932 single base substitution G A upstream_gene_variant ORCA-IN 2 32822937 32822937 single base substitution C G downstream_gene_variant ORCA-IN 2 32822937 32822937 single base substitution C G exon_variant ORCA-IN 2 32822937 32822937 single base substitution C G missense_variant L4578V 13732C>G ORCA-IN 2 32822937 32822937 single base substitution C G upstream_gene_variant ORCA-IN 2 32823198 32823198 insertion of <=200bp - CC downstream_gene_variant ORCA-IN 2 32823198 32823198 insertion of <=200bp - CC intron_variant ORCA-IN 2 32823198 32823198 insertion of <=200bp - CC upstream_gene_variant OV-AU 2 32578730 32578730 single base substitution C G upstream_gene_variant OV-AU 2 32579250 32579250 single base substitution C A upstream_gene_variant OV-AU 2 32587934 32587934 single base substitution C A intron_variant OV-AU 2 32591228 32591228 single base substitution C G intron_variant OV-AU 2 32596142 32596142 single base substitution G A intron_variant OV-AU 2 32596567 32596567 single base substitution C G intron_variant OV-AU 2 32602555 32602555 single base substitution A C intron_variant OV-AU 2 32602744 32602744 single base substitution G A synonymous_variant K138K 414G>A OV-AU 2 32608137 32608137 single base substitution C T intron_variant OV-AU 2 32622015 32622015 single base substitution C T intron_variant OV-AU 2 32622016 32622016 single base substitution G T intron_variant OV-AU 2 32624167 32624167 single base substitution T A intron_variant OV-AU 2 32641858 32641858 single base substitution C A intron_variant OV-AU 2 32645240 32645240 single base substitution T C intron_variant OV-AU 2 32645430 32645430 single base substitution T C intron_variant OV-AU 2 32647293 32647293 single base substitution T C intron_variant OV-AU 2 32654015 32654015 single base substitution T C intron_variant OV-AU 2 32654015 32654015 single base substitution T C upstream_gene_variant OV-AU 2 32658208 32658208 single base substitution C T intron_variant OV-AU 2 32658208 32658208 single base substitution C T upstream_gene_variant OV-AU 2 32663366 32663366 single base substitution C A intron_variant OV-AU 2 32666256 32666256 single base substitution G T intron_variant OV-AU 2 32666256 32666256 single base substitution G T upstream_gene_variant OV-AU 2 32670431 32670431 single base substitution G A downstream_gene_variant OV-AU 2 32670431 32670431 single base substitution G A intron_variant OV-AU 2 32675959 32675959 single base substitution A G downstream_gene_variant OV-AU 2 32675959 32675959 single base substitution A G intron_variant OV-AU 2 32677720 32677720 single base substitution C G downstream_gene_variant OV-AU 2 32677720 32677720 single base substitution C G intron_variant OV-AU 2 32686857 32686857 single base substitution C A intron_variant OV-AU 2 32688513 32688513 single base substitution T C intron_variant OV-AU 2 32688998 32688998 single base substitution C G intron_variant OV-AU 2 32689996 32689996 single base substitution G A intron_variant OV-AU 2 32691676 32691676 single base substitution C G intron_variant OV-AU 2 32692446 32692446 single base substitution G C intron_variant OV-AU 2 32695530 32695530 single base substitution C T intron_variant OV-AU 2 32695530 32695530 single base substitution C T upstream_gene_variant OV-AU 2 32701896 32701896 single base substitution A G downstream_gene_variant OV-AU 2 32701896 32701896 single base substitution A G intron_variant OV-AU 2 32705442 32705442 single base substitution C G downstream_gene_variant OV-AU 2 32705442 32705442 single base substitution C G intron_variant OV-AU 2 32706619 32706619 single base substitution G A intron_variant OV-AU 2 32711439 32711439 single base substitution G T intron_variant OV-AU 2 32712181 32712181 single base substitution A C intron_variant OV-AU 2 32725807 32725807 single base substitution G C intron_variant OV-AU 2 32725807 32725807 single base substitution G C upstream_gene_variant OV-AU 2 32726149 32726149 single base substitution T C intron_variant OV-AU 2 32726149 32726149 single base substitution T C upstream_gene_variant OV-AU 2 32733628 32733628 single base substitution G C downstream_gene_variant OV-AU 2 32733628 32733628 single base substitution G C intron_variant OV-AU 2 32733628 32733628 single base substitution G C upstream_gene_variant OV-AU 2 32734684 32734684 single base substitution T C downstream_gene_variant OV-AU 2 32734684 32734684 single base substitution T C intron_variant OV-AU 2 32734684 32734684 single base substitution T C upstream_gene_variant OV-AU 2 32737511 32737511 single base substitution T G intron_variant OV-AU 2 32737511 32737511 single base substitution T G upstream_gene_variant OV-AU 2 32738723 32738723 single base substitution A T downstream_gene_variant OV-AU 2 32738723 32738723 single base substitution A T intron_variant OV-AU 2 32738723 32738723 single base substitution A T upstream_gene_variant OV-AU 2 32741780 32741780 single base substitution T C downstream_gene_variant OV-AU 2 32741780 32741780 single base substitution T C intron_variant OV-AU 2 32744591 32744591 single base substitution T C downstream_gene_variant OV-AU 2 32744591 32744591 single base substitution T C intron_variant OV-AU 2 32753430 32753430 single base substitution A G intron_variant OV-AU 2 32754343 32754343 single base substitution C A intron_variant OV-AU 2 32757608 32757608 single base substitution C T intron_variant OV-AU 2 32758211 32758211 single base substitution G T intron_variant OV-AU 2 32775762 32775762 single base substitution G T intron_variant OV-AU 2 32778303 32778303 single base substitution A G intron_variant OV-AU 2 32784646 32784646 single base substitution T C intron_variant OV-AU 2 32787423 32787423 single base substitution G C intron_variant OV-AU 2 32789123 32789123 single base substitution C T intron_variant OV-AU 2 32796003 32796003 single base substitution T C intron_variant OV-AU 2 32796003 32796003 single base substitution T C upstream_gene_variant OV-AU 2 32799041 32799041 single base substitution T C intron_variant OV-AU 2 32799041 32799041 single base substitution T C upstream_gene_variant OV-AU 2 32799045 32799045 single base substitution C A intron_variant OV-AU 2 32799045 32799045 single base substitution C A upstream_gene_variant OV-AU 2 32800924 32800924 single base substitution G C intron_variant OV-AU 2 32804931 32804931 single base substitution T A intron_variant OV-AU 2 32805511 32805511 single base substitution A T intron_variant OV-AU 2 32814591 32814591 single base substitution T A intron_variant OV-AU 2 32815164 32815164 single base substitution T G intron_variant OV-AU 2 32818360 32818360 single base substitution T G intron_variant OV-AU 2 32819028 32819028 single base substitution G C exon_variant OV-AU 2 32819028 32819028 single base substitution G C missense_variant D4468H 13402G>C OV-AU 2 32821404 32821404 single base substitution G A downstream_gene_variant OV-AU 2 32821404 32821404 single base substitution G A intron_variant OV-AU 2 32823219 32823219 single base substitution G A downstream_gene_variant OV-AU 2 32823219 32823219 single base substitution G A intron_variant OV-AU 2 32823219 32823219 single base substitution G A upstream_gene_variant OV-AU 2 32835109 32835109 single base substitution G A intron_variant OV-AU 2 32836188 32836188 single base substitution T C intron_variant OV-AU 2 32841202 32841202 single base substitution G C downstream_gene_variant OV-AU 2 32841202 32841202 single base substitution G C intron_variant OV-AU 2 32841769 32841769 single base substitution G C intron_variant OV-AU 2 32844325 32844325 single base substitution G A downstream_gene_variant PACA-AU 2 32582259 32582259 single base substitution C T synonymous_variant P10P 30C>T PACA-AU 2 32582302 32582302 single base substitution G A missense_variant A25T 73G>A PACA-AU 2 32593389 32593389 single base substitution T C intron_variant PACA-AU 2 32597844 32597844 single base substitution G A intron_variant PACA-AU 2 32601016 32601016 single base substitution G T intron_variant PACA-AU 2 32601017 32601017 single base substitution G T intron_variant PACA-AU 2 32603089 32603089 deletion of <=200bp A - intron_variant PACA-AU 2 32604958 32604958 single base substitution T C intron_variant PACA-AU 2 32605734 32605734 single base substitution C T intron_variant PACA-AU 2 32606457 32606457 single base substitution G A intron_variant PACA-AU 2 32611503 32611504 deletion of <=200bp TC - intron_variant PACA-AU 2 32611503 32611504 deletion of <=200bp TC - upstream_gene_variant PACA-AU 2 32618468 32618468 single base substitution G A intron_variant PACA-AU 2 32618938 32618938 single base substitution T G intron_variant PACA-AU 2 32620941 32620941 single base substitution G A intron_variant PACA-AU 2 32629396 32629396 single base substitution C T downstream_gene_variant PACA-AU 2 32629396 32629396 single base substitution C T intron_variant PACA-AU 2 32629397 32629397 single base substitution T C downstream_gene_variant PACA-AU 2 32629397 32629397 single base substitution T C intron_variant PACA-AU 2 32629739 32629739 single base substitution T C downstream_gene_variant PACA-AU 2 32629739 32629739 single base substitution T C intron_variant PACA-AU 2 32638580 32638580 single base substitution T G intron_variant PACA-AU 2 32641392 32641392 insertion of <=200bp - T intron_variant PACA-AU 2 32641931 32641931 single base substitution T G intron_variant PACA-AU 2 32652974 32652977 deletion of <=200bp AAAC - intron_variant PACA-AU 2 32653514 32653514 single base substitution A T intron_variant PACA-AU 2 32655894 32655894 single base substitution T C intron_variant PACA-AU 2 32655894 32655894 single base substitution T C upstream_gene_variant PACA-AU 2 32656396 32656396 single base substitution T A intron_variant PACA-AU 2 32656396 32656396 single base substitution T A upstream_gene_variant PACA-AU 2 32661201 32661201 single base substitution C A exon_variant PACA-AU 2 32661201 32661201 single base substitution C A missense_variant L1194I 3580C>A PACA-AU 2 32661201 32661201 single base substitution C A missense_variant L80I 238C>A PACA-AU 2 32664877 32664877 single base substitution A G intron_variant PACA-AU 2 32664877 32664877 single base substitution A G upstream_gene_variant PACA-AU 2 32666716 32666716 single base substitution C T downstream_gene_variant PACA-AU 2 32666716 32666716 single base substitution C T intron_variant PACA-AU 2 32666716 32666716 single base substitution C T upstream_gene_variant PACA-AU 2 32675390 32675390 single base substitution C G downstream_gene_variant PACA-AU 2 32675390 32675390 single base substitution C G intron_variant PACA-AU 2 32679770 32679770 single base substitution G A intron_variant PACA-AU 2 32681268 32681268 single base substitution T C intron_variant PACA-AU 2 32681665 32681665 single base substitution C T intron_variant PACA-AU 2 32685188 32685188 single base substitution T C intron_variant PACA-AU 2 32688702 32688702 single base substitution C A intron_variant PACA-AU 2 32688970 32688970 single base substitution C T intron_variant PACA-AU 2 32691165 32691165 single base substitution T A intron_variant PACA-AU 2 32693478 32693487 deletion of <=200bp ATTTTGTTCA - intron_variant PACA-AU 2 32693478 32693487 deletion of <=200bp ATTTTGTTCA - upstream_gene_variant PACA-AU 2 32701451 32701451 single base substitution G T downstream_gene_variant PACA-AU 2 32701451 32701451 single base substitution G T intron_variant PACA-AU 2 32708506 32708506 single base substitution T C intron_variant PACA-AU 2 32717413 32717413 single base substitution A G intron_variant PACA-AU 2 32725117 32725117 single base substitution T A missense_variant M2991K 8972T>A PACA-AU 2 32725117 32725117 single base substitution T A upstream_gene_variant PACA-AU 2 32730107 32730114 deletion of <=200bp GCTGAAGT - exon_variant PACA-AU 2 32730107 32730114 deletion of <=200bp GCTGAAGT - frameshift_variant AEV3179 PACA-AU 2 32730107 32730114 deletion of <=200bp GCTGAAGT - upstream_gene_variant PACA-AU 2 32732174 32732174 single base substitution T A downstream_gene_variant PACA-AU 2 32732174 32732174 single base substitution T A intron_variant PACA-AU 2 32732174 32732174 single base substitution T A upstream_gene_variant PACA-AU 2 32733862 32733862 single base substitution G A downstream_gene_variant PACA-AU 2 32733862 32733862 single base substitution G A intron_variant PACA-AU 2 32733862 32733862 single base substitution G A upstream_gene_variant PACA-AU 2 32747025 32747025 single base substitution G A downstream_gene_variant PACA-AU 2 32747025 32747025 single base substitution G A intron_variant PACA-AU 2 32747025 32747025 single base substitution G A upstream_gene_variant PACA-AU 2 32750864 32750864 single base substitution G A intron_variant PACA-AU 2 32755011 32755011 single base substitution T C intron_variant PACA-AU 2 32763372 32763372 single base substitution A G intron_variant PACA-AU 2 32767185 32767185 single base substitution A C intron_variant PACA-AU 2 32768807 32768807 single base substitution A G intron_variant PACA-AU 2 32770301 32770301 deletion of <=200bp A - intron_variant PACA-AU 2 32781065 32781065 single base substitution C A intron_variant PACA-AU 2 32782263 32782263 single base substitution T G intron_variant PACA-AU 2 32783943 32783943 single base substitution T A intron_variant PACA-AU 2 32786503 32786503 single base substitution C T intron_variant PACA-AU 2 32795094 32795094 single base substitution T G intron_variant PACA-AU 2 32802228 32802228 single base substitution C T intron_variant PACA-AU 2 32803869 32803869 insertion of <=200bp - AAAT intron_variant PACA-AU 2 32808878 32808878 single base substitution G A intron_variant PACA-AU 2 32809039 32809049 deletion of <=200bp TCTGCCCATCT - intron_variant PACA-AU 2 32810068 32810068 single base substitution A C intron_variant PACA-AU 2 32823123 32823123 single base substitution A G downstream_gene_variant PACA-AU 2 32823123 32823123 single base substitution A G intron_variant PACA-AU 2 32823123 32823123 single base substitution A G upstream_gene_variant PACA-AU 2 32828504 32828504 single base substitution A C intron_variant PACA-AU 2 32828553 32828553 single base substitution G T intron_variant PACA-AU 2 32829967 32829967 single base substitution T C intron_variant PACA-AU 2 32832241 32832241 single base substitution T C intron_variant PACA-AU 2 32833880 32833880 single base substitution C G intron_variant PACA-AU 2 32834473 32834473 single base substitution T G intron_variant PACA-AU 2 32838446 32838446 single base substitution T A downstream_gene_variant PACA-AU 2 32838446 32838446 single base substitution T A intron_variant PACA-CA 2 32577604 32577604 single base substitution T C upstream_gene_variant PACA-CA 2 32577687 32577687 single base substitution C T upstream_gene_variant PACA-CA 2 32579613 32579613 single base substitution C T upstream_gene_variant PACA-CA 2 32581081 32581081 single base substitution T C upstream_gene_variant PACA-CA 2 32586551 32586551 single base substitution G C intron_variant PACA-CA 2 32587492 32587492 single base substitution T A intron_variant PACA-CA 2 32587854 32587854 insertion of <=200bp - A intron_variant PACA-CA 2 32587873 32587873 single base substitution A T intron_variant PACA-CA 2 32587978 32587978 single base substitution G T intron_variant PACA-CA 2 32589544 32589544 single base substitution C G intron_variant PACA-CA 2 32592374 32592374 single base substitution T C intron_variant PACA-CA 2 32596024 32596024 single base substitution T G intron_variant PACA-CA 2 32604913 32604913 single base substitution T A intron_variant PACA-CA 2 32605520 32605520 single base substitution G A intron_variant PACA-CA 2 32606162 32606162 single base substitution C G intron_variant PACA-CA 2 32618012 32618012 insertion of <=200bp - T intron_variant PACA-CA 2 32620169 32620169 single base substitution C T intron_variant PACA-CA 2 32621049 32621049 single base substitution G T intron_variant PACA-CA 2 32622076 32622076 single base substitution G A intron_variant PACA-CA 2 32622749 32622749 single base substitution C T intron_variant PACA-CA 2 32622751 32622751 single base substitution C T intron_variant PACA-CA 2 32622948 32622948 single base substitution C G intron_variant PACA-CA 2 32625324 32625324 single base substitution A G intron_variant PACA-CA 2 32625856 32625856 single base substitution T G intron_variant PACA-CA 2 32627677 32627677 single base substitution A G downstream_gene_variant PACA-CA 2 32627677 32627677 single base substitution A G intron_variant PACA-CA 2 32629798 32629798 single base substitution C T downstream_gene_variant PACA-CA 2 32629798 32629798 single base substitution C T intron_variant PACA-CA 2 32632651 32632651 single base substitution G A intron_variant PACA-CA 2 32633696 32633696 single base substitution T A intron_variant PACA-CA 2 32638138 32638138 single base substitution G A intron_variant PACA-CA 2 32638343 32638343 single base substitution G C intron_variant PACA-CA 2 32640517 32640517 single base substitution T C synonymous_variant L720L 2158T>C PACA-CA 2 32645469 32645469 single base substitution C G intron_variant PACA-CA 2 32646043 32646043 single base substitution T A intron_variant PACA-CA 2 32659579 32659579 deletion of <=200bp A - intron_variant PACA-CA 2 32659579 32659579 deletion of <=200bp A - upstream_gene_variant PACA-CA 2 32661929 32661929 deletion of <=200bp C - intron_variant PACA-CA 2 32663819 32663819 single base substitution G A intron_variant PACA-CA 2 32663819 32663819 single base substitution G A upstream_gene_variant PACA-CA 2 32664258 32664258 insertion of <=200bp - GTGCGT intron_variant PACA-CA 2 32664258 32664258 insertion of <=200bp - GTGCGT upstream_gene_variant PACA-CA 2 32667119 32667119 single base substitution T G downstream_gene_variant PACA-CA 2 32667119 32667119 single base substitution T G intron_variant PACA-CA 2 32667119 32667119 single base substitution T G upstream_gene_variant PACA-CA 2 32669287 32669287 single base substitution C T downstream_gene_variant PACA-CA 2 32669287 32669287 single base substitution C T intron_variant PACA-CA 2 32671603 32671603 single base substitution G A downstream_gene_variant PACA-CA 2 32671603 32671603 single base substitution G A intron_variant PACA-CA 2 32674767 32674767 single base substitution C G downstream_gene_variant PACA-CA 2 32674767 32674767 single base substitution C G intron_variant PACA-CA 2 32678394 32678394 single base substitution G A downstream_gene_variant PACA-CA 2 32678394 32678394 single base substitution G A intron_variant PACA-CA 2 32679323 32679323 single base substitution G C intron_variant PACA-CA 2 32679416 32679416 single base substitution G T intron_variant PACA-CA 2 32679824 32679824 single base substitution G T intron_variant PACA-CA 2 32679900 32679900 single base substitution G T intron_variant PACA-CA 2 32680071 32680071 single base substitution G C intron_variant PACA-CA 2 32681685 32681685 single base substitution C T intron_variant PACA-CA 2 32682238 32682238 single base substitution C A intron_variant PACA-CA 2 32682915 32682915 single base substitution G T intron_variant PACA-CA 2 32698536 32698536 single base substitution A G intron_variant PACA-CA 2 32698829 32698829 single base substitution T A intron_variant PACA-CA 2 32699932 32699932 deletion of <=200bp T - intron_variant PACA-CA 2 32699942 32699942 single base substitution C T intron_variant PACA-CA 2 32700518 32700518 single base substitution G T intron_variant PACA-CA 2 32701024 32701024 single base substitution T A intron_variant PACA-CA 2 32707475 32707475 insertion of <=200bp - T intron_variant PACA-CA 2 32707607 32707607 deletion of <=200bp G - frameshift_variant T2551 PACA-CA 2 32715833 32715833 single base substitution G T intron_variant PACA-CA 2 32719250 32719250 deletion of <=200bp T - intron_variant PACA-CA 2 32721647 32721647 single base substitution A G intron_variant PACA-CA 2 32722497 32722497 single base substitution G T intron_variant PACA-CA 2 32726313 32726313 single base substitution T A intron_variant PACA-CA 2 32726313 32726313 single base substitution T A upstream_gene_variant PACA-CA 2 32730932 32730932 single base substitution T C downstream_gene_variant PACA-CA 2 32730932 32730932 single base substitution T C intron_variant PACA-CA 2 32730932 32730932 single base substitution T C upstream_gene_variant PACA-CA 2 32731104 32731104 single base substitution C T downstream_gene_variant PACA-CA 2 32731104 32731104 single base substitution C T intron_variant PACA-CA 2 32731104 32731104 single base substitution C T upstream_gene_variant PACA-CA 2 32733261 32733261 single base substitution T C downstream_gene_variant PACA-CA 2 32733261 32733261 single base substitution T C synonymous_variant G3305G 9915T>C PACA-CA 2 32733261 32733261 single base substitution T C upstream_gene_variant PACA-CA 2 32737597 32737597 deletion of <=200bp A - intron_variant PACA-CA 2 32737597 32737597 deletion of <=200bp A - upstream_gene_variant PACA-CA 2 32742689 32742689 single base substitution C T downstream_gene_variant PACA-CA 2 32742689 32742689 single base substitution C T intron_variant PACA-CA 2 32743730 32743730 single base substitution G A intron_variant PACA-CA 2 32747138 32747138 deletion of <=200bp C - downstream_gene_variant PACA-CA 2 32747138 32747138 deletion of <=200bp C - intron_variant PACA-CA 2 32747138 32747138 deletion of <=200bp C - upstream_gene_variant PACA-CA 2 32749258 32749258 single base substitution G T downstream_gene_variant PACA-CA 2 32749258 32749258 single base substitution G T intron_variant PACA-CA 2 32749258 32749258 single base substitution G T upstream_gene_variant PACA-CA 2 32751016 32751016 single base substitution G A intron_variant PACA-CA 2 32756475 32756475 single base substitution G T exon_variant PACA-CA 2 32756475 32756475 single base substitution G T missense_variant D4050Y 12148G>T PACA-CA 2 32758581 32758581 single base substitution T G intron_variant PACA-CA 2 32770577 32770577 single base substitution T C intron_variant PACA-CA 2 32770895 32770895 single base substitution C T exon_variant PACA-CA 2 32770895 32770895 single base substitution C T stop_gained R4260* 12778C>T PACA-CA 2 32772666 32772666 single base substitution A G intron_variant PACA-CA 2 32778620 32778620 insertion of <=200bp - T intron_variant PACA-CA 2 32778789 32778789 single base substitution G A intron_variant PACA-CA 2 32778858 32778858 single base substitution T C intron_variant PACA-CA 2 32782763 32782763 single base substitution G A intron_variant PACA-CA 2 32786808 32786808 single base substitution T A intron_variant PACA-CA 2 32791564 32791564 single base substitution C T intron_variant PACA-CA 2 32797306 32797306 single base substitution A T intron_variant PACA-CA 2 32797306 32797306 single base substitution A T upstream_gene_variant PACA-CA 2 32799058 32799058 deletion of <=200bp T - intron_variant PACA-CA 2 32799058 32799058 deletion of <=200bp T - upstream_gene_variant PACA-CA 2 32800336 32800336 single base substitution G A exon_variant PACA-CA 2 32800336 32800336 single base substitution G A missense_variant G4420S 13258G>A PACA-CA 2 32800336 32800336 single base substitution G A upstream_gene_variant PACA-CA 2 32801623 32801623 single base substitution G A intron_variant PACA-CA 2 32803892 32803892 single base substitution T C intron_variant PACA-CA 2 32804063 32804063 insertion of <=200bp - T intron_variant PACA-CA 2 32804077 32804078 deletion of <=200bp CC - intron_variant PACA-CA 2 32805106 32805106 single base substitution C T intron_variant PACA-CA 2 32806162 32806162 single base substitution C T intron_variant PACA-CA 2 32807587 32807587 single base substitution T C intron_variant PACA-CA 2 32808886 32808886 single base substitution C T intron_variant PACA-CA 2 32812797 32812797 single base substitution A G intron_variant PACA-CA 2 32814571 32814571 single base substitution C T intron_variant PACA-CA 2 32815893 32815893 single base substitution T C exon_variant PACA-CA 2 32815893 32815893 single base substitution T C intron_variant PACA-CA 2 32817668 32817668 single base substitution T C intron_variant PACA-CA 2 32822912 32822912 single base substitution G A downstream_gene_variant PACA-CA 2 32822912 32822912 single base substitution G A exon_variant PACA-CA 2 32822912 32822912 single base substitution G A synonymous_variant A4569A 13707G>A PACA-CA 2 32822912 32822912 single base substitution G A upstream_gene_variant PACA-CA 2 32835307 32835307 single base substitution T C intron_variant PACA-CA 2 32835314 32835314 single base substitution T G intron_variant PACA-CA 2 32838167 32838167 single base substitution T C downstream_gene_variant PACA-CA 2 32838167 32838167 single base substitution T C intron_variant PACA-CA 2 32841298 32841298 single base substitution T A downstream_gene_variant PACA-CA 2 32841298 32841298 single base substitution T A intron_variant PACA-CA 2 32842691 32842691 single base substitution A C intron_variant PACA-CA 2 32844066 32844066 single base substitution C T downstream_gene_variant PACA-CA 2 32848478 32848478 single base substitution G A downstream_gene_variant PACA-CA 2 32848649 32848649 insertion of <=200bp - T downstream_gene_variant PAEN-AU 2 32577772 32577772 single base substitution C T upstream_gene_variant PAEN-AU 2 32597528 32597528 single base substitution T C intron_variant PAEN-AU 2 32673714 32673714 single base substitution G A intron_variant PAEN-AU 2 32710347 32710347 single base substitution A G intron_variant PAEN-AU 2 32726975 32726975 single base substitution A G intron_variant PAEN-AU 2 32726975 32726975 single base substitution A G upstream_gene_variant PAEN-AU 2 32768730 32768730 single base substitution G A intron_variant PAEN-AU 2 32788788 32788788 single base substitution C T intron_variant PAEN-AU 2 32797979 32797979 single base substitution C A intron_variant PAEN-AU 2 32797979 32797979 single base substitution C A upstream_gene_variant PAEN-AU 2 32823554 32823554 single base substitution C T downstream_gene_variant PAEN-AU 2 32823554 32823554 single base substitution C T intron_variant PAEN-AU 2 32823554 32823554 single base substitution C T upstream_gene_variant PAEN-AU 2 32842273 32842273 single base substitution C T intron_variant PAEN-AU 2 32846075 32846075 single base substitution G C downstream_gene_variant PAEN-AU 2 32848718 32848718 single base substitution A G downstream_gene_variant PAEN-IT 2 32589264 32589264 single base substitution G T intron_variant PAEN-IT 2 32599969 32599969 single base substitution C T intron_variant PAEN-IT 2 32616458 32616458 single base substitution C T intron_variant PAEN-IT 2 32729853 32729853 single base substitution A T intron_variant PAEN-IT 2 32729853 32729853 single base substitution A T upstream_gene_variant PAEN-IT 2 32779997 32779997 single base substitution A G intron_variant PAEN-IT 2 32791384 32791384 single base substitution C A intron_variant PBCA-DE 2 32592585 32592585 single base substitution G A intron_variant PBCA-DE 2 32595130 32595131 deletion of <=200bp AC - intron_variant PBCA-DE 2 32600426 32600426 single base substitution T C intron_variant PBCA-DE 2 32602282 32602282 insertion of <=200bp - TG intron_variant PBCA-DE 2 32611371 32611371 single base substitution C A intron_variant PBCA-DE 2 32611371 32611371 single base substitution C A upstream_gene_variant PBCA-DE 2 32622643 32622643 insertion of <=200bp - TG intron_variant PBCA-DE 2 32640418 32640418 single base substitution T A missense_variant Y687N 2059T>A PBCA-DE 2 32670018 32670018 single base substitution C T downstream_gene_variant PBCA-DE 2 32670018 32670018 single base substitution C T intron_variant PBCA-DE 2 32670858 32670858 single base substitution T G downstream_gene_variant PBCA-DE 2 32670858 32670858 single base substitution T G intron_variant PBCA-DE 2 32671436 32671436 single base substitution G A downstream_gene_variant PBCA-DE 2 32671436 32671436 single base substitution G A intron_variant PBCA-DE 2 32679280 32679280 insertion of <=200bp - C intron_variant PBCA-DE 2 32689175 32689175 single base substitution G T intron_variant PBCA-DE 2 32694043 32694043 single base substitution G T intron_variant PBCA-DE 2 32694043 32694043 single base substitution G T upstream_gene_variant PBCA-DE 2 32714449 32714449 single base substitution C T intron_variant PBCA-DE 2 32723383 32723383 single base substitution C A intron_variant PBCA-DE 2 32723383 32723383 single base substitution C A upstream_gene_variant PBCA-DE 2 32726089 32726089 single base substitution T A intron_variant PBCA-DE 2 32726089 32726089 single base substitution T A upstream_gene_variant PBCA-DE 2 32730394 32730394 single base substitution G T exon_variant PBCA-DE 2 32730394 32730394 single base substitution G T intron_variant PBCA-DE 2 32730394 32730394 single base substitution G T upstream_gene_variant PBCA-DE 2 32732685 32732685 single base substitution A T downstream_gene_variant PBCA-DE 2 32732685 32732685 single base substitution A T intron_variant PBCA-DE 2 32732685 32732685 single base substitution A T upstream_gene_variant PBCA-DE 2 32739894 32739895 deletion of <=200bp TA - downstream_gene_variant PBCA-DE 2 32739894 32739895 deletion of <=200bp TA - intron_variant PBCA-DE 2 32739894 32739895 deletion of <=200bp TA - upstream_gene_variant PBCA-DE 2 32742979 32742979 single base substitution A T downstream_gene_variant PBCA-DE 2 32742979 32742979 single base substitution A T intron_variant PBCA-DE 2 32745840 32745840 single base substitution C T downstream_gene_variant PBCA-DE 2 32745840 32745840 single base substitution C T intron_variant PBCA-DE 2 32745840 32745840 single base substitution C T upstream_gene_variant PBCA-DE 2 32750241 32750241 insertion of <=200bp - T intron_variant PBCA-DE 2 32767184 32767185 deletion of <=200bp TA - intron_variant PBCA-DE 2 32770570 32770570 single base substitution T A intron_variant PBCA-DE 2 32770619 32770619 single base substitution C T intron_variant PBCA-DE 2 32789120 32789120 single base substitution G T intron_variant PBCA-DE 2 32802091 32802091 insertion of <=200bp - C intron_variant PBCA-DE 2 32802647 32802647 insertion of <=200bp - TA intron_variant PBCA-DE 2 32804018 32804018 single base substitution G A intron_variant PBCA-DE 2 32811948 32811951 deletion of <=200bp AAAC - intron_variant PBCA-DE 2 32819255 32819255 single base substitution T G exon_variant PBCA-DE 2 32819255 32819255 single base substitution T G intron_variant PBCA-DE 2 32827449 32827449 single base substitution T A intron_variant PBCA-DE 2 32827449 32827449 single base substitution T A upstream_gene_variant PBCA-DE 2 32837017 32837017 single base substitution T C downstream_gene_variant PBCA-DE 2 32837017 32837017 single base substitution T C intron_variant PBCA-DE 2 32842468 32842468 insertion of <=200bp - A intron_variant PBCA-DE 2 32847971 32847971 deletion of <=200bp T - downstream_gene_variant PRAD-CA 2 32597130 32597130 single base substitution C G intron_variant PRAD-CA 2 32605168 32605168 single base substitution T G intron_variant PRAD-CA 2 32613779 32613779 single base substitution A C intron_variant PRAD-CA 2 32613779 32613779 single base substitution A C upstream_gene_variant PRAD-CA 2 32626859 32626859 single base substitution A G downstream_gene_variant PRAD-CA 2 32626859 32626859 single base substitution A G intron_variant PRAD-CA 2 32644219 32644219 single base substitution G A intron_variant PRAD-CA 2 32647337 32647337 single base substitution C T intron_variant PRAD-CA 2 32661764 32661764 single base substitution C T intron_variant PRAD-CA 2 32687809 32687809 single base substitution A C intron_variant PRAD-CA 2 32715090 32715090 single base substitution T C intron_variant PRAD-CA 2 32720034 32720034 single base substitution T A intron_variant PRAD-CA 2 32770122 32770122 single base substitution A C intron_variant PRAD-CA 2 32772976 32772976 single base substitution C G exon_variant PRAD-CA 2 32772976 32772976 single base substitution C G synonymous_variant A4290A 12870C>G PRAD-CA 2 32796747 32796747 single base substitution T G intron_variant PRAD-CA 2 32796747 32796747 single base substitution T G upstream_gene_variant PRAD-CA 2 32804093 32804093 single base substitution C T intron_variant PRAD-CA 2 32821852 32821852 single base substitution G A downstream_gene_variant PRAD-CA 2 32821852 32821852 single base substitution G A intron_variant PRAD-CA 2 32823018 32823018 single base substitution C G downstream_gene_variant PRAD-CA 2 32823018 32823018 single base substitution C G exon_variant PRAD-CA 2 32823018 32823018 single base substitution C G missense_variant R4605G 13813C>G PRAD-CA 2 32823018 32823018 single base substitution C G upstream_gene_variant PRAD-CA 2 32830110 32830110 single base substitution C A intron_variant PRAD-UK 2 32579572 32579572 single base substitution A T upstream_gene_variant PRAD-UK 2 32581777 32581777 single base substitution C G upstream_gene_variant PRAD-UK 2 32586420 32586420 insertion of <=200bp - T intron_variant PRAD-UK 2 32588884 32588884 single base substitution G A intron_variant PRAD-UK 2 32603479 32603479 insertion of <=200bp - T intron_variant PRAD-UK 2 32609227 32609227 single base substitution A G intron_variant PRAD-UK 2 32609227 32609227 single base substitution A G upstream_gene_variant PRAD-UK 2 32615630 32615630 single base substitution C T intron_variant PRAD-UK 2 32616474 32616478 deletion of <=200bp TTCTG - intron_variant PRAD-UK 2 32618339 32618341 deletion of <=200bp GAG - intron_variant PRAD-UK 2 32618652 32618652 single base substitution T A intron_variant PRAD-UK 2 32619564 32619564 single base substitution T C intron_variant PRAD-UK 2 32636479 32636479 single base substitution A G intron_variant PRAD-UK 2 32643223 32643223 single base substitution T C intron_variant PRAD-UK 2 32645481 32645481 insertion of <=200bp - T intron_variant PRAD-UK 2 32650139 32650139 single base substitution T G intron_variant PRAD-UK 2 32652897 32652897 single base substitution T A intron_variant PRAD-UK 2 32655667 32655671 deletion of <=200bp GGTTG - intron_variant PRAD-UK 2 32655667 32655671 deletion of <=200bp GGTTG - upstream_gene_variant PRAD-UK 2 32657930 32657930 single base substitution T G intron_variant PRAD-UK 2 32657930 32657930 single base substitution T G upstream_gene_variant PRAD-UK 2 32673714 32673714 single base substitution G A intron_variant PRAD-UK 2 32685724 32685776 deletion of <=200bp TTGTGCAAAAGATTTCTGATTAGTTCTATAGTATCAGGATGGCTTATTTTTCC - intron_variant PRAD-UK 2 32697708 32697708 single base substitution A T intron_variant PRAD-UK 2 32697708 32697708 single base substitution A T upstream_gene_variant PRAD-UK 2 32699022 32699022 single base substitution G A intron_variant PRAD-UK 2 32701533 32701533 single base substitution G A downstream_gene_variant PRAD-UK 2 32701533 32701533 single base substitution G A intron_variant PRAD-UK 2 32712679 32712679 single base substitution T G intron_variant PRAD-UK 2 32753436 32753436 single base substitution G A intron_variant PRAD-UK 2 32760814 32760814 single base substitution A G intron_variant PRAD-UK 2 32767957 32767957 single base substitution C T intron_variant PRAD-UK 2 32778414 32778414 single base substitution G T intron_variant PRAD-UK 2 32805462 32805462 single base substitution G A intron_variant PRAD-UK 2 32814856 32814856 single base substitution G C intron_variant PRAD-UK 2 32826984 32826984 single base substitution A G intron_variant PRAD-UK 2 32826984 32826984 single base substitution A G upstream_gene_variant PRAD-UK 2 32832847 32832847 single base substitution C G intron_variant PRAD-UK 2 32833844 32833844 single base substitution A G intron_variant PRAD-UK 2 32837298 32837298 single base substitution T C downstream_gene_variant PRAD-UK 2 32837298 32837298 single base substitution T C intron_variant PRAD-US 2 32667453 32667453 single base substitution C T downstream_gene_variant PRAD-US 2 32667453 32667453 single base substitution C T missense_variant R1390C 4168C>T PRAD-US 2 32667453 32667453 single base substitution C T upstream_gene_variant PRAD-US 2 32712725 32712725 single base substitution C A missense_variant P2609T 7825C>A PRAD-US 2 32824954 32824954 single base substitution A C exon_variant PRAD-US 2 32824954 32824954 single base substitution A C missense_variant Y4660S 13979A>C PRAD-US 2 32824954 32824954 single base substitution A C upstream_gene_variant READ-US 2 32641017 32641017 single base substitution G T missense_variant K886N 2658G>T READ-US 2 32654233 32654233 single base substitution C T synonymous_variant L964L 2892C>T READ-US 2 32654233 32654233 single base substitution C T upstream_gene_variant READ-US 2 32656134 32656134 single base substitution G A missense_variant R1075Q 3224G>A READ-US 2 32656134 32656134 single base substitution G A upstream_gene_variant READ-US 2 32696179 32696179 single base substitution G T missense_variant K2193N 6579G>T READ-US 2 32696179 32696179 single base substitution G T upstream_gene_variant READ-US 2 32702649 32702649 single base substitution A G downstream_gene_variant READ-US 2 32702649 32702649 single base substitution A G missense_variant K2356E 7066A>G READ-US 2 32704532 32704532 single base substitution G A downstream_gene_variant READ-US 2 32704532 32704532 single base substitution G A missense_variant E2419K 7255G>A READ-US 2 32724866 32724866 single base substitution A G synonymous_variant K2907K 8721A>G READ-US 2 32724866 32724866 single base substitution A G upstream_gene_variant READ-US 2 32733143 32733143 single base substitution A C downstream_gene_variant READ-US 2 32733143 32733143 single base substitution A C missense_variant K3266T 9797A>C READ-US 2 32733143 32733143 single base substitution A C upstream_gene_variant READ-US 2 32733163 32733163 single base substitution G A downstream_gene_variant READ-US 2 32733163 32733163 single base substitution G A missense_variant E3273K 9817G>A READ-US 2 32733163 32733163 single base substitution G A upstream_gene_variant READ-US 2 32740529 32740529 single base substitution G A downstream_gene_variant READ-US 2 32740529 32740529 single base substitution G A missense_variant D3681N 11041G>A READ-US 2 32740529 32740529 single base substitution G A upstream_gene_variant READ-US 2 32754802 32754802 single base substitution T A exon_variant READ-US 2 32754802 32754802 single base substitution T A missense_variant I4002K 12005T>A READ-US 2 32820100 32820100 insertion of <=200bp - A downstream_gene_variant READ-US 2 32820100 32820100 insertion of <=200bp - A splice_acceptor_variant RECA-CN 2 32692607 32692607 single base substitution G T missense_variant V1791L 5371G>T RECA-EU 2 32607816 32607816 single base substitution G C intron_variant RECA-EU 2 32617613 32617613 single base substitution C T intron_variant RECA-EU 2 32631365 32631365 single base substitution G C downstream_gene_variant RECA-EU 2 32631365 32631365 single base substitution G C intron_variant RECA-EU 2 32632027 32632027 single base substitution C T intron_variant RECA-EU 2 32633474 32633474 single base substitution G C intron_variant RECA-EU 2 32636965 32636965 single base substitution G A intron_variant RECA-EU 2 32638915 32638915 single base substitution C T intron_variant RECA-EU 2 32640490 32640490 single base substitution C T missense_variant P711S 2131C>T RECA-EU 2 32640962 32640962 single base substitution A G missense_variant D868G 2603A>G RECA-EU 2 32645347 32645347 single base substitution A C intron_variant RECA-EU 2 32656081 32656081 single base substitution G T missense_variant R1057S 3171G>T RECA-EU 2 32656081 32656081 single base substitution G T upstream_gene_variant RECA-EU 2 32681057 32681057 single base substitution A T intron_variant RECA-EU 2 32687721 32687721 single base substitution A T intron_variant RECA-EU 2 32698821 32698821 single base substitution T G intron_variant RECA-EU 2 32699148 32699148 single base substitution A T intron_variant RECA-EU 2 32699870 32699870 single base substitution A T intron_variant RECA-EU 2 32704547 32704547 single base substitution G A downstream_gene_variant RECA-EU 2 32704547 32704547 single base substitution G A missense_variant V2424I 7270G>A RECA-EU 2 32704711 32704711 single base substitution T C downstream_gene_variant RECA-EU 2 32704711 32704711 single base substitution T C intron_variant RECA-EU 2 32712562 32712562 single base substitution C A intron_variant RECA-EU 2 32715510 32715510 single base substitution G A intron_variant RECA-EU 2 32738313 32738313 single base substitution G T downstream_gene_variant RECA-EU 2 32738313 32738313 single base substitution G T intron_variant RECA-EU 2 32738313 32738313 single base substitution G T upstream_gene_variant RECA-EU 2 32745227 32745227 single base substitution A G downstream_gene_variant RECA-EU 2 32745227 32745227 single base substitution A G intron_variant RECA-EU 2 32745227 32745227 single base substitution A G upstream_gene_variant RECA-EU 2 32768510 32768510 single base substitution T C exon_variant RECA-EU 2 32768510 32768510 single base substitution T C missense_variant L4165P 12494T>C RECA-EU 2 32782550 32782550 single base substitution C T intron_variant RECA-EU 2 32786993 32786993 single base substitution C G intron_variant RECA-EU 2 32791510 32791510 single base substitution C T intron_variant RECA-EU 2 32796989 32796989 single base substitution C T intron_variant RECA-EU 2 32796989 32796989 single base substitution C T upstream_gene_variant RECA-EU 2 32801717 32801717 single base substitution C A intron_variant RECA-EU 2 32801837 32801837 single base substitution T G intron_variant RECA-EU 2 32810508 32810508 single base substitution G A intron_variant RECA-EU 2 32825969 32825969 single base substitution T C intron_variant RECA-EU 2 32825969 32825969 single base substitution T C upstream_gene_variant RECA-EU 2 32834724 32834724 single base substitution C T intron_variant RECA-EU 2 32843730 32843730 single base substitution T A 3_prime_UTR_variant RECA-EU 2 32843730 32843730 single base substitution T A exon_variant SKCA-BR 2 32579295 32579295 single base substitution T G upstream_gene_variant SKCA-BR 2 32579381 32579381 single base substitution C T upstream_gene_variant SKCA-BR 2 32579411 32579411 single base substitution G A upstream_gene_variant SKCA-BR 2 32580455 32580455 single base substitution T G upstream_gene_variant SKCA-BR 2 32580723 32580723 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 2 32580756 32580756 single base substitution T A upstream_gene_variant SKCA-BR 2 32582128 32582128 single base substitution C T 5_prime_UTR_variant SKCA-BR 2 32585091 32585091 single base substitution C T intron_variant SKCA-BR 2 32595010 32595017 deletion of <=200bp AAAAATAT - intron_variant SKCA-BR 2 32599274 32599274 single base substitution A G intron_variant SKCA-BR 2 32604279 32604279 single base substitution C T intron_variant SKCA-BR 2 32604362 32604362 single base substitution C T intron_variant SKCA-BR 2 32606096 32606096 single base substitution A G intron_variant SKCA-BR 2 32612369 32612370 deletion of <=200bp CT - intron_variant SKCA-BR 2 32612369 32612370 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 2 32613862 32613862 single base substitution C T synonymous_variant S230S 690C>T SKCA-BR 2 32613862 32613862 single base substitution C T upstream_gene_variant SKCA-BR 2 32620888 32620888 single base substitution G A intron_variant SKCA-BR 2 32621265 32621265 single base substitution C T intron_variant SKCA-BR 2 32622239 32622239 single base substitution A G intron_variant SKCA-BR 2 32622431 32622431 single base substitution T A intron_variant SKCA-BR 2 32624163 32624163 insertion of <=200bp - AT intron_variant SKCA-BR 2 32624714 32624715 deletion of <=200bp AG - intron_variant SKCA-BR 2 32626628 32626628 single base substitution C T downstream_gene_variant SKCA-BR 2 32626628 32626628 single base substitution C T missense_variant P452L 1355C>T SKCA-BR 2 32630484 32630484 single base substitution T C downstream_gene_variant SKCA-BR 2 32630484 32630484 single base substitution T C intron_variant SKCA-BR 2 32631475 32631475 single base substitution C T downstream_gene_variant SKCA-BR 2 32631475 32631475 single base substitution C T intron_variant SKCA-BR 2 32633056 32633056 single base substitution G A intron_variant SKCA-BR 2 32638575 32638575 insertion of <=200bp - CG intron_variant SKCA-BR 2 32640053 32640053 single base substitution C T missense_variant P565L 1694C>T SKCA-BR 2 32648000 32648000 single base substitution G A intron_variant SKCA-BR 2 32649212 32649212 single base substitution A G intron_variant SKCA-BR 2 32649705 32649705 single base substitution C T intron_variant SKCA-BR 2 32650502 32650502 insertion of <=200bp - CTT intron_variant SKCA-BR 2 32653769 32653769 single base substitution C T intron_variant SKCA-BR 2 32653769 32653769 single base substitution C T upstream_gene_variant SKCA-BR 2 32658942 32658942 single base substitution C T intron_variant SKCA-BR 2 32658942 32658942 single base substitution C T upstream_gene_variant SKCA-BR 2 32661954 32661955 deletion of <=200bp CT - intron_variant SKCA-BR 2 32663626 32663626 single base substitution C T intron_variant SKCA-BR 2 32663626 32663626 single base substitution C T upstream_gene_variant SKCA-BR 2 32669768 32669768 single base substitution C T downstream_gene_variant SKCA-BR 2 32669768 32669768 single base substitution C T intron_variant SKCA-BR 2 32669859 32669859 single base substitution A G downstream_gene_variant SKCA-BR 2 32669859 32669859 single base substitution A G intron_variant SKCA-BR 2 32672619 32672619 single base substitution G T intron_variant SKCA-BR 2 32672730 32672730 single base substitution C T intron_variant SKCA-BR 2 32679092 32679092 single base substitution C T downstream_gene_variant SKCA-BR 2 32679092 32679092 single base substitution C T intron_variant SKCA-BR 2 32680448 32680448 single base substitution A C intron_variant SKCA-BR 2 32685342 32685342 single base substitution T A intron_variant SKCA-BR 2 32686824 32686824 single base substitution C T intron_variant SKCA-BR 2 32695191 32695191 single base substitution C T intron_variant SKCA-BR 2 32695191 32695191 single base substitution C T upstream_gene_variant SKCA-BR 2 32697376 32697376 single base substitution A C intron_variant SKCA-BR 2 32697376 32697376 single base substitution A C upstream_gene_variant SKCA-BR 2 32700227 32700227 insertion of <=200bp - TA intron_variant SKCA-BR 2 32701373 32701373 single base substitution C T downstream_gene_variant SKCA-BR 2 32701373 32701373 single base substitution C T synonymous_variant L2271L 6813C>T SKCA-BR 2 32701999 32701999 single base substitution G C downstream_gene_variant SKCA-BR 2 32701999 32701999 single base substitution G C intron_variant SKCA-BR 2 32707988 32707988 insertion of <=200bp - GT intron_variant SKCA-BR 2 32709351 32709351 insertion of <=200bp - TA intron_variant SKCA-BR 2 32709352 32709352 single base substitution G A intron_variant SKCA-BR 2 32710228 32710228 single base substitution C T intron_variant SKCA-BR 2 32711324 32711324 single base substitution C T intron_variant SKCA-BR 2 32712421 32712421 single base substitution C T intron_variant SKCA-BR 2 32712422 32712422 single base substitution C T intron_variant SKCA-BR 2 32719743 32719743 single base substitution A G intron_variant SKCA-BR 2 32725487 32725487 insertion of <=200bp - AT intron_variant SKCA-BR 2 32725487 32725487 insertion of <=200bp - AT upstream_gene_variant SKCA-BR 2 32725673 32725673 insertion of <=200bp - GT intron_variant SKCA-BR 2 32725673 32725673 insertion of <=200bp - GT upstream_gene_variant SKCA-BR 2 32729028 32729028 single base substitution C T intron_variant SKCA-BR 2 32729584 32729585 deletion of <=200bp AT - intron_variant SKCA-BR 2 32729667 32729667 single base substitution G T intron_variant SKCA-BR 2 32731740 32731740 single base substitution C T downstream_gene_variant SKCA-BR 2 32731740 32731740 single base substitution C T intron_variant SKCA-BR 2 32731740 32731740 single base substitution C T upstream_gene_variant SKCA-BR 2 32732271 32732271 single base substitution T G downstream_gene_variant SKCA-BR 2 32732271 32732271 single base substitution T G intron_variant SKCA-BR 2 32732271 32732271 single base substitution T G upstream_gene_variant SKCA-BR 2 32732928 32732928 single base substitution C T downstream_gene_variant SKCA-BR 2 32732928 32732928 single base substitution C T intron_variant SKCA-BR 2 32732928 32732928 single base substitution C T upstream_gene_variant SKCA-BR 2 32733899 32733899 single base substitution C T downstream_gene_variant SKCA-BR 2 32733899 32733899 single base substitution C T intron_variant SKCA-BR 2 32733899 32733899 single base substitution C T upstream_gene_variant SKCA-BR 2 32743955 32743955 single base substitution C T exon_variant SKCA-BR 2 32743955 32743955 single base substitution C T synonymous_variant F3855F 11565C>T SKCA-BR 2 32748091 32748091 single base substitution C T downstream_gene_variant SKCA-BR 2 32748091 32748091 single base substitution C T intron_variant SKCA-BR 2 32748091 32748091 single base substitution C T upstream_gene_variant SKCA-BR 2 32755585 32755585 single base substitution C T intron_variant SKCA-BR 2 32757201 32757201 insertion of <=200bp - CGTGTGTGTGT intron_variant SKCA-BR 2 32759441 32759441 insertion of <=200bp - CA intron_variant SKCA-BR 2 32761196 32761196 single base substitution C T intron_variant SKCA-BR 2 32763453 32763453 single base substitution C T intron_variant SKCA-BR 2 32763929 32763929 single base substitution C T intron_variant SKCA-BR 2 32769033 32769033 single base substitution G A intron_variant SKCA-BR 2 32770766 32770766 single base substitution C T exon_variant SKCA-BR 2 32770766 32770766 single base substitution C T missense_variant L4217F 12649C>T SKCA-BR 2 32773382 32773383 deletion of <=200bp CT - intron_variant SKCA-BR 2 32774554 32774554 single base substitution T G splice_region_variant SKCA-BR 2 32778086 32778087 deletion of <=200bp TA - intron_variant SKCA-BR 2 32783319 32783319 single base substitution T A intron_variant SKCA-BR 2 32794049 32794049 insertion of <=200bp - CT intron_variant SKCA-BR 2 32804046 32804046 insertion of <=200bp - AATATATATATATATATATATATATATATAT intron_variant SKCA-BR 2 32804056 32804063 deletion of <=200bp TACACTTA - intron_variant SKCA-BR 2 32804077 32804077 single base substitution C T intron_variant SKCA-BR 2 32804078 32804078 single base substitution C A intron_variant SKCA-BR 2 32804090 32804090 single base substitution T C intron_variant SKCA-BR 2 32804586 32804586 single base substitution C T intron_variant SKCA-BR 2 32810302 32810302 single base substitution C T intron_variant SKCA-BR 2 32810451 32810451 insertion of <=200bp - GT intron_variant SKCA-BR 2 32811490 32811491 deletion of <=200bp CT - intron_variant SKCA-BR 2 32812410 32812410 single base substitution C T intron_variant SKCA-BR 2 32812579 32812579 single base substitution T G intron_variant SKCA-BR 2 32823188 32823188 insertion of <=200bp - TC downstream_gene_variant SKCA-BR 2 32823188 32823188 insertion of <=200bp - TC intron_variant SKCA-BR 2 32823188 32823188 insertion of <=200bp - TC upstream_gene_variant SKCA-BR 2 32823193 32823193 single base substitution A C downstream_gene_variant SKCA-BR 2 32823193 32823193 single base substitution A C intron_variant SKCA-BR 2 32823193 32823193 single base substitution A C upstream_gene_variant SKCA-BR 2 32823198 32823198 single base substitution T C downstream_gene_variant SKCA-BR 2 32823198 32823198 single base substitution T C intron_variant SKCA-BR 2 32823198 32823198 single base substitution T C upstream_gene_variant SKCA-BR 2 32823206 32823206 single base substitution T C downstream_gene_variant SKCA-BR 2 32823206 32823206 single base substitution T C intron_variant SKCA-BR 2 32823206 32823206 single base substitution T C upstream_gene_variant SKCA-BR 2 32829763 32829763 single base substitution C T intron_variant SKCA-BR 2 32832907 32832907 single base substitution C T intron_variant SKCA-BR 2 32836059 32836059 single base substitution T G intron_variant SKCA-BR 2 32840922 32840922 single base substitution G A downstream_gene_variant SKCA-BR 2 32840922 32840922 single base substitution G A intron_variant SKCA-BR 2 32846213 32846213 single base substitution G A downstream_gene_variant SKCA-BR 2 32846579 32846579 single base substitution C T downstream_gene_variant SKCM-US 2 32602682 32602682 single base substitution C T stop_gained Q118* 352C>T SKCM-US 2 32605261 32605261 single base substitution T A missense_variant I183N 548T>A SKCM-US 2 32626358 32626358 single base substitution A G exon_variant SKCM-US 2 32626358 32626358 single base substitution A G missense_variant I388V 1162A>G SKCM-US 2 32640055 32640055 single base substitution T A missense_variant C566S 1696T>A SKCM-US 2 32640219 32640219 single base substitution T G synonymous_variant S620S 1860T>G SKCM-US 2 32640294 32640294 single base substitution C T synonymous_variant I645I 1935C>T SKCM-US 2 32640582 32640582 single base substitution C A missense_variant D741E 2223C>A SKCM-US 2 32654243 32654243 single base substitution G A missense_variant G968R 2902G>A SKCM-US 2 32654243 32654243 single base substitution G A upstream_gene_variant SKCM-US 2 32666457 32666457 single base substitution C T intron_variant SKCM-US 2 32666457 32666457 single base substitution C T missense_variant R1291W 3871C>T SKCM-US 2 32666457 32666457 single base substitution C T missense_variant R177W 529C>T SKCM-US 2 32666457 32666457 single base substitution C T upstream_gene_variant SKCM-US 2 32689700 32689700 single base substitution C T missense_variant H1689Y 5065C>T SKCM-US 2 32689721 32689721 single base substitution C T missense_variant P1696S 5086C>T SKCM-US 2 32689819 32689819 single base substitution C T synonymous_variant F1728F 5184C>T SKCM-US 2 32696142 32696142 single base substitution A G missense_variant Y2181C 6542A>G SKCM-US 2 32696142 32696142 single base substitution A G upstream_gene_variant SKCM-US 2 32706501 32706501 single base substitution C T missense_variant L2508F 7522C>T SKCM-US 2 32710717 32710717 single base substitution T A missense_variant D2568E 7704T>A SKCM-US 2 32712717 32712717 single base substitution C T missense_variant S2606L 7817C>T SKCM-US 2 32712786 32712786 single base substitution T G missense_variant L2629R 7886T>G SKCM-US 2 32712801 32712801 single base substitution C T missense_variant S2634L 7901C>T SKCM-US 2 32715118 32715118 single base substitution T C synonymous_variant T2702T 8106T>C SKCM-US 2 32718649 32718649 single base substitution C T stop_gained R2795* 8383C>T SKCM-US 2 32724761 32724761 single base substitution T C synonymous_variant T2872T 8616T>C SKCM-US 2 32724761 32724761 single base substitution T C upstream_gene_variant SKCM-US 2 32724764 32724764 single base substitution C T synonymous_variant C2873C 8619C>T SKCM-US 2 32724764 32724764 single base substitution C T upstream_gene_variant SKCM-US 2 32724803 32724803 single base substitution C T synonymous_variant S2886S 8658C>T SKCM-US 2 32724803 32724803 single base substitution C T upstream_gene_variant SKCM-US 2 32724814 32724814 single base substitution G A missense_variant R2890Q 8669G>A SKCM-US 2 32724814 32724814 single base substitution G A upstream_gene_variant SKCM-US 2 32724849 32724849 single base substitution C T missense_variant R2902C 8704C>T SKCM-US 2 32724849 32724849 single base substitution C T upstream_gene_variant SKCM-US 2 32724999 32724999 single base substitution G A missense_variant D2952N 8854G>A SKCM-US 2 32724999 32724999 single base substitution G A upstream_gene_variant SKCM-US 2 32726811 32726811 single base substitution A T missense_variant E3021D 9063A>T SKCM-US 2 32726811 32726811 single base substitution A T upstream_gene_variant SKCM-US 2 32733298 32733298 single base substitution C T downstream_gene_variant SKCM-US 2 32733298 32733298 single base substitution C T missense_variant P3318S 9952C>T SKCM-US 2 32733298 32733298 single base substitution C T upstream_gene_variant SKCM-US 2 32738066 32738066 single base substitution G A exon_variant SKCM-US 2 32738066 32738066 single base substitution G A synonymous_variant R3471R 10413G>A SKCM-US 2 32738066 32738066 single base substitution G A upstream_gene_variant SKCM-US 2 32738123 32738123 single base substitution T A exon_variant SKCM-US 2 32738123 32738123 single base substitution T A synonymous_variant S3490S 10470T>A SKCM-US 2 32738123 32738123 single base substitution T A upstream_gene_variant SKCM-US 2 32740464 32740464 single base substitution T A downstream_gene_variant SKCM-US 2 32740464 32740464 single base substitution T A missense_variant I3659N 10976T>A SKCM-US 2 32740464 32740464 single base substitution T A upstream_gene_variant SKCM-US 2 32740546 32740546 single base substitution T C downstream_gene_variant SKCM-US 2 32740546 32740546 single base substitution T C synonymous_variant I3686I 11058T>C SKCM-US 2 32740546 32740546 single base substitution T C upstream_gene_variant SKCM-US 2 32740645 32740645 single base substitution G T downstream_gene_variant SKCM-US 2 32740645 32740645 single base substitution G T missense_variant L3719F 11157G>T SKCM-US 2 32740645 32740645 single base substitution G T upstream_gene_variant SKCM-US 2 32750561 32750561 single base substitution C T exon_variant SKCM-US 2 32750561 32750561 single base substitution C T missense_variant S3929L 11786C>T SKCM-US 2 32754816 32754816 single base substitution A T exon_variant SKCM-US 2 32754816 32754816 single base substitution A T stop_gained K4007* 12019A>T SKCM-US 2 32768346 32768346 single base substitution G A exon_variant SKCM-US 2 32768346 32768346 single base substitution G A synonymous_variant K4110K 12330G>A SKCM-US 2 32768572 32768572 single base substitution C T exon_variant SKCM-US 2 32768572 32768572 single base substitution C T stop_gained R4186* 12556C>T SKCM-US 2 32772969 32772969 single base substitution A T exon_variant SKCM-US 2 32772969 32772969 single base substitution A T missense_variant Y4288F 12863A>T SKCM-US 2 32773047 32773047 single base substitution G A exon_variant SKCM-US 2 32773047 32773047 single base substitution G A missense_variant R4314K 12941G>A SKCM-US 2 32774474 32774474 single base substitution C T exon_variant SKCM-US 2 32774474 32774474 single base substitution C T missense_variant P4357L 13070C>T SKCM-US 2 32800257 32800257 single base substitution G A exon_variant SKCM-US 2 32800257 32800257 single base substitution G A synonymous_variant R4393R 13179G>A SKCM-US 2 32800257 32800257 single base substitution G A upstream_gene_variant SKCM-US 2 32800289 32800289 single base substitution C T exon_variant SKCM-US 2 32800289 32800289 single base substitution C T missense_variant S4404F 13211C>T SKCM-US 2 32800289 32800289 single base substitution C T upstream_gene_variant SKCM-US 2 32824950 32824950 single base substitution C T exon_variant SKCM-US 2 32824950 32824950 single base substitution C T missense_variant L4659F 13975C>T SKCM-US 2 32824950 32824950 single base substitution C T upstream_gene_variant SKCM-US 2 32828074 32828074 deletion of <=200bp T - exon_variant SKCM-US 2 32828074 32828074 deletion of <=200bp T - frameshift_variant V4665 SKCM-US 2 32828074 32828074 deletion of <=200bp T - splice_region_variant SKCM-US 2 32828126 32828126 single base substitution T G exon_variant SKCM-US 2 32828126 32828126 single base substitution T G missense_variant N4682K 14046T>G SKCM-US 2 32832604 32832604 single base substitution C T exon_variant SKCM-US 2 32832604 32832604 single base substitution C T missense_variant P4718L 14153C>T STAD-US 2 32602775 32602775 single base substitution G A missense_variant A149T 445G>A STAD-US 2 32626306 32626306 single base substitution C A exon_variant STAD-US 2 32626306 32626306 single base substitution C A synonymous_variant V370V 1110C>A STAD-US 2 32626547 32626547 single base substitution A T downstream_gene_variant STAD-US 2 32626547 32626547 single base substitution A T missense_variant E425V 1274A>T STAD-US 2 32626574 32626574 single base substitution T C downstream_gene_variant STAD-US 2 32626574 32626574 single base substitution T C missense_variant V434A 1301T>C STAD-US 2 32640080 32640080 single base substitution C A missense_variant T574K 1721C>A STAD-US 2 32640462 32640462 single base substitution G A synonymous_variant P701P 2103G>A STAD-US 2 32640623 32640623 single base substitution A C missense_variant E755A 2264A>C STAD-US 2 32641161 32641161 single base substitution T C synonymous_variant T934T 2802T>C STAD-US 2 32658760 32658760 single base substitution T C synonymous_variant C1099C 3297T>C STAD-US 2 32658760 32658760 single base substitution T C synonymous_variant C15C 45T>C STAD-US 2 32658760 32658760 single base substitution T C upstream_gene_variant STAD-US 2 32658787 32658787 single base substitution C T synonymous_variant F1108F 3324C>T STAD-US 2 32658787 32658787 single base substitution C T synonymous_variant F24F 72C>T STAD-US 2 32658787 32658787 single base substitution C T upstream_gene_variant STAD-US 2 32664624 32664624 single base substitution T C exon_variant STAD-US 2 32664624 32664624 single base substitution T C missense_variant V113A 338T>C STAD-US 2 32664624 32664624 single base substitution T C missense_variant V1227A 3680T>C STAD-US 2 32664624 32664624 single base substitution T C upstream_gene_variant STAD-US 2 32668623 32668623 single base substitution A G downstream_gene_variant STAD-US 2 32668623 32668623 single base substitution A G exon_variant STAD-US 2 32668623 32668623 single base substitution A G missense_variant N1435D 4303A>G STAD-US 2 32670603 32670603 single base substitution T C downstream_gene_variant STAD-US 2 32670603 32670603 single base substitution T C exon_variant STAD-US 2 32670603 32670603 single base substitution T C missense_variant Y1451H 4351T>C STAD-US 2 32673876 32673876 insertion of <=200bp - A exon_variant STAD-US 2 32673876 32673876 insertion of <=200bp - A frameshift_variant S1500K? STAD-US 2 32673903 32673903 single base substitution G A exon_variant STAD-US 2 32673903 32673903 single base substitution G A missense_variant D1509N 4525G>A STAD-US 2 32678936 32678936 single base substitution T C downstream_gene_variant STAD-US 2 32678936 32678936 single base substitution T C missense_variant L1560P 4679T>C STAD-US 2 32678971 32678971 single base substitution T C downstream_gene_variant STAD-US 2 32678971 32678971 single base substitution T C missense_variant S1572P 4714T>C STAD-US 2 32688342 32688342 single base substitution G A missense_variant A1612T 4834G>A STAD-US 2 32693612 32693612 single base substitution C T missense_variant A1963V 5888C>T STAD-US 2 32693612 32693612 single base substitution C T upstream_gene_variant STAD-US 2 32694625 32694625 single base substitution C T missense_variant S2097F 6290C>T STAD-US 2 32694625 32694625 single base substitution C T upstream_gene_variant STAD-US 2 32695244 32695244 single base substitution T C missense_variant M2119T 6356T>C STAD-US 2 32695244 32695244 single base substitution T C upstream_gene_variant STAD-US 2 32703728 32703728 single base substitution C T downstream_gene_variant STAD-US 2 32703728 32703728 single base substitution C T missense_variant T2365M 7094C>T STAD-US 2 32703759 32703759 single base substitution G A downstream_gene_variant STAD-US 2 32703759 32703759 single base substitution G A synonymous_variant V2375V 7125G>A STAD-US 2 32704595 32704595 single base substitution G A downstream_gene_variant STAD-US 2 32704595 32704595 single base substitution G A missense_variant A2440T 7318G>A STAD-US 2 32707635 32707635 single base substitution G A missense_variant V2561I 7681G>A STAD-US 2 32715111 32715111 single base substitution C G stop_gained S2700* 8099C>G STAD-US 2 32715152 32715152 single base substitution A C missense_variant T2714P 8140A>C STAD-US 2 32724640 32724640 single base substitution C A missense_variant P2832H 8495C>A STAD-US 2 32724640 32724640 single base substitution C A upstream_gene_variant STAD-US 2 32724719 32724719 single base substitution C T synonymous_variant A2858A 8574C>T STAD-US 2 32724719 32724719 single base substitution C T upstream_gene_variant STAD-US 2 32728208 32728208 single base substitution C G exon_variant STAD-US 2 32728208 32728208 single base substitution C G missense_variant S3135C 9404C>G STAD-US 2 32740737 32740740 deletion of <=200bp GACT - downstream_gene_variant STAD-US 2 32740737 32740740 deletion of <=200bp GACT - frameshift_variant GL3750 STAD-US 2 32740737 32740740 deletion of <=200bp GACT - upstream_gene_variant STAD-US 2 32740783 32740783 single base substitution G A downstream_gene_variant STAD-US 2 32740783 32740783 single base substitution G A synonymous_variant A3765A 11295G>A STAD-US 2 32740783 32740783 single base substitution G A upstream_gene_variant STAD-US 2 32750029 32750029 single base substitution G T exon_variant STAD-US 2 32750029 32750029 single base substitution G T stop_gained E3900* 11698G>T STAD-US 2 32750576 32750576 single base substitution G A exon_variant STAD-US 2 32750576 32750576 single base substitution G A missense_variant R3934H 11801G>A STAD-US 2 32750641 32750641 single base substitution G A exon_variant STAD-US 2 32750641 32750641 single base substitution G A missense_variant A3956T 11866G>A STAD-US 2 32754810 32754810 single base substitution A C exon_variant STAD-US 2 32754810 32754810 single base substitution A C missense_variant T4005P 12013A>C STAD-US 2 32756560 32756560 single base substitution G A exon_variant STAD-US 2 32756560 32756560 single base substitution G A missense_variant G4078D 12233G>A STAD-US 2 32768549 32768549 single base substitution G T exon_variant STAD-US 2 32768549 32768549 single base substitution G T missense_variant R4178I 12533G>T STAD-US 2 32768566 32768568 deletion of <=200bp CTT - exon_variant STAD-US 2 32768566 32768568 deletion of <=200bp CTT - inframe_deletion L4184 STAD-US 2 32800229 32800229 single base substitution A G exon_variant STAD-US 2 32800229 32800229 single base substitution A G missense_variant D4384G 13151A>G STAD-US 2 32800229 32800229 single base substitution A G upstream_gene_variant STAD-US 2 32800338 32800338 single base substitution T C exon_variant STAD-US 2 32800338 32800338 single base substitution T C synonymous_variant G4420G 13260T>C STAD-US 2 32800338 32800338 single base substitution T C upstream_gene_variant STAD-US 2 32820140 32820140 single base substitution A C downstream_gene_variant STAD-US 2 32820140 32820140 single base substitution A C exon_variant STAD-US 2 32820140 32820140 single base substitution A C missense_variant K4514T 13541A>C STAD-US 2 32824836 32824836 single base substitution T A exon_variant STAD-US 2 32824836 32824836 single base substitution T A missense_variant Y4621N 13861T>A STAD-US 2 32824836 32824836 single base substitution T A upstream_gene_variant STAD-US 2 32824935 32824935 single base substitution C T exon_variant STAD-US 2 32824935 32824935 single base substitution C T stop_gained R4654* 13960C>T STAD-US 2 32824935 32824935 single base substitution C T upstream_gene_variant STAD-US 2 32828139 32828139 single base substitution A C exon_variant STAD-US 2 32828139 32828139 single base substitution A C missense_variant S4687R 14059A>C STAD-US 2 32836529 32836529 insertion of <=200bp - T exon_variant STAD-US 2 32836529 32836529 insertion of <=200bp - T frameshift_variant H4758H? THCA-US 2 32694627 32694627 single base substitution A T missense_variant N2098Y 6292A>T THCA-US 2 32694627 32694627 single base substitution A T upstream_gene_variant UCEC-US 2 32613983 32613983 single base substitution G A exon_variant UCEC-US 2 32613983 32613983 single base substitution G A missense_variant G271R 811G>A UCEC-US 2 32620633 32620633 single base substitution G A exon_variant UCEC-US 2 32620633 32620633 single base substitution G A missense_variant V336I 1006G>A UCEC-US 2 32620642 32620642 single base substitution G A exon_variant UCEC-US 2 32620642 32620642 single base substitution G A missense_variant E339K 1015G>A UCEC-US 2 32626420 32626420 single base substitution G T exon_variant UCEC-US 2 32626420 32626420 single base substitution G T missense_variant K408N 1224G>T UCEC-US 2 32639968 32639968 single base substitution G T stop_gained E537* 1609G>T UCEC-US 2 32640218 32640218 single base substitution C T missense_variant S620F 1859C>T UCEC-US 2 32640284 32640284 single base substitution C T missense_variant A642V 1925C>T UCEC-US 2 32640323 32640323 single base substitution A C missense_variant K655T 1964A>C UCEC-US 2 32640326 32640326 single base substitution G T missense_variant S656I 1967G>T UCEC-US 2 32640546 32640546 single base substitution G T missense_variant E729D 2187G>T UCEC-US 2 32640615 32640615 single base substitution C T synonymous_variant C752C 2256C>T UCEC-US 2 32640863 32640863 single base substitution G A missense_variant R835Q 2504G>A UCEC-US 2 32640933 32640933 single base substitution G A synonymous_variant S858S 2574G>A UCEC-US 2 32640968 32640968 single base substitution G A missense_variant R870Q 2609G>A UCEC-US 2 32641017 32641017 single base substitution G T missense_variant K886N 2658G>T UCEC-US 2 32641122 32641122 single base substitution A C missense_variant E921D 2763A>C UCEC-US 2 32656134 32656134 single base substitution G A missense_variant R1075Q 3224G>A UCEC-US 2 32656134 32656134 single base substitution G A upstream_gene_variant UCEC-US 2 32658722 32658722 single base substitution G A missense_variant D1087N 3259G>A UCEC-US 2 32658722 32658722 single base substitution G A missense_variant D3N 7G>A UCEC-US 2 32658722 32658722 single base substitution G A upstream_gene_variant UCEC-US 2 32658772 32658772 single base substitution T C synonymous_variant H1103H 3309T>C UCEC-US 2 32658772 32658772 single base substitution T C synonymous_variant H19H 57T>C UCEC-US 2 32658772 32658772 single base substitution T C upstream_gene_variant UCEC-US 2 32660609 32660609 single base substitution A G intron_variant UCEC-US 2 32660609 32660609 single base substitution A G missense_variant D1152G 3455A>G UCEC-US 2 32660609 32660609 single base substitution A G upstream_gene_variant UCEC-US 2 32664657 32664657 single base substitution G T exon_variant UCEC-US 2 32664657 32664657 single base substitution G T missense_variant G1238V 3713G>T UCEC-US 2 32664657 32664657 single base substitution G T missense_variant G124V 371G>T UCEC-US 2 32664657 32664657 single base substitution G T upstream_gene_variant UCEC-US 2 32666457 32666457 single base substitution C T intron_variant UCEC-US 2 32666457 32666457 single base substitution C T missense_variant R1291W 3871C>T UCEC-US 2 32666457 32666457 single base substitution C T missense_variant R177W 529C>T UCEC-US 2 32666457 32666457 single base substitution C T upstream_gene_variant UCEC-US 2 32667224 32667224 single base substitution G T 3_prime_UTR_variant UCEC-US 2 32667224 32667224 single base substitution G T downstream_gene_variant UCEC-US 2 32667224 32667224 single base substitution G T stop_gained E1346* 4036G>T UCEC-US 2 32667224 32667224 single base substitution G T upstream_gene_variant UCEC-US 2 32667398 32667398 single base substitution G T 3_prime_UTR_variant UCEC-US 2 32667398 32667398 single base substitution G T downstream_gene_variant UCEC-US 2 32667398 32667398 single base substitution G T missense_variant K1371N 4113G>T UCEC-US 2 32667398 32667398 single base substitution G T upstream_gene_variant UCEC-US 2 32667407 32667407 single base substitution T C 3_prime_UTR_variant UCEC-US 2 32667407 32667407 single base substitution T C downstream_gene_variant UCEC-US 2 32667407 32667407 single base substitution T C synonymous_variant N1374N 4122T>C UCEC-US 2 32667407 32667407 single base substitution T C upstream_gene_variant UCEC-US 2 32667430 32667430 single base substitution G A 3_prime_UTR_variant UCEC-US 2 32667430 32667430 single base substitution G A downstream_gene_variant UCEC-US 2 32667430 32667430 single base substitution G A missense_variant R1382Q 4145G>A UCEC-US 2 32667430 32667430 single base substitution G A upstream_gene_variant UCEC-US 2 32667448 32667448 single base substitution T G 3_prime_UTR_variant UCEC-US 2 32667448 32667448 single base substitution T G downstream_gene_variant UCEC-US 2 32667448 32667448 single base substitution T G missense_variant I1388S 4163T>G UCEC-US 2 32667448 32667448 single base substitution T G upstream_gene_variant UCEC-US 2 32668621 32668623 deletion of <=200bp ATA - downstream_gene_variant UCEC-US 2 32668621 32668623 deletion of <=200bp ATA - exon_variant UCEC-US 2 32668621 32668623 deletion of <=200bp ATA - inframe_deletion DN1434D UCEC-US 2 32689802 32689802 single base substitution G A missense_variant E1723K 5167G>A UCEC-US 2 32690159 32690159 single base substitution T C synonymous_variant L1761L 5283T>C UCEC-US 2 32690174 32690174 single base substitution T C synonymous_variant A1766A 5298T>C UCEC-US 2 32690221 32690221 single base substitution G A missense_variant R1782Q 5345G>A UCEC-US 2 32692602 32692602 single base substitution G T missense_variant R1789I 5366G>T UCEC-US 2 32692987 32692987 single base substitution G A missense_variant R1863H 5588G>A UCEC-US 2 32693581 32693581 single base substitution G A missense_variant A1953T 5857G>A UCEC-US 2 32693581 32693581 single base substitution G A upstream_gene_variant UCEC-US 2 32693798 32693798 single base substitution C A missense_variant T2025N 6074C>A UCEC-US 2 32693798 32693798 single base substitution C A upstream_gene_variant UCEC-US 2 32696115 32696115 single base substitution T C missense_variant V2172A 6515T>C UCEC-US 2 32696115 32696115 single base substitution T C upstream_gene_variant UCEC-US 2 32702455 32702455 single base substitution G A downstream_gene_variant UCEC-US 2 32702455 32702455 single base substitution G A missense_variant R2291H 6872G>A UCEC-US 2 32703729 32703729 single base substitution G A downstream_gene_variant UCEC-US 2 32703729 32703729 single base substitution G A synonymous_variant T2365T 7095G>A UCEC-US 2 32704676 32704676 single base substitution G T downstream_gene_variant UCEC-US 2 32704676 32704676 single base substitution G T missense_variant D2467Y 7399G>T UCEC-US 2 32704682 32704682 single base substitution A C downstream_gene_variant UCEC-US 2 32704682 32704682 single base substitution A C missense_variant T2469P 7405A>C UCEC-US 2 32707515 32707515 single base substitution T C missense_variant Y2521H 7561T>C UCEC-US 2 32707634 32707634 single base substitution C T synonymous_variant S2560S 7680C>T UCEC-US 2 32715171 32715171 single base substitution G A missense_variant C2720Y 8159G>A UCEC-US 2 32724627 32724627 single base substitution A T missense_variant T2828S 8482A>T UCEC-US 2 32724627 32724627 single base substitution A T upstream_gene_variant UCEC-US 2 32724666 32724666 single base substitution G T stop_gained E2841* 8521G>T UCEC-US 2 32724666 32724666 single base substitution G T upstream_gene_variant UCEC-US 2 32724695 32724695 single base substitution C T synonymous_variant V2850V 8550C>T UCEC-US 2 32724695 32724695 single base substitution C T upstream_gene_variant UCEC-US 2 32724749 32724749 single base substitution C T synonymous_variant H2868H 8604C>T UCEC-US 2 32724749 32724749 single base substitution C T upstream_gene_variant UCEC-US 2 32724814 32724814 single base substitution G A missense_variant R2890Q 8669G>A UCEC-US 2 32724814 32724814 single base substitution G A upstream_gene_variant UCEC-US 2 32724960 32724960 single base substitution G A missense_variant E2939K 8815G>A UCEC-US 2 32724960 32724960 single base substitution G A upstream_gene_variant UCEC-US 2 32724990 32724990 single base substitution A C missense_variant N2949H 8845A>C UCEC-US 2 32724990 32724990 single base substitution A C upstream_gene_variant UCEC-US 2 32725073 32725073 single base substitution G A synonymous_variant S2976S 8928G>A UCEC-US 2 32725073 32725073 single base substitution G A upstream_gene_variant UCEC-US 2 32726952 32726952 single base substitution A G synonymous_variant R3068R 9204A>G UCEC-US 2 32726952 32726952 single base substitution A G upstream_gene_variant UCEC-US 2 32730161 32730161 single base substitution T C exon_variant UCEC-US 2 32730161 32730161 single base substitution T C missense_variant W3197R 9589T>C UCEC-US 2 32730161 32730161 single base substitution T C upstream_gene_variant UCEC-US 2 32733118 32733118 single base substitution G T downstream_gene_variant UCEC-US 2 32733118 32733118 single base substitution G T missense_variant V3258F 9772G>T UCEC-US 2 32733118 32733118 single base substitution G T upstream_gene_variant UCEC-US 2 32733196 32733196 single base substitution C T downstream_gene_variant UCEC-US 2 32733196 32733196 single base substitution C T missense_variant R3284C 9850C>T UCEC-US 2 32733196 32733196 single base substitution C T upstream_gene_variant UCEC-US 2 32735613 32735613 single base substitution T C exon_variant UCEC-US 2 32735613 32735613 single base substitution T C missense_variant F3420L 10258T>C UCEC-US 2 32735613 32735613 single base substitution T G exon_variant UCEC-US 2 32735613 32735613 single base substitution T G missense_variant F3420V 10258T>G UCEC-US 2 32735648 32735648 single base substitution G A exon_variant UCEC-US 2 32735648 32735648 single base substitution G A synonymous_variant T3431T 10293G>A UCEC-US 2 32735649 32735649 single base substitution A C exon_variant UCEC-US 2 32735649 32735649 single base substitution A C missense_variant I3432L 10294A>C UCEC-US 2 32740507 32740507 single base substitution T C downstream_gene_variant UCEC-US 2 32740507 32740507 single base substitution T C synonymous_variant C3673C 11019T>C UCEC-US 2 32740507 32740507 single base substitution T C upstream_gene_variant UCEC-US 2 32740650 32740650 single base substitution A G downstream_gene_variant UCEC-US 2 32740650 32740650 single base substitution A G missense_variant H3721R 11162A>G UCEC-US 2 32740650 32740650 single base substitution A G upstream_gene_variant UCEC-US 2 32740803 32740803 single base substitution C T downstream_gene_variant UCEC-US 2 32740803 32740803 single base substitution C T missense_variant S3772L 11315C>T UCEC-US 2 32740803 32740803 single base substitution C T upstream_gene_variant UCEC-US 2 32740826 32740826 single base substitution C T downstream_gene_variant UCEC-US 2 32740826 32740826 single base substitution C T exon_variant UCEC-US 2 32740826 32740826 single base substitution C T synonymous_variant L3780L 11338C>T UCEC-US 2 32750029 32750029 single base substitution G T exon_variant UCEC-US 2 32750029 32750029 single base substitution G T stop_gained E3900* 11698G>T UCEC-US 2 32750576 32750576 single base substitution G A exon_variant UCEC-US 2 32750576 32750576 single base substitution G A missense_variant R3934H 11801G>A UCEC-US 2 32756613 32756613 single base substitution C A exon_variant UCEC-US 2 32756613 32756613 single base substitution C A missense_variant Q4096K 12286C>A UCEC-US 2 32768495 32768495 single base substitution C T exon_variant UCEC-US 2 32768495 32768495 single base substitution C T missense_variant A4160V 12479C>T UCEC-US 2 32768509 32768509 single base substitution C A exon_variant UCEC-US 2 32768509 32768509 single base substitution C A missense_variant L4165I 12493C>A UCEC-US 2 32770803 32770803 single base substitution A G exon_variant UCEC-US 2 32770803 32770803 single base substitution A G missense_variant D4229G 12686A>G UCEC-US 2 32770829 32770829 single base substitution G A exon_variant UCEC-US 2 32770829 32770829 single base substitution G A missense_variant A4238T 12712G>A UCEC-US 2 32770835 32770835 single base substitution G T exon_variant UCEC-US 2 32770835 32770835 single base substitution G T stop_gained E4240* 12718G>T UCEC-US 2 32774537 32774537 single base substitution G A exon_variant UCEC-US 2 32774537 32774537 single base substitution G A missense_variant R4378Q 13133G>A UCEC-US 2 32774544 32774544 single base substitution T G exon_variant UCEC-US 2 32774544 32774544 single base substitution T G missense_variant D4380E 13140T>G UCEC-US 2 32800276 32800276 single base substitution C T exon_variant UCEC-US 2 32800276 32800276 single base substitution C T missense_variant R4400W 13198C>T UCEC-US 2 32800276 32800276 single base substitution C T upstream_gene_variant UCEC-US 2 32819113 32819113 single base substitution G A exon_variant UCEC-US 2 32819113 32819113 single base substitution G A missense_variant R4496Q 13487G>A UCEC-US 2 32820188 32820188 single base substitution C T downstream_gene_variant UCEC-US 2 32820188 32820188 single base substitution C T exon_variant UCEC-US 2 32820188 32820188 single base substitution C T missense_variant A4530V 13589C>T UCEC-US 2 32822821 32822821 single base substitution C T downstream_gene_variant UCEC-US 2 32822821 32822821 single base substitution C T exon_variant UCEC-US 2 32822821 32822821 single base substitution C T missense_variant T4539M 13616C>T UCEC-US 2 32822821 32822821 single base substitution C T upstream_gene_variant UCEC-US 2 32822934 32822934 single base substitution C T downstream_gene_variant UCEC-US 2 32822934 32822934 single base substitution C T exon_variant UCEC-US 2 32822934 32822934 single base substitution C T missense_variant R4577C 13729C>T UCEC-US 2 32822934 32822934 single base substitution C T upstream_gene_variant UCEC-US 2 32822950 32822950 single base substitution C A downstream_gene_variant UCEC-US 2 32822950 32822950 single base substitution C A exon_variant UCEC-US 2 32822950 32822950 single base substitution C A missense_variant A4582D 13745C>A UCEC-US 2 32822950 32822950 single base substitution C A upstream_gene_variant UCEC-US 2 32824935 32824935 single base substitution C T exon_variant UCEC-US 2 32824935 32824935 single base substitution C T stop_gained R4654* 13960C>T UCEC-US 2 32824935 32824935 single base substitution C T upstream_gene_variant UCEC-US 2 32832617 32832617 single base substitution G T exon_variant UCEC-US 2 32832617 32832617 single base substitution G T missense_variant Q4722H 14166G>T UCEC-US 2 32832645 32832645 single base substitution C T exon_variant UCEC-US 2 32832645 32832645 single base substitution C T stop_gained R4732* 14194C>T UCEC-US 2 32832646 32832646 single base substitution G A exon_variant UCEC-US 2 32832646 32832646 single base substitution G A missense_variant R4732Q 14195G>A UCEC-US 2 32836583 32836583 single base substitution T C exon_variant UCEC-US 2 32836583 32836583 single base substitution T C synonymous_variant D4776D 14328T>C

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-B5-A1MY-01 COSM1020461 c.14296A>T p.I4766L Substitution - Missense 2:32611484-32611484 + ccRCC-15 COSM1660778 c.4805T>G p.V1602G Substitution - Missense 2:32463245-32463245 + BD190T COSM5517749 c.13356-2A>G p.? Unknown 2:32593913-32593913 + SWE-20 COSM1179065 c.6663T>C p.S2221S Substitution - coding silent 2:32473182-32473182 + pfg057T COSM4752328 c.7091C>T p.A2364V Substitution - Missense 2:32478657-32478657 + TCGA-FW-A3R5-06 COSM1407820 c.8658C>T p.S2886S Substitution - coding silent 2:32499736-32499736 + TCGA-J9-A52C-01 COSM4877377 c.4168C>T p.R1390C Substitution - Missense 2:32442385-32442385 + TCGA-DD-A1EG-01 COSM4915778 c.9831T>C p.A3277A Substitution - coding silent 2:32508110-32508110 + TCGA-A7-A13F-01 COSM442829 c.13787G>T p.S4596I Substitution - Missense 2:32597925-32597925 + TCGA-CM-6170-01 COSM1407798 c.4818G>A p.S1606S Substitution - coding silent 2:32463258-32463258 + TCGA-AP-A059-01 COSM1020342 c.8604C>T p.H2868H Substitution - coding silent 2:32499682-32499682 + UM-SCC-4 COSM4591362 c.3994G>C p.V1332L Substitution - Missense CHC2216T COSM4805993 c.14368A>T p.M4790L Substitution - Missense 2:32611556-32611556 + TCGA-AP-A056-01 COSM1020376 c.10293G>A p.T3431T Substitution - coding silent 2:32510581-32510581 + RK126_C01 COSM1631982 c.4679T>G p.L1560R Substitution - Missense 2:32453868-32453868 + BK0043 COSM4187365 c.12073A>G p.K4025E Substitution - Missense 2:32529803-32529803 + BK0022 COSM4186321 c.4604C>T p.S1535L Substitution - Missense 2:32448914-32448914 + Pat_59_B COSM5862448 c.8920C>T p.Q2974* Substitution - Nonsense 2:32499998-32499998 + K3-Tumor COSM249146 c.5371G>T p.V1791L Substitution - Missense 2:32467539-32467539 + 019T COSM1727922 c.3997A>C p.N1333H Substitution - Missense 2:32442117-32442117 + BD110T COSM5514125 c.2295C>A p.A765A Substitution - coding silent 2:32415586-32415586 + T2269 COSM4665765 c.14212T>C p.W4738R Substitution - Missense 2:32607596-32607596 + ATL044 COSM5708195 c.14539A>T p.S4847C Substitution - Missense 2:32617869-32617869 + CSCC-37-T COSM4550306 c.4981G>T p.A1661S Substitution - Missense 2:32464548-32464548 + C0097T COSM4164511 c.3171G>T p.R1057S Substitution - Missense 2:32431013-32431013 + HCC25T COSM1614786 c.4541G>T p.G1514V Substitution - Missense 2:32448851-32448851 + D-10 COSM4766218 c.7904C>A p.S2635Y Substitution - Missense 2:32487737-32487737 + BK0021 COSM4186271 c.4004_4005delTT p.C1336fs*5 Deletion - Frameshift 2:32442124-32442125 + 2492729 COSM5726303 c.7423T>C p.S2475P Substitution - Missense 2:32481334-32481334 + 18 COSM5744716 c.7042G>A p.A2348T Substitution - Missense 2:32477557-32477557 + CML010T COSM5802801 c.4166T>G p.V1389G Substitution - Missense 2:32442383-32442383 + ORL-48 COSM4592548 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + TCGA-D1-A17D-01 COSM1020252 c.3309T>C p.H1103H Substitution - coding silent 2:32433704-32433704 + TCGA-G4-6297-01 COSM3695480 c.7264G>T p.A2422S Substitution - Missense 2:32479473-32479473 + TCGA-BT-A3PH-01 COSM1306748 c.10882G>C p.D3628H Substitution - Missense 2:32515303-32515303 + HCT8 COSM2942606 c.10430C>A p.P3477H Substitution - Missense 2:32513016-32513016 + SJHYPO020 COSM4775509 c.6713A>G p.H2238R Substitution - Missense 2:32473232-32473232 + TCGA-AG-A002-01 COSM259643 c.11698G>T p.E3900* Substitution - Nonsense 2:32524962-32524962 + CHC1600T COSM4791532 c.13318A>G p.M4440V Substitution - Missense 2:32575329-32575329 + LP6005500-DNA_D01 COSM5036181 c.4531G>A p.E1511K Substitution - Missense 2:32448841-32448841 + 2492723 COSM5719570 c.12489A>C p.L4163F Substitution - Missense 2:32543438-32543438 + 381_T COSM3962785 c.3151C>G p.Q1051E Substitution - Missense 2:32430993-32430993 + pfg143T COSM4752342 c.13331T>A p.V4444D Substitution - Missense 2:32575342-32575342 + TCGA-EK-A2RA-01 COSM159376 c.11600C>T p.S3867L Substitution - Missense 2:32518923-32518923 + TCGA-DK-A1AC-01 COSM1306757 c.12614C>T p.S4205L Substitution - Missense 2:32545664-32545664 + ESO-114 COSM1246115 c.10477C>A p.H3493N Substitution - Missense 2:32513063-32513063 + BN41 COSM1614784 c.729T>G p.N243K Substitution - Missense 2:32388833-32388833 + pfg057T COSM4765143 c.12045_12046insC p.S4017fs*9 Insertion - Frameshift 2:32529775-32529776 + TCGA-B5-A0JY-01 COSM259638 c.4145G>A p.R1382Q Substitution - Missense 2:32442362-32442362 + TCGA-AO-A0J5-01 COSM442824 c.7036T>A p.C2346S Substitution - Missense 2:32477551-32477551 + TCGA-A8-A097-01 COSM442831 c.13846C>A p.P4616T Substitution - Missense 2:32599754-32599754 + TCGA-AP-A0LM-01 COSM1020437 c.13729C>T p.R4577C Substitution - Missense 2:32597867-32597867 + TCGA-37-3789-01 COSM721191 c.10861G>C p.E3621Q Substitution - Missense 2:32515282-32515282 + TCGA-CG-5721-01 COSM4093870 c.3680T>C p.V1227A Substitution - Missense 2:32439556-32439556 + 2173_T COSM3962792 c.9688G>A p.A3230T Substitution - Missense 2:32505193-32505193 + HCT8 COSM4634835 c.11054C>A p.P3685H Substitution - Missense 2:32515475-32515475 + TCGA-BQ-7058-01 COSM3991279 c.9097G>A p.G3033R Substitution - Missense 2:32501778-32501778 + 2492723 COSM1690428 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + 587376 COSM1184743 c.11590A>G p.T3864A Substitution - Missense 2:32518913-32518913 + TCGA-AA-3492-01 COSM1407772 c.609A>T p.T203T Substitution - coding silent 2:32380254-32380254 + CSCC-57-T COSM4571951 c.594T>C p.D198D Substitution - coding silent 2:32380239-32380239 + TCGA-66-2758-01 COSM721207 c.7193C>A p.S2398Y Substitution - Missense 2:32478759-32478759 + TCGA-G2-A2EO-01 COSM1306739 c.4662C>T p.F1554F Substitution - coding silent 2:32453851-32453851 + TCGA-B5-A11O-01 COSM1020282 c.4301_4303delATA p.N1435delN Deletion - In frame 2:32443553-32443555 + C086 COSM5527363 c.13897C>T p.P4633S Substitution - Missense 2:32599805-32599805 + TCGA-B5-A11E-01 COSM1020406 c.12479C>T p.A4160V Substitution - Missense 2:32543428-32543428 + TCGA-60-2723-01 COSM721214 c.4047G>C p.Q1349H Substitution - Missense 2:32442167-32442167 + 116 COSM5010805 c.11498A>G p.Y3833C Substitution - Missense 2:32518821-32518821 + ESO-0292 COSM1240895 c.7421T>G p.L2474R Substitution - Missense 2:32481332-32481332 + T2284 COSM4665762 c.11778T>C p.R3926R Substitution - coding silent 2:32525486-32525486 + BD114T COSM5502462 c.5044G>A p.A1682T Substitution - Missense 2:32464611-32464611 + TCGA-A5-A0GB-01 COSM185701 c.7095G>A p.T2365T Substitution - coding silent 2:32478661-32478661 + CSCC-44-T COSM4507471 c.7471C>T p.L2491L Substitution - coding silent 2:32481382-32481382 + UPCI:SCC090 COSM4591363 c.3994G>C p.V1332L Substitution - Missense TCGA-EE-A20C-06 COSM3581220 c.12941G>A p.R4314K Substitution - Missense 2:32547980-32547980 + AOCS-086-3-2 COSM4141072 c.414G>A p.K138K Substitution - coding silent 2:32377676-32377676 + 587228 COSM1184726 c.5783A>T p.Y1928F Substitution - Missense 2:32468439-32468439 + HCC037T COSM5811828 c.9704G>C p.C3235S Substitution - Missense 2:32507983-32507983 + TCGA-AA-3672-01 COSM266096 c.10706C>A p.P3569H Substitution - Missense 2:32515127-32515127 + T2269 COSM4665757 c.10810G>A p.A3604T Substitution - Missense 2:32515231-32515231 + CHC1602T COSM4789050 c.4813G>A p.A1605T Substitution - Missense 2:32463253-32463253 + HCC25 COSM1614786 c.4541G>T p.G1514V Substitution - Missense 2:32448851-32448851 + LIM1899 COSM4640434 c.6765G>A p.Q2255Q Substitution - coding silent 2:32476257-32476257 + TCGA-BR-7723-01 COSM4093851 c.445G>A p.A149T Substitution - Missense 2:32377707-32377707 + TCGA-AR-A256-01 COSM1483062 c.2971T>C p.S991P Substitution - Missense 2:32429244-32429244 + TCGA-AP-A056-01 COSM1020422 c.13140T>G p.D4380E Substitution - Missense 2:32549477-32549477 + BRC42 COSM5025604 c.3881A>G p.D1294G Substitution - Missense 2:32441399-32441399 + CSCC-19-T COSM4469525 c.1603C>T p.L535F Substitution - Missense 2:32414894-32414894 + TCGA-D1-A103-01 COSM1020348 c.8815G>A p.E2939K Substitution - Missense 2:32499893-32499893 + I2L-P19Ta-Tumor-Biopsy COSM5354156 c.2843G>A p.G948D Substitution - Missense 2:32416134-32416134 + PT23_2 COSM5903381 c.7968+1G>A p.? Unknown 2:32487802-32487802 + TCGA-HE-7130-01 COSM3991270 c.1306C>T p.Q436* Substitution - Nonsense 2:32401511-32401511 + UM-SCC-11B COSM4591362 c.3994G>C p.V1332L Substitution - Missense UD-SCC-2 COSM4591362 c.3994G>C p.V1332L Substitution - Missense TCGA-B0-5705-01 COSM477328 c.1923A>G p.K641K Substitution - coding silent 2:32415214-32415214 + ESO-1670 COSM1246122 c.14354G>A p.R4785Q Substitution - Missense 2:32611542-32611542 + TCGA-AR-A2LE-01 COSM3839435 c.12584G>T p.G4195V Substitution - Missense 2:32543533-32543533 + HCC87 COSM1614794 c.8530C>G p.L2844V Substitution - Missense 2:32499608-32499608 + TCGA-AA-A00N-01 COSM274138 c.14174G>A p.R4725Q Substitution - Missense 2:32607558-32607558 + TCGA-CA-6718-01 COSM1020240 c.2658G>T p.K886N Substitution - Missense 2:32415949-32415949 + TCGA-CM-4743-01 COSM1407788 c.3605C>T p.T1202M Substitution - Missense 2:32436158-32436158 + 8013912 COSM3391708 c.3580C>A p.L1194I Substitution - Missense 2:32436133-32436133 + pfg053T COSM4765142 c.7968_7968+1insGAAC p.L2657fs*17 Unknown 2:32487801-32487802 + pfg143T COSM4752321 c.1558C>T p.Q520* Substitution - Nonsense 2:32414849-32414849 + PDA_067 COSM1483065 c.8020A>T p.T2674S Substitution - Missense 2:32488639-32488639 + TCGA-AP-A0LM-01 COSM1020273 c.4122T>C p.N1374N Substitution - coding silent 2:32442339-32442339 + TCGA-66-2754-01 COSM721211 c.5473G>C p.E1825Q Substitution - Missense 2:32467641-32467641 + PT38 COSM5922136 c.2717C>T p.T906I Substitution - Missense 2:32416008-32416008 + LUAD_E00522 COSM353129 c.14024G>T p.G4675V Substitution - Missense 2:32603037-32603037 + T56 COSM1177511 c.10436_10437insT p.S3480fs*25 Insertion - Frameshift 2:32513022-32513023 + TCGA-AG-A036-01 COSM5075323 c.7854G>T p.G2618G Substitution - coding silent 2:32487687-32487687 + LUAD-S01467 COSM399462 c.11002C>G p.H3668D Substitution - Missense 2:32515423-32515423 + 2492729 COSM5726306 c.11819G>A p.G3940E Substitution - Missense 2:32525527-32525527 + WSU-HN8 COSM4591362 c.3994G>C p.V1332L Substitution - Missense TCGA-AN-A0AK-01 COSM3839420 c.380T>C p.I127T Substitution - Missense 2:32377642-32377642 + TCGA-B5-A0JY-01 COSM259639 c.4145G>A p.R1382Q Substitution - Missense 2:32442362-32442362 + TCGA-FU-A3HZ-01 COSM4840924 c.6219G>T p.K2073N Substitution - Missense 2:32469486-32469486 + TCGA-DJ-A3VJ-01 COSM3372763 c.6292A>T p.N2098Y Substitution - Missense 2:32469559-32469559 + Pat_65_A COSM5862441 c.7079G>A p.R2360H Substitution - Missense 2:32478645-32478645 + CSCC-49-T COSM3581187 c.5184C>T p.F1728F Substitution - coding silent 2:32464751-32464751 + 388 COSM3720974 c.4085T>G p.V1362G Substitution - Missense 2:32442205-32442205 + HCC134T COSM5818972 c.4962G>T p.K1654N Substitution - Missense 2:32464529-32464529 + TCGA-AP-A056-01 COSM1020387 c.11162A>G p.H3721R Substitution - Missense 2:32515583-32515583 + TCGA-AP-A059-01 COSM1020263 c.3713G>T p.G1238V Substitution - Missense 2:32439589-32439589 + TCGA-D1-A16Y-01 COSM1020283 c.5167G>A p.E1723K Substitution - Missense 2:32464734-32464734 + 472 COSM4437991 c.14540G>A p.S4847N Substitution - Missense 2:32617870-32617870 + TCGA-JW-A5VL-01 COSM4846932 c.524C>T p.S175L Substitution - Missense 2:32380169-32380169 + WSU-HN6 COSM4591363 c.3994G>C p.V1332L Substitution - Missense LUAD-S01315 COSM345318 c.9889A>T p.K3297* Substitution - Nonsense 2:32508168-32508168 + TCGA-FW-A3R5-06 COSM3910256 c.11786C>T p.S3929L Substitution - Missense 2:32525494-32525494 + TCGA-CJ-4893-01 COSM3364725 c.5457T>G p.I1819M Substitution - Missense 2:32467625-32467625 + LIM1215 COSM4312902 c.336T>C p.G112G Substitution - coding silent 2:32377598-32377598 + 2293782 COSM4608879 c.769G>T p.D257Y Substitution - Missense 2:32388873-32388873 + YUDIALE COSM1690437 c.10597C>T p.P3533S Substitution - Missense 2:32515018-32515018 + TCGA-AK-3458-01 COSM477343 c.8403T>C p.S2801S Substitution - coding silent 2:32493602-32493602 + PD4601a COSM159384 c.5323C>T p.H1775Y Substitution - Missense 2:32465131-32465131 + LIM2405 COSM4642665 c.8220T>C p.S2740S Substitution - coding silent 2:32491438-32491438 + TCGA-AP-A056-01 COSM1020385 c.11162A>G p.H3721R Substitution - Missense 2:32515583-32515583 + TCGA-CM-6162-01 COSM1407850 c.13349G>A p.R4450H Substitution - Missense 2:32575360-32575360 + TCGA-B0-5092-01 COSM477329 c.2357C>A p.S786* Substitution - Nonsense 2:32415648-32415648 + TCGA-21-1070-01 COSM721169 c.13096C>G p.Q4366E Substitution - Missense 2:32549433-32549433 + T56 COSM1177512 c.10436_10437insT p.S3480fs*25 Insertion - Frameshift 2:32513022-32513023 + TCGA-G4-6297-01 COSM3695481 c.7265C>T p.A2422V Substitution - Missense 2:32479474-32479474 + TCGA-EB-A3Y7-01 COSM3581226 c.13975C>T p.L4659F Substitution - Missense 2:32599883-32599883 + TCGA-EI-6917-01 COSM3749658 c.7255G>A p.E2419K Substitution - Missense 2:32479464-32479464 + VCB-PH-05T COSM4770665 c.3931A>G p.I1311V Substitution - Missense 2:32441449-32441449 + TCGA-BR-8680-01 COSM4093918 c.13541A>C p.K4514T Substitution - Missense 2:32595073-32595073 + 1910787 COSM1293101 c.2182G>T p.E728* Substitution - Nonsense 2:32415473-32415473 + TCGA-43-6771-01 COSM721185 c.11821A>T p.R3941W Substitution - Missense 2:32525529-32525529 + TCGA-F1-6177-01 COSM4093907 c.11295G>A p.A3765A Substitution - coding silent 2:32515716-32515716 + BCN11 COSM4172303 c.2689A>T p.I897F Substitution - Missense 2:32415980-32415980 + TCGA-DK-A1A7-01 COSM419194 c.4499G>A p.S1500N Substitution - Missense 2:32448809-32448809 + 98 COSM5010803 c.8299T>A p.S2767T Substitution - Missense 2:32491517-32491517 + ESO-0292 COSM1240896 c.7421T>G p.L2474R Substitution - Missense 2:32481332-32481332 + TCGA-CD-5801-01 COSM4093878 c.4679T>C p.L1560P Substitution - Missense 2:32453868-32453868 + TCGA-BR-4184-01 COSM4093912 c.12233G>A p.G4078D Substitution - Missense 2:32531493-32531493 + 88 COSM5014215 c.9621G>A p.W3207* Substitution - Nonsense 2:32505126-32505126 + SC_9090 COSM5569495 c.6845C>A p.T2282N Substitution - Missense 2:32476337-32476337 + TCGA-BR-4184-01 COSM4093881 c.4714T>C p.S1572P Substitution - Missense 2:32453903-32453903 + TCGA-A8-A07R-01 COSM3839424 c.2294C>A p.A765D Substitution - Missense 2:32415585-32415585 + 343 COSM1742234 c.12791C>T p.S4264F Substitution - Missense 2:32545841-32545841 + TCGA-AX-A0J0-01 COSM1020464 c.14328T>C p.D4776D Substitution - coding silent 2:32611516-32611516 + TCGA-G2-A2EF-01 COSM1306727 c.1342G>A p.D448N Substitution - Missense 2:32401547-32401547 + CSCC-44-T COSM4507472 c.7471C>T p.L2491L Substitution - coding silent 2:32481382-32481382 + T578 COSM4665755 c.10098G>T p.L3366F Substitution - Missense 2:32509855-32509855 + YUFERY COSM5396935 c.5530C>T p.L1844F Substitution - Missense 2:32467698-32467698 + TCGA-CD-5801-01 COSM4093879 c.4679T>C p.L1560P Substitution - Missense 2:32453868-32453868 + TCGA-BS-A0TG-01 COSM1020307 c.6349G>T p.V2117F Substitution - Missense 2:32470169-32470169 + I2L-P10-Tumor-Organoid COSM5354029 c.6191A>T p.K2064I Substitution - Missense 2:32469458-32469458 + TCGA-BH-A1FJ-01 COSM1483059 c.2308_2310delAAT p.N770delN Deletion - In frame 2:32415599-32415601 + YUKRIN COSM1690441 c.14046T>G p.N4682K Substitution - Missense 2:32603059-32603059 + ESO-1594 COSM1246119 c.11729A>G p.D3910G Substitution - Missense 2:32524993-32524993 + TCGA-DD-A1EK-01 COSM4934336 c.376G>T p.V126F Substitution - Missense 2:32377638-32377638 + 1_PRE-TREATMENT COSM1718161 c.4931T>G p.L1644R Substitution - Missense 2:32463371-32463371 + SNUH_G16_S1 COSM4001649 c.13344C>A p.T4448T Substitution - coding silent 2:32575355-32575355 + TCGA-D1-A17A-01 COSM1020236 c.2574G>A p.S858S Substitution - coding silent 2:32415865-32415865 + RKO COSM2942505 c.8449C>T p.H2817Y Substitution - Missense 2:32493648-32493648 + ESCC_25 COSM5626768 c.13602A>G p.K4534K Substitution - coding silent 2:32595134-32595134 + TCGA-B5-A11E-01 COSM1020200 c.1015G>A p.E339K Substitution - Missense 2:32395574-32395574 + 2173_T COSM3962793 c.9688G>A p.A3230T Substitution - Missense 2:32505193-32505193 + YUBER COSM1690440 c.11153T>C p.L3718S Substitution - Missense 2:32515574-32515574 + BN02 COSM1614793 c.6955C>T p.L2319F Substitution - Missense 2:32477470-32477470 + TCGA-AA-A010-01 COSM279171 c.13323G>T p.K4441N Substitution - Missense 2:32575334-32575334 + PD22360a COSM5784264 c.6868A>G p.I2290V Substitution - Missense 2:32477383-32477383 + pfg129T COSM4746920 c.10276_10277delCT p.S3427fs*2 Deletion - Frameshift 2:32510564-32510565 + H838 COSM1193103 c.5225C>T p.A1742V Substitution - Missense 2:32464792-32464792 + TCGA-BR-7851-01 COSM1407782 c.2103G>A p.P701P Substitution - coding silent 2:32415394-32415394 + ESO-1154 COSM1246118 c.1130C>T p.A377V Substitution - Missense 2:32401258-32401258 + TCGA-AG-3902-01 COSM5069735 c.5908_5909insT p.S1972fs*18 Insertion - Frameshift 2:32468564-32468565 + TCGA-EE-A2GN-06 COSM3581222 c.13179G>A p.R4393R Substitution - coding silent 2:32575190-32575190 + TCGA-34-5928-01 COSM721197 c.10090G>T p.A3364S Substitution - Missense 2:32509847-32509847 + YUGATOR COSM5396928 c.828T>C p.R276R Substitution - coding silent 2:32388932-32388932 + PT23_2 COSM5903380 c.7968+1G>A p.? Unknown 2:32487802-32487802 + TCGA-B5-A0JY-01 COSM1020391 c.11338C>T p.L3780L Substitution - coding silent 2:32515759-32515759 + TCGA-BH-A0EE-01 COSM5216378 c.4552delA p.N1519fs*61 Deletion - Frameshift 2:32448862-32448862 + CSCC-19-T COSM4469524 c.1603C>T p.L535F Substitution - Missense 2:32414894-32414894 + TCGA-21-1077-01 COSM721157 c.14171C>T p.S4724F Substitution - Missense 2:32607555-32607555 + 381_T COSM3962784 c.3151C>G p.Q1051E Substitution - Missense 2:32430993-32430993 + TCGA-EI-6917-01 COSM3749657 c.7255G>A p.E2419K Substitution - Missense 2:32479464-32479464 + TCGA-EQ-A4SO-01 COSM4093905 c.9404C>G p.S3135C Substitution - Missense 2:32503141-32503141 + TCGA-BH-A18G-01 COSM3839433 c.11140G>A p.A3714T Substitution - Missense 2:32515561-32515561 + TCGA-AZ-4615-01 COSM2942749 c.13502delA p.K4503fs*11 Deletion - Frameshift 2:32595034-32595034 + HT115 COSM2942363 c.4610T>C p.V1537A Substitution - Missense 2:32448920-32448920 + S02328 COSM5692026 c.11340G>T p.L3780L Substitution - coding silent 2:32515761-32515761 + TCGA-EE-A3AC-06 COSM3581184 c.5086C>T p.P1696S Substitution - Missense 2:32464653-32464653 + PD23550a COSM5784371 c.5873G>A p.R1958Q Substitution - Missense 2:32468529-32468529 + C086 COSM1690428 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + RK326_C01 COSM4779084 c.11070G>T p.L3690F Substitution - Missense 2:32515491-32515491 + TCGA-BT-A3PH-01 COSM1306747 c.10882G>C p.D3628H Substitution - Missense 2:32515303-32515303 + CML010T COSM5802807 c.13717G>A p.A4573T Substitution - Missense 2:32597855-32597855 + TCGA-H4-A2HQ-01 COSM1306752 c.11572C>T p.L3858F Substitution - Missense 2:32518895-32518895 + S02328 COSM5692025 c.11340G>T p.L3780L Substitution - coding silent 2:32515761-32515761 + C0075T COSM4164514 c.7270G>A p.V2424I Substitution - Missense 2:32479479-32479479 + TCGA-DK-A2I6-01 COSM1306745 c.10453_10454GG>AT p.G3485I Substitution - Missense 2:32513039-32513040 + KM12 COSM2942330 c.3759T>C p.S1253S Substitution - coding silent 2:32439635-32439635 + TCGA-BS-A0UV-01 COSM1020345 c.8669G>A p.R2890Q Substitution - Missense 2:32499747-32499747 + 343 COSM1742233 c.12791C>T p.S4264F Substitution - Missense 2:32545841-32545841 + RK212_C01 COSM3743779 c.2199A>G p.I733M Substitution - Missense 2:32415490-32415490 + TCGA-ER-A194-01 COSM3581213 c.11058T>C p.I3686I Substitution - coding silent 2:32515479-32515479 + YUBER COSM1690433 c.8704C>T p.R2902C Substitution - Missense 2:32499782-32499782 + TCGA-AX-A05Z-01 COSM259639 c.4145G>A p.R1382Q Substitution - Missense 2:32442362-32442362 + TCGA-BR-8679-01 COSM4093875 c.4351T>C p.Y1451H Substitution - Missense 2:32445535-32445535 + CPCG0185-F1 COSM4966479 c.13813C>G p.R4605G Substitution - Missense 2:32597951-32597951 + CLL024 COSM1291500 c.6809A>G p.K2270R Substitution - Missense 2:32476301-32476301 + TCGA-66-2770-01 COSM721178 c.11946A>G p.T3982T Substitution - coding silent 2:32529676-32529676 + TCGA-EB-A44O-01 COSM3581218 c.12863A>T p.Y4288F Substitution - Missense 2:32547902-32547902 + CSCC-31-T COSM4499962 c.5549C>T p.P1850L Substitution - Missense 2:32467717-32467717 + CHC892T COSM4796730 c.5256+1G>A p.? Unknown 2:32464824-32464824 + DN110CD COSM5795597 c.6977A>T p.E2326V Substitution - Missense 2:32477492-32477492 + 1910786 COSM1293102 c.2182G>T p.E728* Substitution - Nonsense 2:32415473-32415473 + TCGA-21-1070-01 COSM721168 c.13096C>G p.Q4366E Substitution - Missense 2:32549433-32549433 + TCGA-JX-A3Q0-01 COSM4824566 c.5609G>A p.R1870K Substitution - Missense 2:32467940-32467940 + PCSI_0083_Pa_P_526 COSM3380142 c.12778C>T p.R4260* Substitution - Nonsense 2:32545828-32545828 + 19M COSM5578122 c.8903G>A p.G2968E Substitution - Missense 2:32499981-32499981 + BD49T COSM1020327 c.7680C>T p.S2560S Substitution - coding silent 2:32482566-32482566 + YUBER COSM1690439 c.11153T>C p.L3718S Substitution - Missense 2:32515574-32515574 + TCGA-BS-A0UF-01 COSM1020419 c.13133G>A p.R4378Q Substitution - Missense 2:32549470-32549470 + TCGA-B0-5092-01 COSM477330 c.2357C>A p.S786* Substitution - Nonsense 2:32415648-32415648 + 2 COSM4172306 c.10514A>G p.Y3505C Substitution - Missense 2:32513100-32513100 + YULOCUS COSM5396940 c.12244C>T p.L4082F Substitution - Missense 2:32531504-32531504 + 1_RESISTANT COSM1718161 c.4931T>G p.L1644R Substitution - Missense 2:32463371-32463371 + TCGA-G3-A3CK-01 COSM4922333 c.2957A>C p.K986T Substitution - Missense 2:32429230-32429230 + TCGA-AX-A0J0-01 COSM1020425 c.13198C>T p.R4400W Substitution - Missense 2:32575209-32575209 + TCGA-B5-A11E-01 COSM1020430 c.13487G>A p.R4496Q Substitution - Missense 2:32594046-32594046 + J80_T COSM3962789 c.5534A>C p.H1845P Substitution - Missense 2:32467702-32467702 + CSCC-11-T COSM4557437 c.7295G>A p.G2432E Substitution - Missense 2:32479504-32479504 + OSCC-GB_00530111 COSM4883495 c.5748G>C p.M1916I Substitution - Missense 2:32468079-32468079 + TCGA-42-2589-01 COSM1327096 c.3488A>C p.E1163A Substitution - Missense 2:32435574-32435574 + ACINAR25 COSM1734255 c.4259G>A p.C1420Y Substitution - Missense 2:32443511-32443511 + TCGA-D1-A103-01 COSM1020358 c.9204A>G p.R3068R Substitution - coding silent 2:32501885-32501885 + TCGA-AX-A0J1-01 COSM1020413 c.12712G>A p.A4238T Substitution - Missense 2:32545762-32545762 + TCGA-A8-A09Z-01 COSM3839422 c.1455T>C p.H485H Substitution - coding silent 2:32406535-32406535 + TCGA-F4-6856-01 COSM1407794 c.4214delC p.R1406fs*3 Deletion - Frameshift 2:32442431-32442431 + TCGA-66-2756-01 COSM721182 c.11890G>T p.V3964L Substitution - Missense 2:32525598-32525598 + Pat_41_B COSM5862446 c.8141C>T p.T2714I Substitution - Missense 2:32490086-32490086 + CAL27 COSM4591362 c.3994G>C p.V1332L Substitution - Missense PDA_067 COSM148833 c.8020A>T p.T2674S Substitution - Missense 2:32488639-32488639 + TCGA-AA-3492-01 COSM1407770 c.607A>C p.T203P Substitution - Missense 2:32380252-32380252 + 2492710 COSM2942294 c.3120G>A p.A1040A Substitution - coding silent 2:32430962-32430962 + pfg143T COSM4752341 c.13331T>A p.V4444D Substitution - Missense 2:32575342-32575342 + TCGA-D1-A17A-01 COSM1020234 c.2574G>A p.S858S Substitution - coding silent 2:32415865-32415865 + LUAD-B01811 COSM334456 c.12810+1G>T p.? Unknown 2:32545861-32545861 + KM12 COSM2942733 c.13199G>C p.R4400P Substitution - Missense 2:32575210-32575210 + TCGA-EE-A2GR-06 COSM3581191 c.7522C>T p.L2508F Substitution - Missense 2:32481433-32481433 + TCGA-DK-A3WW-01 COSM3798964 c.962C>G p.S321C Substitution - Missense 2:32395521-32395521 + TCGA-EI-6884-01 COSM5079627 c.4205A>G p.H1402R Substitution - Missense 2:32442422-32442422 + BN01T COSM1614789 c.4835C>A p.A1612E Substitution - Missense 2:32463275-32463275 + YUDATE COSM1690422 c.4792T>C p.S1598P Substitution - Missense 2:32463232-32463232 + TCGA-43-6771-01 COSM721186 c.10918G>T p.A3640S Substitution - Missense 2:32515339-32515339 + 17143 COSM5029117 c.9143C>G p.S3048C Substitution - Missense 2:32501824-32501824 + ESO-114 COSM1246116 c.10477C>A p.H3493N Substitution - Missense 2:32513063-32513063 + TCGA-EI-6917-01 COSM3426398 c.7066A>G p.K2356E Substitution - Missense 2:32477581-32477581 + Gp5D COSM2942498 c.8392G>A p.V2798M Substitution - Missense 2:32493591-32493591 + HCC013T COSM5807541 c.4652A>T p.E1551V Substitution - Missense 2:32453841-32453841 + TCGA-AX-A0J0-01 COSM1020207 c.1609G>T p.E537* Substitution - Nonsense 2:32414900-32414900 + TCGA-AU-6004-01 COSM1407777 c.1251_1252insA p.M418fs*8 Insertion - Frameshift 2:32401379-32401380 + CDGLIV0504A0086_T COSM5041841 c.7828A>T p.T2610S Substitution - Missense 2:32487661-32487661 + TCGA-43-6771-01 COSM721187 c.10918G>T p.A3640S Substitution - Missense 2:32515339-32515339 + BN01 COSM1614788 c.4835C>A p.A1612E Substitution - Missense 2:32463275-32463275 + 1N04-VS-1T04 COSM4972738 c.5034C>T p.S1678S Substitution - coding silent 2:32464601-32464601 + TCGA-BG-A0M4-01 COSM1020192 c.811G>A p.G271R Substitution - Missense 2:32388915-32388915 + TCGA-BR-7723-01 COSM4093902 c.8574C>T p.A2858A Substitution - coding silent 2:32499652-32499652 + LP6005409-DNA_E01 COSM4409232 c.1085A>C p.H362P Substitution - Missense 2:32401213-32401213 + PD24195a COSM5795124 c.10737G>T p.M3579I Substitution - Missense 2:32515158-32515158 + DN110CD COSM5779916 c.6976G>T p.E2326* Substitution - Nonsense 2:32477491-32477491 + C467 COSM4442111 c.7937T>C p.L2646P Substitution - Missense 2:32487770-32487770 + TCGA-AA-3492-01 COSM1407827 c.9156G>T p.M3052I Substitution - Missense 2:32501837-32501837 + sysucc-311T COSM5465543 c.5078T>C p.V1693A Substitution - Missense 2:32464645-32464645 + TCGA-G4-6586-01 COSM1407839 c.11951C>T p.A3984V Substitution - Missense 2:32529681-32529681 + HT115 COSM2942273 c.2618A>C p.D873A Substitution - Missense 2:32415909-32415909 + YULAN COSM1690436 c.9143C>T p.S3048F Substitution - Missense 2:32501824-32501824 + TCGA-BR-7957-01 COSM4093920 c.13861T>A p.Y4621N Substitution - Missense 2:32599769-32599769 + BRC5 COSM5025602 c.2620T>G p.C874G Substitution - Missense 2:32415911-32415911 + 16135 COSM5029119 c.14057C>G p.S4686* Substitution - Nonsense 2:32603070-32603070 + HCC013T COSM5807542 c.4652A>T p.E1551V Substitution - Missense 2:32453841-32453841 + TCGA-D1-A103-01 COSM1020350 c.8815G>A p.E2939K Substitution - Missense 2:32499893-32499893 + PCSI_0047_Pa_P COSM3782191 c.12148G>T p.D4050Y Substitution - Missense 2:32531408-32531408 + BRC51 COSM5025609 c.10439C>G p.S3480* Substitution - Nonsense 2:32513025-32513025 + TCGA-EI-6917-01 COSM3426402 c.9797A>C p.K3266T Substitution - Missense 2:32508076-32508076 + pfg008T COSM4752346 c.13688T>C p.V4563A Substitution - Missense 2:32597826-32597826 + TCGA-Q1-A73P-01 COSM4825831 c.12819G>T p.V4273V Substitution - coding silent 2:32547858-32547858 + GB19 COSM1742854 c.8150G>A p.R2717Q Substitution - Missense 2:32490095-32490095 + TCGA-CM-4746-01 COSM1407793 c.4051C>A p.L1351I Substitution - Missense 2:32442171-32442171 + TCGA-AP-A059-01 COSM1020261 c.3713G>T p.G1238V Substitution - Missense 2:32439589-32439589 + 587224 COSM1184728 c.2000T>A p.I667N Substitution - Missense 2:32415291-32415291 + TCGA-CZ-5465-01 COSM477323 c.523T>C p.S175P Substitution - Missense 2:32380168-32380168 + HCC160 COSM3709624 c.11755+3A>T p.? Unknown 2:32525022-32525022 + 1N04-VS-1T04 COSM4972739 c.5034C>T p.S1678S Substitution - coding silent 2:32464601-32464601 + RKO COSM2942504 c.8449C>T p.H2817Y Substitution - Missense 2:32493648-32493648 + TCGA-E5-A2PC-01 COSM1306724 c.1149T>C p.D383D Substitution - coding silent 2:32401277-32401277 + CML010T COSM5802802 c.4166T>G p.V1389G Substitution - Missense 2:32442383-32442383 + I2L-P19Ta-Tumor-Organoid COSM5354155 c.2843G>A p.G948D Substitution - Missense 2:32416134-32416134 + PD4202a COSM159379 c.4169G>A p.R1390H Substitution - Missense 2:32442386-32442386 + TCGA-AA-3510-01 COSM185743 c.14548G>T p.E4850* Substitution - Nonsense 2:32617878-32617878 + TCGA-EB-A41A-01 COSM3581181 c.2223C>A p.D741E Substitution - Missense 2:32415514-32415514 + LP6005409-DNA_F03 COSM4408878 c.2710G>C p.V904L Substitution - Missense 2:32416001-32416001 + CHC2362T COSM5348586 c.3470_3471insT p.M1157fs*13 Insertion - Frameshift 2:32435556-32435557 + CHC1595T COSM4801766 c.1039G>C p.E347Q Substitution - Missense 2:32401167-32401167 + S29-pre COSM5574257 c.12829C>G p.H4277D Substitution - Missense 2:32547868-32547868 + BN41T COSM1614784 c.729T>G p.N243K Substitution - Missense 2:32388833-32388833 + TCGA-BR-7851-01 COSM1407783 c.2103G>A p.P701P Substitution - coding silent 2:32415394-32415394 + T84 COSM2942654 c.11509A>G p.I3837V Substitution - Missense 2:32518832-32518832 + RK169_C01 COSM3702180 c.1656A>G p.T552T Substitution - coding silent 2:32414947-32414947 + CHC892T COSM4796729 c.5256+1G>A p.? Unknown 2:32464824-32464824 + ESCC_40 COSM5629370 c.3308A>T p.H1103L Substitution - Missense 2:32433703-32433703 + TCGA-BP-4762-01 COSM574914 c.826C>T p.R276C Substitution - Missense 2:32388930-32388930 + TCGA-DK-A2I4-01 COSM3798965 c.2160G>A p.L720L Substitution - coding silent 2:32415451-32415451 + TCGA-D1-A17Q-01 COSM1020245 c.2763A>C p.E921D Substitution - Missense 2:32416054-32416054 + TCGA-FP-A4BF-01 COSM4093890 c.7125G>A p.V2375V Substitution - coding silent 2:32478691-32478691 + TCGA-G2-A2ES-01 COSM1306726 c.1254G>A p.M418I Substitution - Missense 2:32401382-32401382 + 49M COSM5589818 c.10733C>T p.S3578F Substitution - Missense 2:32515154-32515154 + LIM1899 COSM4640433 c.6765G>A p.Q2255Q Substitution - coding silent 2:32476257-32476257 + TCGA-HW-8320-01 COSM3933635 c.13469C>T p.A4490V Substitution - Missense 2:32594028-32594028 + TCGA-CM-6674-01 COSM1407840 c.12035T>C p.V4012A Substitution - Missense 2:32529765-32529765 + TCGA-EE-A3AC-06 COSM3581185 c.5086C>T p.P1696S Substitution - Missense 2:32464653-32464653 + S02209 COSM5675303 c.7880G>T p.S2627I Substitution - Missense 2:32487713-32487713 + TCGA-AP-A059-01 COSM1020344 c.8604C>T p.H2868H Substitution - coding silent 2:32499682-32499682 + TCGA-AM-5821-01 COSM148834 c.13752G>A p.T4584T Substitution - coding silent 2:32597890-32597890 + UM-SCC-17B COSM4592548 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + TCGA-AR-A2LE-01 COSM3839428 c.6134C>T p.S2045F Substitution - Missense 2:32469401-32469401 + WA15 COSM238966 c.5571G>T p.K1857N Substitution - Missense 2:32467739-32467739 + TCGA-BS-A0UJ-01 COSM1020335 c.8482A>T p.T2828S Substitution - Missense 2:32499560-32499560 + S48_pre COSM5574435 c.4864_4865delCA p.H1622fs*70 Deletion - Frameshift 2:32463304-32463305 + CHC2216T COSM4805994 c.14368A>T p.M4790L Substitution - Missense 2:32611556-32611556 + TCGA-AX-A0J0-01 COSM1020403 c.12286C>A p.Q4096K Substitution - Missense 2:32531546-32531546 + TCGA-BR-7723-01 COSM4093903 c.8574C>T p.A2858A Substitution - coding silent 2:32499652-32499652 + CHC605T COSM3668665 c.8582A>G p.E2861G Substitution - Missense 2:32499660-32499660 + T3118 COSM4665743 c.4434_4437delCAGA p.R1479fs*6 Deletion - Frameshift 2:32445618-32445621 + RK326_C01 COSM4779083 c.11070G>T p.L3690F Substitution - Missense 2:32515491-32515491 + TCGA-AX-A060-01 COSM1020443 c.13960C>T p.R4654* Substitution - Nonsense 2:32599868-32599868 + 2492722 COSM1690427 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + 2293782 COSM4608878 c.769G>T p.D257Y Substitution - Missense 2:32388873-32388873 + HT29 COSM4638589 c.7880G>A p.S2627N Substitution - Missense 2:32487713-32487713 + T26 COSM5344196 c.1478-1G>A p.? Unknown 2:32414768-32414768 + PD18730a COSM5787182 c.9700+3G>C p.? Unknown 2:32505208-32505208 + OSCC-GB_00740111 COSM4890892 c.8698C>G p.L2900V Substitution - Missense 2:32499776-32499776 + 18_tFL COSM4171161 c.1004T>C p.L335P Substitution - Missense 2:32395563-32395563 + TCGA-AA-3930-01 COSM296554 c.3318C>T p.F1106F Substitution - coding silent 2:32433713-32433713 + TCGA-DJ-A3VJ-01 COSM3372764 c.6292A>T p.N2098Y Substitution - Missense 2:32469559-32469559 + TCGA-DA-A1IA-06 COSM1690442 c.14046T>G p.N4682K Substitution - Missense 2:32603059-32603059 + TCGA-AC-A23H-01 COSM1306757 c.12614C>T p.S4205L Substitution - Missense 2:32545664-32545664 + HCC49 COSM1614791 c.5595G>T p.G1865G Substitution - coding silent 2:32467926-32467926 + Au4 COSM5602906 c.8213C>T p.S2738F Substitution - Missense 2:32491431-32491431 + TCGA-EE-A2MR-06 COSM1690434 c.8704C>T p.R2902C Substitution - Missense 2:32499782-32499782 + pfg057T COSM4765144 c.12045_12046insC p.S4017fs*9 Insertion - Frameshift 2:32529775-32529776 + H838 COSM1193102 c.5225C>T p.A1742V Substitution - Missense 2:32464792-32464792 + TCGA-DD-A11C-01 COSM4925607 c.12954A>G p.E4318E Substitution - coding silent 2:32547993-32547993 + S48_post COSM5574436 c.4864_4865delCA p.H1622fs*70 Deletion - Frameshift 2:32463304-32463305 + TCGA-43-6770-01 COSM721209 c.7156C>G p.L2386V Substitution - Missense 2:32478722-32478722 + TCGA-BS-A0UV-01 COSM1020347 c.8669G>A p.R2890Q Substitution - Missense 2:32499747-32499747 + CSCC-31-T COSM4562633 c.9368G>A p.R3123K Substitution - Missense 2:32503105-32503105 + BHY COSM4592548 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + TCGA-37-5819-01 COSM721181 c.11900T>C p.L3967P Substitution - Missense 2:32525608-32525608 + H1155 COSM1195529 c.2518G>A p.E840K Substitution - Missense 2:32415809-32415809 + WSU-HN13 COSM4591363 c.3994G>C p.V1332L Substitution - Missense PT23_2 COSM5903378 c.7968G>A p.Q2656Q Substitution - coding silent 2:32487801-32487801 + TCGA-AP-A056-01 COSM1020382 c.11019T>C p.C3673C Substitution - coding silent 2:32515440-32515440 + TCGA-GN-A266-06 COSM3581204 c.9063A>T p.E3021D Substitution - Missense 2:32501744-32501744 + TCGA-ER-A194-01 COSM3581212 c.11058T>C p.I3686I Substitution - coding silent 2:32515479-32515479 + EGC3 COSM1020313 c.6872G>A p.R2291H Substitution - Missense 2:32477387-32477387 + TCGA-AP-A059-01 COSM1020194 c.811G>A p.G271R Substitution - Missense 2:32388915-32388915 + ACINAR01 COSM1734254 c.2909G>A p.C970Y Substitution - Missense 2:32429182-32429182 + PT33 COSM5908066 c.1693C>T p.P565S Substitution - Missense 2:32414984-32414984 + TCGA-G4-6294-01 COSM3695483 c.9821T>C p.V3274A Substitution - Missense 2:32508100-32508100 + 17143 COSM5029116 c.9143C>G p.S3048C Substitution - Missense 2:32501824-32501824 + PD3989a COSM159374 c.1398A>G p.I466M Substitution - Missense 2:32401603-32401603 + sysucc-311T COSM5465546 c.13612+10A>C p.? Unknown 2:32595154-32595154 + TCGA-34-5928-01 COSM721196 c.10090G>T p.A3364S Substitution - Missense 2:32509847-32509847 + HCC87T COSM1614794 c.8530C>G p.L2844V Substitution - Missense 2:32499608-32499608 + TCGA-AX-A060-01 COSM1020445 c.13960C>T p.R4654* Substitution - Nonsense 2:32599868-32599868 + TCGA-CG-5721-01 COSM4093866 c.3297T>C p.C1099C Substitution - coding silent 2:32433692-32433692 + CSCC-11-T COSM4555374 c.6525G>T p.V2175V Substitution - coding silent 2:32471057-32471057 + YUFERY COSM5396936 c.5530C>T p.L1844F Substitution - Missense 2:32467698-32467698 + 2521259 COSM5889655 c.1055C>T p.S352F Substitution - Missense 2:32401183-32401183 + TCGA-CA-6717-01 COSM1407816 c.7167A>G p.G2389G Substitution - coding silent 2:32478733-32478733 + ESCC_157 COSM5646336 c.10864G>C p.A3622P Substitution - Missense 2:32515285-32515285 + TCGA-A2-A0D0-01 COSM442826 c.10511G>A p.S3504N Substitution - Missense 2:32513097-32513097 + TCGA-AG-3892-01 COSM256400 c.9967G>A p.V3323I Substitution - Missense 2:32508246-32508246 + TCGA-AX-A05Z-01 COSM1020246 c.3224G>A p.R1075Q Substitution - Missense 2:32431066-32431066 + 472 COSM4437990 c.14540G>A p.S4847N Substitution - Missense 2:32617870-32617870 + TCGA-BL-A13I-01 COSM419191 c.6321A>G p.E2107E Substitution - coding silent 2:32469588-32469588 + TCGA-AA-A010-01 COSM279164 c.2360A>C p.N787T Substitution - Missense 2:32415651-32415651 + TCGA-AP-A0LT-01 COSM1020213 c.1925C>T p.A642V Substitution - Missense 2:32415216-32415216 + TCGA-AP-A0LM-01 COSM1020267 c.4036G>T p.E1346* Substitution - Nonsense 2:32442156-32442156 + RK126_C01 COSM1631981 c.4679T>G p.L1560R Substitution - Missense 2:32453868-32453868 + 8012321 COSM3391710 c.8972T>A p.M2991K Substitution - Missense 2:32500050-32500050 + ESCC-190T COSM3939075 c.2557C>G p.Q853E Substitution - Missense 2:32415848-32415848 + TCGA-DD-A1EG-01 COSM4915779 c.9831T>C p.A3277A Substitution - coding silent 2:32508110-32508110 + K3 COSM249146 c.5371G>T p.V1791L Substitution - Missense 2:32467539-32467539 + TCGA-FW-A3R5-06 COSM3910250 c.5065C>T p.H1689Y Substitution - Missense 2:32464632-32464632 + 108 COSM5016775 c.12592+2T>G p.? Unknown 2:32543543-32543543 + TCGA-EE-A20C-06 COSM3581221 c.12941G>A p.R4314K Substitution - Missense 2:32547980-32547980 + LUAD-YINHD COSM350632 c.4424C>G p.T1475S Substitution - Missense 2:32445608-32445608 + TCGA-AG-A002-01 COSM259636 c.2005G>T p.E669* Substitution - Nonsense 2:32415296-32415296 + OSCC-GB_00990111 COSM4885715 c.13727G>A p.R4576H Substitution - Missense 2:32597865-32597865 + LIM1215 COSM4312903 c.336T>C p.G112G Substitution - coding silent 2:32377598-32377598 + TCGA-AP-A05A-01 COSM1020366 c.9772G>T p.V3258F Substitution - Missense 2:32508051-32508051 + SNUH_G76_S1 COSM4419497 c.3642A>G p.G1214G Substitution - coding silent 2:32439518-32439518 + TCGA-B8-5163-01 COSM477332 c.2566A>G p.I856V Substitution - Missense 2:32415857-32415857 + TCGA-D9-A6EC-06 COSM4401235 c.12556C>T p.R4186* Substitution - Nonsense 2:32543505-32543505 + 40M COSM5584554 c.6461C>T p.P2154L Substitution - Missense 2:32470281-32470281 + DLD1 COSM2942607 c.10430C>A p.P3477H Substitution - Missense 2:32513016-32513016 + GC8_T COSM148835 c.13752G>A p.T4584T Substitution - coding silent 2:32597890-32597890 + TCGA-DI-A0WH-01 COSM1020398 c.12190A>G p.T4064A Substitution - Missense 2:32531450-32531450 + TCGA-DK-A1AC-01 COSM1306749 c.11479C>T p.Q3827* Substitution - Nonsense 2:32518383-32518383 + ESO-752 COSM1246128 c.5568G>A p.M1856I Substitution - Missense 2:32467736-32467736 + TCGA-EP-A2KA-01 COSM4917249 c.4654G>T p.G1552C Substitution - Missense 2:32453843-32453843 + TCGA-AX-A0J1-01 COSM1020415 c.12712G>A p.A4238T Substitution - Missense 2:32545762-32545762 + TCGA-AG-3892-01 COSM256398 c.6916G>T p.E2306* Substitution - Nonsense 2:32477431-32477431 + HCC2998 COSM2942356 c.4193G>A p.R1398Q Substitution - Missense 2:32442410-32442410 + UM-SCC-11B COSM4592547 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + 8057482 COSM3391706 c.73G>A p.A25T Substitution - Missense 2:32357234-32357234 + 457 COSM4436194 c.13771C>T p.L4591L Substitution - coding silent 2:32597909-32597909 + TCGA-FW-A3R5-06 COSM3910257 c.11786C>T p.S3929L Substitution - Missense 2:32525494-32525494 + BCN23 COSM4172308 c.12793A>G p.S4265G Substitution - Missense 2:32545843-32545843 + UM-SCC-17B COSM4591362 c.3994G>C p.V1332L Substitution - Missense T3094 COSM4665759 c.11643T>G p.A3881A Substitution - coding silent 2:32524907-32524907 + TCGA-CW-5585-01 COSM477346 c.9317T>C p.L3106P Substitution - Missense 2:32503054-32503054 + TCGA-18-3409-01 COSM721177 c.12379G>A p.E4127K Substitution - Missense 2:32543328-32543328 + TCGA-AG-A002-01 COSM259641 c.9063A>C p.E3021D Substitution - Missense 2:32501744-32501744 + LUAD-S01306 COSM343615 c.4069T>C p.C1357R Substitution - Missense 2:32442189-32442189 + 85 COSM5010807 c.13885G>A p.D4629N Substitution - Missense 2:32599793-32599793 + TCGA-85-6560-01 COSM721202 c.8928G>A p.S2976S Substitution - coding silent 2:32500006-32500006 + BK0019 COSM4186122 c.1750A>T p.S584C Substitution - Missense 2:32415041-32415041 + TCGA-D3-A2JH-06 COSM3581229 c.14153C>T p.P4718L Substitution - Missense 2:32607537-32607537 + TCGA-AP-A059-01 COSM1020433 c.13589C>T p.A4530V Substitution - Missense 2:32595121-32595121 + ccRCC-29 COSM1660780 c.6707T>C p.V2236A Substitution - Missense 2:32473226-32473226 + LUAD_E00522 COSM353128 c.14024G>T p.G4675V Substitution - Missense 2:32603037-32603037 + TCGA-EB-A3XD-01 COSM3581198 c.8383C>T p.R2795* Substitution - Nonsense 2:32493582-32493582 + DLD1 COSM4624788 c.14528T>C p.V4843A Substitution - Missense 2:32617858-32617858 + TCGA-BR-6452-01 COSM4093914 c.13151A>G p.D4384G Substitution - Missense 2:32575162-32575162 + SC_9090 COSM5569496 c.6845C>A p.T2282N Substitution - Missense 2:32476337-32476337 + 2250161 COSM5029765 c.10346+4C>T p.? Unknown 2:32510638-32510638 + LUAD-S01346 COSM397723 c.9740G>A p.G3247E Substitution - Missense 2:32508019-32508019 + LUAD-RT-S01711 COSM380155 c.8705G>T p.R2902L Substitution - Missense 2:32499783-32499783 + TCGA-AR-A0TX-01 COSM442828 c.12755C>T p.S4252F Substitution - Missense 2:32545805-32545805 + TCGA-FS-A1ZE-06 COSM1020345 c.8669G>A p.R2890Q Substitution - Missense 2:32499747-32499747 + 18_tFL COSM4171159 c.985T>C p.F329L Substitution - Missense 2:32395544-32395544 + 43_tFL COSM4171166 c.11815A>G p.R3939G Substitution - Missense 2:32525523-32525523 + SNU-C4 COSM4653552 c.6703C>A p.L2235I Substitution - Missense 2:32473222-32473222 + TCGA-AA-A010-01 COSM279168 c.9798A>C p.K3266N Substitution - Missense 2:32508077-32508077 + 587344 COSM1184731 c.1121C>G p.T374R Substitution - Missense 2:32401249-32401249 + J30_T COSM3962786 c.4645G>A p.A1549T Substitution - Missense 2:32453834-32453834 + TCGA-BR-8487-01 COSM4093892 c.7318G>A p.A2440T Substitution - Missense 2:32479527-32479527 + pfg143T COSM4752322 c.1558C>T p.Q520* Substitution - Nonsense 2:32414849-32414849 + U2940 COSM5620355 c.12694G>A p.V4232I Substitution - Missense 2:32545744-32545744 + CSCC-47-T COSM4559362 c.8023G>A p.G2675R Substitution - Missense 2:32488642-32488642 + ORL-48 COSM4591362 c.3994G>C p.V1332L Substitution - Missense TCGA-BP-4173-01 COSM3773970 c.2681C>T p.T894M Substitution - Missense 2:32415972-32415972 + 28 COSM148833 c.8020A>T p.T2674S Substitution - Missense 2:32488639-32488639 + TCGA-EB-A41A-01 COSM3581169 c.352C>T p.Q118* Substitution - Nonsense 2:32377614-32377614 + PCSI_0083_Pa_P COSM3380143 c.12778C>T p.R4260* Substitution - Nonsense 2:32545828-32545828 + TCGA-EB-A3Y7-01 COSM3581187 c.5184C>T p.F1728F Substitution - coding silent 2:32464751-32464751 + TCGA-BR-8589-01 COSM4093923 c.14059A>C p.S4687R Substitution - Missense 2:32603072-32603072 + C008 COSM1690427 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + YUWAND COSM1690427 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + HCT8 COSM2942607 c.10430C>A p.P3477H Substitution - Missense 2:32513016-32513016 + HCC090T COSM5810786 c.3200A>G p.H1067R Substitution - Missense 2:32431042-32431042 + S0075 COSM5883444 c.425G>C p.G142A Substitution - Missense 2:32377687-32377687 + TCGA-CM-6674-01 COSM1407800 c.5026G>A p.V1676M Substitution - Missense 2:32464593-32464593 + TCGA-BS-A0UV-01 COSM1020240 c.2658G>T p.K886N Substitution - Missense 2:32415949-32415949 + TCGA-AP-A0LM-01 COSM1020275 c.4122T>C p.N1374N Substitution - coding silent 2:32442339-32442339 + TCGA-37-3789-01 COSM721194 c.10430C>T p.P3477L Substitution - Missense 2:32513016-32513016 + PTC-7C COSM4133814 c.1487C>A p.S496* Substitution - Nonsense 2:32414778-32414778 + CSCC-31-T COSM4562632 c.9368G>A p.R3123K Substitution - Missense 2:32503105-32503105 + 28 COSM1483065 c.8020A>T p.T2674S Substitution - Missense 2:32488639-32488639 + TCGA-Q1-A73P-01 COSM4825830 c.12819G>T p.V4273V Substitution - coding silent 2:32547858-32547858 + TCGA-ER-A198-06 COSM3581208 c.10413G>A p.R3471R Substitution - coding silent 2:32512999-32512999 + TCGA-AP-A0LM-01 COSM1020332 c.8159G>A p.C2720Y Substitution - Missense 2:32490104-32490104 + TCGA-F5-6814-01 COSM2942583 c.9817G>A p.E3273K Substitution - Missense 2:32508096-32508096 + TCGA-AR-A24H-01 COSM1483064 c.3097A>G p.T1033A Substitution - Missense 2:32430939-32430939 + TCGA-BQ-7058-01 COSM3991278 c.9097G>A p.G3033R Substitution - Missense 2:32501778-32501778 + 2493722 COSM5731611 c.9816C>T p.A3272A Substitution - coding silent 2:32508095-32508095 + S00825 COSM5659192 c.3205G>A p.D1069N Substitution - Missense 2:32431047-32431047 + CSCC-37-T COSM4550307 c.4981G>T p.A1661S Substitution - Missense 2:32464548-32464548 + TCGA-AC-A23H-01 COSM3839440 c.13264G>A p.E4422K Substitution - Missense 2:32575275-32575275 + TCGA-GD-A3OS-01 COSM1306731 c.2577C>G p.L859L Substitution - coding silent 2:32415868-32415868 + BK0022 COSM4186322 c.4604C>T p.S1535L Substitution - Missense 2:32448914-32448914 + TCGA-AX-A0J1-01 COSM1020233 c.2504G>A p.R835Q Substitution - Missense 2:32415795-32415795 + LC_C6 COSM1185875 c.9710C>T p.S3237F Substitution - Missense 2:32507989-32507989 + TCGA-FW-A3TV-06 COSM3581171 c.548T>A p.I183N Substitution - Missense 2:32380193-32380193 + TCGA-BR-7851-01 COSM4093909 c.11866G>A p.A3956T Substitution - Missense 2:32525574-32525574 + TCGA-BQ-5881-01 COSM3991272 c.3144A>C p.E1048D Substitution - Missense 2:32430986-32430986 + BK0019 COSM4186121 c.1750A>T p.S584C Substitution - Missense 2:32415041-32415041 + U343 COSM5712084 c.6550A>G p.T2184A Substitution - Missense 2:32471082-32471082 + 61 COSM5736005 c.5465T>C p.L1822S Substitution - Missense 2:32467633-32467633 + 2521259 COSM5889657 c.656T>G p.V219G Substitution - Missense 2:32388760-32388760 + BN01 COSM1614789 c.4835C>A p.A1612E Substitution - Missense 2:32463275-32463275 + J30_T COSM3962790 c.8002A>T p.S2668C Substitution - Missense 2:32488621-32488621 + 10-P8045 COSM4583471 c.1378T>C p.S460P Substitution - Missense 2:32401583-32401583 + TCGA-AN-A046-01 COSM3839429 c.6674G>T p.R2225I Substitution - Missense 2:32473193-32473193 + sysucc-311T COSM5465542 c.5078T>C p.V1693A Substitution - Missense 2:32464645-32464645 + TCGA-EI-6917-01 COSM3426399 c.7066A>G p.K2356E Substitution - Missense 2:32477581-32477581 + TCGA-AX-A05Z-01 COSM1020407 c.12493C>A p.L4165I Substitution - Missense 2:32543442-32543442 + BN19T COSM1614799 c.10374T>G p.S3458R Substitution - Missense 2:32512960-32512960 + TCGA-GD-A3OS-01 COSM1306732 c.2577C>G p.L859L Substitution - coding silent 2:32415868-32415868 + TCGA-AP-A056-01 COSM1020320 c.7405A>C p.T2469P Substitution - Missense 2:32479614-32479614 + TCGA-AA-3492-01 COSM1407773 c.609A>T p.T203T Substitution - coding silent 2:32380254-32380254 + PR-3036 COSM243208 c.3878G>T p.C1293F Substitution - Missense 2:32441396-32441396 + TCGA-E5-A2PC-01 COSM1306723 c.1149T>C p.D383D Substitution - coding silent 2:32401277-32401277 + U2940 COSM5620352 c.4255C>T p.P1419S Substitution - Missense 2:32443507-32443507 + TCGA-K4-A3WS-01 COSM3798971 c.11302C>G p.L3768V Substitution - Missense 2:32515723-32515723 + LUAD-F00162 COSM391675 c.6347delG p.V2117fs*19 Deletion - Frameshift 2:32469614-32469614 + TCGA-EB-A41A-01 COSM3581180 c.2223C>A p.D741E Substitution - Missense 2:32415514-32415514 + TCGA-AP-A0LM-01 COSM1020436 c.13616C>T p.T4539M Substitution - Missense 2:32597754-32597754 + WSU-HN12 COSM4591362 c.3994G>C p.V1332L Substitution - Missense LOVO COSM2942632 c.11041G>A p.D3681N Substitution - Missense 2:32515462-32515462 + TCGA-HW-8320-01 COSM3933636 c.13469C>T p.A4490V Substitution - Missense 2:32594028-32594028 + TCGA-A8-A081-01 COSM442833 c.14260-1G>T p.? Unknown 2:32611447-32611447 + PCSI_0098_Pa_P COSM216588 c.9915T>C p.G3305G Substitution - coding silent 2:32508194-32508194 + 1_PRE-TREATMENT COSM1718162 c.13084G>C p.E4362Q Substitution - Missense 2:32549421-32549421 + NCI-H1395 COSM13999 c.1111A>T p.T371S Substitution - Missense 2:32401239-32401239 + pfg076T COSM4765148 c.13502_13503insA p.L4504fs*3 Insertion - Frameshift 2:32595034-32595035 + ESCC_BICR_014T COSM5436223 c.3910C>G p.R1304G Substitution - Missense 2:32441428-32441428 + ESO-2143 COSM1246124 c.13931A>T p.N4644I Substitution - Missense 2:32599839-32599839 + BHY COSM4592547 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + TCGA-CH-5767-01 COSM1130795 c.13979A>C p.Y4660S Substitution - Missense 2:32599887-32599887 + ccRCC-56 COSM1659566 c.2170A>G p.K724E Substitution - Missense 2:32415461-32415461 + TCGA-37-3789-01 COSM721195 c.10430C>T p.P3477L Substitution - Missense 2:32513016-32513016 + TCGA-25-1324-01 COSM79339 c.5661G>A p.W1887* Substitution - Nonsense 2:32467992-32467992 + PD18730a COSM5787183 c.9700+3G>C p.? Unknown 2:32505208-32505208 + SCC-9 COSM4591362 c.3994G>C p.V1332L Substitution - Missense SCC-15 COSM4591362 c.3994G>C p.V1332L Substitution - Missense pfg103T COSM4752324 c.2091C>G p.N697K Substitution - Missense 2:32415382-32415382 + TCGA-16-0861-01 COSM3407834 c.13007G>A p.S4336N Substitution - Missense 2:32549344-32549344 + TCGA-66-2758-01 COSM721206 c.7193C>A p.S2398Y Substitution - Missense 2:32478759-32478759 + HX24T COSM3709622 c.5549C>A p.P1850H Substitution - Missense 2:32467717-32467717 + TCGA-60-2698-01 COSM721212 c.4606G>T p.D1536Y Substitution - Missense 2:32448916-32448916 + 587222 COSM1184733 c.4810G>T p.E1604* Substitution - Nonsense 2:32463250-32463250 + 1_PRE-TREATMENT COSM1718160 c.4931T>G p.L1644R Substitution - Missense 2:32463371-32463371 + pfg053T COSM4765141 c.7968_7968+1insGAAC p.L2657fs*17 Unknown 2:32487801-32487802 + PDA_063 COSM5001224 c.6979C>T p.R2327C Substitution - Missense 2:32477494-32477494 + MB_Exm23 COSM215876 c.2059T>A p.Y687N Substitution - Missense 2:32415350-32415350 + TCGA-AX-A0J0-01 COSM1020327 c.7680C>T p.S2560S Substitution - coding silent 2:32482566-32482566 + BRC15 COSM5025607 c.9208-1G>A p.? Unknown 2:32502794-32502794 + TCGA-CJ-4893-01 COSM3364726 c.5457T>G p.I1819M Substitution - Missense 2:32467625-32467625 + TCGA-EB-A3XC-01 COSM3581188 c.6542A>G p.Y2181C Substitution - Missense 2:32471074-32471074 + TCGA-AP-A0LG-01 COSM1020204 c.1413A>G p.G471G Substitution - coding silent 2:32401618-32401618 + C086 COSM1690427 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + TCGA-FP-A4BF-01 COSM4093891 c.7125G>A p.V2375V Substitution - coding silent 2:32478691-32478691 + 2521259 COSM5889653 c.6163C>T p.H2055Y Substitution - Missense 2:32469430-32469430 + RK119_C01 COSM3743776 c.1089A>G p.T363T Substitution - coding silent 2:32401217-32401217 + sysucc-773T COSM1483065 c.8020A>T p.T2674S Substitution - Missense 2:32488639-32488639 + C008 COSM5522190 c.6067T>C p.L2023L Substitution - coding silent 2:32468723-32468723 + TCGA-AX-A05Z-01 COSM1020251 c.3259G>A p.D1087N Substitution - Missense 2:32433654-32433654 + TCGA-AD-5900-01 COSM1407820 c.8658C>T p.S2886S Substitution - coding silent 2:32499736-32499736 + TCGA-AA-A00N-01 COSM274136 c.12277G>T p.E4093* Substitution - Nonsense 2:32531537-32531537 + TCGA-JW-A5VL-01 COSM4846931 c.524C>T p.S175L Substitution - Missense 2:32380169-32380169 + RK023_C01 COSM1631984 c.5101A>T p.T1701S Substitution - Missense 2:32464668-32464668 + sysucc-1135T COSM1020452 c.14194C>T p.R4732* Substitution - Nonsense 2:32607578-32607578 + TCGA-HU-A4GN-01 COSM4093885 c.5888C>T p.A1963V Substitution - Missense 2:32468544-32468544 + AOCS-086-3-2 COSM4141071 c.414G>A p.K138K Substitution - coding silent 2:32377676-32377676 + TCGA-B0-5081-01 COSM477347 c.11923C>T p.Q3975* Substitution - Nonsense 2:32529653-32529653 + WSU-HN6 COSM4602001 c.8164delG p.V2722fs*5 Deletion - Frameshift 2:32490109-32490109 + BN02 COSM1614792 c.6955C>T p.L2319F Substitution - Missense 2:32477470-32477470 + ccRCC-56 COSM1659567 c.2170A>G p.K724E Substitution - Missense 2:32415461-32415461 + PR-3127 COSM243204 c.2825C>T p.S942F Substitution - Missense 2:32416116-32416116 + SWE-19 COSM1179032 c.3551G>T p.G1184V Substitution - Missense 2:32436104-32436104 + TCGA-GN-A266-06 COSM3581205 c.9063A>T p.E3021D Substitution - Missense 2:32501744-32501744 + ZZUFHECRKL-G067T COSM5438715 c.7475T>C p.M2492T Substitution - Missense 2:32481386-32481386 + 39 COSM5733749 c.2994A>C p.L998F Substitution - Missense 2:32429267-32429267 + KM12 COSM2942734 c.13199G>C p.R4400P Substitution - Missense 2:32575210-32575210 + TCGA-D3-A51G-06 COSM3910259 c.13070C>T p.P4357L Substitution - Missense 2:32549407-32549407 + TCGA-AP-A059-01 COSM1020431 c.13589C>T p.A4530V Substitution - Missense 2:32595121-32595121 + TCGA-UB-A7MB-01 COSM4931233 c.11869A>C p.N3957H Substitution - Missense 2:32525577-32525577 + PT23_1 COSM5902535 c.11129C>T p.P3710L Substitution - Missense 2:32515550-32515550 + TCGA-B5-A1MY-01 COSM1020460 c.14290G>T p.V4764F Substitution - Missense 2:32611478-32611478 + TCGA-AP-A056-01 COSM1020378 c.10293G>A p.T3431T Substitution - coding silent 2:32510581-32510581 + TCGA-AP-A056-01 COSM1020384 c.11019T>C p.C3673C Substitution - coding silent 2:32515440-32515440 + TCGA-37-5819-01 COSM721180 c.11900T>C p.L3967P Substitution - Missense 2:32525608-32525608 + TCGA-34-5240-01 COSM721192 c.10494A>G p.A3498A Substitution - coding silent 2:32513080-32513080 + TCGA-AZ-4615-01 COSM2942750 c.13502delA p.K4503fs*11 Deletion - Frameshift 2:32595034-32595034 + AOCS-001-1-7 COSM4141074 c.13402G>C p.D4468H Substitution - Missense 2:32593961-32593961 + CSCC-47-T COSM4559363 c.8023G>A p.G2675R Substitution - Missense 2:32488642-32488642 + SCC-25 COSM4591363 c.3994G>C p.V1332L Substitution - Missense 39 COSM5733750 c.2994A>C p.L998F Substitution - Missense 2:32429267-32429267 + TCGA-AG-3906-01 COSM5070268 c.5424T>C p.T1808T Substitution - coding silent 2:32467592-32467592 + TCGA-DK-A1AC-01 COSM1306758 c.12614C>T p.S4205L Substitution - Missense 2:32545664-32545664 + PCSI_0098_Pa_P COSM216589 c.9915T>C p.G3305G Substitution - coding silent 2:32508194-32508194 + DLD1 COSM4624787 c.14528T>C p.V4843A Substitution - Missense 2:32617858-32617858 + TCGA-CH-5767-01 COSM1130797 c.13979A>C p.Y4660S Substitution - Missense 2:32599887-32599887 + TCGA-EI-6917-01 COSM1020246 c.3224G>A p.R1075Q Substitution - Missense 2:32431066-32431066 + LUAD-QY22Z COSM394761 c.2442G>T p.Q814H Substitution - Missense 2:32415733-32415733 + LUAD-B01970 COSM356083 c.7339G>A p.D2447N Substitution - Missense 2:32479548-32479548 + TCGA-AA-A010-01 COSM279170 c.13323G>T p.K4441N Substitution - Missense 2:32575334-32575334 + TCGA-G2-A2ES-01 COSM1306744 c.10416G>T p.M3472I Substitution - Missense 2:32513002-32513002 + HCC46T COSM3709618 c.1170C>T p.C390C Substitution - coding silent 2:32401298-32401298 + HCC160T COSM3709623 c.11755+3A>T p.? Unknown 2:32525022-32525022 + TCGA-BR-4362-01 COSM4093859 c.1301T>C p.V434A Substitution - Missense 2:32401506-32401506 + TCGA-BR-6565-01 COSM4093861 c.1721C>A p.T574K Substitution - Missense 2:32415012-32415012 + PD4120a COSM159376 c.11600C>T p.S3867L Substitution - Missense 2:32518923-32518923 + PT33 COSM5908065 c.1693C>T p.P565S Substitution - Missense 2:32414984-32414984 + sysucc-311T COSM1020313 c.6872G>A p.R2291H Substitution - Missense 2:32477387-32477387 + HCC25T COSM1614787 c.4541G>T p.G1514V Substitution - Missense 2:32448851-32448851 + 2275_T COSM3962795 c.12146G>T p.G4049V Substitution - Missense 2:32531406-32531406 + Pat_28_B COSM5862444 c.7316G>A p.G2439D Substitution - Missense 2:32479525-32479525 + 019T COSM1727923 c.3997A>C p.N1333H Substitution - Missense 2:32442117-32442117 + BRC51 COSM5025610 c.10439C>G p.S3480* Substitution - Nonsense 2:32513025-32513025 + TCGA-EK-A2RA-01 COSM159375 c.11600C>T p.S3867L Substitution - Missense 2:32518923-32518923 + U2940 COSM5620354 c.12694G>A p.V4232I Substitution - Missense 2:32545744-32545744 + TCGA-D1-A103-01 COSM1020360 c.9204A>G p.R3068R Substitution - coding silent 2:32501885-32501885 + HCC139T COSM1614797 c.9980+10G>T p.? Unknown 2:32508269-32508269 + TCGA-ER-A1A1-06 COSM3581225 c.13211C>T p.S4404F Substitution - Missense 2:32575222-32575222 + PD13162a COSM5795596 c.6977A>T p.E2326V Substitution - Missense 2:32477492-32477492 + CHC918T COSM3668663 c.6668T>C p.L2223P Substitution - Missense 2:32473187-32473187 + TCGA-AG-3902-01 COSM5069736 c.5908_5909insT p.S1972fs*18 Insertion - Frameshift 2:32468564-32468565 + CSCC-27-T COSM1020367 c.9850C>T p.R3284C Substitution - Missense 2:32508129-32508129 + TCGA-AG-A002-01 COSM259642 c.11698G>T p.E3900* Substitution - Nonsense 2:32524962-32524962 + TCGA-D3-A5GO-06 COSM3581216 c.12330G>A p.K4110K Substitution - coding silent 2:32543279-32543279 + C0075T COSM4164513 c.7270G>A p.V2424I Substitution - Missense 2:32479479-32479479 + Br27P COSM39874 c.2965G>A p.E989K Substitution - Missense 2:32429238-32429238 + TCGA-06-0142-01 COSM3407833 c.10918G>A p.A3640T Substitution - Missense 2:32515339-32515339 + TCGA-AX-A05Z-01 COSM1020216 c.1964A>C p.K655T Substitution - Missense 2:32415255-32415255 + EGC15 COSM5058876 c.1257+2T>C p.? Unknown 2:32401387-32401387 + UM-SCC-17B COSM4591363 c.3994G>C p.V1332L Substitution - Missense BCM723T COSM4956330 c.5990C>T p.A1997V Substitution - Missense 2:32468646-32468646 + SWE-16 COSM1178947 c.8238G>T p.E2746D Substitution - Missense 2:32491456-32491456 + TCGA-AA-3930-01 COSM296553 c.3318C>T p.F1106F Substitution - coding silent 2:32433713-32433713 + TCGA-34-5239-01 COSM721217 c.3752A>T p.H1251L Substitution - Missense 2:32439628-32439628 + TCGA-HU-8604-01 COSM4093894 c.7681G>A p.V2561I Substitution - Missense 2:32482567-32482567 + TCGA-HU-8604-01 COSM4093895 c.7681G>A p.V2561I Substitution - Missense 2:32482567-32482567 + T3094 COSM4665760 c.11643T>G p.A3881A Substitution - coding silent 2:32524907-32524907 + LIM2405 COSM4642666 c.8220T>C p.S2740S Substitution - coding silent 2:32491438-32491438 + 2493722 COSM5731612 c.9816C>T p.A3272A Substitution - coding silent 2:32508095-32508095 + C467 COSM4442110 c.7937T>C p.L2646P Substitution - Missense 2:32487770-32487770 + TCGA-D1-A0ZS-01 COSM1020279 c.4163T>G p.I1388S Substitution - Missense 2:32442380-32442380 + TCGA-AG-A002-01 COSM259644 c.12780A>G p.R4260R Substitution - coding silent 2:32545830-32545830 + 2492720 COSM1690427 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + 2492709 COSM2942294 c.3120G>A p.A1040A Substitution - coding silent 2:32430962-32430962 + 2492722 COSM5719569 c.12489A>C p.L4163F Substitution - Missense 2:32543438-32543438 + Ad1 COSM4440800 c.5152G>A p.V1718I Substitution - Missense 2:32464719-32464719 + LUAD-QY22Z COSM394758 c.1337G>C p.G446A Substitution - Missense 2:32401542-32401542 + TCGA-D1-A16D-01 COSM1020351 c.8838G>T p.V2946V Substitution - coding silent 2:32499916-32499916 + sysucc-311T COSM1020311 c.6872G>A p.R2291H Substitution - Missense 2:32477387-32477387 + ESO-0292 COSM1240893 c.4996G>A p.A1666T Substitution - Missense 2:32464563-32464563 + C0097T COSM4164512 c.3171G>T p.R1057S Substitution - Missense 2:32431013-32431013 + NCI-H2009 COSM14053 c.11049_11061del13 p.A3684fs*3 Deletion - Frameshift 2:32515470-32515482 + TCGA-A8-A07R-01 COSM3839423 c.2294C>A p.A765D Substitution - Missense 2:32415585-32415585 + TCGA-CG-5718-01 COSM4093896 c.8099C>G p.S2700* Substitution - Nonsense 2:32490044-32490044 + CSCC-27-T COSM1020369 c.9850C>T p.R3284C Substitution - Missense 2:32508129-32508129 + WSU-HN6 COSM4602002 c.8164delG p.V2722fs*5 Deletion - Frameshift 2:32490109-32490109 + YULOCUS COSM5396939 c.12244C>T p.L4082F Substitution - Missense 2:32531504-32531504 + CHC909T COSM5348152 c.2680delA p.T894fs*11 Deletion - Frameshift 2:32415971-32415971 + TCGA-HU-A4GU-01 COSM4093854 c.1110C>A p.V370V Substitution - coding silent 2:32401238-32401238 + TCGA-C5-A7CL-01 COSM4837866 c.2573C>T p.S858L Substitution - Missense 2:32415864-32415864 + BCN11 COSM4172302 c.2689A>T p.I897F Substitution - Missense 2:32415980-32415980 + 40M COSM5584553 c.6461C>T p.P2154L Substitution - Missense 2:32470281-32470281 + SCC-9 COSM4591363 c.3994G>C p.V1332L Substitution - Missense TCGA-BR-8680-01 COSM4093919 c.13541A>C p.K4514T Substitution - Missense 2:32595073-32595073 + CHOL40 COSM1744974 c.11822_11823GG>AC p.R3941N Substitution - Missense 2:32525530-32525531 + TCGA-18-3419-01 COSM721189 c.10900C>G p.L3634V Substitution - Missense 2:32515321-32515321 + LUAD-CHTN-Z4716A COSM391416 c.1235delG p.D413fs*6 Deletion - Frameshift 2:32401363-32401363 + TCGA-AA-3492-01 COSM1407768 c.599_600insA p.N202fs*5 Insertion - Frameshift 2:32380244-32380245 + TCGA-AZ-4315-01 COSM1407782 c.2103G>A p.P701P Substitution - coding silent 2:32415394-32415394 + 062T COSM1730129 c.4973C>G p.T1658R Substitution - Missense 2:32464540-32464540 + T84 COSM2942653 c.11509A>G p.I3837V Substitution - Missense 2:32518832-32518832 + TCGA-06-0749-01 COSM3407828 c.6468T>A p.H2156Q Substitution - Missense 2:32470288-32470288 + RK169_C01 COSM3702181 c.1656A>G p.T552T Substitution - coding silent 2:32414947-32414947 + TCGA-D9-A6EC-06 COSM4404174 c.7886T>G p.L2629R Substitution - Missense 2:32487719-32487719 + 46M COSM5587293 c.7663G>A p.G2555R Substitution - Missense 2:32482549-32482549 + UM-SCC-4 COSM4591363 c.3994G>C p.V1332L Substitution - Missense CSCC-27-T COSM4497827 c.5061C>T p.F1687F Substitution - coding silent 2:32464628-32464628 + C0058T COSM4164509 c.2603A>G p.D868G Substitution - Missense 2:32415894-32415894 + TCGA-B5-A11O-01 COSM1020228 c.2353G>T p.E785* Substitution - Nonsense 2:32415644-32415644 + TCGA-AP-A059-01 COSM1020222 c.2187G>T p.E729D Substitution - Missense 2:32415478-32415478 + PD4203a COSM159382 c.2722C>G p.Q908E Substitution - Missense 2:32416013-32416013 + TCGA-B5-A0K2-01 COSM1020299 c.5857G>A p.A1953T Substitution - Missense 2:32468513-32468513 + I2L-P10-Tumor-Organoid COSM5354030 c.6191A>T p.K2064I Substitution - Missense 2:32469458-32469458 + YUGOE COSM1690427 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + TCGA-AP-A0LM-01 COSM1020439 c.13729C>T p.R4577C Substitution - Missense 2:32597867-32597867 + TCGA-DK-A2I4-01 COSM3798966 c.2160G>A p.L720L Substitution - coding silent 2:32415451-32415451 + SJHYPO020 COSM4775508 c.6713A>G p.H2238R Substitution - Missense 2:32473232-32473232 + Pat_44_B COSM5862450 c.12145G>A p.G4049S Substitution - Missense 2:32531405-32531405 + PD22360a COSM5784263 c.6868A>G p.I2290V Substitution - Missense 2:32477383-32477383 + 457 COSM4436195 c.13771C>T p.L4591L Substitution - coding silent 2:32597909-32597909 + sysucc-773T COSM148833 c.8020A>T p.T2674S Substitution - Missense 2:32488639-32488639 + TCGA-EI-6917-01 COSM3426403 c.9797A>C p.K3266T Substitution - Missense 2:32508076-32508076 + TCGA-CG-4305-01 COSM2942461 c.7094C>T p.T2365M Substitution - Missense 2:32478660-32478660 + BN01T COSM1614788 c.4835C>A p.A1612E Substitution - Missense 2:32463275-32463275 + TCGA-CJ-5681-01 COSM477350 c.14196A>G p.R4732R Substitution - coding silent 2:32607580-32607580 + TCGA-BS-A0UF-01 COSM1020372 c.10258T>G p.F3420V Substitution - Missense 2:32510546-32510546 + TCGA-66-2754-01 COSM721210 c.5473G>C p.E1825Q Substitution - Missense 2:32467641-32467641 + 587376 COSM1184739 c.6028A>T p.N2010Y Substitution - Missense 2:32468684-32468684 + RK228_C01 COSM4944800 c.3632-1G>C p.? Unknown 2:32439507-32439507 + LUAD-QY22Z COSM394759 c.1337G>C p.G446A Substitution - Missense 2:32401542-32401542 + NOKSI COSM4595658 c.3116C>T p.S1039L Substitution - Missense 2:32430958-32430958 + S15_post COSM5574434 c.7960C>G p.H2654D Substitution - Missense 2:32487793-32487793 + TCGA-B5-A11E-01 COSM721202 c.8928G>A p.S2976S Substitution - coding silent 2:32500006-32500006 + 875-01-3TD COSM2942208 c.1542A>G p.Q514Q Substitution - coding silent 2:32414833-32414833 + TCGA-CG-5728-01 COSM4093916 c.13260T>C p.G4420G Substitution - coding silent 2:32575271-32575271 + PT53 COSM5941179 c.2243G>A p.G748E Substitution - Missense 2:32415534-32415534 + 2521244 COSM5887204 c.1744C>T p.P582S Substitution - Missense 2:32415035-32415035 + TCGA-AX-A06H-01 COSM1020286 c.5283T>C p.L1761L Substitution - coding silent 2:32465091-32465091 + T578 COSM4665739 c.1505A>G p.E502G Substitution - Missense 2:32414796-32414796 + BCN23 COSM4172309 c.12793A>G p.S4265G Substitution - Missense 2:32545843-32545843 + TCGA-EE-A2A2-06 COSM3581196 c.8106T>C p.T2702T Substitution - coding silent 2:32490051-32490051 + TCGA-CG-4306-01 COSM1020443 c.13960C>T p.R4654* Substitution - Nonsense 2:32599868-32599868 + TCGA-FW-A3R5-06 COSM3910252 c.7901C>T p.S2634L Substitution - Missense 2:32487734-32487734 + TCGA-AO-A0J5-01 COSM442823 c.7036T>A p.C2346S Substitution - Missense 2:32477551-32477551 + LUAD-NYU284 COSM372970 c.12343G>A p.D4115N Substitution - Missense 2:32543292-32543292 + TCGA-AX-A0J0-01 COSM1020210 c.1859C>T p.S620F Substitution - Missense 2:32415150-32415150 + BD40T COSM5509171 c.3451G>T p.V1151F Substitution - Missense 2:32435537-32435537 + PT37 COSM5917537 c.1825G>T p.D609Y Substitution - Missense 2:32415116-32415116 + sysucc-783T COSM5484547 c.12706C>T p.R4236W Substitution - Missense 2:32545756-32545756 + CHC892T COSM4795047 c.2413G>A p.A805T Substitution - Missense 2:32415704-32415704 + 10-P8045 COSM2942208 c.1542A>G p.Q514Q Substitution - coding silent 2:32414833-32414833 + SNUH_G16_S1 COSM4001646 c.6407A>G p.E2136G Substitution - Missense 2:32470227-32470227 + YULAN COSM1690435 c.9143C>T p.S3048F Substitution - Missense 2:32501824-32501824 + TCGA-AP-A051-01 COSM1020451 c.14166G>T p.Q4722H Substitution - Missense 2:32607550-32607550 + VCB-PH-05T COSM4770664 c.3931A>G p.I1311V Substitution - Missense 2:32441449-32441449 + TCGA-B5-A0JY-01 COSM1020246 c.3224G>A p.R1075Q Substitution - Missense 2:32431066-32431066 + 587376 COSM1184742 c.11590A>G p.T3864A Substitution - Missense 2:32518913-32518913 + LUAD-CHTN-Z4716A COSM391415 c.1235delG p.D413fs*6 Deletion - Frameshift 2:32401363-32401363 + LUAD-YINHD COSM350631 c.4424C>G p.T1475S Substitution - Missense 2:32445608-32445608 + TCGA-60-2723-01 COSM721215 c.4047G>C p.Q1349H Substitution - Missense 2:32442167-32442167 + TCGA-G4-6304-01 COSM1407767 c.542T>C p.V181A Substitution - Missense 2:32380187-32380187 + TCGA-AA-3492-01 COSM1407771 c.607A>C p.T203P Substitution - Missense 2:32380252-32380252 + TCGA-FP-A4BE-01 COSM4093865 c.2802T>C p.T934T Substitution - coding silent 2:32416093-32416093 + TCGA-C5-A7CL-01 COSM4837867 c.2573C>T p.S858L Substitution - Missense 2:32415864-32415864 + 2250172 COSM5030152 c.13400C>T p.S4467F Substitution - Missense 2:32593959-32593959 + DN110CD COSM5795596 c.6977A>T p.E2326V Substitution - Missense 2:32477492-32477492 + UD-SCC-2 COSM4591363 c.3994G>C p.V1332L Substitution - Missense TCGA-A8-A0A6-01 COSM3839425 c.4802C>T p.T1601I Substitution - Missense 2:32463242-32463242 + C0091T COSM4164515 c.12494T>C p.L4165P Substitution - Missense 2:32543443-32543443 + TCGA-CM-5861-01 COSM1407831 c.10725T>C p.H3575H Substitution - coding silent 2:32515146-32515146 + pfg106T COSM4765146 c.12108_12109insA p.L4037fs*3 Insertion - Frameshift 2:32531368-32531369 + TCGA-BT-A3PJ-01 COSM1020452 c.14194C>T p.R4732* Substitution - Nonsense 2:32607578-32607578 + TCGA-DK-A1A3-01 COSM419187 c.10795G>A p.A3599T Substitution - Missense 2:32515216-32515216 + PD4202a COSM159380 c.4169G>A p.R1390H Substitution - Missense 2:32442386-32442386 + TCGA-EP-A2KA-01 COSM4917248 c.4654G>T p.G1552C Substitution - Missense 2:32453843-32453843 + H1155 COSM1195528 c.2518G>A p.E840K Substitution - Missense 2:32415809-32415809 + TCGA-EE-A3JE-06 COSM3910255 c.11157G>T p.L3719F Substitution - Missense 2:32515578-32515578 + 449 COSM4435502 c.7974G>A p.E2658E Substitution - coding silent 2:32488593-32488593 + LUAD-S01467 COSM399463 c.11002C>G p.H3668D Substitution - Missense 2:32515423-32515423 + TCGA-13-0883-01 COSM69821 c.905G>C p.R302T Substitution - Missense 2:32392104-32392104 + TCGA-09-1670-01 COSM1327098 c.1973A>T p.H658L Substitution - Missense 2:32415264-32415264 + TCGA-B6-A0IJ-01 COSM442822 c.2286A>G p.Q762Q Substitution - coding silent 2:32415577-32415577 + TCGA-EI-6884-01 COSM5079628 c.4205A>G p.H1402R Substitution - Missense 2:32442422-32442422 + TCGA-G4-6586-01 COSM1407834 c.11086A>G p.S3696G Substitution - Missense 2:32515507-32515507 + LUAD-YINHD COSM350634 c.10015A>T p.T3339S Substitution - Missense 2:32509772-32509772 + C135 COSM4618231 c.10119G>A p.M3373I Substitution - Missense 2:32509876-32509876 + TCGA-HC-7210-01 COSM4391750 c.7825C>A p.P2609T Substitution - Missense 2:32487658-32487658 + TCGA-B5-A0JY-01 COSM1020317 c.7399G>T p.D2467Y Substitution - Missense 2:32479608-32479608 + TCGA-D1-A103-01 COSM1020418 c.12718G>T p.E4240* Substitution - Nonsense 2:32545768-32545768 + TCGA-BG-A0M3-01 COSM1020296 c.5588G>A p.R1863H Substitution - Missense 2:32467919-32467919 + TCGA-CA-6718-01 COSM1407849 c.13189G>A p.E4397K Substitution - Missense 2:32575200-32575200 + 2367454 COSM5004078 c.11470A>G p.M3824V Substitution - Missense 2:32518374-32518374 + TCGA-AC-A23H-01 COSM3839439 c.13264G>A p.E4422K Substitution - Missense 2:32575275-32575275 + CHC1744T COSM4792299 c.12573G>A p.V4191V Substitution - coding silent 2:32543522-32543522 + TCGA-24-2030-01 COSM69823 c.12758C>T p.A4253V Substitution - Missense 2:32545808-32545808 + LUAD-RT-S01711 COSM380154 c.8705G>T p.R2902L Substitution - Missense 2:32499783-32499783 + 49M COSM5589819 c.10733C>T p.S3578F Substitution - Missense 2:32515154-32515154 + BD190T COSM5517750 c.13356-2A>G p.? Unknown 2:32593913-32593913 + TCGA-AX-A05Z-01 COSM1020381 c.10294A>C p.I3432L Substitution - Missense 2:32510582-32510582 + CSCC-20-T COSM4505262 c.6884C>T p.T2295I Substitution - Missense 2:32477399-32477399 + YULOCUS COSM5396933 c.5261C>T p.P1754L Substitution - Missense 2:32465069-32465069 + GHE0609 COSM5714180 c.9980+2T>A p.? Unknown 2:32508261-32508261 + HCC055T COSM5823903 c.11924A>T p.Q3975L Substitution - Missense 2:32529654-32529654 + YUWALI COSM1690430 c.7627C>T p.P2543S Substitution - Missense 2:32482513-32482513 + Pat_36_B COSM5862452 c.13027C>T p.Q4343* Substitution - Nonsense 2:32549364-32549364 + TCGA-BH-A18V-06 COSM3839432 c.10527A>G p.V3509V Substitution - coding silent 2:32513113-32513113 + TCGA-AN-A0XW-01 COSM442835 c.14309G>A p.C4770Y Substitution - Missense 2:32611497-32611497 + TCGA-AA-A010-01 COSM279166 c.7789G>A p.A2597T Substitution - Missense 2:32485735-32485735 + TCGA-D3-A51G-06 COSM3910258 c.13070C>T p.P4357L Substitution - Missense 2:32549407-32549407 + WSU-HN13 COSM4591362 c.3994G>C p.V1332L Substitution - Missense CSCC-10-T COSM4498497 c.5210C>T p.A1737V Substitution - Missense 2:32464777-32464777 + Gp5D COSM2942499 c.8392G>A p.V2798M Substitution - Missense 2:32493591-32493591 + TCGA-37-3789-01 COSM721190 c.10861G>C p.E3621Q Substitution - Missense 2:32515282-32515282 + 587344 COSM1184730 c.1121C>G p.T374R Substitution - Missense 2:32401249-32401249 + TCGA-AG-A002-01 COSM259640 c.9063A>C p.E3021D Substitution - Missense 2:32501744-32501744 + C0099T COSM4422522 c.2131C>T p.P711S Substitution - Missense 2:32415422-32415422 + PD4937a COSM159386 c.2446G>C p.E816Q Substitution - Missense 2:32415737-32415737 + TCGA-AM-5821-01 COSM148835 c.13752G>A p.T4584T Substitution - coding silent 2:32597890-32597890 + BN41 COSM1614785 c.729T>G p.N243K Substitution - Missense 2:32388833-32388833 + GB19 COSM1742853 c.8150G>A p.R2717Q Substitution - Missense 2:32490095-32490095 + 88 COSM5014216 c.9621G>A p.W3207* Substitution - Nonsense 2:32505126-32505126 + QC2-34-T2 COSM5655036 c.7674_7677delAGTT p.V2559fs*12 Deletion - Frameshift 2:32482560-32482563 + Pat_41_B COSM5862445 c.8141C>T p.T2714I Substitution - Missense 2:32490086-32490086 + TCGA-FS-A1ZQ-06 COSM3581202 c.8619C>T p.C2873C Substitution - coding silent 2:32499697-32499697 + TCGA-AP-A05A-01 COSM1020364 c.9772G>T p.V3258F Substitution - Missense 2:32508051-32508051 + TCGA-AG-3906-01 COSM5070269 c.5424T>C p.T1808T Substitution - coding silent 2:32467592-32467592 + TCGA-BL-A13I-01 COSM419192 c.6321A>G p.E2107E Substitution - coding silent 2:32469588-32469588 + TCGA-D1-A160-01 COSM1020375 c.10258T>C p.F3420L Substitution - Missense 2:32510546-32510546 + WSU-HN30 COSM4591362 c.3994G>C p.V1332L Substitution - Missense CCK81 COSM2942767 c.13669T>C p.Y4557H Substitution - Missense 2:32597807-32597807 + LUAD-S01302 COSM395974 c.8580A>G p.I2860M Substitution - Missense 2:32499658-32499658 + TCGA-A7-A13F-01 COSM442830 c.13787G>T p.S4596I Substitution - Missense 2:32597925-32597925 + HCC46 COSM3709618 c.1170C>T p.C390C Substitution - coding silent 2:32401298-32401298 + SNU-C4 COSM4653551 c.6703C>A p.L2235I Substitution - Missense 2:32473222-32473222 + SC_9008 COSM5559989 c.2247G>A p.L749L Substitution - coding silent 2:32415538-32415538 + TCGA-18-3406-01 COSM721205 c.7831G>T p.G2611* Substitution - Nonsense 2:32487664-32487664 + SNUH_G16_S1 COSM4001648 c.13344C>A p.T4448T Substitution - coding silent 2:32575355-32575355 + HCC127T COSM5822802 c.1091A>T p.Q364L Substitution - Missense 2:32401219-32401219 + TCGA-BR-8680-01 COSM4093910 c.12013A>C p.T4005P Substitution - Missense 2:32529743-32529743 + TCGA-BS-A0UJ-01 COSM1020308 c.6515T>C p.V2172A Substitution - Missense 2:32471047-32471047 + TCGA-AP-A0LM-01 COSM1020269 c.4036G>T p.E1346* Substitution - Nonsense 2:32442156-32442156 + TCGA-B5-A0JY-01 COSM1020248 c.3224G>A p.R1075Q Substitution - Missense 2:32431066-32431066 + TCGA-BS-A0UA-01 COSM1020194 c.811G>A p.G271R Substitution - Missense 2:32388915-32388915 + TCGA-AF-2693-01 COSM1565588 c.2892C>T p.L964L Substitution - coding silent 2:32429165-32429165 + HCC49 COSM1614790 c.5595G>T p.G1865G Substitution - coding silent 2:32467926-32467926 + GCT27 COSM5749315 c.2161A>G p.R721G Substitution - Missense 2:32415452-32415452 + 2492710 COSM2942293 c.3120G>A p.A1040A Substitution - coding silent 2:32430962-32430962 + PDA_032 COSM4999659 c.2326C>A p.L776I Substitution - Missense 2:32415617-32415617 + HT115 COSM2942323 c.3671T>C p.V1224A Substitution - Missense 2:32439547-32439547 + TCGA-CA-6717-01 COSM1407812 c.6592+2T>G p.? Unknown 2:32471126-32471126 + LP6007401-DNA_A01 COSM5036128 c.2674G>T p.E892* Substitution - Nonsense 2:32415965-32415965 + TCGA-CZ-5451-01 COSM477342 c.5953A>T p.N1985Y Substitution - Missense 2:32468609-32468609 + YUKRIN COSM1690442 c.14046T>G p.N4682K Substitution - Missense 2:32603059-32603059 + TCGA-43-6771-01 COSM721184 c.11821A>T p.R3941W Substitution - Missense 2:32525529-32525529 + TCGA-EI-6917-01 COSM2942632 c.11041G>A p.D3681N Substitution - Missense 2:32515462-32515462 + S02209 COSM5675302 c.7880G>T p.S2627I Substitution - Missense 2:32487713-32487713 + TCGA-G2-A2ES-01 COSM1306759 c.14138G>T p.R4713L Substitution - Missense 2:32607522-32607522 + ESO-0292 COSM1240894 c.4996G>A p.A1666T Substitution - Missense 2:32464563-32464563 + 8013912 COSM3391709 c.3580C>A p.L1194I Substitution - Missense 2:32436133-32436133 + TCGA-BR-6565-01 COSM4093860 c.1721C>A p.T574K Substitution - Missense 2:32415012-32415012 + Pat_65_A COSM5862442 c.7079G>A p.R2360H Substitution - Missense 2:32478645-32478645 + C91 COSM4444782 c.14138G>A p.R4713Q Substitution - Missense 2:32607522-32607522 + PCSI_0083_Pa_X COSM3380143 c.12778C>T p.R4260* Substitution - Nonsense 2:32545828-32545828 + HCC13T COSM3746542 c.3656C>T p.S1219L Substitution - Missense 2:32439532-32439532 + TCGA-AP-A051-01 COSM1020264 c.3871C>T p.R1291W Substitution - Missense 2:32441389-32441389 + 2492720 COSM5719569 c.12489A>C p.L4163F Substitution - Missense 2:32543438-32543438 + TCGA-AG-3892-01 COSM256399 c.9967G>A p.V3323I Substitution - Missense 2:32508246-32508246 + TCGA-BS-A0TG-01 COSM1020305 c.6349G>T p.V2117F Substitution - Missense 2:32470169-32470169 + TCGA-GD-A3OP-01 COSM1306736 c.4394G>A p.G1465E Substitution - Missense 2:32445578-32445578 + CLL132 COSM1291498 c.6496delC p.M2167fs*1 Deletion - Frameshift 2:32471028-32471028 + TCGA-D8-A1JL-01 COSM1483066 c.11594C>T p.T3865I Substitution - Missense 2:32518917-32518917 + ESCC_25 COSM5626767 c.13602A>G p.K4534K Substitution - coding silent 2:32595134-32595134 + TCGA-H4-A2HQ-01 COSM1306754 c.11575C>T p.H3859Y Substitution - Missense 2:32518898-32518898 + TCGA-BT-A20N-01 COSM419189 c.8267C>G p.P2756R Substitution - Missense 2:32491485-32491485 + TCGA-34-5240-01 COSM721193 c.10494A>G p.A3498A Substitution - coding silent 2:32513080-32513080 + TCGA-H4-A2HQ-01 COSM1306756 c.11608C>G p.L3870V Substitution - Missense 2:32518931-32518931 + TCGA-06-0749-01 COSM3407829 c.6468T>A p.H2156Q Substitution - Missense 2:32470288-32470288 + TCGA-BR-8487-01 COSM4093893 c.7318G>A p.A2440T Substitution - Missense 2:32479527-32479527 + UM-SCC-47 COSM4591363 c.3994G>C p.V1332L Substitution - Missense CHC1595T COSM4801765 c.1039G>C p.E347Q Substitution - Missense 2:32401167-32401167 + TCGA-F5-6814-01 COSM2942582 c.9817G>A p.E3273K Substitution - Missense 2:32508096-32508096 + BCN34 COSM4172305 c.5029C>T p.P1677S Substitution - Missense 2:32464596-32464596 + AOCS-001-1-7 COSM4141073 c.13402G>C p.D4468H Substitution - Missense 2:32593961-32593961 + C0058T COSM4164510 c.2603A>G p.D868G Substitution - Missense 2:32415894-32415894 + PD3989a COSM159373 c.1398A>G p.I466M Substitution - Missense 2:32401603-32401603 + TCGA-CA-6718-01 COSM1407842 c.12068C>A p.S4023Y Substitution - Missense 2:32529798-32529798 + BN41T COSM1614785 c.729T>G p.N243K Substitution - Missense 2:32388833-32388833 + B22-Tumor COSM3933633 c.7438G>C p.D2480H Substitution - Missense 2:32481349-32481349 + SWE-20 COSM1179066 c.6663T>C p.S2221S Substitution - coding silent 2:32473182-32473182 + BCM791T COSM4803025 c.7002A>C p.K2334N Substitution - Missense 2:32477517-32477517 + MD-146 COSM301767 c.2624A>G p.E875G Substitution - Missense 2:32415915-32415915 + TCGA-AG-3892-01 COSM256401 c.13486C>T p.R4496W Substitution - Missense 2:32594045-32594045 + CHC1600T COSM4791531 c.13318A>G p.M4440V Substitution - Missense 2:32575329-32575329 + S48_pre COSM5574436 c.4864_4865delCA p.H1622fs*70 Deletion - Frameshift 2:32463304-32463305 + CHC909T COSM5348153 c.2680delA p.T894fs*11 Deletion - Frameshift 2:32415971-32415971 + HCC055T COSM5823902 c.11924A>T p.Q3975L Substitution - Missense 2:32529654-32529654 + TCGA-DB-A64O-01 COSM3972227 c.8590A>T p.T2864S Substitution - Missense 2:32499668-32499668 + TCGA-BR-4184-01 COSM1020397 c.11801G>A p.R3934H Substitution - Missense 2:32525509-32525509 + TCGA-43-6770-01 COSM721208 c.7156C>G p.L2386V Substitution - Missense 2:32478722-32478722 + TCGA-D5-6928-01 COSM1407857 c.13851G>T p.A4617A Substitution - coding silent 2:32599759-32599759 + HT115 COSM2942324 c.3671T>C p.V1224A Substitution - Missense 2:32439547-32439547 + Detroit_562 COSM4591363 c.3994G>C p.V1332L Substitution - Missense SNUH_G16_S1 COSM4001647 c.6407A>G p.E2136G Substitution - Missense 2:32470227-32470227 + UPCI:SCC090 COSM4592547 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + TCGA-G3-A25V-01 COSM4914546 c.1412G>A p.G471E Substitution - Missense 2:32401617-32401617 + TCGA-AR-A256-01 COSM1483061 c.2971T>C p.S991P Substitution - Missense 2:32429244-32429244 + PD24195a COSM5795123 c.10737G>T p.M3579I Substitution - Missense 2:32515158-32515158 + TCGA-BR-8680-01 COSM4093863 c.2264A>C p.E755A Substitution - Missense 2:32415555-32415555 + CHC892T COSM4795048 c.2413G>A p.A805T Substitution - Missense 2:32415704-32415704 + TCGA-EI-6917-01 COSM3426397 c.6579G>T p.K2193N Substitution - Missense 2:32471111-32471111 + 108 COSM5016776 c.12592+2T>G p.? Unknown 2:32543543-32543543 + TCGA-A6-6781-01 COSM1407814 c.6899G>A p.R2300H Substitution - Missense 2:32477414-32477414 + TCGA-EB-A3XC-01 COSM3581189 c.6542A>G p.Y2181C Substitution - Missense 2:32471074-32471074 + 2250161 COSM5029766 c.10346+4C>T p.? Unknown 2:32510638-32510638 + TCGA-AP-A056-01 COSM1020341 c.8550C>T p.V2850V Substitution - coding silent 2:32499628-32499628 + TCGA-CK-5916-01 COSM1407818 c.7588A>T p.T2530S Substitution - Missense 2:32482474-32482474 + MPCC_0032_Pa_C COSM3380145 c.13707G>A p.A4569A Substitution - coding silent 2:32597845-32597845 + 044 COSM145137 c.11060T>G p.L3687R Substitution - Missense 2:32515481-32515481 + BD49T COSM1020329 c.7680C>T p.S2560S Substitution - coding silent 2:32482566-32482566 + TCGA-CI-6623-01 COSM5076206 c.4164C>T p.I1388I Substitution - coding silent 2:32442381-32442381 + TCGA-21-5787-01 COSM721162 c.13605A>G p.L4535L Substitution - coding silent 2:32595137-32595137 + TCGA-33-4538-01 COSM721172 c.12970C>T p.L4324L Substitution - coding silent 2:32548009-32548009 + TCGA-K4-A3WS-01 COSM3798972 c.11302C>G p.L3768V Substitution - Missense 2:32515723-32515723 + TCGA-DD-A1EC-01 COSM4938168 c.5567T>C p.M1856T Substitution - Missense 2:32467735-32467735 + C135 COSM4618232 c.10119G>A p.M3373I Substitution - Missense 2:32509876-32509876 + TCGA-EB-A41A-01 COSM3581168 c.352C>T p.Q118* Substitution - Nonsense 2:32377614-32377614 + TCGA-B5-A1MY-01 COSM1020458 c.14290G>T p.V4764F Substitution - Missense 2:32611478-32611478 + TCGA-AP-A051-01 COSM1020266 c.3871C>T p.R1291W Substitution - Missense 2:32441389-32441389 + 2497766 COSM5750264 c.425G>T p.G142V Substitution - Missense 2:32377687-32377687 + TCGA-CC-A3MC-01 COSM4919534 c.1648G>T p.E550* Substitution - Nonsense 2:32414939-32414939 + U343 COSM5712083 c.6550A>G p.T2184A Substitution - Missense 2:32471082-32471082 + HCC2998 COSM2942355 c.4193G>A p.R1398Q Substitution - Missense 2:32442410-32442410 + TCGA-AA-A00N-01 COSM298592 c.509C>G p.A170G Substitution - Missense 2:32380154-32380154 + TCGA-CA-6717-01 COSM1407817 c.7167A>G p.G2389G Substitution - coding silent 2:32478733-32478733 + TCGA-AP-A059-01 COSM1020304 c.6074C>A p.T2025N Substitution - Missense 2:32468730-32468730 + LS411 COSM2942619 c.10657C>A p.H3553N Substitution - Missense 2:32515078-32515078 + TCGA-BT-A20N-01 COSM419190 c.8267C>G p.P2756R Substitution - Missense 2:32491485-32491485 + TCGA-CZ-5465-01 COSM477324 c.523T>C p.S175P Substitution - Missense 2:32380168-32380168 + PR-3036 COSM243207 c.3878G>T p.C1293F Substitution - Missense 2:32441396-32441396 + TCGA-AA-3672-01 COSM266097 c.10706C>A p.P3569H Substitution - Missense 2:32515127-32515127 + TCGA-CA-6717-01 COSM1407813 c.6592+2T>G p.? Unknown 2:32471126-32471126 + 1_RESISTANT COSM1718162 c.13084G>C p.E4362Q Substitution - Missense 2:32549421-32549421 + TCGA-EB-A3Y7-01 COSM3581186 c.5184C>T p.F1728F Substitution - coding silent 2:32464751-32464751 + TCGA-BR-6452-01 COSM4093915 c.13151A>G p.D4384G Substitution - Missense 2:32575162-32575162 + YULOCUS COSM5396934 c.5261C>T p.P1754L Substitution - Missense 2:32465069-32465069 + ESCC_40 COSM5629371 c.3308A>T p.H1103L Substitution - Missense 2:32433703-32433703 + UM-SCC-11B COSM4591363 c.3994G>C p.V1332L Substitution - Missense TCGA-EI-6917-01 COSM2942633 c.11041G>A p.D3681N Substitution - Missense 2:32515462-32515462 + T3557 COSM4665748 c.7749G>A p.L2583L Substitution - coding silent 2:32485695-32485695 + TCGA-BR-8680-01 COSM4093911 c.12013A>C p.T4005P Substitution - Missense 2:32529743-32529743 + TCGA-EE-A182-06 COSM3581228 c.14153C>T p.P4718L Substitution - Missense 2:32607537-32607537 + 2113171 COSM4167309 c.61A>C p.I21L Substitution - Missense 2:32357222-32357222 + TCGA-B5-A0K9-01 COSM1020448 c.14087A>G p.Q4696R Substitution - Missense 2:32607471-32607471 + ZZUFHECRKL-G003T COSM5430937 c.12168A>G p.I4056M Substitution - Missense 2:32531428-32531428 + ESO-1670 COSM1246121 c.14354G>A p.R4785Q Substitution - Missense 2:32611542-32611542 + 2492721 COSM1690427 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + TCGA-AX-A0J0-01 COSM1020427 c.13198C>T p.R4400W Substitution - Missense 2:32575209-32575209 + EGC15 COSM5058877 c.1257+2T>C p.? Unknown 2:32401387-32401387 + TCGA-F5-6814-01 COSM1020242 c.2658G>T p.K886N Substitution - Missense 2:32415949-32415949 + TCGA-EB-A44O-01 COSM3581219 c.12863A>T p.Y4288F Substitution - Missense 2:32547902-32547902 + BCN34 COSM4172304 c.5029C>T p.P1677S Substitution - Missense 2:32464596-32464596 + CSCC-35-T COSM4514338 c.9719C>T p.S3240F Substitution - Missense 2:32507998-32507998 + BICR_22 COSM2942230 c.1859C>G p.S620C Substitution - Missense 2:32415150-32415150 + PT36 COSM5914878 c.5593G>A p.G1865R Substitution - Missense 2:32467924-32467924 + BICR_22 COSM4591362 c.3994G>C p.V1332L Substitution - Missense TCGA-CA-6718-01 COSM1407784 c.2170A>C p.K724Q Substitution - Missense 2:32415461-32415461 + LP6005500-DNA_D01 COSM5036180 c.4531G>A p.E1511K Substitution - Missense 2:32448841-32448841 + 2492720 COSM5719570 c.12489A>C p.L4163F Substitution - Missense 2:32543438-32543438 + 2492721 COSM5719569 c.12489A>C p.L4163F Substitution - Missense 2:32543438-32543438 + TCGA-DK-A1A3-01 COSM419188 c.10795G>A p.A3599T Substitution - Missense 2:32515216-32515216 + TCGA-AZ-4315-01 COSM1407783 c.2103G>A p.P701P Substitution - coding silent 2:32415394-32415394 + CHC2362T COSM5348585 c.3470_3471insT p.M1157fs*13 Insertion - Frameshift 2:32435556-32435557 + CAL27 COSM4591363 c.3994G>C p.V1332L Substitution - Missense TCGA-D1-A17D-01 COSM1020254 c.3309T>C p.H1103H Substitution - coding silent 2:32433704-32433704 + Pat_59_B COSM5862447 c.8920C>T p.Q2974* Substitution - Nonsense 2:32499998-32499998 + ESCC_156 COSM5646023 c.884C>G p.S295* Substitution - Nonsense 2:32392083-32392083 + NOKSI COSM4595659 c.3116C>T p.S1039L Substitution - Missense 2:32430958-32430958 + 53M COSM5594266 c.7431G>A p.L2477L Substitution - coding silent 2:32481342-32481342 + PD23550a COSM5784370 c.5873G>A p.R1958Q Substitution - Missense 2:32468529-32468529 + BCN34 COSM1614788 c.4835C>A p.A1612E Substitution - Missense 2:32463275-32463275 + TCGA-DK-A1A7-01 COSM419193 c.4499G>A p.S1500N Substitution - Missense 2:32448809-32448809 + GC8_T COSM148834 c.13752G>A p.T4584T Substitution - coding silent 2:32597890-32597890 + TCGA-B0-5110-01 COSM477325 c.1445G>A p.S482N Substitution - Missense 2:32406525-32406525 + TCGA-AX-A0J0-01 COSM1020401 c.12286C>A p.Q4096K Substitution - Missense 2:32531546-32531546 + PT36 COSM5914877 c.5594G>A p.G1865E Substitution - Missense 2:32467925-32467925 + C0099T COSM4422521 c.2131C>T p.P711S Substitution - Missense 2:32415422-32415422 + 19M COSM5578121 c.8903G>A p.G2968E Substitution - Missense 2:32499981-32499981 + TCGA-06-0142-01 COSM3407832 c.10918G>A p.A3640T Substitution - Missense 2:32515339-32515339 + ESCC_BICR_014T COSM5436224 c.3910C>G p.R1304G Substitution - Missense 2:32441428-32441428 + TCGA-AG-3892-01 COSM256402 c.13486C>T p.R4496W Substitution - Missense 2:32594045-32594045 + PCSI_0098_Pa_P_526 COSM216589 c.9915T>C p.G3305G Substitution - coding silent 2:32508194-32508194 + sysucc-311T COSM5465544 c.8371G>T p.E2791* Substitution - Nonsense 2:32493570-32493570 + OSCC-GB_00530111 COSM4883494 c.5748G>C p.M1916I Substitution - Missense 2:32468079-32468079 + BK0030 COSM4186814 c.2068C>T p.Q690* Substitution - Nonsense 2:32415359-32415359 + YUGATOR COSM5396927 c.828T>C p.R276R Substitution - coding silent 2:32388932-32388932 + TCGA-BS-A0UF-01 COSM1020454 c.14194C>T p.R4732* Substitution - Nonsense 2:32607578-32607578 + ESCC_96 COSM5637670 c.5107C>G p.L1703V Substitution - Missense 2:32464674-32464674 + 8064632 COSM3391705 c.30C>T p.P10P Substitution - coding silent 2:32357191-32357191 + TCGA-D3-A3MU-06 COSM3581215 c.12019A>T p.K4007* Substitution - Nonsense 2:32529749-32529749 + 18195 COSM1306724 c.1149T>C p.D383D Substitution - coding silent 2:32401277-32401277 + CA2 COSM1166143 c.11777G>A p.R3926H Substitution - Missense 2:32525485-32525485 + TCGA-BP-5169-01 COSM477338 c.5143G>T p.A1715S Substitution - Missense 2:32464710-32464710 + TCGA-D1-A160-01 COSM1020373 c.10258T>C p.F3420L Substitution - Missense 2:32510546-32510546 + CSCC-49-T COSM3581186 c.5184C>T p.F1728F Substitution - coding silent 2:32464751-32464751 + ESCC-183T COSM3939076 c.4069T>A p.C1357S Substitution - Missense 2:32442189-32442189 + J30_T COSM3962787 c.4645G>A p.A1549T Substitution - Missense 2:32453834-32453834 + SNUH_G76_S1 COSM4419498 c.3642A>G p.G1214G Substitution - coding silent 2:32439518-32439518 + TCGA-BR-6452-01 COSM4093900 c.8495C>A p.P2832H Substitution - Missense 2:32499573-32499573 + ESCC_86 COSM5636571 c.4340C>T p.S1447F Substitution - Missense 2:32445524-32445524 + TCGA-BR-4184-01 COSM1020395 c.11801G>A p.R3934H Substitution - Missense 2:32525509-32525509 + HX24T COSM3709621 c.5549C>A p.P1850H Substitution - Missense 2:32467717-32467717 + ML_06_T_01 COSM5037930 c.13144+6T>G p.? Unknown 2:32549487-32549487 + 1946219 COSM1578218 c.12095-1G>C p.? Unknown 2:32531354-32531354 + TCGA-DK-A3WW-01 COSM3798967 c.4696C>G p.L1566V Substitution - Missense 2:32453885-32453885 + CLL132 COSM1291497 c.6496delC p.M2167fs*1 Deletion - Frameshift 2:32471028-32471028 + U2940 COSM5620353 c.4255C>T p.P1419S Substitution - Missense 2:32443507-32443507 + TCGA-G5-6233-01 COSM5080774 c.13829A>C p.K4610T Substitution - Missense 2:32597967-32597967 + TCGA-BS-A0UF-01 COSM1020421 c.13133G>A p.R4378Q Substitution - Missense 2:32549470-32549470 + UM-SCC-11B COSM4592548 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + TCGA-A8-A081-01 COSM442834 c.14260-1G>T p.? Unknown 2:32611447-32611447 + 18195 COSM1306723 c.1149T>C p.D383D Substitution - coding silent 2:32401277-32401277 + TCGA-EE-A3JE-06 COSM3910254 c.11157G>T p.L3719F Substitution - Missense 2:32515578-32515578 + TCGA-HU-A4H4-01 COSM4093873 c.4303A>G p.N1435D Substitution - Missense 2:32443555-32443555 + CSCC-27-T COSM4497828 c.5061C>T p.F1687F Substitution - coding silent 2:32464628-32464628 + Pat_41_B COSM5862439 c.2771C>T p.A924V Substitution - Missense 2:32416062-32416062 + WSU-HN30 COSM4591363 c.3994G>C p.V1332L Substitution - Missense TCGA-B0-5104-01 COSM477336 c.4581C>A p.V1527V Substitution - coding silent 2:32448891-32448891 + CHC1207T COSM4800186 c.7832G>A p.G2611E Substitution - Missense 2:32487665-32487665 + BD40T COSM5509170 c.3451G>T p.V1151F Substitution - Missense 2:32435537-32435537 + TCGA-H4-A2HQ-01 COSM1306751 c.11572C>T p.L3858F Substitution - Missense 2:32518895-32518895 + C608 COSM4442884 c.5863T>C p.Y1955H Substitution - Missense 2:32468519-32468519 + Pat_44_B COSM5862449 c.12145G>A p.G4049S Substitution - Missense 2:32531405-32531405 + TCGA-EE-A2M5-06 COSM3581175 c.1696T>A p.C566S Substitution - Missense 2:32414987-32414987 + T684 COSM4665750 c.8956G>A p.A2986T Substitution - Missense 2:32500034-32500034 + TCGA-UB-A7MB-01 COSM4931232 c.11869A>C p.N3957H Substitution - Missense 2:32525577-32525577 + pfg129T COSM4752336 c.12544C>T p.Q4182* Substitution - Nonsense 2:32543493-32543493 + TCGA-A6-6781-01 COSM1407815 c.6899G>A p.R2300H Substitution - Missense 2:32477414-32477414 + PT38 COSM5922135 c.2717C>T p.T906I Substitution - Missense 2:32416008-32416008 + pfg106T COSM4765145 c.12108_12109insA p.L4037fs*3 Insertion - Frameshift 2:32531368-32531369 + YUBER COSM1690434 c.8704C>T p.R2902C Substitution - Missense 2:32499782-32499782 + HCT8 COSM4634833 c.4070G>A p.C1357Y Substitution - Missense 2:32442190-32442190 + TCGA-BR-7851-01 COSM4093908 c.11866G>A p.A3956T Substitution - Missense 2:32525574-32525574 + TCGA-AC-A23H-01 COSM1306758 c.12614C>T p.S4205L Substitution - Missense 2:32545664-32545664 + TCGA-AX-A05Z-01 COSM1020218 c.1964A>C p.K655T Substitution - Missense 2:32415255-32415255 + 2250172 COSM5030151 c.13400C>T p.S4467F Substitution - Missense 2:32593959-32593959 + TCGA-CZ-5451-01 COSM477341 c.5953A>T p.N1985Y Substitution - Missense 2:32468609-32468609 + TCGA-EI-6882-01 COSM5079035 c.13502-1_13502insA p.L4504fs*3 Unknown 2:32595033-32595034 + CLL024 COSM1291499 c.6809A>G p.K2270R Substitution - Missense 2:32476301-32476301 + KM12 COSM2942329 c.3759T>C p.S1253S Substitution - coding silent 2:32439635-32439635 + PTC-7C COSM4133813 c.1487C>A p.S496* Substitution - Nonsense 2:32414778-32414778 + TCGA-D9-A6EC-06 COSM4404175 c.7886T>G p.L2629R Substitution - Missense 2:32487719-32487719 + ESCC_132 COSM5642394 c.3347A>G p.N1116S Substitution - Missense 2:32433742-32433742 + TCGA-CG-4305-01 COSM2942462 c.7094C>T p.T2365M Substitution - Missense 2:32478660-32478660 + TCGA-AZ-4315-01 COSM1407811 c.6380G>T p.R2127I Substitution - Missense 2:32470200-32470200 + 2367454 COSM5004077 c.11470A>G p.M3824V Substitution - Missense 2:32518374-32518374 + TCGA-21-5787-01 COSM721163 c.13605A>G p.L4535L Substitution - coding silent 2:32595137-32595137 + 71 COSM4777768 c.1005_1006insC p.V336fs*7 Insertion - Frameshift 2:32395564-32395565 + TCGA-G2-A2ES-01 COSM1306760 c.14138G>T p.R4713L Substitution - Missense 2:32607522-32607522 + TCGA-AP-A056-01 COSM1020239 c.2609G>A p.R870Q Substitution - Missense 2:32415900-32415900 + TCGA-33-4538-01 COSM721173 c.12970C>T p.L4324L Substitution - coding silent 2:32548009-32548009 + TCGA-DB-A64O-01 COSM3972228 c.8590A>T p.T2864S Substitution - Missense 2:32499668-32499668 + RKO COSM4648594 c.5736G>A p.Q1912Q Substitution - coding silent 2:32468067-32468067 + TCGA-G4-6304-01 COSM1407766 c.542T>C p.V181A Substitution - Missense 2:32380187-32380187 + TCGA-AP-A0LM-01 COSM1020270 c.4113G>T p.K1371N Substitution - Missense 2:32442330-32442330 + 3N31-VS-3T31 COSM4980654 c.4550G>T p.C1517F Substitution - Missense 2:32448860-32448860 + TCGA-FS-A1ZQ-06 COSM3581200 c.8616T>C p.T2872T Substitution - coding silent 2:32499694-32499694 + C008 COSM1690428 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + TCGA-AX-A0J1-01 COSM1020395 c.11801G>A p.R3934H Substitution - Missense 2:32525509-32525509 + ATL088 COSM5708190 c.8721A>C p.K2907N Substitution - Missense 2:32499799-32499799 + 49M COSM5589817 c.9661A>G p.K3221E Substitution - Missense 2:32505166-32505166 + J80_T COSM3962788 c.5534A>C p.H1845P Substitution - Missense 2:32467702-32467702 + 399 COSM4429241 c.7942T>G p.S2648A Substitution - Missense 2:32487775-32487775 + 19 COSM5745891 c.5626G>A p.G1876R Substitution - Missense 2:32467957-32467957 + TCGA-B5-A0JY-01 COSM1020315 c.7399G>T p.D2467Y Substitution - Missense 2:32479608-32479608 + CHC892T COSM4959514 c.6750G>A p.K2250K Substitution - coding silent 2:32476242-32476242 + SWE-19 COSM1179031 c.3551G>T p.G1184V Substitution - Missense 2:32436104-32436104 + BRC15 COSM5025608 c.9208-1G>A p.? Unknown 2:32502794-32502794 + LUAD-E00918 COSM365159 c.2410C>T p.P804S Substitution - Missense 2:32415701-32415701 + TCGA-CW-5585-01 COSM477345 c.9317T>C p.L3106P Substitution - Missense 2:32503054-32503054 + ESCC_BICR_023T COSM5436461 c.7213C>T p.Q2405* Substitution - Nonsense 2:32478779-32478779 + TCGA-AX-A0J1-01 COSM1020397 c.11801G>A p.R3934H Substitution - Missense 2:32525509-32525509 + TCGA-46-3767-01 COSM721201 c.9076G>T p.G3026W Substitution - Missense 2:32501757-32501757 + TCGA-DK-A1AC-01 COSM1306729 c.2263G>A p.E755K Substitution - Missense 2:32415554-32415554 + TCGA-CM-6170-01 COSM1407799 c.4818G>A p.S1606S Substitution - coding silent 2:32463258-32463258 + TCGA-G4-6586-01 COSM1407838 c.11951C>T p.A3984V Substitution - Missense 2:32529681-32529681 + 1_RESISTANT COSM1718160 c.4931T>G p.L1644R Substitution - Missense 2:32463371-32463371 + pfg129T COSM4746921 c.10276_10277delCT p.S3427fs*2 Deletion - Frameshift 2:32510564-32510565 + YUQUEST COSM5396931 c.3209C>T p.A1070V Substitution - Missense 2:32431051-32431051 + D28 COSM5544531 c.9477G>A p.G3159G Substitution - coding silent 2:32503214-32503214 + TCGA-AP-A0LM-01 COSM1020356 c.8845A>C p.N2949H Substitution - Missense 2:32499923-32499923 + HCT8 COSM4634836 c.11054C>A p.P3685H Substitution - Missense 2:32515475-32515475 + pfg076T COSM4765149 c.13502_13503insA p.L4504fs*3 Insertion - Frameshift 2:32595034-32595035 + TCGA-AP-A059-01 COSM1020302 c.6074C>A p.T2025N Substitution - Missense 2:32468730-32468730 + B102-Tumor COSM3933635 c.13469C>T p.A4490V Substitution - Missense 2:32594028-32594028 + UM-SCC-2 COSM4591362 c.3994G>C p.V1332L Substitution - Missense TCGA-AA-A010-01 COSM279165 c.2360A>C p.N787T Substitution - Missense 2:32415651-32415651 + TCGA-DK-A3WW-01 COSM3798968 c.4696C>G p.L1566V Substitution - Missense 2:32453885-32453885 + RW2982 COSM4649691 c.13850C>T p.A4617V Substitution - Missense 2:32599758-32599758 + TCGA-D1-A16E-01 COSM1020260 c.3653G>T p.R1218L Substitution - Missense 2:32439529-32439529 + 8012321 COSM3391711 c.8972T>A p.M2991K Substitution - Missense 2:32500050-32500050 + AD63 COSM5966663 c.9940A>G p.N3314D Substitution - Missense 2:32508219-32508219 + TCGA-G4-6297-01 COSM3695479 c.7264G>T p.A2422S Substitution - Missense 2:32479473-32479473 + T684 COSM4665749 c.8956G>A p.A2986T Substitution - Missense 2:32500034-32500034 + TCGA-CG-4306-01 COSM1020445 c.13960C>T p.R4654* Substitution - Nonsense 2:32599868-32599868 + TCGA-BP-4173-01 COSM3773971 c.2681C>T p.T894M Substitution - Missense 2:32415972-32415972 + TCGA-HU-A4GN-01 COSM4093884 c.5888C>T p.A1963V Substitution - Missense 2:32468544-32468544 + TCGA-BR-8589-01 COSM4093922 c.14059A>C p.S4687R Substitution - Missense 2:32603072-32603072 + 18_tFL COSM4171158 c.985T>C p.F329L Substitution - Missense 2:32395544-32395544 + C135 COSM4618234 c.13751C>T p.T4584M Substitution - Missense 2:32597889-32597889 + TCGA-J9-A52C-01 COSM4877376 c.4168C>T p.R1390C Substitution - Missense 2:32442385-32442385 + TCGA-AN-A046-01 COSM274137 c.14174G>A p.R4725Q Substitution - Missense 2:32607558-32607558 + HCC87 COSM1614795 c.8530C>G p.L2844V Substitution - Missense 2:32499608-32499608 + TCGA-BS-A0UF-01 COSM1020452 c.14194C>T p.R4732* Substitution - Nonsense 2:32607578-32607578 + HCC49T COSM1614791 c.5595G>T p.G1865G Substitution - coding silent 2:32467926-32467926 + TCGA-D3-A2JH-06 COSM3581228 c.14153C>T p.P4718L Substitution - Missense 2:32607537-32607537 + CHC2216T COSM4806001 c.14337G>A p.Q4779Q Substitution - coding silent 2:32611525-32611525 + Pat_41_B COSM5862440 c.2771C>T p.A924V Substitution - Missense 2:32416062-32416062 + TCGA-AP-A059-01 COSM1020192 c.811G>A p.G271R Substitution - Missense 2:32388915-32388915 + ESO-2472 COSM1246125 c.13816C>A p.L4606I Substitution - Missense 2:32597954-32597954 + BN19T COSM1614798 c.10374T>G p.S3458R Substitution - Missense 2:32512960-32512960 + PD4264a COSM5768425 c.5780+10G>C p.? Unknown 2:32468121-32468121 + CSCC-35-T COSM4514339 c.9719C>T p.S3240F Substitution - Missense 2:32507998-32507998 + TCGA-UB-A7MB-01 COSM4931747 c.9059A>C p.H3020P Substitution - Missense 2:32501740-32501740 + TCGA-D1-A17Q-01 COSM1020294 c.5345G>A p.R1782Q Substitution - Missense 2:32465153-32465153 + TCGA-60-2724-01 COSM721198 c.9523A>T p.T3175S Substitution - Missense 2:32505028-32505028 + TCGA-46-3767-01 COSM721200 c.9076G>T p.G3026W Substitution - Missense 2:32501757-32501757 + TCGA-H4-A2HQ-01 COSM1306753 c.11575C>T p.H3859Y Substitution - Missense 2:32518898-32518898 + B22-Tumor COSM3933634 c.7438G>C p.D2480H Substitution - Missense 2:32481349-32481349 + TCGA-AD-5900-01 COSM1407821 c.8658C>T p.S2886S Substitution - coding silent 2:32499736-32499736 + TCGA-BH-A0EE-01 COSM5216379 c.4552delA p.N1519fs*61 Deletion - Frameshift 2:32448862-32448862 + TCGA-GN-A267-06 COSM3581177 c.1860T>G p.S620S Substitution - coding silent 2:32415151-32415151 + TCGA-HE-7130-01 COSM3991271 c.1306C>T p.Q436* Substitution - Nonsense 2:32401511-32401511 + ESCC_157 COSM5646335 c.10864G>C p.A3622P Substitution - Missense 2:32515285-32515285 + sysucc-783T COSM5484546 c.12706C>T p.R4236W Substitution - Missense 2:32545756-32545756 + TCGA-AX-A0J0-01 COSM1020209 c.1609G>T p.E537* Substitution - Nonsense 2:32414900-32414900 + 1731645 COSM327777 c.8834C>T p.S2945F Substitution - Missense 2:32499912-32499912 + TCGA-AX-A06H-01 COSM1020288 c.5283T>C p.L1761L Substitution - coding silent 2:32465091-32465091 + LP6005409-DNA_F03 COSM4408879 c.2710G>C p.V904L Substitution - Missense 2:32416001-32416001 + TCGA-18-3406-01 COSM721158 c.14163A>T p.T4721T Substitution - coding silent 2:32607547-32607547 + LOVO COSM2942633 c.11041G>A p.D3681N Substitution - Missense 2:32515462-32515462 + 545 COSM5612636 c.14024G>A p.G4675E Substitution - Missense 2:32603037-32603037 + 2492729 COSM5726305 c.11819G>A p.G3940E Substitution - Missense 2:32525527-32525527 + 1731645 COSM327776 c.8834C>T p.S2945F Substitution - Missense 2:32499912-32499912 + TCGA-33-4582-01 COSM721154 c.14387C>G p.A4796G Substitution - Missense 2:32611575-32611575 + TCGA-EE-A2A2-06 COSM3581197 c.8106T>C p.T2702T Substitution - coding silent 2:32490051-32490051 + TCGA-AG-A036-01 COSM5075324 c.7854G>T p.G2618G Substitution - coding silent 2:32487687-32487687 + ESO-2472 COSM1246126 c.13816C>A p.L4606I Substitution - Missense 2:32597954-32597954 + TCGA-DK-A2I6-01 COSM1306746 c.10453_10454GG>AT p.G3485I Substitution - Missense 2:32513039-32513040 + ACINAR03 COSM1734260 c.12455C>A p.P4152H Substitution - Missense 2:32543404-32543404 + CHOL40 COSM1744973 c.11822_11823GG>AC p.R3941N Substitution - Missense 2:32525530-32525531 + TCGA-FW-A3R5-06 COSM3910253 c.7901C>T p.S2634L Substitution - Missense 2:32487734-32487734 + CSCC-32-T COSM4572265 c.6920T>C p.V2307A Substitution - Missense 2:32477435-32477435 + S01453 COSM5701786 c.11712_11713GG>AT p.E3905* Substitution - Nonsense 2:32524976-32524977 + CHC1600T COSM4791531 c.13318A>G p.M4440V Substitution - Missense 2:32575329-32575329 + TCGA-16-0861-01 COSM3407835 c.13007G>A p.S4336N Substitution - Missense 2:32549344-32549344 + BD110T COSM5514126 c.2295C>A p.A765A Substitution - coding silent 2:32415586-32415586 + Gp2D COSM4628060 c.5753T>C p.V1918A Substitution - Missense 2:32468084-32468084 + TCGA-BR-8078-01 COSM4093888 c.6356T>C p.M2119T Substitution - Missense 2:32470176-32470176 + TCGA-AG-3892-01 COSM256397 c.6916G>T p.E2306* Substitution - Nonsense 2:32477431-32477431 + TCGA-B5-A11G-01 COSM1020289 c.5298T>C p.A1766A Substitution - coding silent 2:32465106-32465106 + HT115 COSM2942627 c.11006T>C p.V3669A Substitution - Missense 2:32515427-32515427 + CHC605T COSM3668666 c.8582A>G p.E2861G Substitution - Missense 2:32499660-32499660 + TCGA-D3-A2JN-06 COSM3581182 c.2902G>A p.G968R Substitution - Missense 2:32429175-32429175 + D28 COSM5544530 c.9477G>A p.G3159G Substitution - coding silent 2:32503214-32503214 + 2 COSM4172307 c.10514A>G p.Y3505C Substitution - Missense 2:32513100-32513100 + UM-SCC-2 COSM4591363 c.3994G>C p.V1332L Substitution - Missense TCGA-A6-6650-01 COSM3695485 c.10796C>T p.A3599V Substitution - Missense 2:32515217-32515217 + GHE0609 COSM5714179 c.9980+2T>A p.? Unknown 2:32508261-32508261 + TCGA-B8-5163-01 COSM477331 c.2566A>G p.I856V Substitution - Missense 2:32415857-32415857 + TCGA-G4-6586-01 COSM1407835 c.11086A>G p.S3696G Substitution - Missense 2:32515507-32515507 + CRC-19T COSM256402 c.13486C>T p.R4496W Substitution - Missense 2:32594045-32594045 + TCGA-BH-A18V-06 COSM3839431 c.10527A>G p.V3509V Substitution - coding silent 2:32513113-32513113 + TCGA-EI-6917-01 COSM3426396 c.6579G>T p.K2193N Substitution - Missense 2:32471111-32471111 + PT37 COSM5917538 c.1825G>T p.D609Y Substitution - Missense 2:32415116-32415116 + TCGA-BG-A0M3-01 COSM1020298 c.5588G>A p.R1863H Substitution - Missense 2:32467919-32467919 + HCC037T COSM5811827 c.9704G>C p.C3235S Substitution - Missense 2:32507983-32507983 + TCGA-ED-A7PY-01 COSM4926558 c.2666T>C p.F889S Substitution - Missense 2:32415957-32415957 + 2_FL COSM4171162 c.9628C>G p.L3210V Substitution - Missense 2:32505133-32505133 + TCGA-66-2756-01 COSM721183 c.11890G>T p.V3964L Substitution - Missense 2:32525598-32525598 + pfg103T COSM4752323 c.2091C>G p.N697K Substitution - Missense 2:32415382-32415382 + TCGA-BR-8680-01 COSM2942690 c.12533G>T p.R4178I Substitution - Missense 2:32543482-32543482 + AD63 COSM5966664 c.9940A>G p.N3314D Substitution - Missense 2:32508219-32508219 + 044 COSM145137 c.11060T>G p.L3687R Substitution - Missense 2:32515481-32515481 + PCSI_0047_Pa_P COSM3782192 c.12148G>T p.D4050Y Substitution - Missense 2:32531408-32531408 + WSU-HN13 COSM4592547 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + TCGA-G2-A2EO-01 COSM1306740 c.4662C>T p.F1554F Substitution - coding silent 2:32453851-32453851 + PD4937a COSM159385 c.2446G>C p.E816Q Substitution - Missense 2:32415737-32415737 + CHC1602T COSM4789050 c.4813G>A p.A1605T Substitution - Missense 2:32463253-32463253 + TCGA-CM-4746-01 COSM1407792 c.4051C>A p.L1351I Substitution - Missense 2:32442171-32442171 + J30_T COSM3962791 c.8002A>T p.S2668C Substitution - Missense 2:32488621-32488621 + 2492722 COSM5719570 c.12489A>C p.L4163F Substitution - Missense 2:32543438-32543438 + TCGA-AP-A0LG-01 COSM1020206 c.1413A>G p.G471G Substitution - coding silent 2:32401618-32401618 + TCGA-AX-A0J0-01 COSM1020363 c.9589T>C p.W3197R Substitution - Missense 2:32505094-32505094 + TCGA-A3-3346-01 COSM1494916 c.10579A>T p.N3527Y Substitution - Missense 2:32515000-32515000 + Ad1 COSM4440799 c.5152G>A p.V1718I Substitution - Missense 2:32464719-32464719 + ESCC-154T COSM3939078 c.9396T>C p.F3132F Substitution - coding silent 2:32503133-32503133 + ATL071 COSM5708192 c.10901T>C p.L3634P Substitution - Missense 2:32515322-32515322 + T578 COSM4665740 c.1505A>G p.E502G Substitution - Missense 2:32414796-32414796 + 2521259 COSM5889656 c.656T>G p.V219G Substitution - Missense 2:32388760-32388760 + TCGA-AX-A0J0-01 COSM1020361 c.9589T>C p.W3197R Substitution - Missense 2:32505094-32505094 + 39 COSM3581198 c.8383C>T p.R2795* Substitution - Nonsense 2:32493582-32493582 + TCGA-BG-A0M4-01 COSM1020194 c.811G>A p.G271R Substitution - Missense 2:32388915-32388915 + TCGA-AU-6004-01 COSM1407776 c.1251_1252insA p.M418fs*8 Insertion - Frameshift 2:32401379-32401380 + 12-P616 COSM4583473 c.12978T>C p.V4326V Substitution - coding silent 2:32549315-32549315 + LUAD-S01405 COSM399100 c.3066G>T p.L1022F Substitution - Missense 2:32430908-32430908 + ccRCC-15 COSM1660779 c.4805T>G p.V1602G Substitution - Missense 2:32463245-32463245 + TCGA-D1-A16X-01 COSM1020412 c.12686A>G p.D4229G Substitution - Missense 2:32545736-32545736 + ACINAR01 COSM1734253 c.2909G>A p.C970Y Substitution - Missense 2:32429182-32429182 + ESCC-190T COSM3939074 c.2557C>G p.Q853E Substitution - Missense 2:32415848-32415848 + 2492708 COSM2942294 c.3120G>A p.A1040A Substitution - coding silent 2:32430962-32430962 + COLO-829 COSM36763 c.9802C>T p.Q3268* Substitution - Nonsense 2:32508081-32508081 + LUAD-NYU195 COSM371095 c.9208-1G>T p.? Unknown 2:32502794-32502794 + 044-0092-01TD COSM145137 c.11060T>G p.L3687R Substitution - Missense 2:32515481-32515481 + WSU-HN12 COSM4591363 c.3994G>C p.V1332L Substitution - Missense HCC2998 COSM2942621 c.10721A>G p.H3574R Substitution - Missense 2:32515142-32515142 + TCGA-BR-7723-01 COSM4093852 c.445G>A p.A149T Substitution - Missense 2:32377707-32377707 + C008 COSM5522191 c.6067T>C p.L2023L Substitution - coding silent 2:32468723-32468723 + TCGA-ER-A1A1-06 COSM3581224 c.13211C>T p.S4404F Substitution - Missense 2:32575222-32575222 + TCGA-AP-A0LM-01 COSM1020354 c.8845A>C p.N2949H Substitution - Missense 2:32499923-32499923 + TCGA-DA-A1HV-06 COSM3581193 c.7704T>A p.D2568E Substitution - Missense 2:32485650-32485650 + TCGA-D9-A6EC-06 COSM4402144 c.10470T>A p.S3490S Substitution - coding silent 2:32513056-32513056 + PD4127a COSM159377 c.7184G>T p.G2395V Substitution - Missense 2:32478750-32478750 + K3 COSM249145 c.5371G>T p.V1791L Substitution - Missense 2:32467539-32467539 + MPCC_0032_Pa_C COSM3380144 c.13707G>A p.A4569A Substitution - coding silent 2:32597845-32597845 + TCGA-43-6647-01 COSM721152 c.14416G>A p.E4806K Substitution - Missense 2:32617746-32617746 + TCGA-D1-A103-01 COSM1020416 c.12718G>T p.E4240* Substitution - Nonsense 2:32545768-32545768 + B65 COSM1745489 c.772_773insGATT p.S260fs*7 Insertion - Frameshift 2:32388876-32388877 + TCGA-CG-5721-01 COSM4093867 c.3297T>C p.C1099C Substitution - coding silent 2:32433692-32433692 + T2284 COSM4665761 c.11778T>C p.R3926R Substitution - coding silent 2:32525486-32525486 + 61 COSM5736006 c.5465T>C p.L1822S Substitution - Missense 2:32467633-32467633 + TCGA-23-1031-01 COSM69822 c.5311C>G p.Q1771E Substitution - Missense 2:32465119-32465119 + TCGA-CJ-5681-01 COSM477333 c.3350T>C p.I1117T Substitution - Missense 2:32433745-32433745 + TCGA-A2-A0D0-01 COSM442825 c.10511G>A p.S3504N Substitution - Missense 2:32513097-32513097 + TCGA-AP-A056-01 COSM1020424 c.13140T>G p.D4380E Substitution - Missense 2:32549477-32549477 + TCGA-AP-A0LT-01 COSM1020215 c.1925C>T p.A642V Substitution - Missense 2:32415216-32415216 + TCGA-BT-A3PH-01 COSM1306742 c.8296C>G p.L2766V Substitution - Missense 2:32491514-32491514 + TCGA-AP-A051-01 COSM1020449 c.14166G>T p.Q4722H Substitution - Missense 2:32607550-32607550 + T3094 COSM4665738 c.600delA p.N202fs*27 Deletion - Frameshift 2:32380245-32380245 + TCGA-D1-A15X-01 COSM1020323 c.7561T>C p.Y2521H Substitution - Missense 2:32482447-32482447 + BRC12 COSM5025605 c.4347T>C p.Y1449Y Substitution - coding silent 2:32445531-32445531 + TCGA-AX-A05Z-01 COSM1020201 c.1224G>T p.K408N Substitution - Missense 2:32401352-32401352 + TCGA-D1-A103-01 COSM1020455 c.14195G>A p.R4732Q Substitution - Missense 2:32607579-32607579 + 587228 COSM1184724 c.3089G>A p.R1030H Substitution - Missense 2:32430931-32430931 + TCGA-DM-A28F-01 COSM1407808 c.6186C>G p.L2062L Substitution - coding silent 2:32469453-32469453 + 2492708 COSM2942293 c.3120G>A p.A1040A Substitution - coding silent 2:32430962-32430962 + PDA_032 COSM4999660 c.2326C>A p.L776I Substitution - Missense 2:32415617-32415617 + BHY COSM4591363 c.3994G>C p.V1332L Substitution - Missense TCGA-EQ-A4SO-01 COSM4093904 c.9404C>G p.S3135C Substitution - Missense 2:32503141-32503141 + LP6005409-DNA_E01 COSM4409231 c.1085A>C p.H362P Substitution - Missense 2:32401213-32401213 + TCGA-CM-6674-01 COSM1407841 c.12035T>C p.V4012A Substitution - Missense 2:32529765-32529765 + TCGA-AF-2693-01 COSM1565587 c.2892C>T p.L964L Substitution - coding silent 2:32429165-32429165 + TCGA-AP-A051-01 COSM1020225 c.2256C>T p.C752C Substitution - coding silent 2:32415547-32415547 + PD4120a COSM159375 c.11600C>T p.S3867L Substitution - Missense 2:32518923-32518923 + HT115 COSM2942274 c.2618A>C p.D873A Substitution - Missense 2:32415909-32415909 + TCGA-D8-A1JL-01 COSM1483067 c.11594C>T p.T3865I Substitution - Missense 2:32518917-32518917 + TCGA-CA-6718-01 COSM1020242 c.2658G>T p.K886N Substitution - Missense 2:32415949-32415949 + TCGA-B5-A11E-01 COSM1020404 c.12479C>T p.A4160V Substitution - Missense 2:32543428-32543428 + TCGA-D5-6927-01 COSM1407803 c.5203delC p.P1736fs*17 Deletion - Frameshift 2:32464770-32464770 + CHC2216T COSM4805994 c.14368A>T p.M4790L Substitution - Missense 2:32611556-32611556 + YUKLAB COSM1690424 c.5663A>G p.E1888G Substitution - Missense 2:32467994-32467994 + BRC42 COSM5025603 c.3881A>G p.D1294G Substitution - Missense 2:32441399-32441399 + TCGA-ER-A198-06 COSM3581209 c.10413G>A p.R3471R Substitution - coding silent 2:32512999-32512999 + TCGA-BR-8078-01 COSM4093889 c.6356T>C p.M2119T Substitution - Missense 2:32470176-32470176 + TCGA-D5-6927-01 COSM1407802 c.5203delC p.P1736fs*17 Deletion - Frameshift 2:32464770-32464770 + LUAD-QY22Z COSM394760 c.2442G>T p.Q814H Substitution - Missense 2:32415733-32415733 + YUKAT COSM5396937 c.9074G>A p.G3025D Substitution - Missense 2:32501755-32501755 + OSCC-GB_00740111 COSM4890891 c.8698C>G p.L2900V Substitution - Missense 2:32499776-32499776 + 3N31-VS-3T31 COSM4980653 c.4550G>T p.C1517F Substitution - Missense 2:32448860-32448860 + TCGA-GF-A6C9-06 COSM4902509 c.8854G>A p.D2952N Substitution - Missense 2:32499932-32499932 + TCGA-EB-A3Y7-01 COSM3581227 c.13975C>T p.L4659F Substitution - Missense 2:32599883-32599883 + TCGA-19-1790-01 COSM3407831 c.7731G>A p.Q2577Q Substitution - coding silent 2:32485677-32485677 + T26 COSM5344197 c.1478-1G>A p.? Unknown 2:32414768-32414768 + BN06 COSM1614800 c.10821A>C p.E3607D Substitution - Missense 2:32515242-32515242 + TCGA-BR-8680-01 COSM4093898 c.8140A>C p.T2714P Substitution - Missense 2:32490085-32490085 + AIMAH5 COSM5961816 c.12264C>T p.P4088P Substitution - coding silent 2:32531524-32531524 + TCGA-B5-A11G-01 COSM1020291 c.5298T>C p.A1766A Substitution - coding silent 2:32465106-32465106 + BN06 COSM1614801 c.10821A>C p.E3607D Substitution - Missense 2:32515242-32515242 + TCGA-EE-A2M5-06 COSM3581174 c.1696T>A p.C566S Substitution - Missense 2:32414987-32414987 + PDA_046 COSM5000523 c.11051C>T p.A3684V Substitution - Missense 2:32515472-32515472 + SC_9008 COSM5559988 c.2247G>A p.L749L Substitution - coding silent 2:32415538-32415538 + S48_post COSM5574435 c.4864_4865delCA p.H1622fs*70 Deletion - Frameshift 2:32463304-32463305 + LS411 COSM2942618 c.10657C>A p.H3553N Substitution - Missense 2:32515078-32515078 + TCGA-FJ-A3ZE-01 COSM3798970 c.8203A>C p.N2735H Substitution - Missense 2:32490148-32490148 + 2275_T COSM3962794 c.12146G>T p.G4049V Substitution - Missense 2:32531406-32531406 + TCGA-AP-A0LM-01 COSM1020330 c.8159G>A p.C2720Y Substitution - Missense 2:32490104-32490104 + TCGA-AG-A002-01 COSM259645 c.12780A>G p.R4260R Substitution - coding silent 2:32545830-32545830 + CML010T COSM5802806 c.13717G>A p.A4573T Substitution - Missense 2:32597855-32597855 + TCGA-AP-A056-01 COSM1020318 c.7405A>C p.T2469P Substitution - Missense 2:32479614-32479614 + TCGA-DD-A11C-01 COSM4925608 c.12954A>G p.E4318E Substitution - coding silent 2:32547993-32547993 + TCGA-BP-5169-01 COSM477337 c.5143G>T p.A1715S Substitution - Missense 2:32464710-32464710 + ATL071 COSM5708193 c.10901T>C p.L3634P Substitution - Missense 2:32515322-32515322 + HT29 COSM4638588 c.7880G>A p.S2627N Substitution - Missense 2:32487713-32487713 + TCGA-D5-6928-01 COSM1407856 c.13851G>T p.A4617A Substitution - coding silent 2:32599759-32599759 + C91 COSM4444781 c.14138G>A p.R4713Q Substitution - Missense 2:32607522-32607522 + sysucc-1247T COSM1020266 c.3871C>T p.R1291W Substitution - Missense 2:32441389-32441389 + 2_FL COSM4171163 c.9628C>G p.L3210V Substitution - Missense 2:32505133-32505133 + I2L-P19Tb-Tumor-Biopsy COSM5354339 c.5094A>C p.P1698P Substitution - coding silent 2:32464661-32464661 + PD24216a COSM5800557 c.14176G>A p.E4726K Substitution - Missense 2:32607560-32607560 + ccRCC-29 COSM1660781 c.6707T>C p.V2236A Substitution - Missense 2:32473226-32473226 + I2L-P19Ta-Tumor-Organoid COSM5354156 c.2843G>A p.G948D Substitution - Missense 2:32416134-32416134 + TCGA-AP-A0LM-01 COSM1020221 c.1967G>T p.S656I Substitution - Missense 2:32415258-32415258 + CHC2216T COSM4806002 c.14337G>A p.Q4779Q Substitution - coding silent 2:32611525-32611525 + STC291 COSM5058880 c.10326G>A p.Q3442Q Substitution - coding silent 2:32510614-32510614 + TCGA-BR-6452-01 COSM4093901 c.8495C>A p.P2832H Substitution - Missense 2:32499573-32499573 + TCGA-EE-A182-06 COSM3581229 c.14153C>T p.P4718L Substitution - Missense 2:32607537-32607537 + DLD1 COSM2942606 c.10430C>A p.P3477H Substitution - Missense 2:32513016-32513016 + Pat_28_B COSM5862443 c.7316G>A p.G2439D Substitution - Missense 2:32479525-32479525 + 93VU147T COSM4591362 c.3994G>C p.V1332L Substitution - Missense ML_06_T_01 COSM5037931 c.13144+6T>G p.? Unknown 2:32549487-32549487 + TCGA-BS-A0UV-01 COSM1020237 c.2609G>A p.R870Q Substitution - Missense 2:32415900-32415900 + 587376 COSM1184738 c.6028A>T p.N2010Y Substitution - Missense 2:32468684-32468684 + TCGA-AX-A0J1-01 COSM1020197 c.1006G>A p.V336I Substitution - Missense 2:32395565-32395565 + TCGA-B5-A0K2-01 COSM1020301 c.5857G>A p.A1953T Substitution - Missense 2:32468513-32468513 + TCGA-DK-A1AC-01 COSM1306730 c.2263G>A p.E755K Substitution - Missense 2:32415554-32415554 + YURTHE COSM1690425 c.6382T>C p.S2128P Substitution - Missense 2:32470202-32470202 + PCSI_0116_Pa_X COSM3380141 c.2158T>C p.L720L Substitution - coding silent 2:32415449-32415449 + TCGA-HU-A4GU-01 COSM4093855 c.1110C>A p.V370V Substitution - coding silent 2:32401238-32401238 + TCGA-HU-A4H4-01 COSM4093872 c.4303A>G p.N1435D Substitution - Missense 2:32443555-32443555 + CRC-19T COSM5482381 c.9500-12_9500-8delTATCT p.? Unknown 2:32504993-32504997 + S01453 COSM5701787 c.11712_11713GG>AT p.E3905* Substitution - Nonsense 2:32524976-32524977 + PD11358a COSM5786280 c.6800C>T p.S2267L Substitution - Missense 2:32476292-32476292 + UM-SCC-17B COSM4592547 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + PD11358a COSM5786279 c.6800C>T p.S2267L Substitution - Missense 2:32476292-32476292 + PD4264a COSM5768424 c.5780+10G>C p.? Unknown 2:32468121-32468121 + 2492723 COSM5719569 c.12489A>C p.L4163F Substitution - Missense 2:32543438-32543438 + UPCI:SCC090 COSM4592548 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + PCSI_0098_Pa_P_526 COSM216588 c.9915T>C p.G3305G Substitution - coding silent 2:32508194-32508194 + TCGA-BR-4184-01 COSM4093913 c.12233G>A p.G4078D Substitution - Missense 2:32531493-32531493 + C0091T COSM4164516 c.12494T>C p.L4165P Substitution - Missense 2:32543443-32543443 + EGC15 COSM5058879 c.9863C>T p.A3288V Substitution - Missense 2:32508142-32508142 + LUAD-S01302 COSM395973 c.8580A>G p.I2860M Substitution - Missense 2:32499658-32499658 + 044-05-01TD COSM145137 c.11060T>G p.L3687R Substitution - Missense 2:32515481-32515481 + TCGA-G3-A3CK-01 COSM4922332 c.2957A>C p.K986T Substitution - Missense 2:32429230-32429230 + TCGA-CC-A3MC-01 COSM4919535 c.1648G>T p.E550* Substitution - Nonsense 2:32414939-32414939 + 2492722 COSM1690428 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + TCGA-C8-A1HE-01 COSM1483068 c.13965C>T p.F4655F Substitution - coding silent 2:32599873-32599873 + HCC160T COSM3709624 c.11755+3A>T p.? Unknown 2:32525022-32525022 + TCGA-AN-A0XW-01 COSM442836 c.14309G>A p.C4770Y Substitution - Missense 2:32611497-32611497 + ESCC-183T COSM3939077 c.4069T>A p.C1357S Substitution - Missense 2:32442189-32442189 + TCGA-UB-A7MB-01 COSM4931748 c.9059A>C p.H3020P Substitution - Missense 2:32501740-32501740 + CHC892T COSM4795048 c.2413G>A p.A805T Substitution - Missense 2:32415704-32415704 + TCGA-EE-A2A0-06 COSM3581173 c.1162A>G p.I388V Substitution - Missense 2:32401290-32401290 + PDA_046 COSM5000524 c.11051C>T p.A3684V Substitution - Missense 2:32515472-32515472 + 587228 COSM1184725 c.3089G>A p.R1030H Substitution - Missense 2:32430931-32430931 + TCGA-D1-A17U-01 COSM1020324 c.7604C>A p.P2535H Substitution - Missense 2:32482490-32482490 + T2949 COSM4093902 c.8574C>T p.A2858A Substitution - coding silent 2:32499652-32499652 + 399 COSM4429242 c.7942T>G p.S2648A Substitution - Missense 2:32487775-32487775 + TCGA-D9-A6EC-06 COSM4401236 c.12556C>T p.R4186* Substitution - Nonsense 2:32543505-32543505 + 116 COSM5010804 c.11498A>G p.Y3833C Substitution - Missense 2:32518821-32518821 + TCGA-BS-A0UF-01 COSM1020370 c.10258T>G p.F3420V Substitution - Missense 2:32510546-32510546 + CRC-19T COSM256401 c.13486C>T p.R4496W Substitution - Missense 2:32594045-32594045 + PT36 COSM5914879 c.5593G>A p.G1865R Substitution - Missense 2:32467924-32467924 + HCC46 COSM3709617 c.1170C>T p.C390C Substitution - coding silent 2:32401298-32401298 + TCGA-BF-A1Q0-01 COSM3581194 c.7817C>T p.S2606L Substitution - Missense 2:32487650-32487650 + EGC15 COSM5058878 c.9863C>T p.A3288V Substitution - Missense 2:32508142-32508142 + TCGA-BR-8363-01 COSM4093883 c.4834G>A p.A1612T Substitution - Missense 2:32463274-32463274 + COLO-829 COSM36763 c.9802C>T p.Q3268* Substitution - Nonsense 2:32508081-32508081 + ESO-1154 COSM1246117 c.1130C>T p.A377V Substitution - Missense 2:32401258-32401258 + TCGA-GN-A267-06 COSM3581176 c.1860T>G p.S620S Substitution - coding silent 2:32415151-32415151 + PDA_063 COSM5001223 c.6979C>T p.R2327C Substitution - Missense 2:32477494-32477494 + Pat_36_B COSM5862451 c.13027C>T p.Q4343* Substitution - Nonsense 2:32549364-32549364 + TCGA-HC-7210-01 COSM4391749 c.7825C>A p.P2609T Substitution - Missense 2:32487658-32487658 + TCGA-AA-3492-01 COSM1407769 c.599_600insA p.N202fs*5 Insertion - Frameshift 2:32380244-32380245 + TCGA-D7-A4YY-01 COSM4093868 c.3324C>T p.F1108F Substitution - coding silent 2:32433719-32433719 + TCGA-BR-8679-01 COSM4093874 c.4351T>C p.Y1451H Substitution - Missense 2:32445535-32445535 + 98 COSM5010802 c.8299T>A p.S2767T Substitution - Missense 2:32491517-32491517 + TCGA-AX-A0J0-01 COSM1020212 c.1859C>T p.S620F Substitution - Missense 2:32415150-32415150 + S29-post COSM5574257 c.12829C>G p.H4277D Substitution - Missense 2:32547868-32547868 + 39 COSM5733751 c.2996C>G p.S999* Substitution - Nonsense 2:32429269-32429269 + TCGA-EE-A2MR-06 COSM1690433 c.8704C>T p.R2902C Substitution - Missense 2:32499782-32499782 + WSU-HN6 COSM4591362 c.3994G>C p.V1332L Substitution - Missense TCGA-D1-A0ZS-01 COSM1020277 c.4163T>G p.I1388S Substitution - Missense 2:32442380-32442380 + HCC2998 COSM2942620 c.10721A>G p.H3574R Substitution - Missense 2:32515142-32515142 + ESCC_96 COSM5637669 c.5107C>G p.L1703V Substitution - Missense 2:32464674-32464674 + ESCC_86 COSM5636572 c.4340C>T p.S1447F Substitution - Missense 2:32445524-32445524 + LUAD-B01970 COSM356082 c.7339G>A p.D2447N Substitution - Missense 2:32479548-32479548 + TCGA-AN-A046-01 COSM274138 c.14174G>A p.R4725Q Substitution - Missense 2:32607558-32607558 + TCGA-B0-5110-01 COSM477326 c.1445G>A p.S482N Substitution - Missense 2:32406525-32406525 + TCGA-BS-A0UJ-01 COSM1020333 c.8482A>T p.T2828S Substitution - Missense 2:32499560-32499560 + TCGA-F4-6856-01 COSM1407795 c.4214delC p.R1406fs*3 Deletion - Frameshift 2:32442431-32442431 + CPCG0242-F1 COSM4880495 c.12870C>G p.A4290A Substitution - coding silent 2:32547909-32547909 + ESCC_132 COSM5642393 c.3347A>G p.N1116S Substitution - Missense 2:32433742-32433742 + ORL-48 COSM4591363 c.3994G>C p.V1332L Substitution - Missense TCGA-AA-A010-01 COSM279167 c.7789G>A p.A2597T Substitution - Missense 2:32485735-32485735 + TCGA-43-6647-01 COSM721153 c.14416G>A p.E4806K Substitution - Missense 2:32617746-32617746 + TCGA-BR-6452-01 COSM4093887 c.6290C>T p.S2097F Substitution - Missense 2:32469557-32469557 + CHC918T COSM3668664 c.6668T>C p.L2223P Substitution - Missense 2:32473187-32473187 + TCGA-AP-A0LM-01 COSM1020369 c.9850C>T p.R3284C Substitution - Missense 2:32508129-32508129 + TCGA-FS-A1ZE-06 COSM1020347 c.8669G>A p.R2890Q Substitution - Missense 2:32499747-32499747 + XHDG38 COSM4769679 c.2444C>A p.P815H Substitution - Missense 2:32415735-32415735 + YUDATE COSM1690421 c.4792T>C p.S1598P Substitution - Missense 2:32463232-32463232 + TCGA-F5-6814-01 COSM3426405 c.12005T>A p.I4002K Substitution - Missense 2:32529735-32529735 + TCGA-D1-A15X-01 COSM1020321 c.7561T>C p.Y2521H Substitution - Missense 2:32482447-32482447 + 587376 COSM1184741 c.9851G>A p.R3284H Substitution - Missense 2:32508130-32508130 + AA1924 COSM4168524 c.8416C>G p.Q2806E Substitution - Missense 2:32493615-32493615 + 49M COSM5589816 c.9661A>G p.K3221E Substitution - Missense 2:32505166-32505166 + WSU-HN8 COSM4591363 c.3994G>C p.V1332L Substitution - Missense PD4203a COSM159381 c.2722C>G p.Q908E Substitution - Missense 2:32416013-32416013 + TCGA-CG-5718-01 COSM4093897 c.8099C>G p.S2700* Substitution - Nonsense 2:32490044-32490044 + TCGA-CA-6718-01 COSM1407843 c.12068C>A p.S4023Y Substitution - Missense 2:32529798-32529798 + TCGA-BP-4977-01 COSM477340 c.5618T>G p.I1873S Substitution - Missense 2:32467949-32467949 + TCGA-A5-A0GB-01 COSM185700 c.7095G>A p.T2365T Substitution - coding silent 2:32478661-32478661 + HCT15 COSM2942606 c.10430C>A p.P3477H Substitution - Missense 2:32513016-32513016 + T578 COSM4665741 c.4038A>C p.E1346D Substitution - Missense 2:32442158-32442158 + TCGA-18-3407-01 COSM721174 c.12926C>T p.A4309V Substitution - Missense 2:32547965-32547965 + HCC134T COSM5818973 c.4962G>T p.K1654N Substitution - Missense 2:32464529-32464529 + LUAD-F00162 COSM391674 c.6347delG p.V2117fs*19 Deletion - Frameshift 2:32469614-32469614 + TCGA-G4-6588-01 COSM1407833 c.10750delA p.K3585fs*8 Deletion - Frameshift 2:32515171-32515171 + TCGA-AX-A0J0-01 COSM1020466 c.14328T>C p.D4776D Substitution - coding silent 2:32611516-32611516 + pfg129T COSM4752337 c.12544C>T p.Q4182* Substitution - Nonsense 2:32543493-32543493 + TCGA-D1-A17Q-01 COSM1020292 c.5345G>A p.R1782Q Substitution - Missense 2:32465153-32465153 + LUAD-LC15C COSM341904 c.3361C>G p.Q1121E Substitution - Missense 2:32433756-32433756 + TCGA-EE-A2GC-06 COSM1020266 c.3871C>T p.R1291W Substitution - Missense 2:32441389-32441389 + CSCC-10-T COSM4498496 c.5210C>T p.A1737V Substitution - Missense 2:32464777-32464777 + OSCC-GB_00630111 COSM4885092 c.1090C>A p.Q364K Substitution - Missense 2:32401218-32401218 + TCGA-66-2759-01 COSM721164 c.13588G>T p.A4530S Substitution - Missense 2:32595120-32595120 + TCGA-GD-A3OP-01 COSM1306734 c.4252G>T p.D1418Y Substitution - Missense 2:32443504-32443504 + RKO COSM4648593 c.5736G>A p.Q1912Q Substitution - coding silent 2:32468067-32468067 + 2492720 COSM1690428 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + TCGA-EI-6917-01 COSM1020248 c.3224G>A p.R1075Q Substitution - Missense 2:32431066-32431066 + pfg057T COSM4752329 c.7091C>T p.A2364V Substitution - Missense 2:32478657-32478657 + 20_tFL COSM4171165 c.10654G>A p.V3552I Substitution - Missense 2:32515075-32515075 + TCGA-BQ-5876-01 COSM3991277 c.5647T>C p.Y1883H Substitution - Missense 2:32467978-32467978 + MD-146 COSM301766 c.2624A>G p.E875G Substitution - Missense 2:32415915-32415915 + TCGA-CJ-5681-01 COSM477349 c.14196A>G p.R4732R Substitution - coding silent 2:32607580-32607580 + TCGA-B5-A11E-01 COSM1020198 c.1015G>A p.E339K Substitution - Missense 2:32395574-32395574 + 388 COSM3720973 c.4085T>G p.V1362G Substitution - Missense 2:32442205-32442205 + TCGA-D3-A5GO-06 COSM3581217 c.12330G>A p.K4110K Substitution - coding silent 2:32543279-32543279 + TCGA-DI-A0WH-01 COSM1020400 c.12190A>G p.T4064A Substitution - Missense 2:32531450-32531450 + 71 COSM4777767 c.1005_1006insC p.V336fs*7 Insertion - Frameshift 2:32395564-32395565 + CAL33 COSM4591363 c.3994G>C p.V1332L Substitution - Missense LUAD-NYU284 COSM372971 c.12343G>A p.D4115N Substitution - Missense 2:32543292-32543292 + NOKSI COSM4591363 c.3994G>C p.V1332L Substitution - Missense TCGA-A8-A0A6-01 COSM3839426 c.4802C>T p.T1601I Substitution - Missense 2:32463242-32463242 + TCGA-AN-A0AK-01 COSM3839419 c.380T>C p.I127T Substitution - Missense 2:32377642-32377642 + TCGA-D1-A16D-01 COSM1020353 c.8838G>T p.V2946V Substitution - coding silent 2:32499916-32499916 + TCGA-BR-7958-01 COSM4093877 c.4525G>A p.D1509N Substitution - Missense 2:32448835-32448835 + PCSI_0116_Pa_X COSM3380140 c.2158T>C p.L720L Substitution - coding silent 2:32415449-32415449 + TCGA-F5-6814-01 COSM3426401 c.8721A>G p.K2907K Substitution - coding silent 2:32499799-32499799 + T3431 COSM4665746 c.7612_7613insGAGGTCT p.G2541fs*22 Insertion - Frameshift 2:32482498-32482499 + 2521244 COSM5887203 c.1744C>T p.P582S Substitution - Missense 2:32415035-32415035 + 575 COSM3720971 c.358A>T p.I120F Substitution - Missense 2:32377620-32377620 + TCGA-D1-A17U-01 COSM1020326 c.7604C>A p.P2535H Substitution - Missense 2:32482490-32482490 + TCGA-DM-A28F-01 COSM1407809 c.6186C>G p.L2062L Substitution - coding silent 2:32469453-32469453 + TCGA-EV-5902-01 COSM3991275 c.4088A>C p.H1363P Substitution - Missense 2:32442208-32442208 + 449 COSM4435501 c.7974G>A p.E2658E Substitution - coding silent 2:32488593-32488593 + TCGA-G3-A25V-01 COSM4914547 c.1412G>A p.G471E Substitution - Missense 2:32401617-32401617 + TCGA-DD-A1EK-01 COSM4934335 c.376G>T p.V126F Substitution - Missense 2:32377638-32377638 + TCGA-AA-3510-01 COSM185744 c.14548G>T p.E4850* Substitution - Nonsense 2:32617878-32617878 + TCGA-CM-6162-01 COSM1407851 c.13349G>A p.R4450H Substitution - Missense 2:32575360-32575360 + TCGA-JX-A3Q0-01 COSM4824565 c.5609G>A p.R1870K Substitution - Missense 2:32467940-32467940 + CHC892T COSM4959513 c.6750G>A p.K2250K Substitution - coding silent 2:32476242-32476242 + TCGA-DK-A3X1-01 COSM3798962 c.949C>G p.Q317E Substitution - Missense 2:32392148-32392148 + TCGA-FW-A3R5-06 COSM1407821 c.8658C>T p.S2886S Substitution - coding silent 2:32499736-32499736 + ESCC_156 COSM5646024 c.884C>G p.S295* Substitution - Nonsense 2:32392083-32392083 + TCGA-DK-A3X1-01 COSM3798961 c.949C>G p.Q317E Substitution - Missense 2:32392148-32392148 + 1946219 COSM1578219 c.12095-1G>C p.? Unknown 2:32531354-32531354 + YURTHE COSM1690426 c.6382T>C p.S2128P Substitution - Missense 2:32470202-32470202 + TCGA-D3-A2JN-06 COSM3581183 c.2902G>A p.G968R Substitution - Missense 2:32429175-32429175 + TCGA-D7-A4YY-01 COSM4093869 c.3324C>T p.F1108F Substitution - coding silent 2:32433719-32433719 + BICR_22 COSM4591363 c.3994G>C p.V1332L Substitution - Missense ATL088 COSM5708191 c.8721A>C p.K2907N Substitution - Missense 2:32499799-32499799 + TCGA-B5-A11O-01 COSM1020230 c.2353G>T p.E785* Substitution - Nonsense 2:32415644-32415644 + ESO-752 COSM1246127 c.5568G>A p.M1856I Substitution - Missense 2:32467736-32467736 + TCGA-BR-A4QL-01 COSM4093856 c.1274A>T p.E425V Substitution - Missense 2:32401479-32401479 + TCGA-AP-A0LM-01 COSM1020434 c.13616C>T p.T4539M Substitution - Missense 2:32597754-32597754 + STC291 COSM5058881 c.10326G>A p.Q3442Q Substitution - coding silent 2:32510614-32510614 + AIMAH5 COSM5961815 c.12264C>T p.P4088P Substitution - coding silent 2:32531524-32531524 + TCGA-BR-8680-01 COSM4093862 c.2264A>C p.E755A Substitution - Missense 2:32415555-32415555 + OSCC-GB_00630111 COSM4885091 c.1090C>A p.Q364K Substitution - Missense 2:32401218-32401218 + P05-3859 COSM243205 c.11294C>T p.A3765V Substitution - Missense 2:32515715-32515715 + 18_tFL COSM4171160 c.1004T>C p.L335P Substitution - Missense 2:32395563-32395563 + HCC074T COSM5810060 c.13954A>T p.S4652C Substitution - Missense 2:32599862-32599862 + TCGA-G2-A2EF-01 COSM1306728 c.1342G>A p.D448N Substitution - Missense 2:32401547-32401547 + TCGA-AP-A0LM-01 COSM1020219 c.1967G>T p.S656I Substitution - Missense 2:32415258-32415258 + T2269 COSM4665766 c.14212T>C p.W4738R Substitution - Missense 2:32607596-32607596 + CA2 COSM1166144 c.11777G>A p.R3926H Substitution - Missense 2:32525485-32525485 + T3094 COSM4665737 c.600delA p.N202fs*27 Deletion - Frameshift 2:32380245-32380245 + CSCC-11-T COSM4555375 c.6525G>T p.V2175V Substitution - coding silent 2:32471057-32471057 + TCGA-FU-A3HZ-01 COSM4840923 c.6219G>T p.K2073N Substitution - Missense 2:32469486-32469486 + T2269 COSM4665758 c.10810G>A p.A3604T Substitution - Missense 2:32515231-32515231 + B102-Tumor COSM3933636 c.13469C>T p.A4490V Substitution - Missense 2:32594028-32594028 + TCGA-BS-A0UV-01 COSM1020242 c.2658G>T p.K886N Substitution - Missense 2:32415949-32415949 + sysucc-707T COSM1614797 c.9980+10G>T p.? Unknown 2:32508269-32508269 + TCGA-AA-3492-01 COSM1407826 c.9156G>T p.M3052I Substitution - Missense 2:32501837-32501837 + TCGA-BR-7958-01 COSM4093876 c.4525G>A p.D1509N Substitution - Missense 2:32448835-32448835 + 85 COSM5010806 c.13885G>A p.D4629N Substitution - Missense 2:32599793-32599793 + T578 COSM4665756 c.10098G>T p.L3366F Substitution - Missense 2:32509855-32509855 + TCGA-D1-A17Q-01 COSM1020243 c.2763A>C p.E921D Substitution - Missense 2:32416054-32416054 + YUGOE COSM1690428 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + ESCC_BICR_052T COSM5434713 c.1056C>T p.S352S Substitution - coding silent 2:32401184-32401184 + TCGA-CG-5721-01 COSM4093871 c.3680T>C p.V1227A Substitution - Missense 2:32439556-32439556 + CHC1744T COSM4792299 c.12573G>A p.V4191V Substitution - coding silent 2:32543522-32543522 + TCGA-AX-A05Z-01 COSM1020203 c.1224G>T p.K408N Substitution - Missense 2:32401352-32401352 + TCGA-B5-A1MY-01 COSM1020463 c.14296A>T p.I4766L Substitution - Missense 2:32611484-32611484 + GC_296T1-GC_296N COSM4772103 c.8174G>A p.S2725N Substitution - Missense 2:32490119-32490119 + HCC25 COSM1614787 c.4541G>T p.G1514V Substitution - Missense 2:32448851-32448851 + TCGA-18-3407-01 COSM721175 c.12926C>T p.A4309V Substitution - Missense 2:32547965-32547965 + HCC127T COSM5822803 c.1091A>T p.Q364L Substitution - Missense 2:32401219-32401219 + PT36 COSM5914876 c.5594G>A p.G1865E Substitution - Missense 2:32467925-32467925 + 587342 COSM1184735 c.13993-2A>C p.? Unknown 2:32603004-32603004 + TCGA-EE-A2GC-06 COSM1020264 c.3871C>T p.R1291W Substitution - Missense 2:32441389-32441389 + BCM723T COSM4956331 c.5990C>T p.A1997V Substitution - Missense 2:32468646-32468646 + LUAD-LC15C COSM341903 c.3361C>G p.Q1121E Substitution - Missense 2:32433756-32433756 + TCGA-AG-A02N-01 COSM5074801 c.7420C>A p.L2474M Substitution - Missense 2:32481331-32481331 + 53M COSM5594265 c.7431G>A p.L2477L Substitution - coding silent 2:32481342-32481342 + S0075 COSM5883445 c.425G>C p.G142A Substitution - Missense 2:32377687-32377687 + TCGA-AA-A00N-01 COSM298593 c.509C>G p.A170G Substitution - Missense 2:32380154-32380154 + TCGA-34-5239-01 COSM721216 c.3752A>T p.H1251L Substitution - Missense 2:32439628-32439628 + HCC46T COSM3709617 c.1170C>T p.C390C Substitution - coding silent 2:32401298-32401298 + CHC892T COSM4959513 c.6750G>A p.K2250K Substitution - coding silent 2:32476242-32476242 + TCGA-G2-A2ES-01 COSM1306725 c.1254G>A p.M418I Substitution - Missense 2:32401382-32401382 + TCGA-37-3789-01 COSM721171 c.13027C>G p.Q4343E Substitution - Missense 2:32549364-32549364 + LUAD-B01811 COSM334457 c.12810+1G>T p.? Unknown 2:32545861-32545861 + 18 COSM5744717 c.7042G>A p.A2348T Substitution - Missense 2:32477557-32477557 + TCGA-A3-3346-01 COSM1494915 c.10579A>T p.N3527Y Substitution - Missense 2:32515000-32515000 + 044-05-01TD COSM1317093 c.11060T>G p.L3687R Substitution - Missense 2:32515481-32515481 + BN02T COSM1614793 c.6955C>T p.L2319F Substitution - Missense 2:32477470-32477470 + UM-SCC-47 COSM4591362 c.3994G>C p.V1332L Substitution - Missense MB_Exm23 COSM215877 c.2059T>A p.Y687N Substitution - Missense 2:32415350-32415350 + TCGA-B6-A0IJ-01 COSM442821 c.2286A>G p.Q762Q Substitution - coding silent 2:32415577-32415577 + SWE-16 COSM1178946 c.8238G>T p.E2746D Substitution - Missense 2:32491456-32491456 + BCM723T COSM4956331 c.5990C>T p.A1997V Substitution - Missense 2:32468646-32468646 + TCGA-D1-A16Y-01 COSM1020285 c.5167G>A p.E1723K Substitution - Missense 2:32464734-32464734 + RK175_C01 COSM3743781 c.4346A>G p.Y1449C Substitution - Missense 2:32445530-32445530 + D-10 COSM4766217 c.7904C>A p.S2635Y Substitution - Missense 2:32487737-32487737 + TCGA-18-3419-01 COSM721188 c.10900C>G p.L3634V Substitution - Missense 2:32515321-32515321 + 10-P8045 COSM2942207 c.1542A>G p.Q514Q Substitution - coding silent 2:32414833-32414833 + SCC-15 COSM4592547 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + TCGA-AZ-4315-01 COSM1407810 c.6380G>T p.R2127I Substitution - Missense 2:32470200-32470200 + TCGA-D1-A16E-01 COSM1020258 c.3653G>T p.R1218L Substitution - Missense 2:32439529-32439529 + YUKIL COSM1690431 c.7667C>T p.S2556L Substitution - Missense 2:32482553-32482553 + CAL33 COSM4591362 c.3994G>C p.V1332L Substitution - Missense CHC892T COSM4959514 c.6750G>A p.K2250K Substitution - coding silent 2:32476242-32476242 + TCGA-BR-4184-01 COSM4093880 c.4714T>C p.S1572P Substitution - Missense 2:32453903-32453903 + T3094 COSM4665764 c.13501+2T>C p.? Unknown 2:32594062-32594062 + PR-3127 COSM243203 c.2825C>T p.S942F Substitution - Missense 2:32416116-32416116 + tumor_4174905 COSM3357581 c.14179T>C p.Y4727H Substitution - Missense 2:32607563-32607563 + TCGA-AG-A02N-01 COSM5074800 c.7420C>A p.L2474M Substitution - Missense 2:32481331-32481331 + TCGA-EI-6882-01 COSM5079034 c.13502-1_13502insA p.L4504fs*3 Unknown 2:32595033-32595034 + PD3181a COSM1659124 c.9339T>C p.T3113T Substitution - coding silent 2:32503076-32503076 + TCGA-BS-A0UF-01 COSM1020255 c.3455A>G p.D1152G Substitution - Missense 2:32435541-32435541 + YUWALI COSM1690429 c.7627C>T p.P2543S Substitution - Missense 2:32482513-32482513 + S15_post COSM5574433 c.7960C>G p.H2654D Substitution - Missense 2:32487793-32487793 + ACINAR03 COSM1734261 c.12455C>A p.P4152H Substitution - Missense 2:32543404-32543404 + TCGA-AA-A00N-01 COSM274135 c.12277G>T p.E4093* Substitution - Nonsense 2:32531537-32531537 + 423 COSM4432526 c.11776C>T p.R3926C Substitution - Missense 2:32525484-32525484 + TCGA-18-3409-01 COSM721176 c.12379G>A p.E4127K Substitution - Missense 2:32543328-32543328 + TCGA-BR-8680-01 COSM4093899 c.8140A>C p.T2714P Substitution - Missense 2:32490085-32490085 + 1910787 COSM1293102 c.2182G>T p.E728* Substitution - Nonsense 2:32415473-32415473 + TCGA-D3-A3MU-06 COSM3581214 c.12019A>T p.K4007* Substitution - Nonsense 2:32529749-32529749 + TCGA-DK-A1AC-01 COSM1306750 c.11479C>T p.Q3827* Substitution - Nonsense 2:32518383-32518383 + TCGA-BS-A0UF-01 COSM1020257 c.3455A>G p.D1152G Substitution - Missense 2:32435541-32435541 + 1_PRE-TREATMENT COSM1718163 c.13084G>C p.E4362Q Substitution - Missense 2:32549421-32549421 + 20_tFL COSM4171164 c.10654G>A p.V3552I Substitution - Missense 2:32515075-32515075 + CHC2216T COSM4806002 c.14337G>A p.Q4779Q Substitution - coding silent 2:32611525-32611525 + TCGA-09-1670-01 COSM1327099 c.1973A>T p.H658L Substitution - Missense 2:32415264-32415264 + TCGA-AX-A0J0-01 COSM1020329 c.7680C>T p.S2560S Substitution - coding silent 2:32482566-32482566 + TCGA-BR-8363-01 COSM4093882 c.4834G>A p.A1612T Substitution - Missense 2:32463274-32463274 + TCGA-AX-A060-01 COSM1020390 c.11315C>T p.S3772L Substitution - Missense 2:32515736-32515736 + SCC-25 COSM4591362 c.3994G>C p.V1332L Substitution - Missense ACA4 COSM5961409 c.12857A>G p.Q4286R Substitution - Missense 2:32547896-32547896 + TCGA-AX-A0J1-01 COSM1020231 c.2504G>A p.R835Q Substitution - Missense 2:32415795-32415795 + BN02T COSM1614792 c.6955C>T p.L2319F Substitution - Missense 2:32477470-32477470 + TCGA-25-1318-01 COSM117136 c.14015C>T p.T4672M Substitution - Missense 2:32603028-32603028 + TCGA-AX-A0J1-01 COSM1020195 c.1006G>A p.V336I Substitution - Missense 2:32395565-32395565 + TCGA-D1-A15X-01 COSM1020311 c.6872G>A p.R2291H Substitution - Missense 2:32477387-32477387 + TCGA-FS-A1ZQ-06 COSM3581201 c.8616T>C p.T2872T Substitution - coding silent 2:32499694-32499694 + TCGA-BR-4362-01 COSM4093858 c.1301T>C p.V434A Substitution - Missense 2:32401506-32401506 + 43_tFL COSM4171167 c.11815A>G p.R3939G Substitution - Missense 2:32525523-32525523 + TCGA-JW-A5VL-01 COSM4847378 c.588C>G p.L196L Substitution - coding silent 2:32380233-32380233 + PD3181a COSM1659125 c.9339T>C p.T3113T Substitution - coding silent 2:32503076-32503076 + CP66-MEL COSM14001 c.9024G>A p.M3008I Substitution - Missense 2:32500102-32500102 + C086 COSM5527364 c.13897C>T p.P4633S Substitution - Missense 2:32599805-32599805 + OSCC-GB_00600111 COSM4890268 c.13732C>G p.L4578V Substitution - Missense 2:32597870-32597870 + OSCC-GB_00990111 COSM4885716 c.13727G>A p.R4576H Substitution - Missense 2:32597865-32597865 + TCGA-DA-A1HV-06 COSM3581192 c.7704T>A p.D2568E Substitution - Missense 2:32485650-32485650 + PD13162a COSM5779915 c.6976G>T p.E2326* Substitution - Nonsense 2:32477491-32477491 + TCGA-G2-A2ES-01 COSM1306743 c.10416G>T p.M3472I Substitution - Missense 2:32513002-32513002 + PD4127a COSM159378 c.7184G>T p.G2395V Substitution - Missense 2:32478750-32478750 + TCGA-D9-A6EC-06 COSM4402143 c.10470T>A p.S3490S Substitution - coding silent 2:32513056-32513056 + ESCC_BICR_046T COSM5441956 c.6656G>T p.G2219V Substitution - Missense 2:32473175-32473175 + CHC1602T COSM4789051 c.4813G>A p.A1605T Substitution - Missense 2:32463253-32463253 + TCGA-FS-A1Z3-06 COSM3581206 c.9952C>T p.P3318S Substitution - Missense 2:32508231-32508231 + TCGA-A8-A09Z-01 COSM3839421 c.1455T>C p.H485H Substitution - coding silent 2:32406535-32406535 + GCT27 COSM5749314 c.2161A>G p.R721G Substitution - Missense 2:32415452-32415452 + TCGA-60-2698-01 COSM721213 c.4606G>T p.D1536Y Substitution - Missense 2:32448916-32448916 + LUAD-RT-S01709 COSM379916 c.2909G>T p.C970F Substitution - Missense 2:32429182-32429182 + T2458 COSM4665754 c.9881C>A p.S3294* Substitution - Nonsense 2:32508160-32508160 + NOKSI COSM4591362 c.3994G>C p.V1332L Substitution - Missense WA15 COSM238967 c.5571G>T p.K1857N Substitution - Missense 2:32467739-32467739 + TCGA-G4-6588-01 COSM1407832 c.10750delA p.K3585fs*8 Deletion - Frameshift 2:32515171-32515171 + CPCG0242-F1 COSM4880494 c.12870C>G p.A4290A Substitution - coding silent 2:32547909-32547909 + GC8_T COSM148833 c.8020A>T p.T2674S Substitution - Missense 2:32488639-32488639 + CRC-19T COSM5482382 c.9500-12_9500-8delTATCT p.? Unknown 2:32504993-32504997 + TCGA-42-2589-01 COSM1327097 c.3488A>C p.E1163A Substitution - Missense 2:32435574-32435574 + TCGA-AR-A24H-01 COSM1483063 c.3097A>G p.T1033A Substitution - Missense 2:32430939-32430939 + EGC3 COSM1020311 c.6872G>A p.R2291H Substitution - Missense 2:32477387-32477387 + RK023_C01 COSM1631983 c.5101A>T p.T1701S Substitution - Missense 2:32464668-32464668 + LP6005334-DNA_E01 COSM4412575 c.6617A>G p.N2206S Substitution - Missense 2:32473136-32473136 + TCGA-JW-A5VL-01 COSM4847377 c.588C>G p.L196L Substitution - coding silent 2:32380233-32380233 + TCGA-BF-A1Q0-01 COSM3581195 c.7817C>T p.S2606L Substitution - Missense 2:32487650-32487650 + CHC1600T COSM4791532 c.13318A>G p.M4440V Substitution - Missense 2:32575329-32575329 + BCM791T COSM4803024 c.7002A>C p.K2334N Substitution - Missense 2:32477517-32477517 + TCGA-60-2724-01 COSM721199 c.9523A>T p.T3175S Substitution - Missense 2:32505028-32505028 + TCGA-F5-6814-01 COSM3426404 c.12005T>A p.I4002K Substitution - Missense 2:32529735-32529735 + T3557 COSM4665747 c.7749G>A p.L2583L Substitution - coding silent 2:32485695-32485695 + TCGA-B5-A0JY-01 COSM1020393 c.11338C>T p.L3780L Substitution - coding silent 2:32515759-32515759 + TCGA-60-2720-01 COSM721160 c.13827G>C p.M4609I Substitution - Missense 2:32597965-32597965 + TCGA-B5-A11E-01 COSM721203 c.8928G>A p.S2976S Substitution - coding silent 2:32500006-32500006 + TCGA-EE-A2GR-06 COSM3581190 c.7522C>T p.L2508F Substitution - Missense 2:32481433-32481433 + TCGA-60-2720-01 COSM721161 c.13827G>C p.M4609I Substitution - Missense 2:32597965-32597965 + 587376 COSM1184740 c.9851G>A p.R3284H Substitution - Missense 2:32508130-32508130 + TCGA-EE-A2M5-06 COSM3581211 c.10976T>A p.I3659N Substitution - Missense 2:32515397-32515397 + TCGA-B0-5104-01 COSM477335 c.4581C>A p.V1527V Substitution - coding silent 2:32448891-32448891 + T3431 COSM4665745 c.7612_7613insGAGGTCT p.G2541fs*22 Insertion - Frameshift 2:32482498-32482499 + LUAD-RT-S01709 COSM379915 c.2909G>T p.C970F Substitution - Missense 2:32429182-32429182 + sysucc-311T COSM5465547 c.13612+10A>C p.? Unknown 2:32595154-32595154 + HCC49T COSM1614790 c.5595G>T p.G1865G Substitution - coding silent 2:32467926-32467926 + ESO-2143 COSM1246123 c.13931A>T p.N4644I Substitution - Missense 2:32599839-32599839 + 423 COSM4432525 c.11776C>T p.R3926C Substitution - Missense 2:32525484-32525484 + TCGA-DA-A1IA-06 COSM1690441 c.14046T>G p.N4682K Substitution - Missense 2:32603059-32603059 + TCGA-F4-6808-01 COSM1407847 c.13180G>T p.A4394S Substitution - Missense 2:32575191-32575191 + CHC892T COSM4796729 c.5256+1G>A p.? Unknown 2:32464824-32464824 + PT53 COSM5941180 c.2243G>A p.G748E Substitution - Missense 2:32415534-32415534 + HCC090T COSM5810785 c.3200A>G p.H1067R Substitution - Missense 2:32431042-32431042 + CDGLIV0504A0086_T COSM5041840 c.7828A>T p.T2610S Substitution - Missense 2:32487661-32487661 + 044-0092-01TD COSM1317093 c.11060T>G p.L3687R Substitution - Missense 2:32515481-32515481 + TCGA-BR-8680-01 COSM259642 c.11698G>T p.E3900* Substitution - Nonsense 2:32524962-32524962 + TCGA-B5-A11E-01 COSM1020428 c.13487G>A p.R4496Q Substitution - Missense 2:32594046-32594046 + ESCC_124 COSM5641003 c.5218C>G p.L1740V Substitution - Missense 2:32464785-32464785 + 2521259 COSM5889654 c.1055C>T p.S352F Substitution - Missense 2:32401183-32401183 + LUAD-YINHD COSM350633 c.10015A>T p.T3339S Substitution - Missense 2:32509772-32509772 + RK220_C01 COSM3743783 c.14229A>T p.Q4743H Substitution - Missense 2:32607613-32607613 + TCGA-B5-A0JY-01 COSM185696 c.5366G>T p.R1789I Substitution - Missense 2:32467534-32467534 + TCGA-CM-4743-01 COSM1407789 c.3605C>T p.T1202M Substitution - Missense 2:32436158-32436158 + T578 COSM4665742 c.4038A>C p.E1346D Substitution - Missense 2:32442158-32442158 + S00825 COSM5659195 c.4832C>T p.S1611L Substitution - Missense 2:32463272-32463272 + 2521259 COSM5889652 c.6163C>T p.H2055Y Substitution - Missense 2:32469430-32469430 + TCGA-A6-6650-01 COSM3695486 c.10796C>T p.A3599V Substitution - Missense 2:32515217-32515217 + YUWAND COSM1690428 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + BD114T COSM5502463 c.5044G>A p.A1682T Substitution - Missense 2:32464611-32464611 + YUQUEST COSM5396932 c.3209C>T p.A1070V Substitution - Missense 2:32431051-32431051 + 2492723 COSM1690427 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + TCGA-A8-A097-01 COSM442832 c.13846C>A p.P4616T Substitution - Missense 2:32599754-32599754 + WSU-HN12 COSM4592548 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + TCGA-85-6560-01 COSM721203 c.8928G>A p.S2976S Substitution - coding silent 2:32500006-32500006 + TCGA-BQ-5876-01 COSM3991276 c.5647T>C p.Y1883H Substitution - Missense 2:32467978-32467978 + 587342 COSM1184734 c.13993-2A>C p.? Unknown 2:32603004-32603004 + TCGA-D1-A103-01 COSM1020457 c.14195G>A p.R4732Q Substitution - Missense 2:32607579-32607579 + TCGA-G4-6294-01 COSM3695484 c.9821T>C p.V3274A Substitution - Missense 2:32508100-32508100 + AA1924 COSM4168523 c.8416C>G p.Q2806E Substitution - Missense 2:32493615-32493615 + TCGA-FS-A1ZQ-06 COSM3581203 c.8619C>T p.C2873C Substitution - coding silent 2:32499697-32499697 + CHC1602T COSM4789051 c.4813G>A p.A1605T Substitution - Missense 2:32463253-32463253 + TCGA-FW-A3R5-06 COSM3910251 c.5065C>T p.H1689Y Substitution - Missense 2:32464632-32464632 + TCGA-AG-A002-01 COSM259637 c.2005G>T p.E669* Substitution - Nonsense 2:32415296-32415296 + TCGA-AG-A002-01 COSM259638 c.4145G>A p.R1382Q Substitution - Missense 2:32442362-32442362 + TCGA-21-1077-01 COSM721156 c.14171C>T p.S4724F Substitution - Missense 2:32607555-32607555 + S00825 COSM5659194 c.4832C>T p.S1611L Substitution - Missense 2:32463272-32463272 + TCGA-66-2795-01 COSM721167 c.13107C>G p.L4369L Substitution - coding silent 2:32549444-32549444 + RK228_C01 COSM4944799 c.3632-1G>C p.? Unknown 2:32439507-32439507 + LP6005334-DNA_E01 COSM4412574 c.6617A>G p.N2206S Substitution - Missense 2:32473136-32473136 + HX23T COSM3709620 c.3258G>A p.W1086* Substitution - Nonsense 2:32433653-32433653 + TCGA-FW-A3TV-06 COSM3581170 c.548T>A p.I183N Substitution - Missense 2:32380193-32380193 + sysucc-1135T COSM1020454 c.14194C>T p.R4732* Substitution - Nonsense 2:32607578-32607578 + ZZUFHECRKL-G003T COSM5430936 c.12168A>G p.I4056M Substitution - Missense 2:32531428-32531428 + TCGA-AP-A051-01 COSM1020227 c.2256C>T p.C752C Substitution - coding silent 2:32415547-32415547 + TCGA-E2-A574-01 COSM3839438 c.13100C>T p.S4367F Substitution - Missense 2:32549437-32549437 + TCGA-AX-A05Z-01 COSM1020409 c.12493C>A p.L4165I Substitution - Missense 2:32543442-32543442 + ATL044 COSM5708194 c.14539A>T p.S4847C Substitution - Missense 2:32617869-32617869 + CHC2216T COSM4805993 c.14368A>T p.M4790L Substitution - Missense 2:32611556-32611556 + 587376 COSM1184737 c.3816A>C p.K1272N Substitution - Missense 2:32441334-32441334 + TCGA-GF-A6C9-06 COSM4902508 c.8854G>A p.D2952N Substitution - Missense 2:32499932-32499932 + TCGA-CM-5861-01 COSM1407830 c.10725T>C p.H3575H Substitution - coding silent 2:32515146-32515146 + TCGA-E2-A574-01 COSM3839437 c.13100C>T p.S4367F Substitution - Missense 2:32549437-32549437 + HT115 COSM2942364 c.4610T>C p.V1537A Substitution - Missense 2:32448920-32448920 + ESCC-154T COSM3939079 c.9396T>C p.F3132F Substitution - coding silent 2:32503133-32503133 + 2492721 COSM1690428 c.6871C>T p.R2291C Substitution - Missense 2:32477386-32477386 + T3118 COSM4665744 c.4434_4437delCAGA p.R1479fs*6 Deletion - Frameshift 2:32445618-32445621 + 587228 COSM1184727 c.5783A>T p.Y1928F Substitution - Missense 2:32468439-32468439 + BK0030 COSM4186815 c.2068C>T p.Q690* Substitution - Nonsense 2:32415359-32415359 + YUKLAB COSM1690423 c.5663A>G p.E1888G Substitution - Missense 2:32467994-32467994 + TCGA-BP-4762-01 COSM574915 c.826C>T p.R276C Substitution - Missense 2:32388930-32388930 + HX23T COSM3709619 c.3258G>A p.W1086* Substitution - Nonsense 2:32433653-32433653 + TCGA-D1-A103-01 COSM1020336 c.8521G>T p.E2841* Substitution - Nonsense 2:32499599-32499599 + RK212_C01 COSM3743778 c.2199A>G p.I733M Substitution - Missense 2:32415490-32415490 + HCT15 COSM2942607 c.10430C>A p.P3477H Substitution - Missense 2:32513016-32513016 + HT115 COSM2942776 c.13961G>A p.R4654Q Substitution - Missense 2:32599869-32599869 + sysucc-707T COSM1614796 c.9980+10G>T p.? Unknown 2:32508269-32508269 + TCGA-D3-A3MV-06 COSM3581178 c.1935C>T p.I645I Substitution - coding silent 2:32415226-32415226 + TCGA-BR-A4QL-01 COSM4093857 c.1274A>T p.E425V Substitution - Missense 2:32401479-32401479 + TCGA-ED-A7PY-01 COSM4926557 c.2666T>C p.F889S Substitution - Missense 2:32415957-32415957 + PT23_2 COSM5903379 c.7968G>A p.Q2656Q Substitution - coding silent 2:32487801-32487801 + S00825 COSM5659193 c.3205G>A p.D1069N Substitution - Missense 2:32431047-32431047 + 12-P616 COSM4583474 c.12978T>C p.V4326V Substitution - coding silent 2:32549315-32549315 + TCGA-59-2352-01 COSM78882 c.2061C>G p.Y687* Substitution - Nonsense 2:32415352-32415352 + TCGA-EK-A3GK-01 COSM1306740 c.4662C>T p.F1554F Substitution - coding silent 2:32453851-32453851 + TCGA-A5-A0GP-01 COSM259642 c.11698G>T p.E3900* Substitution - Nonsense 2:32524962-32524962 + Detroit_562 COSM4591362 c.3994G>C p.V1332L Substitution - Missense YUDIALE COSM1690438 c.10597C>T p.P3533S Substitution - Missense 2:32515018-32515018 + ESCC-148T COSM3939072 c.1216C>T p.R406* Substitution - Nonsense 2:32401344-32401344 + SCC-15 COSM4592548 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + 10-P8045 COSM4583472 c.1378T>C p.S460P Substitution - Missense 2:32401583-32401583 + HCC139T COSM1614796 c.9980+10G>T p.? Unknown 2:32508269-32508269 + MZ1-PC COSM21790 c.11474T>C p.F3825S Substitution - Missense 2:32518378-32518378 + TCGA-D3-A3MV-06 COSM3581179 c.1935C>T p.I645I Substitution - coding silent 2:32415226-32415226 + 1910786 COSM1293101 c.2182G>T p.E728* Substitution - Nonsense 2:32415473-32415473 + TCGA-37-3789-01 COSM721170 c.13027C>G p.Q4343E Substitution - Missense 2:32549364-32549364 + TCGA-BH-A1FJ-01 COSM1483060 c.2308_2310delAAT p.N770delN Deletion - In frame 2:32415599-32415601 + TCGA-DD-A1EC-01 COSM4938169 c.5567T>C p.M1856T Substitution - Missense 2:32467735-32467735 + CCK81 COSM2942766 c.13669T>C p.Y4557H Substitution - Missense 2:32597807-32597807 + Au4 COSM5602905 c.8213C>T p.S2738F Substitution - Missense 2:32491431-32491431 + 2492729 COSM5726304 c.7423T>C p.S2475P Substitution - Missense 2:32481334-32481334 + YUKIL COSM1690432 c.7667C>T p.S2556L Substitution - Missense 2:32482553-32482553 + I2L-P19Ta-Tumor-Biopsy COSM5354155 c.2843G>A p.G948D Substitution - Missense 2:32416134-32416134 + TCGA-F5-6814-01 COSM1020240 c.2658G>T p.K886N Substitution - Missense 2:32415949-32415949 + TCGA-G4-6297-01 COSM3695482 c.7265C>T p.A2422V Substitution - Missense 2:32479474-32479474 + TCGA-BR-7957-01 COSM4093921 c.13861T>A p.Y4621N Substitution - Missense 2:32599769-32599769 + CHC892T COSM4796730 c.5256+1G>A p.? Unknown 2:32464824-32464824 + HCT8 COSM4634834 c.4070G>A p.C1357Y Substitution - Missense 2:32442190-32442190 + TCGA-GD-A3OP-01 COSM1306735 c.4394G>A p.G1465E Substitution - Missense 2:32445578-32445578 + CHC1207T COSM4800186 c.7832G>A p.G2611E Substitution - Missense 2:32487665-32487665 + TCGA-D1-A103-01 COSM1020442 c.13745C>A p.A4582D Substitution - Missense 2:32597883-32597883 + CSCC-31-T COSM4499963 c.5549C>T p.P1850L Substitution - Missense 2:32467717-32467717 + TCGA-AP-A0LM-01 COSM1020367 c.9850C>T p.R3284C Substitution - Missense 2:32508129-32508129 + HCC87T COSM1614795 c.8530C>G p.L2844V Substitution - Missense 2:32499608-32499608 + CHC1744T COSM4792298 c.12573G>A p.V4191V Substitution - coding silent 2:32543522-32543522 + TCGA-AX-A060-01 COSM1020388 c.11315C>T p.S3772L Substitution - Missense 2:32515736-32515736 + 8057482 COSM3391707 c.73G>A p.A25T Substitution - Missense 2:32357234-32357234 + 587222 COSM1184732 c.4810G>T p.E1604* Substitution - Nonsense 2:32463250-32463250 + WSU-HN13 COSM4592548 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + 1_RESISTANT COSM1718163 c.13084G>C p.E4362Q Substitution - Missense 2:32549421-32549421 + 062T COSM1730128 c.4973C>G p.T1658R Substitution - Missense 2:32464540-32464540 + YUKAT COSM5396929 c.934G>A p.A312T Substitution - Missense 2:32392133-32392133 + LUAD-NYU195 COSM371096 c.9208-1G>T p.? Unknown 2:32502794-32502794 + DN110CD COSM5779915 c.6976G>T p.E2326* Substitution - Nonsense 2:32477491-32477491 + TCGA-EE-A2A0-06 COSM3581172 c.1162A>G p.I388V Substitution - Missense 2:32401290-32401290 + CHC2216T COSM4806001 c.14337G>A p.Q4779Q Substitution - coding silent 2:32611525-32611525 + ESCC-148T COSM3939073 c.1216C>T p.R406* Substitution - Nonsense 2:32401344-32401344 + 2492721 COSM5719570 c.12489A>C p.L4163F Substitution - Missense 2:32543438-32543438 + TCGA-B5-A11O-01 COSM1020280 c.4301_4303delATA p.N1435delN Deletion - In frame 2:32443553-32443555 + TCGA-D1-A103-01 COSM1020338 c.8521G>T p.E2841* Substitution - Nonsense 2:32499599-32499599 + TCGA-CK-5916-01 COSM1407819 c.7588A>T p.T2530S Substitution - Missense 2:32482474-32482474 + OSCC-GB_00600111 COSM4890267 c.13732C>G p.L4578V Substitution - Missense 2:32597870-32597870 + ESCC_BICR_023T COSM5436462 c.7213C>T p.Q2405* Substitution - Nonsense 2:32478779-32478779 + PD24216a COSM5800558 c.14176G>A p.E4726K Substitution - Missense 2:32607560-32607560 + tumor_4174905 COSM3357582 c.14179T>C p.Y4727H Substitution - Missense 2:32607563-32607563 + TCGA-AA-A00N-01 COSM274137 c.14174G>A p.R4725Q Substitution - Missense 2:32607558-32607558 + TCGA-BS-A0UJ-01 COSM1020310 c.6515T>C p.V2172A Substitution - Missense 2:32471047-32471047 + TCGA-19-1790-01 COSM3407830 c.7731G>A p.Q2577Q Substitution - coding silent 2:32485677-32485677 + LUAD-S01346 COSM397722 c.9740G>A p.G3247E Substitution - Missense 2:32508019-32508019 + CSCC-57-T COSM4571952 c.594T>C p.D198D Substitution - coding silent 2:32380239-32380239 + PCSI_0083_Pa_P COSM3380142 c.12778C>T p.R4260* Substitution - Nonsense 2:32545828-32545828 + HCC13T COSM3746541 c.3656C>T p.S1219L Substitution - Missense 2:32439532-32439532 + TCGA-66-2759-01 COSM721165 c.13588G>T p.A4530S Substitution - Missense 2:32595120-32595120 + T2258 COSM4665751 c.9094G>T p.V3032F Substitution - Missense 2:32501775-32501775 + TCGA-BS-A0UA-01 COSM1020192 c.811G>A p.G271R Substitution - Missense 2:32388915-32388915 + RK119_C01 COSM3743777 c.1089A>G p.T363T Substitution - coding silent 2:32401217-32401217 + T2458 COSM4665753 c.9881C>A p.S3294* Substitution - Nonsense 2:32508160-32508160 + BRC5 COSM5025601 c.2620T>G p.C874G Substitution - Missense 2:32415911-32415911 + TCGA-66-2770-01 COSM721179 c.11946A>G p.T3982T Substitution - coding silent 2:32529676-32529676 + LUAD-S01405 COSM399099 c.3066G>T p.L1022F Substitution - Missense 2:32430908-32430908 + 2497766 COSM5750265 c.425G>T p.G142V Substitution - Missense 2:32377687-32377687 + 044 COSM1317093 c.11060T>G p.L3687R Substitution - Missense 2:32515481-32515481 + TCGA-61-2109-01 COSM118356 c.4893A>C p.L1631L Substitution - coding silent 2:32463333-32463333 + TCGA-EV-5902-01 COSM3991274 c.4088A>C p.H1363P Substitution - Missense 2:32442208-32442208 + YUKAT COSM5396930 c.934G>A p.A312T Substitution - Missense 2:32392133-32392133 + TCGA-D1-A15X-01 COSM1020313 c.6872G>A p.R2291H Substitution - Missense 2:32477387-32477387 + TCGA-BT-A3PJ-01 COSM1020454 c.14194C>T p.R4732* Substitution - Nonsense 2:32607578-32607578 + TCGA-EE-A2GN-06 COSM3581223 c.13179G>A p.R4393R Substitution - coding silent 2:32575190-32575190 + ZZUFHECRKL-G067T COSM5438716 c.7475T>C p.M2492T Substitution - Missense 2:32481386-32481386 + ACA4 COSM5961408 c.12857A>G p.Q4286R Substitution - Missense 2:32547896-32547896 + PCSI_0083_Pa_P_526 COSM3380143 c.12778C>T p.R4260* Substitution - Nonsense 2:32545828-32545828 + RK175_C01 COSM3743780 c.4346A>G p.Y1449C Substitution - Missense 2:32445530-32445530 + 16135 COSM5029118 c.14057C>G p.S4686* Substitution - Nonsense 2:32603070-32603070 + TCGA-D1-A16X-01 COSM1020410 c.12686A>G p.D4229G Substitution - Missense 2:32545736-32545736 + 39 COSM3581199 c.8383C>T p.R2795* Substitution - Nonsense 2:32493582-32493582 + HCC160 COSM3709623 c.11755+3A>T p.? Unknown 2:32525022-32525022 + TCGA-EE-A2M5-06 COSM3581210 c.10976T>A p.I3659N Substitution - Missense 2:32515397-32515397 + 545 COSM5612635 c.14024G>A p.G4675E Substitution - Missense 2:32603037-32603037 + BICR_22 COSM2942229 c.1859C>G p.S620C Substitution - Missense 2:32415150-32415150 + TCGA-B0-5081-01 COSM477348 c.11923C>T p.Q3975* Substitution - Nonsense 2:32529653-32529653 + TCGA-AX-A05Z-01 COSM1020249 c.3259G>A p.D1087N Substitution - Missense 2:32433654-32433654 + TCGA-AP-A059-01 COSM1020224 c.2187G>T p.E729D Substitution - Missense 2:32415478-32415478 + TCGA-AR-A2LE-01 COSM3839436 c.12584G>T p.G4195V Substitution - Missense 2:32543533-32543533 + TCGA-66-2795-01 COSM721166 c.13107C>G p.L4369L Substitution - coding silent 2:32549444-32549444 + BN06T COSM1614800 c.10821A>C p.E3607D Substitution - Missense 2:32515242-32515242 + TCGA-18-3406-01 COSM721159 c.14163A>T p.T4721T Substitution - coding silent 2:32607547-32607547 + TCGA-AR-A0TX-01 COSM442827 c.12755C>T p.S4252F Substitution - Missense 2:32545805-32545805 + ACINAR25 COSM1734256 c.4259G>A p.C1420Y Substitution - Missense 2:32443511-32443511 + TCGA-AP-A0LM-01 COSM1020272 c.4113G>T p.K1371N Substitution - Missense 2:32442330-32442330 + ESCC_BICR_046T COSM5441957 c.6656G>T p.G2219V Substitution - Missense 2:32473175-32473175 + PD13162a COSM5779916 c.6976G>T p.E2326* Substitution - Nonsense 2:32477491-32477491 + TCGA-BH-A18G-01 COSM3839434 c.11140G>A p.A3714T Substitution - Missense 2:32515561-32515561 + CHC1595T COSM4801765 c.1039G>C p.E347Q Substitution - Missense 2:32401167-32401167 + TCGA-D1-A103-01 COSM1020440 c.13745C>A p.A4582D Substitution - Missense 2:32597883-32597883 + TCGA-F5-6814-01 COSM3426400 c.8721A>G p.K2907K Substitution - coding silent 2:32499799-32499799 + PT23_1 COSM5902536 c.11129C>T p.P3710L Substitution - Missense 2:32515550-32515550 + TCGA-BR-8680-01 COSM259643 c.11698G>T p.E3900* Substitution - Nonsense 2:32524962-32524962 + TCGA-AK-3427-01 COSM1494914 c.14071-2A>T p.? Unknown 2:32607453-32607453 + 39 COSM5733752 c.2996C>G p.S999* Substitution - Nonsense 2:32429269-32429269 + TCGA-CM-6674-01 COSM1407801 c.5026G>A p.V1676M Substitution - Missense 2:32464593-32464593 + K3-Tumor COSM249145 c.5371G>T p.V1791L Substitution - Missense 2:32467539-32467539 + BHY COSM4591362 c.3994G>C p.V1332L Substitution - Missense TCGA-CJ-5681-01 COSM477334 c.3350T>C p.I1117T Substitution - Missense 2:32433745-32433745 + TCGA-CG-5728-01 COSM4093917 c.13260T>C p.G4420G Substitution - coding silent 2:32575271-32575271 + TCGA-AP-A056-01 COSM1020237 c.2609G>A p.R870Q Substitution - Missense 2:32415900-32415900 + QC2-34-T2 COSM5655035 c.7674_7677delAGTT p.V2559fs*12 Deletion - Frameshift 2:32482560-32482563 + TCGA-G5-6233-01 COSM5080773 c.13829A>C p.K4610T Substitution - Missense 2:32597967-32597967 + I2L-P19Tb-Tumor-Biopsy COSM5354338 c.5094A>C p.P1698P Substitution - coding silent 2:32464661-32464661 + TCGA-C8-A1HE-01 COSM1483069 c.13965C>T p.F4655F Substitution - coding silent 2:32599873-32599873 + PD3989a COSM159374 c.1398A>G p.I466M Substitution - Missense 2:32401603-32401603 + BN19 COSM1614798 c.10374T>G p.S3458R Substitution - Missense 2:32512960-32512960 + TCGA-CA-6718-01 COSM1407848 c.13189G>A p.E4397K Substitution - Missense 2:32575200-32575200 + TCGA-AR-A2LE-01 COSM3839427 c.6134C>T p.S2045F Substitution - Missense 2:32469401-32469401 + CSCC-20-T COSM4505263 c.6884C>T p.T2295I Substitution - Missense 2:32477399-32477399 + TCGA-CI-6623-01 COSM5076205 c.4164C>T p.I1388I Substitution - coding silent 2:32442381-32442381 + SCC-15 COSM4591363 c.3994G>C p.V1332L Substitution - Missense BCN34 COSM1614789 c.4835C>A p.A1612E Substitution - Missense 2:32463275-32463275 + BCM791T COSM4803025 c.7002A>C p.K2334N Substitution - Missense 2:32477517-32477517 + PD4601a COSM159383 c.5323C>T p.H1775Y Substitution - Missense 2:32465131-32465131 + 875-01-3TD COSM2942207 c.1542A>G p.Q514Q Substitution - coding silent 2:32414833-32414833 + C608 COSM4442885 c.5863T>C p.Y1955H Substitution - Missense 2:32468519-32468519 + BCM723T COSM4956330 c.5990C>T p.A1997V Substitution - Missense 2:32468646-32468646 + TCGA-EK-A3GK-01 COSM1306739 c.4662C>T p.F1554F Substitution - coding silent 2:32453851-32453851 + ESCC_92 COSM5637086 c.13879G>C p.E4627Q Substitution - Missense 2:32599787-32599787 + CSCC-11-T COSM4557436 c.7295G>A p.G2432E Substitution - Missense 2:32479504-32479504 + LP6007401-DNA_A01 COSM5036127 c.2674G>T p.E892* Substitution - Nonsense 2:32415965-32415965 + TCGA-AX-A05Z-01 COSM1020248 c.3224G>A p.R1075Q Substitution - Missense 2:32431066-32431066 + LUAD-E00918 COSM365160 c.2410C>T p.P804S Substitution - Missense 2:32415701-32415701 + LUAD-S01315 COSM345317 c.9889A>T p.K3297* Substitution - Nonsense 2:32508168-32508168 + T2258 COSM4665752 c.9094G>T p.V3032F Substitution - Missense 2:32501775-32501775 + TCGA-AP-A056-01 COSM1020339 c.8550C>T p.V2850V Substitution - coding silent 2:32499628-32499628 + TCGA-GD-A3OP-01 COSM1306737 c.4510G>A p.D1504N Substitution - Missense 2:32448820-32448820 + TCGA-GD-A3OP-01 COSM1306738 c.4510G>A p.D1504N Substitution - Missense 2:32448820-32448820 + ESO-1594 COSM1246120 c.11729A>G p.D3910G Substitution - Missense 2:32524993-32524993 + HT115 COSM2942626 c.11006T>C p.V3669A Substitution - Missense 2:32515427-32515427 + 19 COSM5745890 c.5626G>A p.G1876R Substitution - Missense 2:32467957-32467957 + PD7243a COSM5779141 c.12010C>G p.L4004V Substitution - Missense 2:32529740-32529740 + PD3989a COSM159373 c.1398A>G p.I466M Substitution - Missense 2:32401603-32401603 + 8064632 COSM3391704 c.30C>T p.P10P Substitution - coding silent 2:32357191-32357191 + RK220_C01 COSM3743782 c.14229A>T p.Q4743H Substitution - Missense 2:32607613-32607613 + TCGA-FJ-A3ZE-01 COSM3798969 c.8203A>C p.N2735H Substitution - Missense 2:32490148-32490148 + YUKAT COSM5396938 c.9074G>A p.G3025D Substitution - Missense 2:32501755-32501755 + HT115 COSM2942777 c.13961G>A p.R4654Q Substitution - Missense 2:32599869-32599869 + pfg008T COSM4752345 c.13688T>C p.V4563A Substitution - Missense 2:32597826-32597826 + CPCG0185-F1 COSM4966480 c.13813C>G p.R4605G Substitution - Missense 2:32597951-32597951 + TCGA-33-4582-01 COSM721155 c.14387C>G p.A4796G Substitution - Missense 2:32611575-32611575 + MZ7-mel COSM14000 c.7717G>A p.V2573I Substitution - Missense 2:32485663-32485663 + TCGA-AX-A05Z-01 COSM1020379 c.10294A>C p.I3432L Substitution - Missense 2:32510582-32510582 + BN06T COSM1614801 c.10821A>C p.E3607D Substitution - Missense 2:32515242-32515242 + TCGA-F4-6808-01 COSM1407846 c.13180G>T p.A4394S Substitution - Missense 2:32575191-32575191 + PD13162a COSM5795597 c.6977A>T p.E2326V Substitution - Missense 2:32477492-32477492 + 93VU147T COSM4591363 c.3994G>C p.V1332L Substitution - Missense LC_C6 COSM1185876 c.9710C>T p.S3237F Substitution - Missense 2:32507989-32507989 + WSU-HN12 COSM4592547 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + BK0043 COSM4187364 c.12073A>G p.K4025E Substitution - Missense 2:32529803-32529803 + CHC1744T COSM4792298 c.12573G>A p.V4191V Substitution - coding silent 2:32543522-32543522 + CSCC-32-T COSM4572264 c.6920T>C p.V2307A Substitution - Missense 2:32477435-32477435 + 587224 COSM1184729 c.2000T>A p.I667N Substitution - Missense 2:32415291-32415291 + CSCC-40-T COSM4506091 c.7108C>T p.H2370Y Substitution - Missense 2:32478674-32478674 + BCM791T COSM4803024 c.7002A>C p.K2334N Substitution - Missense 2:32477517-32477517 + 575 COSM3720972 c.358A>T p.I120F Substitution - Missense 2:32377620-32377620 + B65 COSM1745488 c.772_773insGATT p.S260fs*7 Insertion - Frameshift 2:32388876-32388877 + PCSI_0083_Pa_X COSM3380142 c.12778C>T p.R4260* Substitution - Nonsense 2:32545828-32545828 + UPCI:SCC090 COSM4591362 c.3994G>C p.V1332L Substitution - Missense 46M COSM5587294 c.7663G>A p.G2555R Substitution - Missense 2:32482549-32482549 + TCGA-BS-A0UV-01 COSM1020239 c.2609G>A p.R870Q Substitution - Missense 2:32415900-32415900 + TCGA-BP-4977-01 COSM477339 c.5618T>G p.I1873S Substitution - Missense 2:32467949-32467949 + ESCC_92 COSM5637085 c.13879G>C p.E4627Q Substitution - Missense 2:32599787-32599787 + CHC1207T COSM4800187 c.7832G>A p.G2611E Substitution - Missense 2:32487665-32487665 + TCGA-DK-A3WW-01 COSM3798963 c.962C>G p.S321C Substitution - Missense 2:32395521-32395521 + LUAD-S01306 COSM343614 c.4069T>C p.C1357R Substitution - Missense 2:32442189-32442189 + TCGA-BR-8680-01 COSM2942689 c.12533G>T p.R4178I Substitution - Missense 2:32543482-32543482 + TCGA-EB-A3XD-01 COSM3581199 c.8383C>T p.R2795* Substitution - Nonsense 2:32493582-32493582 + TCGA-F1-6177-01 COSM4093906 c.11295G>A p.A3765A Substitution - coding silent 2:32515716-32515716 + Gp2D COSM4628059 c.5753T>C p.V1918A Substitution - Missense 2:32468084-32468084 + GC_296T1-GC_296N COSM4772102 c.8174G>A p.S2725N Substitution - Missense 2:32490119-32490119 + CHC892T COSM4795047 c.2413G>A p.A805T Substitution - Missense 2:32415704-32415704 + BRC12 COSM5025606 c.4347T>C p.Y1449Y Substitution - coding silent 2:32445531-32445531 + PD7243a COSM5779142 c.12010C>G p.L4004V Substitution - Missense 2:32529740-32529740 + TCGA-A5-A0GP-01 COSM259643 c.11698G>T p.E3900* Substitution - Nonsense 2:32524962-32524962 + ESCC_124 COSM5641004 c.5218C>G p.L1740V Substitution - Missense 2:32464785-32464785 + TCGA-H4-A2HQ-01 COSM1306755 c.11608C>G p.L3870V Substitution - Missense 2:32518931-32518931 + C135 COSM4618233 c.13751C>T p.T4584M Substitution - Missense 2:32597889-32597889 + BN19 COSM1614799 c.10374T>G p.S3458R Substitution - Missense 2:32512960-32512960 + CHC1207T COSM4800187 c.7832G>A p.G2611E Substitution - Missense 2:32487665-32487665 + TCGA-AK-3427-01 COSM1494913 c.14071-2A>T p.? Unknown 2:32607453-32607453 + HCC2218 COSM14002 c.13509A>C p.K4503N Substitution - Missense 2:32595041-32595041 + TCGA-AX-A05Z-01 COSM259638 c.4145G>A p.R1382Q Substitution - Missense 2:32442362-32442362 + TCGA-18-3406-01 COSM721204 c.7831G>T p.G2611* Substitution - Nonsense 2:32487664-32487664 + TCGA-CA-6718-01 COSM1407785 c.2170A>C p.K724Q Substitution - Missense 2:32415461-32415461 + TCGA-FS-A1Z3-06 COSM3581207 c.9952C>T p.P3318S Substitution - Missense 2:32508231-32508231 + P05-3859 COSM243206 c.11294C>T p.A3765V Substitution - Missense 2:32515715-32515715 + CHC1595T COSM4801766 c.1039G>C p.E347Q Substitution - Missense 2:32401167-32401167 + TCGA-FP-A4BE-01 COSM4093864 c.2802T>C p.T934T Substitution - coding silent 2:32416093-32416093 + CSCC-40-T COSM4506090 c.7108C>T p.H2370Y Substitution - Missense 2:32478674-32478674 + TCGA-BQ-5881-01 COSM3991273 c.3144A>C p.E1048D Substitution - Missense 2:32430986-32430986 + TCGA-B0-5705-01 COSM477327 c.1923A>G p.K641K Substitution - coding silent 2:32415214-32415214 + TCGA-AG-A002-01 COSM259639 c.4145G>A p.R1382Q Substitution - Missense 2:32442362-32442362 + T3094 COSM4665763 c.13501+2T>C p.? Unknown 2:32594062-32594062 + BK0021 COSM4186270 c.4004_4005delTT p.C1336fs*5 Deletion - Frameshift 2:32442124-32442125 + RW2982 COSM4649692 c.13850C>T p.A4617V Substitution - Missense 2:32599758-32599758 + sysucc-1247T COSM1020264 c.3871C>T p.R1291W Substitution - Missense 2:32441389-32441389 + TCGA-GD-A3OP-01 COSM1306733 c.4252G>T p.D1418Y Substitution - Missense 2:32443504-32443504 + TCGA-B5-A0JY-01 COSM185695 c.5366G>T p.R1789I Substitution - Missense 2:32467534-32467534 + 587376 COSM1184736 c.3816A>C p.K1272N Substitution - Missense 2:32441334-32441334 + 2492709 COSM2942293 c.3120G>A p.A1040A Substitution - coding silent 2:32430962-32430962 + 2113171 COSM4167310 c.61A>C p.I21L Substitution - Missense 2:32357222-32357222 + XHDG38 COSM4769678 c.2444C>A p.P815H Substitution - Missense 2:32415735-32415735 + ESCC_BICR_052T COSM5434714 c.1056C>T p.S352S Substitution - coding silent 2:32401184-32401184 + TCGA-B5-A0K9-01 COSM1020446 c.14087A>G p.Q4696R Substitution - Missense 2:32607471-32607471 + HCC074T COSM5810059 c.13954A>T p.S4652C Substitution - Missense 2:32599862-32599862 + ORL-48 COSM4592547 c.9977C>A p.T3326K Substitution - Missense 2:32508256-32508256 + T2949 COSM4093903 c.8574C>T p.A2858A Substitution - coding silent 2:32499652-32499652 + TCGA-AN-A046-01 COSM3839430 c.6674G>T p.R2225I Substitution - Missense 2:32473193-32473193 + sysucc-311T COSM5465545 c.8371G>T p.E2791* Substitution - Nonsense 2:32493570-32493570 + TCGA-AA-A010-01 COSM279169 c.9798A>C p.K3266N Substitution - Missense 2:32508077-32508077 + TCGA-BT-A3PH-01 COSM1306741 c.8296C>G p.L2766V Substitution - Missense 2:32491514-32491514 + TCGA-BR-6452-01 COSM4093886 c.6290C>T p.S2097F Substitution - Missense 2:32469557-32469557 + TCGA-AK-3458-01 COSM477344 c.8403T>C p.S2801S Substitution - coding silent 2:32493602-32493602 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.150092;Hs.150093;Hs.150105;Hs.150107 2p22.3 605638

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAGTTGAAC - MultiAAMissense p.E1562_P1565delinsA c.4685_4693delAAGTTGAAC 2 32678942 LUAD AAT - InFrameDeletion p.N770delN c.2310_2312delTAA 2 32640667 BRCA - AATTA IntronicInsertion . c.9500-306_9500-305insTTAAA 2 32729764 CLL A C Missense p.T4293P c.12877A>C 2 32772983 LUAD A C Missense p.Y4660S c.13979A>C 2 32824954 PRAD A C Synonymous p.L1631L c.4893A>C 2 32688401 OV A G 3-UTRSNV . c.14571+341A>G 2 32843309 HC A G Missense p.D1294G c.3881A>G 2 32666467 BRCA A G Missense p.D3910G c.11729A>G 2 32750060 ESCA A G Missense p.H2238R c.6713A>G 2 32698300 ALL A G Missense p.H4793R c.14378A>G 2 32836633 LUAD A G Missense p.I388V c.1162A>G 2 32626358 CM A G Missense p.I466M c.1398A>G 2 32626671 BRCA A G Missense p.I856V c.2566A>G 2 32640925 RCCC A G Missense p.K2270R c.6809A>G 2 32701369 CLL A G Missense p.T1033A c.3097A>G 2 32656007 BRCA A G Missense p.T3042A c.9124A>G 2 32726872 HNSC A G Missense p.Y2269C c.6806A>G 2 32701366 HNSC A G Missense p.Y824C c.2471A>G 2 32640830 LUAD A G Synonymous p.A3498A c.10494A>G 2 32738147 LUSC A G Synonymous p.E1372E c.4116A>G 2 32667401 CM A G Synonymous p.E2107E c.6321A>G 2 32694656 BLCA A G Synonymous p.L4535L c.13605A>G 2 32820204 LUSC A G Synonymous p.Q762Q c.2286A>G 2 32640645 BRCA A G Synonymous p.T3982T c.11946A>G 2 32754743 LUSC AGTGGAGCCTCCCAAAAAGG - Frameshift p.V926Gfs*3 c.2777_2796delTGGAGCCTCCCAAAAAGGAG 2 32641134 HNSC ATA - InFrameDeletion p.N1435delN c.4304_4306delATA 2 32668621 UCEC A T Missense p.H1159L c.3476A>T 2 32660630 HNSC A T Missense p.H1251L c.3752A>T 2 32664696 LUSC A T Missense p.H4180L c.12539A>T 2 32768555 LUAD A T Missense p.L3081F c.9243A>T 2 32727897 GBM A T Missense p.N1985Y c.5953A>T 2 32693677 RCCC A T Missense p.N2713Y c.8137A>T 2 32715149 LUAD A T Missense p.N4644I c.13931A>T 2 32824906 ESCA A T Missense p.R3941W c.11821A>T 2 32750596 LUSC A T Missense p.T1701S c.5101A>T 2 32689736 HC A T Missense p.T3175S c.9523A>T 2 32730095 LUSC A T Nonsense p.K4007* c.12019A>T 2 32754816 CM A T Synonymous p.S3590S c.10770A>T 2 32740258 LUAD A T Synonymous p.T4721T c.14163A>T 2 32832614 LUSC C A IntronicSNV . c.13612+507C>A 2 32820718 CLL C A Missense p.H3493N c.10477C>A 2 32738130 ESCA C A Missense p.L3858I c.11572C>A 2 32743962 LUAD C A Missense p.L4606I c.13816C>A 2 32823021 ESCA C A Missense p.P2609T c.7825C>A 2 32712725 PRAD C A Missense p.P4616T c.13846C>A 2 32824821 BRCA C A Missense p.S2398Y c.7193C>A 2 32703827 LUSC C A Missense p.T574K c.1721C>A 2 32640080 STAD C A Nonsense p.S3740* c.11219C>A 2 32740707 CM C A Nonsense p.S786* c.2357C>A 2 32640716 RCCC C A Synonymous p.V1527V c.4581C>A 2 32673959 RCCC C A Synonymous p.V1732V c.5196C>A 2 32689831 MM CC TT Missense p.P4641S c.13920_13921delinsTT 2 32824895 CM CC TT Missense p.S3198F c.9593_9594delinsTT 2 32730165 LUAD C - Frameshift p.K712Sfs*9 c.2133delC 2 32640490 LUAD C - Frameshift p.M2167*fs*1 c.6495delT 2 32696095 CLL C G Missense p.A4796G c.14387C>G 2 32836642 LUSC C G Missense p.L2386V c.7156C>G 2 32703790 LUSC C G Missense p.L2766V c.8296C>G 2 32716581 BLCA C G Missense p.L3634V c.10900C>G 2 32740388 LUSC C G Missense p.L3870V c.11608C>G 2 32743998 BLCA C G Missense p.P2756R c.8267C>G 2 32716552 BLCA C G Missense p.P4152R c.12455C>G 2 32768471 LUAD C G Missense p.Q1771E c.5311C>G 2 32690187 OV C G Missense p.Q4343E c.13027C>G 2 32774431 LUSC C G Missense p.Q4366E c.13096C>G 2 32774500 LUSC C G Missense p.Q908E c.2722C>G 2 32641081 BRCA C G Missense p.S2608C c.7823C>G 2 32712723 HNSC C G Missense p.S389C c.1166C>G 2 32626362 HNSC C G Nonsense p.S2700* c.8099C>G 2 32715111 STAD C G Nonsense p.S2874* c.8621C>G 2 32724766 HNSC C G Nonsense p.S3294* c.9881C>G 2 32733227 HNSC C G Nonsense p.S3480* c.10439C>G 2 32738092 BRCA C G Nonsense p.Y687* c.2061C>G 2 32640420 OV C G Synonymous p.L4369L c.13107C>G 2 32774511 LUSC C G Synonymous p.L859L c.2577C>G 2 32640936 BLCA C T IntronicSNV . c.12094+337C>T 2 32755228 CLL C T Missense p.A1661V c.4982C>T 2 32689617 LUAD C T Missense p.A377V c.1130C>T 2 32626326 ESCA C T Missense p.A4253V c.12758C>T 2 32770875 OV C T Missense p.A4309V c.12926C>T 2 32773032 LUSC C T Missense p.A642V c.1925C>T 2 32640284 UCEC C T Missense p.H1622Y c.4864C>T 2 32688372 LUAD C T Missense p.H1775Y c.5323C>T 2 32690199 BRCA C T Missense p.H226Y c.676C>T 2 32613848 LUAD C T Missense p.H3859Y c.11575C>T 2 32743965 BLCA C T Missense p.L140F c.418C>T 2 32602748 LUAD C T Missense p.L223F c.667C>T 2 32613839 HNSC C T Missense p.L2508F c.7522C>T 2 32706501 CM C T Missense p.L3858F c.11572C>T 2 32743962 BLCA C T Missense p.P1696S c.5086C>T 2 32689721 CM C T Missense p.P1736S c.5206C>T 2 32689841 CM C T Missense p.P2473S c.7417C>T 2 32706396 CM C T Missense p.P3318S c.9952C>T 2 32733298 CM C T Missense p.P3477L c.10430C>T 2 32738083 LUSC C T Missense p.P3620S c.10858C>T 2 32740346 CM C T Missense p.P3829S c.11485C>T 2 32743456 CM C T Missense p.P4718L c.14153C>T 2 32832604 CM C T Missense p.R1291W c.3871C>T 2 32666457 CM C T Missense p.R276C c.826C>T 2 32613998 LUAD C T Missense p.R276C c.826C>T 2 32613998 RCCC C T Missense p.S1364L c.4091C>T 2 32667279 HNSC C T Missense p.S1539L c.4616C>T 2 32673994 LUAD C T Missense p.S2606L c.7817C>T 2 32712717 CM C T Missense p.S3608L c.10823C>T 2 32740311 CM C T Missense p.S3772L c.11315C>T 2 32740803 UCEC C T Missense p.S3867L c.11600C>T 2 32743990 BRCA C T Missense p.S4404F c.13211C>T 2 32800289 CM C T Missense p.S4724F c.14171C>T 2 32832622 LUSC C T Missense p.T2365M c.7094C>T 2 32703728 STAD C T Missense p.T3865I c.11594C>T 2 32743984 BRCA C T Missense p.T4672M c.14015C>T 2 32828095 OV C T Nonsense p.Q1645* c.4933C>T 2 32688441 HNSC C T Nonsense p.Q2974* c.8920C>T 2 32725065 CM C T Nonsense p.R4654* c.13960C>T 2 32824935 STAD C T Nonsense p.R4654* c.13960C>T 2 32824935 UCEC C T Nonsense p.R4732* c.14194C>T 2 32832645 BLCA C T Synonymous p.C2873C c.8619C>T 2 32724764 CM C T Synonymous p.F1106F c.3318C>T 2 32658781 COREAD C T Synonymous p.F1554F c.4662C>T 2 32678919 BLCA C T Synonymous p.F1728F c.5184C>T 2 32689819 CM C T Synonymous p.F192F c.576C>T 2 32605289 HNSC C T Synonymous p.F4655F c.13965C>T 2 32824940 BRCA C T Synonymous p.I645I c.1935C>T 2 32640294 CM C T Synonymous p.L4324L c.12970C>T 2 32773076 LUSC G A Missense p.A1953T c.5857G>A 2 32693581 UCEC G A Missense p.A3599T c.10795G>A 2 32740283 BLCA G A Missense p.A3640T c.10918G>A 2 32740406 GBM G A Missense p.C4770Y c.14309G>A 2 32836564 BRCA G A Missense p.D1504N c.4510G>A 2 32673888 BLCA G A Missense p.D448N c.1342G>A 2 32626615 BLCA G A Missense p.E1723K c.5167G>A 2 32689802 UCEC G A Missense p.E3158K c.9472G>A 2 32728276 HNSC G A Missense p.E4526K c.13576G>A 2 32820175 HNSC G A Missense p.E4806K c.14416G>A 2 32842813 LUSC G A Missense p.E989K c.2965G>A 2 32654306 GBM G A Missense p.G1465E c.4394G>A 2 32670646 BLCA G A Missense p.G271R c.811G>A 2 32613983 UCEC G A Missense p.G394E c.1181G>A 2 32626377 LUAD G A Missense p.G968R c.2902G>A 2 32654243 CM G A Missense p.M1856I c.5568G>A 2 32692804 ESCA G A Missense p.M418I c.1254G>A 2 32626450 BLCA G A Missense p.M649I c.1947G>A 2 32640306 LUAD G A Missense p.R1390H c.4169G>A 2 32667454 BRCA G A Missense p.R1863H c.5588G>A 2 32692987 UCEC G A Missense p.R2890Q c.8669G>A 2 32724814 CM G A Missense p.R4314K c.12941G>A 2 32773047 CM G A Missense p.R4785Q c.14354G>A 2 32836609 ESCA G A Missense p.S1500N c.4499G>A 2 32673877 BLCA G A Missense p.S3504N c.10511G>A 2 32738164 BRCA G A Missense p.S4336N c.13007G>A 2 32774411 GBM G A Missense p.S482N c.1445G>A 2 32631593 RCCC G A Missense p.V2850I c.8548G>A 2 32724693 LUAD G A Nonsense p.W1887* c.5661G>A 2 32693060 OV G A SpliceAcceptorSNV . c.9208-1G>A 2 32727861 BRCA G A Synonymous p.A3765A c.11295G>A 2 32740783 STAD G A Synonymous p.E1329E c.3987G>A 2 32667175 HNSC G A Synonymous p.L720L c.2160G>A 2 32640519 BLCA G A Synonymous p.Q2577Q c.7731G>A 2 32710744 GBM G A Synonymous p.R3471R c.10413G>A 2 32738066 CM G A Synonymous p.R4393R c.13179G>A 2 32800257 CM G A Synonymous p.S2976S c.8928G>A 2 32725073 LUSC G A Synonymous p.S858S c.2574G>A 2 32640933 UCEC G A Synonymous p.T2365T c.7095G>A 2 32703729 UCEC G C Missense p.D3628H c.10882G>C 2 32740370 BLCA G C Missense p.E1825Q c.5473G>C 2 32692709 LUSC G C Missense p.E3621Q c.10861G>C 2 32740349 LUSC G C Missense p.E816Q c.2446G>C 2 32640805 BRCA G C Missense p.M4609I c.13827G>C 2 32823032 LUSC G C Missense p.Q1349H c.4047G>C 2 32667235 LUSC G C Missense p.R302T c.905G>C 2 32617172 OV G C Missense p.W2710C c.8130G>C 2 32715142 LUAD GG AA Missense p.G2895K c.8683_8684delinsAA 2 32724828 CM GG AT Missense p.D2568Y c.7701_7702delinsAT 2 32710714 CM GG AT Missense p.G3485I c.10453_10454delinsAT 2 32738106 BLCA G T IntronicSNV . c.9700+122G>T 2 32730394 MB G T Missense p.A1715S c.5143G>T 2 32689778 RCCC G T Missense p.A3364S c.10090G>T 2 32734914 LUSC G T Missense p.A3640S c.10918G>T 2 32740406 LUSC G T Missense p.A4530S c.13588G>T 2 32820187 LUSC G T Missense p.D1418Y c.4252G>T 2 32668572 BLCA G T Missense p.G1214V c.3641G>T 2 32664585 CM G T Missense p.G2395V c.7184G>T 2 32703818 BRCA G T Missense p.G3026W c.9076G>T 2 32726824 LUSC G T Missense p.G493V c.1478G>T 2 32639837 LUAD G T Missense p.L3719F c.11157G>T 2 32740645 CM G T Missense p.L4551F c.13653G>T 2 32822858 LUAD G T Missense p.M1100I c.3300G>T 2 32658763 LUAD G T Missense p.M3472I c.10416G>T 2 32738069 BLCA G T Missense p.Q2051H c.6153G>T 2 32694488 LUAD G T Missense p.R2890L c.8669G>T 2 32724814 LUAD G T Missense p.R3068I c.9203G>T 2 32726951 LUAD G T Missense p.R4713L c.14138G>T 2 32832589 BLCA G T Missense p.R818S c.2454G>T 2 32640813 LUAD G T Missense p.S4596I c.13787G>T 2 32822992 BRCA G T Missense p.V1243L c.3727G>T 2 32664671 HNSC G T Missense p.V3258F c.9772G>T 2 32733118 UCEC G T Missense p.V3964L c.11890G>T 2 32750665 LUSC G T Missense p.V4216F c.12646G>T 2 32770763 HNSC G T Nonsense p.E3204* c.9610G>T 2 32730182 HNSC G T Nonsense p.E3900* c.11698G>T 2 32750029 UCEC G T Nonsense p.G2611* c.7831G>T 2 32712731 LUSC G T SpliceAcceptorSNV . c.14260-1G>T 2 32836514 BRCA T A IntronicSNV . c.4754-3019T>A 2 32685243 CLL T A Missense p.C2346S c.7036T>A 2 32702619 BRCA T A Missense p.C566S c.1696T>A 2 32640055 CM T A Missense p.D2568E c.7704T>A 2 32710717 CM T A Missense p.H2156Q c.6468T>A 2 32695356 GBM T A Missense p.I3659N c.10976T>A 2 32740464 CM T A Missense p.L1322I c.3964T>A 2 32667152 LUAD T A Missense p.Y687N c.2059T>A 2 32640418 MB T C IntronicSNV . c.13355+4459T>C 2 32804892 CLL T C Missense p.F3420L c.10258T>C 2 32735613 UCEC T C Missense p.L1560P c.4679T>C 2 32678936 STAD T C Missense p.L3967P c.11900T>C 2 32750675 LUSC T C Missense p.S175P c.523T>C 2 32605236 RCCC T C Missense p.S991P c.2971T>C 2 32654312 BRCA T C Synonymous p.A1766A c.5298T>C 2 32690174 UCEC T C Synonymous p.D383D c.1149T>C 2 32626345 BLCA T C Synonymous p.G3305G c.9915T>C 2 32733261 PAAD T C Synonymous p.G4420G c.13260T>C 2 32800338 STAD T C Synonymous p.G782G c.2346T>C 2 32640705 STAD T C Synonymous p.H1103H c.3309T>C 2 32658772 UCEC T C Synonymous p.I3686I c.11058T>C 2 32740546 CM T C Synonymous p.L1761L c.5283T>C 2 32690159 UCEC T C Synonymous p.L2605L c.7813T>C 2 32710826 CM T C Synonymous p.S654S c.1962T>C 2 32640321 CM T C Synonymous p.T2702T c.8106T>C 2 32715118 CM T C Synonymous p.T2872T c.8616T>C 2 32724761 CM T C Synonymous p.Y1449Y c.4347T>C 2 32670599 BRCA T - Frameshift p.C4666Vfs*2 c.13996delT 2 32828074 CM T - Frameshift p.L2477Wfs*15 c.7430delT 2 32706407 LGG - T Frameshift p.W1086Lfs*3 c.3256dupT 2 32658719 LUAD T G IntronicSNV . c.13501+128T>G 2 32819255 MB T G Missense p.C874G c.2620T>G 2 32640979 BRCA T G Missense p.I1388S c.4163T>G 2 32667448 UCEC T G Missense p.I1819M c.5457T>G 2 32692693 RCCC T G Missense p.I1873S c.5618T>G 2 32693017 RCCC T G Missense p.L1560R c.4679T>G 2 32678936 HC T G Missense p.L3687R c.11060T>G 2 32740548 CLL T G Missense p.N1541K c.4623T>G 2 32678880 BRCA T G Missense p.N4682K c.14046T>G 2 32828126 CM T G Missense p.S2852A c.8554T>G 2 32724699 CM T G Synonymous p.S620S c.1860T>G 2 32640219 CM - TGTGTG IntronicInsertion . c.9499+843_9499+844insGTGTGT 2 32729145 CLL