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 13 77780870 77780870 + Silent SNP A A G TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr13:77780870A>G c.3393T>C c.(3391-3393)tgT>tgC p.C1131C ACC 13 77837809 77837809 + Missense_Mutation SNP A A G TCGA-OR-A5JI-01A-11D-A29I-10 TCGA-OR-A5JI-10A-01D-A29L-10 g.chr13:77837809A>G c.1433T>C c.(1432-1434)cTg>cCg p.L478P ACC 13 77870754 77870754 + Missense_Mutation SNP T T C TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr13:77870754T>C c.244A>G c.(244-246)Aaa>Gaa p.K82E BLCA 13 77625965 77625965 + Missense_Mutation SNP G G C TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr13:77625965G>C c.13622C>G c.(13621-13623)tCt>tGt p.S4541C BLCA 13 77629765 77629765 + Silent SNP C C G TCGA-XF-AAN5-01A-11D-A42E-08 TCGA-XF-AAN5-10A-01D-A42H-08 g.chr13:77629765C>G c.13461G>C c.(13459-13461)gtG>gtC p.V4487V BLCA 13 77631124 77631124 + Missense_Mutation SNP G G C TCGA-XF-A9ST-01A-11D-A42E-08 TCGA-XF-A9ST-10A-01D-A42H-08 g.chr13:77631124G>C c.13320C>G c.(13318-13320)tgC>tgG p.C4440W BLCA 13 77641780 77641780 + Missense_Mutation SNP T T C TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr13:77641780T>C c.12277A>G c.(12277-12279)Aca>Gca p.T4093A BLCA 13 77641943 77641943 + Silent SNP G G A TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr13:77641943G>A c.12114C>T c.(12112-12114)agC>agT p.S4038S BLCA 13 77641944 77641944 + Missense_Mutation SNP C C A TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr13:77641944C>A c.12113G>T c.(12112-12114)aGc>aTc p.S4038I BLCA 13 77641954 77641954 + Missense_Mutation SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr13:77641954G>A c.12103C>T c.(12103-12105)Cgt>Tgt p.R4035C BLCA 13 77642913 77642913 + Silent SNP T T C TCGA-E7-A97P-01A-11D-A38G-08 TCGA-E7-A97P-10A-01D-A38J-08 g.chr13:77642913T>C c.11844A>G c.(11842-11844)gaA>gaG p.E3948E BLCA 13 77642919 77642919 + Silent SNP G G C TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr13:77642919G>C c.11838C>G c.(11836-11838)gtC>gtG p.V3946V BLCA 13 77644815 77644815 + Missense_Mutation SNP A A G TCGA-ZF-AA54-01A-11D-A391-08 TCGA-ZF-AA54-10A-01D-A394-08 g.chr13:77644815A>G c.11741T>C c.(11740-11742)aTg>aCg p.M3914T BLCA 13 77644831 77644831 + Missense_Mutation SNP C C G TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr13:77644831C>G c.11725G>C c.(11725-11727)Gac>Cac p.D3909H BLCA 13 77651312 77651312 + Missense_Mutation SNP G G T TCGA-DK-A6AV-01A-12D-A30E-08 TCGA-DK-A6AV-10A-01D-A30H-08 g.chr13:77651312G>T c.11581C>A c.(11581-11583)Ctg>Atg p.L3861M BLCA 13 77651516 77651516 + Silent SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr13:77651516G>A c.11377C>T c.(11377-11379)Ctg>Ttg p.L3793L BLCA 13 77652990 77652990 + Missense_Mutation SNP T T C TCGA-5N-A9KM-01A-11D-A42E-08 TCGA-5N-A9KM-10A-01D-A42H-08 g.chr13:77652990T>C c.11339A>G c.(11338-11340)aAa>aGa p.K3780R BLCA 13 77656085 77656085 + Missense_Mutation SNP G G A TCGA-GC-A3I6-01A-11D-A20D-08 TCGA-GC-A3I6-10A-01D-A20D-08 g.chr13:77656085G>A c.10966C>T c.(10966-10968)Cat>Tat p.H3656Y BLCA 13 77664333 77664333 + Missense_Mutation SNP G G A TCGA-ZF-AA58-01A-12D-A42E-08 TCGA-ZF-AA58-10A-01D-A42H-08 g.chr13:77664333G>A c.10319C>T c.(10318-10320)tCa>tTa p.S3440L BLCA 13 77667465 77667465 + Missense_Mutation SNP T T C TCGA-DK-A3IS-01A-21D-A21A-08 TCGA-DK-A3IS-10A-01D-A21A-08 g.chr13:77667465T>C c.10088A>G c.(10087-10089)cAt>cGt p.H3363R BLCA 13 77669735 77669735 + Silent SNP G G A TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr13:77669735G>A c.9843C>T c.(9841-9843)gtC>gtT p.V3281V BLCA 13 77670490 77670490 + Missense_Mutation SNP C C T TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr13:77670490C>T c.9797G>A c.(9796-9798)aGa>aAa p.R3266K BLCA 13 77671712 77671712 + Missense_Mutation SNP G G T TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr13:77671712G>T c.9463C>A c.(9463-9465)Ctt>Att p.L3155I BLCA 13 77671944 77671944 + Silent SNP G G A TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr13:77671944G>A c.9231C>T c.(9229-9231)atC>atT p.I3077I BLCA 13 77671968 77671968 + Silent SNP T T C TCGA-YF-AA3L-01A-11D-A38G-08 TCGA-YF-AA3L-10A-01D-A38J-08 g.chr13:77671968T>C c.9207A>G c.(9205-9207)ccA>ccG p.P3069P BLCA 13 77672613 77672613 + Missense_Mutation SNP C C G TCGA-ZF-AA4X-01A-11D-A38G-08 TCGA-ZF-AA4X-10A-01D-A38J-08 g.chr13:77672613C>G c.8562G>C c.(8560-8562)ttG>ttC p.L2854F BLCA 13 77672741 77672741 + Missense_Mutation SNP G G C TCGA-K4-A3WU-01B-11D-A23M-08 TCGA-K4-A3WU-10A-01D-A23K-08 g.chr13:77672741G>C c.8434C>G c.(8434-8436)Cta>Gta p.L2812V BLCA 13 77673121 77673121 + Missense_Mutation SNP G G A TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr13:77673121G>A c.8054C>T c.(8053-8055)tCt>tTt p.S2685F BLCA 13 77673132 77673132 + Missense_Mutation SNP G G C TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr13:77673132G>C c.8043C>G c.(8041-8043)atC>atG p.I2681M BLCA 13 77714227 77714227 + Silent SNP C C T TCGA-G2-A3IE-01A-11D-A20D-08 TCGA-G2-A3IE-10A-01D-A20D-08 g.chr13:77714227C>T c.7359G>A c.(7357-7359)caG>caA p.Q2453Q BLCA 13 77725015 77725015 + Missense_Mutation SNP G G C TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr13:77725015G>C c.6871C>G c.(6871-6873)Caa>Gaa p.Q2291E BLCA 13 77736073 77736073 + Missense_Mutation SNP C C G TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr13:77736073C>G c.6451G>C c.(6451-6453)Gac>Cac p.D2151H BLCA 13 77739431 77739431 + Missense_Mutation SNP C C T TCGA-4Z-AA89-01A-11D-A391-08 TCGA-4Z-AA89-10A-01D-A394-08 g.chr13:77739431C>T c.6322G>A c.(6322-6324)Gaa>Aaa p.E2108K BLCA 13 77742607 77742607 + Missense_Mutation SNP C C G TCGA-CF-A9FF-01A-11D-A38G-08 TCGA-CF-A9FF-10A-01D-A38J-08 g.chr13:77742607C>G c.5956G>C c.(5956-5958)Gag>Cag p.E1986Q BLCA 13 77743819 77743819 + Missense_Mutation SNP G G A TCGA-BT-A20Q-01A-11D-A14W-08 TCGA-BT-A20Q-11A-11D-A14W-08 g.chr13:77743819G>A c.5711C>T c.(5710-5712)tCc>tTc p.S1904F BLCA 13 77743843 77743843 + Missense_Mutation SNP T T C TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr13:77743843T>C c.5687A>G c.(5686-5688)gAc>gGc p.D1896G BLCA 13 77743847 77743847 + Missense_Mutation SNP C C T TCGA-BT-A3PJ-01A-21D-A21Z-08 TCGA-BT-A3PJ-10A-01D-A21Z-08 g.chr13:77743847C>T c.5683G>A c.(5683-5685)Gat>Aat p.D1895N BLCA 13 77748454 77748454 + Silent SNP G G C TCGA-ZF-A9RL-01A-11D-A38G-08 TCGA-ZF-A9RL-10A-01D-A38J-08 g.chr13:77748454G>C c.5529C>G c.(5527-5529)ctC>ctG p.L1843L BLCA 13 77750673 77750673 + Missense_Mutation SNP C C T TCGA-FT-A3EE-01A-11D-A202-08 TCGA-FT-A3EE-10A-01D-A202-08 g.chr13:77750673C>T c.5317G>A c.(5317-5319)Gat>Aat p.D1773N BLCA 13 77754343 77754343 + Missense_Mutation SNP G G C TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr13:77754343G>C c.4938C>G c.(4936-4938)ttC>ttG p.F1646L BLCA 13 77759261 77759261 + Missense_Mutation SNP C C T TCGA-XF-A9ST-01A-11D-A42E-08 TCGA-XF-A9ST-10A-01D-A42H-08 g.chr13:77759261C>T c.4582G>A c.(4582-4584)Gat>Aat p.D1528N BLCA 13 77759426 77759426 + Nonsense_Mutation SNP C C A TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr13:77759426C>A c.4417G>T c.(4417-4419)Gaa>Taa p.E1473* BLCA 13 77765949 77765949 + Splice_Site SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr13:77765949C>G c.e28-1 BLCA 13 77779435 77779435 + Missense_Mutation SNP G G A TCGA-FD-A43U-01A-11D-A23U-08 TCGA-FD-A43U-10A-01D-A23U-08 g.chr13:77779435G>A c.3685C>T c.(3685-3687)Ctt>Ttt p.L1229F BLCA 13 77780798 77780798 + Silent SNP C C T TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr13:77780798C>T c.3465G>A c.(3463-3465)ttG>ttA p.L1155L BLCA 13 77786175 77786175 + Missense_Mutation SNP G G T TCGA-FD-A3B6-01A-21D-A20D-08 TCGA-FD-A3B6-10A-01D-A20D-08 g.chr13:77786175G>T c.3064C>A c.(3064-3066)Caa>Aaa p.Q1022K BLCA 13 77792079 77792079 + Missense_Mutation SNP G G C TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr13:77792079G>C c.2839C>G c.(2839-2841)Ctt>Gtt p.L947V BLCA 13 77807357 77807357 + Missense_Mutation SNP C C G TCGA-GU-A763-01A-11D-A32B-08 TCGA-GU-A763-10A-01D-A329-08 g.chr13:77807357C>G c.2557G>C c.(2557-2559)Gaa>Caa p.E853Q BLCA 13 77807357 77807357 + Missense_Mutation SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr13:77807357C>G c.2557G>C c.(2557-2559)Gaa>Caa p.E853Q BLCA 13 77807378 77807378 + Missense_Mutation SNP G G A TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr13:77807378G>A c.2536C>T c.(2536-2538)Cct>Tct p.P846S BLCA 13 77825292 77825292 + Missense_Mutation SNP G G C TCGA-CF-A1HS-01A-11D-A13W-08 TCGA-CF-A1HS-10A-01D-A13W-08 g.chr13:77825292G>C c.2261C>G c.(2260-2262)cCc>cGc p.P754R BLCA 13 77825302 77825302 + Missense_Mutation SNP C C T TCGA-GD-A2C5-01A-12D-A17V-08 TCGA-GD-A2C5-10A-01D-A17V-08 g.chr13:77825302C>T c.2251G>A c.(2251-2253)Gac>Aac p.D751N BLCA 13 77825389 77825389 + Missense_Mutation SNP T T G TCGA-E7-A4XJ-01A-11D-A26M-08 TCGA-E7-A4XJ-10A-01D-A26K-08 g.chr13:77825389T>G c.2164A>C c.(2164-2166)Aaa>Caa p.K722Q BLCA 13 77842012 77842012 + Missense_Mutation SNP C C T TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr13:77842012C>T c.1207G>A c.(1207-1209)Gaa>Aaa p.E403K BLCA 13 77847640 77847640 + Silent SNP G G T TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr13:77847640G>T c.798C>A c.(796-798)acC>acA p.T266T BLCA 13 77852999 77852999 + Silent SNP T T C TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr13:77852999T>C c.528A>G c.(526-528)acA>acG p.T176T BLCA 13 77862308 77862308 + Missense_Mutation SNP G G C TCGA-2F-A9KO-01A-11D-A38G-08 TCGA-2F-A9KO-11A-12D-A38J-08 g.chr13:77862308G>C c.468C>G c.(466-468)atC>atG p.I156M BLCA 13 77862371 77862371 + Missense_Mutation SNP C C G TCGA-ZF-AA4X-01A-11D-A38G-08 TCGA-ZF-AA4X-10A-01D-A38J-08 g.chr13:77862371C>G c.405G>C c.(403-405)aaG>aaC p.K135N BRCA 13 77636761 77636761 + Missense_Mutation SNP C C A TCGA-E2-A15D-01A-11D-A10Y-09 TCGA-E2-A15D-10A-01D-A110-09 g.chr13:77636761C>A c.12630G>T c.(12628-12630)tgG>tgT p.W4210C BRCA 13 77644815 77644815 + Missense_Mutation SNP A A G TCGA-E2-A158-01A-11D-A12B-09 TCGA-E2-A158-11A-22D-A12B-09 g.chr13:77644815A>G c.11741T>C c.(11740-11742)aTg>aCg p.M3914T BRCA 13 77644827 77644827 + Missense_Mutation SNP A A G TCGA-C8-A12O-01A-11D-A10Y-09 TCGA-C8-A12O-10A-01D-A110-09 g.chr13:77644827A>G c.11729T>C c.(11728-11730)cTg>cCg p.L3910P BRCA 13 77651360 77651360 + Nonsense_Mutation SNP G G A TCGA-A8-A06Q-01A-11W-A050-09 TCGA-A8-A06Q-10A-01W-A055-09 g.chr13:77651360G>A c.11533C>T c.(11533-11535)Cag>Tag p.Q3845* BRCA 13 77655719 77655719 + Missense_Mutation SNP G G A TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr13:77655719G>A c.11147C>T c.(11146-11148)cCt>cTt p.P3716L BRCA 13 77655723 77655723 + Nonsense_Mutation SNP G G A TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr13:77655723G>A c.11143C>T c.(11143-11145)Cga>Tga p.R3715* BRCA 13 77656125 77656125 + Missense_Mutation SNP G G C TCGA-EW-A1PA-01A-11D-A142-09 TCGA-EW-A1PA-10A-01D-A142-09 g.chr13:77656125G>C c.10926C>G c.(10924-10926)tgC>tgG p.C3642W BRCA 13 77663147 77663147 + Missense_Mutation SNP C C G TCGA-E9-A1R4-01A-21D-A14G-09 TCGA-E9-A1R4-10A-01D-A14G-09 g.chr13:77663147C>G c.10431G>C c.(10429-10431)ttG>ttC p.L3477F BRCA 13 77667317 77667317 + Missense_Mutation SNP C C T TCGA-GM-A2DO-01A-11D-A19Y-09 TCGA-GM-A2DO-10D-01D-A18P-09 g.chr13:77667317C>T c.10236G>A c.(10234-10236)atG>atA p.M3412I BRCA 13 77669522 77669522 + Missense_Mutation SNP C C T TCGA-EW-A1IZ-01A-11D-A188-09 TCGA-EW-A1IZ-10A-01D-A13O-09 g.chr13:77669522C>T c.10056G>A c.(10054-10056)atG>atA p.M3352I BRCA 13 77670474 77670474 + Silent SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:77670474G>A c.9813C>T c.(9811-9813)cgC>cgT p.R3271R BRCA 13 77671823 77671823 + Missense_Mutation SNP G G C TCGA-AR-A251-01A-12D-A167-09 TCGA-AR-A251-10A-01D-A167-09 g.chr13:77671823G>C c.9352C>G c.(9352-9354)Ctt>Gtt p.L3118V BRCA 13 77671946 77671946 + Missense_Mutation SNP T T C TCGA-A8-A06P-01A-11W-A019-09 TCGA-A8-A06P-10A-01W-A021-09 g.chr13:77671946T>C c.9229A>G c.(9229-9231)Atc>Gtc p.I3077V BRCA 13 77672548 77672548 + Missense_Mutation SNP G G A TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chr13:77672548G>A c.8627C>T c.(8626-8628)tCt>tTt p.S2876F BRCA 13 77673021 77673021 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr13:77673021C>G c.8154G>C c.(8152-8154)aaG>aaC p.K2718N BRCA 13 77673130 77673130 + Nonsense_Mutation SNP G G C TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chr13:77673130G>C c.8045C>G c.(8044-8046)tCa>tGa p.S2682* BRCA 13 77695616 77695616 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr13:77695616C>G c.7918G>C c.(7918-7920)Gat>Cat p.D2640H BRCA 13 77724895 77724895 + Nonsense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:77724895G>A c.6991C>T c.(6991-6993)Cga>Tga p.R2331* BRCA 13 77740653 77740653 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:77740653C>T c.6037G>A c.(6037-6039)Gaa>Aaa p.E2013K BRCA 13 77742767 77742767 + Silent SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:77742767G>T c.5796C>A c.(5794-5796)gtC>gtA p.V1932V BRCA 13 77748601 77748601 + Silent SNP G G A TCGA-D8-A1JU-01A-11D-A13L-09 TCGA-D8-A1JU-10A-01D-A188-09 g.chr13:77748601G>A c.5382C>T c.(5380-5382)cgC>cgT p.R1794R BRCA 13 77764443 77764443 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr13:77764443C>G c.3984G>C c.(3982-3984)aaG>aaC p.K1328N BRCA 13 77779677 77779677 + Missense_Mutation SNP C C G TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr13:77779677C>G c.3532G>C c.(3532-3534)Gag>Cag p.E1178Q BRCA 13 77791998 77791998 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:77791998C>T c.2920G>A c.(2920-2922)Gtc>Atc p.V974I BRCA 13 77817214 77817214 + Missense_Mutation SNP T T C TCGA-C8-A12Z-01A-11D-A10Y-09 TCGA-C8-A12Z-10A-01D-A110-09 g.chr13:77817214T>C c.2495A>G c.(2494-2496)cAc>cGc p.H832R BRCA 13 77836235 77836235 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:77836235G>T c.1486C>A c.(1486-1488)Ctt>Att p.L496I BRCA 13 77862348 77862348 + Nonsense_Mutation SNP G G C TCGA-A8-A085-01A-11W-A019-09 TCGA-A8-A085-10A-01W-A021-09 g.chr13:77862348G>C c.428C>G c.(427-429)tCa>tGa p.S143* CESC 13 77625989 77625989 + Missense_Mutation SNP C C G TCGA-EK-A2PG-01A-11D-A18J-09 TCGA-EK-A2PG-10A-01D-A18J-09 g.chr13:77625989C>G c.13598G>C c.(13597-13599)aGa>aCa p.R4533T CESC 13 77633672 77633672 + Missense_Mutation SNP C C G TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr13:77633672C>G c.13012G>C c.(13012-13014)Gat>Cat p.D4338H CESC 13 77640190 77640190 + Missense_Mutation SNP C C T TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr13:77640190C>T c.12375G>A c.(12373-12375)atG>atA p.M4125I CESC 13 77670497 77670497 + Missense_Mutation SNP G G A TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr13:77670497G>A c.9790C>T c.(9790-9792)Cgc>Tgc p.R3264C CESC 13 77695598 77695598 + Missense_Mutation SNP G G C TCGA-C5-A1BQ-01C-11D-A20U-09 TCGA-C5-A1BQ-10A-01D-A20U-09 g.chr13:77695598G>C c.7936C>G c.(7936-7938)Cct>Gct p.P2646A CESC 13 77754359 77754359 + Missense_Mutation SNP C C T TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr13:77754359C>T c.4922G>A c.(4921-4923)aGa>aAa p.R1641K CESC 13 77754364 77754364 + Silent SNP C C T TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr13:77754364C>T c.4917G>A c.(4915-4917)ctG>ctA p.L1639L CESC 13 77817203 77817203 + Missense_Mutation SNP C C T TCGA-EK-A2RJ-01A-11D-A18J-09 TCGA-EK-A2RJ-10A-01D-A18J-09 g.chr13:77817203C>T c.2506G>A c.(2506-2508)Gaa>Aaa p.E836K CESC 13 77817206 77817206 + Missense_Mutation SNP C C T TCGA-EK-A2RJ-01A-11D-A18J-09 TCGA-EK-A2RJ-10A-01D-A18J-09 g.chr13:77817206C>T c.2503G>A c.(2503-2505)Gag>Aag p.E835K CESC 13 77834572 77834572 + Missense_Mutation SNP C C T TCGA-C5-A1M8-01A-21D-A13W-08 TCGA-C5-A1M8-10A-01D-A13W-08 g.chr13:77834572C>T c.1894G>A c.(1894-1896)Gat>Aat p.D632N CESC 13 77862415 77862415 + Missense_Mutation SNP G G C TCGA-C5-A1MN-01A-11D-A14W-08 TCGA-C5-A1MN-10A-01D-A14W-08 g.chr13:77862415G>C c.361C>G c.(361-363)Ctg>Gtg p.L121V CHOL 13 77672823 77672823 + Silent SNP A A C TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr13:77672823A>C c.8352T>G c.(8350-8352)ccT>ccG p.P2784P CHOL 13 77818052 77818052 + Missense_Mutation SNP C C T TCGA-YR-A95A-01A-12D-A417-09 TCGA-YR-A95A-10A-01D-A41A-09 g.chr13:77818052C>T c.2302G>A c.(2302-2304)Gct>Act p.A768T COAD 13 77625227 77625227 + Frame_Shift_Del DEL A A - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr13:77625227delA c.13712delT c.(13711-13713)ttcfs p.F4571fs COAD 13 77626011 77626011 + Missense_Mutation SNP G G A TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr13:77626011G>A c.13576C>T c.(13576-13578)Cgg>Tgg p.R4526W COAD 13 77626053 77626053 + Splice_Site SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr13:77626053C>T c.13534G>A c.(13534-13536)Gca>Aca p.A4512T COAD 13 77631119 77631119 + Splice_Site SNP A A G TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr13:77631119A>G c.e79+1 COAD 13 77632488 77632488 + Silent SNP C C A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr13:77632488C>A c.13080G>T c.(13078-13080)ggG>ggT p.G4360G COAD 13 77635825 77635825 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr13:77635825T>C c.12761A>G c.(12760-12762)cAt>cGt p.H4254R COAD 13 77635909 77635909 + Missense_Mutation SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr13:77635909T>C c.12677A>G c.(12676-12678)cAt>cGt p.H4226R COAD 13 77636817 77636817 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr13:77636817C>T c.12574G>A c.(12574-12576)Gca>Aca p.A4192T COAD 13 77641849 77641849 + Missense_Mutation SNP T T C TCGA-AA-A00Q-01A-01W-A005-10 TCGA-AA-A00Q-10A-01W-A005-10 g.chr13:77641849T>C c.12208A>G c.(12208-12210)Atg>Gtg p.M4070V COAD 13 77641917 77641917 + Frame_Shift_Del DEL G G - TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr13:77641917delG c.12140delC c.(12139-12141)ccafs p.P4047fs COAD 13 77641953 77641953 + Missense_Mutation SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr13:77641953C>T c.12104G>A c.(12103-12105)cGt>cAt p.R4035H COAD 13 77642770 77642770 + Missense_Mutation SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr13:77642770G>A c.11987C>T c.(11986-11988)gCt>gTt p.A3996V COAD 13 77642918 77642918 + Missense_Mutation SNP G G A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr13:77642918G>A c.11839C>T c.(11839-11841)Cgt>Tgt p.R3947C COAD 13 77642939 77642939 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:77642939G>A c.11818C>T c.(11818-11820)Cgc>Tgc p.R3940C COAD 13 77644772 77644772 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:77644772T>G c.11784A>C c.(11782-11784)caA>caC p.Q3928H COAD 13 77644799 77644799 + Missense_Mutation SNP G G T TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr13:77644799G>T c.11757C>A c.(11755-11757)ttC>ttA p.F3919L COAD 13 77651459 77651459 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr13:77651459T>C c.11434A>G c.(11434-11436)Atc>Gtc p.I3812V COAD 13 77655626 77655626 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:77655626T>C c.11240A>G c.(11239-11241)aAc>aGc p.N3747S COAD 13 77657196 77657196 + Silent SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr13:77657196G>A c.10893C>T c.(10891-10893)agC>agT p.S3631S COAD 13 77664369 77664369 + Missense_Mutation SNP T T C TCGA-AA-3852-01A-01W-0900-09 TCGA-AA-3852-10A-01W-0900-09 g.chr13:77664369T>C c.10283A>G c.(10282-10284)gAt>gGt p.D3428G COAD 13 77669576 77669576 + Silent SNP T T C TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr13:77669576T>C c.10002A>G c.(10000-10002)caA>caG p.Q3334Q COAD 13 77671639 77671639 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:77671639A>C c.9536T>G c.(9535-9537)gTt>gGt p.V3179G COAD 13 77671938 77671938 + Silent SNP T T C TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr13:77671938T>C c.9237A>G c.(9235-9237)aaA>aaG p.K3079K COAD 13 77672277 77672277 + Missense_Mutation SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr13:77672277C>T c.1465G>A c.(1465-1467)Gag>Aag p.E489K COAD 13 77672278 77672278 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:77672278G>A c.8897C>T c.(8896-8898)tCg>tTg p.S2966L COAD 13 77672651 77672652 + Frame_Shift_Ins INS - - G TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr13:77672651_77672652insG c.8523_8524insC c.(8521-8526)gataccfs p.T2842fs COAD 13 77672658 77672658 + Missense_Mutation SNP A A T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr13:77672658A>T c.8517T>A c.(8515-8517)gaT>gaA p.D2839E COAD 13 77672768 77672768 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr13:77672768G>A c.8407C>T c.(8407-8409)Cgc>Tgc p.R2803C COAD 13 77695605 77695605 + Silent SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr13:77695605A>G c.7929T>C c.(7927-7929)tcT>tcC p.S2643S COAD 13 77695607 77695607 + Missense_Mutation SNP A A G TCGA-D5-6929-01A-31D-1924-10 TCGA-D5-6929-10A-01D-1924-10 g.chr13:77695607A>G c.7927T>C c.(7927-7929)Tct>Cct p.S2643P COAD 13 77699498 77699498 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr13:77699498C>T c.7876G>A c.(7876-7878)Gga>Aga p.G2626R COAD 13 77700455 77700455 + Nonsense_Mutation SNP C C A TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chr13:77700455C>A c.7768G>T c.(7768-7770)Gag>Tag p.E2590* COAD 13 77700630 77700630 + Silent SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr13:77700630G>A c.7593C>T c.(7591-7593)tgC>tgT p.C2531C COAD 13 77713363 77713363 + Missense_Mutation SNP G G C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr13:77713363G>C c.7513C>G c.(7513-7515)Cat>Gat p.H2505D COAD 13 77720341 77720341 + Missense_Mutation SNP A A T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr13:77720341A>T c.7029T>A c.(7027-7029)aaT>aaA p.N2343K COAD 13 77724946 77724946 + Missense_Mutation SNP C C A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr13:77724946C>A c.6940G>T c.(6940-6942)Gca>Tca p.A2314S COAD 13 77730270 77730270 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr13:77730270G>A c.6724C>T c.(6724-6726)Cgt>Tgt p.R2242C COAD 13 77730329 77730329 + Missense_Mutation SNP T T C TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr13:77730329T>C c.6665A>G c.(6664-6666)cAg>cGg p.Q2222R COAD 13 77740558 77740558 + Silent SNP T T C TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr13:77740558T>C c.6132A>G c.(6130-6132)aaA>aaG p.K2044K COAD 13 77740566 77740566 + Missense_Mutation SNP C C T TCGA-A6-4105-01A-02D-1771-10 TCGA-A6-4105-10A-01D-1771-10 g.chr13:77740566C>T c.6124G>A c.(6124-6126)Gga>Aga p.G2042R COAD 13 77740566 77740566 + Missense_Mutation SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr13:77740566C>T c.6124G>A c.(6124-6126)Gga>Aga p.G2042R COAD 13 77740566 77740566 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr13:77740566C>T c.6124G>A c.(6124-6126)Gga>Aga p.G2042R COAD 13 77742582 77742582 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr13:77742582G>A c.5981C>T c.(5980-5982)gCc>gTc p.A1994V COAD 13 77742631 77742631 + Missense_Mutation SNP T T C TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr13:77742631T>C c.5932A>G c.(5932-5934)Acc>Gcc p.T1978A COAD 13 77742708 77742708 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr13:77742708G>A c.5855C>T c.(5854-5856)cCg>cTg p.P1952L COAD 13 77743778 77743778 + Missense_Mutation SNP T T A TCGA-AA-3858-01A-01W-0900-09 TCGA-AA-3858-10A-01W-0900-09 g.chr13:77743778T>A c.5752A>T c.(5752-5754)Ata>Tta p.I1918L COAD 13 77745750 77745750 + De_novo_Start_OutOfFrame SNP A A C TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:77745750A>C COAD 13 77748601 77748601 + Silent SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr13:77748601G>A c.5382C>T c.(5380-5382)cgC>cgT p.R1794R COAD 13 77750702 77750702 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr13:77750702C>T c.5288G>A c.(5287-5289)gGa>gAa p.G1763E COAD 13 77750754 77750754 + Missense_Mutation SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr13:77750754C>T c.5236G>A c.(5236-5238)Gca>Aca p.A1746T COAD 13 77754358 77754358 + Silent SNP T T C TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr13:77754358T>C c.4923A>G c.(4921-4923)agA>agG p.R1641R COAD 13 77754360 77754360 + Missense_Mutation SNP T T C TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr13:77754360T>C c.4921A>G c.(4921-4923)Aga>Gga p.R1641G COAD 13 77755924 77755924 + Nonsense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr13:77755924G>T c.4739C>A c.(4738-4740)tCa>tAa p.S1580* COAD 13 77760025 77760025 + Silent SNP A A G TCGA-DM-A0X9-01A-11D-A152-10 TCGA-DM-A0X9-10A-01D-A152-10 g.chr13:77760025A>G c.4311T>C c.(4309-4311)tgT>tgC p.C1437C COAD 13 77760025 77760025 + Silent SNP A A G TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr13:77760025A>G c.4311T>C c.(4309-4311)tgT>tgC p.C1437C COAD 13 77760026 77760026 + De_novo_Start_OutOfFrame SNP C C T TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr13:77760026C>T COAD 13 77760027 77760027 + Missense_Mutation SNP A A G TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr13:77760027A>G c.4309T>C c.(4309-4311)Tgt>Cgt p.C1437R COAD 13 77779614 77779614 + Missense_Mutation SNP A A C TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr13:77779614A>C c.3595T>G c.(3595-3597)Ttt>Gtt p.F1199V COAD 13 77780956 77780956 + Nonsense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr13:77780956G>A c.3307C>T c.(3307-3309)Cga>Tga p.R1103* COAD 13 77785378 77785378 + Missense_Mutation SNP T T A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr13:77785378T>A c.3226A>T c.(3226-3228)Act>Tct p.T1076S COAD 13 77786240 77786240 + Missense_Mutation SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr13:77786240G>A c.2999C>T c.(2998-3000)gCt>gTt p.A1000V COAD 13 77786285 77786285 + Missense_Mutation SNP A A G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr13:77786285A>G c.2954T>C c.(2953-2955)cTg>cCg p.L985P COAD 13 77792004 77792004 + Nonsense_Mutation SNP C C A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr13:77792004C>A c.2914G>T c.(2914-2916)Gga>Tga p.G972* COAD 13 77792023 77792023 + Silent SNP C C T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr13:77792023C>T c.2895G>A c.(2893-2895)acG>acA p.T965T COAD 13 77798654 77798654 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:77798654T>G c.2757A>C c.(2755-2757)gaA>gaC p.E919D COAD 13 77817968 77817968 + Nonsense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr13:77817968C>A c.2386G>T c.(2386-2388)Gaa>Taa p.E796* COAD 13 77831879 77831879 + De_novo_Start_OutOfFrame SNP C C A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr13:77831879C>A COAD 13 77834649 77834649 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr13:77834649G>A c.1817C>T c.(1816-1818)gCc>gTc p.A606V COAD 13 77841995 77841995 + Silent SNP A A G TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr13:77841995A>G c.1224T>C c.(1222-1224)gaT>gaC p.D408D COAD 13 77842067 77842067 + Silent SNP A A G TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr13:77842067A>G c.1152T>C c.(1150-1152)taT>taC p.Y384Y COAD 13 77844149 77844149 + Frame_Shift_Del DEL T T - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr13:77844149delT c.1124delA c.(1123-1125)aagfs p.K375fs COAD 13 77853004 77853004 + Nonsense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr13:77853004C>A c.523G>T c.(523-525)Gag>Tag p.E175* COAD 13 77862314 77862314 + Silent SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr13:77862314G>A c.462C>T c.(460-462)ccC>ccT p.P154P COAD 13 77862352 77862352 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:77862352C>T c.424G>A c.(424-426)Gaa>Aaa p.E142K COAD 13 77870783 77870783 + Missense_Mutation SNP T T C TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr13:77870783T>C c.215A>G c.(214-216)aAa>aGa p.K72R COAD 13 77900636 77900636 + Frame_Shift_Del DEL C C - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr13:77900636delC c.161delG c.(160-162)ggcfs p.G55fs COAD 13 77900686 77900686 + Missense_Mutation SNP G G T TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr13:77900686G>T c.111C>A c.(109-111)gaC>gaA p.D37E COADREAD 13 77625227 77625227 + Frame_Shift_Del DEL A A - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr13:77625227delA c.13712delT c.(13711-13713)ttcfs p.F4571fs COADREAD 13 77626011 77626011 + Missense_Mutation SNP G G A TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr13:77626011G>A c.13576C>T c.(13576-13578)Cgg>Tgg p.R4526W COADREAD 13 77626053 77626053 + Splice_Site SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr13:77626053C>T c.13534G>A c.(13534-13536)Gca>Aca p.A4512T COADREAD 13 77631119 77631119 + Splice_Site SNP A A G TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr13:77631119A>G c.e79+1 COADREAD 13 77632488 77632488 + Silent SNP C C A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr13:77632488C>A c.13080G>T c.(13078-13080)ggG>ggT p.G4360G COADREAD 13 77635825 77635825 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr13:77635825T>C c.12761A>G c.(12760-12762)cAt>cGt p.H4254R COADREAD 13 77635909 77635909 + Missense_Mutation SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr13:77635909T>C c.12677A>G c.(12676-12678)cAt>cGt p.H4226R COADREAD 13 77636817 77636817 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr13:77636817C>T c.12574G>A c.(12574-12576)Gca>Aca p.A4192T COADREAD 13 77641849 77641849 + Missense_Mutation SNP T T C TCGA-AA-A00Q-01A-01W-A005-10 TCGA-AA-A00Q-10A-01W-A005-10 g.chr13:77641849T>C c.12208A>G c.(12208-12210)Atg>Gtg p.M4070V COADREAD 13 77641917 77641917 + Frame_Shift_Del DEL G G - TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr13:77641917delG c.12140delC c.(12139-12141)ccafs p.P4047fs COADREAD 13 77641953 77641953 + Missense_Mutation SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr13:77641953C>T c.12104G>A c.(12103-12105)cGt>cAt p.R4035H COADREAD 13 77642770 77642770 + Missense_Mutation SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr13:77642770G>A c.11987C>T c.(11986-11988)gCt>gTt p.A3996V COADREAD 13 77642918 77642918 + Missense_Mutation SNP G G A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr13:77642918G>A c.11839C>T c.(11839-11841)Cgt>Tgt p.R3947C COADREAD 13 77642939 77642939 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:77642939G>A c.11818C>T c.(11818-11820)Cgc>Tgc p.R3940C COADREAD 13 77644772 77644772 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:77644772T>G c.11784A>C c.(11782-11784)caA>caC p.Q3928H COADREAD 13 77644799 77644799 + Missense_Mutation SNP G G T TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr13:77644799G>T c.11757C>A c.(11755-11757)ttC>ttA p.F3919L COADREAD 13 77651459 77651459 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr13:77651459T>C c.11434A>G c.(11434-11436)Atc>Gtc p.I3812V COADREAD 13 77655626 77655626 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:77655626T>C c.11240A>G c.(11239-11241)aAc>aGc p.N3747S COADREAD 13 77657196 77657196 + Silent SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr13:77657196G>A c.10893C>T c.(10891-10893)agC>agT p.S3631S COADREAD 13 77657240 77657240 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:77657240G>A c.10849C>T c.(10849-10851)Cgc>Tgc p.R3617C COADREAD 13 77664369 77664369 + Missense_Mutation SNP T T C TCGA-AA-3852-01A-01W-0900-09 TCGA-AA-3852-10A-01W-0900-09 g.chr13:77664369T>C c.10283A>G c.(10282-10284)gAt>gGt p.D3428G COADREAD 13 77669576 77669576 + Silent SNP T T C TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr13:77669576T>C c.10002A>G c.(10000-10002)caA>caG p.Q3334Q COADREAD 13 77671639 77671639 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:77671639A>C c.9536T>G c.(9535-9537)gTt>gGt p.V3179G COADREAD 13 77671938 77671938 + Silent SNP T T C TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr13:77671938T>C c.9237A>G c.(9235-9237)aaA>aaG p.K3079K COADREAD 13 77672277 77672277 + Missense_Mutation SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr13:77672277C>T c.1465G>A c.(1465-1467)Gag>Aag p.E489K COADREAD 13 77672278 77672278 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:77672278G>A c.8897C>T c.(8896-8898)tCg>tTg p.S2966L COADREAD 13 77672651 77672652 + Frame_Shift_Ins INS - - G TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr13:77672651_77672652insG c.8523_8524insC c.(8521-8526)gataccfs p.T2842fs COADREAD 13 77672658 77672658 + Missense_Mutation SNP A A T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr13:77672658A>T c.8517T>A c.(8515-8517)gaT>gaA p.D2839E COADREAD 13 77672768 77672768 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr13:77672768G>A c.8407C>T c.(8407-8409)Cgc>Tgc p.R2803C COADREAD 13 77695605 77695605 + Silent SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr13:77695605A>G c.7929T>C c.(7927-7929)tcT>tcC p.S2643S COADREAD 13 77695607 77695607 + Missense_Mutation SNP A A G TCGA-D5-6929-01A-31D-1924-10 TCGA-D5-6929-10A-01D-1924-10 g.chr13:77695607A>G c.7927T>C c.(7927-7929)Tct>Cct p.S2643P COADREAD 13 77695607 77695607 + Missense_Mutation SNP A A T TCGA-DY-A1DF-01A-11D-A152-10 TCGA-DY-A1DF-10A-01D-A152-10 g.chr13:77695607A>T c.7927T>A c.(7927-7929)Tct>Act p.S2643T COADREAD 13 77699498 77699498 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr13:77699498C>T c.7876G>A c.(7876-7878)Gga>Aga p.G2626R COADREAD 13 77700455 77700455 + Nonsense_Mutation SNP C C A TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chr13:77700455C>A c.7768G>T c.(7768-7770)Gag>Tag p.E2590* COADREAD 13 77700630 77700630 + Silent SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr13:77700630G>A c.7593C>T c.(7591-7593)tgC>tgT p.C2531C COADREAD 13 77713363 77713363 + Missense_Mutation SNP G G C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr13:77713363G>C c.7513C>G c.(7513-7515)Cat>Gat p.H2505D COADREAD 13 77718581 77718581 + Splice_Site SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:77718581G>A c.7188C>T c.(7186-7188)atC>atT p.I2396I COADREAD 13 77720341 77720341 + Missense_Mutation SNP A A T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr13:77720341A>T c.7029T>A c.(7027-7029)aaT>aaA p.N2343K COADREAD 13 77724946 77724946 + Missense_Mutation SNP C C A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr13:77724946C>A c.6940G>T c.(6940-6942)Gca>Tca p.A2314S COADREAD 13 77730270 77730270 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr13:77730270G>A c.6724C>T c.(6724-6726)Cgt>Tgt p.R2242C COADREAD 13 77730329 77730329 + Missense_Mutation SNP T T C TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr13:77730329T>C c.6665A>G c.(6664-6666)cAg>cGg p.Q2222R COADREAD 13 77740558 77740558 + Silent SNP T T C TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr13:77740558T>C c.6132A>G c.(6130-6132)aaA>aaG p.K2044K COADREAD 13 77740564 77740564 + Silent SNP T T C TCGA-DY-A1DG-01A-11D-A152-10 TCGA-DY-A1DG-10A-01D-A152-10 g.chr13:77740564T>C c.6126A>G c.(6124-6126)ggA>ggG p.G2042G COADREAD 13 77740566 77740566 + Missense_Mutation SNP C C T TCGA-A6-4105-01A-02D-1771-10 TCGA-A6-4105-10A-01D-1771-10 g.chr13:77740566C>T c.6124G>A c.(6124-6126)Gga>Aga p.G2042R COADREAD 13 77740566 77740566 + Missense_Mutation SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr13:77740566C>T c.6124G>A c.(6124-6126)Gga>Aga p.G2042R COADREAD 13 77740566 77740566 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr13:77740566C>T c.6124G>A c.(6124-6126)Gga>Aga p.G2042R COADREAD 13 77742582 77742582 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr13:77742582G>A c.5981C>T c.(5980-5982)gCc>gTc p.A1994V COADREAD 13 77742631 77742631 + Missense_Mutation SNP T T C TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr13:77742631T>C c.5932A>G c.(5932-5934)Acc>Gcc p.T1978A COADREAD 13 77742708 77742708 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr13:77742708G>A c.5855C>T c.(5854-5856)cCg>cTg p.P1952L COADREAD 13 77743778 77743778 + Missense_Mutation SNP T T A TCGA-AA-3858-01A-01W-0900-09 TCGA-AA-3858-10A-01W-0900-09 g.chr13:77743778T>A c.5752A>T c.(5752-5754)Ata>Tta p.I1918L COADREAD 13 77745750 77745750 + De_novo_Start_OutOfFrame SNP A A C TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:77745750A>C COADREAD 13 77748601 77748601 + Silent SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr13:77748601G>A c.5382C>T c.(5380-5382)cgC>cgT p.R1794R COADREAD 13 77750702 77750702 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr13:77750702C>T c.5288G>A c.(5287-5289)gGa>gAa p.G1763E COADREAD 13 77750754 77750754 + Missense_Mutation SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr13:77750754C>T c.5236G>A c.(5236-5238)Gca>Aca p.A1746T COADREAD 13 77754358 77754358 + Silent SNP T T C TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr13:77754358T>C c.4923A>G c.(4921-4923)agA>agG p.R1641R COADREAD 13 77754360 77754360 + Missense_Mutation SNP T T C TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr13:77754360T>C c.4921A>G c.(4921-4923)Aga>Gga p.R1641G COADREAD 13 77755924 77755924 + Nonsense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr13:77755924G>T c.4739C>A c.(4738-4740)tCa>tAa p.S1580* COADREAD 13 77760025 77760025 + Silent SNP A A G TCGA-DM-A0X9-01A-11D-A152-10 TCGA-DM-A0X9-10A-01D-A152-10 g.chr13:77760025A>G c.4311T>C c.(4309-4311)tgT>tgC p.C1437C COADREAD 13 77760025 77760025 + Silent SNP A A G TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr13:77760025A>G c.4311T>C c.(4309-4311)tgT>tgC p.C1437C COADREAD 13 77760026 77760026 + De_novo_Start_OutOfFrame SNP C C T TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr13:77760026C>T COADREAD 13 77760027 77760027 + Missense_Mutation SNP A A G TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr13:77760027A>G c.4309T>C c.(4309-4311)Tgt>Cgt p.C1437R COADREAD 13 77779614 77779614 + Missense_Mutation SNP A A C TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr13:77779614A>C c.3595T>G c.(3595-3597)Ttt>Gtt p.F1199V COADREAD 13 77780956 77780956 + Nonsense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr13:77780956G>A c.3307C>T c.(3307-3309)Cga>Tga p.R1103* COADREAD 13 77785378 77785378 + Missense_Mutation SNP T T A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr13:77785378T>A c.3226A>T c.(3226-3228)Act>Tct p.T1076S COADREAD 13 77786240 77786240 + Missense_Mutation SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr13:77786240G>A c.2999C>T c.(2998-3000)gCt>gTt p.A1000V COADREAD 13 77786285 77786285 + Missense_Mutation SNP A A G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr13:77786285A>G c.2954T>C c.(2953-2955)cTg>cCg p.L985P COADREAD 13 77792004 77792004 + Nonsense_Mutation SNP C C A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr13:77792004C>A c.2914G>T c.(2914-2916)Gga>Tga p.G972* COADREAD 13 77792023 77792023 + Silent SNP C C T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr13:77792023C>T c.2895G>A c.(2893-2895)acG>acA p.T965T COADREAD 13 77798654 77798654 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:77798654T>G c.2757A>C c.(2755-2757)gaA>gaC p.E919D COADREAD 13 77817968 77817968 + Nonsense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr13:77817968C>A c.2386G>T c.(2386-2388)Gaa>Taa p.E796* COADREAD 13 77831879 77831879 + De_novo_Start_OutOfFrame SNP C C A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr13:77831879C>A COADREAD 13 77834649 77834649 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr13:77834649G>A c.1817C>T c.(1816-1818)gCc>gTc p.A606V COADREAD 13 77838066 77838066 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:77838066C>A c.1315G>T c.(1315-1317)Gat>Tat p.D439Y COADREAD 13 77841995 77841995 + Silent SNP A A G TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr13:77841995A>G c.1224T>C c.(1222-1224)gaT>gaC p.D408D COADREAD 13 77842067 77842067 + Silent SNP A A G TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr13:77842067A>G c.1152T>C c.(1150-1152)taT>taC p.Y384Y COADREAD 13 77844149 77844149 + Frame_Shift_Del DEL T T - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr13:77844149delT c.1124delA c.(1123-1125)aagfs p.K375fs COADREAD 13 77853004 77853004 + Nonsense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr13:77853004C>A c.523G>T c.(523-525)Gag>Tag p.E175* COADREAD 13 77862314 77862314 + Silent SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr13:77862314G>A c.462C>T c.(460-462)ccC>ccT p.P154P COADREAD 13 77862352 77862352 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:77862352C>T c.424G>A c.(424-426)Gaa>Aaa p.E142K COADREAD 13 77870783 77870783 + Missense_Mutation SNP T T C TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr13:77870783T>C c.215A>G c.(214-216)aAa>aGa p.K72R COADREAD 13 77900636 77900636 + Frame_Shift_Del DEL C C - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr13:77900636delC c.161delG c.(160-162)ggcfs p.G55fs COADREAD 13 77900686 77900686 + Missense_Mutation SNP G G T TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr13:77900686G>T c.111C>A c.(109-111)gaC>gaA p.D37E DLBC 13 77657173 77657173 + Missense_Mutation SNP G G A TCGA-FF-8041-01A-11D-2210-10 TCGA-FF-8041-10A-01D-2210-10 g.chr13:77657173G>A c.10916C>T c.(10915-10917)gCc>gTc p.A3639V DLBC 13 77740577 77740577 + Missense_Mutation SNP T T C TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr13:77740577T>C c.6113A>G c.(6112-6114)aAt>aGt p.N2038S DLBC 13 77754319 77754319 + De_novo_Start_OutOfFrame SNP G G T TCGA-GS-A9TW-01A-11D-A382-10 TCGA-GS-A9TW-10A-01D-A385-10 g.chr13:77754319G>T ESCA 13 77636817 77636817 + Missense_Mutation SNP C C T TCGA-L5-A8NE-01A-11D-A37C-09 TCGA-L5-A8NE-11A-11D-A37F-09 g.chr13:77636817C>T c.12574G>A c.(12574-12576)Gca>Aca p.A4192T ESCA 13 77641876 77641876 + Missense_Mutation SNP C C G TCGA-LN-A9FO-01A-11D-A387-09 TCGA-LN-A9FO-10A-01D-A38A-09 g.chr13:77641876C>G c.12181G>C c.(12181-12183)Gac>Cac p.D4061H ESCA 13 77657220 77657220 + Silent SNP T T G TCGA-JY-A6FG-01A-11D-A33E-09 TCGA-JY-A6FG-10A-01D-A33H-09 g.chr13:77657220T>G c.10869A>C c.(10867-10869)tcA>tcC p.S3623S ESCA 13 77663012 77663012 + Missense_Mutation SNP C C A TCGA-R6-A6XG-01B-11D-A33E-09 TCGA-R6-A6XG-10A-01D-A33H-09 g.chr13:77663012C>A c.10566G>T c.(10564-10566)atG>atT p.M3522I ESCA 13 77671764 77671764 + Missense_Mutation SNP G G C TCGA-Z6-AAPN-01A-11D-A403-09 TCGA-Z6-AAPN-10A-01D-A403-09 g.chr13:77671764G>C c.9411C>G c.(9409-9411)atC>atG p.I3137M ESCA 13 77672299 77672299 + Missense_Mutation SNP G G A TCGA-L5-A8NV-01A-11D-A37C-09 TCGA-L5-A8NV-11A-11D-A37F-09 g.chr13:77672299G>A c.8876C>T c.(8875-8877)aCc>aTc p.T2959I ESCA 13 77673005 77673005 + Missense_Mutation SNP C C T TCGA-R6-A8W8-01B-11D-A37C-09 TCGA-R6-A8W8-10A-01D-A37F-09 g.chr13:77673005C>T c.8170G>A c.(8170-8172)Gaa>Aaa p.E2724K ESCA 13 77673124 77673124 + Missense_Mutation SNP G G A TCGA-LN-A49Y-01A-11D-A27G-09 TCGA-LN-A49Y-10A-01D-A27G-09 g.chr13:77673124G>A c.8051C>T c.(8050-8052)tCt>tTt p.S2684F ESCA 13 77724939 77724939 + Missense_Mutation SNP G G A TCGA-L5-A4OR-01A-11D-A27G-09 TCGA-L5-A4OR-11A-11D-A27G-09 g.chr13:77724939G>A c.6947C>T c.(6946-6948)cCa>cTa p.P2316L ESCA 13 77738652 77738652 + Missense_Mutation SNP A A T TCGA-JY-A938-01A-11D-A37C-09 TCGA-JY-A938-10A-01D-A37F-09 g.chr13:77738652A>T c.6370T>A c.(6370-6372)Tta>Ata p.L2124I ESCA 13 77739439 77739439 + Missense_Mutation SNP A A G TCGA-VR-AA4D-01A-11D-A37C-09 TCGA-VR-AA4D-10A-01D-A37F-09 g.chr13:77739439A>G c.6314T>C c.(6313-6315)aTt>aCt p.I2105T ESCA 13 77739514 77739514 + Missense_Mutation SNP A A T TCGA-XP-A8T7-01A-11D-A36J-09 TCGA-XP-A8T7-10A-01D-A36M-09 g.chr13:77739514A>T c.6239T>A c.(6238-6240)cTt>cAt p.L2080H ESCA 13 77740653 77740653 + Missense_Mutation SNP C C T TCGA-JY-A93D-01A-11D-A387-09 TCGA-JY-A93D-10A-01D-A38A-09 g.chr13:77740653C>T c.6037G>A c.(6037-6039)Gaa>Aaa p.E2013K ESCA 13 77764414 77764414 + Missense_Mutation SNP G G A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr13:77764414G>A c.4013C>T c.(4012-4014)gCg>gTg p.A1338V ESCA 13 77792007 77792007 + Missense_Mutation SNP C C A TCGA-L5-A4OR-01A-11D-A27G-09 TCGA-L5-A4OR-11A-11D-A27G-09 g.chr13:77792007C>A c.2911G>T c.(2911-2913)Gat>Tat p.D971Y ESCA 13 77807343 77807343 + Silent SNP G G T TCGA-L5-A4OJ-01A-11D-A27G-09 TCGA-L5-A4OJ-11A-12D-A27G-09 g.chr13:77807343G>T c.2571C>A c.(2569-2571)gcC>gcA p.A857A ESCA 13 77835366 77835366 + Missense_Mutation SNP C C T TCGA-VR-A8EY-01A-11D-A36J-09 TCGA-VR-A8EY-10A-01D-A36M-09 g.chr13:77835366C>T c.1678G>A c.(1678-1680)Gca>Aca p.A560T ESCA 13 77842008 77842008 + Missense_Mutation SNP G G A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr13:77842008G>A c.1211C>T c.(1210-1212)aCa>aTa p.T404I GBM 13 77835447 77835447 + Missense_Mutation SNP A A G TCGA-06-0745-01A-01W-0348-08 TCGA-06-0745-10A-01W-0348-08 g.chr13:77835447A>G c.1597T>C c.(1597-1599)Tgg>Cgg p.W533R GBMLGG 13 77631174 77631174 + Nonsense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77631174G>A c.13270C>T c.(13270-13272)Cga>Tga p.R4424* GBMLGG 13 77632512 77632512 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77632512C>T c.13056G>A c.(13054-13056)acG>acA p.T4352T GBMLGG 13 77661658 77661658 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77661658C>A c.10722G>T c.(10720-10722)gaG>gaT p.E3574D GBMLGG 13 77663122 77663122 + Missense_Mutation SNP G G A TCGA-P5-A780-01A-12D-A32B-08 TCGA-P5-A780-10A-01D-A329-08 g.chr13:77663122G>A c.10456C>T c.(10456-10458)Cgg>Tgg p.R3486W GBMLGG 13 77667377 77667377 + Silent SNP C C T TCGA-VW-A7QS-01A-12D-A33T-08 TCGA-VW-A7QS-10A-02D-A33W-08 g.chr13:77667377C>T c.10176G>A c.(10174-10176)ccG>ccA p.P3392P GBMLGG 13 77670496 77670496 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77670496C>T c.9791G>A c.(9790-9792)cGc>cAc p.R3264H GBMLGG 13 77671996 77671996 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77671996T>C c.9179A>G c.(9178-9180)aAt>aGt p.N3060S GBMLGG 13 77714188 77714188 + Missense_Mutation SNP A A C TCGA-DB-5281-01A-01D-1468-08 TCGA-DB-5281-10A-01D-1468-08 g.chr13:77714188A>C c.7398T>G c.(7396-7398)atT>atG p.I2466M GBMLGG 13 77755901 77755901 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77755901C>T c.4762G>A c.(4762-4764)Gag>Aag p.E1588K GBMLGG 13 77807397 77807397 + Splice_Site SNP G G C TCGA-HT-7684-01A-11D-2253-08 TCGA-HT-7684-10A-01D-2253-08 g.chr13:77807397G>C c.2517C>G c.(2515-2517)ggC>ggG p.G839G GBMLGG 13 77835374 77835374 + Missense_Mutation SNP A A G TCGA-P5-A5EZ-01A-11D-A27K-08 TCGA-P5-A5EZ-10A-01D-A27N-08 g.chr13:77835374A>G c.1670T>C c.(1669-1671)cTt>cCt p.L557P GBMLGG 13 77835447 77835447 + Missense_Mutation SNP A A G TCGA-06-0745-01A-01W-0348-08 TCGA-06-0745-10A-01W-0348-08 g.chr13:77835447A>G c.1597T>C c.(1597-1599)Tgg>Cgg p.W533R GBMLGG 13 77844139 77844139 + Missense_Mutation SNP T T G TCGA-VM-A8C8-01A-11D-A36O-08 TCGA-VM-A8C8-10A-01D-A367-08 g.chr13:77844139T>G c.1134A>C c.(1132-1134)ttA>ttC p.L378F GBMLGG 13 77862494 77862494 + Missense_Mutation SNP A A T TCGA-HT-8106-01A-11D-2395-08 TCGA-HT-8106-10A-01D-2396-08 g.chr13:77862494A>T c.282T>A c.(280-282)aaT>aaA p.N94K HNSC 13 77619532 77619532 + Missense_Mutation SNP C C G TCGA-CQ-A4C9-01A-11D-A25D-08 TCGA-CQ-A4C9-10A-01D-A25E-08 g.chr13:77619532C>G c.13904G>C c.(13903-13905)aGa>aCa p.R4635T HNSC 13 77625189 77625190 + Frame_Shift_Ins INS - - A TCGA-BA-5556-01A-01D-1512-08 TCGA-BA-5556-10A-01D-1512-08 g.chr13:77625189_77625190insA c.13749_13750insT c.(13747-13752)catgatfs p.D4584fs HNSC 13 77625998 77625998 + Missense_Mutation SNP T T C TCGA-CV-5966-01A-11D-1683-08 TCGA-CV-5966-10A-01D-1870-08 g.chr13:77625998T>C c.13589A>G c.(13588-13590)tAt>tGt p.Y4530C HNSC 13 77629732 77629732 + Missense_Mutation SNP C C G TCGA-CV-A45Q-01A-11D-A24D-08 TCGA-CV-A45Q-10A-01D-A24F-08 g.chr13:77629732C>G c.13494G>C c.(13492-13494)atG>atC p.M4498I HNSC 13 77632376 77632376 + Missense_Mutation SNP G G A TCGA-CV-6956-01A-21D-2012-08 TCGA-CV-6956-10A-01D-2013-08 g.chr13:77632376G>A c.13192C>T c.(13192-13194)Ctc>Ttc p.L4398F HNSC 13 77633702 77633702 + Missense_Mutation SNP C C T TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr13:77633702C>T c.12982G>A c.(12982-12984)Gag>Aag p.E4328K HNSC 13 77633756 77633756 + Missense_Mutation SNP G G C TCGA-CN-5360-01A-01D-1434-08 TCGA-CN-5360-10A-01D-1434-08 g.chr13:77633756G>C c.12928C>G c.(12928-12930)Ccc>Gcc p.P4310A HNSC 13 77635394 77635394 + Missense_Mutation SNP C C G TCGA-MT-A67F-01A-11D-A30E-08 TCGA-MT-A67F-10A-01D-A30H-08 g.chr13:77635394C>G c.12832G>C c.(12832-12834)Gaa>Caa p.E4278Q HNSC 13 77641807 77641807 + Missense_Mutation SNP T T C TCGA-T2-A6WX-01A-12D-A34J-08 TCGA-T2-A6WX-10B-01D-A34M-08 g.chr13:77641807T>C c.12250A>G c.(12250-12252)Aaa>Gaa p.K4084E HNSC 13 77644815 77644815 + Missense_Mutation SNP A A G TCGA-CV-A463-01A-11D-A25Y-08 TCGA-CV-A463-10A-01D-A25Y-08 g.chr13:77644815A>G c.11741T>C c.(11740-11742)aTg>aCg p.M3914T HNSC 13 77650977 77650977 + Missense_Mutation SNP C C A TCGA-HD-A633-01A-11D-A28R-08 TCGA-HD-A633-10A-01D-A28U-08 g.chr13:77650977C>A c.11618G>T c.(11617-11619)gGa>gTa p.G3873V HNSC 13 77651324 77651324 + Missense_Mutation SNP C C T TCGA-H7-7774-01A-21D-2078-08 TCGA-H7-7774-10A-01D-2078-08 g.chr13:77651324C>T c.11569G>A c.(11569-11571)Gaa>Aaa p.E3857K HNSC 13 77661767 77661767 + Splice_Site SNP G G A TCGA-C9-A47Z-01A-11D-A24D-08 TCGA-C9-A47Z-10A-01D-A24F-08 g.chr13:77661767G>A c.10613C>T c.(10612-10614)gCt>gTt p.A3538V HNSC 13 77662989 77662989 + Missense_Mutation SNP G G A TCGA-CV-6950-01A-11D-1912-08 TCGA-CV-6950-10A-01D-1912-08 g.chr13:77662989G>A c.10589C>T c.(10588-10590)gCt>gTt p.A3530V HNSC 13 77667369 77667369 + Missense_Mutation SNP G G A TCGA-CV-7099-01A-41D-2012-08 TCGA-CV-7099-10A-01D-2013-08 g.chr13:77667369G>A c.10184C>T c.(10183-10185)tCa>tTa p.S3395L HNSC 13 77670523 77670523 + Missense_Mutation SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr13:77670523C>T c.9764G>A c.(9763-9765)gGa>gAa p.G3255E HNSC 13 77671556 77671556 + Missense_Mutation SNP C C G TCGA-CV-6948-01A-11D-1912-08 TCGA-CV-6948-10A-01D-1912-08 g.chr13:77671556C>G c.9619G>C c.(9619-9621)Ggg>Cgg p.G3207R HNSC 13 77672447 77672447 + Missense_Mutation SNP C C A TCGA-CR-7364-01A-11D-2012-08 TCGA-CR-7364-10A-01D-2013-08 g.chr13:77672447C>A c.8728G>T c.(8728-8730)Gac>Tac p.D2910Y HNSC 13 77672743 77672743 + Missense_Mutation SNP T T C TCGA-CV-5966-01A-11D-1683-08 TCGA-CV-5966-10A-01D-1870-08 g.chr13:77672743T>C c.8432A>G c.(8431-8433)aAt>aGt p.N2811S HNSC 13 77699528 77699528 + Missense_Mutation SNP C C G TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr13:77699528C>G c.7846G>C c.(7846-7848)Gag>Cag p.E2616Q HNSC 13 77715011 77715011 + Silent SNP G G C TCGA-CR-7373-01A-11D-2012-08 TCGA-CR-7373-10A-01D-2013-08 g.chr13:77715011G>C c.7257C>G c.(7255-7257)gtC>gtG p.V2419V HNSC 13 77742684 77742684 + Missense_Mutation SNP G G C TCGA-CV-7091-01A-11D-2012-08 TCGA-CV-7091-10A-01D-2013-08 g.chr13:77742684G>C c.5879C>G c.(5878-5880)tCg>tGg p.S1960W HNSC 13 77748593 77748593 + Missense_Mutation SNP T T A TCGA-CQ-A4CA-01A-11D-A25D-08 TCGA-CQ-A4CA-10A-01D-A25E-08 g.chr13:77748593T>A c.5390A>T c.(5389-5391)aAc>aTc p.N1797I HNSC 13 77751900 77751900 + Missense_Mutation SNP C C T TCGA-CN-6023-01A-11D-1683-08 TCGA-CN-6023-10A-01D-1683-08 g.chr13:77751900C>T c.5209G>A c.(5209-5211)Gag>Aag p.E1737K HNSC 13 77754439 77754439 + Silent SNP G G T TCGA-CV-A45Z-01A-21D-A25D-08 TCGA-CV-A45Z-10A-01D-A25E-08 g.chr13:77754439G>T c.4842C>A c.(4840-4842)atC>atA p.I1614I HNSC 13 77759426 77759426 + Missense_Mutation SNP C C G TCGA-DQ-5624-01A-01D-1870-08 TCGA-DQ-5624-10A-01D-1870-08 g.chr13:77759426C>G c.4417G>C c.(4417-4419)Gaa>Caa p.E1473Q HNSC 13 77765925 77765925 + Missense_Mutation SNP T T C TCGA-CV-A6JM-01A-11D-A31L-08 TCGA-CV-A6JM-10A-01D-A31J-08 g.chr13:77765925T>C c.3845A>G c.(3844-3846)gAt>gGt p.D1282G HNSC 13 77779509 77779509 + Missense_Mutation SNP C C T TCGA-CQ-7072-01A-21D-A30E-08 TCGA-CQ-7072-10A-01D-A30H-08 g.chr13:77779509C>T c.3611G>A c.(3610-3612)gGa>gAa p.G1204E HNSC 13 77791957 77791989 + Splice_Site DEL GTTTTAAAAATTCCTTACAGAAAAACTTCCAAA GTTTTAAAAATTCCTTACAGAAAAACTTCCAAA - TCGA-IQ-A61K-01A-11D-A30E-08 TCGA-IQ-A61K-10A-01D-A30H-08 g.chr13:77791957_77791989delGTTTTAAAAATTCCTTACAGAAAAACTTCCAAA c.2929_2944delTTTGGAAGTTTTTCTGTAAGGAATTTTTAAAAC c.(2929-2946)tttggaagtttttctgta>ta p.FGSFSV977del HNSC 13 77792089 77792089 + Silent SNP T T C TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chr13:77792089T>C c.2829A>G c.(2827-2829)ggA>ggG p.G943G HNSC 13 77847776 77847776 + Missense_Mutation SNP A A G TCGA-CV-A6JN-01A-11D-A31L-08 TCGA-CV-A6JN-10A-01D-A31J-08 g.chr13:77847776A>G c.662T>C c.(661-663)aTc>aCc p.I221T HNSC 13 77870791 77870791 + Silent SNP A A G TCGA-CN-A6V3-01A-12D-A34J-08 TCGA-CN-A6V3-10A-01D-A34M-08 g.chr13:77870791A>G c.207T>C c.(205-207)aaT>aaC p.N69N KICH 13 77714270 77714270 + Missense_Mutation SNP G G A TCGA-KN-8423-01A-11D-2310-10 TCGA-KN-8423-11A-01D-2310-10 g.chr13:77714270G>A c.7316C>T c.(7315-7317)gCg>gTg p.A2439V KICH 13 77799637 77799637 + Silent SNP A A G TCGA-KL-8343-01A-11D-2310-10 TCGA-KL-8343-11A-01D-2310-10 g.chr13:77799637A>G c.2676T>C c.(2674-2676)ccT>ccC p.P892P KIPAN 13 77629761 77629761 + Missense_Mutation SNP A A G TCGA-B0-5709-01A-11D-1534-10 TCGA-B0-5709-11A-01D-1534-10 g.chr13:77629761A>G c.13465T>C c.(13465-13467)Ttt>Ctt p.F4489L KIPAN 13 77642846 77642846 + Missense_Mutation SNP A A C TCGA-4A-A93W-01A-11D-A36X-10 TCGA-4A-A93W-10A-01D-A370-10 g.chr13:77642846A>C c.11911T>G c.(11911-11913)Tct>Gct p.S3971A KIPAN 13 77657271 77657272 + Missense_Mutation DNP TT TT CG TCGA-UZ-A9PZ-01A-11D-A42J-10 TCGA-UZ-A9PZ-10A-01D-A42M-10 g.chr13:77657271_77657272TT>CG c.10817_10818AA>CG c.(10816-10818)gAA>gCG p.E3606A KIPAN 13 77669615 77669615 + Silent SNP T T C TCGA-B0-4691-01A-01D-1361-10 TCGA-B0-4691-11A-01D-1361-10 g.chr13:77669615T>C c.9963A>G c.(9961-9963)gaA>gaG p.E3321E KIPAN 13 77714270 77714270 + Missense_Mutation SNP G G A TCGA-KN-8423-01A-11D-2310-10 TCGA-KN-8423-11A-01D-2310-10 g.chr13:77714270G>A c.7316C>T c.(7315-7317)gCg>gTg p.A2439V KIPAN 13 77714290 77714290 + Frame_Shift_Del DEL T T - TCGA-CZ-5462-01A-01D-1501-10 TCGA-CZ-5462-11A-01D-1501-10 g.chr13:77714290delT c.7296delA c.(7294-7296)aaafs p.K2432fs KIPAN 13 77714983 77714983 + De_novo_Start_OutOfFrame SNP T T C TCGA-B9-A5W9-01A-11D-A28G-10 TCGA-B9-A5W9-10A-01D-A28G-10 g.chr13:77714983T>C KIPAN 13 77730192 77730192 + Splice_Site SNP C C A TCGA-BP-4331-01A-01D-1366-10 TCGA-BP-4331-11A-01D-1366-10 g.chr13:77730192C>A c.e46+1 KIPAN 13 77732194 77732194 + Silent SNP A A G TCGA-F9-A7VF-01A-11D-A33Q-10 TCGA-F9-A7VF-10A-01D-A33Q-10 g.chr13:77732194A>G c.6534T>C c.(6532-6534)caT>caC p.H2178H KIPAN 13 77742691 77742691 + Missense_Mutation SNP T T C TCGA-5P-A9K3-01A-11D-A42J-10 TCGA-5P-A9K3-10A-01D-A42M-10 g.chr13:77742691T>C c.5872A>G c.(5872-5874)Aat>Gat p.N1958D KIPAN 13 77759324 77759326 + In_Frame_Del DEL TAT TAT - TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr13:77759324_77759326delTAT c.4517_4519delATA c.(4516-4521)aatact>act p.N1506del KIPAN 13 77785318 77785318 + Missense_Mutation SNP A A G TCGA-CJ-5684-01A-11D-1534-10 TCGA-CJ-5684-11A-01D-1535-10 g.chr13:77785318A>G c.3286T>C c.(3286-3288)Tat>Cat p.Y1096H KIPAN 13 77798620 77798620 + Missense_Mutation SNP G G T TCGA-A3-3313-01A-01D-0966-08 TCGA-A3-3313-11A-01D-0966-08 g.chr13:77798620G>T c.2791C>A c.(2791-2793)Cat>Aat p.H931N KIPAN 13 77799637 77799637 + Silent SNP A A G TCGA-KL-8343-01A-11D-2310-10 TCGA-KL-8343-11A-01D-2310-10 g.chr13:77799637A>G c.2676T>C c.(2674-2676)ccT>ccC p.P892P KIPAN 13 77799654 77799654 + Missense_Mutation SNP T T C TCGA-EV-5902-01A-11D-1589-08 TCGA-EV-5902-10A-01D-1589-08 g.chr13:77799654T>C c.2659A>G c.(2659-2661)Aaa>Gaa p.K887E KIPAN 13 77817235 77817235 + Missense_Mutation SNP C C G TCGA-B0-5109-01A-02D-1421-08 TCGA-B0-5109-11A-01D-1421-08 g.chr13:77817235C>G c.2474G>C c.(2473-2475)cGg>cCg p.R825P KIPAN 13 77853046 77853046 + Splice_Site SNP T T G TCGA-SX-A7SR-01A-12D-A35Z-10 TCGA-SX-A7SR-10A-01D-A35Z-10 g.chr13:77853046T>G c.481A>C c.(481-483)Att>Ctt p.I161L KIRC 13 77629761 77629761 + Missense_Mutation SNP A A G TCGA-B0-5709-01A-11D-1534-10 TCGA-B0-5709-11A-01D-1534-10 g.chr13:77629761A>G c.13465T>C c.(13465-13467)Ttt>Ctt p.F4489L KIRC 13 77669615 77669615 + Silent SNP T T C TCGA-B0-4691-01A-01D-1361-10 TCGA-B0-4691-11A-01D-1361-10 g.chr13:77669615T>C c.9963A>G c.(9961-9963)gaA>gaG p.E3321E KIRC 13 77714290 77714290 + Frame_Shift_Del DEL T T - TCGA-CZ-5462-01A-01D-1501-10 TCGA-CZ-5462-11A-01D-1501-10 g.chr13:77714290delT c.7296delA c.(7294-7296)aaafs p.K2432fs KIRC 13 77730192 77730192 + Splice_Site SNP C C A TCGA-BP-4331-01A-01D-1366-10 TCGA-BP-4331-11A-01D-1366-10 g.chr13:77730192C>A c.e46+1 KIRC 13 77759324 77759326 + In_Frame_Del DEL TAT TAT - TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr13:77759324_77759326delTAT c.4517_4519delATA c.(4516-4521)aatact>act p.N1506del KIRC 13 77785318 77785318 + Missense_Mutation SNP A A G TCGA-CJ-5684-01A-11D-1534-10 TCGA-CJ-5684-11A-01D-1535-10 g.chr13:77785318A>G c.3286T>C c.(3286-3288)Tat>Cat p.Y1096H KIRC 13 77798620 77798620 + Missense_Mutation SNP G G T TCGA-A3-3313-01A-01D-0966-08 TCGA-A3-3313-11A-01D-0966-08 g.chr13:77798620G>T c.2791C>A c.(2791-2793)Cat>Aat p.H931N KIRC 13 77817235 77817235 + Missense_Mutation SNP C C G TCGA-B0-5109-01A-02D-1421-08 TCGA-B0-5109-11A-01D-1421-08 g.chr13:77817235C>G c.2474G>C c.(2473-2475)cGg>cCg p.R825P KIRP 13 77642846 77642846 + Missense_Mutation SNP A A C TCGA-4A-A93W-01A-11D-A36X-10 TCGA-4A-A93W-10A-01D-A370-10 g.chr13:77642846A>C c.11911T>G c.(11911-11913)Tct>Gct p.S3971A KIRP 13 77657271 77657272 + Missense_Mutation DNP TT TT CG TCGA-UZ-A9PZ-01A-11D-A42J-10 TCGA-UZ-A9PZ-10A-01D-A42M-10 g.chr13:77657271_77657272TT>CG c.10817_10818AA>CG c.(10816-10818)gAA>gCG p.E3606A KIRP 13 77714983 77714983 + De_novo_Start_OutOfFrame SNP T T C TCGA-B9-A5W9-01A-11D-A28G-10 TCGA-B9-A5W9-10A-01D-A28G-10 g.chr13:77714983T>C KIRP 13 77732194 77732194 + Silent SNP A A G TCGA-F9-A7VF-01A-11D-A33Q-10 TCGA-F9-A7VF-10A-01D-A33Q-10 g.chr13:77732194A>G c.6534T>C c.(6532-6534)caT>caC p.H2178H KIRP 13 77742691 77742691 + Missense_Mutation SNP T T C TCGA-5P-A9K3-01A-11D-A42J-10 TCGA-5P-A9K3-10A-01D-A42M-10 g.chr13:77742691T>C c.5872A>G c.(5872-5874)Aat>Gat p.N1958D KIRP 13 77799654 77799654 + Missense_Mutation SNP T T C TCGA-EV-5902-01A-11D-1589-08 TCGA-EV-5902-10A-01D-1589-08 g.chr13:77799654T>C c.2659A>G c.(2659-2661)Aaa>Gaa p.K887E KIRP 13 77853046 77853046 + Splice_Site SNP T T G TCGA-SX-A7SR-01A-12D-A35Z-10 TCGA-SX-A7SR-10A-01D-A35Z-10 g.chr13:77853046T>G c.481A>C c.(481-483)Att>Ctt p.I161L LAML 13 77730270 77730270 + Missense_Mutation SNP G G A TCGA-AB-2991-03A-01D-0739-09 TCGA-AB-2991-11A-01D-0739-09 g.chr13:77730270G>A c.6724C>T c.(6724-6726)Cgt>Tgt p.R2242C LGG 13 77631174 77631174 + Nonsense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77631174G>A c.13270C>T c.(13270-13272)Cga>Tga p.R4424* LGG 13 77632512 77632512 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77632512C>T c.13056G>A c.(13054-13056)acG>acA p.T4352T LGG 13 77661658 77661658 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77661658C>A c.10722G>T c.(10720-10722)gaG>gaT p.E3574D LGG 13 77663122 77663122 + Missense_Mutation SNP G G A TCGA-P5-A780-01A-12D-A32B-08 TCGA-P5-A780-10A-01D-A329-08 g.chr13:77663122G>A c.10456C>T c.(10456-10458)Cgg>Tgg p.R3486W LGG 13 77667377 77667377 + Silent SNP C C T TCGA-VW-A7QS-01A-12D-A33T-08 TCGA-VW-A7QS-10A-02D-A33W-08 g.chr13:77667377C>T c.10176G>A c.(10174-10176)ccG>ccA p.P3392P LGG 13 77670496 77670496 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77670496C>T c.9791G>A c.(9790-9792)cGc>cAc p.R3264H LGG 13 77671996 77671996 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77671996T>C c.9179A>G c.(9178-9180)aAt>aGt p.N3060S LGG 13 77714188 77714188 + Missense_Mutation SNP A A C TCGA-DB-5281-01A-01D-1468-08 TCGA-DB-5281-10A-01D-1468-08 g.chr13:77714188A>C c.7398T>G c.(7396-7398)atT>atG p.I2466M LGG 13 77755901 77755901 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:77755901C>T c.4762G>A c.(4762-4764)Gag>Aag p.E1588K LGG 13 77807397 77807397 + Splice_Site SNP G G C TCGA-HT-7684-01A-11D-2253-08 TCGA-HT-7684-10A-01D-2253-08 g.chr13:77807397G>C c.2517C>G c.(2515-2517)ggC>ggG p.G839G LGG 13 77835374 77835374 + Missense_Mutation SNP A A G TCGA-P5-A5EZ-01A-11D-A27K-08 TCGA-P5-A5EZ-10A-01D-A27N-08 g.chr13:77835374A>G c.1670T>C c.(1669-1671)cTt>cCt p.L557P LGG 13 77844139 77844139 + Missense_Mutation SNP T T G TCGA-VM-A8C8-01A-11D-A36O-08 TCGA-VM-A8C8-10A-01D-A367-08 g.chr13:77844139T>G c.1134A>C c.(1132-1134)ttA>ttC p.L378F LGG 13 77862494 77862494 + Missense_Mutation SNP A A T TCGA-HT-8106-01A-11D-2395-08 TCGA-HT-8106-10A-01D-2396-08 g.chr13:77862494A>T c.282T>A c.(280-282)aaT>aaA p.N94K LIHC 13 77636737 77636737 + Frame_Shift_Del DEL T T - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr13:77636737delT c.12654delA c.(12652-12654)aaafs p.K4218fs LIHC 13 77642923 77642923 + Missense_Mutation SNP C C G TCGA-CC-A7IE-01A-21D-A382-10 TCGA-CC-A7IE-10A-01D-A385-10 g.chr13:77642923C>G c.11834G>C c.(11833-11835)aGa>aCa p.R3945T LIHC 13 77656079 77656079 + Missense_Mutation SNP T T C TCGA-DD-A73B-01A-12D-A32G-10 TCGA-DD-A73B-10A-01D-A32G-10 g.chr13:77656079T>C c.10972A>G c.(10972-10974)Agc>Ggc p.S3658G LIHC 13 77661633 77661633 + Missense_Mutation SNP C C T TCGA-DD-AACV-01A-11D-A40R-10 TCGA-DD-AACV-10A-01D-A40U-10 g.chr13:77661633C>T c.10747G>A c.(10747-10749)Gaa>Aaa p.E3583K LIHC 13 77671529 77671529 + Missense_Mutation SNP A A C TCGA-DD-AAD8-01A-11D-A40R-10 TCGA-DD-AAD8-10A-01D-A40U-10 g.chr13:77671529A>C c.9646T>G c.(9646-9648)Tat>Gat p.Y3216D LIHC 13 77672195 77672195 + Nonsense_Mutation SNP T T A TCGA-DD-AACT-01A-11D-A40R-10 TCGA-DD-AACT-10A-01D-A40U-10 g.chr13:77672195T>A c.8980A>T c.(8980-8982)Aga>Tga p.R2994* LIHC 13 77672359 77672359 + Missense_Mutation SNP T T C TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr13:77672359T>C c.8816A>G c.(8815-8817)aAa>aGa p.K2939R LIHC 13 77700507 77700507 + Missense_Mutation SNP T T A TCGA-CC-A8HV-01A-11D-A35Z-10 TCGA-CC-A8HV-10A-01D-A35Z-10 g.chr13:77700507T>A c.7716A>T c.(7714-7716)agA>agT p.R2572S LIHC 13 77740659 77740659 + Missense_Mutation SNP T T C TCGA-DD-A3A1-01A-11D-A20W-10 TCGA-DD-A3A1-11A-11D-A20W-10 g.chr13:77740659T>C c.6031A>G c.(6031-6033)Aca>Gca p.T2011A LIHC 13 77743838 77743838 + Missense_Mutation SNP G G C TCGA-CC-A7IE-01A-21D-A382-10 TCGA-CC-A7IE-10A-01D-A385-10 g.chr13:77743838G>C c.5692C>G c.(5692-5694)Cca>Gca p.P1898A LIHC 13 77750664 77750664 + Nonsense_Mutation SNP C C A TCGA-MI-A75E-01A-11D-A32G-10 TCGA-MI-A75E-10A-01D-A32G-10 g.chr13:77750664C>A c.5326G>T c.(5326-5328)Gag>Tag p.E1776* LIHC 13 77751932 77751932 + Missense_Mutation SNP T T C TCGA-DD-AACX-01A-11D-A40R-10 TCGA-DD-AACX-10A-01D-A40U-10 g.chr13:77751932T>C c.5177A>G c.(5176-5178)tAt>tGt p.Y1726C LIHC 13 77755971 77755971 + Silent SNP C C A TCGA-DD-AAC8-01A-11D-A40R-10 TCGA-DD-AAC8-10A-01D-A40U-10 g.chr13:77755971C>A c.4692G>T c.(4690-4692)ctG>ctT p.L1564L LIHC 13 77763108 77763108 + Missense_Mutation SNP G G T TCGA-CC-A5UD-01A-11D-A28X-10 TCGA-CC-A5UD-10A-01D-A28X-10 g.chr13:77763108G>T c.4115C>A c.(4114-4116)tCt>tAt p.S1372Y LIHC 13 77798633 77798633 + Frame_Shift_Del DEL A A - TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr13:77798633delA c.2778delT c.(2776-2778)tttfs p.F926fs LIHC 13 77836229 77836229 + Missense_Mutation SNP C C T TCGA-5C-A9VH-01A-11D-A36X-10 TCGA-5C-A9VH-10A-01D-A370-10 g.chr13:77836229C>T c.1492G>A c.(1492-1494)Gca>Aca p.A498T LIHC 13 77842001 77842001 + Missense_Mutation SNP C C A TCGA-DD-AADW-01A-11D-A38X-10 TCGA-DD-AADW-10A-01D-A38X-10 g.chr13:77842001C>A c.1218G>T c.(1216-1218)gaG>gaT p.E406D LIHC 13 77844588 77844588 + Missense_Mutation SNP C C T TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr13:77844588C>T c.917G>A c.(916-918)gGc>gAc p.G306D LUAD 13 77631213 77631213 + Missense_Mutation SNP T T C TCGA-05-4415-01A-22D-1855-08 TCGA-05-4415-10A-01D-1855-08 g.chr13:77631213T>C c.13231A>G c.(13231-13233)Ata>Gta p.I4411V LUAD 13 77632489 77632489 + Missense_Mutation SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr13:77632489C>A c.13079G>T c.(13078-13080)gGg>gTg p.G4360V LUAD 13 77640183 77640183 + Missense_Mutation SNP A A G TCGA-67-4679-01B-01D-1753-08 TCGA-67-4679-10A-01D-1753-08 g.chr13:77640183A>G c.12382T>C c.(12382-12384)Tca>Cca p.S4128P LUAD 13 77642954 77642954 + Missense_Mutation SNP T T C TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr13:77642954T>C c.11803A>G c.(11803-11805)Att>Gtt p.I3935V LUAD 13 77655572 77655572 + Missense_Mutation SNP C C T TCGA-50-6591-01A-11D-1753-08 TCGA-50-6591-11A-01D-1753-08 g.chr13:77655572C>T c.11294G>A c.(11293-11295)cGa>cAa p.R3765Q LUAD 13 77655608 77655608 + Missense_Mutation SNP T T C TCGA-62-A46S-01A-11D-A24D-08 TCGA-62-A46S-10A-01D-A24F-08 g.chr13:77655608T>C c.11258A>G c.(11257-11259)aAt>aGt p.N3753S LUAD 13 77655991 77655991 + Missense_Mutation SNP C C A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr13:77655991C>A c.11060G>T c.(11059-11061)gGc>gTc p.G3687V LUAD 13 77656020 77656020 + Missense_Mutation SNP T T G TCGA-05-4418-01A-01D-1265-08 TCGA-05-4418-10A-01D-1265-08 g.chr13:77656020T>G c.11031A>C c.(11029-11031)gaA>gaC p.E3677D LUAD 13 77656071 77656071 + Silent SNP G G C TCGA-55-7910-01A-11D-2167-08 TCGA-55-7910-11A-01D-2167-08 g.chr13:77656071G>C c.10980C>G c.(10978-10980)gtC>gtG p.V3660V LUAD 13 77663000 77663000 + Silent SNP T T A TCGA-50-5049-01A-01D-1625-08 TCGA-50-5049-10A-01D-1625-08 g.chr13:77663000T>A c.10578A>T c.(10576-10578)ctA>ctT p.L3526L LUAD 13 77663032 77663032 + Missense_Mutation SNP C C G TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr13:77663032C>G c.10546G>C c.(10546-10548)Gaa>Caa p.E3516Q LUAD 13 77664249 77664249 + Missense_Mutation SNP C C G TCGA-J2-A4AD-01A-11D-A24D-08 TCGA-J2-A4AD-10A-01D-A24F-08 g.chr13:77664249C>G c.10403G>C c.(10402-10404)gGa>gCa p.G3468A LUAD 13 77664259 77664259 + Missense_Mutation SNP C C A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr13:77664259C>A c.10393G>T c.(10393-10395)Gtt>Ttt p.V3465F LUAD 13 77669555 77669555 + Missense_Mutation SNP T T A TCGA-MN-A4N1-01A-11D-A24P-08 TCGA-MN-A4N1-10A-01D-A24P-08 g.chr13:77669555T>A c.10023A>T c.(10021-10023)aaA>aaT p.K3341N LUAD 13 77669677 77669677 + Missense_Mutation SNP C C G TCGA-50-5049-01A-01D-1625-08 TCGA-50-5049-10A-01D-1625-08 g.chr13:77669677C>G c.9901G>C c.(9901-9903)Gaa>Caa p.E3301Q LUAD 13 77669711 77669711 + Missense_Mutation SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr13:77669711C>A c.9867G>T c.(9865-9867)atG>atT p.M3289I LUAD 13 77670506 77670506 + Missense_Mutation SNP C C A TCGA-55-7914-01A-11D-2167-08 TCGA-55-7914-10A-01D-2167-08 g.chr13:77670506C>A c.9781G>T c.(9781-9783)Gta>Tta p.V3261L LUAD 13 77670575 77670575 + Missense_Mutation SNP C C A TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr13:77670575C>A c.9712G>T c.(9712-9714)Ggg>Tgg p.G3238W LUAD 13 77671766 77671766 + Missense_Mutation SNP T T C TCGA-17-Z030-01A-01W-0746-08 TCGA-17-Z030-11A-01W-0746-08 g.chr13:77671766T>C c.9409A>G c.(9409-9411)Atc>Gtc p.I3137V LUAD 13 77671869 77671869 + Silent SNP G G C TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr13:77671869G>C c.9306C>G c.(9304-9306)acC>acG p.T3102T LUAD 13 77671932 77671932 + Missense_Mutation SNP C C A TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr13:77671932C>A c.9243G>T c.(9241-9243)aaG>aaT p.K3081N LUAD 13 77672295 77672295 + Missense_Mutation SNP C C A TCGA-91-7771-01A-11D-2167-08 TCGA-91-7771-10A-01D-2167-08 g.chr13:77672295C>A c.8880G>T c.(8878-8880)agG>agT p.R2960S LUAD 13 77695587 77695587 + Missense_Mutation SNP G G T TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr13:77695587G>T c.7947C>A c.(7945-7947)agC>agA p.S2649R LUAD 13 77699604 77699604 + Splice_Site SNP C C A TCGA-91-6848-01A-11D-1945-08 TCGA-91-6848-11A-01D-1945-08 g.chr13:77699604C>A c.e54-1 LUAD 13 77713445 77713445 + Silent SNP C C T TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr13:77713445C>T c.7431G>A c.(7429-7431)ctG>ctA p.L2477L LUAD 13 77714190 77714190 + Missense_Mutation SNP T T A TCGA-17-Z030-01A-01W-0746-08 TCGA-17-Z030-11A-01W-0746-08 g.chr13:77714190T>A c.7396A>T c.(7396-7398)Att>Ttt p.I2466F LUAD 13 77724985 77724985 + Missense_Mutation SNP C C T TCGA-62-8399-01A-21D-2323-08 TCGA-62-8399-10A-01D-2323-08 g.chr13:77724985C>T c.6901G>A c.(6901-6903)Gct>Act p.A2301T LUAD 13 77738625 77738625 + Missense_Mutation SNP C C A TCGA-91-A4BC-01A-11D-A24D-08 TCGA-91-A4BC-10A-01D-A24F-08 g.chr13:77738625C>A c.6397G>T c.(6397-6399)Gca>Tca p.A2133S LUAD 13 77739436 77739436 + Missense_Mutation SNP C C T TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr13:77739436C>T c.6317G>A c.(6316-6318)gGa>gAa p.G2106E LUAD 13 77748446 77748446 + Splice_Site SNP C C T TCGA-17-Z049-01A-01W-0746-08 TCGA-17-Z049-11A-01W-0747-08 g.chr13:77748446C>T c.5537G>A c.(5536-5538)aGg>aAg p.R1846K LUAD 13 77748563 77748563 + Missense_Mutation SNP C C T TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr13:77748563C>T c.5420G>A c.(5419-5421)gGa>gAa p.G1807E LUAD 13 77754433 77754433 + Silent SNP C C A TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr13:77754433C>A c.4848G>T c.(4846-4848)ggG>ggT p.G1616G LUAD 13 77755891 77755891 + Missense_Mutation SNP G G A TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chr13:77755891G>A c.4772C>T c.(4771-4773)tCa>tTa p.S1591L LUAD 13 77755944 77755944 + Silent SNP A A G TCGA-38-4628-01A-01D-1265-08 TCGA-38-4628-11A-01D-1265-08 g.chr13:77755944A>G c.4719T>C c.(4717-4719)gaT>gaC p.D1573D LUAD 13 77759467 77759467 + Missense_Mutation SNP C C T TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr13:77759467C>T c.4376G>A c.(4375-4377)tGt>tAt p.C1459Y LUAD 13 77765894 77765894 + Missense_Mutation SNP C C A TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr13:77765894C>A c.3876G>T c.(3874-3876)tgG>tgT p.W1292C LUAD 13 77779485 77779485 + Missense_Mutation SNP G G A TCGA-86-7955-01A-11D-2184-08 TCGA-86-7955-10A-01D-2184-08 g.chr13:77779485G>A c.3635C>T c.(3634-3636)tCa>tTa p.S1212L LUAD 13 77779653 77779653 + Missense_Mutation SNP T T G TCGA-49-4487-01A-21D-1855-08 TCGA-49-4487-11A-01D-1855-08 g.chr13:77779653T>G c.3556A>C c.(3556-3558)Aag>Cag p.K1186Q LUAD 13 77786258 77786258 + De_novo_Start_OutOfFrame SNP T T C TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr13:77786258T>C LUAD 13 77799691 77799691 + Splice_Site SNP T T C TCGA-MP-A4SY-01A-21D-A24P-08 TCGA-MP-A4SY-10A-01D-A24P-08 g.chr13:77799691T>C c.e19-2 LUAD 13 77817201 77817201 + De_novo_Start_OutOfFrame SNP T T A TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr13:77817201T>A LUAD 13 77831824 77831824 + Missense_Mutation SNP T T A TCGA-86-8672-01A-21D-2393-08 TCGA-86-8672-10A-01D-2393-08 g.chr13:77831824T>A c.2044A>T c.(2044-2046)Atg>Ttg p.M682L LUAD 13 77831856 77831856 + Missense_Mutation SNP T T C TCGA-78-7148-01A-11D-2036-08 TCGA-78-7148-10A-01D-2036-08 g.chr13:77831856T>C c.2012A>G c.(2011-2013)aAt>aGt p.N671S LUAD 13 77847655 77847655 + Silent SNP G G A TCGA-55-7903-01A-11D-2167-08 TCGA-55-7903-10A-01D-2167-08 g.chr13:77847655G>A c.783C>T c.(781-783)atC>atT p.I261I LUAD 13 77847731 77847731 + Missense_Mutation SNP A A G TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr13:77847731A>G c.707T>C c.(706-708)tTa>tCa p.L236S LUAD 13 77900726 77900726 + Missense_Mutation SNP C C A TCGA-78-7159-01A-11D-2036-08 TCGA-78-7159-10A-01D-2036-08 g.chr13:77900726C>A c.71G>T c.(70-72)gGt>gTt p.G24V LUSC 13 77629779 77629779 + Missense_Mutation SNP T T C TCGA-39-5036-01A-01D-1441-08 TCGA-39-5036-11A-01D-1441-08 g.chr13:77629779T>C c.13447A>G c.(13447-13449)Aca>Gca p.T4483A LUSC 13 77636830 77636830 + Silent SNP G G A TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr13:77636830G>A c.12561C>T c.(12559-12561)ctC>ctT p.L4187L LUSC 13 77641898 77641898 + Silent SNP G G A TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr13:77641898G>A c.12159C>T c.(12157-12159)atC>atT p.I4053I LUSC 13 77644818 77644818 + Missense_Mutation SNP T T G TCGA-63-5128-01A-01D-1441-08 TCGA-63-5128-10A-01D-1441-08 g.chr13:77644818T>G c.11738A>C c.(11737-11739)cAt>cCt p.H3913P LUSC 13 77657221 77657221 + Missense_Mutation SNP G G A TCGA-66-2778-01A-02D-1522-08 TCGA-66-2778-11A-01D-1522-08 g.chr13:77657221G>A c.10868C>T c.(10867-10869)tCa>tTa p.S3623L LUSC 13 77657256 77657256 + Silent SNP T T C TCGA-34-5231-01A-21D-1817-08 TCGA-34-5231-10A-01D-1817-08 g.chr13:77657256T>C c.10833A>G c.(10831-10833)ttA>ttG p.L3611L LUSC 13 77669539 77669539 + Missense_Mutation SNP C C A TCGA-18-3410-01A-01D-0983-08 TCGA-18-3410-11A-01D-0983-08 g.chr13:77669539C>A c.10039G>T c.(10039-10041)Gat>Tat p.D3347Y LUSC 13 77670488 77670488 + Missense_Mutation SNP C C G TCGA-66-2789-01A-01D-0983-08 TCGA-66-2789-11A-01D-0983-08 g.chr13:77670488C>G c.9799G>C c.(9799-9801)Gaa>Caa p.E3267Q LUSC 13 77672487 77672487 + Silent SNP T T C TCGA-39-5024-01A-21D-1817-08 TCGA-39-5024-11A-01D-1817-08 g.chr13:77672487T>C c.8688A>G c.(8686-8688)gaA>gaG p.E2896E LUSC 13 77672952 77672952 + Silent SNP C C T TCGA-43-3920-01A-01D-0983-08 TCGA-43-3920-10A-01D-0983-08 g.chr13:77672952C>T c.8223G>A c.(8221-8223)ttG>ttA p.L2741L LUSC 13 77695532 77695532 + Missense_Mutation SNP C C G TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr13:77695532C>G c.8002G>C c.(8002-8004)Gat>Cat p.D2668H LUSC 13 77699588 77699588 + Missense_Mutation SNP C C T TCGA-66-2734-01A-01D-0983-08 TCGA-66-2734-11A-01D-0983-08 g.chr13:77699588C>T c.7786G>A c.(7786-7788)Ggg>Agg p.G2596R LUSC 13 77714292 77714292 + Missense_Mutation SNP T T G TCGA-33-4582-01A-01D-1441-08 TCGA-33-4582-11A-01D-1441-08 g.chr13:77714292T>G c.7294A>C c.(7294-7296)Aaa>Caa p.K2432Q LUSC 13 77724879 77724879 + Missense_Mutation SNP G G T TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr13:77724879G>T c.7007C>A c.(7006-7008)aCa>aAa p.T2336K LUSC 13 77724913 77724913 + Missense_Mutation SNP T T C TCGA-66-2758-01A-02D-1522-08 TCGA-66-2758-11A-01D-1522-08 g.chr13:77724913T>C c.6973A>G c.(6973-6975)Atg>Gtg p.M2325V LUSC 13 77739409 77739409 + Splice_Site SNP T T A TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr13:77739409T>A c.6344A>T c.(6343-6345)gAg>gTg p.E2115V LUSC 13 77740591 77740591 + Silent SNP G G C TCGA-56-6545-01A-11D-1817-08 TCGA-56-6545-10A-01D-1817-08 g.chr13:77740591G>C c.6099C>G c.(6097-6099)gtC>gtG p.V2033V LUSC 13 77743836 77743836 + Silent SNP T T C TCGA-39-5019-01A-01D-1817-08 TCGA-39-5019-11A-01D-1817-08 g.chr13:77743836T>C c.5694A>G c.(5692-5694)ccA>ccG p.P1898P LUSC 13 77748533 77748533 + Missense_Mutation SNP C C G TCGA-18-4083-01A-01D-1352-08 TCGA-18-4083-11A-01D-1352-08 g.chr13:77748533C>G c.5450G>C c.(5449-5451)gGt>gCt p.G1817A LUSC 13 77748550 77748550 + Silent SNP T T A TCGA-37-4135-01A-01D-1352-08 TCGA-37-4135-10A-01D-1352-08 g.chr13:77748550T>A c.5433A>T c.(5431-5433)acA>acT p.T1811T LUSC 13 77759384 77759384 + Nonsense_Mutation SNP G G A TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr13:77759384G>A c.4459C>T c.(4459-4461)Caa>Taa p.Q1487* LUSC 13 77760022 77760022 + Missense_Mutation SNP T T A TCGA-66-2781-01A-01D-1522-08 TCGA-66-2781-11A-01D-1522-08 g.chr13:77760022T>A c.4314A>T c.(4312-4314)gaA>gaT p.E1438D LUSC 13 77760039 77760039 + Missense_Mutation SNP G G A TCGA-51-4080-01A-01D-1458-08 TCGA-51-4080-11A-01D-1458-08 g.chr13:77760039G>A c.4297C>T c.(4297-4299)Cgt>Tgt p.R1433C LUSC 13 77760189 77760189 + Missense_Mutation SNP C C G TCGA-60-2715-01A-01D-1522-08 TCGA-60-2715-11A-01D-1522-08 g.chr13:77760189C>G c.4147G>C c.(4147-4149)Gag>Cag p.E1383Q LUSC 13 77835401 77835401 + Nonsense_Mutation SNP G G C TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr13:77835401G>C c.1643C>G c.(1642-1644)tCa>tGa p.S548* LUSC 13 77844568 77844568 + Missense_Mutation SNP T T A TCGA-18-3406-01A-01D-0983-08 TCGA-18-3406-11A-01D-0983-08 g.chr13:77844568T>A c.937A>T c.(937-939)Atg>Ttg p.M313L LUSC 13 77900608 77900608 + Splice_Site SNP C C T TCGA-39-5024-01A-21D-1817-08 TCGA-39-5024-11A-01D-1817-08 g.chr13:77900608C>T c.e1+1 LUSC 13 77900796 77900796 + Missense_Mutation SNP T T A TCGA-33-4538-01A-01D-1267-08 TCGA-33-4538-11A-01D-1267-08 g.chr13:77900796T>A c.115A>T c.(115-117)Atg>Ttg p.M39L OV 13 77625229 77625229 + Silent SNP A A G TCGA-36-2552-01A-01D-1526-09 TCGA-36-2552-10A-01D-1526-09 g.chr13:77625229A>G c.13710T>C c.(13708-13710)ttT>ttC p.F4570F OV 13 77629819 77629819 + Missense_Mutation SNP C C G TCGA-23-1124-01A-01W-0488-09 TCGA-23-1124-10A-01W-0488-09 g.chr13:77629819C>G c.13407G>C c.(13405-13407)atG>atC p.M4469I OV 13 77638760 77638760 + Missense_Mutation SNP G G C TCGA-13-1483-01A-01W-0549-09 TCGA-13-1483-10A-01W-0549-09 g.chr13:77638760G>C c.12548C>G c.(12547-12549)gCa>gGa p.A4183G OV 13 77695606 77695606 + Missense_Mutation SNP G G A TCGA-13-0889-01A-01W-0419-10 TCGA-13-0889-10A-01W-0419-10 g.chr13:77695606G>A c.7928C>T c.(7927-7929)tCt>tTt p.S2643F OV 13 77740565 77740565 + Missense_Mutation SNP C C G TCGA-13-1403-01A-01W-0494-09 TCGA-13-1403-10A-01W-0495-09 g.chr13:77740565C>G c.6125G>C c.(6124-6126)gGa>gCa p.G2042A OV 13 77754358 77754358 + Missense_Mutation SNP T T G TCGA-24-1470-01A-01W-0553-09 TCGA-24-1470-10A-01W-0553-09 g.chr13:77754358T>G c.4923A>C c.(4921-4923)agA>agC p.R1641S OV 13 77798611 77798611 + Missense_Mutation SNP G G C TCGA-13-0885-01A-02W-0421-09 TCGA-13-0885-10A-01W-0421-09 g.chr13:77798611G>C c.2800C>G c.(2800-2802)Cta>Gta p.L934V PAAD 13 77625140 77625140 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:77625140C>T c.13799G>A c.(13798-13800)tGt>tAt p.C4600Y PAAD 13 77632491 77632491 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:77632491G>A c.13077C>T c.(13075-13077)tgC>tgT p.C4359C PAAD 13 77635368 77635368 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:77635368G>T c.12858C>A c.(12856-12858)ttC>ttA p.F4286L PAAD 13 77671856 77671856 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:77671856A>G c.9319T>C c.(9319-9321)Tcc>Ccc p.S3107P PAAD 13 77672965 77672965 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:77672965T>C c.8210A>G c.(8209-8211)gAt>gGt p.D2737G PAAD 13 77699592 77699592 + Silent SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:77699592A>G c.7782T>C c.(7780-7782)tcT>tcC p.S2594S PAAD 13 77736067 77736067 + Nonsense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:77736067C>A c.6457G>T c.(6457-6459)Gaa>Taa p.E2153* PAAD 13 77742684 77742684 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:77742684G>A c.5879C>T c.(5878-5880)tCg>tTg p.S1960L PAAD 13 77779470 77779470 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:77779470C>T c.3650G>A c.(3649-3651)cGt>cAt p.R1217H PAAD 13 77825349 77825349 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:77825349C>A c.2204G>T c.(2203-2205)gGa>gTa p.G735V PRAD 13 77629784 77629784 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr13:77629784G>A c.13442C>T c.(13441-13443)gCt>gTt p.A4481V PRAD 13 77642776 77642776 + Missense_Mutation SNP T T A TCGA-G9-6354-01A-11D-A30X-08 TCGA-G9-6354-10A-01D-A30X-08 g.chr13:77642776T>A c.11981A>T c.(11980-11982)tAt>tTt p.Y3994F PRAD 13 77664342 77664342 + Missense_Mutation SNP C C A TCGA-EJ-5519-01A-01D-1576-08 TCGA-EJ-5519-10A-01D-1577-08 g.chr13:77664342C>A c.10310G>T c.(10309-10311)aGa>aTa p.R3437I PRAD 13 77671856 77671856 + Missense_Mutation SNP A A G TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr13:77671856A>G c.9319T>C c.(9319-9321)Tcc>Ccc p.S3107P PRAD 13 77672530 77672530 + Missense_Mutation SNP G G C TCGA-XA-A8JR-01A-11D-A364-08 TCGA-XA-A8JR-10A-01D-A362-08 g.chr13:77672530G>C c.8645C>G c.(8644-8646)tCt>tGt p.S2882C PRAD 13 77713379 77713379 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr13:77713379G>A c.7497C>T c.(7495-7497)tgC>tgT p.C2499C PRAD 13 77718680 77718680 + Missense_Mutation SNP C C T TCGA-EJ-5525-01A-01D-1576-08 TCGA-EJ-5525-10A-01D-1577-08 g.chr13:77718680C>T c.7089G>A c.(7087-7089)atG>atA p.M2363I PRAD 13 77738587 77738587 + Splice_Site SNP A A G TCGA-HC-A76X-01A-11D-A33T-08 TCGA-HC-A76X-10A-01D-A33W-08 g.chr13:77738587A>G c.e43+1 PRAD 13 77765887 77765887 + Missense_Mutation SNP C C T TCGA-FC-A6HD-01A-11D-A31L-08 TCGA-FC-A6HD-10A-01D-A31J-08 g.chr13:77765887C>T c.3883G>A c.(3883-3885)Gca>Aca p.A1295T PRAD 13 77835490 77835490 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr13:77835490G>A c.1554C>T c.(1552-1554)taC>taT p.Y518Y PRAD 13 77844149 77844149 + Frame_Shift_Del DEL T T - TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr13:77844149delT c.1124delA c.(1123-1125)aagfs p.K375fs PRAD 13 77853046 77853046 + Splice_Site SNP T T C TCGA-FC-A4JI-01A-11D-A257-08 TCGA-FC-A4JI-10A-01D-A25A-08 g.chr13:77853046T>C c.481A>G c.(481-483)Att>Gtt p.I161V READ 13 77657240 77657240 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:77657240G>A c.10849C>T c.(10849-10851)Cgc>Tgc p.R3617C READ 13 77695607 77695607 + Missense_Mutation SNP A A T TCGA-DY-A1DF-01A-11D-A152-10 TCGA-DY-A1DF-10A-01D-A152-10 g.chr13:77695607A>T c.7927T>A c.(7927-7929)Tct>Act p.S2643T READ 13 77718581 77718581 + Splice_Site SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:77718581G>A c.7188C>T c.(7186-7188)atC>atT p.I2396I READ 13 77740564 77740564 + Silent SNP T T C TCGA-DY-A1DG-01A-11D-A152-10 TCGA-DY-A1DG-10A-01D-A152-10 g.chr13:77740564T>C c.6126A>G c.(6124-6126)ggA>ggG p.G2042G READ 13 77838066 77838066 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:77838066C>A c.1315G>T c.(1315-1317)Gat>Tat p.D439Y SARC 13 77629706 77629730 + Frame_Shift_Del DEL TAGCACACATAATATGCATATCTAT TAGCACACATAATATGCATATCTAT - TCGA-DX-A8BU-01A-11D-A37C-09 TCGA-DX-A8BU-10A-01D-A37F-09 g.chr13:77629706_77629730delTAGCACACATAATATGCATATCTAT c.13496_13520delATAGATATGCATATTATGTGTGCTA c.(13495-13521)aatagatatgcatattatgtgtgctacfs p.NRYAYYVCY4499fs SARC 13 77798600 77798600 + Silent SNP T T C TCGA-X6-A7WC-01A-12D-A351-09 TCGA-X6-A7WC-10A-01D-A351-09 g.chr13:77798600T>C c.2811A>G c.(2809-2811)ggA>ggG p.G937G SARC 13 77799597 77799597 + Nonsense_Mutation SNP G G A TCGA-DX-A6BB-01A-12D-A32I-09 TCGA-DX-A6BB-10A-01D-A32I-09 g.chr13:77799597G>A c.2716C>T c.(2716-2718)Caa>Taa p.Q906* SKCM 13 77619581 77619581 + Missense_Mutation SNP C C A TCGA-EE-A2MU-06A-21D-A196-08 TCGA-EE-A2MU-10A-01D-A198-08 g.chr13:77619581C>A c.13855G>T c.(13855-13857)Gtt>Ttt p.V4619F SKCM 13 77635390 77635390 + Missense_Mutation SNP C C T TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr13:77635390C>T c.12836G>A c.(12835-12837)gGt>gAt p.G4279D SKCM 13 77636771 77636771 + Missense_Mutation SNP G G A TCGA-EE-A2A6-06A-11D-A197-08 TCGA-EE-A2A6-10A-01D-A199-08 g.chr13:77636771G>A c.12620C>T c.(12619-12621)tCg>tTg p.S4207L SKCM 13 77636804 77636804 + Missense_Mutation SNP A A G TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr13:77636804A>G c.12587T>C c.(12586-12588)gTt>gCt p.V4196A SKCM 13 77638818 77638818 + Missense_Mutation SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr13:77638818T>C c.12490A>G c.(12490-12492)Acc>Gcc p.T4164A SKCM 13 77641724 77641724 + Silent SNP G G A TCGA-EE-A17X-06A-11D-A197-08 TCGA-EE-A17X-10A-01D-A199-08 g.chr13:77641724G>A c.12333C>T c.(12331-12333)ttC>ttT p.F4111F SKCM 13 77642739 77642739 + Silent SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr13:77642739G>A c.12018C>T c.(12016-12018)ttC>ttT p.F4006F SKCM 13 77642739 77642739 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr13:77642739G>A c.12018C>T c.(12016-12018)ttC>ttT p.F4006F SKCM 13 77642817 77642817 + Silent SNP A A G TCGA-RP-A694-06A-11D-A30X-08 TCGA-RP-A694-10A-01D-A30X-08 g.chr13:77642817A>G c.11940T>C c.(11938-11940)tcT>tcC p.S3980S SKCM 13 77642939 77642939 + Missense_Mutation SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr13:77642939G>A c.11818C>T c.(11818-11820)Cgc>Tgc p.R3940C SKCM 13 77651353 77651353 + Missense_Mutation SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr13:77651353G>A c.11540C>T c.(11539-11541)tCa>tTa p.S3847L SKCM 13 77651477 77651477 + Missense_Mutation SNP G G A TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr13:77651477G>A c.11416C>T c.(11416-11418)Cca>Tca p.P3806S SKCM 13 77655567 77655567 + Missense_Mutation SNP G G A TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr13:77655567G>A c.11299C>T c.(11299-11301)Ctt>Ttt p.L3767F SKCM 13 77655574 77655574 + Silent SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr13:77655574G>A c.11292C>T c.(11290-11292)tcC>tcT p.S3764S SKCM 13 77656067 77656067 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr13:77656067G>A c.10984C>T c.(10984-10986)Cat>Tat p.H3662Y SKCM 13 77661649 77661649 + Silent SNP T T C TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr13:77661649T>C c.10731A>G c.(10729-10731)gaA>gaG p.E3577E SKCM 13 77663163 77663163 + Missense_Mutation SNP A A G TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr13:77663163A>G c.10415T>C c.(10414-10416)gTt>gCt p.V3472A SKCM 13 77671818 77671818 + Silent SNP G G A TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr13:77671818G>A c.9357C>T c.(9355-9357)ccC>ccT p.P3119P SKCM 13 77671825 77671825 + Missense_Mutation SNP G G A TCGA-EE-A2A5-06A-11D-A197-08 TCGA-EE-A2A5-10A-01D-A199-08 g.chr13:77671825G>A c.9350C>T c.(9349-9351)cCt>cTt p.P3117L SKCM 13 77671906 77671906 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr13:77671906G>A c.9269C>T c.(9268-9270)cCt>cTt p.P3090L SKCM 13 77672094 77672094 + Frame_Shift_Del DEL A A - TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr13:77672094delA c.9081delT c.(9079-9081)catfs p.H3027fs SKCM 13 77672117 77672117 + Missense_Mutation SNP G G A TCGA-EE-A2ML-06A-11D-A197-08 TCGA-EE-A2ML-10A-01D-A199-08 g.chr13:77672117G>A c.9058C>T c.(9058-9060)Cat>Tat p.H3020Y SKCM 13 77672272 77672272 + Missense_Mutation SNP A A G TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr13:77672272A>G c.8903T>C c.(8902-8904)tTt>tCt p.F2968S SKCM 13 77672656 77672656 + Missense_Mutation SNP G G A TCGA-ER-A19S-06A-11D-A196-08 TCGA-ER-A19S-10A-01D-A198-08 g.chr13:77672656G>A c.8519C>T c.(8518-8520)cCa>cTa p.P2840L SKCM 13 77672695 77672695 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr13:77672695G>A c.8480C>T c.(8479-8481)cCt>cTt p.P2827L SKCM 13 77672723 77672723 + Missense_Mutation SNP C C T TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr13:77672723C>T c.8452G>A c.(8452-8454)Gct>Act p.A2818T SKCM 13 77673139 77673139 + Missense_Mutation SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr13:77673139C>T c.8036G>A c.(8035-8037)gGa>gAa p.G2679E SKCM 13 77700588 77700588 + Silent SNP G G A TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr13:77700588G>A c.7635C>T c.(7633-7635)ttC>ttT p.F2545F SKCM 13 77718653 77718653 + Silent SNP A A G TCGA-D3-A3MV-06A-11D-A21A-08 TCGA-D3-A3MV-10A-01D-A21A-08 g.chr13:77718653A>G c.7116T>C c.(7114-7116)acT>acC p.T2372T SKCM 13 77725060 77725060 + Missense_Mutation SNP A A T TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr13:77725060A>T c.6826T>A c.(6826-6828)Tct>Act p.S2276T SKCM 13 77730262 77730262 + Silent SNP A A G TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr13:77730262A>G c.6732T>C c.(6730-6732)ggT>ggC p.G2244G SKCM 13 77730270 77730270 + Missense_Mutation SNP G G A TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr13:77730270G>A c.6724C>T c.(6724-6726)Cgt>Tgt p.R2242C SKCM 13 77742742 77742742 + Missense_Mutation SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr13:77742742G>A c.5821C>T c.(5821-5823)Ccg>Tcg p.P1941S SKCM 13 77745767 77745767 + De_novo_Start_OutOfFrame SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr13:77745767C>T SKCM 13 77748454 77748454 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr13:77748454G>A c.5529C>T c.(5527-5529)ctC>ctT p.L1843L SKCM 13 77751993 77751993 + Missense_Mutation SNP G G A TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr13:77751993G>A c.5116C>T c.(5116-5118)Cct>Tct p.P1706S SKCM 13 77754364 77754364 + Silent SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr13:77754364C>T c.4917G>A c.(4915-4917)ctG>ctA p.L1639L SKCM 13 77779516 77779516 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr13:77779516G>A c.3604C>T c.(3604-3606)Cat>Tat p.H1202Y SKCM 13 77779699 77779699 + Silent SNP T T C TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr13:77779699T>C c.3510A>G c.(3508-3510)ttA>ttG p.L1170L SKCM 13 77785366 77785366 + Missense_Mutation SNP A A T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr13:77785366A>T c.3238T>A c.(3238-3240)Tca>Aca p.S1080T SKCM 13 77786261 77786261 + Missense_Mutation SNP G G A TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr13:77786261G>A c.2978C>T c.(2977-2979)cCa>cTa p.P993L SKCM 13 77799638 77799638 + Missense_Mutation SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr13:77799638G>A c.2675C>T c.(2674-2676)cCt>cTt p.P892L SKCM 13 77799640 77799640 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr13:77799640G>A c.2673C>T c.(2671-2673)taC>taT p.Y891Y SKCM 13 77807327 77807327 + Missense_Mutation SNP G G A TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr13:77807327G>A c.2587C>T c.(2587-2589)Cca>Tca p.P863S SKCM 13 77817289 77817289 + Missense_Mutation SNP G G A TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr13:77817289G>A c.2420C>T c.(2419-2421)cCa>cTa p.P807L SKCM 13 77835375 77835375 + Missense_Mutation SNP G G A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr13:77835375G>A c.1669C>T c.(1669-1671)Ctt>Ttt p.L557F SKCM 13 77844493 77844493 + Missense_Mutation SNP G G A TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr13:77844493G>A c.1012C>T c.(1012-1014)Ctt>Ttt p.L338F SKCM 13 77852997 77852997 + Missense_Mutation SNP C C T TCGA-EE-A2A1-06A-11D-A197-08 TCGA-EE-A2A1-10A-01D-A199-08 g.chr13:77852997C>T c.530G>A c.(529-531)cGa>cAa p.R177Q SKCM 13 77862314 77862314 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr13:77862314G>A c.462C>T c.(460-462)ccC>ccT p.P154P ACC 5 102340902 102340903 + Frame_Shift_Ins INS - - T TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr5:102340902_102340903insT c.1775_1776insT c.(1774-1779)tattggfs p.W593fs BLCA 5 102309957 102309957 + Missense_Mutation SNP G G A TCGA-4Z-AA82-01A-11D-A391-08 TCGA-4Z-AA82-10A-01D-A394-08 g.chr5:102309957G>A c.1300G>A c.(1300-1302)Gat>Aat p.D434N BLCA 5 102326096 102326096 + Missense_Mutation SNP G G T TCGA-5N-A9KM-01A-11D-A42E-08 TCGA-5N-A9KM-10A-01D-A42H-08 g.chr5:102326096G>T c.1604G>T c.(1603-1605)tGg>tTg p.W535L BLCA 5 102343301 102343301 + Missense_Mutation SNP G G A TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr5:102343301G>A c.2155G>A c.(2155-2157)Gtg>Atg p.V719M BLCA 5 102360917 102360917 + Silent SNP G G A TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr5:102360917G>A c.2568G>A c.(2566-2568)ctG>ctA p.L856L BLCA 5 102364618 102364618 + Missense_Mutation SNP G G A TCGA-CF-A9FL-01A-11D-A38G-08 TCGA-CF-A9FL-10A-01D-A38J-08 g.chr5:102364618G>A c.2771G>A c.(2770-2772)gGt>gAt p.G924D BRCA 5 102203071 102203071 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr5:102203071C>T c.184C>T c.(184-186)Cgc>Tgc p.R62C BRCA 5 102237088 102237088 + Missense_Mutation SNP G G C TCGA-BH-A0AW-01A-11W-A071-09 TCGA-BH-A0AW-10A-01W-A071-09 g.chr5:102237088G>C c.239G>C c.(238-240)cGa>cCa p.R80P BRCA 5 102343195 102343195 + Silent SNP C C T TCGA-A8-A09G-01A-21W-A019-09 TCGA-A8-A09G-10A-01W-A021-09 g.chr5:102343195C>T c.2049C>T c.(2047-2049)ttC>ttT p.F683F BRCA 5 102343295 102343295 + Nonsense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr5:102343295G>T c.2149G>T c.(2149-2151)Gaa>Taa p.E717* BRCA 5 102353039 102353039 + Splice_Site SNP A A G TCGA-C8-A1HK-01A-21D-A13L-09 TCGA-C8-A1HK-10A-01D-A13O-09 g.chr5:102353039A>G c.2333A>G c.(2332-2334)cAc>cGc p.H778R BRCA 5 102355495 102355495 + Splice_Site SNP A A C TCGA-EW-A1PC-01B-11D-A21Q-09 TCGA-EW-A1PC-10A-01D-A21Q-09 g.chr5:102355495A>C c.2433A>C c.(2431-2433)aaA>aaC p.K811N BRCA 5 102363906 102363906 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr5:102363906G>A c.2707G>A c.(2707-2709)Gag>Aag p.E903K CESC 5 102262314 102262314 + Silent SNP G G A TCGA-C5-A1BI-01B-11D-A13W-08 TCGA-C5-A1BI-10A-01D-A13W-08 g.chr5:102262314G>A c.468G>A c.(466-468)gaG>gaA p.E156E CESC 5 102309832 102309832 + Missense_Mutation SNP C C T TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr5:102309832C>T c.1175C>T c.(1174-1176)tCa>tTa p.S392L COAD 5 102260707 102260707 + Missense_Mutation SNP G G A TCGA-AA-3688-01A-01W-0900-09 TCGA-AA-3688-10A-01W-0900-09 g.chr5:102260707G>A c.403G>A c.(403-405)Gcc>Acc p.A135T COAD 5 102282575 102282575 + Missense_Mutation SNP C C A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr5:102282575C>A c.561C>A c.(559-561)caC>caA p.H187Q COAD 5 102285290 102285290 + Silent SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr5:102285290C>A c.693C>A c.(691-693)gtC>gtA p.V231V COAD 5 102285661 102285661 + Silent SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr5:102285661G>A c.780G>A c.(778-780)cgG>cgA p.R260R COAD 5 102286446 102286446 + Missense_Mutation SNP T T G TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr5:102286446T>G c.827T>G c.(826-828)gTt>gGt p.V276G COAD 5 102295581 102295581 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr5:102295581G>A c.908G>A c.(907-909)gGc>gAc p.G303D COAD 5 102295706 102295706 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr5:102295706G>A c.1033G>A c.(1033-1035)Gcc>Acc p.A345T COAD 5 102295711 102295711 + Silent SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr5:102295711C>T c.1038C>T c.(1036-1038)aaC>aaT p.N346N COAD 5 102295723 102295723 + Silent SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr5:102295723C>T c.1050C>T c.(1048-1050)ccC>ccT p.P350P COAD 5 102309960 102309960 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:102309960C>A c.1303C>A c.(1303-1305)Ctt>Att p.L435I COAD 5 102342600 102342600 + Silent SNP C C A TCGA-DM-A1D8-01A-11D-A152-10 TCGA-DM-A1D8-10A-01D-A152-10 g.chr5:102342600C>A c.1899C>A c.(1897-1899)ccC>ccA p.P633P COAD 5 102343184 102343184 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr5:102343184C>T c.2038C>T c.(2038-2040)Cca>Tca p.P680S COAD 5 102343266 102343266 + Missense_Mutation SNP G G A TCGA-AA-3522-01A-01W-0831-10 TCGA-AA-3522-10A-01W-0831-10 g.chr5:102343266G>A c.2120G>A c.(2119-2121)cGg>cAg p.R707Q COAD 5 102345565 102345565 + Missense_Mutation SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr5:102345565C>T c.2326C>T c.(2326-2328)Cgc>Tgc p.R776C COAD 5 102353054 102353054 + Missense_Mutation SNP A A G TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr5:102353054A>G c.2348A>G c.(2347-2349)cAt>cGt p.H783R COAD 5 102353125 102353125 + Missense_Mutation SNP A A G TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr5:102353125A>G c.2419A>G c.(2419-2421)Acc>Gcc p.T807A COAD 5 102355501 102355501 + Silent SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:102355501A>G c.2439A>G c.(2437-2439)gaA>gaG p.E813E COAD 5 102360976 102360976 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr5:102360976C>T c.2627C>T c.(2626-2628)cCg>cTg p.P876L COAD 5 102361013 102361013 + Silent SNP G G T TCGA-AA-3511-01A-21D-1835-10 TCGA-AA-3511-11A-01D-1835-10 g.chr5:102361013G>T c.2664G>T c.(2662-2664)cgG>cgT p.R888R COAD 5 102361017 102361017 + Frame_Shift_Del DEL A A - TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr5:102361017delA c.2668delA c.(2668-2670)aaafs p.K891fs COAD 5 102363910 102363910 + Missense_Mutation SNP C C T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr5:102363910C>T c.2711C>T c.(2710-2712)aCg>aTg p.T904M COAD 5 102364651 102364651 + Missense_Mutation SNP G G A TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr5:102364651G>A c.2804G>A c.(2803-2805)cGa>cAa p.R935Q COAD 5 102364672 102364672 + Missense_Mutation SNP G G T TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr5:102364672G>T c.2825G>T c.(2824-2826)aGc>aTc p.S942I COAD 5 102364751 102364751 + Silent SNP C C T TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr5:102364751C>T c.2904C>T c.(2902-2904)ctC>ctT p.L968L COADREAD 5 102260707 102260707 + Missense_Mutation SNP G G A TCGA-AA-3688-01A-01W-0900-09 TCGA-AA-3688-10A-01W-0900-09 g.chr5:102260707G>A c.403G>A c.(403-405)Gcc>Acc p.A135T COADREAD 5 102282575 102282575 + Missense_Mutation SNP C C A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr5:102282575C>A c.561C>A c.(559-561)caC>caA p.H187Q COADREAD 5 102285290 102285290 + Silent SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr5:102285290C>A c.693C>A c.(691-693)gtC>gtA p.V231V COADREAD 5 102285661 102285661 + Silent SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr5:102285661G>A c.780G>A c.(778-780)cgG>cgA p.R260R COADREAD 5 102286446 102286446 + Missense_Mutation SNP T T G TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr5:102286446T>G c.827T>G c.(826-828)gTt>gGt p.V276G COADREAD 5 102295581 102295581 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr5:102295581G>A c.908G>A c.(907-909)gGc>gAc p.G303D COADREAD 5 102295706 102295706 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr5:102295706G>A c.1033G>A c.(1033-1035)Gcc>Acc p.A345T COADREAD 5 102295711 102295711 + Silent SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr5:102295711C>T c.1038C>T c.(1036-1038)aaC>aaT p.N346N COADREAD 5 102295723 102295723 + Silent SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr5:102295723C>T c.1050C>T c.(1048-1050)ccC>ccT p.P350P COADREAD 5 102309960 102309960 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:102309960C>A c.1303C>A c.(1303-1305)Ctt>Att p.L435I COADREAD 5 102326074 102326074 + Missense_Mutation SNP T T A TCGA-AG-4008-01A-01W-1073-09 TCGA-AG-4008-10A-01W-1073-09 g.chr5:102326074T>A c.1582T>A c.(1582-1584)Ttc>Atc p.F528I COADREAD 5 102342600 102342600 + Silent SNP C C A TCGA-DM-A1D8-01A-11D-A152-10 TCGA-DM-A1D8-10A-01D-A152-10 g.chr5:102342600C>A c.1899C>A c.(1897-1899)ccC>ccA p.P633P COADREAD 5 102343184 102343184 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr5:102343184C>T c.2038C>T c.(2038-2040)Cca>Tca p.P680S COADREAD 5 102343266 102343266 + Missense_Mutation SNP G G A TCGA-AA-3522-01A-01W-0831-10 TCGA-AA-3522-10A-01W-0831-10 g.chr5:102343266G>A c.2120G>A c.(2119-2121)cGg>cAg p.R707Q COADREAD 5 102343348 102343348 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:102343348T>G c.2202T>G c.(2200-2202)atT>atG p.I734M COADREAD 5 102345565 102345565 + Missense_Mutation SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr5:102345565C>T c.2326C>T c.(2326-2328)Cgc>Tgc p.R776C COADREAD 5 102353054 102353054 + Missense_Mutation SNP A A G TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr5:102353054A>G c.2348A>G c.(2347-2349)cAt>cGt p.H783R COADREAD 5 102353125 102353125 + Missense_Mutation SNP A A G TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr5:102353125A>G c.2419A>G c.(2419-2421)Acc>Gcc p.T807A COADREAD 5 102355501 102355501 + Silent SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:102355501A>G c.2439A>G c.(2437-2439)gaA>gaG p.E813E COADREAD 5 102360976 102360976 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr5:102360976C>T c.2627C>T c.(2626-2628)cCg>cTg p.P876L COADREAD 5 102361013 102361013 + Silent SNP G G T TCGA-AA-3511-01A-21D-1835-10 TCGA-AA-3511-11A-01D-1835-10 g.chr5:102361013G>T c.2664G>T c.(2662-2664)cgG>cgT p.R888R COADREAD 5 102361017 102361017 + Frame_Shift_Del DEL A A - TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr5:102361017delA c.2668delA c.(2668-2670)aaafs p.K891fs COADREAD 5 102363910 102363910 + Missense_Mutation SNP C C T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr5:102363910C>T c.2711C>T c.(2710-2712)aCg>aTg p.T904M COADREAD 5 102364651 102364651 + Missense_Mutation SNP G G A TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr5:102364651G>A c.2804G>A c.(2803-2805)cGa>cAa p.R935Q COADREAD 5 102364672 102364672 + Missense_Mutation SNP G G T TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr5:102364672G>T c.2825G>T c.(2824-2826)aGc>aTc p.S942I COADREAD 5 102364751 102364751 + Silent SNP C C T TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr5:102364751C>T c.2904C>T c.(2902-2904)ctC>ctT p.L968L ESCA 5 102363888 102363888 + Splice_Site SNP G G T TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chr5:102363888G>T c.e24-1 GBM 5 102284128 102284128 + Missense_Mutation SNP G G C TCGA-06-0214-01A-02D-1491-08 TCGA-06-0214-10A-01D-1491-08 g.chr5:102284128G>C c.622G>C c.(622-624)Gtt>Ctt p.V208L GBM 5 102360910 102360911 + Frame_Shift_Del DEL AG AG - TCGA-27-1833-01A-01W-0643-08 TCGA-27-1833-10A-01W-0644-08 g.chr5:102360910_102360911delAG c.2561_2562delAG c.(2560-2562)cagfs p.Q854fs GBMLGG 5 102284128 102284128 + Missense_Mutation SNP G G C TCGA-06-0214-01A-02D-1491-08 TCGA-06-0214-10A-01D-1491-08 g.chr5:102284128G>C c.622G>C c.(622-624)Gtt>Ctt p.V208L GBMLGG 5 102295742 102295742 + Missense_Mutation SNP A A C TCGA-E1-A7YV-01A-11D-A34J-08 TCGA-E1-A7YV-10A-01D-A34M-08 g.chr5:102295742A>C c.1069A>C c.(1069-1071)Atg>Ctg p.M357L GBMLGG 5 102296885 102296885 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:102296885C>T c.1114C>T c.(1114-1116)Cct>Tct p.P372S GBMLGG 5 102360910 102360911 + Frame_Shift_Del DEL AG AG - TCGA-27-1833-01A-01W-0643-08 TCGA-27-1833-10A-01W-0644-08 g.chr5:102360910_102360911delAG c.2561_2562delAG c.(2560-2562)cagfs p.Q854fs HNSC 5 102286460 102286460 + Missense_Mutation SNP G G T TCGA-CN-5360-01A-01D-1434-08 TCGA-CN-5360-10A-01D-1434-08 g.chr5:102286460G>T c.841G>T c.(841-843)Ggt>Tgt p.G281C HNSC 5 102296933 102296933 + Splice_Site SNP G G C TCGA-CQ-6219-01A-11D-1912-08 TCGA-CQ-6219-10A-01D-1912-08 g.chr5:102296933G>C c.1162G>C c.(1162-1164)Ggt>Cgt p.G388R HNSC 5 102342554 102342554 + Missense_Mutation SNP G G T TCGA-D6-A6EK-01A-11D-A31L-08 TCGA-D6-A6EK-10A-01D-A31J-08 g.chr5:102342554G>T c.1853G>T c.(1852-1854)gGa>gTa p.G618V HNSC 5 102342680 102342680 + Missense_Mutation SNP C C T TCGA-D6-6826-01A-11D-1912-08 TCGA-D6-6826-10A-01D-1912-08 g.chr5:102342680C>T c.1979C>T c.(1978-1980)tCa>tTa p.S660L HNSC 5 102343267 102343267 + Silent SNP G G T TCGA-DQ-5629-01A-01D-1870-08 TCGA-DQ-5629-10A-01D-1870-08 g.chr5:102343267G>T c.2121G>T c.(2119-2121)cgG>cgT p.R707R HNSC 5 102353044 102353044 + Missense_Mutation SNP G G C TCGA-F7-A61V-01A-11D-A28R-08 TCGA-F7-A61V-10A-01D-A28U-08 g.chr5:102353044G>C c.2338G>C c.(2338-2340)Gat>Cat p.D780H HNSC 5 102363940 102363940 + Missense_Mutation SNP G G C TCGA-CN-5359-01A-01D-1434-08 TCGA-CN-5359-10A-01D-1434-08 g.chr5:102363940G>C c.2741G>C c.(2740-2742)aGa>aCa p.R914T KIPAN 5 102203042 102203042 + Frame_Shift_Del DEL T T - TCGA-HE-A5NI-01A-11D-A26P-10 TCGA-HE-A5NI-10A-01D-A26P-10 g.chr5:102203042delT c.155delT c.(154-156)attfs p.I52fs KIPAN 5 102203043 102203044 + Frame_Shift_Del DEL TG TG - TCGA-HE-A5NI-01A-11D-A26P-10 TCGA-HE-A5NI-10A-01D-A26P-10 g.chr5:102203043_102203044delTG c.156_157delTG c.(154-159)attgatfs p.D53fs KIPAN 5 102203044 102203044 + Missense_Mutation SNP G G A TCGA-HE-A5NI-01A-11D-A26P-10 TCGA-HE-A5NI-10A-01D-A26P-10 g.chr5:102203044G>A c.157G>A c.(157-159)Gat>Aat p.D53N KIPAN 5 102237063 102237063 + Missense_Mutation SNP G G A TCGA-IA-A40U-01A-11D-A25F-10 TCGA-IA-A40U-10A-01D-A25F-10 g.chr5:102237063G>A c.214G>A c.(214-216)Gat>Aat p.D72N KIPAN 5 102285295 102285295 + Missense_Mutation SNP C C T TCGA-P4-A5E6-01A-11D-A28G-10 TCGA-P4-A5E6-11A-22D-A28G-10 g.chr5:102285295C>T c.698C>T c.(697-699)gCc>gTc p.A233V KIPAN 5 102326008 102326008 + Missense_Mutation SNP G G A TCGA-B0-5707-01A-11D-1534-10 TCGA-B0-5707-11A-01D-1534-10 g.chr5:102326008G>A c.1516G>A c.(1516-1518)Gga>Aga p.G506R KIRC 5 102326008 102326008 + Missense_Mutation SNP G G A TCGA-B0-5707-01A-11D-1534-10 TCGA-B0-5707-11A-01D-1534-10 g.chr5:102326008G>A c.1516G>A c.(1516-1518)Gga>Aga p.G506R KIRP 5 102203042 102203042 + Frame_Shift_Del DEL T T - TCGA-HE-A5NI-01A-11D-A26P-10 TCGA-HE-A5NI-10A-01D-A26P-10 g.chr5:102203042delT c.155delT c.(154-156)attfs p.I52fs KIRP 5 102203043 102203044 + Frame_Shift_Del DEL TG TG - TCGA-HE-A5NI-01A-11D-A26P-10 TCGA-HE-A5NI-10A-01D-A26P-10 g.chr5:102203043_102203044delTG c.156_157delTG c.(154-159)attgatfs p.D53fs KIRP 5 102203044 102203044 + Missense_Mutation SNP G G A TCGA-HE-A5NI-01A-11D-A26P-10 TCGA-HE-A5NI-10A-01D-A26P-10 g.chr5:102203044G>A c.157G>A c.(157-159)Gat>Aat p.D53N KIRP 5 102237063 102237063 + Missense_Mutation SNP G G A TCGA-IA-A40U-01A-11D-A25F-10 TCGA-IA-A40U-10A-01D-A25F-10 g.chr5:102237063G>A c.214G>A c.(214-216)Gat>Aat p.D72N KIRP 5 102285295 102285295 + Missense_Mutation SNP C C T TCGA-P4-A5E6-01A-11D-A28G-10 TCGA-P4-A5E6-11A-22D-A28G-10 g.chr5:102285295C>T c.698C>T c.(697-699)gCc>gTc p.A233V LGG 5 102295742 102295742 + Missense_Mutation SNP A A C TCGA-E1-A7YV-01A-11D-A34J-08 TCGA-E1-A7YV-10A-01D-A34M-08 g.chr5:102295742A>C c.1069A>C c.(1069-1071)Atg>Ctg p.M357L LGG 5 102296885 102296885 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:102296885C>T c.1114C>T c.(1114-1116)Cct>Tct p.P372S LIHC 5 102203011 102203011 + Missense_Mutation SNP T T A TCGA-DD-A1EA-01A-11D-A12Z-10 TCGA-DD-A1EA-10A-01D-A12Z-10 g.chr5:102203011T>A c.124T>A c.(124-126)Tgt>Agt p.C42S LIHC 5 102237061 102237061 + Splice_Site SNP C C A TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr5:102237061C>A c.212C>A c.(211-213)tCc>tAc p.S71Y LIHC 5 102326046 102326046 + Silent SNP T T C TCGA-DD-AACI-01A-11D-A40R-10 TCGA-DD-AACI-10A-01D-A40U-10 g.chr5:102326046T>C c.1554T>C c.(1552-1554)gcT>gcC p.A518A LIHC 5 102326066 102326066 + Missense_Mutation SNP T T C TCGA-ZS-A9CE-01A-11D-A36X-10 TCGA-ZS-A9CE-10A-01D-A370-10 g.chr5:102326066T>C c.1574T>C c.(1573-1575)cTg>cCg p.L525P LIHC 5 102360941 102360941 + Silent SNP G G T TCGA-DD-AAW1-01A-11D-A40P-10 TCGA-DD-AAW1-10A-01D-A40P-10 g.chr5:102360941G>T c.2592G>T c.(2590-2592)gtG>gtT p.V864V LIHC 5 102360991 102360991 + Missense_Mutation SNP T T A TCGA-DD-A73A-01A-12D-A32G-10 TCGA-DD-A73A-10A-01D-A32G-10 g.chr5:102360991T>A c.2642T>A c.(2641-2643)cTg>cAg p.L881Q LUAD 5 102260668 102260668 + Missense_Mutation SNP G G T TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr5:102260668G>T c.364G>T c.(364-366)Gat>Tat p.D122Y LUAD 5 102260736 102260736 + Silent SNP G G A TCGA-97-A4M6-01A-11D-A24P-08 TCGA-97-A4M6-10A-01D-A24P-08 g.chr5:102260736G>A c.432G>A c.(430-432)cgG>cgA p.R144R LUAD 5 102285239 102285239 + Splice_Site SNP A A G TCGA-64-5778-01A-01D-1625-08 TCGA-64-5778-10A-01D-1625-08 g.chr5:102285239A>G c.e9-1 LUAD 5 102309956 102309956 + Missense_Mutation SNP G G C TCGA-44-7667-01A-31D-2063-08 TCGA-44-7667-10A-01D-2063-08 g.chr5:102309956G>C c.1299G>C c.(1297-1299)aaG>aaC p.K433N LUAD 5 102309984 102309984 + Missense_Mutation SNP G G T TCGA-55-8614-01A-11D-2393-08 TCGA-55-8614-10A-01D-2393-08 g.chr5:102309984G>T c.1327G>T c.(1327-1329)Ggt>Tgt p.G443C LUAD 5 102326009 102326009 + Missense_Mutation SNP G G C TCGA-49-4514-01A-21D-1855-08 TCGA-49-4514-11A-01D-1855-08 g.chr5:102326009G>C c.1517G>C c.(1516-1518)gGa>gCa p.G506A LUAD 5 102361025 102361025 + Silent SNP A A C TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr5:102361025A>C c.2676A>C c.(2674-2676)tcA>tcC p.S892S LUAD 5 102364680 102364680 + Missense_Mutation SNP G G T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr5:102364680G>T c.2833G>T c.(2833-2835)Ggc>Tgc p.G945C LUSC 5 102295636 102295636 + Missense_Mutation SNP G G T TCGA-43-6770-01A-11D-1817-08 TCGA-43-6770-11A-01D-1817-08 g.chr5:102295636G>T c.963G>T c.(961-963)aaG>aaT p.K321N LUSC 5 102309957 102309957 + Missense_Mutation SNP G G C TCGA-22-1011-01A-01D-1521-08 TCGA-22-1011-11A-01D-1521-08 g.chr5:102309957G>C c.1300G>C c.(1300-1302)Gat>Cat p.D434H LUSC 5 102363902 102363902 + Missense_Mutation SNP A A T TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr5:102363902A>T c.2703A>T c.(2701-2703)aaA>aaT p.K901N PAAD 5 102284122 102284122 + Missense_Mutation SNP G G T TCGA-YB-A89D-01A-12D-A36O-08 TCGA-YB-A89D-11A-11D-A36O-08 g.chr5:102284122G>T c.616G>T c.(616-618)Gac>Tac p.D206Y PAAD 5 102295657 102295657 + Silent SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr5:102295657C>A c.984C>A c.(982-984)acC>acA p.T328T PAAD 5 102309949 102309949 + Frame_Shift_Del DEL A A - TCGA-IB-A5SP-01A-11D-A32N-08 TCGA-IB-A5SP-10A-01D-A32N-08 g.chr5:102309949delA c.1292delA c.(1291-1293)caafs p.Q431fs PAAD 5 102343346 102343346 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr5:102343346A>G c.2200A>G c.(2200-2202)Att>Gtt p.I734V PAAD 5 102364643 102364643 + Silent SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr5:102364643C>A c.2796C>A c.(2794-2796)ggC>ggA p.G932G READ 5 102326074 102326074 + Missense_Mutation SNP T T A TCGA-AG-4008-01A-01W-1073-09 TCGA-AG-4008-10A-01W-1073-09 g.chr5:102326074T>A c.1582T>A c.(1582-1584)Ttc>Atc p.F528I READ 5 102343348 102343348 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:102343348T>G c.2202T>G c.(2200-2202)atT>atG p.I734M SKCM 5 102203051 102203051 + Missense_Mutation SNP C C T TCGA-D3-A3MV-06A-11D-A21A-08 TCGA-D3-A3MV-10A-01D-A21A-08 g.chr5:102203051C>T c.164C>T c.(163-165)tCa>tTa p.S55L SKCM 5 102260734 102260734 + Missense_Mutation SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr5:102260734C>T c.430C>T c.(430-432)Cgg>Tgg p.R144W SKCM 5 102282552 102282552 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr5:102282552G>A c.538G>A c.(538-540)Gac>Aac p.D180N SKCM 5 102284087 102284087 + Missense_Mutation SNP C C T TCGA-FR-A3YO-06A-11D-A23B-08 TCGA-FR-A3YO-10A-01D-A23B-08 g.chr5:102284087C>T c.581C>T c.(580-582)cCt>cTt p.P194L SKCM 5 102285616 102285616 + Silent SNP A A G TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr5:102285616A>G c.735A>G c.(733-735)gtA>gtG p.V245V SKCM 5 102309921 102309921 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr5:102309921C>T c.1264C>T c.(1264-1266)Ctg>Ttg p.L422L SKCM 5 102310054 102310054 + Missense_Mutation SNP C C T TCGA-FS-A1ZC-06A-11D-A197-08 TCGA-FS-A1ZC-10A-01D-A199-08 g.chr5:102310054C>T c.1397C>T c.(1396-1398)tCt>tTt p.S466F SKCM 5 102310099 102310099 + Missense_Mutation SNP C C T TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr5:102310099C>T c.1442C>T c.(1441-1443)cCc>cTc p.P481L SKCM 5 102326039 102326039 + Missense_Mutation SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr5:102326039G>A c.1547G>A c.(1546-1548)gGg>gAg p.G516E SKCM 5 102338740 102338740 + Silent SNP G G A TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr5:102338740G>A c.1617G>A c.(1615-1617)tcG>tcA p.S539S SKCM 5 102340891 102340891 + Silent SNP A A G TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr5:102340891A>G c.1764A>G c.(1762-1764)aaA>aaG p.K588K SKCM 5 102340892 102340892 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr5:102340892G>A c.1765G>A c.(1765-1767)Gat>Aat p.D589N SKCM 5 102343270 102343270 + Silent SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr5:102343270C>T c.2124C>T c.(2122-2124)atC>atT p.I708I SKCM 5 102361011 102361011 + Missense_Mutation SNP C C T TCGA-DA-A1I7-06A-22D-A197-08 TCGA-DA-A1I7-10A-01D-A199-08 g.chr5:102361011C>T c.2662C>T c.(2662-2664)Cgg>Tgg p.R888W SKCM 5 102361015 102361015 + Nonsense_Mutation SNP G G A TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr5:102361015G>A c.2666G>A c.(2665-2667)tGg>tAg p.W889* SKCM 5 102361024 102361024 + Missense_Mutation SNP C C T TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr5:102361024C>T c.2675C>T c.(2674-2676)tCa>tTa p.S892L SKCM 5 102363938 102363938 + Silent SNP T T C TCGA-EE-A3J4-06A-11D-A20D-08 TCGA-EE-A3J4-10A-01D-A20D-08 g.chr5:102363938T>C c.2739T>C c.(2737-2739)ttT>ttC p.F913F

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 13 77642816 77642816 single base substitution T C missense_variant M3981V 11941A>G BLCA-CN 13 77642816 77642816 single base substitution T C missense_variant M4019V 12055A>G BLCA-CN 13 77642816 77642816 single base substitution T C missense_variant M401V 1201A>G BLCA-CN 13 77720346 77720346 single base substitution C A 5_prime_UTR_variant BLCA-CN 13 77720346 77720346 single base substitution C A exon_variant BLCA-CN 13 77720346 77720346 single base substitution C A stop_gained E2342* 7024G>T BLCA-CN 13 77720346 77720346 single base substitution C A stop_gained E2380* 7138G>T BLCA-CN 13 77742655 77742655 single base substitution C T 5_prime_UTR_variant BLCA-CN 13 77742655 77742655 single base substitution C T missense_variant E1970K 5908G>A BLCA-CN 13 77742655 77742655 single base substitution C T missense_variant E2008K 6022G>A BLCA-CN 13 77807371 77807371 single base substitution A G 5_prime_UTR_variant BLCA-CN 13 77807371 77807371 single base substitution A G missense_variant F848S 2543T>C BLCA-CN 13 77807371 77807371 single base substitution A G missense_variant F886S 2657T>C BLCA-US 13 77642919 77642919 single base substitution G C synonymous_variant V366V 1098C>G BLCA-US 13 77642919 77642919 single base substitution G C synonymous_variant V3946V 11838C>G BLCA-US 13 77642919 77642919 single base substitution G C synonymous_variant V3984V 11952C>G BLCA-US 13 77651516 77651516 single base substitution G A synonymous_variant L216L 646C>T BLCA-US 13 77651516 77651516 single base substitution G A synonymous_variant L3793L 11377C>T BLCA-US 13 77651516 77651516 single base substitution G A synonymous_variant L3831L 11491C>T BLCA-US 13 77656085 77656085 single base substitution G A missense_variant H3656Y 10966C>T BLCA-US 13 77656085 77656085 single base substitution G A missense_variant H3694Y 11080C>T BLCA-US 13 77656085 77656085 single base substitution G A missense_variant H79Y 235C>T BLCA-US 13 77667465 77667465 single base substitution T C downstream_gene_variant BLCA-US 13 77667465 77667465 single base substitution T C missense_variant H3363R 10088A>G BLCA-US 13 77667465 77667465 single base substitution T C missense_variant H3401R 10202A>G BLCA-US 13 77667465 77667465 single base substitution T C splice_region_variant BLCA-US 13 77669735 77669735 single base substitution G A downstream_gene_variant BLCA-US 13 77669735 77669735 single base substitution G A splice_region_variant BLCA-US 13 77672741 77672741 single base substitution G C downstream_gene_variant BLCA-US 13 77672741 77672741 single base substitution G C exon_variant BLCA-US 13 77672741 77672741 single base substitution G C missense_variant L2812V 8434C>G BLCA-US 13 77672741 77672741 single base substitution G C missense_variant L2850V 8548C>G BLCA-US 13 77672741 77672741 single base substitution G C missense_variant L335V 1003C>G BLCA-US 13 77672741 77672741 single base substitution G C upstream_gene_variant BLCA-US 13 77714227 77714227 single base substitution C T 5_prime_UTR_variant BLCA-US 13 77714227 77714227 single base substitution C T downstream_gene_variant BLCA-US 13 77714227 77714227 single base substitution C T exon_variant BLCA-US 13 77714227 77714227 single base substitution C T synonymous_variant Q2453Q 7359G>A BLCA-US 13 77714227 77714227 single base substitution C T synonymous_variant Q2491Q 7473G>A BLCA-US 13 77736073 77736073 single base substitution C G 5_prime_UTR_variant BLCA-US 13 77736073 77736073 single base substitution C G missense_variant D2151H 6451G>C BLCA-US 13 77736073 77736073 single base substitution C G missense_variant D2189H 6565G>C BLCA-US 13 77743819 77743819 single base substitution G A 5_prime_UTR_variant BLCA-US 13 77743819 77743819 single base substitution G A missense_variant S1904F 5711C>T BLCA-US 13 77743819 77743819 single base substitution G A missense_variant S1942F 5825C>T BLCA-US 13 77743847 77743847 single base substitution C T missense_variant D1895N 5683G>A BLCA-US 13 77743847 77743847 single base substitution C T missense_variant D1933N 5797G>A BLCA-US 13 77743847 77743847 single base substitution C T splice_region_variant BLCA-US 13 77750673 77750673 single base substitution C T 5_prime_UTR_variant BLCA-US 13 77750673 77750673 single base substitution C T missense_variant D1773N 5317G>A BLCA-US 13 77750673 77750673 single base substitution C T missense_variant D1811N 5431G>A BLCA-US 13 77786175 77786175 single base substitution G T 5_prime_UTR_variant BLCA-US 13 77786175 77786175 single base substitution G T missense_variant Q1022K 3064C>A BLCA-US 13 77786175 77786175 single base substitution G T missense_variant Q1060K 3178C>A BLCA-US 13 77825292 77825292 single base substitution G C 5_prime_UTR_variant BLCA-US 13 77825292 77825292 single base substitution G C missense_variant P754R 2261C>G BLCA-US 13 77825292 77825292 single base substitution G C missense_variant P792R 2375C>G BLCA-US 13 77825302 77825302 single base substitution C T 5_prime_UTR_variant BLCA-US 13 77825302 77825302 single base substitution C T missense_variant D751N 2251G>A BLCA-US 13 77825302 77825302 single base substitution C T missense_variant D789N 2365G>A BLCA-US 13 77852999 77852999 single base substitution T C 5_prime_UTR_variant BLCA-US 13 77852999 77852999 single base substitution T C synonymous_variant T176T 528A>G BLCA-US 13 77852999 77852999 single base substitution T C synonymous_variant T214T 642A>G BOCA-FR 13 77662930 77662930 single base substitution A T downstream_gene_variant BOCA-FR 13 77662930 77662930 single base substitution A T intron_variant BOCA-FR 13 77662930 77662930 single base substitution A T upstream_gene_variant BOCA-FR 13 77737738 77737738 single base substitution A G intron_variant BRCA-EU 13 77614071 77614071 single base substitution C G downstream_gene_variant BRCA-EU 13 77614365 77614365 single base substitution C G downstream_gene_variant BRCA-EU 13 77614768 77614768 single base substitution C A downstream_gene_variant BRCA-EU 13 77616844 77616844 single base substitution A C downstream_gene_variant BRCA-EU 13 77618150 77618150 single base substitution G A downstream_gene_variant BRCA-EU 13 77618594 77618595 deletion of <=200bp AT - downstream_gene_variant BRCA-EU 13 77619972 77619972 single base substitution C G intron_variant BRCA-EU 13 77625227 77625227 deletion of <=200bp A - frameshift_variant F4571 BRCA-EU 13 77625227 77625227 deletion of <=200bp A - frameshift_variant F4609 BRCA-EU 13 77625227 77625227 deletion of <=200bp A - frameshift_variant F991 BRCA-EU 13 77626356 77626356 single base substitution C T intron_variant BRCA-EU 13 77627043 77627043 single base substitution T G intron_variant BRCA-EU 13 77627488 77627488 single base substitution G A intron_variant BRCA-EU 13 77628584 77628584 single base substitution G A intron_variant BRCA-EU 13 77628938 77628938 single base substitution C G intron_variant BRCA-EU 13 77629262 77629262 single base substitution T C intron_variant BRCA-EU 13 77629641 77629641 single base substitution C A intron_variant BRCA-EU 13 77629963 77629963 single base substitution T C intron_variant BRCA-EU 13 77633788 77633788 single base substitution C A intron_variant BRCA-EU 13 77634275 77634275 single base substitution A T intron_variant BRCA-EU 13 77634893 77634893 single base substitution C T intron_variant BRCA-EU 13 77636620 77636620 single base substitution C A intron_variant BRCA-EU 13 77636657 77636657 single base substitution T C intron_variant BRCA-EU 13 77637826 77637826 single base substitution C G intron_variant BRCA-EU 13 77639069 77639069 single base substitution G A intron_variant BRCA-EU 13 77642907 77642932 deletion of <=200bp CCATTCTTCACGGACTCTGGTAGCTT - frameshift_variant EATRVREEW362 BRCA-EU 13 77642907 77642932 deletion of <=200bp CCATTCTTCACGGACTCTGGTAGCTT - frameshift_variant EATRVREEW3942 BRCA-EU 13 77642907 77642932 deletion of <=200bp CCATTCTTCACGGACTCTGGTAGCTT - frameshift_variant EATRVREEW3980 BRCA-EU 13 77642984 77642984 single base substitution A T intron_variant BRCA-EU 13 77644655 77644655 single base substitution G T intron_variant BRCA-EU 13 77644806 77644806 single base substitution A T missense_variant I337N 1010T>A BRCA-EU 13 77644806 77644806 single base substitution A T missense_variant I3917N 11750T>A BRCA-EU 13 77644806 77644806 single base substitution A T missense_variant I3955N 11864T>A BRCA-EU 13 77644839 77644839 single base substitution G A missense_variant S326L 977C>T BRCA-EU 13 77644839 77644839 single base substitution G A missense_variant S3906L 11717C>T BRCA-EU 13 77644839 77644839 single base substitution G A missense_variant S3944L 11831C>T BRCA-EU 13 77645250 77645250 single base substitution G T intron_variant BRCA-EU 13 77645251 77645251 single base substitution C G intron_variant BRCA-EU 13 77645453 77645453 single base substitution C G intron_variant BRCA-EU 13 77645652 77645652 deletion of <=200bp T - intron_variant BRCA-EU 13 77645733 77645733 single base substitution T C intron_variant BRCA-EU 13 77647060 77647060 single base substitution C G intron_variant BRCA-EU 13 77647089 77647092 deletion of <=200bp CTCT - intron_variant BRCA-EU 13 77647584 77647584 single base substitution T C intron_variant BRCA-EU 13 77647852 77647852 single base substitution C G intron_variant BRCA-EU 13 77648698 77648698 single base substitution C T intron_variant BRCA-EU 13 77649004 77649004 single base substitution G C intron_variant BRCA-EU 13 77649805 77649805 single base substitution T G intron_variant BRCA-EU 13 77649809 77649809 single base substitution T G intron_variant BRCA-EU 13 77649810 77649810 deletion of <=200bp G - intron_variant BRCA-EU 13 77650157 77650157 single base substitution G C intron_variant BRCA-EU 13 77650359 77650359 single base substitution C G intron_variant BRCA-EU 13 77651508 77651508 single base substitution G C synonymous_variant S218S 654C>G BRCA-EU 13 77651508 77651508 single base substitution G C synonymous_variant S3795S 11385C>G BRCA-EU 13 77651508 77651508 single base substitution G C synonymous_variant S3833S 11499C>G BRCA-EU 13 77652066 77652066 deletion of <=200bp T - intron_variant BRCA-EU 13 77654328 77654328 single base substitution T A intron_variant BRCA-EU 13 77655003 77655003 single base substitution G C intron_variant BRCA-EU 13 77655246 77655247 deletion of <=200bp GG - intron_variant BRCA-EU 13 77655697 77655697 deletion of <=200bp T - frameshift_variant T146 BRCA-EU 13 77655697 77655697 deletion of <=200bp T - frameshift_variant T3723 BRCA-EU 13 77655697 77655697 deletion of <=200bp T - frameshift_variant T3761 BRCA-EU 13 77655797 77655797 single base substitution C A intron_variant BRCA-EU 13 77656895 77656902 multiple base substitution (>=2bp and <=200bp) GTAGGAGA GTGAT intron_variant BRCA-EU 13 77661431 77661431 single base substitution C T intron_variant BRCA-EU 13 77661859 77661859 single base substitution C T intron_variant BRCA-EU 13 77661859 77661859 single base substitution C T upstream_gene_variant BRCA-EU 13 77662662 77662662 single base substitution C T downstream_gene_variant BRCA-EU 13 77662662 77662662 single base substitution C T intron_variant BRCA-EU 13 77662662 77662662 single base substitution C T upstream_gene_variant BRCA-EU 13 77662698 77662698 single base substitution A T downstream_gene_variant BRCA-EU 13 77662698 77662698 single base substitution A T intron_variant BRCA-EU 13 77662698 77662698 single base substitution A T upstream_gene_variant BRCA-EU 13 77663784 77663784 single base substitution T C downstream_gene_variant BRCA-EU 13 77663784 77663784 single base substitution T C intron_variant BRCA-EU 13 77663784 77663784 single base substitution T C upstream_gene_variant BRCA-EU 13 77663785 77663785 single base substitution T C downstream_gene_variant BRCA-EU 13 77663785 77663785 single base substitution T C intron_variant BRCA-EU 13 77663785 77663785 single base substitution T C upstream_gene_variant BRCA-EU 13 77664608 77664608 single base substitution G A downstream_gene_variant BRCA-EU 13 77664608 77664608 single base substitution G A intron_variant BRCA-EU 13 77664608 77664608 single base substitution G A upstream_gene_variant BRCA-EU 13 77666929 77666929 single base substitution G T downstream_gene_variant BRCA-EU 13 77666929 77666929 single base substitution G T intron_variant BRCA-EU 13 77667378 77667378 single base substitution G A downstream_gene_variant BRCA-EU 13 77667378 77667378 single base substitution G A missense_variant P3392L 10175C>T BRCA-EU 13 77667378 77667378 single base substitution G A missense_variant P3430L 10289C>T BRCA-EU 13 77670318 77670318 single base substitution T G downstream_gene_variant BRCA-EU 13 77670318 77670318 single base substitution T G intron_variant BRCA-EU 13 77679718 77679718 single base substitution C A intron_variant BRCA-EU 13 77680678 77680678 single base substitution A T intron_variant BRCA-EU 13 77683289 77683289 single base substitution G T intron_variant BRCA-EU 13 77684107 77684107 single base substitution A G intron_variant BRCA-EU 13 77684543 77684543 single base substitution C A intron_variant BRCA-EU 13 77684843 77684843 single base substitution C T intron_variant BRCA-EU 13 77685522 77685522 single base substitution G T intron_variant BRCA-EU 13 77685743 77685743 single base substitution G C intron_variant BRCA-EU 13 77685947 77685947 single base substitution C T intron_variant BRCA-EU 13 77686240 77686240 single base substitution C G intron_variant BRCA-EU 13 77686758 77686758 single base substitution G C intron_variant BRCA-EU 13 77686865 77686865 deletion of <=200bp C - intron_variant BRCA-EU 13 77686971 77686971 single base substitution A G intron_variant BRCA-EU 13 77687991 77687991 single base substitution T G intron_variant BRCA-EU 13 77689414 77689414 single base substitution C T intron_variant BRCA-EU 13 77689534 77689534 single base substitution A T intron_variant BRCA-EU 13 77690040 77690040 single base substitution C G intron_variant BRCA-EU 13 77690186 77690186 single base substitution C A intron_variant BRCA-EU 13 77691560 77691560 single base substitution C A downstream_gene_variant BRCA-EU 13 77691560 77691560 single base substitution C A intron_variant BRCA-EU 13 77691927 77691927 single base substitution C G downstream_gene_variant BRCA-EU 13 77691927 77691927 single base substitution C G intron_variant BRCA-EU 13 77694947 77694948 deletion of <=200bp TT - downstream_gene_variant BRCA-EU 13 77694947 77694948 deletion of <=200bp TT - intron_variant BRCA-EU 13 77694947 77694948 deletion of <=200bp TT - upstream_gene_variant BRCA-EU 13 77695699 77695699 single base substitution G A intron_variant BRCA-EU 13 77695699 77695699 single base substitution G A upstream_gene_variant BRCA-EU 13 77696424 77696424 single base substitution G T intron_variant BRCA-EU 13 77696424 77696424 single base substitution G T upstream_gene_variant BRCA-EU 13 77700906 77700906 single base substitution G A intron_variant BRCA-EU 13 77700906 77700906 single base substitution G A upstream_gene_variant BRCA-EU 13 77701077 77701077 deletion of <=200bp A - intron_variant BRCA-EU 13 77701077 77701077 deletion of <=200bp A - upstream_gene_variant BRCA-EU 13 77701377 77701377 single base substitution G C intron_variant BRCA-EU 13 77701377 77701377 single base substitution G C upstream_gene_variant BRCA-EU 13 77702961 77702961 single base substitution G T intron_variant BRCA-EU 13 77702961 77702961 single base substitution G T upstream_gene_variant BRCA-EU 13 77703202 77703202 single base substitution A G intron_variant BRCA-EU 13 77703202 77703202 single base substitution A G upstream_gene_variant BRCA-EU 13 77706762 77706762 single base substitution C T intron_variant BRCA-EU 13 77709614 77709614 deletion of <=200bp A - intron_variant BRCA-EU 13 77711046 77711046 single base substitution C G intron_variant BRCA-EU 13 77711784 77711784 single base substitution C T intron_variant BRCA-EU 13 77713625 77713625 deletion of <=200bp A - downstream_gene_variant BRCA-EU 13 77713625 77713625 deletion of <=200bp A - intron_variant BRCA-EU 13 77713647 77713647 single base substitution C T downstream_gene_variant BRCA-EU 13 77713647 77713647 single base substitution C T intron_variant BRCA-EU 13 77714278 77714278 single base substitution C G 5_prime_UTR_variant BRCA-EU 13 77714278 77714278 single base substitution C G downstream_gene_variant BRCA-EU 13 77714278 77714278 single base substitution C G exon_variant BRCA-EU 13 77714278 77714278 single base substitution C G missense_variant K2436N 7308G>C BRCA-EU 13 77714278 77714278 single base substitution C G missense_variant K2474N 7422G>C BRCA-EU 13 77714340 77714340 single base substitution G A downstream_gene_variant BRCA-EU 13 77714340 77714340 single base substitution G A intron_variant BRCA-EU 13 77715762 77715762 single base substitution C T downstream_gene_variant BRCA-EU 13 77715762 77715762 single base substitution C T intron_variant BRCA-EU 13 77715762 77715762 single base substitution C T upstream_gene_variant BRCA-EU 13 77715864 77715864 single base substitution C G downstream_gene_variant BRCA-EU 13 77715864 77715864 single base substitution C G intron_variant BRCA-EU 13 77715864 77715864 single base substitution C G upstream_gene_variant BRCA-EU 13 77717777 77717777 single base substitution A G downstream_gene_variant BRCA-EU 13 77717777 77717777 single base substitution A G intron_variant BRCA-EU 13 77717777 77717777 single base substitution A G upstream_gene_variant BRCA-EU 13 77720173 77720173 single base substitution G A intron_variant BRCA-EU 13 77720885 77720885 single base substitution C G intron_variant BRCA-EU 13 77721210 77721210 single base substitution C G intron_variant BRCA-EU 13 77722064 77722064 single base substitution C G intron_variant BRCA-EU 13 77722730 77722730 single base substitution G C intron_variant BRCA-EU 13 77723084 77723084 single base substitution C G intron_variant BRCA-EU 13 77727435 77727435 single base substitution G A intron_variant BRCA-EU 13 77727435 77727435 single base substitution G A upstream_gene_variant BRCA-EU 13 77727925 77727925 single base substitution G A intron_variant BRCA-EU 13 77727925 77727925 single base substitution G A upstream_gene_variant BRCA-EU 13 77729293 77729293 single base substitution A T intron_variant BRCA-EU 13 77729293 77729293 single base substitution A T upstream_gene_variant BRCA-EU 13 77730001 77730001 deletion of <=200bp A - intron_variant BRCA-EU 13 77730001 77730001 insertion of <=200bp - A intron_variant BRCA-EU 13 77730812 77730812 deletion of <=200bp T - intron_variant BRCA-EU 13 77731122 77731122 single base substitution C G intron_variant BRCA-EU 13 77731971 77731971 insertion of <=200bp - T intron_variant BRCA-EU 13 77732248 77732248 single base substitution T C splice_region_variant BRCA-EU 13 77733155 77733155 single base substitution G A intron_variant BRCA-EU 13 77733885 77733885 single base substitution T C intron_variant BRCA-EU 13 77734865 77734865 single base substitution T A intron_variant BRCA-EU 13 77735144 77735144 single base substitution G C intron_variant BRCA-EU 13 77735589 77735589 single base substitution T C intron_variant BRCA-EU 13 77736292 77736292 single base substitution C G intron_variant BRCA-EU 13 77737150 77737150 single base substitution A C intron_variant BRCA-EU 13 77742131 77742135 deletion of <=200bp ATTTT - intron_variant BRCA-EU 13 77743284 77743284 single base substitution C A intron_variant BRCA-EU 13 77746968 77746968 single base substitution G A intron_variant BRCA-EU 13 77749337 77749337 single base substitution G A intron_variant BRCA-EU 13 77749515 77749515 deletion of <=200bp A - intron_variant BRCA-EU 13 77749678 77749678 single base substitution C G intron_variant BRCA-EU 13 77752991 77752991 single base substitution T C intron_variant BRCA-EU 13 77753452 77753452 single base substitution G A intron_variant BRCA-EU 13 77753467 77753467 single base substitution A G intron_variant BRCA-EU 13 77754776 77754776 single base substitution G C intron_variant BRCA-EU 13 77755971 77755971 single base substitution C T 5_prime_UTR_variant BRCA-EU 13 77755971 77755971 single base substitution C T synonymous_variant L1564L 4692G>A BRCA-EU 13 77755971 77755971 single base substitution C T synonymous_variant L1602L 4806G>A BRCA-EU 13 77756548 77756548 single base substitution C T intron_variant BRCA-EU 13 77757270 77757270 single base substitution C T intron_variant BRCA-EU 13 77758907 77758907 single base substitution C T intron_variant BRCA-EU 13 77759724 77759724 single base substitution C G intron_variant BRCA-EU 13 77761585 77761585 single base substitution G A intron_variant BRCA-EU 13 77762886 77762886 single base substitution A G intron_variant BRCA-EU 13 77763117 77763117 single base substitution A G 5_prime_UTR_variant BRCA-EU 13 77763117 77763117 single base substitution A G missense_variant L1369S 4106T>C BRCA-EU 13 77763117 77763117 single base substitution A G missense_variant L1407S 4220T>C BRCA-EU 13 77764133 77764133 single base substitution A C intron_variant BRCA-EU 13 77765675 77765675 single base substitution G A intron_variant BRCA-EU 13 77766406 77766406 insertion of <=200bp - A intron_variant BRCA-EU 13 77766558 77766558 single base substitution G C intron_variant BRCA-EU 13 77767073 77767073 single base substitution G C intron_variant BRCA-EU 13 77767241 77767241 single base substitution G C intron_variant BRCA-EU 13 77767251 77767251 single base substitution G A intron_variant BRCA-EU 13 77767354 77767354 single base substitution A T intron_variant BRCA-EU 13 77768907 77768907 single base substitution A T intron_variant BRCA-EU 13 77769307 77769307 single base substitution G C intron_variant BRCA-EU 13 77769570 77769570 deletion of <=200bp A - intron_variant BRCA-EU 13 77771302 77771302 single base substitution A G intron_variant BRCA-EU 13 77773132 77773132 single base substitution T A intron_variant BRCA-EU 13 77773161 77773161 deletion of <=200bp G - intron_variant BRCA-EU 13 77775801 77775801 single base substitution A G intron_variant BRCA-EU 13 77775905 77775905 single base substitution G C intron_variant BRCA-EU 13 77776655 77776655 single base substitution G A intron_variant BRCA-EU 13 77779051 77779051 single base substitution G A intron_variant BRCA-EU 13 77779916 77779916 single base substitution G C intron_variant BRCA-EU 13 77780725 77780725 deletion of <=200bp A - intron_variant BRCA-EU 13 77781040 77781040 single base substitution C T intron_variant BRCA-EU 13 77781228 77781228 single base substitution G A intron_variant BRCA-EU 13 77787612 77787612 single base substitution C T intron_variant BRCA-EU 13 77788488 77788488 single base substitution A G intron_variant BRCA-EU 13 77788855 77788855 single base substitution G A intron_variant BRCA-EU 13 77789193 77789193 single base substitution G C intron_variant BRCA-EU 13 77790579 77790579 single base substitution C G intron_variant BRCA-EU 13 77791052 77791052 deletion of <=200bp A - intron_variant BRCA-EU 13 77792285 77792285 single base substitution A C intron_variant BRCA-EU 13 77796260 77796260 single base substitution G C intron_variant BRCA-EU 13 77796633 77796633 deletion of <=200bp T - intron_variant BRCA-EU 13 77797417 77797417 single base substitution C A intron_variant BRCA-EU 13 77798397 77798397 single base substitution C G intron_variant BRCA-EU 13 77799500 77799500 deletion of <=200bp A - intron_variant BRCA-EU 13 77801047 77801047 single base substitution T A intron_variant BRCA-EU 13 77804544 77804544 single base substitution G C intron_variant BRCA-EU 13 77805848 77805848 single base substitution G A intron_variant BRCA-EU 13 77805855 77805855 single base substitution G A intron_variant BRCA-EU 13 77806351 77806351 deletion of <=200bp A - intron_variant BRCA-EU 13 77809619 77809619 single base substitution A G intron_variant BRCA-EU 13 77810245 77810245 single base substitution G A intron_variant BRCA-EU 13 77812504 77812504 single base substitution A T intron_variant BRCA-EU 13 77812988 77812988 single base substitution G A intron_variant BRCA-EU 13 77813331 77813331 single base substitution A T intron_variant BRCA-EU 13 77816070 77816070 single base substitution T C intron_variant BRCA-EU 13 77816100 77816100 insertion of <=200bp - T intron_variant BRCA-EU 13 77816278 77816278 single base substitution C G intron_variant BRCA-EU 13 77816645 77816645 single base substitution C T intron_variant BRCA-EU 13 77817023 77817023 single base substitution G A intron_variant BRCA-EU 13 77817591 77817591 single base substitution T C intron_variant BRCA-EU 13 77820698 77820698 single base substitution G C intron_variant BRCA-EU 13 77822676 77822676 single base substitution G A intron_variant BRCA-EU 13 77826005 77826005 single base substitution C T intron_variant BRCA-EU 13 77826510 77826510 single base substitution G A intron_variant BRCA-EU 13 77827597 77827597 single base substitution T C intron_variant BRCA-EU 13 77827967 77827967 single base substitution G A intron_variant BRCA-EU 13 77828627 77828627 single base substitution G A intron_variant BRCA-EU 13 77829403 77829403 single base substitution C A intron_variant BRCA-EU 13 77829494 77829494 single base substitution G T intron_variant BRCA-EU 13 77829682 77829682 single base substitution A T intron_variant BRCA-EU 13 77830006 77830010 deletion of <=200bp AACCA - intron_variant BRCA-EU 13 77830225 77830225 single base substitution G A intron_variant BRCA-EU 13 77830678 77830678 single base substitution C G intron_variant BRCA-EU 13 77830999 77830999 single base substitution A C intron_variant BRCA-EU 13 77831335 77831335 single base substitution A G intron_variant BRCA-EU 13 77832010 77832010 single base substitution C A intron_variant BRCA-EU 13 77832506 77832506 single base substitution A G intron_variant BRCA-EU 13 77835185 77835185 insertion of <=200bp - AT intron_variant BRCA-EU 13 77835902 77835902 single base substitution G A intron_variant BRCA-EU 13 77838068 77838068 single base substitution C G 5_prime_UTR_variant BRCA-EU 13 77838068 77838068 single base substitution C G missense_variant R438T 1313G>C BRCA-EU 13 77838068 77838068 single base substitution C G missense_variant R476T 1427G>C BRCA-EU 13 77839462 77839462 single base substitution A T downstream_gene_variant BRCA-EU 13 77839462 77839462 single base substitution A T intron_variant BRCA-EU 13 77840041 77840041 single base substitution G A downstream_gene_variant BRCA-EU 13 77840041 77840041 single base substitution G A intron_variant BRCA-EU 13 77841080 77841080 single base substitution G C downstream_gene_variant BRCA-EU 13 77841080 77841080 single base substitution G C intron_variant BRCA-EU 13 77842161 77842161 single base substitution G A downstream_gene_variant BRCA-EU 13 77842161 77842161 single base substitution G A intron_variant BRCA-EU 13 77842916 77842916 single base substitution A C downstream_gene_variant BRCA-EU 13 77842916 77842916 single base substitution A C intron_variant BRCA-EU 13 77842930 77842930 single base substitution A T downstream_gene_variant BRCA-EU 13 77842930 77842930 single base substitution A T intron_variant BRCA-EU 13 77845177 77845177 insertion of <=200bp - T intron_variant BRCA-EU 13 77845589 77845589 single base substitution A G intron_variant BRCA-EU 13 77846129 77846129 single base substitution T G intron_variant BRCA-EU 13 77847548 77847548 single base substitution G A intron_variant BRCA-EU 13 77848564 77848564 single base substitution T C intron_variant BRCA-EU 13 77848564 77848564 single base substitution T C upstream_gene_variant BRCA-EU 13 77850738 77850738 single base substitution G C intron_variant BRCA-EU 13 77850738 77850738 single base substitution G C upstream_gene_variant BRCA-EU 13 77852276 77852276 single base substitution C T intron_variant BRCA-EU 13 77852276 77852276 single base substitution C T upstream_gene_variant BRCA-EU 13 77852913 77852913 single base substitution G C 5_prime_UTR_variant BRCA-EU 13 77852913 77852913 single base substitution G C missense_variant S205C 614C>G BRCA-EU 13 77852913 77852913 single base substitution G C missense_variant S243C 728C>G BRCA-EU 13 77856285 77856285 single base substitution C T intron_variant BRCA-EU 13 77856836 77856836 single base substitution A G intron_variant BRCA-EU 13 77857488 77857488 single base substitution C G intron_variant BRCA-EU 13 77858620 77858620 single base substitution G A intron_variant BRCA-EU 13 77858660 77858660 single base substitution C T intron_variant BRCA-EU 13 77860250 77860250 single base substitution G T intron_variant BRCA-EU 13 77861804 77861804 single base substitution C T intron_variant BRCA-EU 13 77861832 77861832 single base substitution T C intron_variant BRCA-EU 13 77862280 77862280 single base substitution G A intron_variant BRCA-EU 13 77862543 77862543 single base substitution C A intron_variant BRCA-EU 13 77863417 77863417 single base substitution G A intron_variant BRCA-EU 13 77863644 77863644 single base substitution G C intron_variant BRCA-EU 13 77863916 77863916 single base substitution G C intron_variant BRCA-EU 13 77864118 77864118 single base substitution G T intron_variant BRCA-EU 13 77864906 77864906 single base substitution T G intron_variant BRCA-EU 13 77867745 77867745 single base substitution A G downstream_gene_variant BRCA-EU 13 77867745 77867745 single base substitution A G intron_variant BRCA-EU 13 77869020 77869020 single base substitution G A downstream_gene_variant BRCA-EU 13 77869020 77869020 single base substitution G A intron_variant BRCA-EU 13 77869191 77869191 single base substitution T A downstream_gene_variant BRCA-EU 13 77869191 77869191 single base substitution T A intron_variant BRCA-EU 13 77871664 77871664 single base substitution T A intron_variant BRCA-EU 13 77871888 77871888 single base substitution T G intron_variant BRCA-EU 13 77874503 77874503 single base substitution C T intron_variant BRCA-EU 13 77875075 77875075 single base substitution G A intron_variant BRCA-EU 13 77875913 77875913 single base substitution G C intron_variant BRCA-EU 13 77879490 77879490 deletion of <=200bp A - intron_variant BRCA-EU 13 77880802 77880802 single base substitution C T intron_variant BRCA-EU 13 77882468 77882468 single base substitution C T intron_variant BRCA-EU 13 77882922 77882922 single base substitution G A intron_variant BRCA-EU 13 77883243 77883251 deletion of <=200bp AGCTACTGC - intron_variant BRCA-EU 13 77883379 77883379 single base substitution A T intron_variant BRCA-EU 13 77884741 77884741 insertion of <=200bp - AT intron_variant BRCA-EU 13 77885239 77885239 single base substitution G T intron_variant BRCA-EU 13 77885940 77885940 single base substitution C T intron_variant BRCA-EU 13 77886238 77886238 single base substitution G A intron_variant BRCA-EU 13 77886449 77886449 deletion of <=200bp G - intron_variant BRCA-EU 13 77887536 77887536 single base substitution G C intron_variant BRCA-EU 13 77888944 77888944 single base substitution T C intron_variant BRCA-EU 13 77896524 77896524 single base substitution T C intron_variant BRCA-EU 13 77896836 77896836 single base substitution G C intron_variant BRCA-EU 13 77896852 77896852 insertion of <=200bp - A intron_variant BRCA-EU 13 77901479 77901479 single base substitution G C upstream_gene_variant BRCA-EU 13 77901676 77901676 single base substitution T G upstream_gene_variant BRCA-EU 13 77901876 77901876 deletion of <=200bp A - upstream_gene_variant BRCA-EU 13 77903125 77903125 single base substitution C A upstream_gene_variant BRCA-EU 13 77903126 77903126 single base substitution C T upstream_gene_variant BRCA-EU 13 77903925 77903925 single base substitution G A upstream_gene_variant BRCA-EU 13 77904824 77904824 single base substitution G A upstream_gene_variant BRCA-FR 13 77627261 77627261 single base substitution A C intron_variant BRCA-FR 13 77627488 77627488 single base substitution G A intron_variant BRCA-FR 13 77628584 77628584 single base substitution G A intron_variant BRCA-FR 13 77644655 77644655 single base substitution G T intron_variant BRCA-FR 13 77647852 77647852 single base substitution C G intron_variant BRCA-FR 13 77648698 77648698 single base substitution C T intron_variant BRCA-FR 13 77650157 77650157 single base substitution G C intron_variant BRCA-FR 13 77654328 77654328 single base substitution T A intron_variant BRCA-FR 13 77685947 77685947 single base substitution C T intron_variant BRCA-FR 13 77686758 77686758 single base substitution G C intron_variant BRCA-FR 13 77689534 77689534 single base substitution A T intron_variant BRCA-FR 13 77691560 77691560 single base substitution C A downstream_gene_variant BRCA-FR 13 77691560 77691560 single base substitution C A intron_variant BRCA-FR 13 77715864 77715864 single base substitution C G downstream_gene_variant BRCA-FR 13 77715864 77715864 single base substitution C G intron_variant BRCA-FR 13 77715864 77715864 single base substitution C G upstream_gene_variant BRCA-FR 13 77717928 77717928 single base substitution C T downstream_gene_variant BRCA-FR 13 77717928 77717928 single base substitution C T intron_variant BRCA-FR 13 77717928 77717928 single base substitution C T upstream_gene_variant BRCA-FR 13 77728953 77728953 single base substitution C G intron_variant BRCA-FR 13 77728953 77728953 single base substitution C G upstream_gene_variant BRCA-FR 13 77729389 77729389 single base substitution G A intron_variant BRCA-FR 13 77729389 77729389 single base substitution G A upstream_gene_variant BRCA-FR 13 77744063 77744063 single base substitution C G intron_variant BRCA-FR 13 77749337 77749337 single base substitution G A intron_variant BRCA-FR 13 77755971 77755971 single base substitution C T 5_prime_UTR_variant BRCA-FR 13 77755971 77755971 single base substitution C T synonymous_variant L1564L 4692G>A BRCA-FR 13 77755971 77755971 single base substitution C T synonymous_variant L1602L 4806G>A BRCA-FR 13 77767251 77767251 single base substitution G A intron_variant BRCA-FR 13 77776655 77776655 single base substitution G A intron_variant BRCA-FR 13 77794974 77794974 single base substitution C G intron_variant BRCA-FR 13 77796260 77796260 single base substitution G C intron_variant BRCA-FR 13 77810245 77810245 single base substitution G A intron_variant BRCA-FR 13 77822676 77822676 single base substitution G A intron_variant BRCA-FR 13 77838068 77838068 single base substitution C G 5_prime_UTR_variant BRCA-FR 13 77838068 77838068 single base substitution C G missense_variant R438T 1313G>C BRCA-FR 13 77838068 77838068 single base substitution C G missense_variant R476T 1427G>C BRCA-FR 13 77842161 77842161 single base substitution G A downstream_gene_variant BRCA-FR 13 77842161 77842161 single base substitution G A intron_variant BRCA-FR 13 77844786 77844786 single base substitution G A intron_variant BRCA-FR 13 77847180 77847180 single base substitution C T intron_variant BRCA-FR 13 77882922 77882922 single base substitution G A intron_variant BRCA-FR 13 77885825 77885825 single base substitution A G intron_variant BRCA-FR 13 77896836 77896836 single base substitution G C intron_variant BRCA-FR 13 77901676 77901676 single base substitution T G upstream_gene_variant BRCA-FR 13 77902773 77902773 single base substitution G A upstream_gene_variant BRCA-KR 13 77818084 77818084 single base substitution A G missense_variant I757T 2270T>C BRCA-KR 13 77818084 77818084 single base substitution A G missense_variant I795T 2384T>C BRCA-KR 13 77818084 77818084 single base substitution A G splice_region_variant BRCA-UK 13 77619972 77619972 single base substitution C G intron_variant BRCA-UK 13 77627043 77627043 single base substitution T G intron_variant BRCA-UK 13 77630226 77630226 single base substitution C G intron_variant BRCA-UK 13 77631192 77631192 single base substitution G A missense_variant R4418W 13252C>T BRCA-UK 13 77631192 77631192 single base substitution G A missense_variant R4456W 13366C>T BRCA-UK 13 77631192 77631192 single base substitution G A missense_variant R838W 2512C>T BRCA-UK 13 77632395 77632395 single base substitution C G missense_variant M4391I 13173G>C BRCA-UK 13 77632395 77632395 single base substitution C G missense_variant M4429I 13287G>C BRCA-UK 13 77632395 77632395 single base substitution C G missense_variant M811I 2433G>C BRCA-UK 13 77632449 77632449 single base substitution G A synonymous_variant H4373H 13119C>T BRCA-UK 13 77632449 77632449 single base substitution G A synonymous_variant H4411H 13233C>T BRCA-UK 13 77632449 77632449 single base substitution G A synonymous_variant H793H 2379C>T BRCA-UK 13 77636620 77636620 single base substitution C A intron_variant BRCA-UK 13 77655797 77655797 single base substitution C A intron_variant BRCA-UK 13 77670318 77670318 single base substitution T G downstream_gene_variant BRCA-UK 13 77670318 77670318 single base substitution T G intron_variant BRCA-UK 13 77707954 77707954 single base substitution C G intron_variant BRCA-UK 13 77716270 77716270 single base substitution G C downstream_gene_variant BRCA-UK 13 77716270 77716270 single base substitution G C intron_variant BRCA-UK 13 77716270 77716270 single base substitution G C upstream_gene_variant BRCA-UK 13 77750644 77750644 single base substitution C T 5_prime_UTR_variant BRCA-UK 13 77750644 77750644 single base substitution C T synonymous_variant V1782V 5346G>A BRCA-UK 13 77750644 77750644 single base substitution C T synonymous_variant V1820V 5460G>A BRCA-UK 13 77762886 77762886 single base substitution A G intron_variant BRCA-UK 13 77791556 77791556 single base substitution G A intron_variant BRCA-UK 13 77823484 77823484 single base substitution G C intron_variant BRCA-UK 13 77823946 77823946 single base substitution G C intron_variant BRCA-UK 13 77839462 77839462 single base substitution A T downstream_gene_variant BRCA-UK 13 77839462 77839462 single base substitution A T intron_variant BRCA-UK 13 77844581 77844581 single base substitution C G 5_prime_UTR_variant BRCA-UK 13 77844581 77844581 single base substitution C G exon_variant BRCA-UK 13 77844581 77844581 single base substitution C G missense_variant K308N 924G>C BRCA-UK 13 77844581 77844581 single base substitution C G missense_variant K346N 1038G>C BRCA-UK 13 77844845 77844845 single base substitution C G intron_variant BRCA-UK 13 77857336 77857336 single base substitution C T intron_variant BRCA-UK 13 77896524 77896524 single base substitution T C intron_variant BRCA-US 13 77636761 77636761 single base substitution C A missense_variant W4210C 12630G>T BRCA-US 13 77636761 77636761 single base substitution C A missense_variant W4248C 12744G>T BRCA-US 13 77636761 77636761 single base substitution C A missense_variant W630C 1890G>T BRCA-US 13 77644815 77644815 single base substitution A G missense_variant M334T 1001T>C BRCA-US 13 77644815 77644815 single base substitution A G missense_variant M3914T 11741T>C BRCA-US 13 77644815 77644815 single base substitution A G missense_variant M3952T 11855T>C BRCA-US 13 77644827 77644827 single base substitution A G missense_variant L330P 989T>C BRCA-US 13 77644827 77644827 single base substitution A G missense_variant L3910P 11729T>C BRCA-US 13 77644827 77644827 single base substitution A G missense_variant L3948P 11843T>C BRCA-US 13 77651360 77651360 single base substitution G A stop_gained Q268* 802C>T BRCA-US 13 77651360 77651360 single base substitution G A stop_gained Q3845* 11533C>T BRCA-US 13 77651360 77651360 single base substitution G A stop_gained Q3883* 11647C>T BRCA-US 13 77655719 77655719 single base substitution G A missense_variant P139L 416C>T BRCA-US 13 77655719 77655719 single base substitution G A missense_variant P3716L 11147C>T BRCA-US 13 77655719 77655719 single base substitution G A missense_variant P3754L 11261C>T BRCA-US 13 77655723 77655723 single base substitution G A stop_gained R138* 412C>T BRCA-US 13 77655723 77655723 single base substitution G A stop_gained R3715* 11143C>T BRCA-US 13 77655723 77655723 single base substitution G A stop_gained R3753* 11257C>T BRCA-US 13 77656125 77656125 single base substitution G C missense_variant C3642W 10926C>G BRCA-US 13 77656125 77656125 single base substitution G C missense_variant C3680W 11040C>G BRCA-US 13 77656125 77656125 single base substitution G C missense_variant C65W 195C>G BRCA-US 13 77663147 77663147 single base substitution C G downstream_gene_variant BRCA-US 13 77663147 77663147 single base substitution C G missense_variant L3477F 10431G>C BRCA-US 13 77663147 77663147 single base substitution C G missense_variant L3515F 10545G>C BRCA-US 13 77663147 77663147 single base substitution C G upstream_gene_variant BRCA-US 13 77667317 77667317 single base substitution C T downstream_gene_variant BRCA-US 13 77667317 77667317 single base substitution C T missense_variant M3412I 10236G>A BRCA-US 13 77667317 77667317 single base substitution C T missense_variant M3450I 10350G>A BRCA-US 13 77669522 77669522 single base substitution C T downstream_gene_variant BRCA-US 13 77669522 77669522 single base substitution C T intron_variant BRCA-US 13 77669522 77669522 single base substitution C T missense_variant M3352I 10056G>A BRCA-US 13 77669522 77669522 single base substitution C T missense_variant M3390I 10170G>A BRCA-US 13 77670474 77670474 single base substitution G A downstream_gene_variant BRCA-US 13 77670474 77670474 single base substitution G A exon_variant BRCA-US 13 77670474 77670474 single base substitution G A synonymous_variant R3271R 9813C>T BRCA-US 13 77670474 77670474 single base substitution G A synonymous_variant R3309R 9927C>T BRCA-US 13 77671823 77671823 single base substitution G C downstream_gene_variant BRCA-US 13 77671823 77671823 single base substitution G C missense_variant L3118V 9352C>G BRCA-US 13 77671823 77671823 single base substitution G C missense_variant L3156V 9466C>G BRCA-US 13 77671823 77671823 single base substitution G C upstream_gene_variant BRCA-US 13 77671946 77671946 single base substitution T C downstream_gene_variant BRCA-US 13 77671946 77671946 single base substitution T C missense_variant I3077V 9229A>G BRCA-US 13 77671946 77671946 single base substitution T C missense_variant I3115V 9343A>G BRCA-US 13 77671946 77671946 single base substitution T C upstream_gene_variant BRCA-US 13 77672548 77672548 single base substitution G A downstream_gene_variant BRCA-US 13 77672548 77672548 single base substitution G A exon_variant BRCA-US 13 77672548 77672548 single base substitution G A missense_variant S2876F 8627C>T BRCA-US 13 77672548 77672548 single base substitution G A missense_variant S2914F 8741C>T BRCA-US 13 77672548 77672548 single base substitution G A missense_variant S399F 1196C>T BRCA-US 13 77672548 77672548 single base substitution G A upstream_gene_variant BRCA-US 13 77673021 77673021 single base substitution C G exon_variant BRCA-US 13 77673021 77673021 single base substitution C G missense_variant K241N 723G>C BRCA-US 13 77673021 77673021 single base substitution C G missense_variant K2718N 8154G>C BRCA-US 13 77673021 77673021 single base substitution C G missense_variant K2756N 8268G>C BRCA-US 13 77673021 77673021 single base substitution C G upstream_gene_variant BRCA-US 13 77673130 77673130 single base substitution G C exon_variant BRCA-US 13 77673130 77673130 single base substitution G C stop_gained S205* 614C>G BRCA-US 13 77673130 77673130 single base substitution G C stop_gained S2682* 8045C>G BRCA-US 13 77673130 77673130 single base substitution G C stop_gained S2720* 8159C>G BRCA-US 13 77673130 77673130 single base substitution G C upstream_gene_variant BRCA-US 13 77692650 77692650 single base substitution C G downstream_gene_variant BRCA-US 13 77692650 77692650 single base substitution C G exon_variant BRCA-US 13 77692650 77692650 single base substitution C G intron_variant BRCA-US 13 77692650 77692650 single base substitution C G missense_variant L140F 420G>C BRCA-US 13 77692650 77692650 single base substitution C G upstream_gene_variant BRCA-US 13 77695616 77695616 single base substitution C G exon_variant BRCA-US 13 77695616 77695616 single base substitution C G missense_variant D103H 307G>C BRCA-US 13 77695616 77695616 single base substitution C G missense_variant D2640H 7918G>C BRCA-US 13 77695616 77695616 single base substitution C G missense_variant D2678H 8032G>C BRCA-US 13 77695616 77695616 single base substitution C G upstream_gene_variant BRCA-US 13 77724895 77724895 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 13 77724895 77724895 single base substitution G A exon_variant BRCA-US 13 77724895 77724895 single base substitution G A stop_gained R2331* 6991C>T BRCA-US 13 77724895 77724895 single base substitution G A stop_gained R2369* 7105C>T BRCA-US 13 77740653 77740653 single base substitution C T 5_prime_UTR_variant BRCA-US 13 77740653 77740653 single base substitution C T missense_variant E2013K 6037G>A BRCA-US 13 77740653 77740653 single base substitution C T missense_variant E2051K 6151G>A BRCA-US 13 77742767 77742767 single base substitution G T 5_prime_UTR_variant BRCA-US 13 77742767 77742767 single base substitution G T synonymous_variant V1932V 5796C>A BRCA-US 13 77742767 77742767 single base substitution G T synonymous_variant V1970V 5910C>A BRCA-US 13 77748601 77748601 single base substitution G A 5_prime_UTR_variant BRCA-US 13 77748601 77748601 single base substitution G A synonymous_variant R1794R 5382C>T BRCA-US 13 77748601 77748601 single base substitution G A synonymous_variant R1832R 5496C>T BRCA-US 13 77764443 77764443 single base substitution C G 5_prime_UTR_variant BRCA-US 13 77764443 77764443 single base substitution C G missense_variant K1328N 3984G>C BRCA-US 13 77764443 77764443 single base substitution C G missense_variant K1366N 4098G>C BRCA-US 13 77779677 77779677 single base substitution C G 5_prime_UTR_variant BRCA-US 13 77779677 77779677 single base substitution C G missense_variant E1178Q 3532G>C BRCA-US 13 77779677 77779677 single base substitution C G missense_variant E1216Q 3646G>C BRCA-US 13 77791998 77791998 single base substitution C T 5_prime_UTR_variant BRCA-US 13 77791998 77791998 single base substitution C T missense_variant V1012I 3034G>A BRCA-US 13 77791998 77791998 single base substitution C T missense_variant V974I 2920G>A BRCA-US 13 77817214 77817214 single base substitution T C 5_prime_UTR_variant BRCA-US 13 77817214 77817214 single base substitution T C missense_variant H832R 2495A>G BRCA-US 13 77817214 77817214 single base substitution T C missense_variant H870R 2609A>G BRCA-US 13 77836235 77836235 single base substitution G T 5_prime_UTR_variant BRCA-US 13 77836235 77836235 single base substitution G T missense_variant L496I 1486C>A BRCA-US 13 77836235 77836235 single base substitution G T missense_variant L534I 1600C>A BRCA-US 13 77862348 77862348 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 13 77862348 77862348 single base substitution G C stop_gained S143* 428C>G BRCA-US 13 77862348 77862348 single base substitution G C stop_gained S181* 542C>G BTCA-JP 13 77629697 77629697 single base substitution C A missense_variant R4510I 13529G>T BTCA-JP 13 77629697 77629697 single base substitution C A missense_variant R4548I 13643G>T BTCA-JP 13 77629697 77629697 single base substitution C A missense_variant R930I 2789G>T BTCA-JP 13 77629724 77629724 single base substitution T C missense_variant Y4501C 13502A>G BTCA-JP 13 77629724 77629724 single base substitution T C missense_variant Y4539C 13616A>G BTCA-JP 13 77629724 77629724 single base substitution T C missense_variant Y921C 2762A>G BTCA-JP 13 77632513 77632513 single base substitution G A missense_variant T4352M 13055C>T BTCA-JP 13 77632513 77632513 single base substitution G A missense_variant T4390M 13169C>T BTCA-JP 13 77632513 77632513 single base substitution G A missense_variant T772M 2315C>T BTCA-JP 13 77635306 77635306 single base substitution G A missense_variant T4307I 12920C>T BTCA-JP 13 77635306 77635306 single base substitution G A missense_variant T4345I 13034C>T BTCA-JP 13 77635306 77635306 single base substitution G A missense_variant T727I 2180C>T BTCA-JP 13 77644863 77644863 deletion of <=200bp A - intron_variant BTCA-JP 13 77651324 77651324 single base substitution C T missense_variant E280K 838G>A BTCA-JP 13 77651324 77651324 single base substitution C T missense_variant E3857K 11569G>A BTCA-JP 13 77651324 77651324 single base substitution C T missense_variant E3895K 11683G>A BTCA-JP 13 77670607 77670607 single base substitution C T downstream_gene_variant BTCA-JP 13 77670607 77670607 single base substitution C T exon_variant BTCA-JP 13 77670607 77670607 single base substitution C T missense_variant R3227Q 9680G>A BTCA-JP 13 77670607 77670607 single base substitution C T missense_variant R3265Q 9794G>A BTCA-JP 13 77672993 77672993 single base substitution C A downstream_gene_variant BTCA-JP 13 77672993 77672993 single base substitution C A exon_variant BTCA-JP 13 77672993 77672993 single base substitution C A missense_variant A251S 751G>T BTCA-JP 13 77672993 77672993 single base substitution C A missense_variant A2728S 8182G>T BTCA-JP 13 77672993 77672993 single base substitution C A missense_variant A2766S 8296G>T BTCA-JP 13 77672993 77672993 single base substitution C A upstream_gene_variant BTCA-JP 13 77673226 77673226 deletion of <=200bp A - intron_variant BTCA-JP 13 77673226 77673226 deletion of <=200bp A - upstream_gene_variant BTCA-JP 13 77695440 77695440 single base substitution G A exon_variant BTCA-JP 13 77695440 77695440 single base substitution G A intron_variant BTCA-JP 13 77695440 77695440 single base substitution G A upstream_gene_variant BTCA-JP 13 77713625 77713625 deletion of <=200bp A - downstream_gene_variant BTCA-JP 13 77713625 77713625 deletion of <=200bp A - intron_variant BTCA-JP 13 77714962 77714962 single base substitution C G downstream_gene_variant BTCA-JP 13 77714962 77714962 single base substitution C G intron_variant BTCA-JP 13 77715107 77715107 single base substitution T G downstream_gene_variant BTCA-JP 13 77715107 77715107 single base substitution T G intron_variant BTCA-JP 13 77715107 77715107 single base substitution T G upstream_gene_variant BTCA-JP 13 77718621 77718621 single base substitution C G 5_prime_UTR_variant BTCA-JP 13 77718621 77718621 single base substitution C G exon_variant BTCA-JP 13 77718621 77718621 single base substitution C G missense_variant G2383A 7148G>C BTCA-JP 13 77718621 77718621 single base substitution C G missense_variant G2421A 7262G>C BTCA-JP 13 77718621 77718621 single base substitution C G upstream_gene_variant BTCA-JP 13 77718655 77718655 single base substitution T C 5_prime_UTR_variant BTCA-JP 13 77718655 77718655 single base substitution T C exon_variant BTCA-JP 13 77718655 77718655 single base substitution T C missense_variant T2372A 7114A>G BTCA-JP 13 77718655 77718655 single base substitution T C missense_variant T2410A 7228A>G BTCA-JP 13 77718655 77718655 single base substitution T C upstream_gene_variant BTCA-JP 13 77750766 77750766 deletion of <=200bp A - splice_region_variant BTCA-JP 13 77751820 77751820 single base substitution A G intron_variant BTCA-JP 13 77759988 77759988 insertion of <=200bp - A intron_variant BTCA-JP 13 77780725 77780725 deletion of <=200bp A - intron_variant BTCA-JP 13 77780854 77780854 single base substitution C G 5_prime_UTR_variant BTCA-JP 13 77780854 77780854 single base substitution C G missense_variant E1137Q 3409G>C BTCA-JP 13 77780854 77780854 single base substitution C G missense_variant E1175Q 3523G>C BTCA-JP 13 77780911 77780911 single base substitution C T 5_prime_UTR_variant BTCA-JP 13 77780911 77780911 single base substitution C T missense_variant D1118N 3352G>A BTCA-JP 13 77780911 77780911 single base substitution C T missense_variant D1156N 3466G>A BTCA-JP 13 77792101 77792101 single base substitution A G intron_variant BTCA-JP 13 77799624 77799624 single base substitution G A 5_prime_UTR_variant BTCA-JP 13 77799624 77799624 single base substitution G A stop_gained R897* 2689C>T BTCA-JP 13 77799624 77799624 single base substitution G A stop_gained R935* 2803C>T BTCA-JP 13 77831891 77831891 single base substitution C G 5_prime_UTR_variant BTCA-JP 13 77831891 77831891 single base substitution C G missense_variant M659I 1977G>C BTCA-JP 13 77831891 77831891 single base substitution C G missense_variant M697I 2091G>C BTCA-JP 13 77870658 77870658 deletion of <=200bp T - downstream_gene_variant BTCA-JP 13 77870658 77870658 deletion of <=200bp T - intron_variant BTCA-JP 13 77900798 77900798 single base substitution A G 5_prime_UTR_variant BTCA-JP 13 77900798 77900798 single base substitution A G exon_variant BTCA-JP 13 77900798 77900798 single base substitution A G missense_variant F38S 113T>C CESC-US 13 77625989 77625989 single base substitution C G missense_variant R4533T 13598G>C CESC-US 13 77625989 77625989 single base substitution C G missense_variant R4571T 13712G>C CESC-US 13 77625989 77625989 single base substitution C G missense_variant R953T 2858G>C CESC-US 13 77633672 77633672 single base substitution C G missense_variant D4338H 13012G>C CESC-US 13 77633672 77633672 single base substitution C G missense_variant D4376H 13126G>C CESC-US 13 77633672 77633672 single base substitution C G missense_variant D758H 2272G>C CESC-US 13 77640190 77640190 single base substitution C T missense_variant M4125I 12375G>A CESC-US 13 77640190 77640190 single base substitution C T missense_variant M4163I 12489G>A CESC-US 13 77640190 77640190 single base substitution C T missense_variant M545I 1635G>A CESC-US 13 77651182 77651182 single base substitution G T intron_variant CESC-US 13 77651193 77651193 single base substitution C T intron_variant CESC-US 13 77670497 77670497 single base substitution G A downstream_gene_variant CESC-US 13 77670497 77670497 single base substitution G A exon_variant CESC-US 13 77670497 77670497 single base substitution G A missense_variant R3264C 9790C>T CESC-US 13 77670497 77670497 single base substitution G A missense_variant R3302C 9904C>T CESC-US 13 77677374 77677374 single base substitution C A exon_variant CESC-US 13 77677374 77677374 single base substitution C A intron_variant CESC-US 13 77695487 77695487 single base substitution G T exon_variant CESC-US 13 77695487 77695487 single base substitution G T intron_variant CESC-US 13 77695487 77695487 single base substitution G T upstream_gene_variant CESC-US 13 77695598 77695598 single base substitution G C exon_variant CESC-US 13 77695598 77695598 single base substitution G C missense_variant P109A 325C>G CESC-US 13 77695598 77695598 single base substitution G C missense_variant P2646A 7936C>G CESC-US 13 77695598 77695598 single base substitution G C missense_variant P2684A 8050C>G CESC-US 13 77695598 77695598 single base substitution G C upstream_gene_variant CESC-US 13 77754359 77754359 single base substitution C T 5_prime_UTR_variant CESC-US 13 77754359 77754359 single base substitution C T missense_variant R1641K 4922G>A CESC-US 13 77754359 77754359 single base substitution C T missense_variant R1679K 5036G>A CESC-US 13 77754364 77754364 single base substitution C T 5_prime_UTR_variant CESC-US 13 77754364 77754364 single base substitution C T synonymous_variant L1639L 4917G>A CESC-US 13 77754364 77754364 single base substitution C T synonymous_variant L1677L 5031G>A CESC-US 13 77817203 77817203 single base substitution C T 5_prime_UTR_variant CESC-US 13 77817203 77817203 single base substitution C T missense_variant E836K 2506G>A CESC-US 13 77817203 77817203 single base substitution C T missense_variant E874K 2620G>A CESC-US 13 77817206 77817206 single base substitution C T 5_prime_UTR_variant CESC-US 13 77817206 77817206 single base substitution C T missense_variant E835K 2503G>A CESC-US 13 77817206 77817206 single base substitution C T missense_variant E873K 2617G>A CESC-US 13 77834572 77834572 single base substitution C T 5_prime_UTR_variant CESC-US 13 77834572 77834572 single base substitution C T missense_variant D632N 1894G>A CESC-US 13 77834572 77834572 single base substitution C T missense_variant D670N 2008G>A CESC-US 13 77862415 77862415 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant CESC-US 13 77862415 77862415 single base substitution G C missense_variant L121V 361C>G CESC-US 13 77862415 77862415 single base substitution G C missense_variant L159V 475C>G CLLE-ES 13 77644827 77644827 single base substitution A G missense_variant L330P 989T>C CLLE-ES 13 77644827 77644827 single base substitution A G missense_variant L3910P 11729T>C CLLE-ES 13 77644827 77644827 single base substitution A G missense_variant L3948P 11843T>C CLLE-ES 13 77676725 77676725 single base substitution A T intron_variant CLLE-ES 13 77676725 77676725 single base substitution A T upstream_gene_variant CLLE-ES 13 77699728 77699728 single base substitution A G intron_variant CLLE-ES 13 77699728 77699728 single base substitution A G upstream_gene_variant CLLE-ES 13 77759524 77759524 single base substitution A G intron_variant CLLE-ES 13 77786257 77786257 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant CLLE-ES 13 77786257 77786257 single base substitution A G synonymous_variant Y1032Y 3096T>C CLLE-ES 13 77786257 77786257 single base substitution A G synonymous_variant Y994Y 2982T>C CLLE-ES 13 77804510 77804510 single base substitution T C intron_variant CLLE-ES 13 77840419 77840419 single base substitution A G downstream_gene_variant CLLE-ES 13 77840419 77840419 single base substitution A G intron_variant CLLE-ES 13 77863100 77863100 single base substitution G A intron_variant CLLE-ES 13 77864072 77864072 single base substitution G C intron_variant CLLE-ES 13 77890041 77890041 single base substitution A G intron_variant CLLE-ES 13 77890100 77890100 single base substitution A G intron_variant CLLE-ES 13 77892154 77892154 single base substitution A C intron_variant CLLE-ES 13 77893428 77893429 multiple base substitution (>=2bp and <=200bp) AA GC intron_variant CLLE-ES 13 77895211 77895211 single base substitution T C intron_variant COAD-US 13 77631119 77631119 single base substitution A G splice_donor_variant COAD-US 13 77632470 77632470 single base substitution C T synonymous_variant E4366E 13098G>A COAD-US 13 77632470 77632470 single base substitution C T synonymous_variant E4404E 13212G>A COAD-US 13 77632470 77632470 single base substitution C T synonymous_variant E786E 2358G>A COAD-US 13 77632488 77632488 single base substitution C A synonymous_variant G4360G 13080G>T COAD-US 13 77632488 77632488 single base substitution C A synonymous_variant G4398G 13194G>T COAD-US 13 77632488 77632488 single base substitution C A synonymous_variant G780G 2340G>T COAD-US 13 77632521 77632521 single base substitution A G synonymous_variant C4349C 13047T>C COAD-US 13 77632521 77632521 single base substitution A G synonymous_variant C4387C 13161T>C COAD-US 13 77632521 77632521 single base substitution A G synonymous_variant C769C 2307T>C COAD-US 13 77635825 77635825 single base substitution T C missense_variant H4254R 12761A>G COAD-US 13 77635825 77635825 single base substitution T C missense_variant H4292R 12875A>G COAD-US 13 77635825 77635825 single base substitution T C missense_variant H674R 2021A>G COAD-US 13 77636817 77636817 single base substitution C T missense_variant A4192T 12574G>A COAD-US 13 77636817 77636817 single base substitution C T missense_variant A4230T 12688G>A COAD-US 13 77636817 77636817 single base substitution C T missense_variant A612T 1834G>A COAD-US 13 77641953 77641953 single base substitution C T missense_variant R4035H 12104G>A COAD-US 13 77641953 77641953 single base substitution C T missense_variant R4073H 12218G>A COAD-US 13 77641953 77641953 single base substitution C T missense_variant R455H 1364G>A COAD-US 13 77642770 77642770 single base substitution G A missense_variant A3996V 11987C>T COAD-US 13 77642770 77642770 single base substitution G A missense_variant A4034V 12101C>T COAD-US 13 77642770 77642770 single base substitution G A missense_variant A416V 1247C>T COAD-US 13 77642918 77642918 single base substitution G A missense_variant R367C 1099C>T COAD-US 13 77642918 77642918 single base substitution G A missense_variant R3947C 11839C>T COAD-US 13 77642918 77642918 single base substitution G A missense_variant R3985C 11953C>T COAD-US 13 77644772 77644772 single base substitution T G missense_variant Q348H 1044A>C COAD-US 13 77644772 77644772 single base substitution T G missense_variant Q3928H 11784A>C COAD-US 13 77644772 77644772 single base substitution T G missense_variant Q3966H 11898A>C COAD-US 13 77644799 77644799 single base substitution G T missense_variant F339L 1017C>A COAD-US 13 77644799 77644799 single base substitution G T missense_variant F3919L 11757C>A COAD-US 13 77644799 77644799 single base substitution G T missense_variant F3957L 11871C>A COAD-US 13 77651459 77651459 single base substitution T C missense_variant I235V 703A>G COAD-US 13 77651459 77651459 single base substitution T C missense_variant I3812V 11434A>G COAD-US 13 77651459 77651459 single base substitution T C missense_variant I3850V 11548A>G COAD-US 13 77655626 77655626 single base substitution T C missense_variant N170S 509A>G COAD-US 13 77655626 77655626 single base substitution T C missense_variant N3747S 11240A>G COAD-US 13 77655626 77655626 single base substitution T C missense_variant N3785S 11354A>G COAD-US 13 77657196 77657196 single base substitution G A synonymous_variant S3631S 10893C>T COAD-US 13 77657196 77657196 single base substitution G A synonymous_variant S3669S 11007C>T COAD-US 13 77657196 77657196 single base substitution G A synonymous_variant S54S 162C>T COAD-US 13 77671639 77671639 single base substitution A C downstream_gene_variant COAD-US 13 77671639 77671639 single base substitution A C exon_variant COAD-US 13 77671639 77671639 single base substitution A C missense_variant V3179G 9536T>G COAD-US 13 77671639 77671639 single base substitution A C missense_variant V3217G 9650T>G COAD-US 13 77671938 77671938 single base substitution T C downstream_gene_variant COAD-US 13 77671938 77671938 single base substitution T C synonymous_variant K3079K 9237A>G COAD-US 13 77671938 77671938 single base substitution T C synonymous_variant K3117K 9351A>G COAD-US 13 77671938 77671938 single base substitution T C upstream_gene_variant COAD-US 13 77672277 77672277 single base substitution C T downstream_gene_variant COAD-US 13 77672277 77672277 single base substitution C T exon_variant COAD-US 13 77672277 77672277 single base substitution C T missense_variant E489K 1465G>A COAD-US 13 77672277 77672277 single base substitution C T synonymous_variant S2966S 8898G>A COAD-US 13 77672277 77672277 single base substitution C T synonymous_variant S3004S 9012G>A COAD-US 13 77672277 77672277 single base substitution C T upstream_gene_variant COAD-US 13 77672278 77672278 single base substitution G A downstream_gene_variant COAD-US 13 77672278 77672278 single base substitution G A exon_variant COAD-US 13 77672278 77672278 single base substitution G A missense_variant S2966L 8897C>T COAD-US 13 77672278 77672278 single base substitution G A missense_variant S3004L 9011C>T COAD-US 13 77672278 77672278 single base substitution G A synonymous_variant I488I 1464C>T COAD-US 13 77672278 77672278 single base substitution G A upstream_gene_variant COAD-US 13 77672768 77672768 single base substitution G A downstream_gene_variant COAD-US 13 77672768 77672768 single base substitution G A exon_variant COAD-US 13 77672768 77672768 single base substitution G A missense_variant R2803C 8407C>T COAD-US 13 77672768 77672768 single base substitution G A missense_variant R2841C 8521C>T COAD-US 13 77672768 77672768 single base substitution G A missense_variant R326C 976C>T COAD-US 13 77672768 77672768 single base substitution G A upstream_gene_variant COAD-US 13 77699498 77699498 single base substitution C T exon_variant COAD-US 13 77699498 77699498 single base substitution C T missense_variant G2626R 7876G>A COAD-US 13 77699498 77699498 single base substitution C T missense_variant G2664R 7990G>A COAD-US 13 77699498 77699498 single base substitution C T missense_variant G89R 265G>A COAD-US 13 77700455 77700455 single base substitution C A splice_region_variant COAD-US 13 77700455 77700455 single base substitution C A stop_gained E2590* 7768G>T COAD-US 13 77700455 77700455 single base substitution C A stop_gained E2628* 7882G>T COAD-US 13 77700455 77700455 single base substitution C A stop_gained E53* 157G>T COAD-US 13 77700455 77700455 single base substitution C A upstream_gene_variant COAD-US 13 77700630 77700630 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 13 77700630 77700630 single base substitution G A exon_variant COAD-US 13 77700630 77700630 single base substitution G A synonymous_variant C2531C 7593C>T COAD-US 13 77700630 77700630 single base substitution G A synonymous_variant C2569C 7707C>T COAD-US 13 77700630 77700630 single base substitution G A upstream_gene_variant COAD-US 13 77720341 77720341 single base substitution A T 5_prime_UTR_variant COAD-US 13 77720341 77720341 single base substitution A T exon_variant COAD-US 13 77720341 77720341 single base substitution A T missense_variant N2343K 7029T>A COAD-US 13 77720341 77720341 single base substitution A T missense_variant N2381K 7143T>A COAD-US 13 77743845 77743845 single base substitution A T 5_prime_UTR_variant COAD-US 13 77743845 77743845 single base substitution A T missense_variant D1895E 5685T>A COAD-US 13 77743845 77743845 single base substitution A T missense_variant D1933E 5799T>A COAD-US 13 77745750 77745750 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant COAD-US 13 77745750 77745750 single base substitution A C missense_variant L1853V 5557T>G COAD-US 13 77745750 77745750 single base substitution A C missense_variant L1891V 5671T>G COAD-US 13 77748601 77748601 single base substitution G A 5_prime_UTR_variant COAD-US 13 77748601 77748601 single base substitution G A synonymous_variant R1794R 5382C>T COAD-US 13 77748601 77748601 single base substitution G A synonymous_variant R1832R 5496C>T COAD-US 13 77750766 77750767 deletion of <=200bp AA - splice_region_variant COAD-US 13 77750766 77750768 deletion of <=200bp AAA - splice_region_variant COAD-US 13 77779614 77779614 single base substitution A C 5_prime_UTR_variant COAD-US 13 77779614 77779614 single base substitution A C missense_variant F1199V 3595T>G COAD-US 13 77779614 77779614 single base substitution A C missense_variant F1237V 3709T>G COAD-US 13 77779661 77779661 single base substitution G A 5_prime_UTR_variant COAD-US 13 77779661 77779661 single base substitution G A missense_variant A1183V 3548C>T COAD-US 13 77779661 77779661 single base substitution G A missense_variant A1221V 3662C>T COAD-US 13 77785378 77785378 single base substitution T A 5_prime_UTR_variant COAD-US 13 77785378 77785378 single base substitution T A missense_variant T1076S 3226A>T COAD-US 13 77785378 77785378 single base substitution T A missense_variant T1114S 3340A>T COAD-US 13 77786240 77786240 single base substitution G A 5_prime_UTR_variant COAD-US 13 77786240 77786240 single base substitution G A missense_variant A1000V 2999C>T COAD-US 13 77786240 77786240 single base substitution G A missense_variant A1038V 3113C>T COAD-US 13 77786285 77786285 single base substitution A G 5_prime_UTR_variant COAD-US 13 77786285 77786285 single base substitution A G missense_variant L1023P 3068T>C COAD-US 13 77786285 77786285 single base substitution A G missense_variant L985P 2954T>C COAD-US 13 77798654 77798654 single base substitution T G 5_prime_UTR_variant COAD-US 13 77798654 77798654 single base substitution T G missense_variant E919D 2757A>C COAD-US 13 77798654 77798654 single base substitution T G missense_variant E957D 2871A>C COAD-US 13 77817229 77817229 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant COAD-US 13 77817229 77817229 single base substitution C T missense_variant R827H 2480G>A COAD-US 13 77817229 77817229 single base substitution C T missense_variant R865H 2594G>A COAD-US 13 77817958 77817958 single base substitution G T 5_prime_UTR_variant COAD-US 13 77817958 77817958 single base substitution G T missense_variant P799H 2396C>A COAD-US 13 77817958 77817958 single base substitution G T missense_variant P837H 2510C>A COAD-US 13 77831879 77831879 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 13 77831879 77831879 single base substitution C A missense_variant E663D 1989G>T COAD-US 13 77831879 77831879 single base substitution C A missense_variant E701D 2103G>T COAD-US 13 77834649 77834649 single base substitution G A 5_prime_UTR_variant COAD-US 13 77834649 77834649 single base substitution G A missense_variant A606V 1817C>T COAD-US 13 77834649 77834649 single base substitution G A missense_variant A644V 1931C>T COAD-US 13 77844149 77844149 deletion of <=200bp T - 5_prime_UTR_variant COAD-US 13 77844149 77844149 deletion of <=200bp T - downstream_gene_variant COAD-US 13 77844149 77844149 deletion of <=200bp T - frameshift_variant K375 COAD-US 13 77844149 77844149 deletion of <=200bp T - frameshift_variant K413 COAD-US 13 77862314 77862314 single base substitution G A 5_prime_UTR_variant COAD-US 13 77862314 77862314 single base substitution G A synonymous_variant P154P 462C>T COAD-US 13 77862314 77862314 single base substitution G A synonymous_variant P192P 576C>T COAD-US 13 77870783 77870783 single base substitution T C 5_prime_UTR_variant COAD-US 13 77870783 77870783 single base substitution T C exon_variant COAD-US 13 77870783 77870783 single base substitution T C missense_variant K110R 329A>G COAD-US 13 77870783 77870783 single base substitution T C missense_variant K72R 215A>G COAD-US 13 77900636 77900636 deletion of <=200bp C - 5_prime_UTR_variant COAD-US 13 77900636 77900636 deletion of <=200bp C - exon_variant COAD-US 13 77900636 77900636 deletion of <=200bp C - frameshift_variant G54 COAD-US 13 77900636 77900636 deletion of <=200bp C - frameshift_variant G92 COAD-US 13 77900686 77900686 single base substitution G T 5_prime_UTR_variant COAD-US 13 77900686 77900686 single base substitution G T exon_variant COAD-US 13 77900686 77900686 single base substitution G T missense_variant D37E 111C>A COAD-US 13 77900686 77900686 single base substitution G T missense_variant D75E 225C>A COCA-CN 13 77625338 77625338 single base substitution G A intron_variant COCA-CN 13 77630994 77630994 single base substitution T G intron_variant COCA-CN 13 77631076 77631076 single base substitution G T intron_variant COCA-CN 13 77635462 77635462 single base substitution A G intron_variant COCA-CN 13 77636716 77636716 single base substitution A T intron_variant COCA-CN 13 77641668 77641668 single base substitution T C intron_variant COCA-CN 13 77663069 77663069 single base substitution C T downstream_gene_variant COCA-CN 13 77663069 77663069 single base substitution C T stop_gained W3503* 10509G>A COCA-CN 13 77663069 77663069 single base substitution C T stop_gained W3541* 10623G>A COCA-CN 13 77663069 77663069 single base substitution C T upstream_gene_variant COCA-CN 13 77667450 77667450 single base substitution A C downstream_gene_variant COCA-CN 13 77667450 77667450 single base substitution A C exon_variant COCA-CN 13 77667450 77667450 single base substitution A C missense_variant F3368C 10103T>G COCA-CN 13 77667450 77667450 single base substitution A C missense_variant F3406C 10217T>G COCA-CN 13 77672321 77672321 single base substitution G A downstream_gene_variant COCA-CN 13 77672321 77672321 single base substitution G A exon_variant COCA-CN 13 77672321 77672321 single base substitution G A stop_gained R2952* 8854C>T COCA-CN 13 77672321 77672321 single base substitution G A stop_gained R2990* 8968C>T COCA-CN 13 77672321 77672321 single base substitution G A stop_gained R475* 1423C>T COCA-CN 13 77672321 77672321 single base substitution G A upstream_gene_variant COCA-CN 13 77672423 77672423 single base substitution C A downstream_gene_variant COCA-CN 13 77672423 77672423 single base substitution C A exon_variant COCA-CN 13 77672423 77672423 single base substitution C A stop_gained E2918* 8752G>T COCA-CN 13 77672423 77672423 single base substitution C A stop_gained E2956* 8866G>T COCA-CN 13 77672423 77672423 single base substitution C A stop_gained E441* 1321G>T COCA-CN 13 77672423 77672423 single base substitution C A upstream_gene_variant COCA-CN 13 77672450 77672450 single base substitution T C downstream_gene_variant COCA-CN 13 77672450 77672450 single base substitution T C exon_variant COCA-CN 13 77672450 77672450 single base substitution T C missense_variant T2909A 8725A>G COCA-CN 13 77672450 77672450 single base substitution T C missense_variant T2947A 8839A>G COCA-CN 13 77672450 77672450 single base substitution T C missense_variant T432A 1294A>G COCA-CN 13 77672450 77672450 single base substitution T C upstream_gene_variant COCA-CN 13 77695625 77695625 single base substitution C T exon_variant COCA-CN 13 77695625 77695625 single base substitution C T missense_variant A100T 298G>A COCA-CN 13 77695625 77695625 single base substitution C T missense_variant A2637T 7909G>A COCA-CN 13 77695625 77695625 single base substitution C T missense_variant A2675T 8023G>A COCA-CN 13 77695625 77695625 single base substitution C T upstream_gene_variant COCA-CN 13 77695761 77695761 single base substitution A G intron_variant COCA-CN 13 77695761 77695761 single base substitution A G upstream_gene_variant COCA-CN 13 77714835 77714835 single base substitution G T downstream_gene_variant COCA-CN 13 77714835 77714835 single base substitution G T intron_variant COCA-CN 13 77720287 77720287 single base substitution C T intron_variant COCA-CN 13 77720437 77720437 single base substitution G T intron_variant COCA-CN 13 77725162 77725162 single base substitution T C intron_variant COCA-CN 13 77725162 77725162 single base substitution T C upstream_gene_variant COCA-CN 13 77736061 77736061 single base substitution G T 5_prime_UTR_variant COCA-CN 13 77736061 77736061 single base substitution G T missense_variant L2155I 6463C>A COCA-CN 13 77736061 77736061 single base substitution G T missense_variant L2193I 6577C>A COCA-CN 13 77740760 77740760 insertion of <=200bp - TG intron_variant COCA-CN 13 77742772 77742772 single base substitution C A 5_prime_UTR_variant COCA-CN 13 77742772 77742772 single base substitution C A stop_gained E1931* 5791G>T COCA-CN 13 77742772 77742772 single base substitution C A stop_gained E1969* 5905G>T COCA-CN 13 77742918 77742918 single base substitution G T intron_variant COCA-CN 13 77743733 77743733 single base substitution G T intron_variant COCA-CN 13 77745668 77745668 single base substitution C T 5_prime_UTR_variant COCA-CN 13 77745668 77745668 single base substitution C T missense_variant R1880Q 5639G>A COCA-CN 13 77745668 77745668 single base substitution C T missense_variant R1918Q 5753G>A COCA-CN 13 77750710 77750710 single base substitution T G 5_prime_UTR_variant COCA-CN 13 77750710 77750710 single base substitution T G missense_variant L1760F 5280A>C COCA-CN 13 77750710 77750710 single base substitution T G missense_variant L1798F 5394A>C COCA-CN 13 77751940 77751940 single base substitution G T 5_prime_UTR_variant COCA-CN 13 77751940 77751940 single base substitution G T missense_variant F1723L 5169C>A COCA-CN 13 77751940 77751940 single base substitution G T missense_variant F1761L 5283C>A COCA-CN 13 77756040 77756040 single base substitution G T 5_prime_UTR_variant COCA-CN 13 77756040 77756040 single base substitution G T missense_variant N1541K 4623C>A COCA-CN 13 77756040 77756040 single base substitution G T missense_variant N1579K 4737C>A COCA-CN 13 77768247 77768247 single base substitution A C intron_variant COCA-CN 13 77779749 77779749 single base substitution A T intron_variant COCA-CN 13 77789075 77789075 single base substitution C A intron_variant COCA-CN 13 77792099 77792099 single base substitution T C splice_region_variant COCA-CN 13 77792101 77792101 single base substitution A C intron_variant COCA-CN 13 77792102 77792102 single base substitution A C intron_variant COCA-CN 13 77798594 77798594 single base substitution G C 5_prime_UTR_variant COCA-CN 13 77798594 77798594 single base substitution G C synonymous_variant V939V 2817C>G COCA-CN 13 77798594 77798594 single base substitution G C synonymous_variant V977V 2931C>G COCA-CN 13 77798845 77798845 single base substitution T G intron_variant COCA-CN 13 77799468 77799468 single base substitution T G intron_variant COCA-CN 13 77799481 77799481 single base substitution T C intron_variant COCA-CN 13 77799540 77799540 single base substitution G A intron_variant COCA-CN 13 77807345 77807345 single base substitution C T 5_prime_UTR_variant COCA-CN 13 77807345 77807345 single base substitution C T missense_variant A857T 2569G>A COCA-CN 13 77807345 77807345 single base substitution C T missense_variant A895T 2683G>A COCA-CN 13 77817359 77817359 single base substitution A C intron_variant COCA-CN 13 77817968 77817968 single base substitution C A 5_prime_UTR_variant COCA-CN 13 77817968 77817968 single base substitution C A stop_gained E796* 2386G>T COCA-CN 13 77817968 77817968 single base substitution C A stop_gained E834* 2500G>T COCA-CN 13 77831731 77831731 single base substitution A G intron_variant COCA-CN 13 77834735 77834735 single base substitution A G splice_region_variant COCA-CN 13 77835529 77835530 multiple base substitution (>=2bp and <=200bp) AA GG intron_variant COCA-CN 13 77837854 77837854 single base substitution A G 5_prime_UTR_variant COCA-CN 13 77837854 77837854 single base substitution A G missense_variant L463P 1388T>C COCA-CN 13 77837854 77837854 single base substitution A G missense_variant L501P 1502T>C COCA-CN 13 77841899 77841899 single base substitution C A downstream_gene_variant COCA-CN 13 77841899 77841899 single base substitution C A intron_variant COCA-CN 13 77844174 77844174 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 13 77844174 77844174 single base substitution G A exon_variant COCA-CN 13 77844174 77844174 single base substitution G A missense_variant R367C 1099C>T COCA-CN 13 77844174 77844174 single base substitution G A missense_variant R405C 1213C>T COCA-CN 13 77844581 77844581 single base substitution C A 5_prime_UTR_variant COCA-CN 13 77844581 77844581 single base substitution C A exon_variant COCA-CN 13 77844581 77844581 single base substitution C A missense_variant K308N 924G>T COCA-CN 13 77844581 77844581 single base substitution C A missense_variant K346N 1038G>T COCA-CN 13 77847768 77847768 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 13 77847768 77847768 single base substitution G A stop_gained R224* 670C>T COCA-CN 13 77847768 77847768 single base substitution G A stop_gained R262* 784C>T COCA-CN 13 77847768 77847768 single base substitution G A upstream_gene_variant COCA-CN 13 77862497 77862497 single base substitution C A 5_prime_UTR_variant COCA-CN 13 77862497 77862497 single base substitution C A missense_variant E131D 393G>T COCA-CN 13 77862497 77862497 single base substitution C A missense_variant E93D 279G>T EOPC-DE 13 77621061 77621061 single base substitution G A intron_variant EOPC-DE 13 77690076 77690076 single base substitution T A intron_variant EOPC-DE 13 77816381 77816381 single base substitution T G intron_variant EOPC-DE 13 77825932 77825932 single base substitution G A intron_variant EOPC-DE 13 77860019 77860019 single base substitution G C intron_variant ESAD-UK 13 77614311 77614311 single base substitution C T downstream_gene_variant ESAD-UK 13 77614565 77614565 single base substitution T G downstream_gene_variant ESAD-UK 13 77614635 77614635 single base substitution T C downstream_gene_variant ESAD-UK 13 77615252 77615252 single base substitution G C downstream_gene_variant ESAD-UK 13 77616011 77616011 single base substitution C T downstream_gene_variant ESAD-UK 13 77620153 77620153 single base substitution A C intron_variant ESAD-UK 13 77620748 77620748 single base substitution C G intron_variant ESAD-UK 13 77620749 77620749 single base substitution A T intron_variant ESAD-UK 13 77623303 77623303 single base substitution T C intron_variant ESAD-UK 13 77624663 77624663 single base substitution C T intron_variant ESAD-UK 13 77627917 77627918 deletion of <=200bp TG - intron_variant ESAD-UK 13 77628465 77628465 single base substitution A G intron_variant ESAD-UK 13 77628896 77628896 single base substitution T G intron_variant ESAD-UK 13 77629896 77629896 single base substitution T C missense_variant I4444V 13330A>G ESAD-UK 13 77629896 77629896 single base substitution T C missense_variant I4482V 13444A>G ESAD-UK 13 77629896 77629896 single base substitution T C missense_variant I864V 2590A>G ESAD-UK 13 77631370 77631370 single base substitution G A intron_variant ESAD-UK 13 77632483 77632483 single base substitution A G missense_variant V4362A 13085T>C ESAD-UK 13 77632483 77632483 single base substitution A G missense_variant V4400A 13199T>C ESAD-UK 13 77632483 77632483 single base substitution A G missense_variant V782A 2345T>C ESAD-UK 13 77632682 77632682 single base substitution T C intron_variant ESAD-UK 13 77633317 77633317 single base substitution C G intron_variant ESAD-UK 13 77634087 77634087 insertion of <=200bp - A intron_variant ESAD-UK 13 77634356 77634356 single base substitution T G intron_variant ESAD-UK 13 77637082 77637082 single base substitution T C intron_variant ESAD-UK 13 77638759 77638759 single base substitution T C synonymous_variant A4183A 12549A>G ESAD-UK 13 77638759 77638759 single base substitution T C synonymous_variant A4221A 12663A>G ESAD-UK 13 77638759 77638759 single base substitution T C synonymous_variant A603A 1809A>G ESAD-UK 13 77639850 77639850 single base substitution T G intron_variant ESAD-UK 13 77641051 77641051 single base substitution T C intron_variant ESAD-UK 13 77642405 77642405 single base substitution C A intron_variant ESAD-UK 13 77642616 77642616 single base substitution C T intron_variant ESAD-UK 13 77642939 77642939 single base substitution G A missense_variant R360C 1078C>T ESAD-UK 13 77642939 77642939 single base substitution G A missense_variant R3940C 11818C>T ESAD-UK 13 77642939 77642939 single base substitution G A missense_variant R3978C 11932C>T ESAD-UK 13 77643190 77643190 single base substitution C A intron_variant ESAD-UK 13 77643741 77643741 single base substitution C A intron_variant ESAD-UK 13 77648291 77648291 single base substitution C A intron_variant ESAD-UK 13 77648990 77648990 single base substitution G C intron_variant ESAD-UK 13 77649395 77649395 single base substitution C A intron_variant ESAD-UK 13 77649474 77649475 deletion of <=200bp AA - intron_variant ESAD-UK 13 77650533 77650533 single base substitution G C intron_variant ESAD-UK 13 77653826 77653826 insertion of <=200bp - T intron_variant ESAD-UK 13 77654091 77654091 single base substitution C T intron_variant ESAD-UK 13 77655838 77655838 single base substitution G T intron_variant ESAD-UK 13 77657503 77657503 single base substitution G A intron_variant ESAD-UK 13 77657797 77657797 single base substitution A G intron_variant ESAD-UK 13 77658867 77658867 single base substitution C T intron_variant ESAD-UK 13 77659923 77659923 single base substitution A C intron_variant ESAD-UK 13 77663879 77663879 single base substitution C T downstream_gene_variant ESAD-UK 13 77663879 77663879 single base substitution C T intron_variant ESAD-UK 13 77663879 77663879 single base substitution C T upstream_gene_variant ESAD-UK 13 77664987 77664987 single base substitution A G downstream_gene_variant ESAD-UK 13 77664987 77664987 single base substitution A G intron_variant ESAD-UK 13 77664987 77664987 single base substitution A G upstream_gene_variant ESAD-UK 13 77669486 77669486 single base substitution T C downstream_gene_variant ESAD-UK 13 77669486 77669486 single base substitution T C intron_variant ESAD-UK 13 77669486 77669486 single base substitution T C splice_region_variant ESAD-UK 13 77669674 77669674 single base substitution C T downstream_gene_variant ESAD-UK 13 77669674 77669674 single base substitution C T exon_variant ESAD-UK 13 77669674 77669674 single base substitution C T missense_variant A3302T 9904G>A ESAD-UK 13 77669674 77669674 single base substitution C T missense_variant A3340T 10018G>A ESAD-UK 13 77669998 77669998 insertion of <=200bp - T downstream_gene_variant ESAD-UK 13 77669998 77669998 insertion of <=200bp - T intron_variant ESAD-UK 13 77672693 77672693 single base substitution G A downstream_gene_variant ESAD-UK 13 77672693 77672693 single base substitution G A exon_variant ESAD-UK 13 77672693 77672693 single base substitution G A missense_variant R2828W 8482C>T ESAD-UK 13 77672693 77672693 single base substitution G A missense_variant R2866W 8596C>T ESAD-UK 13 77672693 77672693 single base substitution G A missense_variant R351W 1051C>T ESAD-UK 13 77672693 77672693 single base substitution G A upstream_gene_variant ESAD-UK 13 77673322 77673322 single base substitution C T intron_variant ESAD-UK 13 77673322 77673322 single base substitution C T upstream_gene_variant ESAD-UK 13 77675279 77675279 single base substitution C G intron_variant ESAD-UK 13 77675279 77675279 single base substitution C G upstream_gene_variant ESAD-UK 13 77675912 77675912 single base substitution G C intron_variant ESAD-UK 13 77675912 77675912 single base substitution G C upstream_gene_variant ESAD-UK 13 77678155 77678155 deletion of <=200bp T - intron_variant ESAD-UK 13 77678440 77678440 single base substitution G T intron_variant ESAD-UK 13 77681689 77681689 single base substitution T C intron_variant ESAD-UK 13 77682317 77682317 single base substitution A T intron_variant ESAD-UK 13 77682740 77682740 single base substitution C T intron_variant ESAD-UK 13 77687219 77687219 single base substitution A G intron_variant ESAD-UK 13 77689698 77689698 single base substitution C A intron_variant ESAD-UK 13 77689829 77689829 single base substitution A C intron_variant ESAD-UK 13 77689932 77689932 single base substitution C T intron_variant ESAD-UK 13 77691068 77691068 single base substitution G T downstream_gene_variant ESAD-UK 13 77691068 77691068 single base substitution G T intron_variant ESAD-UK 13 77694029 77694029 single base substitution G A downstream_gene_variant ESAD-UK 13 77694029 77694029 single base substitution G A intron_variant ESAD-UK 13 77694029 77694029 single base substitution G A upstream_gene_variant ESAD-UK 13 77694732 77694732 single base substitution G C downstream_gene_variant ESAD-UK 13 77694732 77694732 single base substitution G C intron_variant ESAD-UK 13 77694732 77694732 single base substitution G C upstream_gene_variant ESAD-UK 13 77697790 77697790 single base substitution A G intron_variant ESAD-UK 13 77700041 77700041 single base substitution G T intron_variant ESAD-UK 13 77700041 77700041 single base substitution G T upstream_gene_variant ESAD-UK 13 77701077 77701077 deletion of <=200bp A - intron_variant ESAD-UK 13 77701077 77701077 deletion of <=200bp A - upstream_gene_variant ESAD-UK 13 77703465 77703465 single base substitution C T intron_variant ESAD-UK 13 77703465 77703465 single base substitution C T upstream_gene_variant ESAD-UK 13 77703930 77703930 single base substitution T A intron_variant ESAD-UK 13 77703930 77703930 single base substitution T A upstream_gene_variant ESAD-UK 13 77704542 77704542 insertion of <=200bp - ATAT intron_variant ESAD-UK 13 77704542 77704542 insertion of <=200bp - ATAT upstream_gene_variant ESAD-UK 13 77704742 77704742 single base substitution C G intron_variant ESAD-UK 13 77704742 77704742 single base substitution C G upstream_gene_variant ESAD-UK 13 77704918 77704918 deletion of <=200bp T - intron_variant ESAD-UK 13 77704918 77704918 deletion of <=200bp T - upstream_gene_variant ESAD-UK 13 77705218 77705218 single base substitution G A intron_variant ESAD-UK 13 77705218 77705218 single base substitution G A upstream_gene_variant ESAD-UK 13 77705340 77705340 single base substitution G T intron_variant ESAD-UK 13 77705340 77705340 single base substitution G T upstream_gene_variant ESAD-UK 13 77706818 77706818 single base substitution G C intron_variant ESAD-UK 13 77708417 77708417 single base substitution C T intron_variant ESAD-UK 13 77710707 77710707 single base substitution T C intron_variant ESAD-UK 13 77712561 77712561 single base substitution C T intron_variant ESAD-UK 13 77713620 77713620 single base substitution C T downstream_gene_variant ESAD-UK 13 77713620 77713620 single base substitution C T intron_variant ESAD-UK 13 77714034 77714034 single base substitution A G downstream_gene_variant ESAD-UK 13 77714034 77714034 single base substitution A G intron_variant ESAD-UK 13 77714566 77714566 single base substitution G A downstream_gene_variant ESAD-UK 13 77714566 77714566 single base substitution G A intron_variant ESAD-UK 13 77714612 77714612 single base substitution C A downstream_gene_variant ESAD-UK 13 77714612 77714612 single base substitution C A intron_variant ESAD-UK 13 77715084 77715084 single base substitution A G downstream_gene_variant ESAD-UK 13 77715084 77715084 single base substitution A G splice_region_variant ESAD-UK 13 77715084 77715084 single base substitution A G upstream_gene_variant ESAD-UK 13 77715256 77715256 single base substitution C T downstream_gene_variant ESAD-UK 13 77715256 77715256 single base substitution C T intron_variant ESAD-UK 13 77715256 77715256 single base substitution C T upstream_gene_variant ESAD-UK 13 77715363 77715363 single base substitution A G downstream_gene_variant ESAD-UK 13 77715363 77715363 single base substitution A G intron_variant ESAD-UK 13 77715363 77715363 single base substitution A G upstream_gene_variant ESAD-UK 13 77717814 77717814 single base substitution A T downstream_gene_variant ESAD-UK 13 77717814 77717814 single base substitution A T intron_variant ESAD-UK 13 77717814 77717814 single base substitution A T upstream_gene_variant ESAD-UK 13 77718311 77718311 single base substitution C T exon_variant ESAD-UK 13 77718311 77718311 single base substitution C T intron_variant ESAD-UK 13 77718311 77718311 single base substitution C T upstream_gene_variant ESAD-UK 13 77720412 77720412 single base substitution C T intron_variant ESAD-UK 13 77725102 77725102 single base substitution G T intron_variant ESAD-UK 13 77725102 77725102 single base substitution G T upstream_gene_variant ESAD-UK 13 77725730 77725741 deletion of <=200bp TAACTCTACAGT - intron_variant ESAD-UK 13 77725730 77725741 deletion of <=200bp TAACTCTACAGT - upstream_gene_variant ESAD-UK 13 77725788 77725788 single base substitution A G intron_variant ESAD-UK 13 77725788 77725788 single base substitution A G upstream_gene_variant ESAD-UK 13 77726771 77726771 single base substitution C T intron_variant ESAD-UK 13 77726771 77726771 single base substitution C T upstream_gene_variant ESAD-UK 13 77727094 77727094 single base substitution G A intron_variant ESAD-UK 13 77727094 77727094 single base substitution G A upstream_gene_variant ESAD-UK 13 77727243 77727243 single base substitution C A intron_variant ESAD-UK 13 77727243 77727243 single base substitution C A upstream_gene_variant ESAD-UK 13 77732429 77732429 single base substitution A T intron_variant ESAD-UK 13 77732761 77732761 single base substitution T G intron_variant ESAD-UK 13 77734382 77734382 single base substitution C G intron_variant ESAD-UK 13 77736929 77736929 single base substitution C T intron_variant ESAD-UK 13 77738168 77738168 single base substitution C T intron_variant ESAD-UK 13 77739255 77739255 single base substitution C G intron_variant ESAD-UK 13 77740074 77740074 single base substitution G A intron_variant ESAD-UK 13 77741930 77741930 single base substitution A G intron_variant ESAD-UK 13 77744924 77744924 single base substitution C T intron_variant ESAD-UK 13 77746293 77746293 single base substitution C T intron_variant ESAD-UK 13 77749325 77749325 single base substitution T C intron_variant ESAD-UK 13 77752359 77752359 single base substitution G T intron_variant ESAD-UK 13 77753200 77753200 single base substitution G A intron_variant ESAD-UK 13 77756478 77756478 single base substitution G A intron_variant ESAD-UK 13 77757042 77757042 single base substitution T C intron_variant ESAD-UK 13 77758307 77758307 single base substitution A T intron_variant ESAD-UK 13 77759754 77759754 single base substitution T G intron_variant ESAD-UK 13 77759988 77759988 deletion of <=200bp A - intron_variant ESAD-UK 13 77763280 77763280 single base substitution A G intron_variant ESAD-UK 13 77765993 77765993 single base substitution C T intron_variant ESAD-UK 13 77766280 77766280 single base substitution A T intron_variant ESAD-UK 13 77766297 77766297 single base substitution A G intron_variant ESAD-UK 13 77766418 77766418 single base substitution C G intron_variant ESAD-UK 13 77766590 77766590 single base substitution T G intron_variant ESAD-UK 13 77770207 77770207 single base substitution G A intron_variant ESAD-UK 13 77770638 77770638 single base substitution G A intron_variant ESAD-UK 13 77780006 77780006 single base substitution G A intron_variant ESAD-UK 13 77780673 77780673 insertion of <=200bp - ATG intron_variant ESAD-UK 13 77780705 77780705 single base substitution C T intron_variant ESAD-UK 13 77781582 77781582 single base substitution C T intron_variant ESAD-UK 13 77785672 77785672 single base substitution A G intron_variant ESAD-UK 13 77787347 77787347 single base substitution C T intron_variant ESAD-UK 13 77787652 77787652 single base substitution A G intron_variant ESAD-UK 13 77787714 77787714 single base substitution T C intron_variant ESAD-UK 13 77791123 77791123 single base substitution A C intron_variant ESAD-UK 13 77796510 77796510 single base substitution G C intron_variant ESAD-UK 13 77796840 77796840 single base substitution T C intron_variant ESAD-UK 13 77797007 77797007 single base substitution C T intron_variant ESAD-UK 13 77797115 77797115 single base substitution A C intron_variant ESAD-UK 13 77800346 77800346 insertion of <=200bp - T intron_variant ESAD-UK 13 77801955 77801955 single base substitution G A intron_variant ESAD-UK 13 77803811 77803811 single base substitution A C intron_variant ESAD-UK 13 77805034 77805034 single base substitution A G intron_variant ESAD-UK 13 77805195 77805195 deletion of <=200bp A - intron_variant ESAD-UK 13 77808267 77808272 deletion of <=200bp TTTATT - intron_variant ESAD-UK 13 77811963 77811963 single base substitution C T intron_variant ESAD-UK 13 77812771 77812771 insertion of <=200bp - T intron_variant ESAD-UK 13 77812792 77812792 single base substitution T C intron_variant ESAD-UK 13 77812912 77812912 single base substitution A T intron_variant ESAD-UK 13 77813201 77813201 single base substitution G A intron_variant ESAD-UK 13 77814646 77814646 single base substitution T C intron_variant ESAD-UK 13 77814915 77814916 deletion of <=200bp TC - intron_variant ESAD-UK 13 77815429 77815429 deletion of <=200bp T - intron_variant ESAD-UK 13 77815764 77815764 single base substitution T C intron_variant ESAD-UK 13 77816415 77816415 single base substitution A T intron_variant ESAD-UK 13 77817823 77817823 single base substitution G T intron_variant ESAD-UK 13 77818068 77818068 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 13 77818068 77818068 single base substitution G A synonymous_variant S762S 2286C>T ESAD-UK 13 77818068 77818068 single base substitution G A synonymous_variant S800S 2400C>T ESAD-UK 13 77821913 77821913 single base substitution A G intron_variant ESAD-UK 13 77821921 77821921 single base substitution C G intron_variant ESAD-UK 13 77826005 77826005 single base substitution C T intron_variant ESAD-UK 13 77830440 77830440 single base substitution A T intron_variant ESAD-UK 13 77831776 77831776 single base substitution A T intron_variant ESAD-UK 13 77832041 77832041 single base substitution G A intron_variant ESAD-UK 13 77833115 77833115 single base substitution C T intron_variant ESAD-UK 13 77835411 77835411 single base substitution C A 5_prime_UTR_variant ESAD-UK 13 77835411 77835411 single base substitution C A missense_variant V545L 1633G>T ESAD-UK 13 77835411 77835411 single base substitution C A missense_variant V583L 1747G>T ESAD-UK 13 77835497 77835497 single base substitution C G 5_prime_UTR_variant ESAD-UK 13 77835497 77835497 single base substitution C G missense_variant G516A 1547G>C ESAD-UK 13 77835497 77835497 single base substitution C G missense_variant G554A 1661G>C ESAD-UK 13 77837992 77837992 single base substitution C G intron_variant ESAD-UK 13 77838879 77838880 deletion of <=200bp AG - intron_variant ESAD-UK 13 77840955 77840955 single base substitution A C downstream_gene_variant ESAD-UK 13 77840955 77840955 single base substitution A C intron_variant ESAD-UK 13 77841564 77841564 single base substitution A T downstream_gene_variant ESAD-UK 13 77841564 77841564 single base substitution A T intron_variant ESAD-UK 13 77842779 77842789 deletion of <=200bp TGGTGGGCACC - downstream_gene_variant ESAD-UK 13 77842779 77842789 deletion of <=200bp TGGTGGGCACC - intron_variant ESAD-UK 13 77843729 77843729 single base substitution C G downstream_gene_variant ESAD-UK 13 77843729 77843729 single base substitution C G intron_variant ESAD-UK 13 77845282 77845282 single base substitution C T intron_variant ESAD-UK 13 77845318 77845318 single base substitution T C intron_variant ESAD-UK 13 77845791 77845791 single base substitution G C intron_variant ESAD-UK 13 77849813 77849813 single base substitution T A intron_variant ESAD-UK 13 77849813 77849813 single base substitution T A upstream_gene_variant ESAD-UK 13 77851741 77851741 deletion of <=200bp A - intron_variant ESAD-UK 13 77851741 77851741 deletion of <=200bp A - upstream_gene_variant ESAD-UK 13 77852261 77852261 deletion of <=200bp A - intron_variant ESAD-UK 13 77852261 77852261 deletion of <=200bp A - upstream_gene_variant ESAD-UK 13 77854474 77854474 single base substitution G C intron_variant ESAD-UK 13 77858023 77858023 single base substitution A C intron_variant ESAD-UK 13 77858068 77858068 single base substitution G T intron_variant ESAD-UK 13 77859373 77859373 single base substitution A C intron_variant ESAD-UK 13 77860123 77860123 single base substitution T C intron_variant ESAD-UK 13 77860663 77860663 single base substitution C T intron_variant ESAD-UK 13 77862363 77862363 single base substitution A G 5_prime_UTR_variant ESAD-UK 13 77862363 77862363 single base substitution A G missense_variant V138A 413T>C ESAD-UK 13 77862363 77862363 single base substitution A G missense_variant V176A 527T>C ESAD-UK 13 77863359 77863362 deletion of <=200bp AAGA - intron_variant ESAD-UK 13 77865176 77865176 single base substitution C A intron_variant ESAD-UK 13 77866274 77866274 single base substitution A T downstream_gene_variant ESAD-UK 13 77866274 77866274 single base substitution A T intron_variant ESAD-UK 13 77867617 77867617 single base substitution G A downstream_gene_variant ESAD-UK 13 77867617 77867617 single base substitution G A intron_variant ESAD-UK 13 77873123 77873123 single base substitution C A intron_variant ESAD-UK 13 77873193 77873193 single base substitution C T intron_variant ESAD-UK 13 77876364 77876365 deletion of <=200bp CC - intron_variant ESAD-UK 13 77877265 77877265 single base substitution C T intron_variant ESAD-UK 13 77879179 77879179 single base substitution G A intron_variant ESAD-UK 13 77880011 77880011 single base substitution T G intron_variant ESAD-UK 13 77881891 77881891 single base substitution A G intron_variant ESAD-UK 13 77882861 77882861 single base substitution A G intron_variant ESAD-UK 13 77883185 77883185 single base substitution A C intron_variant ESAD-UK 13 77885495 77885495 single base substitution C A intron_variant ESAD-UK 13 77888173 77888173 single base substitution C G intron_variant ESAD-UK 13 77893386 77893386 single base substitution G A intron_variant ESAD-UK 13 77895286 77895286 insertion of <=200bp - A intron_variant ESAD-UK 13 77897355 77897355 single base substitution G A intron_variant ESAD-UK 13 77897985 77897985 single base substitution C G intron_variant ESAD-UK 13 77900486 77900486 single base substitution A G intron_variant ESAD-UK 13 77901732 77901732 single base substitution G T upstream_gene_variant ESAD-UK 13 77903867 77903867 single base substitution C T upstream_gene_variant ESAD-UK 13 77905352 77905352 single base substitution A G upstream_gene_variant ESAD-UK 13 77905491 77905491 single base substitution T G upstream_gene_variant ESCA-CN 13 77629881 77629881 single base substitution G C missense_variant L4449V 13345C>G ESCA-CN 13 77629881 77629881 single base substitution G C missense_variant L4487V 13459C>G ESCA-CN 13 77629881 77629881 single base substitution G C missense_variant L869V 2605C>G ESCA-CN 13 77661879 77661879 single base substitution T G intron_variant ESCA-CN 13 77661879 77661879 single base substitution T G upstream_gene_variant ESCA-CN 13 77713429 77713429 single base substitution T A 5_prime_UTR_variant ESCA-CN 13 77713429 77713429 single base substitution T A downstream_gene_variant ESCA-CN 13 77713429 77713429 single base substitution T A exon_variant ESCA-CN 13 77713429 77713429 single base substitution T A missense_variant T2483S 7447A>T ESCA-CN 13 77713429 77713429 single base substitution T A missense_variant T2521S 7561A>T ESCA-CN 13 77720324 77720324 single base substitution A G 5_prime_UTR_variant ESCA-CN 13 77720324 77720324 single base substitution A G exon_variant ESCA-CN 13 77720324 77720324 single base substitution A G missense_variant L2349P 7046T>C ESCA-CN 13 77720324 77720324 single base substitution A G missense_variant L2387P 7160T>C ESCA-CN 13 77835347 77835347 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant ESCA-CN 13 77835347 77835347 single base substitution A C missense_variant F566C 1697T>G ESCA-CN 13 77835347 77835347 single base substitution A C missense_variant F604C 1811T>G GACA-CN 13 77765945 77765945 single base substitution T G 5_prime_UTR_variant GACA-CN 13 77765945 77765945 single base substitution T G missense_variant E1275D 3825A>C GACA-CN 13 77765945 77765945 single base substitution T G missense_variant E1313D 3939A>C GBM-US 13 77835447 77835447 single base substitution A G 5_prime_UTR_variant GBM-US 13 77835447 77835447 single base substitution A G missense_variant W533R 1597T>C GBM-US 13 77835447 77835447 single base substitution A G missense_variant W571R 1711T>C KIRC-US 13 77629761 77629761 single base substitution A G missense_variant F4489L 13465T>C KIRC-US 13 77629761 77629761 single base substitution A G missense_variant F4527L 13579T>C KIRC-US 13 77629761 77629761 single base substitution A G missense_variant F909L 2725T>C KIRC-US 13 77669615 77669615 single base substitution T C downstream_gene_variant KIRC-US 13 77669615 77669615 single base substitution T C intron_variant KIRC-US 13 77669615 77669615 single base substitution T C synonymous_variant E3321E 9963A>G KIRC-US 13 77669615 77669615 single base substitution T C synonymous_variant E3359E 10077A>G KIRC-US 13 77714290 77714290 deletion of <=200bp T - 5_prime_UTR_variant KIRC-US 13 77714290 77714290 deletion of <=200bp T - downstream_gene_variant KIRC-US 13 77714290 77714290 deletion of <=200bp T - exon_variant KIRC-US 13 77714290 77714290 deletion of <=200bp T - frameshift_variant K2432 KIRC-US 13 77714290 77714290 deletion of <=200bp T - frameshift_variant K2470 KIRC-US 13 77730192 77730192 single base substitution C A splice_donor_variant KIRC-US 13 77785318 77785318 single base substitution A G 5_prime_UTR_variant KIRC-US 13 77785318 77785318 single base substitution A G missense_variant Y1096H 3286T>C KIRC-US 13 77785318 77785318 single base substitution A G missense_variant Y1134H 3400T>C KIRC-US 13 77817235 77817235 single base substitution C G 5_prime_UTR_variant KIRC-US 13 77817235 77817235 single base substitution C G missense_variant R825P 2474G>C KIRC-US 13 77817235 77817235 single base substitution C G missense_variant R863P 2588G>C KIRP-US 13 77714983 77714983 single base substitution T C downstream_gene_variant KIRP-US 13 77714983 77714983 single base substitution T C missense_variant K2429E 7285A>G KIRP-US 13 77714983 77714983 single base substitution T C missense_variant K2467E 7399A>G KIRP-US 13 77714983 77714983 single base substitution T C splice_region_variant KIRP-US 13 77799654 77799654 single base substitution T C 5_prime_UTR_variant KIRP-US 13 77799654 77799654 single base substitution T C missense_variant K887E 2659A>G KIRP-US 13 77799654 77799654 single base substitution T C missense_variant K925E 2773A>G LAML-KR 13 77643679 77643679 single base substitution T C intron_variant LAML-KR 13 77657475 77657475 single base substitution T C intron_variant LAML-KR 13 77728246 77728246 single base substitution T G intron_variant LAML-KR 13 77728246 77728246 single base substitution T G upstream_gene_variant LAML-KR 13 77778615 77778615 single base substitution G A intron_variant LAML-KR 13 77861563 77861563 single base substitution A G intron_variant LAML-KR 13 77885725 77885725 single base substitution A T intron_variant LGG-US 13 77714188 77714188 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant LGG-US 13 77714188 77714188 single base substitution A C downstream_gene_variant LGG-US 13 77714188 77714188 single base substitution A C exon_variant LGG-US 13 77714188 77714188 single base substitution A C missense_variant I2466M 7398T>G LGG-US 13 77714188 77714188 single base substitution A C missense_variant I2504M 7512T>G LGG-US 13 77807397 77807397 single base substitution G C splice_region_variant LGG-US 13 77862494 77862494 single base substitution A T 5_prime_UTR_variant LGG-US 13 77862494 77862494 single base substitution A T missense_variant N132K 396T>A LGG-US 13 77862494 77862494 single base substitution A T missense_variant N94K 282T>A LICA-CN 13 77619612 77619612 single base substitution C A missense_variant Q1028H 3084G>T LICA-CN 13 77619612 77619612 single base substitution C A missense_variant Q4608H 13824G>T LICA-CN 13 77619612 77619612 single base substitution C A missense_variant Q4646H 13938G>T LICA-CN 13 77672395 77672395 single base substitution T C downstream_gene_variant LICA-CN 13 77672395 77672395 single base substitution T C exon_variant LICA-CN 13 77672395 77672395 single base substitution T C missense_variant N2927S 8780A>G LICA-CN 13 77672395 77672395 single base substitution T C missense_variant N2965S 8894A>G LICA-CN 13 77672395 77672395 single base substitution T C missense_variant N450S 1349A>G LICA-CN 13 77672395 77672395 single base substitution T C upstream_gene_variant LICA-CN 13 77763172 77763172 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant LICA-CN 13 77763172 77763172 single base substitution T A missense_variant S1351C 4051A>T LICA-CN 13 77763172 77763172 single base substitution T A missense_variant S1389C 4165A>T LICA-CN 13 77786106 77786106 single base substitution T C 5_prime_UTR_variant LICA-CN 13 77786106 77786106 single base substitution T C missense_variant S1045G 3133A>G LICA-CN 13 77786106 77786106 single base substitution T C missense_variant S1083G 3247A>G LICA-CN 13 77817273 77817273 single base substitution G C 5_prime_UTR_variant LICA-CN 13 77817273 77817273 single base substitution G C missense_variant N812K 2436C>G LICA-CN 13 77817273 77817273 single base substitution G C missense_variant N850K 2550C>G LICA-FR 13 77642704 77642704 single base substitution C A missense_variant R4018I 12053G>T LICA-FR 13 77642704 77642704 single base substitution C A missense_variant R4056I 12167G>T LICA-FR 13 77642704 77642704 single base substitution C A missense_variant R438I 1313G>T LICA-FR 13 77655628 77655628 single base substitution G C missense_variant I169M 507C>G LICA-FR 13 77655628 77655628 single base substitution G C missense_variant I3746M 11238C>G LICA-FR 13 77655628 77655628 single base substitution G C missense_variant I3784M 11352C>G LICA-FR 13 77660481 77660481 single base substitution T A intron_variant LICA-FR 13 77671560 77671560 single base substitution C G downstream_gene_variant LICA-FR 13 77671560 77671560 single base substitution C G exon_variant LICA-FR 13 77671560 77671560 single base substitution C G synonymous_variant L3205L 9615G>C LICA-FR 13 77671560 77671560 single base substitution C G synonymous_variant L3243L 9729G>C LICA-FR 13 77677710 77677710 single base substitution T C intron_variant LICA-FR 13 77695068 77695068 single base substitution T C downstream_gene_variant LICA-FR 13 77695068 77695068 single base substitution T C intron_variant LICA-FR 13 77695068 77695068 single base substitution T C upstream_gene_variant LICA-FR 13 77700602 77700602 single base substitution G A exon_variant LICA-FR 13 77700602 77700602 single base substitution G A stop_gained Q2541* 7621C>T LICA-FR 13 77700602 77700602 single base substitution G A stop_gained Q2579* 7735C>T LICA-FR 13 77700602 77700602 single base substitution G A stop_gained Q4* 10C>T LICA-FR 13 77700602 77700602 single base substitution G A upstream_gene_variant LICA-FR 13 77713218 77713218 single base substitution T C intron_variant LICA-FR 13 77718616 77718616 single base substitution A T 5_prime_UTR_variant LICA-FR 13 77718616 77718616 single base substitution A T exon_variant LICA-FR 13 77718616 77718616 single base substitution A T missense_variant Y2385N 7153T>A LICA-FR 13 77718616 77718616 single base substitution A T missense_variant Y2423N 7267T>A LICA-FR 13 77718616 77718616 single base substitution A T upstream_gene_variant LICA-FR 13 77718681 77718681 single base substitution A G 5_prime_UTR_variant LICA-FR 13 77718681 77718681 single base substitution A G exon_variant LICA-FR 13 77718681 77718681 single base substitution A G missense_variant M2363T 7088T>C LICA-FR 13 77718681 77718681 single base substitution A G missense_variant M2401T 7202T>C LICA-FR 13 77718681 77718681 single base substitution A G upstream_gene_variant LICA-FR 13 77732871 77732871 single base substitution C T intron_variant LICA-FR 13 77741112 77741119 deletion of <=200bp ACACACAC - intron_variant LICA-FR 13 77745707 77745707 single base substitution T A 5_prime_UTR_variant LICA-FR 13 77745707 77745707 single base substitution T A missense_variant N1867I 5600A>T LICA-FR 13 77745707 77745707 single base substitution T A missense_variant N1905I 5714A>T LICA-FR 13 77751927 77751927 single base substitution C T 5_prime_UTR_variant LICA-FR 13 77751927 77751927 single base substitution C T missense_variant G1728R 5182G>A LICA-FR 13 77751927 77751927 single base substitution C T missense_variant G1766R 5296G>A LICA-FR 13 77774792 77774792 single base substitution C T intron_variant LICA-FR 13 77775826 77775826 single base substitution G A intron_variant LICA-FR 13 77779515 77779515 single base substitution T C 5_prime_UTR_variant LICA-FR 13 77779515 77779515 single base substitution T C missense_variant H1202R 3605A>G LICA-FR 13 77779515 77779515 single base substitution T C missense_variant H1240R 3719A>G LICA-FR 13 77788824 77788824 single base substitution C T intron_variant LICA-FR 13 77791052 77791052 insertion of <=200bp - A intron_variant LICA-FR 13 77813993 77813993 single base substitution T C intron_variant LICA-FR 13 77835364 77835364 single base substitution T C 5_prime_UTR_variant LICA-FR 13 77835364 77835364 single base substitution T C synonymous_variant A560A 1680A>G LICA-FR 13 77835364 77835364 single base substitution T C synonymous_variant A598A 1794A>G LICA-FR 13 77840672 77840672 single base substitution T C downstream_gene_variant LICA-FR 13 77840672 77840672 single base substitution T C intron_variant LICA-FR 13 77841368 77841368 single base substitution A G downstream_gene_variant LICA-FR 13 77841368 77841368 single base substitution A G intron_variant LICA-FR 13 77842047 77842047 single base substitution T C 5_prime_UTR_variant LICA-FR 13 77842047 77842047 single base substitution T C downstream_gene_variant LICA-FR 13 77842047 77842047 single base substitution T C missense_variant N391S 1172A>G LICA-FR 13 77842047 77842047 single base substitution T C missense_variant N429S 1286A>G LICA-FR 13 77847657 77847657 single base substitution T G 5_prime_UTR_variant LICA-FR 13 77847657 77847657 single base substitution T G missense_variant I261L 781A>C LICA-FR 13 77847657 77847657 single base substitution T G missense_variant I299L 895A>C LICA-FR 13 77847657 77847657 single base substitution T G upstream_gene_variant LICA-FR 13 77849701 77849701 single base substitution A G intron_variant LICA-FR 13 77849701 77849701 single base substitution A G upstream_gene_variant LICA-FR 13 77852493 77852493 single base substitution T C intron_variant LICA-FR 13 77852493 77852493 single base substitution T C upstream_gene_variant LICA-FR 13 77865354 77865354 single base substitution C A intron_variant LICA-FR 13 77877018 77877018 single base substitution C T intron_variant LICA-FR 13 77888191 77888197 deletion of <=200bp AAATGAA - intron_variant LICA-FR 13 77899432 77899432 single base substitution T C intron_variant LICA-FR 13 77900848 77900848 single base substitution T A exon_variant LICA-FR 13 77900848 77900848 single base substitution T A intron_variant LICA-FR 13 77900848 77900848 single base substitution T A synonymous_variant G21G 63A>T LICA-FR 13 77900848 77900848 single base substitution T A upstream_gene_variant LIHC-US 13 77641991 77641991 single base substitution A G synonymous_variant S4022S 12066T>C LIHC-US 13 77641991 77641991 single base substitution A G synonymous_variant S4060S 12180T>C LIHC-US 13 77641991 77641991 single base substitution A G synonymous_variant S442S 1326T>C LIHC-US 13 77656079 77656079 single base substitution T C missense_variant S3658G 10972A>G LIHC-US 13 77656079 77656079 single base substitution T C missense_variant S3696G 11086A>G LIHC-US 13 77656079 77656079 single base substitution T C missense_variant S81G 241A>G LIHC-US 13 77740568 77740568 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant LIHC-US 13 77740568 77740568 single base substitution T C missense_variant Y2041C 6122A>G LIHC-US 13 77740568 77740568 single base substitution T C missense_variant Y2079C 6236A>G LIHC-US 13 77750664 77750664 single base substitution C A 5_prime_UTR_variant LIHC-US 13 77750664 77750664 single base substitution C A stop_gained E1776* 5326G>T LIHC-US 13 77750664 77750664 single base substitution C A stop_gained E1814* 5440G>T LIHC-US 13 77844588 77844588 single base substitution C T 5_prime_UTR_variant LIHC-US 13 77844588 77844588 single base substitution C T exon_variant LIHC-US 13 77844588 77844588 single base substitution C T missense_variant G306D 917G>A LIHC-US 13 77844588 77844588 single base substitution C T missense_variant G344D 1031G>A LINC-JP 13 77624787 77624787 insertion of <=200bp - A intron_variant LINC-JP 13 77629462 77629462 single base substitution T C intron_variant LINC-JP 13 77635907 77635907 single base substitution C T missense_variant D4227N 12679G>A LINC-JP 13 77635907 77635907 single base substitution C T missense_variant D4265N 12793G>A LINC-JP 13 77635907 77635907 single base substitution C T missense_variant D647N 1939G>A LINC-JP 13 77636619 77636619 single base substitution T A intron_variant LINC-JP 13 77642595 77642595 single base substitution T A intron_variant LINC-JP 13 77656066 77656066 single base substitution T C missense_variant H3662R 10985A>G LINC-JP 13 77656066 77656066 single base substitution T C missense_variant H3700R 11099A>G LINC-JP 13 77656066 77656066 single base substitution T C missense_variant H85R 254A>G LINC-JP 13 77658019 77658019 single base substitution T C intron_variant LINC-JP 13 77661716 77661716 single base substitution A C missense_variant I3555S 10664T>G LINC-JP 13 77661716 77661716 single base substitution A C missense_variant I3593S 10778T>G LINC-JP 13 77661716 77661716 single base substitution A C upstream_gene_variant LINC-JP 13 77662972 77662972 single base substitution T A downstream_gene_variant LINC-JP 13 77662972 77662972 single base substitution T A missense_variant M3536L 10606A>T LINC-JP 13 77662972 77662972 single base substitution T A missense_variant M3574L 10720A>T LINC-JP 13 77662972 77662972 single base substitution T A upstream_gene_variant LINC-JP 13 77684167 77684167 single base substitution T A intron_variant LINC-JP 13 77688111 77688111 single base substitution C G intron_variant LINC-JP 13 77701168 77701168 single base substitution T A intron_variant LINC-JP 13 77701168 77701168 single base substitution T A upstream_gene_variant LINC-JP 13 77708544 77708544 single base substitution C T intron_variant LINC-JP 13 77715182 77715182 single base substitution C T downstream_gene_variant LINC-JP 13 77715182 77715182 single base substitution C T intron_variant LINC-JP 13 77715182 77715182 single base substitution C T upstream_gene_variant LINC-JP 13 77718260 77718260 single base substitution A T exon_variant LINC-JP 13 77718260 77718260 single base substitution A T intron_variant LINC-JP 13 77718260 77718260 single base substitution A T upstream_gene_variant LINC-JP 13 77722346 77722346 single base substitution T C intron_variant LINC-JP 13 77725789 77725789 single base substitution T C intron_variant LINC-JP 13 77725789 77725789 single base substitution T C upstream_gene_variant LINC-JP 13 77731931 77731931 single base substitution C A intron_variant LINC-JP 13 77741727 77741727 single base substitution C A intron_variant LINC-JP 13 77743388 77743388 single base substitution G A intron_variant LINC-JP 13 77749253 77749253 single base substitution G C intron_variant LINC-JP 13 77753516 77753516 single base substitution G C intron_variant LINC-JP 13 77758518 77758518 single base substitution G C intron_variant LINC-JP 13 77759436 77759436 single base substitution T C 5_prime_UTR_variant LINC-JP 13 77759436 77759436 single base substitution T C synonymous_variant K1469K 4407A>G LINC-JP 13 77759436 77759436 single base substitution T C synonymous_variant K1507K 4521A>G LINC-JP 13 77760378 77760378 single base substitution C T intron_variant LINC-JP 13 77762058 77762058 single base substitution T C intron_variant LINC-JP 13 77766051 77766051 single base substitution T C intron_variant LINC-JP 13 77779525 77779525 single base substitution T C splice_region_variant LINC-JP 13 77780725 77780725 deletion of <=200bp A - intron_variant LINC-JP 13 77780803 77780803 single base substitution C T 5_prime_UTR_variant LINC-JP 13 77780803 77780803 single base substitution C T missense_variant A1154T 3460G>A LINC-JP 13 77780803 77780803 single base substitution C T missense_variant A1192T 3574G>A LINC-JP 13 77784337 77784337 single base substitution T C intron_variant LINC-JP 13 77784338 77784338 single base substitution C T intron_variant LINC-JP 13 77791348 77791348 single base substitution T C intron_variant LINC-JP 13 77802184 77802184 single base substitution T C intron_variant LINC-JP 13 77807384 77807384 single base substitution C A 5_prime_UTR_variant LINC-JP 13 77807384 77807384 single base substitution C A missense_variant A844S 2530G>T LINC-JP 13 77807384 77807384 single base substitution C A missense_variant A882S 2644G>T LINC-JP 13 77825307 77825307 single base substitution C T 5_prime_UTR_variant LINC-JP 13 77825307 77825307 single base substitution C T missense_variant R749Q 2246G>A LINC-JP 13 77825307 77825307 single base substitution C T missense_variant R787Q 2360G>A LINC-JP 13 77831742 77831742 single base substitution T C intron_variant LINC-JP 13 77839811 77839811 single base substitution G A downstream_gene_variant LINC-JP 13 77839811 77839811 single base substitution G A intron_variant LINC-JP 13 77844079 77844079 single base substitution T G downstream_gene_variant LINC-JP 13 77844079 77844079 single base substitution T G intron_variant LINC-JP 13 77844690 77844690 single base substitution A G intron_variant LINC-JP 13 77849760 77849760 single base substitution C A intron_variant LINC-JP 13 77849760 77849760 single base substitution C A upstream_gene_variant LINC-JP 13 77862166 77862166 single base substitution C T intron_variant LINC-JP 13 77862173 77862173 single base substitution C A intron_variant LINC-JP 13 77871375 77871375 single base substitution G T intron_variant LINC-JP 13 77875038 77875038 single base substitution T C intron_variant LINC-JP 13 77900545 77900545 single base substitution C G intron_variant LINC-JP 13 77902145 77902145 single base substitution T C upstream_gene_variant LIRI-JP 13 77614755 77614755 single base substitution G C downstream_gene_variant LIRI-JP 13 77615993 77615993 single base substitution A T downstream_gene_variant LIRI-JP 13 77616541 77616541 single base substitution G A downstream_gene_variant LIRI-JP 13 77616544 77616544 single base substitution T C downstream_gene_variant LIRI-JP 13 77619239 77619239 single base substitution A G 3_prime_UTR_variant LIRI-JP 13 77619874 77619874 single base substitution G A intron_variant LIRI-JP 13 77627517 77627517 single base substitution G T intron_variant LIRI-JP 13 77628423 77628423 single base substitution T C intron_variant LIRI-JP 13 77629387 77629387 single base substitution G C intron_variant LIRI-JP 13 77631446 77631446 single base substitution T G intron_variant LIRI-JP 13 77632197 77632197 single base substitution G A intron_variant LIRI-JP 13 77634367 77634367 single base substitution T C intron_variant LIRI-JP 13 77635994 77635994 single base substitution T C intron_variant LIRI-JP 13 77638627 77638627 single base substitution G A intron_variant LIRI-JP 13 77639227 77639227 single base substitution C A intron_variant LIRI-JP 13 77640155 77640155 single base substitution A G missense_variant I4137T 12410T>C LIRI-JP 13 77640155 77640155 single base substitution A G missense_variant I4175T 12524T>C LIRI-JP 13 77640155 77640155 single base substitution A G missense_variant I557T 1670T>C LIRI-JP 13 77640158 77640158 single base substitution A G missense_variant I4136T 12407T>C LIRI-JP 13 77640158 77640158 single base substitution A G missense_variant I4174T 12521T>C LIRI-JP 13 77640158 77640158 single base substitution A G missense_variant I556T 1667T>C LIRI-JP 13 77640329 77640329 single base substitution T C intron_variant LIRI-JP 13 77641143 77641143 single base substitution T C intron_variant LIRI-JP 13 77641225 77641225 single base substitution A T intron_variant LIRI-JP 13 77641905 77641905 single base substitution C T missense_variant S4051N 12152G>A LIRI-JP 13 77641905 77641905 single base substitution C T missense_variant S4089N 12266G>A LIRI-JP 13 77641905 77641905 single base substitution C T missense_variant S471N 1412G>A LIRI-JP 13 77642921 77642921 single base substitution C A missense_variant V366F 1096G>T LIRI-JP 13 77642921 77642921 single base substitution C A missense_variant V3946F 11836G>T LIRI-JP 13 77642921 77642921 single base substitution C A missense_variant V3984F 11950G>T LIRI-JP 13 77644170 77644170 single base substitution A T intron_variant LIRI-JP 13 77644676 77644676 single base substitution A G intron_variant LIRI-JP 13 77647584 77647584 single base substitution T C intron_variant LIRI-JP 13 77648630 77648630 single base substitution A T intron_variant LIRI-JP 13 77649432 77649432 single base substitution G A intron_variant LIRI-JP 13 77651180 77651180 single base substitution T C intron_variant LIRI-JP 13 77651806 77651806 single base substitution C G intron_variant LIRI-JP 13 77654063 77654063 single base substitution A C intron_variant LIRI-JP 13 77657493 77657493 single base substitution T C intron_variant LIRI-JP 13 77660089 77660089 single base substitution A C intron_variant LIRI-JP 13 77663782 77663782 deletion of <=200bp G - downstream_gene_variant LIRI-JP 13 77663782 77663782 deletion of <=200bp G - intron_variant LIRI-JP 13 77663782 77663782 deletion of <=200bp G - upstream_gene_variant LIRI-JP 13 77663891 77663891 single base substitution A C downstream_gene_variant LIRI-JP 13 77663891 77663891 single base substitution A C intron_variant LIRI-JP 13 77663891 77663891 single base substitution A C upstream_gene_variant LIRI-JP 13 77664668 77664668 single base substitution T C downstream_gene_variant LIRI-JP 13 77664668 77664668 single base substitution T C intron_variant LIRI-JP 13 77664668 77664668 single base substitution T C upstream_gene_variant LIRI-JP 13 77665740 77665740 single base substitution G A downstream_gene_variant LIRI-JP 13 77665740 77665740 single base substitution G A intron_variant LIRI-JP 13 77665740 77665740 single base substitution G A upstream_gene_variant LIRI-JP 13 77666287 77666288 deletion of <=200bp TA - downstream_gene_variant LIRI-JP 13 77666287 77666288 deletion of <=200bp TA - intron_variant LIRI-JP 13 77666287 77666288 deletion of <=200bp TA - upstream_gene_variant LIRI-JP 13 77666469 77666469 single base substitution T C downstream_gene_variant LIRI-JP 13 77666469 77666469 single base substitution T C intron_variant LIRI-JP 13 77666469 77666469 single base substitution T C upstream_gene_variant LIRI-JP 13 77668134 77668134 single base substitution T A downstream_gene_variant LIRI-JP 13 77668134 77668134 single base substitution T A intron_variant LIRI-JP 13 77668449 77668449 single base substitution A C downstream_gene_variant LIRI-JP 13 77668449 77668449 single base substitution A C intron_variant LIRI-JP 13 77669719 77669719 single base substitution T C downstream_gene_variant LIRI-JP 13 77669719 77669719 single base substitution T C exon_variant LIRI-JP 13 77669719 77669719 single base substitution T C missense_variant K3287E 9859A>G LIRI-JP 13 77669719 77669719 single base substitution T C missense_variant K3325E 9973A>G LIRI-JP 13 77670053 77670053 single base substitution G C downstream_gene_variant LIRI-JP 13 77670053 77670053 single base substitution G C intron_variant LIRI-JP 13 77671170 77671170 single base substitution T C downstream_gene_variant LIRI-JP 13 77671170 77671170 single base substitution T C intron_variant LIRI-JP 13 77671229 77671229 single base substitution G C downstream_gene_variant LIRI-JP 13 77671229 77671229 single base substitution G C intron_variant LIRI-JP 13 77671286 77671286 single base substitution T C downstream_gene_variant LIRI-JP 13 77671286 77671286 single base substitution T C intron_variant LIRI-JP 13 77673285 77673285 single base substitution T C intron_variant LIRI-JP 13 77673285 77673285 single base substitution T C upstream_gene_variant LIRI-JP 13 77673718 77673718 single base substitution A G intron_variant LIRI-JP 13 77673718 77673718 single base substitution A G upstream_gene_variant LIRI-JP 13 77678330 77678330 single base substitution A C intron_variant LIRI-JP 13 77679034 77679034 single base substitution T C intron_variant LIRI-JP 13 77681216 77681216 single base substitution G A intron_variant LIRI-JP 13 77683693 77683693 deletion of <=200bp A - intron_variant LIRI-JP 13 77688611 77688611 single base substitution A G intron_variant LIRI-JP 13 77689247 77689247 single base substitution C A intron_variant LIRI-JP 13 77690553 77690553 single base substitution T G downstream_gene_variant LIRI-JP 13 77690553 77690553 single base substitution T G intron_variant LIRI-JP 13 77691640 77691640 single base substitution T C downstream_gene_variant LIRI-JP 13 77691640 77691640 single base substitution T C intron_variant LIRI-JP 13 77694600 77694600 single base substitution T C downstream_gene_variant LIRI-JP 13 77694600 77694600 single base substitution T C intron_variant LIRI-JP 13 77694600 77694600 single base substitution T C upstream_gene_variant LIRI-JP 13 77695255 77695255 single base substitution T C downstream_gene_variant LIRI-JP 13 77695255 77695255 single base substitution T C intron_variant LIRI-JP 13 77695255 77695255 single base substitution T C upstream_gene_variant LIRI-JP 13 77695757 77695757 single base substitution G A intron_variant LIRI-JP 13 77695757 77695757 single base substitution G A upstream_gene_variant LIRI-JP 13 77695976 77695976 single base substitution A G intron_variant LIRI-JP 13 77695976 77695976 single base substitution A G upstream_gene_variant LIRI-JP 13 77698279 77698279 single base substitution T C intron_variant LIRI-JP 13 77700009 77700009 single base substitution C T intron_variant LIRI-JP 13 77700009 77700009 single base substitution C T upstream_gene_variant LIRI-JP 13 77702255 77702255 single base substitution T C intron_variant LIRI-JP 13 77702255 77702255 single base substitution T C upstream_gene_variant LIRI-JP 13 77702432 77702432 single base substitution C A intron_variant LIRI-JP 13 77702432 77702432 single base substitution C A upstream_gene_variant LIRI-JP 13 77704882 77704882 single base substitution T C intron_variant LIRI-JP 13 77704882 77704882 single base substitution T C upstream_gene_variant LIRI-JP 13 77704938 77704938 single base substitution T C intron_variant LIRI-JP 13 77704938 77704938 single base substitution T C upstream_gene_variant LIRI-JP 13 77706223 77706223 single base substitution T C intron_variant LIRI-JP 13 77706626 77706626 insertion of <=200bp - A intron_variant LIRI-JP 13 77707896 77707896 single base substitution G A intron_variant LIRI-JP 13 77708470 77708470 single base substitution G A intron_variant LIRI-JP 13 77713418 77713418 single base substitution C T 5_prime_UTR_variant LIRI-JP 13 77713418 77713418 single base substitution C T downstream_gene_variant LIRI-JP 13 77713418 77713418 single base substitution C T exon_variant LIRI-JP 13 77713418 77713418 single base substitution C T synonymous_variant K2486K 7458G>A LIRI-JP 13 77713418 77713418 single base substitution C T synonymous_variant K2524K 7572G>A LIRI-JP 13 77713647 77713647 single base substitution C T downstream_gene_variant LIRI-JP 13 77713647 77713647 single base substitution C T intron_variant LIRI-JP 13 77713678 77713678 single base substitution C A downstream_gene_variant LIRI-JP 13 77713678 77713678 single base substitution C A intron_variant LIRI-JP 13 77713888 77713888 single base substitution T C downstream_gene_variant LIRI-JP 13 77713888 77713888 single base substitution T C intron_variant LIRI-JP 13 77715410 77715410 single base substitution T C downstream_gene_variant LIRI-JP 13 77715410 77715410 single base substitution T C intron_variant LIRI-JP 13 77715410 77715410 single base substitution T C upstream_gene_variant LIRI-JP 13 77718067 77718067 single base substitution C T downstream_gene_variant LIRI-JP 13 77718067 77718067 single base substitution C T intron_variant LIRI-JP 13 77718067 77718067 single base substitution C T upstream_gene_variant LIRI-JP 13 77720014 77720014 single base substitution C A intron_variant LIRI-JP 13 77720014 77720014 single base substitution C A upstream_gene_variant LIRI-JP 13 77721908 77721908 single base substitution G A intron_variant LIRI-JP 13 77722036 77722036 single base substitution T C intron_variant LIRI-JP 13 77723126 77723126 single base substitution T G intron_variant LIRI-JP 13 77723874 77723874 single base substitution T C intron_variant LIRI-JP 13 77725420 77725420 single base substitution T C intron_variant LIRI-JP 13 77725420 77725420 single base substitution T C upstream_gene_variant LIRI-JP 13 77725624 77725624 single base substitution G A intron_variant LIRI-JP 13 77725624 77725624 single base substitution G A upstream_gene_variant LIRI-JP 13 77729739 77729739 single base substitution T A intron_variant LIRI-JP 13 77729739 77729739 single base substitution T A upstream_gene_variant LIRI-JP 13 77730198 77730198 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant LIRI-JP 13 77730198 77730198 single base substitution T C missense_variant M2266V 6796A>G LIRI-JP 13 77730198 77730198 single base substitution T C missense_variant M2304V 6910A>G LIRI-JP 13 77731218 77731218 single base substitution T C intron_variant LIRI-JP 13 77732050 77732050 single base substitution A T intron_variant LIRI-JP 13 77732649 77732649 single base substitution C G intron_variant LIRI-JP 13 77735162 77735162 single base substitution C T intron_variant LIRI-JP 13 77735179 77735179 single base substitution T A intron_variant LIRI-JP 13 77736337 77736337 single base substitution T C intron_variant LIRI-JP 13 77736482 77736482 single base substitution G A intron_variant LIRI-JP 13 77738189 77738189 single base substitution A G intron_variant LIRI-JP 13 77739027 77739027 single base substitution G A intron_variant LIRI-JP 13 77741699 77741699 single base substitution A C intron_variant LIRI-JP 13 77741726 77741726 single base substitution T A intron_variant LIRI-JP 13 77745355 77745355 single base substitution T C intron_variant LIRI-JP 13 77746647 77746647 single base substitution G A intron_variant LIRI-JP 13 77746656 77746656 single base substitution T C intron_variant LIRI-JP 13 77749394 77749394 single base substitution A G intron_variant LIRI-JP 13 77749906 77749906 single base substitution G T intron_variant LIRI-JP 13 77751379 77751379 single base substitution T C intron_variant LIRI-JP 13 77751534 77751534 single base substitution T C intron_variant LIRI-JP 13 77751827 77751827 single base substitution T C intron_variant LIRI-JP 13 77752320 77752320 single base substitution T C intron_variant LIRI-JP 13 77754024 77754024 single base substitution C G intron_variant LIRI-JP 13 77755745 77755745 single base substitution T C intron_variant LIRI-JP 13 77758228 77758228 single base substitution A C intron_variant LIRI-JP 13 77760486 77760486 deletion of <=200bp C - intron_variant LIRI-JP 13 77761916 77761916 single base substitution T G intron_variant LIRI-JP 13 77762712 77762712 single base substitution A T intron_variant LIRI-JP 13 77762843 77762843 single base substitution T C intron_variant LIRI-JP 13 77766230 77766230 single base substitution T C intron_variant LIRI-JP 13 77768681 77768681 single base substitution T A intron_variant LIRI-JP 13 77769914 77769914 single base substitution T G intron_variant LIRI-JP 13 77770301 77770301 single base substitution A C intron_variant LIRI-JP 13 77772330 77772330 single base substitution T C intron_variant LIRI-JP 13 77776096 77776096 single base substitution C A intron_variant LIRI-JP 13 77783477 77783477 single base substitution G T intron_variant LIRI-JP 13 77784015 77784015 single base substitution G T intron_variant LIRI-JP 13 77784970 77784970 single base substitution T C intron_variant LIRI-JP 13 77785806 77785806 single base substitution A G intron_variant LIRI-JP 13 77786290 77786290 single base substitution T C 5_prime_UTR_variant LIRI-JP 13 77786290 77786290 single base substitution T C synonymous_variant G1021G 3063A>G LIRI-JP 13 77786290 77786290 single base substitution T C synonymous_variant G983G 2949A>G LIRI-JP 13 77786489 77786489 single base substitution T C intron_variant LIRI-JP 13 77786720 77786720 single base substitution C G intron_variant LIRI-JP 13 77787048 77787049 deletion of <=200bp CT - intron_variant LIRI-JP 13 77797974 77797974 single base substitution C G intron_variant LIRI-JP 13 77798141 77798141 single base substitution G C intron_variant LIRI-JP 13 77798197 77798197 single base substitution T C intron_variant LIRI-JP 13 77798235 77798235 single base substitution C T intron_variant LIRI-JP 13 77798822 77798822 single base substitution A T intron_variant LIRI-JP 13 77799304 77799304 single base substitution T C intron_variant LIRI-JP 13 77799846 77799846 single base substitution C T intron_variant LIRI-JP 13 77801022 77801022 single base substitution G C intron_variant LIRI-JP 13 77803250 77803250 single base substitution G T intron_variant LIRI-JP 13 77803289 77803289 single base substitution C A intron_variant LIRI-JP 13 77803681 77803681 insertion of <=200bp - AA intron_variant LIRI-JP 13 77805222 77805222 single base substitution T A intron_variant LIRI-JP 13 77808533 77808533 single base substitution G C intron_variant LIRI-JP 13 77809115 77809115 single base substitution A C intron_variant LIRI-JP 13 77810083 77810083 single base substitution G C intron_variant LIRI-JP 13 77810523 77810523 single base substitution G A intron_variant LIRI-JP 13 77811543 77811543 single base substitution T G intron_variant LIRI-JP 13 77813336 77813336 single base substitution A G intron_variant LIRI-JP 13 77813747 77813747 single base substitution T A intron_variant LIRI-JP 13 77814443 77814443 single base substitution T C intron_variant LIRI-JP 13 77815032 77815032 single base substitution A T intron_variant LIRI-JP 13 77816949 77816949 single base substitution T C intron_variant LIRI-JP 13 77817155 77817155 single base substitution T G intron_variant LIRI-JP 13 77819554 77819554 single base substitution G C intron_variant LIRI-JP 13 77820823 77820823 single base substitution T A intron_variant LIRI-JP 13 77821385 77821385 single base substitution C A intron_variant LIRI-JP 13 77825107 77825107 single base substitution T C intron_variant LIRI-JP 13 77825635 77825635 single base substitution A G intron_variant LIRI-JP 13 77827291 77827291 single base substitution A G intron_variant LIRI-JP 13 77827788 77827788 single base substitution T C intron_variant LIRI-JP 13 77828627 77828627 single base substitution G A intron_variant LIRI-JP 13 77828667 77828667 single base substitution T C intron_variant LIRI-JP 13 77829351 77829351 single base substitution T C intron_variant LIRI-JP 13 77829495 77829495 single base substitution T C intron_variant LIRI-JP 13 77829982 77829982 deletion of <=200bp A - intron_variant LIRI-JP 13 77832920 77832920 single base substitution T C intron_variant LIRI-JP 13 77836861 77836861 single base substitution T C intron_variant LIRI-JP 13 77836936 77836936 single base substitution T C intron_variant LIRI-JP 13 77838788 77838788 single base substitution A G intron_variant LIRI-JP 13 77839858 77839858 single base substitution C T downstream_gene_variant LIRI-JP 13 77839858 77839858 single base substitution C T intron_variant LIRI-JP 13 77839896 77839896 single base substitution A G downstream_gene_variant LIRI-JP 13 77839896 77839896 single base substitution A G intron_variant LIRI-JP 13 77842073 77842073 single base substitution C T downstream_gene_variant LIRI-JP 13 77842073 77842073 single base substitution C T splice_acceptor_variant LIRI-JP 13 77842631 77842631 single base substitution C G downstream_gene_variant LIRI-JP 13 77842631 77842631 single base substitution C G intron_variant LIRI-JP 13 77844460 77844460 single base substitution T C 5_prime_UTR_variant LIRI-JP 13 77844460 77844460 single base substitution T C exon_variant LIRI-JP 13 77844460 77844460 single base substitution T C missense_variant I349V 1045A>G LIRI-JP 13 77844460 77844460 single base substitution T C missense_variant I387V 1159A>G LIRI-JP 13 77845609 77845609 single base substitution G T intron_variant LIRI-JP 13 77845765 77845765 single base substitution A G intron_variant LIRI-JP 13 77846762 77846762 single base substitution A G intron_variant LIRI-JP 13 77849847 77849847 single base substitution A G intron_variant LIRI-JP 13 77849847 77849847 single base substitution A G upstream_gene_variant LIRI-JP 13 77850085 77850085 single base substitution T C intron_variant LIRI-JP 13 77850085 77850085 single base substitution T C upstream_gene_variant LIRI-JP 13 77850233 77850233 single base substitution T G intron_variant LIRI-JP 13 77850233 77850233 single base substitution T G upstream_gene_variant LIRI-JP 13 77852631 77852631 single base substitution G C intron_variant LIRI-JP 13 77852631 77852631 single base substitution G C upstream_gene_variant LIRI-JP 13 77855939 77855939 single base substitution G C intron_variant LIRI-JP 13 77856437 77856437 single base substitution T C intron_variant LIRI-JP 13 77856511 77856511 single base substitution C G intron_variant LIRI-JP 13 77856595 77856595 deletion of <=200bp C - intron_variant LIRI-JP 13 77859137 77859137 single base substitution T C intron_variant LIRI-JP 13 77860674 77860674 single base substitution G T intron_variant LIRI-JP 13 77861812 77861814 deletion of <=200bp CTA - intron_variant LIRI-JP 13 77863037 77863037 single base substitution T A intron_variant LIRI-JP 13 77864050 77864050 single base substitution T C intron_variant LIRI-JP 13 77864202 77864202 single base substitution T C intron_variant LIRI-JP 13 77866309 77866309 single base substitution T C downstream_gene_variant LIRI-JP 13 77866309 77866309 single base substitution T C intron_variant LIRI-JP 13 77866503 77866503 single base substitution T C downstream_gene_variant LIRI-JP 13 77866503 77866503 single base substitution T C intron_variant LIRI-JP 13 77867069 77867069 single base substitution G A downstream_gene_variant LIRI-JP 13 77867069 77867069 single base substitution G A intron_variant LIRI-JP 13 77870011 77870011 single base substitution C A downstream_gene_variant LIRI-JP 13 77870011 77870011 single base substitution C A intron_variant LIRI-JP 13 77871340 77871340 single base substitution T G intron_variant LIRI-JP 13 77871747 77871747 single base substitution G A intron_variant LIRI-JP 13 77874143 77874143 single base substitution C T intron_variant LIRI-JP 13 77879460 77879460 single base substitution C T intron_variant LIRI-JP 13 77880577 77880577 single base substitution T C intron_variant LIRI-JP 13 77880658 77880658 single base substitution C T intron_variant LIRI-JP 13 77880920 77880920 single base substitution T C intron_variant LIRI-JP 13 77881175 77881175 single base substitution T C intron_variant LIRI-JP 13 77882012 77882012 single base substitution A G intron_variant LIRI-JP 13 77882460 77882460 single base substitution C A intron_variant LIRI-JP 13 77883228 77883228 single base substitution T G intron_variant LIRI-JP 13 77886717 77886717 single base substitution A G intron_variant LIRI-JP 13 77887721 77887721 single base substitution A G intron_variant LIRI-JP 13 77887971 77887971 single base substitution G A intron_variant LIRI-JP 13 77888807 77888807 single base substitution C T intron_variant LIRI-JP 13 77889683 77889683 single base substitution T G intron_variant LIRI-JP 13 77889819 77889819 single base substitution C T intron_variant LIRI-JP 13 77891435 77891435 single base substitution G C intron_variant LIRI-JP 13 77891665 77891665 single base substitution G C intron_variant LIRI-JP 13 77893388 77893388 single base substitution G A intron_variant LIRI-JP 13 77894994 77894994 single base substitution T C intron_variant LIRI-JP 13 77897212 77897212 single base substitution T A intron_variant LIRI-JP 13 77902292 77902292 single base substitution T C upstream_gene_variant LIRI-JP 13 77904823 77904823 single base substitution G C upstream_gene_variant LIRI-JP 13 77905403 77905403 single base substitution A G upstream_gene_variant LIRI-JP 13 77905501 77905501 single base substitution A G upstream_gene_variant LIRI-JP 13 77905575 77905575 single base substitution G A upstream_gene_variant LUSC-KR 13 77623502 77623502 single base substitution T G intron_variant LUSC-KR 13 77627870 77627870 single base substitution C G intron_variant LUSC-KR 13 77631071 77631071 single base substitution A G intron_variant LUSC-KR 13 77632569 77632569 single base substitution C A intron_variant LUSC-KR 13 77641954 77641954 single base substitution G A missense_variant R4035C 12103C>T LUSC-KR 13 77641954 77641954 single base substitution G A missense_variant R4073C 12217C>T LUSC-KR 13 77641954 77641954 single base substitution G A missense_variant R455C 1363C>T LUSC-KR 13 77648148 77648148 single base substitution T C intron_variant LUSC-KR 13 77653081 77653081 single base substitution A G intron_variant LUSC-KR 13 77655548 77655548 single base substitution G A intron_variant LUSC-KR 13 77657398 77657398 single base substitution T C intron_variant LUSC-KR 13 77662540 77662540 single base substitution T C downstream_gene_variant LUSC-KR 13 77662540 77662540 single base substitution T C intron_variant LUSC-KR 13 77662540 77662540 single base substitution T C upstream_gene_variant LUSC-KR 13 77664045 77664045 single base substitution C T downstream_gene_variant LUSC-KR 13 77664045 77664045 single base substitution C T intron_variant LUSC-KR 13 77664045 77664045 single base substitution C T upstream_gene_variant LUSC-KR 13 77667960 77667960 single base substitution C A downstream_gene_variant LUSC-KR 13 77667960 77667960 single base substitution C A intron_variant LUSC-KR 13 77670939 77670939 single base substitution T A downstream_gene_variant LUSC-KR 13 77670939 77670939 single base substitution T A intron_variant LUSC-KR 13 77672776 77672776 single base substitution C T downstream_gene_variant LUSC-KR 13 77672776 77672776 single base substitution C T exon_variant LUSC-KR 13 77672776 77672776 single base substitution C T missense_variant S2800N 8399G>A LUSC-KR 13 77672776 77672776 single base substitution C T missense_variant S2838N 8513G>A LUSC-KR 13 77672776 77672776 single base substitution C T missense_variant S323N 968G>A LUSC-KR 13 77672776 77672776 single base substitution C T upstream_gene_variant LUSC-KR 13 77680664 77680664 single base substitution T C intron_variant LUSC-KR 13 77685406 77685406 single base substitution T C intron_variant LUSC-KR 13 77686147 77686147 single base substitution C A intron_variant LUSC-KR 13 77691390 77691390 single base substitution C T downstream_gene_variant LUSC-KR 13 77691390 77691390 single base substitution C T intron_variant LUSC-KR 13 77693683 77693683 single base substitution A T downstream_gene_variant LUSC-KR 13 77693683 77693683 single base substitution A T intron_variant LUSC-KR 13 77693683 77693683 single base substitution A T upstream_gene_variant LUSC-KR 13 77697515 77697515 single base substitution C A intron_variant LUSC-KR 13 77697515 77697515 single base substitution C A upstream_gene_variant LUSC-KR 13 77699656 77699656 single base substitution A C intron_variant LUSC-KR 13 77699656 77699656 single base substitution A C upstream_gene_variant LUSC-KR 13 77710803 77710803 single base substitution C G intron_variant LUSC-KR 13 77714412 77714412 single base substitution C G downstream_gene_variant LUSC-KR 13 77714412 77714412 single base substitution C G intron_variant LUSC-KR 13 77719954 77719954 single base substitution T C intron_variant LUSC-KR 13 77719954 77719954 single base substitution T C upstream_gene_variant LUSC-KR 13 77722311 77722311 single base substitution G A intron_variant LUSC-KR 13 77724463 77724463 single base substitution G A intron_variant LUSC-KR 13 77725324 77725324 single base substitution G A intron_variant LUSC-KR 13 77725324 77725324 single base substitution G A upstream_gene_variant LUSC-KR 13 77728520 77728520 single base substitution T A intron_variant LUSC-KR 13 77728520 77728520 single base substitution T A upstream_gene_variant LUSC-KR 13 77728579 77728579 single base substitution T A intron_variant LUSC-KR 13 77728579 77728579 single base substitution T A upstream_gene_variant LUSC-KR 13 77736049 77736049 single base substitution C A 5_prime_UTR_variant LUSC-KR 13 77736049 77736049 single base substitution C A missense_variant A2159S 6475G>T LUSC-KR 13 77736049 77736049 single base substitution C A missense_variant A2197S 6589G>T LUSC-KR 13 77738664 77738664 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 13 77738664 77738664 single base substitution A G synonymous_variant L2120L 6358T>C LUSC-KR 13 77738664 77738664 single base substitution A G synonymous_variant L2158L 6472T>C LUSC-KR 13 77741400 77741400 single base substitution T C intron_variant LUSC-KR 13 77745293 77745293 single base substitution C T intron_variant LUSC-KR 13 77749164 77749164 single base substitution C A intron_variant LUSC-KR 13 77754115 77754115 single base substitution G C intron_variant LUSC-KR 13 77754346 77754346 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 13 77754346 77754346 single base substitution G C synonymous_variant L1645L 4935C>G LUSC-KR 13 77754346 77754346 single base substitution G C synonymous_variant L1683L 5049C>G LUSC-KR 13 77755660 77755660 single base substitution A C intron_variant LUSC-KR 13 77757773 77757773 single base substitution A T intron_variant LUSC-KR 13 77762818 77762818 single base substitution G A intron_variant LUSC-KR 13 77765481 77765481 single base substitution C G intron_variant LUSC-KR 13 77771613 77771613 single base substitution C A intron_variant LUSC-KR 13 77773698 77773698 single base substitution C T intron_variant LUSC-KR 13 77775364 77775364 single base substitution C A intron_variant LUSC-KR 13 77777720 77777720 single base substitution C G intron_variant LUSC-KR 13 77778031 77778031 single base substitution C A intron_variant LUSC-KR 13 77781009 77781009 single base substitution A T intron_variant LUSC-KR 13 77783083 77783083 single base substitution C A intron_variant LUSC-KR 13 77783996 77783996 single base substitution G A intron_variant LUSC-KR 13 77792427 77792427 single base substitution T C intron_variant LUSC-KR 13 77805822 77805822 single base substitution G C intron_variant LUSC-KR 13 77808306 77808306 single base substitution C T intron_variant LUSC-KR 13 77810687 77810687 single base substitution C G intron_variant LUSC-KR 13 77816759 77816759 single base substitution G C intron_variant LUSC-KR 13 77818553 77818553 single base substitution C A intron_variant LUSC-KR 13 77826117 77826117 single base substitution T G intron_variant LUSC-KR 13 77829310 77829310 single base substitution T C intron_variant LUSC-KR 13 77831488 77831488 single base substitution T C intron_variant LUSC-KR 13 77843754 77843754 single base substitution C A downstream_gene_variant LUSC-KR 13 77843754 77843754 single base substitution C A intron_variant LUSC-KR 13 77844198 77844198 single base substitution C A missense_variant G359C 1075G>T LUSC-KR 13 77844198 77844198 single base substitution C A missense_variant G397C 1189G>T LUSC-KR 13 77844198 77844198 single base substitution C A splice_region_variant LUSC-KR 13 77854940 77854940 single base substitution G A intron_variant LUSC-KR 13 77860024 77860024 single base substitution G C intron_variant LUSC-KR 13 77864045 77864045 single base substitution T A intron_variant LUSC-KR 13 77864671 77864671 single base substitution A C intron_variant LUSC-KR 13 77872865 77872865 single base substitution C T intron_variant LUSC-KR 13 77875098 77875098 single base substitution G A intron_variant LUSC-KR 13 77875583 77875583 single base substitution A C intron_variant LUSC-KR 13 77876678 77876678 single base substitution G C intron_variant LUSC-KR 13 77886773 77886773 single base substitution C A intron_variant LUSC-KR 13 77890667 77890667 single base substitution T G intron_variant LUSC-KR 13 77891032 77891032 single base substitution C A intron_variant LUSC-KR 13 77892522 77892522 single base substitution C A intron_variant LUSC-US 13 77629779 77629779 single base substitution T C missense_variant T4483A 13447A>G LUSC-US 13 77629779 77629779 single base substitution T C missense_variant T4521A 13561A>G LUSC-US 13 77629779 77629779 single base substitution T C missense_variant T903A 2707A>G LUSC-US 13 77636830 77636830 single base substitution G A splice_region_variant LUSC-US 13 77641898 77641898 single base substitution G A synonymous_variant I4053I 12159C>T LUSC-US 13 77641898 77641898 single base substitution G A synonymous_variant I4091I 12273C>T LUSC-US 13 77641898 77641898 single base substitution G A synonymous_variant I473I 1419C>T LUSC-US 13 77644818 77644818 single base substitution T G missense_variant H333P 998A>C LUSC-US 13 77644818 77644818 single base substitution T G missense_variant H3913P 11738A>C LUSC-US 13 77644818 77644818 single base substitution T G missense_variant H3951P 11852A>C LUSC-US 13 77657221 77657221 single base substitution G A missense_variant S3623L 10868C>T LUSC-US 13 77657221 77657221 single base substitution G A missense_variant S3661L 10982C>T LUSC-US 13 77657221 77657221 single base substitution G A missense_variant S46L 137C>T LUSC-US 13 77657256 77657256 single base substitution T C synonymous_variant L34L 102A>G LUSC-US 13 77657256 77657256 single base substitution T C synonymous_variant L3611L 10833A>G LUSC-US 13 77657256 77657256 single base substitution T C synonymous_variant L3649L 10947A>G LUSC-US 13 77669539 77669539 single base substitution C A downstream_gene_variant LUSC-US 13 77669539 77669539 single base substitution C A intron_variant LUSC-US 13 77669539 77669539 single base substitution C A missense_variant D3347Y 10039G>T LUSC-US 13 77669539 77669539 single base substitution C A missense_variant D3385Y 10153G>T LUSC-US 13 77670488 77670488 single base substitution C G downstream_gene_variant LUSC-US 13 77670488 77670488 single base substitution C G exon_variant LUSC-US 13 77670488 77670488 single base substitution C G missense_variant E3267Q 9799G>C LUSC-US 13 77670488 77670488 single base substitution C G missense_variant E3305Q 9913G>C LUSC-US 13 77672487 77672487 single base substitution T C downstream_gene_variant LUSC-US 13 77672487 77672487 single base substitution T C exon_variant LUSC-US 13 77672487 77672487 single base substitution T C synonymous_variant E2896E 8688A>G LUSC-US 13 77672487 77672487 single base substitution T C synonymous_variant E2934E 8802A>G LUSC-US 13 77672487 77672487 single base substitution T C synonymous_variant E419E 1257A>G LUSC-US 13 77672487 77672487 single base substitution T C upstream_gene_variant LUSC-US 13 77672952 77672952 single base substitution C T downstream_gene_variant LUSC-US 13 77672952 77672952 single base substitution C T exon_variant LUSC-US 13 77672952 77672952 single base substitution C T synonymous_variant L264L 792G>A LUSC-US 13 77672952 77672952 single base substitution C T synonymous_variant L2741L 8223G>A LUSC-US 13 77672952 77672952 single base substitution C T synonymous_variant L2779L 8337G>A LUSC-US 13 77672952 77672952 single base substitution C T upstream_gene_variant LUSC-US 13 77695532 77695532 single base substitution C G exon_variant LUSC-US 13 77695532 77695532 single base substitution C G missense_variant D131H 391G>C LUSC-US 13 77695532 77695532 single base substitution C G missense_variant D2668H 8002G>C LUSC-US 13 77695532 77695532 single base substitution C G missense_variant D2706H 8116G>C LUSC-US 13 77695532 77695532 single base substitution C G upstream_gene_variant LUSC-US 13 77699588 77699588 single base substitution C T exon_variant LUSC-US 13 77699588 77699588 single base substitution C T missense_variant G2596R 7786G>A LUSC-US 13 77699588 77699588 single base substitution C T missense_variant G2634R 7900G>A LUSC-US 13 77699588 77699588 single base substitution C T missense_variant G59R 175G>A LUSC-US 13 77699588 77699588 single base substitution C T upstream_gene_variant LUSC-US 13 77714292 77714292 single base substitution T G 5_prime_UTR_variant LUSC-US 13 77714292 77714292 single base substitution T G downstream_gene_variant LUSC-US 13 77714292 77714292 single base substitution T G exon_variant LUSC-US 13 77714292 77714292 single base substitution T G missense_variant K2432Q 7294A>C LUSC-US 13 77714292 77714292 single base substitution T G missense_variant K2470Q 7408A>C LUSC-US 13 77724879 77724879 single base substitution G T 5_prime_UTR_variant LUSC-US 13 77724879 77724879 single base substitution G T exon_variant LUSC-US 13 77724879 77724879 single base substitution G T missense_variant T2336K 7007C>A LUSC-US 13 77724879 77724879 single base substitution G T missense_variant T2374K 7121C>A LUSC-US 13 77724913 77724913 single base substitution T C 5_prime_UTR_variant LUSC-US 13 77724913 77724913 single base substitution T C exon_variant LUSC-US 13 77724913 77724913 single base substitution T C missense_variant M2325V 6973A>G LUSC-US 13 77724913 77724913 single base substitution T C missense_variant M2363V 7087A>G LUSC-US 13 77739409 77739409 single base substitution T A missense_variant E2115V 6344A>T LUSC-US 13 77739409 77739409 single base substitution T A missense_variant E2153V 6458A>T LUSC-US 13 77739409 77739409 single base substitution T A splice_region_variant LUSC-US 13 77740591 77740591 single base substitution G C 5_prime_UTR_variant LUSC-US 13 77740591 77740591 single base substitution G C synonymous_variant V2033V 6099C>G LUSC-US 13 77740591 77740591 single base substitution G C synonymous_variant V2071V 6213C>G LUSC-US 13 77743836 77743836 single base substitution T C 5_prime_UTR_variant LUSC-US 13 77743836 77743836 single base substitution T C synonymous_variant P1898P 5694A>G LUSC-US 13 77743836 77743836 single base substitution T C synonymous_variant P1936P 5808A>G LUSC-US 13 77748533 77748533 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant LUSC-US 13 77748533 77748533 single base substitution C G missense_variant G1817A 5450G>C LUSC-US 13 77748533 77748533 single base substitution C G missense_variant G1855A 5564G>C LUSC-US 13 77748550 77748550 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant LUSC-US 13 77748550 77748550 single base substitution T A synonymous_variant T1811T 5433A>T LUSC-US 13 77748550 77748550 single base substitution T A synonymous_variant T1849T 5547A>T LUSC-US 13 77759384 77759384 single base substitution G A 5_prime_UTR_variant LUSC-US 13 77759384 77759384 single base substitution G A stop_gained Q1487* 4459C>T LUSC-US 13 77759384 77759384 single base substitution G A stop_gained Q1525* 4573C>T LUSC-US 13 77760022 77760022 single base substitution T A 5_prime_UTR_variant LUSC-US 13 77760022 77760022 single base substitution T A missense_variant E1438D 4314A>T LUSC-US 13 77760022 77760022 single base substitution T A missense_variant E1476D 4428A>T LUSC-US 13 77760039 77760039 single base substitution G A 5_prime_UTR_variant LUSC-US 13 77760039 77760039 single base substitution G A missense_variant R1433C 4297C>T LUSC-US 13 77760039 77760039 single base substitution G A missense_variant R1471C 4411C>T LUSC-US 13 77760189 77760189 single base substitution C G 5_prime_UTR_variant LUSC-US 13 77760189 77760189 single base substitution C G missense_variant E1383Q 4147G>C LUSC-US 13 77760189 77760189 single base substitution C G missense_variant E1421Q 4261G>C LUSC-US 13 77835401 77835401 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant LUSC-US 13 77835401 77835401 single base substitution G C stop_gained S548* 1643C>G LUSC-US 13 77835401 77835401 single base substitution G C stop_gained S586* 1757C>G LUSC-US 13 77844568 77844568 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant LUSC-US 13 77844568 77844568 single base substitution T A exon_variant LUSC-US 13 77844568 77844568 single base substitution T A missense_variant M313L 937A>T LUSC-US 13 77844568 77844568 single base substitution T A missense_variant M351L 1051A>T LUSC-US 13 77900608 77900608 single base substitution C T splice_donor_variant LUSC-US 13 77900796 77900796 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant LUSC-US 13 77900796 77900796 single base substitution T A exon_variant LUSC-US 13 77900796 77900796 single base substitution T A initiator_codon_variant M1L 1A>T LUSC-US 13 77900796 77900796 single base substitution T A missense_variant M39L 115A>T MALY-DE 13 77620320 77620324 deletion of <=200bp TTATT - intron_variant MALY-DE 13 77633210 77633210 single base substitution A T intron_variant MALY-DE 13 77633217 77633217 single base substitution T G intron_variant MALY-DE 13 77646723 77646723 single base substitution C A intron_variant MALY-DE 13 77649820 77649820 single base substitution A G intron_variant MALY-DE 13 77653775 77653775 single base substitution G C intron_variant MALY-DE 13 77664294 77664294 single base substitution A C downstream_gene_variant MALY-DE 13 77664294 77664294 single base substitution A C stop_gained L3453* 10358T>G MALY-DE 13 77664294 77664294 single base substitution A C stop_gained L3491* 10472T>G MALY-DE 13 77664294 77664294 single base substitution A C upstream_gene_variant MALY-DE 13 77664704 77664704 single base substitution T A downstream_gene_variant MALY-DE 13 77664704 77664704 single base substitution T A intron_variant MALY-DE 13 77664704 77664704 single base substitution T A upstream_gene_variant MALY-DE 13 77665223 77665223 single base substitution C T downstream_gene_variant MALY-DE 13 77665223 77665223 single base substitution C T intron_variant MALY-DE 13 77665223 77665223 single base substitution C T upstream_gene_variant MALY-DE 13 77665642 77665642 single base substitution T G downstream_gene_variant MALY-DE 13 77665642 77665642 single base substitution T G intron_variant MALY-DE 13 77665642 77665642 single base substitution T G upstream_gene_variant MALY-DE 13 77666885 77666885 single base substitution T G downstream_gene_variant MALY-DE 13 77666885 77666885 single base substitution T G intron_variant MALY-DE 13 77666990 77666990 single base substitution T C downstream_gene_variant MALY-DE 13 77666990 77666990 single base substitution T C intron_variant MALY-DE 13 77667059 77667059 single base substitution G A downstream_gene_variant MALY-DE 13 77667059 77667059 single base substitution G A intron_variant MALY-DE 13 77667060 77667060 single base substitution T G downstream_gene_variant MALY-DE 13 77667060 77667060 single base substitution T G intron_variant MALY-DE 13 77681272 77681272 single base substitution T G intron_variant MALY-DE 13 77686092 77686092 single base substitution A T intron_variant MALY-DE 13 77689081 77689081 single base substitution T G intron_variant MALY-DE 13 77691182 77691182 single base substitution T C downstream_gene_variant MALY-DE 13 77691182 77691182 single base substitution T C intron_variant MALY-DE 13 77700415 77700415 single base substitution G A intron_variant MALY-DE 13 77700415 77700415 single base substitution G A upstream_gene_variant MALY-DE 13 77704542 77704542 insertion of <=200bp - AT intron_variant MALY-DE 13 77704542 77704542 insertion of <=200bp - AT upstream_gene_variant MALY-DE 13 77720952 77720952 single base substitution C T intron_variant MALY-DE 13 77740816 77740816 single base substitution A G intron_variant MALY-DE 13 77745217 77745217 single base substitution A G intron_variant MALY-DE 13 77753394 77753394 single base substitution A G intron_variant MALY-DE 13 77753419 77753419 single base substitution A G intron_variant MALY-DE 13 77767281 77767281 single base substitution A C intron_variant MALY-DE 13 77789189 77789189 single base substitution T C intron_variant MALY-DE 13 77791783 77791783 single base substitution G C intron_variant MALY-DE 13 77800533 77800533 single base substitution A G intron_variant MALY-DE 13 77803937 77803937 single base substitution A G intron_variant MALY-DE 13 77804989 77804989 single base substitution A G intron_variant MALY-DE 13 77812260 77812260 deletion of <=200bp C - intron_variant MALY-DE 13 77813406 77813406 single base substitution A C intron_variant MALY-DE 13 77823823 77823823 single base substitution C T intron_variant MALY-DE 13 77831347 77831347 single base substitution A G intron_variant MALY-DE 13 77833144 77833144 single base substitution C T intron_variant MALY-DE 13 77839003 77839004 deletion of <=200bp CA - intron_variant MALY-DE 13 77841031 77841031 single base substitution T A downstream_gene_variant MALY-DE 13 77841031 77841031 single base substitution T A intron_variant MALY-DE 13 77841574 77841574 single base substitution T A downstream_gene_variant MALY-DE 13 77841574 77841574 single base substitution T A intron_variant MALY-DE 13 77845659 77845659 single base substitution G A intron_variant MALY-DE 13 77848203 77848203 insertion of <=200bp - T intron_variant MALY-DE 13 77848203 77848203 insertion of <=200bp - T upstream_gene_variant MALY-DE 13 77854927 77854927 single base substitution T C intron_variant MALY-DE 13 77873766 77873766 single base substitution T C intron_variant MALY-DE 13 77880402 77880402 single base substitution A T intron_variant MALY-DE 13 77881125 77881125 single base substitution A T intron_variant MALY-DE 13 77896273 77896273 single base substitution C T intron_variant MALY-DE 13 77905540 77905540 insertion of <=200bp - A upstream_gene_variant MELA-AU 13 77614045 77614045 single base substitution G A downstream_gene_variant MELA-AU 13 77614502 77614502 single base substitution C T downstream_gene_variant MELA-AU 13 77614747 77614747 single base substitution T C downstream_gene_variant MELA-AU 13 77615100 77615100 single base substitution G A downstream_gene_variant MELA-AU 13 77615107 77615107 single base substitution C T downstream_gene_variant MELA-AU 13 77615947 77615947 single base substitution G A downstream_gene_variant MELA-AU 13 77617816 77617816 single base substitution G A downstream_gene_variant MELA-AU 13 77618019 77618019 single base substitution C A downstream_gene_variant MELA-AU 13 77618250 77618251 deletion of <=200bp TT - downstream_gene_variant MELA-AU 13 77619331 77619331 single base substitution G A 3_prime_UTR_variant MELA-AU 13 77619654 77619654 single base substitution G A intron_variant MELA-AU 13 77620123 77620123 single base substitution G A intron_variant MELA-AU 13 77620553 77620553 single base substitution G A intron_variant MELA-AU 13 77621561 77621561 single base substitution G A intron_variant MELA-AU 13 77621569 77621569 single base substitution G A intron_variant MELA-AU 13 77623501 77623501 single base substitution G A intron_variant MELA-AU 13 77623510 77623510 single base substitution G A intron_variant MELA-AU 13 77623896 77623896 single base substitution G A intron_variant MELA-AU 13 77623906 77623906 single base substitution G A intron_variant MELA-AU 13 77624351 77624351 single base substitution G A intron_variant MELA-AU 13 77624578 77624578 single base substitution G A intron_variant MELA-AU 13 77626108 77626108 single base substitution G A intron_variant MELA-AU 13 77626428 77626428 single base substitution G A intron_variant MELA-AU 13 77626787 77626787 single base substitution C T intron_variant MELA-AU 13 77627170 77627170 single base substitution G A intron_variant MELA-AU 13 77627488 77627488 single base substitution G A intron_variant MELA-AU 13 77627599 77627599 single base substitution G A intron_variant MELA-AU 13 77628035 77628035 single base substitution G A intron_variant MELA-AU 13 77628582 77628582 single base substitution G A intron_variant MELA-AU 13 77628752 77628752 single base substitution T C intron_variant MELA-AU 13 77628846 77628846 single base substitution C T intron_variant MELA-AU 13 77628894 77628894 single base substitution C T intron_variant MELA-AU 13 77629242 77629242 single base substitution G A intron_variant MELA-AU 13 77629258 77629258 single base substitution G A intron_variant MELA-AU 13 77629313 77629313 single base substitution G A intron_variant MELA-AU 13 77630188 77630188 single base substitution G A intron_variant MELA-AU 13 77631002 77631002 single base substitution G A intron_variant MELA-AU 13 77632107 77632107 single base substitution G A intron_variant MELA-AU 13 77632942 77632942 single base substitution A T intron_variant MELA-AU 13 77633036 77633036 single base substitution C T intron_variant MELA-AU 13 77633378 77633378 single base substitution G A intron_variant MELA-AU 13 77633798 77633798 single base substitution G A intron_variant MELA-AU 13 77633871 77633871 single base substitution G A intron_variant MELA-AU 13 77634226 77634226 single base substitution G A intron_variant MELA-AU 13 77634907 77634907 single base substitution A G intron_variant MELA-AU 13 77634925 77634925 single base substitution G A intron_variant MELA-AU 13 77636277 77636277 single base substitution G A intron_variant MELA-AU 13 77636702 77636702 single base substitution G A intron_variant MELA-AU 13 77637061 77637061 single base substitution C T intron_variant MELA-AU 13 77637102 77637102 single base substitution C T intron_variant MELA-AU 13 77637524 77637524 single base substitution C T intron_variant MELA-AU 13 77638059 77638059 single base substitution G A intron_variant MELA-AU 13 77638399 77638399 single base substitution G A intron_variant MELA-AU 13 77638846 77638846 single base substitution G A synonymous_variant S4154S 12462C>T MELA-AU 13 77638846 77638846 single base substitution G A synonymous_variant S4192S 12576C>T MELA-AU 13 77638846 77638846 single base substitution G A synonymous_variant S574S 1722C>T MELA-AU 13 77638960 77638960 single base substitution G A intron_variant MELA-AU 13 77639769 77639770 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77639865 77639865 single base substitution G A intron_variant MELA-AU 13 77641604 77641604 single base substitution G A intron_variant MELA-AU 13 77642185 77642185 single base substitution C T intron_variant MELA-AU 13 77642296 77642296 single base substitution G A intron_variant MELA-AU 13 77642394 77642394 single base substitution G A intron_variant MELA-AU 13 77643295 77643295 single base substitution G A intron_variant MELA-AU 13 77643373 77643373 single base substitution G A intron_variant MELA-AU 13 77643772 77643772 single base substitution A G intron_variant MELA-AU 13 77644914 77644914 single base substitution G A intron_variant MELA-AU 13 77645315 77645315 deletion of <=200bp T - intron_variant MELA-AU 13 77645374 77645374 single base substitution A G intron_variant MELA-AU 13 77645406 77645406 single base substitution G A intron_variant MELA-AU 13 77645797 77645820 deletion of <=200bp TAAGGCTCTTAAAGACTTGAATAT - intron_variant MELA-AU 13 77647586 77647586 single base substitution G A intron_variant MELA-AU 13 77648147 77648147 single base substitution C T intron_variant MELA-AU 13 77648576 77648576 single base substitution A G intron_variant MELA-AU 13 77648637 77648637 single base substitution G A intron_variant MELA-AU 13 77649251 77649251 single base substitution G A intron_variant MELA-AU 13 77649267 77649267 single base substitution C T intron_variant MELA-AU 13 77649646 77649646 single base substitution C T intron_variant MELA-AU 13 77649974 77649974 single base substitution C T intron_variant MELA-AU 13 77650719 77650719 single base substitution G A intron_variant MELA-AU 13 77650846 77650846 single base substitution A G intron_variant MELA-AU 13 77650854 77650854 single base substitution G A intron_variant MELA-AU 13 77651009 77651009 single base substitution G A intron_variant MELA-AU 13 77651064 77651064 single base substitution C T intron_variant MELA-AU 13 77651215 77651215 single base substitution T A intron_variant MELA-AU 13 77654080 77654080 single base substitution G A intron_variant MELA-AU 13 77654290 77654290 single base substitution G A intron_variant MELA-AU 13 77654291 77654291 single base substitution G T intron_variant MELA-AU 13 77654421 77654421 single base substitution G A intron_variant MELA-AU 13 77655185 77655185 single base substitution T C intron_variant MELA-AU 13 77655507 77655507 single base substitution G A intron_variant MELA-AU 13 77655526 77655526 single base substitution G A intron_variant MELA-AU 13 77655835 77655835 single base substitution C T intron_variant MELA-AU 13 77656169 77656169 single base substitution T G intron_variant MELA-AU 13 77656268 77656268 single base substitution G A intron_variant MELA-AU 13 77657503 77657503 single base substitution G A intron_variant MELA-AU 13 77657990 77657990 single base substitution C T intron_variant MELA-AU 13 77658032 77658032 single base substitution G A intron_variant MELA-AU 13 77658348 77658348 single base substitution G A intron_variant MELA-AU 13 77659593 77659593 single base substitution C T intron_variant MELA-AU 13 77659898 77659898 single base substitution G A intron_variant MELA-AU 13 77660563 77660563 single base substitution G A intron_variant MELA-AU 13 77660883 77660883 single base substitution A T intron_variant MELA-AU 13 77660950 77660950 single base substitution T C intron_variant MELA-AU 13 77661439 77661439 single base substitution T C intron_variant MELA-AU 13 77661533 77661533 single base substitution G A intron_variant MELA-AU 13 77661847 77661847 single base substitution G A intron_variant MELA-AU 13 77661847 77661847 single base substitution G A upstream_gene_variant MELA-AU 13 77661931 77661931 single base substitution T C intron_variant MELA-AU 13 77661931 77661931 single base substitution T C upstream_gene_variant MELA-AU 13 77662007 77662007 single base substitution C T intron_variant MELA-AU 13 77662007 77662007 single base substitution C T upstream_gene_variant MELA-AU 13 77662090 77662090 single base substitution A G intron_variant MELA-AU 13 77662090 77662090 single base substitution A G upstream_gene_variant MELA-AU 13 77662698 77662698 single base substitution A G downstream_gene_variant MELA-AU 13 77662698 77662698 single base substitution A G intron_variant MELA-AU 13 77662698 77662698 single base substitution A G upstream_gene_variant MELA-AU 13 77663139 77663139 single base substitution G A downstream_gene_variant MELA-AU 13 77663139 77663139 single base substitution G A missense_variant P3480L 10439C>T MELA-AU 13 77663139 77663139 single base substitution G A missense_variant P3518L 10553C>T MELA-AU 13 77663139 77663139 single base substitution G A upstream_gene_variant MELA-AU 13 77663344 77663344 single base substitution C T downstream_gene_variant MELA-AU 13 77663344 77663344 single base substitution C T intron_variant MELA-AU 13 77663344 77663344 single base substitution C T upstream_gene_variant MELA-AU 13 77663783 77663783 single base substitution T C downstream_gene_variant MELA-AU 13 77663783 77663783 single base substitution T C intron_variant MELA-AU 13 77663783 77663783 single base substitution T C upstream_gene_variant MELA-AU 13 77664271 77664271 single base substitution G A downstream_gene_variant MELA-AU 13 77664271 77664271 single base substitution G A missense_variant P3461S 10381C>T MELA-AU 13 77664271 77664271 single base substitution G A missense_variant P3499S 10495C>T MELA-AU 13 77664271 77664271 single base substitution G A upstream_gene_variant MELA-AU 13 77664714 77664714 single base substitution G A downstream_gene_variant MELA-AU 13 77664714 77664714 single base substitution G A intron_variant MELA-AU 13 77664714 77664714 single base substitution G A upstream_gene_variant MELA-AU 13 77665439 77665439 single base substitution G A downstream_gene_variant MELA-AU 13 77665439 77665439 single base substitution G A intron_variant MELA-AU 13 77665439 77665439 single base substitution G A upstream_gene_variant MELA-AU 13 77665816 77665816 single base substitution C T downstream_gene_variant MELA-AU 13 77665816 77665816 single base substitution C T intron_variant MELA-AU 13 77665816 77665816 single base substitution C T upstream_gene_variant MELA-AU 13 77665880 77665880 single base substitution G A downstream_gene_variant MELA-AU 13 77665880 77665880 single base substitution G A intron_variant MELA-AU 13 77665880 77665880 single base substitution G A upstream_gene_variant MELA-AU 13 77666796 77666796 single base substitution G A downstream_gene_variant MELA-AU 13 77666796 77666796 single base substitution G A intron_variant MELA-AU 13 77666912 77666912 single base substitution G A downstream_gene_variant MELA-AU 13 77666912 77666912 single base substitution G A intron_variant MELA-AU 13 77666927 77666927 single base substitution C T downstream_gene_variant MELA-AU 13 77666927 77666927 single base substitution C T intron_variant MELA-AU 13 77667786 77667786 single base substitution T C downstream_gene_variant MELA-AU 13 77667786 77667786 single base substitution T C intron_variant MELA-AU 13 77667945 77667945 single base substitution G A downstream_gene_variant MELA-AU 13 77667945 77667945 single base substitution G A intron_variant MELA-AU 13 77668568 77668568 single base substitution T G downstream_gene_variant MELA-AU 13 77668568 77668568 single base substitution T G intron_variant MELA-AU 13 77668909 77668909 single base substitution G A downstream_gene_variant MELA-AU 13 77668909 77668909 single base substitution G A intron_variant MELA-AU 13 77669243 77669243 single base substitution C T downstream_gene_variant MELA-AU 13 77669243 77669243 single base substitution C T intron_variant MELA-AU 13 77669634 77669634 single base substitution G A downstream_gene_variant MELA-AU 13 77669634 77669634 single base substitution G A intron_variant MELA-AU 13 77669634 77669634 single base substitution G A missense_variant S3315F 9944C>T MELA-AU 13 77669634 77669634 single base substitution G A missense_variant S3353F 10058C>T MELA-AU 13 77669697 77669698 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 13 77669697 77669698 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 13 77669697 77669698 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P3294F 9880CC>TT MELA-AU 13 77669697 77669698 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P3332F 9994CC>TT MELA-AU 13 77670251 77670251 single base substitution C T downstream_gene_variant MELA-AU 13 77670251 77670251 single base substitution C T intron_variant MELA-AU 13 77670390 77670390 single base substitution A T downstream_gene_variant MELA-AU 13 77670390 77670390 single base substitution A T intron_variant MELA-AU 13 77670539 77670539 single base substitution C T downstream_gene_variant MELA-AU 13 77670539 77670539 single base substitution C T exon_variant MELA-AU 13 77670539 77670539 single base substitution C T missense_variant D3250N 9748G>A MELA-AU 13 77670539 77670539 single base substitution C T missense_variant D3288N 9862G>A MELA-AU 13 77670909 77670909 single base substitution G A downstream_gene_variant MELA-AU 13 77670909 77670909 single base substitution G A intron_variant MELA-AU 13 77671112 77671112 single base substitution G A downstream_gene_variant MELA-AU 13 77671112 77671112 single base substitution G A intron_variant MELA-AU 13 77671412 77671413 multiple base substitution (>=2bp and <=200bp) TC AT downstream_gene_variant MELA-AU 13 77671412 77671413 multiple base substitution (>=2bp and <=200bp) TC AT intron_variant MELA-AU 13 77672117 77672117 single base substitution G A downstream_gene_variant MELA-AU 13 77672117 77672117 single base substitution G A missense_variant H3020Y 9058C>T MELA-AU 13 77672117 77672117 single base substitution G A missense_variant H3058Y 9172C>T MELA-AU 13 77672117 77672117 single base substitution G A upstream_gene_variant MELA-AU 13 77672719 77672719 single base substitution G A downstream_gene_variant MELA-AU 13 77672719 77672719 single base substitution G A exon_variant MELA-AU 13 77672719 77672719 single base substitution G A missense_variant P2819L 8456C>T MELA-AU 13 77672719 77672719 single base substitution G A missense_variant P2857L 8570C>T MELA-AU 13 77672719 77672719 single base substitution G A missense_variant P342L 1025C>T MELA-AU 13 77672719 77672719 single base substitution G A upstream_gene_variant MELA-AU 13 77673085 77673085 single base substitution G A exon_variant MELA-AU 13 77673085 77673085 single base substitution G A missense_variant S220F 659C>T MELA-AU 13 77673085 77673085 single base substitution G A missense_variant S2697F 8090C>T MELA-AU 13 77673085 77673085 single base substitution G A missense_variant S2735F 8204C>T MELA-AU 13 77673085 77673085 single base substitution G A upstream_gene_variant MELA-AU 13 77674107 77674107 single base substitution C T intron_variant MELA-AU 13 77674107 77674107 single base substitution C T upstream_gene_variant MELA-AU 13 77677247 77677247 single base substitution G A intron_variant MELA-AU 13 77677326 77677326 single base substitution G A intron_variant MELA-AU 13 77677454 77677454 single base substitution G A intron_variant MELA-AU 13 77678388 77678388 single base substitution C T intron_variant MELA-AU 13 77680182 77680182 single base substitution C T intron_variant MELA-AU 13 77681879 77681879 single base substitution A T intron_variant MELA-AU 13 77681882 77681882 single base substitution T A intron_variant MELA-AU 13 77682242 77682242 single base substitution A C intron_variant MELA-AU 13 77682576 77682577 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 13 77683607 77683607 single base substitution G A intron_variant MELA-AU 13 77684041 77684041 single base substitution T C intron_variant MELA-AU 13 77684450 77684450 single base substitution G T intron_variant MELA-AU 13 77684501 77684501 single base substitution G A intron_variant MELA-AU 13 77684891 77684891 single base substitution G A intron_variant MELA-AU 13 77684986 77684986 single base substitution G A intron_variant MELA-AU 13 77685654 77685654 single base substitution G A intron_variant MELA-AU 13 77686651 77686652 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 13 77687365 77687365 single base substitution G A intron_variant MELA-AU 13 77688097 77688097 single base substitution C T intron_variant MELA-AU 13 77688407 77688407 single base substitution C T intron_variant MELA-AU 13 77688943 77688943 single base substitution C G intron_variant MELA-AU 13 77689508 77689508 single base substitution A C intron_variant MELA-AU 13 77690079 77690079 single base substitution A T intron_variant MELA-AU 13 77690325 77690325 single base substitution A G intron_variant MELA-AU 13 77690641 77690641 single base substitution G A downstream_gene_variant MELA-AU 13 77690641 77690641 single base substitution G A intron_variant MELA-AU 13 77690914 77690914 single base substitution G A downstream_gene_variant MELA-AU 13 77690914 77690914 single base substitution G A intron_variant MELA-AU 13 77691325 77691325 single base substitution G A downstream_gene_variant MELA-AU 13 77691325 77691325 single base substitution G A intron_variant MELA-AU 13 77692203 77692203 single base substitution G A downstream_gene_variant MELA-AU 13 77692203 77692203 single base substitution G A intron_variant MELA-AU 13 77693263 77693263 single base substitution G A downstream_gene_variant MELA-AU 13 77693263 77693263 single base substitution G A intron_variant MELA-AU 13 77693263 77693263 single base substitution G A upstream_gene_variant MELA-AU 13 77693432 77693432 single base substitution G A downstream_gene_variant MELA-AU 13 77693432 77693432 single base substitution G A intron_variant MELA-AU 13 77693432 77693432 single base substitution G A upstream_gene_variant MELA-AU 13 77694007 77694007 single base substitution G A downstream_gene_variant MELA-AU 13 77694007 77694007 single base substitution G A intron_variant MELA-AU 13 77694007 77694007 single base substitution G A upstream_gene_variant MELA-AU 13 77694231 77694231 single base substitution T C downstream_gene_variant MELA-AU 13 77694231 77694231 single base substitution T C intron_variant MELA-AU 13 77694231 77694231 single base substitution T C upstream_gene_variant MELA-AU 13 77694445 77694445 single base substitution G A downstream_gene_variant MELA-AU 13 77694445 77694445 single base substitution G A intron_variant MELA-AU 13 77694445 77694445 single base substitution G A upstream_gene_variant MELA-AU 13 77694548 77694548 single base substitution A G downstream_gene_variant MELA-AU 13 77694548 77694548 single base substitution A G intron_variant MELA-AU 13 77694548 77694548 single base substitution A G upstream_gene_variant MELA-AU 13 77695134 77695134 single base substitution G A downstream_gene_variant MELA-AU 13 77695134 77695134 single base substitution G A intron_variant MELA-AU 13 77695134 77695134 single base substitution G A upstream_gene_variant MELA-AU 13 77695631 77695631 single base substitution C T splice_acceptor_variant MELA-AU 13 77695631 77695631 single base substitution C T upstream_gene_variant MELA-AU 13 77695986 77696012 deletion of <=200bp GGATAACCTATAAACCAGAAATAAAAG - intron_variant MELA-AU 13 77695986 77696012 deletion of <=200bp GGATAACCTATAAACCAGAAATAAAAG - upstream_gene_variant MELA-AU 13 77696116 77696116 single base substitution G A intron_variant MELA-AU 13 77696116 77696116 single base substitution G A upstream_gene_variant MELA-AU 13 77696383 77696383 single base substitution C T intron_variant MELA-AU 13 77696383 77696383 single base substitution C T upstream_gene_variant MELA-AU 13 77696659 77696659 single base substitution C G intron_variant MELA-AU 13 77696659 77696659 single base substitution C G upstream_gene_variant MELA-AU 13 77697182 77697182 single base substitution G A intron_variant MELA-AU 13 77697182 77697182 single base substitution G A upstream_gene_variant MELA-AU 13 77698419 77698419 single base substitution G A intron_variant MELA-AU 13 77699176 77699176 single base substitution G A intron_variant MELA-AU 13 77699661 77699661 single base substitution G A intron_variant MELA-AU 13 77699661 77699661 single base substitution G A upstream_gene_variant MELA-AU 13 77700151 77700151 single base substitution T C intron_variant MELA-AU 13 77700151 77700151 single base substitution T C upstream_gene_variant MELA-AU 13 77700270 77700270 single base substitution G A intron_variant MELA-AU 13 77700270 77700270 single base substitution G A upstream_gene_variant MELA-AU 13 77700402 77700402 single base substitution T A intron_variant MELA-AU 13 77700402 77700402 single base substitution T A upstream_gene_variant MELA-AU 13 77701231 77701231 single base substitution G A intron_variant MELA-AU 13 77701231 77701231 single base substitution G A upstream_gene_variant MELA-AU 13 77701365 77701365 single base substitution A G intron_variant MELA-AU 13 77701365 77701365 single base substitution A G upstream_gene_variant MELA-AU 13 77701382 77701382 single base substitution G A intron_variant MELA-AU 13 77701382 77701382 single base substitution G A upstream_gene_variant MELA-AU 13 77701382 77701382 single base substitution G T intron_variant MELA-AU 13 77701382 77701382 single base substitution G T upstream_gene_variant MELA-AU 13 77701384 77701384 single base substitution G A intron_variant MELA-AU 13 77701384 77701384 single base substitution G A upstream_gene_variant MELA-AU 13 77701560 77701560 single base substitution C T intron_variant MELA-AU 13 77701560 77701560 single base substitution C T upstream_gene_variant MELA-AU 13 77702606 77702606 single base substitution G A intron_variant MELA-AU 13 77702606 77702606 single base substitution G A upstream_gene_variant MELA-AU 13 77702750 77702750 single base substitution C T intron_variant MELA-AU 13 77702750 77702750 single base substitution C T upstream_gene_variant MELA-AU 13 77703074 77703074 single base substitution T G intron_variant MELA-AU 13 77703074 77703074 single base substitution T G upstream_gene_variant MELA-AU 13 77703532 77703532 single base substitution G A intron_variant MELA-AU 13 77703532 77703532 single base substitution G A upstream_gene_variant MELA-AU 13 77703579 77703579 single base substitution G A intron_variant MELA-AU 13 77703579 77703579 single base substitution G A upstream_gene_variant MELA-AU 13 77703952 77703952 single base substitution T C intron_variant MELA-AU 13 77703952 77703952 single base substitution T C upstream_gene_variant MELA-AU 13 77704434 77704434 single base substitution T A intron_variant MELA-AU 13 77704434 77704434 single base substitution T A upstream_gene_variant MELA-AU 13 77705517 77705517 single base substitution G A intron_variant MELA-AU 13 77705517 77705517 single base substitution G A upstream_gene_variant MELA-AU 13 77706480 77706480 single base substitution G A intron_variant MELA-AU 13 77706653 77706653 single base substitution G A intron_variant MELA-AU 13 77707009 77707009 single base substitution C A intron_variant MELA-AU 13 77707149 77707149 single base substitution A G intron_variant MELA-AU 13 77707447 77707447 single base substitution A G intron_variant MELA-AU 13 77707618 77707618 single base substitution G A intron_variant MELA-AU 13 77708563 77708564 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77710242 77710242 single base substitution C T intron_variant MELA-AU 13 77710313 77710313 single base substitution G A intron_variant MELA-AU 13 77711827 77711827 single base substitution G A intron_variant MELA-AU 13 77712080 77712080 single base substitution G A intron_variant MELA-AU 13 77712841 77712841 single base substitution G A intron_variant MELA-AU 13 77714942 77714942 single base substitution A T downstream_gene_variant MELA-AU 13 77714942 77714942 single base substitution A T intron_variant MELA-AU 13 77715271 77715271 single base substitution G A downstream_gene_variant MELA-AU 13 77715271 77715271 single base substitution G A intron_variant MELA-AU 13 77715271 77715271 single base substitution G A upstream_gene_variant MELA-AU 13 77715483 77715483 single base substitution A G downstream_gene_variant MELA-AU 13 77715483 77715483 single base substitution A G intron_variant MELA-AU 13 77715483 77715483 single base substitution A G upstream_gene_variant MELA-AU 13 77715585 77715585 single base substitution G A downstream_gene_variant MELA-AU 13 77715585 77715585 single base substitution G A intron_variant MELA-AU 13 77715585 77715585 single base substitution G A upstream_gene_variant MELA-AU 13 77716056 77716056 single base substitution G A downstream_gene_variant MELA-AU 13 77716056 77716056 single base substitution G A intron_variant MELA-AU 13 77716056 77716056 single base substitution G A upstream_gene_variant MELA-AU 13 77716644 77716644 single base substitution G A downstream_gene_variant MELA-AU 13 77716644 77716644 single base substitution G A intron_variant MELA-AU 13 77716644 77716644 single base substitution G A upstream_gene_variant MELA-AU 13 77717262 77717262 single base substitution A G downstream_gene_variant MELA-AU 13 77717262 77717262 single base substitution A G intron_variant MELA-AU 13 77717262 77717262 single base substitution A G upstream_gene_variant MELA-AU 13 77717463 77717463 single base substitution G A downstream_gene_variant MELA-AU 13 77717463 77717463 single base substitution G A intron_variant MELA-AU 13 77717463 77717463 single base substitution G A upstream_gene_variant MELA-AU 13 77717520 77717520 single base substitution G A downstream_gene_variant MELA-AU 13 77717520 77717520 single base substitution G A intron_variant MELA-AU 13 77717520 77717520 single base substitution G A upstream_gene_variant MELA-AU 13 77717616 77717616 single base substitution G A downstream_gene_variant MELA-AU 13 77717616 77717616 single base substitution G A intron_variant MELA-AU 13 77717616 77717616 single base substitution G A upstream_gene_variant MELA-AU 13 77717644 77717644 single base substitution G A downstream_gene_variant MELA-AU 13 77717644 77717644 single base substitution G A intron_variant MELA-AU 13 77717644 77717644 single base substitution G A upstream_gene_variant MELA-AU 13 77717691 77717691 single base substitution G A downstream_gene_variant MELA-AU 13 77717691 77717691 single base substitution G A intron_variant MELA-AU 13 77717691 77717691 single base substitution G A upstream_gene_variant MELA-AU 13 77717722 77717722 single base substitution G A downstream_gene_variant MELA-AU 13 77717722 77717722 single base substitution G A intron_variant MELA-AU 13 77717722 77717722 single base substitution G A upstream_gene_variant MELA-AU 13 77717812 77717812 single base substitution G A downstream_gene_variant MELA-AU 13 77717812 77717812 single base substitution G A intron_variant MELA-AU 13 77717812 77717812 single base substitution G A upstream_gene_variant MELA-AU 13 77718039 77718039 single base substitution G A downstream_gene_variant MELA-AU 13 77718039 77718039 single base substitution G A intron_variant MELA-AU 13 77718039 77718039 single base substitution G A upstream_gene_variant MELA-AU 13 77718484 77718484 single base substitution G C exon_variant MELA-AU 13 77718484 77718484 single base substitution G C intron_variant MELA-AU 13 77718484 77718484 single base substitution G C upstream_gene_variant MELA-AU 13 77718720 77718720 single base substitution G A intron_variant MELA-AU 13 77718720 77718720 single base substitution G A upstream_gene_variant MELA-AU 13 77719221 77719221 single base substitution G A intron_variant MELA-AU 13 77719221 77719221 single base substitution G A upstream_gene_variant MELA-AU 13 77719361 77719361 single base substitution C T intron_variant MELA-AU 13 77719361 77719361 single base substitution C T upstream_gene_variant MELA-AU 13 77719480 77719480 single base substitution T C intron_variant MELA-AU 13 77719480 77719480 single base substitution T C upstream_gene_variant MELA-AU 13 77719648 77719648 single base substitution G A intron_variant MELA-AU 13 77719648 77719648 single base substitution G A upstream_gene_variant MELA-AU 13 77720234 77720234 single base substitution G A intron_variant MELA-AU 13 77720267 77720267 single base substitution T G intron_variant MELA-AU 13 77720270 77720270 single base substitution G A intron_variant MELA-AU 13 77720288 77720288 single base substitution G A intron_variant MELA-AU 13 77721382 77721382 single base substitution G A intron_variant MELA-AU 13 77722273 77722273 single base substitution A T intron_variant MELA-AU 13 77722633 77722633 single base substitution C T intron_variant MELA-AU 13 77723042 77723042 single base substitution G A intron_variant MELA-AU 13 77723411 77723411 single base substitution T G intron_variant MELA-AU 13 77723547 77723547 single base substitution C T intron_variant MELA-AU 13 77723951 77723951 single base substitution G A intron_variant MELA-AU 13 77724690 77724690 single base substitution C T intron_variant MELA-AU 13 77725369 77725369 single base substitution G A intron_variant MELA-AU 13 77725369 77725369 single base substitution G A upstream_gene_variant MELA-AU 13 77725551 77725551 single base substitution C T intron_variant MELA-AU 13 77725551 77725551 single base substitution C T upstream_gene_variant MELA-AU 13 77726832 77726832 single base substitution G A intron_variant MELA-AU 13 77726832 77726832 single base substitution G A upstream_gene_variant MELA-AU 13 77727018 77727018 single base substitution G T intron_variant MELA-AU 13 77727018 77727018 single base substitution G T upstream_gene_variant MELA-AU 13 77727187 77727187 single base substitution G A intron_variant MELA-AU 13 77727187 77727187 single base substitution G A upstream_gene_variant MELA-AU 13 77728491 77728491 single base substitution G A intron_variant MELA-AU 13 77728491 77728491 single base substitution G A upstream_gene_variant MELA-AU 13 77730309 77730309 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 13 77730309 77730309 single base substitution G C missense_variant P2229A 6685C>G MELA-AU 13 77730309 77730309 single base substitution G C missense_variant P2267A 6799C>G MELA-AU 13 77732107 77732107 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 13 77732107 77732107 single base substitution G A synonymous_variant A2207A 6621C>T MELA-AU 13 77732107 77732107 single base substitution G A synonymous_variant A2245A 6735C>T MELA-AU 13 77732408 77732408 single base substitution G A intron_variant MELA-AU 13 77733966 77733966 single base substitution G A intron_variant MELA-AU 13 77735266 77735266 single base substitution G A intron_variant MELA-AU 13 77735569 77735569 single base substitution G A intron_variant MELA-AU 13 77735886 77735886 single base substitution G A intron_variant MELA-AU 13 77736026 77736026 single base substitution C A intron_variant MELA-AU 13 77736179 77736179 single base substitution T A intron_variant MELA-AU 13 77738135 77738135 single base substitution A T intron_variant MELA-AU 13 77738921 77738921 single base substitution C T intron_variant MELA-AU 13 77739508 77739508 single base substitution G A 5_prime_UTR_variant MELA-AU 13 77739508 77739508 single base substitution G A missense_variant S2082L 6245C>T MELA-AU 13 77739508 77739508 single base substitution G A missense_variant S2120L 6359C>T MELA-AU 13 77739599 77739599 single base substitution G A intron_variant MELA-AU 13 77739897 77739897 single base substitution G A intron_variant MELA-AU 13 77740067 77740067 single base substitution G A intron_variant MELA-AU 13 77742076 77742076 insertion of <=200bp - A intron_variant MELA-AU 13 77742328 77742329 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77742893 77742893 single base substitution C T intron_variant MELA-AU 13 77742912 77742912 single base substitution C T intron_variant MELA-AU 13 77743267 77743267 single base substitution G A intron_variant MELA-AU 13 77743508 77743508 single base substitution G A intron_variant MELA-AU 13 77743525 77743525 single base substitution C T intron_variant MELA-AU 13 77743664 77743664 single base substitution G A intron_variant MELA-AU 13 77744079 77744079 single base substitution G A intron_variant MELA-AU 13 77744124 77744124 single base substitution A G intron_variant MELA-AU 13 77744335 77744335 single base substitution G A intron_variant MELA-AU 13 77744884 77744884 single base substitution T C intron_variant MELA-AU 13 77745767 77745767 single base substitution C T missense_variant S1847N 5540G>A MELA-AU 13 77745767 77745767 single base substitution C T missense_variant S1885N 5654G>A MELA-AU 13 77745767 77745767 single base substitution C T splice_region_variant MELA-AU 13 77745807 77745807 single base substitution T G intron_variant MELA-AU 13 77746304 77746304 single base substitution G A intron_variant MELA-AU 13 77746344 77746344 single base substitution T C intron_variant MELA-AU 13 77746458 77746458 single base substitution G A intron_variant MELA-AU 13 77746572 77746572 single base substitution G A intron_variant MELA-AU 13 77746824 77746824 single base substitution G A intron_variant MELA-AU 13 77746898 77746898 single base substitution G A intron_variant MELA-AU 13 77747309 77747309 single base substitution T G intron_variant MELA-AU 13 77747739 77747739 single base substitution A G intron_variant MELA-AU 13 77747893 77747893 single base substitution A T intron_variant MELA-AU 13 77747954 77747954 single base substitution G A intron_variant MELA-AU 13 77748465 77748465 single base substitution G A 5_prime_UTR_variant MELA-AU 13 77748465 77748465 single base substitution G A missense_variant P1840S 5518C>T MELA-AU 13 77748465 77748465 single base substitution G A missense_variant P1878S 5632C>T MELA-AU 13 77749297 77749297 single base substitution G T intron_variant MELA-AU 13 77749373 77749373 single base substitution G A intron_variant MELA-AU 13 77749374 77749374 single base substitution G A intron_variant MELA-AU 13 77749679 77749679 single base substitution G A intron_variant MELA-AU 13 77750902 77750902 single base substitution G A intron_variant MELA-AU 13 77751028 77751028 single base substitution G A intron_variant MELA-AU 13 77751282 77751282 single base substitution A G intron_variant MELA-AU 13 77751332 77751332 single base substitution A G intron_variant MELA-AU 13 77751413 77751413 single base substitution G A intron_variant MELA-AU 13 77752424 77752424 single base substitution G A intron_variant MELA-AU 13 77752595 77752595 single base substitution T A intron_variant MELA-AU 13 77752994 77752994 single base substitution G A intron_variant MELA-AU 13 77753088 77753088 single base substitution A G intron_variant MELA-AU 13 77753355 77753355 single base substitution G A intron_variant MELA-AU 13 77753359 77753359 single base substitution T G intron_variant MELA-AU 13 77753526 77753526 single base substitution A T intron_variant MELA-AU 13 77754107 77754107 single base substitution G A intron_variant MELA-AU 13 77754762 77754762 single base substitution A G intron_variant MELA-AU 13 77756415 77756415 single base substitution A G intron_variant MELA-AU 13 77756587 77756587 single base substitution G A intron_variant MELA-AU 13 77759692 77759692 single base substitution A T intron_variant MELA-AU 13 77760264 77760264 single base substitution G A intron_variant MELA-AU 13 77761029 77761029 single base substitution C T intron_variant MELA-AU 13 77761072 77761072 single base substitution A C intron_variant MELA-AU 13 77761074 77761074 single base substitution G A intron_variant MELA-AU 13 77761087 77761087 single base substitution C T intron_variant MELA-AU 13 77761542 77761542 single base substitution G A intron_variant MELA-AU 13 77762382 77762382 single base substitution G A intron_variant MELA-AU 13 77763269 77763269 single base substitution G A intron_variant MELA-AU 13 77763403 77763403 single base substitution A G intron_variant MELA-AU 13 77763617 77763617 single base substitution G A intron_variant MELA-AU 13 77764589 77764589 single base substitution A G intron_variant MELA-AU 13 77764927 77764927 single base substitution G A intron_variant MELA-AU 13 77765767 77765767 single base substitution C T intron_variant MELA-AU 13 77766741 77766741 single base substitution G A intron_variant MELA-AU 13 77766811 77766811 single base substitution G T intron_variant MELA-AU 13 77767718 77767718 single base substitution G A intron_variant MELA-AU 13 77768000 77768000 single base substitution C T intron_variant MELA-AU 13 77768226 77768226 single base substitution T C intron_variant MELA-AU 13 77768245 77768245 single base substitution T G intron_variant MELA-AU 13 77768958 77768958 single base substitution A C intron_variant MELA-AU 13 77768996 77768996 single base substitution G A intron_variant MELA-AU 13 77770683 77770684 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77770684 77770684 single base substitution G A intron_variant MELA-AU 13 77770707 77770707 single base substitution G A intron_variant MELA-AU 13 77771506 77771506 single base substitution G A intron_variant MELA-AU 13 77771688 77771688 single base substitution G A intron_variant MELA-AU 13 77771745 77771745 single base substitution G A intron_variant MELA-AU 13 77771785 77771785 single base substitution G A intron_variant MELA-AU 13 77771810 77771810 single base substitution G A intron_variant MELA-AU 13 77772988 77772988 single base substitution A T intron_variant MELA-AU 13 77773198 77773198 single base substitution C T intron_variant MELA-AU 13 77773237 77773237 single base substitution G A intron_variant MELA-AU 13 77773258 77773258 single base substitution G A intron_variant MELA-AU 13 77774164 77774164 single base substitution A T intron_variant MELA-AU 13 77774465 77774465 single base substitution G A intron_variant MELA-AU 13 77774484 77774484 single base substitution A T intron_variant MELA-AU 13 77775587 77775587 single base substitution T C intron_variant MELA-AU 13 77775927 77775927 single base substitution T A intron_variant MELA-AU 13 77775972 77775972 single base substitution G A intron_variant MELA-AU 13 77776039 77776039 single base substitution G A intron_variant MELA-AU 13 77776191 77776191 single base substitution G A intron_variant MELA-AU 13 77776253 77776253 single base substitution G A intron_variant MELA-AU 13 77779184 77779184 single base substitution A G intron_variant MELA-AU 13 77779749 77779749 single base substitution A C intron_variant MELA-AU 13 77780005 77780005 single base substitution G A intron_variant MELA-AU 13 77780046 77780046 single base substitution A C intron_variant MELA-AU 13 77780165 77780165 single base substitution G A intron_variant MELA-AU 13 77780519 77780519 single base substitution T A intron_variant MELA-AU 13 77780857 77780857 single base substitution G A 5_prime_UTR_variant MELA-AU 13 77780857 77780857 single base substitution G A missense_variant P1136S 3406C>T MELA-AU 13 77780857 77780857 single base substitution G A missense_variant P1174S 3520C>T MELA-AU 13 77782866 77782866 single base substitution G A intron_variant MELA-AU 13 77784521 77784521 single base substitution G A intron_variant MELA-AU 13 77785093 77785093 single base substitution A C intron_variant MELA-AU 13 77785761 77785761 single base substitution C T intron_variant MELA-AU 13 77786021 77786021 single base substitution G T intron_variant MELA-AU 13 77786312 77786312 single base substitution A G intron_variant MELA-AU 13 77786333 77786333 single base substitution T G intron_variant MELA-AU 13 77787044 77787044 single base substitution G A intron_variant MELA-AU 13 77787131 77787144 deletion of <=200bp AGCACAGCAAGAAA - intron_variant MELA-AU 13 77787456 77787456 single base substitution G A intron_variant MELA-AU 13 77787634 77787634 single base substitution T C intron_variant MELA-AU 13 77787677 77787677 single base substitution G A intron_variant MELA-AU 13 77787681 77787681 single base substitution G T intron_variant MELA-AU 13 77788207 77788207 single base substitution G A intron_variant MELA-AU 13 77788251 77788251 single base substitution A G intron_variant MELA-AU 13 77789286 77789286 single base substitution A G intron_variant MELA-AU 13 77789437 77789437 single base substitution C T intron_variant MELA-AU 13 77789560 77789560 single base substitution A G intron_variant MELA-AU 13 77789986 77789986 single base substitution G A intron_variant MELA-AU 13 77790015 77790015 single base substitution C T intron_variant MELA-AU 13 77790236 77790236 single base substitution A T intron_variant MELA-AU 13 77790673 77790673 single base substitution G A intron_variant MELA-AU 13 77791043 77791043 single base substitution G A intron_variant MELA-AU 13 77791549 77791549 single base substitution G A intron_variant MELA-AU 13 77791711 77791711 single base substitution G A intron_variant MELA-AU 13 77792174 77792174 single base substitution G A intron_variant MELA-AU 13 77792268 77792268 single base substitution G A intron_variant MELA-AU 13 77792630 77792630 single base substitution C T intron_variant MELA-AU 13 77792787 77792787 single base substitution G A intron_variant MELA-AU 13 77793102 77793102 single base substitution G A intron_variant MELA-AU 13 77793541 77793541 single base substitution G A intron_variant MELA-AU 13 77793683 77793683 single base substitution G A intron_variant MELA-AU 13 77794167 77794167 single base substitution G A intron_variant MELA-AU 13 77794235 77794235 single base substitution G A intron_variant MELA-AU 13 77794394 77794394 single base substitution G A intron_variant MELA-AU 13 77794742 77794742 single base substitution G A intron_variant MELA-AU 13 77794760 77794760 single base substitution T C intron_variant MELA-AU 13 77794762 77794762 single base substitution C T intron_variant MELA-AU 13 77795189 77795189 single base substitution G A intron_variant MELA-AU 13 77795297 77795297 single base substitution G A intron_variant MELA-AU 13 77795305 77795305 single base substitution G A intron_variant MELA-AU 13 77795504 77795504 single base substitution A G intron_variant MELA-AU 13 77795672 77795672 single base substitution C T intron_variant MELA-AU 13 77795825 77795825 single base substitution A C intron_variant MELA-AU 13 77795956 77795956 single base substitution G A intron_variant MELA-AU 13 77797017 77797017 single base substitution C T intron_variant MELA-AU 13 77797038 77797038 single base substitution C T intron_variant MELA-AU 13 77797469 77797469 single base substitution G A intron_variant MELA-AU 13 77797517 77797517 single base substitution G A intron_variant MELA-AU 13 77797605 77797605 single base substitution G A intron_variant MELA-AU 13 77797691 77797691 single base substitution G A intron_variant MELA-AU 13 77797758 77797758 single base substitution C T intron_variant MELA-AU 13 77798021 77798021 single base substitution G A intron_variant MELA-AU 13 77798316 77798316 single base substitution G A intron_variant MELA-AU 13 77798796 77798796 single base substitution G A intron_variant MELA-AU 13 77799095 77799095 single base substitution G A intron_variant MELA-AU 13 77799099 77799099 single base substitution G A intron_variant MELA-AU 13 77799638 77799638 single base substitution G A 5_prime_UTR_variant MELA-AU 13 77799638 77799638 single base substitution G A missense_variant P892L 2675C>T MELA-AU 13 77799638 77799638 single base substitution G A missense_variant P930L 2789C>T MELA-AU 13 77799680 77799680 single base substitution C T 5_prime_UTR_variant MELA-AU 13 77799680 77799680 single base substitution C T missense_variant G878E 2633G>A MELA-AU 13 77799680 77799680 single base substitution C T missense_variant G916E 2747G>A MELA-AU 13 77800010 77800010 single base substitution G A intron_variant MELA-AU 13 77800257 77800257 single base substitution C T intron_variant MELA-AU 13 77800352 77800352 single base substitution C T intron_variant MELA-AU 13 77800639 77800639 single base substitution G A intron_variant MELA-AU 13 77800883 77800883 single base substitution C T intron_variant MELA-AU 13 77803184 77803184 single base substitution G A intron_variant MELA-AU 13 77803522 77803523 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 13 77804124 77804124 single base substitution G A intron_variant MELA-AU 13 77807032 77807032 single base substitution G A intron_variant MELA-AU 13 77807251 77807251 single base substitution G A intron_variant MELA-AU 13 77807705 77807705 single base substitution C T intron_variant MELA-AU 13 77807995 77807995 single base substitution C A intron_variant MELA-AU 13 77808042 77808042 single base substitution G A intron_variant MELA-AU 13 77808206 77808206 single base substitution G A intron_variant MELA-AU 13 77808616 77808616 single base substitution G A intron_variant MELA-AU 13 77809090 77809090 single base substitution G A intron_variant MELA-AU 13 77809117 77809117 single base substitution G A intron_variant MELA-AU 13 77809321 77809321 single base substitution G A intron_variant MELA-AU 13 77809678 77809678 single base substitution T C intron_variant MELA-AU 13 77809718 77809718 single base substitution A G intron_variant MELA-AU 13 77810007 77810007 single base substitution G A intron_variant MELA-AU 13 77810318 77810318 single base substitution G A intron_variant MELA-AU 13 77810420 77810420 single base substitution G A intron_variant MELA-AU 13 77811414 77811414 single base substitution A G intron_variant MELA-AU 13 77811824 77811824 single base substitution C G intron_variant MELA-AU 13 77812365 77812365 single base substitution G A intron_variant MELA-AU 13 77812485 77812485 single base substitution T C intron_variant MELA-AU 13 77813664 77813664 single base substitution G A intron_variant MELA-AU 13 77814719 77814719 single base substitution G A intron_variant MELA-AU 13 77815310 77815310 single base substitution A G intron_variant MELA-AU 13 77815655 77815655 single base substitution A C intron_variant MELA-AU 13 77816393 77816393 single base substitution C T intron_variant MELA-AU 13 77817050 77817050 single base substitution C T intron_variant MELA-AU 13 77817205 77817205 single base substitution T G 5_prime_UTR_variant MELA-AU 13 77817205 77817205 single base substitution T G missense_variant E835A 2504A>C MELA-AU 13 77817205 77817205 single base substitution T G missense_variant E873A 2618A>C MELA-AU 13 77818092 77818092 single base substitution G A splice_region_variant MELA-AU 13 77818557 77818557 single base substitution C T intron_variant MELA-AU 13 77818864 77818864 single base substitution A G intron_variant MELA-AU 13 77819144 77819144 single base substitution C T intron_variant MELA-AU 13 77819164 77819164 single base substitution G A intron_variant MELA-AU 13 77819234 77819234 single base substitution G A intron_variant MELA-AU 13 77819322 77819322 single base substitution G A intron_variant MELA-AU 13 77819418 77819418 single base substitution C T intron_variant MELA-AU 13 77819545 77819545 single base substitution G A intron_variant MELA-AU 13 77819714 77819715 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77819758 77819758 single base substitution G A intron_variant MELA-AU 13 77819887 77819887 single base substitution C T intron_variant MELA-AU 13 77820000 77820000 single base substitution C T intron_variant MELA-AU 13 77820008 77820008 single base substitution T C intron_variant MELA-AU 13 77820306 77820306 single base substitution C T intron_variant MELA-AU 13 77820731 77820731 single base substitution G A intron_variant MELA-AU 13 77820759 77820759 single base substitution G A intron_variant MELA-AU 13 77820778 77820778 single base substitution A T intron_variant MELA-AU 13 77821459 77821459 single base substitution A T intron_variant MELA-AU 13 77821464 77821464 single base substitution G A intron_variant MELA-AU 13 77822332 77822332 single base substitution G A intron_variant MELA-AU 13 77822334 77822334 single base substitution G A intron_variant MELA-AU 13 77822399 77822400 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77822429 77822429 single base substitution C A intron_variant MELA-AU 13 77823251 77823251 single base substitution G A intron_variant MELA-AU 13 77823858 77823858 single base substitution G A intron_variant MELA-AU 13 77824397 77824397 single base substitution A G intron_variant MELA-AU 13 77824520 77824520 single base substitution G A intron_variant MELA-AU 13 77825761 77825761 single base substitution C T intron_variant MELA-AU 13 77826127 77826127 single base substitution G A intron_variant MELA-AU 13 77826129 77826129 single base substitution G A intron_variant MELA-AU 13 77826192 77826192 single base substitution T G intron_variant MELA-AU 13 77826696 77826696 single base substitution G A intron_variant MELA-AU 13 77827036 77827036 single base substitution C T intron_variant MELA-AU 13 77827132 77827132 single base substitution A G intron_variant MELA-AU 13 77828064 77828064 single base substitution G A intron_variant MELA-AU 13 77828113 77828113 single base substitution G A intron_variant MELA-AU 13 77828481 77828481 single base substitution G A intron_variant MELA-AU 13 77828482 77828482 single base substitution G A intron_variant MELA-AU 13 77828818 77828818 single base substitution G A intron_variant MELA-AU 13 77829317 77829317 single base substitution G A intron_variant MELA-AU 13 77829584 77829584 single base substitution C T intron_variant MELA-AU 13 77830535 77830535 single base substitution G A intron_variant MELA-AU 13 77831048 77831048 single base substitution C T intron_variant MELA-AU 13 77831492 77831492 single base substitution T A intron_variant MELA-AU 13 77831738 77831738 single base substitution A C intron_variant MELA-AU 13 77832710 77832710 single base substitution C A intron_variant MELA-AU 13 77832860 77832860 single base substitution A T intron_variant MELA-AU 13 77833512 77833513 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77833539 77833539 single base substitution C G intron_variant MELA-AU 13 77833804 77833804 single base substitution A G intron_variant MELA-AU 13 77834302 77834302 single base substitution G A intron_variant MELA-AU 13 77834311 77834311 single base substitution C T intron_variant MELA-AU 13 77834423 77834423 single base substitution G A intron_variant MELA-AU 13 77834858 77834858 single base substitution G A intron_variant MELA-AU 13 77835577 77835577 single base substitution G A intron_variant MELA-AU 13 77835785 77835785 single base substitution T G intron_variant MELA-AU 13 77835929 77835929 single base substitution A G intron_variant MELA-AU 13 77836733 77836733 single base substitution G A intron_variant MELA-AU 13 77837760 77837760 single base substitution G A intron_variant MELA-AU 13 77838211 77838211 single base substitution A G intron_variant MELA-AU 13 77838784 77838784 single base substitution C T intron_variant MELA-AU 13 77839043 77839043 single base substitution G A intron_variant MELA-AU 13 77839303 77839303 single base substitution G A downstream_gene_variant MELA-AU 13 77839303 77839303 single base substitution G A intron_variant MELA-AU 13 77839331 77839331 single base substitution G A downstream_gene_variant MELA-AU 13 77839331 77839331 single base substitution G A intron_variant MELA-AU 13 77839513 77839515 deletion of <=200bp AAG - downstream_gene_variant MELA-AU 13 77839513 77839515 deletion of <=200bp AAG - intron_variant MELA-AU 13 77839764 77839764 single base substitution T A downstream_gene_variant MELA-AU 13 77839764 77839764 single base substitution T A intron_variant MELA-AU 13 77839929 77839930 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 13 77839929 77839930 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77840351 77840351 single base substitution G A downstream_gene_variant MELA-AU 13 77840351 77840351 single base substitution G A intron_variant MELA-AU 13 77840603 77840603 single base substitution G A downstream_gene_variant MELA-AU 13 77840603 77840603 single base substitution G A intron_variant MELA-AU 13 77840864 77840864 single base substitution G A downstream_gene_variant MELA-AU 13 77840864 77840864 single base substitution G A intron_variant MELA-AU 13 77842113 77842113 single base substitution C T downstream_gene_variant MELA-AU 13 77842113 77842113 single base substitution C T intron_variant MELA-AU 13 77842601 77842601 single base substitution G A downstream_gene_variant MELA-AU 13 77842601 77842601 single base substitution G A intron_variant MELA-AU 13 77842728 77842728 single base substitution G C downstream_gene_variant MELA-AU 13 77842728 77842728 single base substitution G C intron_variant MELA-AU 13 77843037 77843037 single base substitution G A downstream_gene_variant MELA-AU 13 77843037 77843037 single base substitution G A intron_variant MELA-AU 13 77843748 77843748 single base substitution G A downstream_gene_variant MELA-AU 13 77843748 77843748 single base substitution G A intron_variant MELA-AU 13 77844095 77844095 single base substitution A G downstream_gene_variant MELA-AU 13 77844095 77844095 single base substitution A G intron_variant MELA-AU 13 77844303 77844303 single base substitution G A intron_variant MELA-AU 13 77844786 77844786 single base substitution G A intron_variant MELA-AU 13 77845810 77845810 single base substitution G A intron_variant MELA-AU 13 77845874 77845874 single base substitution C A intron_variant MELA-AU 13 77845961 77845961 single base substitution G A intron_variant MELA-AU 13 77845962 77845962 single base substitution G A intron_variant MELA-AU 13 77846243 77846243 single base substitution C T intron_variant MELA-AU 13 77846308 77846308 single base substitution G A intron_variant MELA-AU 13 77846777 77846778 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77846799 77846799 single base substitution G A intron_variant MELA-AU 13 77846890 77846890 single base substitution G A intron_variant MELA-AU 13 77847313 77847315 multiple base substitution (>=2bp and <=200bp) GGA AAG intron_variant MELA-AU 13 77847809 77847809 single base substitution G A splice_region_variant MELA-AU 13 77847809 77847809 single base substitution G A upstream_gene_variant MELA-AU 13 77847896 77847896 single base substitution G A intron_variant MELA-AU 13 77847896 77847896 single base substitution G A upstream_gene_variant MELA-AU 13 77848139 77848139 single base substitution G A intron_variant MELA-AU 13 77848139 77848139 single base substitution G A upstream_gene_variant MELA-AU 13 77849103 77849103 single base substitution C T intron_variant MELA-AU 13 77849103 77849103 single base substitution C T upstream_gene_variant MELA-AU 13 77849304 77849305 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77849304 77849305 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 13 77849305 77849305 single base substitution G A intron_variant MELA-AU 13 77849305 77849305 single base substitution G A upstream_gene_variant MELA-AU 13 77849911 77849911 single base substitution G A intron_variant MELA-AU 13 77849911 77849911 single base substitution G A upstream_gene_variant MELA-AU 13 77849985 77849985 single base substitution G A intron_variant MELA-AU 13 77849985 77849985 single base substitution G A upstream_gene_variant MELA-AU 13 77850324 77850324 single base substitution G A intron_variant MELA-AU 13 77850324 77850324 single base substitution G A upstream_gene_variant MELA-AU 13 77850508 77850508 single base substitution G A intron_variant MELA-AU 13 77850508 77850508 single base substitution G A upstream_gene_variant MELA-AU 13 77850798 77850798 single base substitution G A intron_variant MELA-AU 13 77850798 77850798 single base substitution G A upstream_gene_variant MELA-AU 13 77851740 77851740 single base substitution G A intron_variant MELA-AU 13 77851740 77851740 single base substitution G A upstream_gene_variant MELA-AU 13 77852256 77852256 single base substitution A C intron_variant MELA-AU 13 77852256 77852256 single base substitution A C upstream_gene_variant MELA-AU 13 77852986 77852986 single base substitution G A 5_prime_UTR_variant MELA-AU 13 77852986 77852986 single base substitution G A missense_variant P181S 541C>T MELA-AU 13 77852986 77852986 single base substitution G A missense_variant P219S 655C>T MELA-AU 13 77853057 77853057 single base substitution G A intron_variant MELA-AU 13 77853383 77853383 single base substitution C T intron_variant MELA-AU 13 77854873 77854873 single base substitution G A intron_variant MELA-AU 13 77855684 77855684 single base substitution G A intron_variant MELA-AU 13 77856265 77856265 single base substitution G A intron_variant MELA-AU 13 77856965 77856965 single base substitution G A intron_variant MELA-AU 13 77857616 77857616 single base substitution T C intron_variant MELA-AU 13 77858304 77858304 single base substitution G A intron_variant MELA-AU 13 77859144 77859144 single base substitution T C intron_variant MELA-AU 13 77859363 77859363 single base substitution A G intron_variant MELA-AU 13 77859938 77859938 single base substitution G A intron_variant MELA-AU 13 77860057 77860057 single base substitution G A intron_variant MELA-AU 13 77860880 77860880 single base substitution G A intron_variant MELA-AU 13 77861454 77861454 single base substitution G A intron_variant MELA-AU 13 77861882 77861882 single base substitution G A intron_variant MELA-AU 13 77862324 77862324 single base substitution G A 5_prime_UTR_variant MELA-AU 13 77862324 77862324 single base substitution G A missense_variant S151F 452C>T MELA-AU 13 77862324 77862324 single base substitution G A missense_variant S189F 566C>T MELA-AU 13 77862715 77862715 single base substitution A G intron_variant MELA-AU 13 77863329 77863329 single base substitution A C intron_variant MELA-AU 13 77863544 77863544 single base substitution C A intron_variant MELA-AU 13 77864287 77864287 single base substitution G A intron_variant MELA-AU 13 77865196 77865196 single base substitution A G intron_variant MELA-AU 13 77865721 77865721 single base substitution G A intron_variant MELA-AU 13 77865890 77865890 single base substitution G A downstream_gene_variant MELA-AU 13 77865890 77865890 single base substitution G A intron_variant MELA-AU 13 77866072 77866072 single base substitution G A downstream_gene_variant MELA-AU 13 77866072 77866072 single base substitution G A intron_variant MELA-AU 13 77866219 77866219 single base substitution G A downstream_gene_variant MELA-AU 13 77866219 77866219 single base substitution G A intron_variant MELA-AU 13 77866372 77866372 single base substitution C T downstream_gene_variant MELA-AU 13 77866372 77866372 single base substitution C T intron_variant MELA-AU 13 77866524 77866524 single base substitution T C downstream_gene_variant MELA-AU 13 77866524 77866524 single base substitution T C intron_variant MELA-AU 13 77867294 77867294 single base substitution G A downstream_gene_variant MELA-AU 13 77867294 77867294 single base substitution G A intron_variant MELA-AU 13 77867985 77867986 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 13 77867985 77867986 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77868335 77868335 single base substitution G A downstream_gene_variant MELA-AU 13 77868335 77868335 single base substitution G A intron_variant MELA-AU 13 77868809 77868809 single base substitution G A downstream_gene_variant MELA-AU 13 77868809 77868809 single base substitution G A intron_variant MELA-AU 13 77869455 77869455 single base substitution G C downstream_gene_variant MELA-AU 13 77869455 77869455 single base substitution G C intron_variant MELA-AU 13 77870823 77870823 single base substitution G A intron_variant MELA-AU 13 77871912 77871912 single base substitution C T intron_variant MELA-AU 13 77873289 77873289 single base substitution G A intron_variant MELA-AU 13 77875194 77875194 single base substitution G A intron_variant MELA-AU 13 77875445 77875445 single base substitution G A intron_variant MELA-AU 13 77875601 77875601 single base substitution G A intron_variant MELA-AU 13 77876969 77876969 single base substitution G A intron_variant MELA-AU 13 77877451 77877451 single base substitution G A intron_variant MELA-AU 13 77877815 77877815 single base substitution G A intron_variant MELA-AU 13 77878276 77878276 single base substitution G A intron_variant MELA-AU 13 77878533 77878533 deletion of <=200bp T - intron_variant MELA-AU 13 77878623 77878623 single base substitution G A intron_variant MELA-AU 13 77878648 77878648 single base substitution G A intron_variant MELA-AU 13 77879087 77879087 single base substitution G A intron_variant MELA-AU 13 77880036 77880036 single base substitution C T intron_variant MELA-AU 13 77880113 77880113 single base substitution G A intron_variant MELA-AU 13 77880477 77880477 single base substitution G A intron_variant MELA-AU 13 77880500 77880500 single base substitution A G intron_variant MELA-AU 13 77880734 77880734 single base substitution G A intron_variant MELA-AU 13 77881570 77881570 single base substitution G A intron_variant MELA-AU 13 77882529 77882529 single base substitution G T intron_variant MELA-AU 13 77883700 77883700 single base substitution C T intron_variant MELA-AU 13 77884326 77884326 single base substitution G A intron_variant MELA-AU 13 77884768 77884768 single base substitution G A intron_variant MELA-AU 13 77884922 77884922 insertion of <=200bp - CA intron_variant MELA-AU 13 77885680 77885680 single base substitution G A intron_variant MELA-AU 13 77886694 77886694 single base substitution A G intron_variant MELA-AU 13 77887624 77887624 single base substitution G A intron_variant MELA-AU 13 77887632 77887632 single base substitution G A intron_variant MELA-AU 13 77887690 77887690 single base substitution C T intron_variant MELA-AU 13 77889444 77889444 single base substitution G A intron_variant MELA-AU 13 77889522 77889522 single base substitution G A intron_variant MELA-AU 13 77891232 77891232 single base substitution G A intron_variant MELA-AU 13 77892305 77892305 single base substitution G A intron_variant MELA-AU 13 77892914 77892914 single base substitution C T intron_variant MELA-AU 13 77893443 77893444 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 77893657 77893657 single base substitution G A intron_variant MELA-AU 13 77894214 77894214 single base substitution G A intron_variant MELA-AU 13 77894676 77894676 single base substitution G A intron_variant MELA-AU 13 77894840 77894840 single base substitution T C intron_variant MELA-AU 13 77895009 77895009 single base substitution G A intron_variant MELA-AU 13 77896006 77896006 single base substitution C T intron_variant MELA-AU 13 77896574 77896574 single base substitution C T intron_variant MELA-AU 13 77899016 77899016 single base substitution A G intron_variant MELA-AU 13 77899019 77899019 single base substitution G A intron_variant MELA-AU 13 77899257 77899257 single base substitution A T intron_variant MELA-AU 13 77899303 77899303 single base substitution A G intron_variant MELA-AU 13 77899640 77899640 single base substitution A G intron_variant MELA-AU 13 77900578 77900578 single base substitution G A intron_variant MELA-AU 13 77900679 77900679 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 13 77900679 77900679 single base substitution G A exon_variant MELA-AU 13 77900679 77900679 single base substitution G A missense_variant R40W 118C>T MELA-AU 13 77900679 77900679 single base substitution G A missense_variant R78W 232C>T MELA-AU 13 77900945 77900945 single base substitution C A 5_prime_UTR_variant MELA-AU 13 77900945 77900945 single base substitution C A exon_variant MELA-AU 13 77900945 77900945 single base substitution C A intron_variant MELA-AU 13 77900945 77900945 single base substitution C A upstream_gene_variant MELA-AU 13 77901283 77901283 single base substitution C T upstream_gene_variant MELA-AU 13 77901289 77901289 single base substitution C T upstream_gene_variant MELA-AU 13 77901317 77901317 single base substitution C T upstream_gene_variant MELA-AU 13 77902214 77902214 single base substitution T A upstream_gene_variant MELA-AU 13 77903113 77903113 single base substitution A T upstream_gene_variant MELA-AU 13 77903995 77903995 single base substitution C T upstream_gene_variant MELA-AU 13 77904279 77904279 single base substitution C T upstream_gene_variant MELA-AU 13 77904731 77904731 single base substitution T A upstream_gene_variant MELA-AU 13 77905503 77905503 single base substitution A G upstream_gene_variant MELA-AU 13 77905527 77905527 single base substitution T A upstream_gene_variant MELA-AU 13 77905802 77905802 single base substitution A G upstream_gene_variant MELA-AU 13 77905944 77905944 single base substitution C T upstream_gene_variant MELA-AU 13 77906085 77906085 single base substitution G A upstream_gene_variant ORCA-IN 13 77629281 77629281 deletion of <=200bp G - intron_variant ORCA-IN 13 77663781 77663781 insertion of <=200bp - C downstream_gene_variant ORCA-IN 13 77663781 77663781 insertion of <=200bp - C intron_variant ORCA-IN 13 77663781 77663781 insertion of <=200bp - C upstream_gene_variant ORCA-IN 13 77681125 77681125 single base substitution G A intron_variant ORCA-IN 13 77722464 77722464 single base substitution G A intron_variant ORCA-IN 13 77793265 77793266 deletion of <=200bp TA - intron_variant ORCA-IN 13 77795052 77795052 single base substitution C T intron_variant ORCA-IN 13 77825622 77825622 single base substitution G T intron_variant ORCA-IN 13 77829910 77829910 single base substitution C T intron_variant ORCA-IN 13 77849660 77849660 single base substitution T A intron_variant ORCA-IN 13 77849660 77849660 single base substitution T A upstream_gene_variant ORCA-IN 13 77849917 77849917 single base substitution G C intron_variant ORCA-IN 13 77849917 77849917 single base substitution G C upstream_gene_variant ORCA-IN 13 77855883 77855883 single base substitution A T intron_variant ORCA-IN 13 77860019 77860019 single base substitution G C intron_variant ORCA-IN 13 77893874 77893874 single base substitution T C intron_variant OV-AU 13 77617109 77617109 single base substitution G A downstream_gene_variant OV-AU 13 77626842 77626842 single base substitution T G intron_variant OV-AU 13 77629091 77629091 single base substitution C T intron_variant OV-AU 13 77630144 77630144 single base substitution T C intron_variant OV-AU 13 77636554 77636554 single base substitution G A intron_variant OV-AU 13 77636704 77636704 single base substitution T G intron_variant OV-AU 13 77643790 77643790 single base substitution G T intron_variant OV-AU 13 77648581 77648581 single base substitution C A intron_variant OV-AU 13 77649810 77649810 single base substitution G T intron_variant OV-AU 13 77649818 77649818 single base substitution T G intron_variant OV-AU 13 77652486 77652486 single base substitution C T intron_variant OV-AU 13 77658396 77658396 single base substitution A C intron_variant OV-AU 13 77667075 77667075 single base substitution T C downstream_gene_variant OV-AU 13 77667075 77667075 single base substitution T C intron_variant OV-AU 13 77667672 77667672 single base substitution C G downstream_gene_variant OV-AU 13 77667672 77667672 single base substitution C G intron_variant OV-AU 13 77686831 77686831 single base substitution T C intron_variant OV-AU 13 77688545 77688545 single base substitution C T intron_variant OV-AU 13 77702162 77702162 single base substitution A G intron_variant OV-AU 13 77702162 77702162 single base substitution A G upstream_gene_variant OV-AU 13 77704953 77704953 single base substitution A C intron_variant OV-AU 13 77704953 77704953 single base substitution A C upstream_gene_variant OV-AU 13 77706998 77706998 single base substitution G T intron_variant OV-AU 13 77715477 77715477 single base substitution C A downstream_gene_variant OV-AU 13 77715477 77715477 single base substitution C A intron_variant OV-AU 13 77715477 77715477 single base substitution C A upstream_gene_variant OV-AU 13 77718432 77718432 single base substitution C T exon_variant OV-AU 13 77718432 77718432 single base substitution C T intron_variant OV-AU 13 77718432 77718432 single base substitution C T upstream_gene_variant OV-AU 13 77722676 77722676 single base substitution T A intron_variant OV-AU 13 77726069 77726069 single base substitution C T intron_variant OV-AU 13 77726069 77726069 single base substitution C T upstream_gene_variant OV-AU 13 77727922 77727922 single base substitution G C intron_variant OV-AU 13 77727922 77727922 single base substitution G C upstream_gene_variant OV-AU 13 77740521 77740521 single base substitution C A 5_prime_UTR_variant OV-AU 13 77740521 77740521 single base substitution C A stop_gained E2057* 6169G>T OV-AU 13 77740521 77740521 single base substitution C A stop_gained E2095* 6283G>T OV-AU 13 77745968 77745968 single base substitution G T intron_variant OV-AU 13 77754394 77754394 single base substitution G C 5_prime_UTR_variant OV-AU 13 77754394 77754394 single base substitution G C synonymous_variant V1629V 4887C>G OV-AU 13 77754394 77754394 single base substitution G C synonymous_variant V1667V 5001C>G OV-AU 13 77762405 77762405 single base substitution A T intron_variant OV-AU 13 77766226 77766226 single base substitution A C intron_variant OV-AU 13 77766798 77766798 single base substitution G A intron_variant OV-AU 13 77771966 77771966 single base substitution C A intron_variant OV-AU 13 77779960 77779960 single base substitution G A intron_variant OV-AU 13 77782087 77782087 single base substitution A C intron_variant OV-AU 13 77808775 77808775 single base substitution T C intron_variant OV-AU 13 77809860 77809860 single base substitution C A intron_variant OV-AU 13 77820905 77820905 single base substitution G T intron_variant OV-AU 13 77827081 77827081 single base substitution G C intron_variant OV-AU 13 77835034 77835034 single base substitution G A intron_variant OV-AU 13 77849498 77849498 single base substitution A C intron_variant OV-AU 13 77849498 77849498 single base substitution A C upstream_gene_variant OV-AU 13 77852154 77852154 single base substitution A T intron_variant OV-AU 13 77852154 77852154 single base substitution A T upstream_gene_variant OV-AU 13 77865712 77865712 single base substitution C T intron_variant OV-AU 13 77865732 77865732 single base substitution G C intron_variant OV-AU 13 77881650 77881650 single base substitution A T intron_variant OV-AU 13 77893583 77893583 single base substitution C G intron_variant OV-AU 13 77893679 77893679 single base substitution A G intron_variant OV-AU 13 77899159 77899159 single base substitution C G intron_variant OV-AU 13 77901708 77901708 single base substitution C A upstream_gene_variant OV-AU 13 77901709 77901709 single base substitution T A upstream_gene_variant OV-US 13 77629819 77629819 single base substitution C G missense_variant M4469I 13407G>C OV-US 13 77629819 77629819 single base substitution C G missense_variant M4507I 13521G>C OV-US 13 77629819 77629819 single base substitution C G missense_variant M889I 2667G>C OV-US 13 77638760 77638760 single base substitution G C missense_variant A4183G 12548C>G OV-US 13 77638760 77638760 single base substitution G C missense_variant A4221G 12662C>G OV-US 13 77638760 77638760 single base substitution G C missense_variant A603G 1808C>G OV-US 13 77740565 77740565 single base substitution C G 5_prime_UTR_variant OV-US 13 77740565 77740565 single base substitution C G missense_variant G2042A 6125G>C OV-US 13 77740565 77740565 single base substitution C G missense_variant G2080A 6239G>C OV-US 13 77754358 77754358 single base substitution T G 5_prime_UTR_variant OV-US 13 77754358 77754358 single base substitution T G missense_variant R1641S 4923A>C OV-US 13 77754358 77754358 single base substitution T G missense_variant R1679S 5037A>C OV-US 13 77798611 77798611 single base substitution G C 5_prime_UTR_variant OV-US 13 77798611 77798611 single base substitution G C missense_variant L934V 2800C>G OV-US 13 77798611 77798611 single base substitution G C missense_variant L972V 2914C>G PACA-AU 13 77614623 77614623 single base substitution T A downstream_gene_variant PACA-AU 13 77631470 77631470 single base substitution C T intron_variant PACA-AU 13 77631661 77631697 deletion of <=200bp TATGTATAGAAGTATGTATCATTATGTATAGATCAAT - intron_variant PACA-AU 13 77633707 77633707 single base substitution C T missense_variant G4326E 12977G>A PACA-AU 13 77633707 77633707 single base substitution C T missense_variant G4364E 13091G>A PACA-AU 13 77633707 77633707 single base substitution C T missense_variant G746E 2237G>A PACA-AU 13 77638533 77638533 single base substitution C T intron_variant PACA-AU 13 77640055 77640055 single base substitution T G intron_variant PACA-AU 13 77642831 77642831 single base substitution A G missense_variant F396L 1186T>C PACA-AU 13 77642831 77642831 single base substitution A G missense_variant F3976L 11926T>C PACA-AU 13 77642831 77642831 single base substitution A G missense_variant F4014L 12040T>C PACA-AU 13 77655693 77655693 single base substitution C T missense_variant G148S 442G>A PACA-AU 13 77655693 77655693 single base substitution C T missense_variant G3725S 11173G>A PACA-AU 13 77655693 77655693 single base substitution C T missense_variant G3763S 11287G>A PACA-AU 13 77663786 77663786 single base substitution T C downstream_gene_variant PACA-AU 13 77663786 77663786 single base substitution T C intron_variant PACA-AU 13 77663786 77663786 single base substitution T C upstream_gene_variant PACA-AU 13 77663787 77663787 single base substitution T C downstream_gene_variant PACA-AU 13 77663787 77663787 single base substitution T C intron_variant PACA-AU 13 77663787 77663787 single base substitution T C upstream_gene_variant PACA-AU 13 77665941 77665941 single base substitution C T downstream_gene_variant PACA-AU 13 77665941 77665941 single base substitution C T intron_variant PACA-AU 13 77665941 77665941 single base substitution C T upstream_gene_variant PACA-AU 13 77668929 77668929 single base substitution T A downstream_gene_variant PACA-AU 13 77668929 77668929 single base substitution T A intron_variant PACA-AU 13 77675289 77675289 single base substitution A G intron_variant PACA-AU 13 77675289 77675289 single base substitution A G upstream_gene_variant PACA-AU 13 77690203 77690203 single base substitution G A intron_variant PACA-AU 13 77697923 77697923 single base substitution C T intron_variant PACA-AU 13 77701237 77701237 single base substitution A G intron_variant PACA-AU 13 77701237 77701237 single base substitution A G upstream_gene_variant PACA-AU 13 77701238 77701238 single base substitution A T intron_variant PACA-AU 13 77701238 77701238 single base substitution A T upstream_gene_variant PACA-AU 13 77706161 77706161 single base substitution C G intron_variant PACA-AU 13 77716342 77716342 single base substitution T C downstream_gene_variant PACA-AU 13 77716342 77716342 single base substitution T C intron_variant PACA-AU 13 77716342 77716342 single base substitution T C upstream_gene_variant PACA-AU 13 77718694 77718694 single base substitution G A missense_variant P2359S 7075C>T PACA-AU 13 77718694 77718694 single base substitution G A missense_variant P2397S 7189C>T PACA-AU 13 77718694 77718694 single base substitution G A splice_region_variant PACA-AU 13 77718694 77718694 single base substitution G A upstream_gene_variant PACA-AU 13 77722622 77722622 single base substitution G A intron_variant PACA-AU 13 77726859 77726859 single base substitution T C intron_variant PACA-AU 13 77726859 77726859 single base substitution T C upstream_gene_variant PACA-AU 13 77727230 77727230 single base substitution G C intron_variant PACA-AU 13 77727230 77727230 single base substitution G C upstream_gene_variant PACA-AU 13 77729045 77729045 deletion of <=200bp A - intron_variant PACA-AU 13 77729045 77729045 deletion of <=200bp A - upstream_gene_variant PACA-AU 13 77730266 77730266 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant PACA-AU 13 77730266 77730266 single base substitution C T missense_variant C2243Y 6728G>A PACA-AU 13 77730266 77730266 single base substitution C T missense_variant C2281Y 6842G>A PACA-AU 13 77733530 77733530 single base substitution T C intron_variant PACA-AU 13 77738829 77738829 single base substitution C T intron_variant PACA-AU 13 77749080 77749080 single base substitution T A intron_variant PACA-AU 13 77751423 77751423 single base substitution A G intron_variant PACA-AU 13 77751473 77751473 single base substitution T C intron_variant PACA-AU 13 77757200 77757200 single base substitution G A intron_variant PACA-AU 13 77761268 77761268 single base substitution T G intron_variant PACA-AU 13 77769674 77769674 single base substitution G C intron_variant PACA-AU 13 77776348 77776348 single base substitution T C intron_variant PACA-AU 13 77785643 77785643 single base substitution A G intron_variant PACA-AU 13 77786551 77786551 single base substitution C T intron_variant PACA-AU 13 77787211 77787211 single base substitution C A intron_variant PACA-AU 13 77789930 77789930 single base substitution G A intron_variant PACA-AU 13 77801634 77801634 single base substitution C T intron_variant PACA-AU 13 77812453 77812453 single base substitution C T intron_variant PACA-AU 13 77818371 77818371 single base substitution C A intron_variant PACA-AU 13 77838530 77838530 insertion of <=200bp - A intron_variant PACA-AU 13 77840783 77840783 single base substitution T C downstream_gene_variant PACA-AU 13 77840783 77840783 single base substitution T C intron_variant PACA-AU 13 77843338 77843338 deletion of <=200bp A - downstream_gene_variant PACA-AU 13 77843338 77843338 deletion of <=200bp A - intron_variant PACA-AU 13 77850992 77850992 single base substitution A C intron_variant PACA-AU 13 77850992 77850992 single base substitution A C upstream_gene_variant PACA-AU 13 77851521 77851521 single base substitution G C intron_variant PACA-AU 13 77851521 77851521 single base substitution G C upstream_gene_variant PACA-AU 13 77851796 77851796 single base substitution T G intron_variant PACA-AU 13 77851796 77851796 single base substitution T G upstream_gene_variant PACA-AU 13 77859014 77859014 single base substitution G A intron_variant PACA-AU 13 77859590 77859590 single base substitution C T intron_variant PACA-AU 13 77865642 77865642 single base substitution A G intron_variant PACA-AU 13 77867109 77867109 single base substitution A G downstream_gene_variant PACA-AU 13 77867109 77867109 single base substitution A G intron_variant PACA-AU 13 77868272 77868272 single base substitution T C downstream_gene_variant PACA-AU 13 77868272 77868272 single base substitution T C intron_variant PACA-AU 13 77879980 77879980 single base substitution T C intron_variant PACA-AU 13 77886231 77886231 single base substitution T C intron_variant PACA-AU 13 77889077 77889077 single base substitution T A intron_variant PACA-AU 13 77891409 77891409 single base substitution A G intron_variant PACA-AU 13 77894218 77894218 single base substitution A G intron_variant PACA-AU 13 77895129 77895129 single base substitution T C intron_variant PACA-AU 13 77900636 77900636 deletion of <=200bp C - 5_prime_UTR_variant PACA-AU 13 77900636 77900636 deletion of <=200bp C - exon_variant PACA-AU 13 77900636 77900636 deletion of <=200bp C - frameshift_variant G54 PACA-AU 13 77900636 77900636 deletion of <=200bp C - frameshift_variant G92 PACA-AU 13 77903519 77903519 single base substitution C T upstream_gene_variant PACA-AU 13 77904663 77904663 single base substitution A G upstream_gene_variant PACA-AU 13 77905595 77905595 single base substitution A G upstream_gene_variant PACA-CA 13 77615968 77615968 single base substitution C T downstream_gene_variant PACA-CA 13 77616073 77616073 single base substitution C T downstream_gene_variant PACA-CA 13 77616789 77616789 single base substitution G A downstream_gene_variant PACA-CA 13 77618580 77618580 single base substitution A G downstream_gene_variant PACA-CA 13 77619150 77619150 single base substitution G A 3_prime_UTR_variant PACA-CA 13 77622046 77622046 single base substitution C T intron_variant PACA-CA 13 77626366 77626366 single base substitution C T intron_variant PACA-CA 13 77629508 77629508 single base substitution A C intron_variant PACA-CA 13 77633942 77633942 deletion of <=200bp A - intron_variant PACA-CA 13 77636324 77636324 single base substitution C A intron_variant PACA-CA 13 77639994 77639994 single base substitution T C intron_variant PACA-CA 13 77641948 77641948 single base substitution C T missense_variant A4037T 12109G>A PACA-CA 13 77641948 77641948 single base substitution C T missense_variant A4075T 12223G>A PACA-CA 13 77641948 77641948 single base substitution C T missense_variant A457T 1369G>A PACA-CA 13 77642436 77642436 single base substitution T C intron_variant PACA-CA 13 77647415 77647415 deletion of <=200bp T - intron_variant PACA-CA 13 77647747 77647747 single base substitution G A intron_variant PACA-CA 13 77649809 77649809 insertion of <=200bp - G intron_variant PACA-CA 13 77651161 77651161 deletion of <=200bp A - intron_variant PACA-CA 13 77658857 77658857 single base substitution C A intron_variant PACA-CA 13 77665809 77665809 single base substitution T A downstream_gene_variant PACA-CA 13 77665809 77665809 single base substitution T A intron_variant PACA-CA 13 77665809 77665809 single base substitution T A upstream_gene_variant PACA-CA 13 77666786 77666786 single base substitution C T downstream_gene_variant PACA-CA 13 77666786 77666786 single base substitution C T intron_variant PACA-CA 13 77667343 77667343 single base substitution C T downstream_gene_variant PACA-CA 13 77667343 77667343 single base substitution C T missense_variant V3404I 10210G>A PACA-CA 13 77667343 77667343 single base substitution C T missense_variant V3442I 10324G>A PACA-CA 13 77671135 77671135 single base substitution T C downstream_gene_variant PACA-CA 13 77671135 77671135 single base substitution T C intron_variant PACA-CA 13 77672836 77672836 single base substitution C T downstream_gene_variant PACA-CA 13 77672836 77672836 single base substitution C T exon_variant PACA-CA 13 77672836 77672836 single base substitution C T missense_variant R2780Q 8339G>A PACA-CA 13 77672836 77672836 single base substitution C T missense_variant R2818Q 8453G>A PACA-CA 13 77672836 77672836 single base substitution C T missense_variant R303Q 908G>A PACA-CA 13 77672836 77672836 single base substitution C T upstream_gene_variant PACA-CA 13 77673517 77673517 single base substitution G A intron_variant PACA-CA 13 77673517 77673517 single base substitution G A upstream_gene_variant PACA-CA 13 77676495 77676495 single base substitution C A intron_variant PACA-CA 13 77676495 77676495 single base substitution C A upstream_gene_variant PACA-CA 13 77677238 77677238 deletion of <=200bp A - intron_variant PACA-CA 13 77677418 77677418 single base substitution C T exon_variant PACA-CA 13 77677418 77677418 single base substitution C T intron_variant PACA-CA 13 77679183 77679183 single base substitution T C intron_variant PACA-CA 13 77679741 77679741 single base substitution C G intron_variant PACA-CA 13 77680184 77680184 single base substitution C A intron_variant PACA-CA 13 77681137 77681137 single base substitution C G intron_variant PACA-CA 13 77684295 77684295 single base substitution C T intron_variant PACA-CA 13 77687381 77687381 single base substitution G T intron_variant PACA-CA 13 77689986 77689986 deletion of <=200bp A - intron_variant PACA-CA 13 77690997 77690997 single base substitution T C downstream_gene_variant PACA-CA 13 77690997 77690997 single base substitution T C intron_variant PACA-CA 13 77715503 77715503 single base substitution A T downstream_gene_variant PACA-CA 13 77715503 77715503 single base substitution A T intron_variant PACA-CA 13 77715503 77715503 single base substitution A T upstream_gene_variant PACA-CA 13 77716014 77716014 single base substitution C T downstream_gene_variant PACA-CA 13 77716014 77716014 single base substitution C T intron_variant PACA-CA 13 77716014 77716014 single base substitution C T upstream_gene_variant PACA-CA 13 77717558 77717558 single base substitution T C downstream_gene_variant PACA-CA 13 77717558 77717558 single base substitution T C intron_variant PACA-CA 13 77717558 77717558 single base substitution T C upstream_gene_variant PACA-CA 13 77717722 77717722 single base substitution G T downstream_gene_variant PACA-CA 13 77717722 77717722 single base substitution G T intron_variant PACA-CA 13 77717722 77717722 single base substitution G T upstream_gene_variant PACA-CA 13 77720256 77720256 single base substitution C T intron_variant PACA-CA 13 77724371 77724371 insertion of <=200bp - A intron_variant PACA-CA 13 77726614 77726614 single base substitution C A intron_variant PACA-CA 13 77726614 77726614 single base substitution C A upstream_gene_variant PACA-CA 13 77726646 77726646 single base substitution G A intron_variant PACA-CA 13 77726646 77726646 single base substitution G A upstream_gene_variant PACA-CA 13 77732065 77732065 single base substitution C T splice_region_variant PACA-CA 13 77742475 77742475 single base substitution T C intron_variant PACA-CA 13 77743176 77743176 single base substitution T C intron_variant PACA-CA 13 77743881 77743881 single base substitution T C intron_variant PACA-CA 13 77746356 77746356 single base substitution A T intron_variant PACA-CA 13 77749408 77749408 single base substitution C G intron_variant PACA-CA 13 77750652 77750652 single base substitution C G 5_prime_UTR_variant PACA-CA 13 77750652 77750652 single base substitution C G missense_variant D1780H 5338G>C PACA-CA 13 77750652 77750652 single base substitution C G missense_variant D1818H 5452G>C PACA-CA 13 77751677 77751677 single base substitution G A intron_variant PACA-CA 13 77752334 77752334 deletion of <=200bp T - intron_variant PACA-CA 13 77752432 77752432 single base substitution A G intron_variant PACA-CA 13 77760240 77760240 single base substitution T C intron_variant PACA-CA 13 77760252 77760252 single base substitution C T intron_variant PACA-CA 13 77764123 77764123 single base substitution A T intron_variant PACA-CA 13 77764662 77764662 single base substitution G A intron_variant PACA-CA 13 77766763 77766763 single base substitution T C intron_variant PACA-CA 13 77769322 77769322 single base substitution C T intron_variant PACA-CA 13 77771036 77771036 single base substitution G A intron_variant PACA-CA 13 77776197 77776197 single base substitution G A intron_variant PACA-CA 13 77777037 77777037 single base substitution A G intron_variant PACA-CA 13 77779159 77779159 single base substitution T G intron_variant PACA-CA 13 77779247 77779247 single base substitution C T intron_variant PACA-CA 13 77780391 77780391 single base substitution A C intron_variant PACA-CA 13 77781009 77781009 single base substitution A T intron_variant PACA-CA 13 77781737 77781737 insertion of <=200bp - T intron_variant PACA-CA 13 77783334 77783334 single base substitution T C intron_variant PACA-CA 13 77795059 77795059 single base substitution T A intron_variant PACA-CA 13 77798277 77798277 single base substitution A G intron_variant PACA-CA 13 77799565 77799565 single base substitution G A splice_region_variant PACA-CA 13 77802751 77802751 single base substitution A T intron_variant PACA-CA 13 77805988 77805988 single base substitution A T intron_variant PACA-CA 13 77813030 77813030 single base substitution C T intron_variant PACA-CA 13 77822288 77822288 single base substitution A G intron_variant PACA-CA 13 77826413 77826413 single base substitution A G intron_variant PACA-CA 13 77829368 77829368 single base substitution C G intron_variant PACA-CA 13 77831839 77831839 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant PACA-CA 13 77831839 77831839 single base substitution G A stop_gained R677* 2029C>T PACA-CA 13 77831839 77831839 single base substitution G A stop_gained R715* 2143C>T PACA-CA 13 77839383 77839383 single base substitution G A downstream_gene_variant PACA-CA 13 77839383 77839383 single base substitution G A intron_variant PACA-CA 13 77843989 77843989 single base substitution A G downstream_gene_variant PACA-CA 13 77843989 77843989 single base substitution A G intron_variant PACA-CA 13 77849042 77849042 single base substitution T C intron_variant PACA-CA 13 77849042 77849042 single base substitution T C upstream_gene_variant PACA-CA 13 77849326 77849326 single base substitution T G intron_variant PACA-CA 13 77849326 77849326 single base substitution T G upstream_gene_variant PACA-CA 13 77849813 77849813 single base substitution T A intron_variant PACA-CA 13 77849813 77849813 single base substitution T A upstream_gene_variant PACA-CA 13 77850118 77850118 insertion of <=200bp - A intron_variant PACA-CA 13 77850118 77850118 insertion of <=200bp - A upstream_gene_variant PACA-CA 13 77854252 77854252 single base substitution A C intron_variant PACA-CA 13 77858699 77858699 single base substitution T G intron_variant PACA-CA 13 77858700 77858700 single base substitution C A intron_variant PACA-CA 13 77862271 77862271 single base substitution A G intron_variant PACA-CA 13 77864345 77864345 single base substitution G A intron_variant PACA-CA 13 77869547 77869547 single base substitution G A downstream_gene_variant PACA-CA 13 77869547 77869547 single base substitution G A intron_variant PACA-CA 13 77871780 77871780 single base substitution A G intron_variant PACA-CA 13 77872302 77872302 single base substitution A G intron_variant PACA-CA 13 77872602 77872602 single base substitution C A intron_variant PACA-CA 13 77877298 77877298 single base substitution T C intron_variant PACA-CA 13 77886927 77886927 single base substitution T A intron_variant PACA-CA 13 77887044 77887044 single base substitution T C intron_variant PACA-CA 13 77889497 77889497 single base substitution C A intron_variant PACA-CA 13 77891056 77891056 deletion of <=200bp C - intron_variant PACA-CA 13 77892839 77892839 single base substitution A T intron_variant PACA-CA 13 77894600 77894600 single base substitution A G intron_variant PACA-CA 13 77903560 77903560 single base substitution C A upstream_gene_variant PAEN-AU 13 77640438 77640438 single base substitution G A intron_variant PAEN-AU 13 77705110 77705110 single base substitution T C intron_variant PAEN-AU 13 77705110 77705110 single base substitution T C upstream_gene_variant PAEN-AU 13 77709531 77709531 single base substitution G T intron_variant PAEN-AU 13 77729994 77729994 single base substitution A C intron_variant PAEN-AU 13 77761175 77761175 single base substitution G C intron_variant PAEN-AU 13 77788359 77788359 single base substitution T A intron_variant PAEN-AU 13 77789243 77789243 single base substitution C T intron_variant PAEN-AU 13 77801899 77801899 single base substitution G A intron_variant PAEN-AU 13 77834770 77834770 insertion of <=200bp - AAT intron_variant PAEN-AU 13 77873654 77873654 single base substitution T C intron_variant PAEN-AU 13 77874434 77874434 single base substitution A T intron_variant PAEN-AU 13 77895701 77895701 single base substitution C T intron_variant PAEN-IT 13 77637680 77637680 single base substitution T C intron_variant PAEN-IT 13 77645595 77645595 single base substitution G T intron_variant PAEN-IT 13 77699603 77699603 single base substitution C T missense_variant V2591I 7771G>A PAEN-IT 13 77699603 77699603 single base substitution C T missense_variant V2629I 7885G>A PAEN-IT 13 77699603 77699603 single base substitution C T missense_variant V54I 160G>A PAEN-IT 13 77699603 77699603 single base substitution C T splice_region_variant PAEN-IT 13 77699603 77699603 single base substitution C T upstream_gene_variant PAEN-IT 13 77770074 77770074 single base substitution C A intron_variant PBCA-DE 13 77620399 77620399 single base substitution T C intron_variant PBCA-DE 13 77638050 77638050 single base substitution C T intron_variant PBCA-DE 13 77645394 77645394 single base substitution G A intron_variant PBCA-DE 13 77650150 77650150 single base substitution G T intron_variant PBCA-DE 13 77656157 77656157 single base substitution G A intron_variant PBCA-DE 13 77662679 77662679 single base substitution A G downstream_gene_variant PBCA-DE 13 77662679 77662679 single base substitution A G intron_variant PBCA-DE 13 77662679 77662679 single base substitution A G upstream_gene_variant PBCA-DE 13 77667720 77667720 single base substitution A G downstream_gene_variant PBCA-DE 13 77667720 77667720 single base substitution A G intron_variant PBCA-DE 13 77693817 77693817 single base substitution A T downstream_gene_variant PBCA-DE 13 77693817 77693817 single base substitution A T intron_variant PBCA-DE 13 77693817 77693817 single base substitution A T upstream_gene_variant PBCA-DE 13 77698538 77698542 deletion of <=200bp TTTGA - intron_variant PBCA-DE 13 77698723 77698723 insertion of <=200bp - AAAGATA intron_variant PBCA-DE 13 77712518 77712518 single base substitution G A intron_variant PBCA-DE 13 77729512 77729512 single base substitution T C intron_variant PBCA-DE 13 77729512 77729512 single base substitution T C upstream_gene_variant PBCA-DE 13 77732328 77732328 single base substitution G A intron_variant PBCA-DE 13 77744398 77744398 single base substitution C T intron_variant PBCA-DE 13 77753548 77753548 single base substitution A T intron_variant PBCA-DE 13 77755480 77755480 single base substitution T A intron_variant PBCA-DE 13 77767309 77767309 single base substitution C T intron_variant PBCA-DE 13 77768887 77768887 insertion of <=200bp - A intron_variant PBCA-DE 13 77789089 77789089 insertion of <=200bp - TA intron_variant PBCA-DE 13 77791537 77791546 deletion of <=200bp AGGGTGGAAA - intron_variant PBCA-DE 13 77808207 77808207 deletion of <=200bp A - intron_variant PBCA-DE 13 77815757 77815760 deletion of <=200bp GTAT - intron_variant PBCA-DE 13 77816158 77816158 deletion of <=200bp A - intron_variant PBCA-DE 13 77839003 77839004 deletion of <=200bp CA - intron_variant PBCA-DE 13 77842134 77842134 single base substitution C T downstream_gene_variant PBCA-DE 13 77842134 77842134 single base substitution C T intron_variant PBCA-DE 13 77860019 77860019 single base substitution G C intron_variant PBCA-DE 13 77868005 77868005 single base substitution C G downstream_gene_variant PBCA-DE 13 77868005 77868005 single base substitution C G intron_variant PBCA-DE 13 77873948 77873948 single base substitution G T intron_variant PBCA-DE 13 77877469 77877472 deletion of <=200bp AAAC - intron_variant PBCA-DE 13 77882053 77882053 single base substitution C A intron_variant PBCA-DE 13 77887379 77887379 single base substitution C A intron_variant PBCA-DE 13 77890159 77890159 insertion of <=200bp - A intron_variant PBCA-DE 13 77895608 77895608 single base substitution C T intron_variant PBCA-DE 13 77896602 77896602 single base substitution C A intron_variant PRAD-CA 13 77617968 77617968 single base substitution G A downstream_gene_variant PRAD-CA 13 77680120 77680120 single base substitution T C intron_variant PRAD-CA 13 77695387 77695387 single base substitution C A exon_variant PRAD-CA 13 77695387 77695387 single base substitution C A intron_variant PRAD-CA 13 77695387 77695387 single base substitution C A upstream_gene_variant PRAD-CA 13 77698803 77698803 single base substitution A G intron_variant PRAD-CA 13 77714392 77714392 single base substitution T C downstream_gene_variant PRAD-CA 13 77714392 77714392 single base substitution T C intron_variant PRAD-CA 13 77717110 77717110 single base substitution G A downstream_gene_variant PRAD-CA 13 77717110 77717110 single base substitution G A intron_variant PRAD-CA 13 77717110 77717110 single base substitution G A upstream_gene_variant PRAD-CA 13 77736883 77736883 single base substitution A C intron_variant PRAD-CA 13 77742786 77742786 single base substitution T C splice_region_variant PRAD-CA 13 77753337 77753337 single base substitution A T intron_variant PRAD-CA 13 77758590 77758590 single base substitution C G intron_variant PRAD-CA 13 77791058 77791058 single base substitution A C intron_variant PRAD-CA 13 77793744 77793744 single base substitution T C intron_variant PRAD-CA 13 77811208 77811208 single base substitution A C intron_variant PRAD-CA 13 77829770 77829770 single base substitution G A intron_variant PRAD-CA 13 77856559 77856559 single base substitution A G intron_variant PRAD-CA 13 77860034 77860034 single base substitution C G intron_variant PRAD-CA 13 77860926 77860926 single base substitution T A intron_variant PRAD-CA 13 77881613 77881613 single base substitution T C intron_variant PRAD-CA 13 77884689 77884689 single base substitution T A intron_variant PRAD-CA 13 77885714 77885714 single base substitution G T intron_variant PRAD-UK 13 77616389 77616389 single base substitution A C downstream_gene_variant PRAD-UK 13 77623431 77623431 insertion of <=200bp - A intron_variant PRAD-UK 13 77635973 77635973 single base substitution G C intron_variant PRAD-UK 13 77638472 77638472 single base substitution C T intron_variant PRAD-UK 13 77651266 77651266 single base substitution G C intron_variant PRAD-UK 13 77665852 77665852 single base substitution T C downstream_gene_variant PRAD-UK 13 77665852 77665852 single base substitution T C intron_variant PRAD-UK 13 77665852 77665852 single base substitution T C upstream_gene_variant PRAD-UK 13 77696514 77696514 single base substitution T G intron_variant PRAD-UK 13 77696514 77696514 single base substitution T G upstream_gene_variant PRAD-UK 13 77706412 77706412 single base substitution G T intron_variant PRAD-UK 13 77708441 77708441 single base substitution G A intron_variant PRAD-UK 13 77716325 77716325 deletion of <=200bp T - downstream_gene_variant PRAD-UK 13 77716325 77716325 deletion of <=200bp T - intron_variant PRAD-UK 13 77716325 77716325 deletion of <=200bp T - upstream_gene_variant PRAD-UK 13 77739362 77739366 deletion of <=200bp GAAAC - intron_variant PRAD-UK 13 77742482 77742482 single base substitution A T intron_variant PRAD-UK 13 77754838 77754838 single base substitution C G intron_variant PRAD-UK 13 77772933 77772933 single base substitution C T intron_variant PRAD-UK 13 77781638 77781638 insertion of <=200bp - A intron_variant PRAD-UK 13 77784019 77784019 single base substitution G A intron_variant PRAD-UK 13 77805793 77805793 single base substitution G C intron_variant PRAD-UK 13 77816081 77816081 single base substitution T A intron_variant PRAD-UK 13 77819577 77819577 single base substitution C T intron_variant PRAD-UK 13 77822126 77822126 single base substitution T C intron_variant PRAD-UK 13 77823032 77823032 single base substitution G A intron_variant PRAD-UK 13 77826765 77826765 single base substitution C T intron_variant PRAD-UK 13 77828313 77828313 single base substitution G C intron_variant PRAD-UK 13 77847109 77847109 single base substitution G T intron_variant PRAD-UK 13 77848324 77848324 single base substitution A G intron_variant PRAD-UK 13 77848324 77848324 single base substitution A G upstream_gene_variant PRAD-UK 13 77853014 77853014 single base substitution T A 5_prime_UTR_variant PRAD-UK 13 77853014 77853014 single base substitution T A missense_variant E171D 513A>T PRAD-UK 13 77853014 77853014 single base substitution T A missense_variant E209D 627A>T PRAD-UK 13 77853035 77853035 single base substitution A T 5_prime_UTR_variant PRAD-UK 13 77853035 77853035 single base substitution A T synonymous_variant V164V 492T>A PRAD-UK 13 77853035 77853035 single base substitution A T synonymous_variant V202V 606T>A PRAD-UK 13 77861519 77861555 multiple base substitution (>=2bp and <=200bp) CATGTTGGCCAGGCTGTTCTCAAACTCCTGACCTCAG CGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTC intron_variant PRAD-UK 13 77866005 77866005 single base substitution G A downstream_gene_variant PRAD-UK 13 77866005 77866005 single base substitution G A intron_variant PRAD-UK 13 77883158 77883158 single base substitution A T intron_variant PRAD-UK 13 77884338 77884338 single base substitution C A intron_variant PRAD-UK 13 77893184 77893184 deletion of <=200bp C - intron_variant PRAD-UK 13 77893324 77893324 single base substitution T A intron_variant PRAD-US 13 77642776 77642776 single base substitution T A missense_variant Y3994F 11981A>T PRAD-US 13 77642776 77642776 single base substitution T A missense_variant Y4032F 12095A>T PRAD-US 13 77642776 77642776 single base substitution T A missense_variant Y414F 1241A>T PRAD-US 13 77664342 77664342 single base substitution C A downstream_gene_variant PRAD-US 13 77664342 77664342 single base substitution C A missense_variant R3437I 10310G>T PRAD-US 13 77664342 77664342 single base substitution C A missense_variant R3475I 10424G>T PRAD-US 13 77664342 77664342 single base substitution C A upstream_gene_variant PRAD-US 13 77718680 77718680 single base substitution C T 5_prime_UTR_variant PRAD-US 13 77718680 77718680 single base substitution C T exon_variant PRAD-US 13 77718680 77718680 single base substitution C T missense_variant M2363I 7089G>A PRAD-US 13 77718680 77718680 single base substitution C T missense_variant M2401I 7203G>A PRAD-US 13 77718680 77718680 single base substitution C T upstream_gene_variant PRAD-US 13 77765887 77765887 single base substitution C T 5_prime_UTR_variant PRAD-US 13 77765887 77765887 single base substitution C T missense_variant A1295T 3883G>A PRAD-US 13 77765887 77765887 single base substitution C T missense_variant A1333T 3997G>A PRAD-US 13 77844149 77844149 deletion of <=200bp T - 5_prime_UTR_variant PRAD-US 13 77844149 77844149 deletion of <=200bp T - downstream_gene_variant PRAD-US 13 77844149 77844149 deletion of <=200bp T - frameshift_variant K375 PRAD-US 13 77844149 77844149 deletion of <=200bp T - frameshift_variant K413 PRAD-US 13 77853046 77853046 single base substitution T C missense_variant I161V 481A>G PRAD-US 13 77853046 77853046 single base substitution T C missense_variant I199V 595A>G PRAD-US 13 77853046 77853046 single base substitution T C splice_region_variant READ-US 13 77671669 77671669 deletion of <=200bp T - downstream_gene_variant READ-US 13 77671669 77671669 deletion of <=200bp T - exon_variant READ-US 13 77671669 77671669 deletion of <=200bp T - frameshift_variant K3169 READ-US 13 77671669 77671669 deletion of <=200bp T - frameshift_variant K3207 READ-US 13 77748566 77748566 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant READ-US 13 77748566 77748566 single base substitution T A missense_variant D1806V 5417A>T READ-US 13 77748566 77748566 single base substitution T A missense_variant D1844V 5531A>T READ-US 13 77780955 77780955 single base substitution C T 5_prime_UTR_variant READ-US 13 77780955 77780955 single base substitution C T missense_variant R1103Q 3308G>A READ-US 13 77780955 77780955 single base substitution C T missense_variant R1141Q 3422G>A READ-US 13 77852892 77852892 single base substitution C T splice_donor_variant RECA-EU 13 77620242 77620242 single base substitution G C intron_variant RECA-EU 13 77625739 77625739 single base substitution T C intron_variant RECA-EU 13 77632418 77632418 single base substitution G A stop_gained Q4384* 13150C>T RECA-EU 13 77632418 77632418 single base substitution G A stop_gained Q4422* 13264C>T RECA-EU 13 77632418 77632418 single base substitution G A stop_gained Q804* 2410C>T RECA-EU 13 77636212 77636212 single base substitution A G intron_variant RECA-EU 13 77637073 77637073 single base substitution C T intron_variant RECA-EU 13 77639662 77639662 single base substitution A G intron_variant RECA-EU 13 77656368 77656368 single base substitution T A intron_variant RECA-EU 13 77658410 77658410 single base substitution A T intron_variant RECA-EU 13 77682237 77682237 single base substitution G C intron_variant RECA-EU 13 77692101 77692101 single base substitution C A downstream_gene_variant RECA-EU 13 77692101 77692101 single base substitution C A intron_variant RECA-EU 13 77710444 77710444 single base substitution G A intron_variant RECA-EU 13 77727016 77727016 single base substitution C T intron_variant RECA-EU 13 77727016 77727016 single base substitution C T upstream_gene_variant RECA-EU 13 77727267 77727267 single base substitution G T intron_variant RECA-EU 13 77727267 77727267 single base substitution G T upstream_gene_variant RECA-EU 13 77729532 77729532 single base substitution A G intron_variant RECA-EU 13 77729532 77729532 single base substitution A G upstream_gene_variant RECA-EU 13 77746082 77746082 single base substitution C A intron_variant RECA-EU 13 77754860 77754860 single base substitution G T intron_variant RECA-EU 13 77756475 77756475 single base substitution C T intron_variant RECA-EU 13 77765097 77765097 single base substitution T C intron_variant RECA-EU 13 77771007 77771007 single base substitution T C intron_variant RECA-EU 13 77777245 77777245 single base substitution T A intron_variant RECA-EU 13 77795950 77795950 single base substitution C A intron_variant RECA-EU 13 77809740 77809740 single base substitution A G intron_variant RECA-EU 13 77851503 77851503 single base substitution C A intron_variant RECA-EU 13 77851503 77851503 single base substitution C A upstream_gene_variant RECA-EU 13 77859876 77859876 single base substitution A T intron_variant RECA-EU 13 77859883 77859883 single base substitution T A intron_variant RECA-EU 13 77860002 77860002 single base substitution A G intron_variant RECA-EU 13 77875583 77875583 single base substitution A C intron_variant RECA-EU 13 77883418 77883418 single base substitution G A intron_variant RECA-EU 13 77889553 77889553 single base substitution C G intron_variant RECA-EU 13 77892448 77892448 single base substitution C G intron_variant RECA-EU 13 77901495 77901495 single base substitution G A upstream_gene_variant RECA-EU 13 77905562 77905562 single base substitution G A upstream_gene_variant SKCA-BR 13 77614206 77614206 single base substitution A T downstream_gene_variant SKCA-BR 13 77615278 77615278 single base substitution G A downstream_gene_variant SKCA-BR 13 77616527 77616527 single base substitution C T downstream_gene_variant SKCA-BR 13 77619987 77619987 single base substitution G A intron_variant SKCA-BR 13 77621415 77621415 single base substitution G A intron_variant SKCA-BR 13 77625153 77625153 single base substitution C T missense_variant E1016K 3046G>A SKCA-BR 13 77625153 77625153 single base substitution C T missense_variant E4596K 13786G>A SKCA-BR 13 77625153 77625153 single base substitution C T missense_variant E4634K 13900G>A SKCA-BR 13 77630757 77630757 single base substitution T G intron_variant SKCA-BR 13 77631084 77631084 single base substitution G A intron_variant SKCA-BR 13 77638325 77638325 single base substitution C T intron_variant SKCA-BR 13 77643118 77643118 single base substitution T G intron_variant SKCA-BR 13 77646002 77646002 single base substitution G A intron_variant SKCA-BR 13 77647249 77647249 single base substitution T C intron_variant SKCA-BR 13 77647378 77647378 single base substitution G A intron_variant SKCA-BR 13 77655122 77655122 single base substitution T A intron_variant SKCA-BR 13 77658838 77658838 single base substitution C T intron_variant SKCA-BR 13 77662081 77662081 single base substitution G A intron_variant SKCA-BR 13 77662081 77662081 single base substitution G A upstream_gene_variant SKCA-BR 13 77669509 77669509 single base substitution G A downstream_gene_variant SKCA-BR 13 77669509 77669509 single base substitution G A intron_variant SKCA-BR 13 77669509 77669509 single base substitution G A synonymous_variant L3357L 10069C>T SKCA-BR 13 77669509 77669509 single base substitution G A synonymous_variant L3395L 10183C>T SKCA-BR 13 77669583 77669583 single base substitution G A downstream_gene_variant SKCA-BR 13 77669583 77669583 single base substitution G A intron_variant SKCA-BR 13 77669583 77669583 single base substitution G A missense_variant P3332L 9995C>T SKCA-BR 13 77669583 77669583 single base substitution G A missense_variant P3370L 10109C>T SKCA-BR 13 77671487 77671487 single base substitution T C downstream_gene_variant SKCA-BR 13 77671487 77671487 single base substitution T C intron_variant SKCA-BR 13 77672012 77672012 single base substitution T G downstream_gene_variant SKCA-BR 13 77672012 77672012 single base substitution T G missense_variant I3055L 9163A>C SKCA-BR 13 77672012 77672012 single base substitution T G missense_variant I3093L 9277A>C SKCA-BR 13 77672012 77672012 single base substitution T G upstream_gene_variant SKCA-BR 13 77673117 77673117 single base substitution T G exon_variant SKCA-BR 13 77673117 77673117 single base substitution T G missense_variant K209N 627A>C SKCA-BR 13 77673117 77673117 single base substitution T G missense_variant K2686N 8058A>C SKCA-BR 13 77673117 77673117 single base substitution T G missense_variant K2724N 8172A>C SKCA-BR 13 77673117 77673117 single base substitution T G upstream_gene_variant SKCA-BR 13 77676368 77676368 single base substitution G A intron_variant SKCA-BR 13 77676368 77676368 single base substitution G A upstream_gene_variant SKCA-BR 13 77683706 77683706 single base substitution G A intron_variant SKCA-BR 13 77684926 77684926 single base substitution C T intron_variant SKCA-BR 13 77684949 77684949 single base substitution C T intron_variant SKCA-BR 13 77693631 77693631 single base substitution G A downstream_gene_variant SKCA-BR 13 77693631 77693631 single base substitution G A intron_variant SKCA-BR 13 77693631 77693631 single base substitution G A upstream_gene_variant SKCA-BR 13 77695135 77695135 single base substitution G A downstream_gene_variant SKCA-BR 13 77695135 77695135 single base substitution G A intron_variant SKCA-BR 13 77695135 77695135 single base substitution G A upstream_gene_variant SKCA-BR 13 77695423 77695423 single base substitution G A exon_variant SKCA-BR 13 77695423 77695423 single base substitution G A intron_variant SKCA-BR 13 77695423 77695423 single base substitution G A upstream_gene_variant SKCA-BR 13 77698541 77698541 single base substitution G A intron_variant SKCA-BR 13 77698804 77698804 single base substitution T C intron_variant SKCA-BR 13 77701586 77701586 single base substitution A C intron_variant SKCA-BR 13 77701586 77701586 single base substitution A C upstream_gene_variant SKCA-BR 13 77708282 77708282 single base substitution T G intron_variant SKCA-BR 13 77709990 77709990 single base substitution G A intron_variant SKCA-BR 13 77710735 77710735 single base substitution T A intron_variant SKCA-BR 13 77710888 77710888 single base substitution G A intron_variant SKCA-BR 13 77712310 77712310 single base substitution C T intron_variant SKCA-BR 13 77712993 77712993 single base substitution G A intron_variant SKCA-BR 13 77713624 77713624 single base substitution G A downstream_gene_variant SKCA-BR 13 77713624 77713624 single base substitution G A intron_variant SKCA-BR 13 77714606 77714606 single base substitution C T downstream_gene_variant SKCA-BR 13 77714606 77714606 single base substitution C T intron_variant SKCA-BR 13 77714622 77714622 single base substitution A C downstream_gene_variant SKCA-BR 13 77714622 77714622 single base substitution A C intron_variant SKCA-BR 13 77727243 77727243 single base substitution C T intron_variant SKCA-BR 13 77727243 77727243 single base substitution C T upstream_gene_variant SKCA-BR 13 77730393 77730393 single base substitution A G intron_variant SKCA-BR 13 77731277 77731277 single base substitution G A intron_variant SKCA-BR 13 77740439 77740439 single base substitution A T intron_variant SKCA-BR 13 77743842 77743842 single base substitution G A 5_prime_UTR_variant SKCA-BR 13 77743842 77743842 single base substitution G A synonymous_variant D1896D 5688C>T SKCA-BR 13 77743842 77743842 single base substitution G A synonymous_variant D1934D 5802C>T SKCA-BR 13 77747729 77747729 single base substitution G A intron_variant SKCA-BR 13 77751610 77751610 single base substitution G A intron_variant SKCA-BR 13 77752301 77752301 single base substitution C T intron_variant SKCA-BR 13 77754338 77754338 single base substitution G A 5_prime_UTR_variant SKCA-BR 13 77754338 77754338 single base substitution G A missense_variant S1648F 4943C>T SKCA-BR 13 77754338 77754338 single base substitution G A missense_variant S1686F 5057C>T SKCA-BR 13 77761214 77761214 single base substitution G A intron_variant SKCA-BR 13 77773600 77773600 single base substitution A G intron_variant SKCA-BR 13 77774725 77774725 single base substitution T A intron_variant SKCA-BR 13 77777498 77777498 single base substitution G A intron_variant SKCA-BR 13 77779079 77779079 single base substitution T A intron_variant SKCA-BR 13 77782092 77782092 single base substitution G C intron_variant SKCA-BR 13 77786848 77786848 single base substitution C T intron_variant SKCA-BR 13 77787456 77787456 single base substitution G A intron_variant SKCA-BR 13 77787859 77787859 single base substitution C T intron_variant SKCA-BR 13 77789521 77789521 single base substitution G A intron_variant SKCA-BR 13 77792673 77792673 single base substitution G A intron_variant SKCA-BR 13 77793625 77793625 single base substitution G A intron_variant SKCA-BR 13 77794833 77794833 single base substitution G A intron_variant SKCA-BR 13 77795349 77795349 single base substitution G A intron_variant SKCA-BR 13 77796928 77796928 single base substitution T C intron_variant SKCA-BR 13 77800999 77800999 single base substitution A C intron_variant SKCA-BR 13 77803050 77803050 single base substitution G A intron_variant SKCA-BR 13 77805515 77805515 single base substitution G A intron_variant SKCA-BR 13 77805911 77805911 single base substitution A C intron_variant SKCA-BR 13 77805970 77805970 single base substitution G C intron_variant SKCA-BR 13 77806884 77806884 single base substitution G A intron_variant SKCA-BR 13 77807262 77807262 single base substitution C A intron_variant SKCA-BR 13 77821182 77821182 single base substitution C T intron_variant SKCA-BR 13 77825185 77825185 single base substitution G A intron_variant SKCA-BR 13 77826251 77826251 single base substitution A G intron_variant SKCA-BR 13 77835908 77835908 single base substitution T A intron_variant SKCA-BR 13 77835937 77835937 single base substitution T G intron_variant SKCA-BR 13 77835964 77835964 single base substitution G A intron_variant SKCA-BR 13 77838311 77838311 single base substitution A G intron_variant SKCA-BR 13 77841159 77841159 single base substitution T A downstream_gene_variant SKCA-BR 13 77841159 77841159 single base substitution T A intron_variant SKCA-BR 13 77841162 77841162 single base substitution C A downstream_gene_variant SKCA-BR 13 77841162 77841162 single base substitution C A intron_variant SKCA-BR 13 77847906 77847906 single base substitution G A intron_variant SKCA-BR 13 77847906 77847906 single base substitution G A upstream_gene_variant SKCA-BR 13 77853403 77853403 single base substitution T G intron_variant SKCA-BR 13 77853445 77853445 single base substitution T A intron_variant SKCA-BR 13 77853540 77853540 single base substitution G A intron_variant SKCA-BR 13 77854694 77854694 single base substitution G A intron_variant SKCA-BR 13 77860924 77860924 single base substitution A T intron_variant SKCA-BR 13 77860924 77860926 deletion of <=200bp AAT - intron_variant SKCA-BR 13 77861198 77861198 single base substitution G A intron_variant SKCA-BR 13 77861447 77861447 single base substitution G A intron_variant SKCA-BR 13 77868239 77868239 insertion of <=200bp - CTATATA downstream_gene_variant SKCA-BR 13 77868239 77868239 insertion of <=200bp - CTATATA intron_variant SKCA-BR 13 77868246 77868246 insertion of <=200bp - TATATATATATATATATATATATAC downstream_gene_variant SKCA-BR 13 77868246 77868246 insertion of <=200bp - TATATATATATATATATATATATAC intron_variant SKCA-BR 13 77868264 77868264 insertion of <=200bp - TATATATATATATAC downstream_gene_variant SKCA-BR 13 77868264 77868264 insertion of <=200bp - TATATATATATATAC intron_variant SKCA-BR 13 77868272 77868272 single base substitution T C downstream_gene_variant SKCA-BR 13 77868272 77868272 single base substitution T C intron_variant SKCA-BR 13 77868278 77868278 single base substitution C T downstream_gene_variant SKCA-BR 13 77868278 77868278 single base substitution C T intron_variant SKCA-BR 13 77868915 77868915 single base substitution G A downstream_gene_variant SKCA-BR 13 77868915 77868915 single base substitution G A intron_variant SKCA-BR 13 77877325 77877325 single base substitution G A intron_variant SKCA-BR 13 77877782 77877782 single base substitution G A intron_variant SKCA-BR 13 77877789 77877789 single base substitution G A intron_variant SKCA-BR 13 77884768 77884768 single base substitution G A intron_variant SKCA-BR 13 77890029 77890030 deletion of <=200bp CA - intron_variant SKCA-BR 13 77895645 77895645 single base substitution T C intron_variant SKCA-BR 13 77903379 77903379 single base substitution G A upstream_gene_variant SKCA-BR 13 77903380 77903380 single base substitution G A upstream_gene_variant SKCA-BR 13 77904724 77904724 single base substitution T G upstream_gene_variant SKCA-BR 13 77905902 77905902 single base substitution C T upstream_gene_variant SKCM-US 13 77619581 77619581 single base substitution C A missense_variant V1039F 3115G>T SKCM-US 13 77619581 77619581 single base substitution C A missense_variant V4619F 13855G>T SKCM-US 13 77619581 77619581 single base substitution C A missense_variant V4657F 13969G>T SKCM-US 13 77635390 77635390 single base substitution C T missense_variant G4279D 12836G>A SKCM-US 13 77635390 77635390 single base substitution C T missense_variant G4317D 12950G>A SKCM-US 13 77635390 77635390 single base substitution C T missense_variant G699D 2096G>A SKCM-US 13 77636771 77636771 single base substitution G A missense_variant S4207L 12620C>T SKCM-US 13 77636771 77636771 single base substitution G A missense_variant S4245L 12734C>T SKCM-US 13 77636771 77636771 single base substitution G A missense_variant S627L 1880C>T SKCM-US 13 77636804 77636804 single base substitution A G missense_variant V4196A 12587T>C SKCM-US 13 77636804 77636804 single base substitution A G missense_variant V4234A 12701T>C SKCM-US 13 77636804 77636804 single base substitution A G missense_variant V616A 1847T>C SKCM-US 13 77638818 77638818 single base substitution T C missense_variant T4164A 12490A>G SKCM-US 13 77638818 77638818 single base substitution T C missense_variant T4202A 12604A>G SKCM-US 13 77638818 77638818 single base substitution T C missense_variant T584A 1750A>G SKCM-US 13 77641724 77641724 single base substitution G A synonymous_variant F4111F 12333C>T SKCM-US 13 77641724 77641724 single base substitution G A synonymous_variant F4149F 12447C>T SKCM-US 13 77641724 77641724 single base substitution G A synonymous_variant F531F 1593C>T SKCM-US 13 77642739 77642739 single base substitution G A synonymous_variant F4006F 12018C>T SKCM-US 13 77642739 77642739 single base substitution G A synonymous_variant F4044F 12132C>T SKCM-US 13 77642739 77642739 single base substitution G A synonymous_variant F426F 1278C>T SKCM-US 13 77642817 77642817 single base substitution A G synonymous_variant S3980S 11940T>C SKCM-US 13 77642817 77642817 single base substitution A G synonymous_variant S400S 1200T>C SKCM-US 13 77642817 77642817 single base substitution A G synonymous_variant S4018S 12054T>C SKCM-US 13 77642939 77642939 single base substitution G A missense_variant R360C 1078C>T SKCM-US 13 77642939 77642939 single base substitution G A missense_variant R3940C 11818C>T SKCM-US 13 77642939 77642939 single base substitution G A missense_variant R3978C 11932C>T SKCM-US 13 77651353 77651353 single base substitution G A missense_variant S270L 809C>T SKCM-US 13 77651353 77651353 single base substitution G A missense_variant S3847L 11540C>T SKCM-US 13 77651353 77651353 single base substitution G A missense_variant S3885L 11654C>T SKCM-US 13 77651477 77651477 single base substitution G A missense_variant P229S 685C>T SKCM-US 13 77651477 77651477 single base substitution G A missense_variant P3806S 11416C>T SKCM-US 13 77651477 77651477 single base substitution G A missense_variant P3844S 11530C>T SKCM-US 13 77655567 77655567 single base substitution G A missense_variant L190F 568C>T SKCM-US 13 77655567 77655567 single base substitution G A missense_variant L3767F 11299C>T SKCM-US 13 77655567 77655567 single base substitution G A missense_variant L3805F 11413C>T SKCM-US 13 77655574 77655574 single base substitution G A synonymous_variant S187S 561C>T SKCM-US 13 77655574 77655574 single base substitution G A synonymous_variant S3764S 11292C>T SKCM-US 13 77655574 77655574 single base substitution G A synonymous_variant S3802S 11406C>T SKCM-US 13 77656067 77656067 single base substitution G A missense_variant H3662Y 10984C>T SKCM-US 13 77656067 77656067 single base substitution G A missense_variant H3700Y 11098C>T SKCM-US 13 77656067 77656067 single base substitution G A missense_variant H85Y 253C>T SKCM-US 13 77661649 77661649 single base substitution T C 5_prime_UTR_variant SKCM-US 13 77661649 77661649 single base substitution T C synonymous_variant E3577E 10731A>G SKCM-US 13 77661649 77661649 single base substitution T C synonymous_variant E3615E 10845A>G SKCM-US 13 77663163 77663163 single base substitution A G downstream_gene_variant SKCM-US 13 77663163 77663163 single base substitution A G missense_variant V3472A 10415T>C SKCM-US 13 77663163 77663163 single base substitution A G missense_variant V3510A 10529T>C SKCM-US 13 77663163 77663163 single base substitution A G upstream_gene_variant SKCM-US 13 77671818 77671818 single base substitution G A downstream_gene_variant SKCM-US 13 77671818 77671818 single base substitution G A synonymous_variant P3119P 9357C>T SKCM-US 13 77671818 77671818 single base substitution G A synonymous_variant P3157P 9471C>T SKCM-US 13 77671818 77671818 single base substitution G A upstream_gene_variant SKCM-US 13 77671825 77671825 single base substitution G A downstream_gene_variant SKCM-US 13 77671825 77671825 single base substitution G A missense_variant P3117L 9350C>T SKCM-US 13 77671825 77671825 single base substitution G A missense_variant P3155L 9464C>T SKCM-US 13 77671825 77671825 single base substitution G A upstream_gene_variant SKCM-US 13 77671906 77671906 single base substitution G A downstream_gene_variant SKCM-US 13 77671906 77671906 single base substitution G A missense_variant P3090L 9269C>T SKCM-US 13 77671906 77671906 single base substitution G A missense_variant P3128L 9383C>T SKCM-US 13 77671906 77671906 single base substitution G A upstream_gene_variant SKCM-US 13 77672094 77672094 deletion of <=200bp A - downstream_gene_variant SKCM-US 13 77672094 77672094 deletion of <=200bp A - frameshift_variant H3027 SKCM-US 13 77672094 77672094 deletion of <=200bp A - frameshift_variant H3065 SKCM-US 13 77672094 77672094 deletion of <=200bp A - upstream_gene_variant SKCM-US 13 77672117 77672117 single base substitution G A downstream_gene_variant SKCM-US 13 77672117 77672117 single base substitution G A missense_variant H3020Y 9058C>T SKCM-US 13 77672117 77672117 single base substitution G A missense_variant H3058Y 9172C>T SKCM-US 13 77672117 77672117 single base substitution G A upstream_gene_variant SKCM-US 13 77672205 77672205 single base substitution G A downstream_gene_variant SKCM-US 13 77672205 77672205 single base substitution G A exon_variant SKCM-US 13 77672205 77672205 single base substitution G A stop_gained R513* 1537C>T SKCM-US 13 77672205 77672205 single base substitution G A synonymous_variant A2990A 8970C>T SKCM-US 13 77672205 77672205 single base substitution G A synonymous_variant A3028A 9084C>T SKCM-US 13 77672205 77672205 single base substitution G A upstream_gene_variant SKCM-US 13 77672272 77672272 single base substitution A G downstream_gene_variant SKCM-US 13 77672272 77672272 single base substitution A G exon_variant SKCM-US 13 77672272 77672272 single base substitution A G missense_variant F2968S 8903T>C SKCM-US 13 77672272 77672272 single base substitution A G missense_variant F3006S 9017T>C SKCM-US 13 77672272 77672272 single base substitution A G synonymous_variant F490F 1470T>C SKCM-US 13 77672272 77672272 single base substitution A G upstream_gene_variant SKCM-US 13 77672557 77672557 single base substitution G A downstream_gene_variant SKCM-US 13 77672557 77672557 single base substitution G A exon_variant SKCM-US 13 77672557 77672557 single base substitution G A missense_variant S2873F 8618C>T SKCM-US 13 77672557 77672557 single base substitution G A missense_variant S2911F 8732C>T SKCM-US 13 77672557 77672557 single base substitution G A missense_variant S396F 1187C>T SKCM-US 13 77672557 77672557 single base substitution G A upstream_gene_variant SKCM-US 13 77672656 77672656 single base substitution G A downstream_gene_variant SKCM-US 13 77672656 77672656 single base substitution G A exon_variant SKCM-US 13 77672656 77672656 single base substitution G A missense_variant P2840L 8519C>T SKCM-US 13 77672656 77672656 single base substitution G A missense_variant P2878L 8633C>T SKCM-US 13 77672656 77672656 single base substitution G A missense_variant P363L 1088C>T SKCM-US 13 77672656 77672656 single base substitution G A upstream_gene_variant SKCM-US 13 77672695 77672695 single base substitution G A downstream_gene_variant SKCM-US 13 77672695 77672695 single base substitution G A exon_variant SKCM-US 13 77672695 77672695 single base substitution G A missense_variant P2827L 8480C>T SKCM-US 13 77672695 77672695 single base substitution G A missense_variant P2865L 8594C>T SKCM-US 13 77672695 77672695 single base substitution G A missense_variant P350L 1049C>T SKCM-US 13 77672695 77672695 single base substitution G A upstream_gene_variant SKCM-US 13 77673139 77673139 single base substitution C T exon_variant SKCM-US 13 77673139 77673139 single base substitution C T missense_variant G202E 605G>A SKCM-US 13 77673139 77673139 single base substitution C T missense_variant G2679E 8036G>A SKCM-US 13 77673139 77673139 single base substitution C T missense_variant G2717E 8150G>A SKCM-US 13 77673139 77673139 single base substitution C T upstream_gene_variant SKCM-US 13 77700588 77700588 single base substitution G A exon_variant SKCM-US 13 77700588 77700588 single base substitution G A synonymous_variant F2545F 7635C>T SKCM-US 13 77700588 77700588 single base substitution G A synonymous_variant F2583F 7749C>T SKCM-US 13 77700588 77700588 single base substitution G A synonymous_variant F8F 24C>T SKCM-US 13 77700588 77700588 single base substitution G A upstream_gene_variant SKCM-US 13 77718653 77718653 single base substitution A G 5_prime_UTR_variant SKCM-US 13 77718653 77718653 single base substitution A G exon_variant SKCM-US 13 77718653 77718653 single base substitution A G synonymous_variant T2372T 7116T>C SKCM-US 13 77718653 77718653 single base substitution A G synonymous_variant T2410T 7230T>C SKCM-US 13 77718653 77718653 single base substitution A G upstream_gene_variant SKCM-US 13 77725060 77725060 single base substitution A T 5_prime_UTR_variant SKCM-US 13 77725060 77725060 single base substitution A T missense_variant S2276T 6826T>A SKCM-US 13 77725060 77725060 single base substitution A T missense_variant S2314T 6940T>A SKCM-US 13 77725060 77725060 single base substitution A T upstream_gene_variant SKCM-US 13 77730262 77730262 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 13 77730262 77730262 single base substitution A G synonymous_variant G2244G 6732T>C SKCM-US 13 77730262 77730262 single base substitution A G synonymous_variant G2282G 6846T>C SKCM-US 13 77730270 77730270 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 13 77730270 77730270 single base substitution G A missense_variant R2242C 6724C>T SKCM-US 13 77730270 77730270 single base substitution G A missense_variant R2280C 6838C>T SKCM-US 13 77742671 77742671 single base substitution G T 5_prime_UTR_variant SKCM-US 13 77742671 77742671 single base substitution G T synonymous_variant T1964T 5892C>A SKCM-US 13 77742671 77742671 single base substitution G T synonymous_variant T2002T 6006C>A SKCM-US 13 77742742 77742742 single base substitution G A 5_prime_UTR_variant SKCM-US 13 77742742 77742742 single base substitution G A missense_variant P1941S 5821C>T SKCM-US 13 77742742 77742742 single base substitution G A missense_variant P1979S 5935C>T SKCM-US 13 77745767 77745767 single base substitution C T missense_variant S1847N 5540G>A SKCM-US 13 77745767 77745767 single base substitution C T missense_variant S1885N 5654G>A SKCM-US 13 77745767 77745767 single base substitution C T splice_region_variant SKCM-US 13 77748454 77748454 single base substitution G A 5_prime_UTR_variant SKCM-US 13 77748454 77748454 single base substitution G A synonymous_variant L1843L 5529C>T SKCM-US 13 77748454 77748454 single base substitution G A synonymous_variant L1881L 5643C>T SKCM-US 13 77751993 77751993 single base substitution G A 5_prime_UTR_variant SKCM-US 13 77751993 77751993 single base substitution G A missense_variant P1706S 5116C>T SKCM-US 13 77751993 77751993 single base substitution G A missense_variant P1744S 5230C>T SKCM-US 13 77754364 77754364 single base substitution C T 5_prime_UTR_variant SKCM-US 13 77754364 77754364 single base substitution C T synonymous_variant L1639L 4917G>A SKCM-US 13 77754364 77754364 single base substitution C T synonymous_variant L1677L 5031G>A SKCM-US 13 77779516 77779516 single base substitution G A missense_variant H1202Y 3604C>T SKCM-US 13 77779516 77779516 single base substitution G A missense_variant H1240Y 3718C>T SKCM-US 13 77779516 77779516 single base substitution G A splice_region_variant SKCM-US 13 77779699 77779699 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 13 77779699 77779699 single base substitution T C synonymous_variant L1170L 3510A>G SKCM-US 13 77779699 77779699 single base substitution T C synonymous_variant L1208L 3624A>G SKCM-US 13 77785366 77785366 single base substitution A T 5_prime_UTR_variant SKCM-US 13 77785366 77785366 single base substitution A T missense_variant S1080T 3238T>A SKCM-US 13 77785366 77785366 single base substitution A T missense_variant S1118T 3352T>A SKCM-US 13 77786261 77786261 single base substitution G A 5_prime_UTR_variant SKCM-US 13 77786261 77786261 single base substitution G A missense_variant P1031L 3092C>T SKCM-US 13 77786261 77786261 single base substitution G A missense_variant P993L 2978C>T SKCM-US 13 77799638 77799638 single base substitution G A 5_prime_UTR_variant SKCM-US 13 77799638 77799638 single base substitution G A missense_variant P892L 2675C>T SKCM-US 13 77799638 77799638 single base substitution G A missense_variant P930L 2789C>T SKCM-US 13 77799640 77799640 single base substitution G A 5_prime_UTR_variant SKCM-US 13 77799640 77799640 single base substitution G A synonymous_variant Y891Y 2673C>T SKCM-US 13 77799640 77799640 single base substitution G A synonymous_variant Y929Y 2787C>T SKCM-US 13 77807327 77807327 single base substitution G A 5_prime_UTR_variant SKCM-US 13 77807327 77807327 single base substitution G A missense_variant P863S 2587C>T SKCM-US 13 77807327 77807327 single base substitution G A missense_variant P901S 2701C>T SKCM-US 13 77817289 77817289 single base substitution G A 5_prime_UTR_variant SKCM-US 13 77817289 77817289 single base substitution G A missense_variant P807L 2420C>T SKCM-US 13 77817289 77817289 single base substitution G A missense_variant P845L 2534C>T SKCM-US 13 77835375 77835375 single base substitution G A 5_prime_UTR_variant SKCM-US 13 77835375 77835375 single base substitution G A missense_variant L557F 1669C>T SKCM-US 13 77835375 77835375 single base substitution G A missense_variant L595F 1783C>T SKCM-US 13 77844167 77844167 single base substitution C T 5_prime_UTR_variant SKCM-US 13 77844167 77844167 single base substitution C T exon_variant SKCM-US 13 77844167 77844167 single base substitution C T missense_variant R369K 1106G>A SKCM-US 13 77844167 77844167 single base substitution C T missense_variant R407K 1220G>A SKCM-US 13 77844493 77844493 single base substitution G A 5_prime_UTR_variant SKCM-US 13 77844493 77844493 single base substitution G A exon_variant SKCM-US 13 77844493 77844493 single base substitution G A missense_variant L338F 1012C>T SKCM-US 13 77844493 77844493 single base substitution G A missense_variant L376F 1126C>T SKCM-US 13 77852997 77852997 single base substitution C T 5_prime_UTR_variant SKCM-US 13 77852997 77852997 single base substitution C T missense_variant R177Q 530G>A SKCM-US 13 77852997 77852997 single base substitution C T missense_variant R215Q 644G>A SKCM-US 13 77862314 77862314 single base substitution G A 5_prime_UTR_variant SKCM-US 13 77862314 77862314 single base substitution G A synonymous_variant P154P 462C>T SKCM-US 13 77862314 77862314 single base substitution G A synonymous_variant P192P 576C>T STAD-US 13 77625209 77625209 single base substitution T C missense_variant H4577R 13730A>G STAD-US 13 77625209 77625209 single base substitution T C missense_variant H4615R 13844A>G STAD-US 13 77625209 77625209 single base substitution T C missense_variant H997R 2990A>G STAD-US 13 77632491 77632491 single base substitution G A synonymous_variant C4359C 13077C>T STAD-US 13 77632491 77632491 single base substitution G A synonymous_variant C4397C 13191C>T STAD-US 13 77632491 77632491 single base substitution G A synonymous_variant C779C 2337C>T STAD-US 13 77632536 77632536 single base substitution G A synonymous_variant Y4344Y 13032C>T STAD-US 13 77632536 77632536 single base substitution G A synonymous_variant Y4382Y 13146C>T STAD-US 13 77632536 77632536 single base substitution G A synonymous_variant Y764Y 2292C>T STAD-US 13 77635848 77635848 single base substitution G A synonymous_variant D4246D 12738C>T STAD-US 13 77635848 77635848 single base substitution G A synonymous_variant D4284D 12852C>T STAD-US 13 77635848 77635848 single base substitution G A synonymous_variant D666D 1998C>T STAD-US 13 77635873 77635873 single base substitution T G missense_variant N4238T 12713A>C STAD-US 13 77635873 77635873 single base substitution T G missense_variant N4276T 12827A>C STAD-US 13 77635873 77635873 single base substitution T G missense_variant N658T 1973A>C STAD-US 13 77636771 77636771 single base substitution G A missense_variant S4207L 12620C>T STAD-US 13 77636771 77636771 single base substitution G A missense_variant S4245L 12734C>T STAD-US 13 77636771 77636771 single base substitution G A missense_variant S627L 1880C>T STAD-US 13 77636799 77636799 single base substitution C G missense_variant D4198H 12592G>C STAD-US 13 77636799 77636799 single base substitution C G missense_variant D4236H 12706G>C STAD-US 13 77636799 77636799 single base substitution C G missense_variant D618H 1852G>C STAD-US 13 77638832 77638832 insertion of <=200bp - T frameshift_variant N4159K? STAD-US 13 77638832 77638832 insertion of <=200bp - T frameshift_variant N4197K? STAD-US 13 77638832 77638832 insertion of <=200bp - T frameshift_variant N579K? STAD-US 13 77641917 77641917 deletion of <=200bp G - frameshift_variant P4047 STAD-US 13 77641917 77641917 deletion of <=200bp G - frameshift_variant P4085 STAD-US 13 77641917 77641917 deletion of <=200bp G - frameshift_variant P467 STAD-US 13 77642784 77642784 single base substitution G A synonymous_variant G3991G 11973C>T STAD-US 13 77642784 77642784 single base substitution G A synonymous_variant G4029G 12087C>T STAD-US 13 77642784 77642784 single base substitution G A synonymous_variant G411G 1233C>T STAD-US 13 77642839 77642839 single base substitution G C missense_variant A393G 1178C>G STAD-US 13 77642839 77642839 single base substitution G C missense_variant A3973G 11918C>G STAD-US 13 77642839 77642839 single base substitution G C missense_variant A4011G 12032C>G STAD-US 13 77651284 77651284 single base substitution T G missense_variant Q293P 878A>C STAD-US 13 77651284 77651284 single base substitution T G missense_variant Q3870P 11609A>C STAD-US 13 77651284 77651284 single base substitution T G missense_variant Q3908P 11723A>C STAD-US 13 77651309 77651309 single base substitution G A stop_gained R285* 853C>T STAD-US 13 77651309 77651309 single base substitution G A stop_gained R3862* 11584C>T STAD-US 13 77651309 77651309 single base substitution G A stop_gained R3900* 11698C>T STAD-US 13 77652957 77652957 single base substitution A G splice_donor_variant STAD-US 13 77656029 77656029 single base substitution G A synonymous_variant G3674G 11022C>T STAD-US 13 77656029 77656029 single base substitution G A synonymous_variant G3712G 11136C>T STAD-US 13 77656029 77656029 single base substitution G A synonymous_variant G97G 291C>T STAD-US 13 77657276 77657276 single base substitution C T missense_variant G28R 82G>A STAD-US 13 77657276 77657276 single base substitution C T missense_variant G3605R 10813G>A STAD-US 13 77657276 77657276 single base substitution C T missense_variant G3643R 10927G>A STAD-US 13 77663139 77663139 single base substitution G A downstream_gene_variant STAD-US 13 77663139 77663139 single base substitution G A missense_variant P3480L 10439C>T STAD-US 13 77663139 77663139 single base substitution G A missense_variant P3518L 10553C>T STAD-US 13 77663139 77663139 single base substitution G A upstream_gene_variant STAD-US 13 77664288 77664288 single base substitution G T downstream_gene_variant STAD-US 13 77664288 77664288 single base substitution G T missense_variant A3455E 10364C>A STAD-US 13 77664288 77664288 single base substitution G T missense_variant A3493E 10478C>A STAD-US 13 77664288 77664288 single base substitution G T upstream_gene_variant STAD-US 13 77664391 77664391 single base substitution T C downstream_gene_variant STAD-US 13 77664391 77664391 single base substitution T C missense_variant T3421A 10261A>G STAD-US 13 77664391 77664391 single base substitution T C missense_variant T3459A 10375A>G STAD-US 13 77664391 77664391 single base substitution T C upstream_gene_variant STAD-US 13 77670602 77670602 single base substitution C T downstream_gene_variant STAD-US 13 77670602 77670602 single base substitution C T exon_variant STAD-US 13 77670602 77670602 single base substitution C T missense_variant A3229T 9685G>A STAD-US 13 77670602 77670602 single base substitution C T missense_variant A3267T 9799G>A STAD-US 13 77670608 77670608 single base substitution G A downstream_gene_variant STAD-US 13 77670608 77670608 single base substitution G A exon_variant STAD-US 13 77670608 77670608 single base substitution G A stop_gained R3227* 9679C>T STAD-US 13 77670608 77670608 single base substitution G A stop_gained R3265* 9793C>T STAD-US 13 77671669 77671669 deletion of <=200bp T - downstream_gene_variant STAD-US 13 77671669 77671669 deletion of <=200bp T - exon_variant STAD-US 13 77671669 77671669 deletion of <=200bp T - frameshift_variant K3169 STAD-US 13 77671669 77671669 deletion of <=200bp T - frameshift_variant K3207 STAD-US 13 77671705 77671705 insertion of <=200bp - T downstream_gene_variant STAD-US 13 77671705 77671705 insertion of <=200bp - T exon_variant STAD-US 13 77671705 77671705 insertion of <=200bp - T frameshift_variant K3157K? STAD-US 13 77671705 77671705 insertion of <=200bp - T frameshift_variant K3195K? STAD-US 13 77671759 77671759 single base substitution G A downstream_gene_variant STAD-US 13 77671759 77671759 single base substitution G A exon_variant STAD-US 13 77671759 77671759 single base substitution G A missense_variant A3139V 9416C>T STAD-US 13 77671759 77671759 single base substitution G A missense_variant A3177V 9530C>T STAD-US 13 77671839 77671839 single base substitution C T downstream_gene_variant STAD-US 13 77671839 77671839 single base substitution C T missense_variant M3112I 9336G>A STAD-US 13 77671839 77671839 single base substitution C T missense_variant M3150I 9450G>A STAD-US 13 77671839 77671839 single base substitution C T upstream_gene_variant STAD-US 13 77671955 77671955 single base substitution T A downstream_gene_variant STAD-US 13 77671955 77671955 single base substitution T A missense_variant M3074L 9220A>T STAD-US 13 77671955 77671955 single base substitution T A missense_variant M3112L 9334A>T STAD-US 13 77671955 77671955 single base substitution T A upstream_gene_variant STAD-US 13 77672167 77672167 single base substitution T C downstream_gene_variant STAD-US 13 77672167 77672167 single base substitution T C missense_variant H3003R 9008A>G STAD-US 13 77672167 77672167 single base substitution T C missense_variant H3041R 9122A>G STAD-US 13 77672167 77672167 single base substitution T C upstream_gene_variant STAD-US 13 77672481 77672481 single base substitution G A downstream_gene_variant STAD-US 13 77672481 77672481 single base substitution G A exon_variant STAD-US 13 77672481 77672481 single base substitution G A synonymous_variant C2898C 8694C>T STAD-US 13 77672481 77672481 single base substitution G A synonymous_variant C2936C 8808C>T STAD-US 13 77672481 77672481 single base substitution G A synonymous_variant C421C 1263C>T STAD-US 13 77672481 77672481 single base substitution G A upstream_gene_variant STAD-US 13 77672621 77672621 single base substitution C A downstream_gene_variant STAD-US 13 77672621 77672621 single base substitution C A exon_variant STAD-US 13 77672621 77672621 single base substitution C A stop_gained E2852* 8554G>T STAD-US 13 77672621 77672621 single base substitution C A stop_gained E2890* 8668G>T STAD-US 13 77672621 77672621 single base substitution C A stop_gained E375* 1123G>T STAD-US 13 77672621 77672621 single base substitution C A upstream_gene_variant STAD-US 13 77672645 77672645 single base substitution G A downstream_gene_variant STAD-US 13 77672645 77672645 single base substitution G A exon_variant STAD-US 13 77672645 77672645 single base substitution G A missense_variant R2844C 8530C>T STAD-US 13 77672645 77672645 single base substitution G A missense_variant R2882C 8644C>T STAD-US 13 77672645 77672645 single base substitution G A missense_variant R367C 1099C>T STAD-US 13 77672645 77672645 single base substitution G A upstream_gene_variant STAD-US 13 77715012 77715012 single base substitution A G 5_prime_UTR_variant STAD-US 13 77715012 77715012 single base substitution A G downstream_gene_variant STAD-US 13 77715012 77715012 single base substitution A G exon_variant STAD-US 13 77715012 77715012 single base substitution A G missense_variant V2419A 7256T>C STAD-US 13 77715012 77715012 single base substitution A G missense_variant V2457A 7370T>C STAD-US 13 77718664 77718664 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant STAD-US 13 77718664 77718664 single base substitution T C exon_variant STAD-US 13 77718664 77718664 single base substitution T C missense_variant N2369D 7105A>G STAD-US 13 77718664 77718664 single base substitution T C missense_variant N2407D 7219A>G STAD-US 13 77718664 77718664 single base substitution T C upstream_gene_variant STAD-US 13 77720321 77720321 single base substitution C T 5_prime_UTR_variant STAD-US 13 77720321 77720321 single base substitution C T exon_variant STAD-US 13 77720321 77720321 single base substitution C T missense_variant R2350H 7049G>A STAD-US 13 77720321 77720321 single base substitution C T missense_variant R2388H 7163G>A STAD-US 13 77724964 77724964 single base substitution T C 5_prime_UTR_variant STAD-US 13 77724964 77724964 single base substitution T C missense_variant M2308V 6922A>G STAD-US 13 77724964 77724964 single base substitution T C missense_variant M2346V 7036A>G STAD-US 13 77724964 77724964 single base substitution T C upstream_gene_variant STAD-US 13 77725048 77725048 deletion of <=200bp T - 5_prime_UTR_variant STAD-US 13 77725048 77725048 deletion of <=200bp T - frameshift_variant M2280 STAD-US 13 77725048 77725048 deletion of <=200bp T - frameshift_variant M2318 STAD-US 13 77725048 77725048 deletion of <=200bp T - upstream_gene_variant STAD-US 13 77725048 77725048 insertion of <=200bp - T 5_prime_UTR_variant STAD-US 13 77725048 77725048 insertion of <=200bp - T frameshift_variant M2280N? STAD-US 13 77725048 77725048 insertion of <=200bp - T frameshift_variant M2318N? STAD-US 13 77725048 77725048 insertion of <=200bp - T upstream_gene_variant STAD-US 13 77725076 77725076 single base substitution C A 5_prime_UTR_variant STAD-US 13 77725076 77725076 single base substitution C A synonymous_variant V2270V 6810G>T STAD-US 13 77725076 77725076 single base substitution C A synonymous_variant V2308V 6924G>T STAD-US 13 77725076 77725076 single base substitution C A upstream_gene_variant STAD-US 13 77732134 77732134 single base substitution T C 5_prime_UTR_variant STAD-US 13 77732134 77732134 single base substitution T C synonymous_variant E2198E 6594A>G STAD-US 13 77732134 77732134 single base substitution T C synonymous_variant E2236E 6708A>G STAD-US 13 77743852 77743852 deletion of <=200bp A - splice_region_variant STAD-US 13 77745688 77745688 single base substitution A T 5_prime_UTR_variant STAD-US 13 77745688 77745688 single base substitution A T synonymous_variant S1873S 5619T>A STAD-US 13 77745688 77745688 single base substitution A T synonymous_variant S1911S 5733T>A STAD-US 13 77751940 77751940 single base substitution G T 5_prime_UTR_variant STAD-US 13 77751940 77751940 single base substitution G T missense_variant F1723L 5169C>A STAD-US 13 77751940 77751940 single base substitution G T missense_variant F1761L 5283C>A STAD-US 13 77754282 77754282 single base substitution C T 5_prime_UTR_variant STAD-US 13 77754282 77754282 single base substitution C T missense_variant A1667T 4999G>A STAD-US 13 77754282 77754282 single base substitution C T missense_variant A1705T 5113G>A STAD-US 13 77754337 77754337 single base substitution G T 5_prime_UTR_variant STAD-US 13 77754337 77754337 single base substitution G T synonymous_variant S1648S 4944C>A STAD-US 13 77754337 77754337 single base substitution G T synonymous_variant S1686S 5058C>A STAD-US 13 77755927 77755927 single base substitution C T 5_prime_UTR_variant STAD-US 13 77755927 77755927 single base substitution C T missense_variant R1579Q 4736G>A STAD-US 13 77755927 77755927 single base substitution C T missense_variant R1617Q 4850G>A STAD-US 13 77755995 77755995 single base substitution A T 5_prime_UTR_variant STAD-US 13 77755995 77755995 single base substitution A T synonymous_variant A1556A 4668T>A STAD-US 13 77755995 77755995 single base substitution A T synonymous_variant A1594A 4782T>A STAD-US 13 77759309 77759309 single base substitution A G 5_prime_UTR_variant STAD-US 13 77759309 77759309 single base substitution A G missense_variant F1512L 4534T>C STAD-US 13 77759309 77759309 single base substitution A G missense_variant F1550L 4648T>C STAD-US 13 77763121 77763121 single base substitution T C 5_prime_UTR_variant STAD-US 13 77763121 77763121 single base substitution T C missense_variant I1368V 4102A>G STAD-US 13 77763121 77763121 single base substitution T C missense_variant I1406V 4216A>G STAD-US 13 77765900 77765900 deletion of <=200bp C - 5_prime_UTR_variant STAD-US 13 77765900 77765900 deletion of <=200bp C - frameshift_variant G1290 STAD-US 13 77765900 77765900 deletion of <=200bp C - frameshift_variant G1328 STAD-US 13 77779459 77779459 single base substitution C T 5_prime_UTR_variant STAD-US 13 77779459 77779459 single base substitution C T missense_variant D1221N 3661G>A STAD-US 13 77779459 77779459 single base substitution C T missense_variant D1259N 3775G>A STAD-US 13 77779485 77779485 single base substitution G T 5_prime_UTR_variant STAD-US 13 77779485 77779485 single base substitution G T stop_gained S1212* 3635C>A STAD-US 13 77779485 77779485 single base substitution G T stop_gained S1250* 3749C>A STAD-US 13 77780843 77780843 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant STAD-US 13 77780843 77780843 single base substitution T C synonymous_variant L1140L 3420A>G STAD-US 13 77780843 77780843 single base substitution T C synonymous_variant L1178L 3534A>G STAD-US 13 77780921 77780921 single base substitution C T 5_prime_UTR_variant STAD-US 13 77780921 77780921 single base substitution C T synonymous_variant A1114A 3342G>A STAD-US 13 77780921 77780921 single base substitution C T synonymous_variant A1152A 3456G>A STAD-US 13 77785411 77785411 single base substitution G A 5_prime_UTR_variant STAD-US 13 77785411 77785411 single base substitution G A missense_variant L1065F 3193C>T STAD-US 13 77785411 77785411 single base substitution G A missense_variant L1103F 3307C>T STAD-US 13 77807298 77807298 single base substitution C T 5_prime_UTR_variant STAD-US 13 77807298 77807298 single base substitution C T synonymous_variant K872K 2616G>A STAD-US 13 77807298 77807298 single base substitution C T synonymous_variant K910K 2730G>A STAD-US 13 77807400 77807400 single base substitution T C splice_acceptor_variant STAD-US 13 77817210 77817210 single base substitution T G 5_prime_UTR_variant STAD-US 13 77817210 77817210 single base substitution T G missense_variant R833S 2499A>C STAD-US 13 77817210 77817210 single base substitution T G missense_variant R871S 2613A>C STAD-US 13 77834716 77834716 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 13 77834716 77834716 single base substitution G A missense_variant R584W 1750C>T STAD-US 13 77834716 77834716 single base substitution G A missense_variant R622W 1864C>T STAD-US 13 77844149 77844149 deletion of <=200bp T - 5_prime_UTR_variant STAD-US 13 77844149 77844149 deletion of <=200bp T - downstream_gene_variant STAD-US 13 77844149 77844149 deletion of <=200bp T - frameshift_variant K375 STAD-US 13 77844149 77844149 deletion of <=200bp T - frameshift_variant K413 STAD-US 13 77847693 77847693 single base substitution C T 5_prime_UTR_variant STAD-US 13 77847693 77847693 single base substitution C T missense_variant A249T 745G>A STAD-US 13 77847693 77847693 single base substitution C T missense_variant A287T 859G>A STAD-US 13 77847693 77847693 single base substitution C T upstream_gene_variant STAD-US 13 77862444 77862444 single base substitution T C 5_prime_UTR_variant STAD-US 13 77862444 77862444 single base substitution T C missense_variant N111S 332A>G STAD-US 13 77862444 77862444 single base substitution T C missense_variant N149S 446A>G STAD-US 13 77900654 77900654 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 13 77900654 77900654 single base substitution T A exon_variant STAD-US 13 77900654 77900654 single base substitution T A missense_variant N48I 143A>T STAD-US 13 77900654 77900654 single base substitution T A missense_variant N86I 257A>T THCA-US 13 77673090 77673090 single base substitution C T exon_variant THCA-US 13 77673090 77673090 single base substitution C T synonymous_variant E218E 654G>A THCA-US 13 77673090 77673090 single base substitution C T synonymous_variant E2695E 8085G>A THCA-US 13 77673090 77673090 single base substitution C T synonymous_variant E2733E 8199G>A THCA-US 13 77673090 77673090 single base substitution C T upstream_gene_variant THCA-US 13 77740543 77740543 single base substitution A T 5_prime_UTR_variant THCA-US 13 77740543 77740543 single base substitution A T missense_variant H2049Q 6147T>A THCA-US 13 77740543 77740543 single base substitution A T missense_variant H2087Q 6261T>A THCA-US 13 77763175 77763175 single base substitution T C 5_prime_UTR_variant THCA-US 13 77763175 77763175 single base substitution T C missense_variant T1350A 4048A>G THCA-US 13 77763175 77763175 single base substitution T C missense_variant T1388A 4162A>G UCEC-US 13 77619573 77619573 single base substitution T G synonymous_variant P1041P 3123A>C UCEC-US 13 77619573 77619573 single base substitution T G synonymous_variant P4621P 13863A>C UCEC-US 13 77619573 77619573 single base substitution T G synonymous_variant P4659P 13977A>C UCEC-US 13 77625255 77625255 single base substitution G A missense_variant R4562C 13684C>T UCEC-US 13 77625255 77625255 single base substitution G A missense_variant R4600C 13798C>T UCEC-US 13 77625255 77625255 single base substitution G A missense_variant R982C 2944C>T UCEC-US 13 77629697 77629697 single base substitution C A missense_variant R4510I 13529G>T UCEC-US 13 77629697 77629697 single base substitution C A missense_variant R4548I 13643G>T UCEC-US 13 77629697 77629697 single base substitution C A missense_variant R930I 2789G>T UCEC-US 13 77629710 77629710 single base substitution A T missense_variant C4506S 13516T>A UCEC-US 13 77629710 77629710 single base substitution A T missense_variant C4544S 13630T>A UCEC-US 13 77629710 77629710 single base substitution A T missense_variant C926S 2776T>A UCEC-US 13 77636781 77636781 single base substitution G A missense_variant R4204C 12610C>T UCEC-US 13 77636781 77636781 single base substitution G A missense_variant R4242C 12724C>T UCEC-US 13 77636781 77636781 single base substitution G A missense_variant R624C 1870C>T UCEC-US 13 77640128 77640128 single base substitution G A missense_variant A4146V 12437C>T UCEC-US 13 77640128 77640128 single base substitution G A missense_variant A4184V 12551C>T UCEC-US 13 77640128 77640128 single base substitution G A missense_variant A566V 1697C>T UCEC-US 13 77640212 77640212 single base substitution C T missense_variant R4118Q 12353G>A UCEC-US 13 77640212 77640212 single base substitution C T missense_variant R4156Q 12467G>A UCEC-US 13 77640212 77640212 single base substitution C T missense_variant R538Q 1613G>A UCEC-US 13 77641765 77641765 single base substitution C T missense_variant V4098M 12292G>A UCEC-US 13 77641765 77641765 single base substitution C T missense_variant V4136M 12406G>A UCEC-US 13 77641765 77641765 single base substitution C T missense_variant V518M 1552G>A UCEC-US 13 77642872 77642872 single base substitution G T missense_variant S382Y 1145C>A UCEC-US 13 77642872 77642872 single base substitution G T missense_variant S3962Y 11885C>A UCEC-US 13 77642872 77642872 single base substitution G T missense_variant S4000Y 11999C>A UCEC-US 13 77651301 77651301 single base substitution G T missense_variant F287L 861C>A UCEC-US 13 77651301 77651301 single base substitution G T missense_variant F3864L 11592C>A UCEC-US 13 77651301 77651301 single base substitution G T missense_variant F3902L 11706C>A UCEC-US 13 77651414 77651414 single base substitution G A stop_gained R250* 748C>T UCEC-US 13 77651414 77651414 single base substitution G A stop_gained R3827* 11479C>T UCEC-US 13 77651414 77651414 single base substitution G A stop_gained R3865* 11593C>T UCEC-US 13 77661630 77661630 single base substitution T G missense_variant N3584H 10750A>C UCEC-US 13 77661630 77661630 single base substitution T G missense_variant N3622H 10864A>C UCEC-US 13 77661630 77661630 single base substitution T G missense_variant N7H 19A>C UCEC-US 13 77661714 77661714 single base substitution G T missense_variant L3556M 10666C>A UCEC-US 13 77661714 77661714 single base substitution G T missense_variant L3594M 10780C>A UCEC-US 13 77661714 77661714 single base substitution G T upstream_gene_variant UCEC-US 13 77662983 77662983 single base substitution C T downstream_gene_variant UCEC-US 13 77662983 77662983 single base substitution C T missense_variant R3532Q 10595G>A UCEC-US 13 77662983 77662983 single base substitution C T missense_variant R3570Q 10709G>A UCEC-US 13 77662983 77662983 single base substitution C T upstream_gene_variant UCEC-US 13 77669695 77669695 single base substitution G A downstream_gene_variant UCEC-US 13 77669695 77669695 single base substitution G A exon_variant UCEC-US 13 77669695 77669695 single base substitution G A missense_variant R3295C 9883C>T UCEC-US 13 77669695 77669695 single base substitution G A missense_variant R3333C 9997C>T UCEC-US 13 77671636 77671636 single base substitution C T downstream_gene_variant UCEC-US 13 77671636 77671636 single base substitution C T exon_variant UCEC-US 13 77671636 77671636 single base substitution C T missense_variant R3180K 9539G>A UCEC-US 13 77671636 77671636 single base substitution C T missense_variant R3218K 9653G>A UCEC-US 13 77671680 77671680 single base substitution C A downstream_gene_variant UCEC-US 13 77671680 77671680 single base substitution C A exon_variant UCEC-US 13 77671680 77671680 single base substitution C A missense_variant K3165N 9495G>T UCEC-US 13 77671680 77671680 single base substitution C A missense_variant K3203N 9609G>T UCEC-US 13 77671712 77671712 single base substitution G T downstream_gene_variant UCEC-US 13 77671712 77671712 single base substitution G T exon_variant UCEC-US 13 77671712 77671712 single base substitution G T missense_variant L3155I 9463C>A UCEC-US 13 77671712 77671712 single base substitution G T missense_variant L3193I 9577C>A UCEC-US 13 77671898 77671898 single base substitution C A downstream_gene_variant UCEC-US 13 77671898 77671898 single base substitution C A stop_gained E3093* 9277G>T UCEC-US 13 77671898 77671898 single base substitution C A stop_gained E3131* 9391G>T UCEC-US 13 77671898 77671898 single base substitution C A upstream_gene_variant UCEC-US 13 77671902 77671902 single base substitution C T downstream_gene_variant UCEC-US 13 77671902 77671902 single base substitution C T synonymous_variant L3091L 9273G>A UCEC-US 13 77671902 77671902 single base substitution C T synonymous_variant L3129L 9387G>A UCEC-US 13 77671902 77671902 single base substitution C T upstream_gene_variant UCEC-US 13 77672321 77672321 single base substitution G T downstream_gene_variant UCEC-US 13 77672321 77672321 single base substitution G T exon_variant UCEC-US 13 77672321 77672321 single base substitution G T synonymous_variant R2952R 8854C>A UCEC-US 13 77672321 77672321 single base substitution G T synonymous_variant R2990R 8968C>A UCEC-US 13 77672321 77672321 single base substitution G T synonymous_variant R475R 1423C>A UCEC-US 13 77672321 77672321 single base substitution G T upstream_gene_variant UCEC-US 13 77672420 77672420 single base substitution A C downstream_gene_variant UCEC-US 13 77672420 77672420 single base substitution A C exon_variant UCEC-US 13 77672420 77672420 single base substitution A C missense_variant F2919V 8755T>G UCEC-US 13 77672420 77672420 single base substitution A C missense_variant F2957V 8869T>G UCEC-US 13 77672420 77672420 single base substitution A C missense_variant F442V 1324T>G UCEC-US 13 77672420 77672420 single base substitution A C upstream_gene_variant UCEC-US 13 77673050 77673050 single base substitution G A exon_variant UCEC-US 13 77673050 77673050 single base substitution G A missense_variant R232C 694C>T UCEC-US 13 77673050 77673050 single base substitution G A missense_variant R2709C 8125C>T UCEC-US 13 77673050 77673050 single base substitution G A missense_variant R2747C 8239C>T UCEC-US 13 77673050 77673050 single base substitution G A upstream_gene_variant UCEC-US 13 77692506 77692506 single base substitution C A downstream_gene_variant UCEC-US 13 77692506 77692506 single base substitution C A exon_variant UCEC-US 13 77692506 77692506 single base substitution C A intron_variant UCEC-US 13 77692506 77692506 single base substitution C A missense_variant Q188H 564G>T UCEC-US 13 77692588 77692588 single base substitution G T downstream_gene_variant UCEC-US 13 77692588 77692588 single base substitution G T exon_variant UCEC-US 13 77692588 77692588 single base substitution G T intron_variant UCEC-US 13 77692588 77692588 single base substitution G T missense_variant P161H 482C>A UCEC-US 13 77714205 77714205 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 13 77714205 77714205 single base substitution C A downstream_gene_variant UCEC-US 13 77714205 77714205 single base substitution C A exon_variant UCEC-US 13 77714205 77714205 single base substitution C A stop_gained G2461* 7381G>T UCEC-US 13 77714205 77714205 single base substitution C A stop_gained G2499* 7495G>T UCEC-US 13 77720322 77720322 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 13 77720322 77720322 single base substitution G A exon_variant UCEC-US 13 77720322 77720322 single base substitution G A missense_variant R2350C 7048C>T UCEC-US 13 77720322 77720322 single base substitution G A missense_variant R2388C 7162C>T UCEC-US 13 77720341 77720341 single base substitution A C 5_prime_UTR_variant UCEC-US 13 77720341 77720341 single base substitution A C exon_variant UCEC-US 13 77720341 77720341 single base substitution A C missense_variant N2343K 7029T>G UCEC-US 13 77720341 77720341 single base substitution A C missense_variant N2381K 7143T>G UCEC-US 13 77724943 77724943 single base substitution A G 5_prime_UTR_variant UCEC-US 13 77724943 77724943 single base substitution A G missense_variant S2315P 6943T>C UCEC-US 13 77724943 77724943 single base substitution A G missense_variant S2353P 7057T>C UCEC-US 13 77724943 77724943 single base substitution A G upstream_gene_variant UCEC-US 13 77725034 77725036 deletion of <=200bp TTG - 5_prime_UTR_variant UCEC-US 13 77725034 77725036 deletion of <=200bp TTG - inframe_deletion Q2284 UCEC-US 13 77725034 77725036 deletion of <=200bp TTG - inframe_deletion Q2322 UCEC-US 13 77725034 77725036 deletion of <=200bp TTG - upstream_gene_variant UCEC-US 13 77725049 77725049 single base substitution T G 5_prime_UTR_variant UCEC-US 13 77725049 77725049 single base substitution T G missense_variant K2279N 6837A>C UCEC-US 13 77725049 77725049 single base substitution T G missense_variant K2317N 6951A>C UCEC-US 13 77725049 77725049 single base substitution T G upstream_gene_variant UCEC-US 13 77730338 77730338 single base substitution C A splice_acceptor_variant UCEC-US 13 77732220 77732220 single base substitution G T 5_prime_UTR_variant UCEC-US 13 77732220 77732220 single base substitution G T missense_variant L2170I 6508C>A UCEC-US 13 77732220 77732220 single base substitution G T missense_variant L2208I 6622C>A UCEC-US 13 77738655 77738655 single base substitution C A 5_prime_UTR_variant UCEC-US 13 77738655 77738655 single base substitution C A stop_gained E2123* 6367G>T UCEC-US 13 77738655 77738655 single base substitution C A stop_gained E2161* 6481G>T UCEC-US 13 77739406 77739406 single base substitution A G splice_donor_variant UCEC-US 13 77739483 77739483 single base substitution C A 5_prime_UTR_variant UCEC-US 13 77739483 77739483 single base substitution C A synonymous_variant V2090V 6270G>T UCEC-US 13 77739483 77739483 single base substitution C A synonymous_variant V2128V 6384G>T UCEC-US 13 77740507 77740507 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 13 77740507 77740507 single base substitution A C missense_variant F2061L 6183T>G UCEC-US 13 77740507 77740507 single base substitution A C missense_variant F2099L 6297T>G UCEC-US 13 77740513 77740513 single base substitution C T 5_prime_UTR_variant UCEC-US 13 77740513 77740513 single base substitution C T synonymous_variant K2059K 6177G>A UCEC-US 13 77740513 77740513 single base substitution C T synonymous_variant K2097K 6291G>A UCEC-US 13 77740590 77740590 single base substitution T G 5_prime_UTR_variant UCEC-US 13 77740590 77740590 single base substitution T G synonymous_variant R2034R 6100A>C UCEC-US 13 77740590 77740590 single base substitution T G synonymous_variant R2072R 6214A>C UCEC-US 13 77740653 77740653 single base substitution C T 5_prime_UTR_variant UCEC-US 13 77740653 77740653 single base substitution C T missense_variant E2013K 6037G>A UCEC-US 13 77740653 77740653 single base substitution C T missense_variant E2051K 6151G>A UCEC-US 13 77743789 77743789 single base substitution A G 5_prime_UTR_variant UCEC-US 13 77743789 77743789 single base substitution A G missense_variant I1914T 5741T>C UCEC-US 13 77743789 77743789 single base substitution A G missense_variant I1952T 5855T>C UCEC-US 13 77745695 77745695 single base substitution G A 5_prime_UTR_variant UCEC-US 13 77745695 77745695 single base substitution G A missense_variant A1871V 5612C>T UCEC-US 13 77745695 77745695 single base substitution G A missense_variant A1909V 5726C>T UCEC-US 13 77748602 77748602 single base substitution C T 5_prime_UTR_variant UCEC-US 13 77748602 77748602 single base substitution C T missense_variant R1794H 5381G>A UCEC-US 13 77748602 77748602 single base substitution C T missense_variant R1832H 5495G>A UCEC-US 13 77750673 77750673 single base substitution C A 5_prime_UTR_variant UCEC-US 13 77750673 77750673 single base substitution C A missense_variant D1773Y 5317G>T UCEC-US 13 77750673 77750673 single base substitution C A missense_variant D1811Y 5431G>T UCEC-US 13 77750698 77750698 single base substitution C T 5_prime_UTR_variant UCEC-US 13 77750698 77750698 single base substitution C T synonymous_variant T1764T 5292G>A UCEC-US 13 77750698 77750698 single base substitution C T synonymous_variant T1802T 5406G>A UCEC-US 13 77751986 77751986 single base substitution G A 5_prime_UTR_variant UCEC-US 13 77751986 77751986 single base substitution G A missense_variant A1708V 5123C>T UCEC-US 13 77751986 77751986 single base substitution G A missense_variant A1746V 5237C>T UCEC-US 13 77752032 77752032 single base substitution T C 5_prime_UTR_variant UCEC-US 13 77752032 77752032 single base substitution T C missense_variant T1693A 5077A>G UCEC-US 13 77752032 77752032 single base substitution T C missense_variant T1731A 5191A>G UCEC-US 13 77752058 77752058 single base substitution T C 5_prime_UTR_variant UCEC-US 13 77752058 77752058 single base substitution T C missense_variant K1684R 5051A>G UCEC-US 13 77752058 77752058 single base substitution T C missense_variant K1722R 5165A>G UCEC-US 13 77754340 77754340 single base substitution G T 5_prime_UTR_variant UCEC-US 13 77754340 77754340 single base substitution G T synonymous_variant S1647S 4941C>A UCEC-US 13 77754340 77754340 single base substitution G T synonymous_variant S1685S 5055C>A UCEC-US 13 77754433 77754433 single base substitution C T 5_prime_UTR_variant UCEC-US 13 77754433 77754433 single base substitution C T synonymous_variant G1616G 4848G>A UCEC-US 13 77754433 77754433 single base substitution C T synonymous_variant G1654G 4962G>A UCEC-US 13 77760086 77760086 single base substitution T C 5_prime_UTR_variant UCEC-US 13 77760086 77760086 single base substitution T C missense_variant D1417G 4250A>G UCEC-US 13 77760086 77760086 single base substitution T C missense_variant D1455G 4364A>G UCEC-US 13 77763183 77763183 single base substitution C A splice_acceptor_variant UCEC-US 13 77764431 77764431 single base substitution A G 5_prime_UTR_variant UCEC-US 13 77764431 77764431 single base substitution A G synonymous_variant N1332N 3996T>C UCEC-US 13 77764431 77764431 single base substitution A G synonymous_variant N1370N 4110T>C UCEC-US 13 77764443 77764443 single base substitution C A 5_prime_UTR_variant UCEC-US 13 77764443 77764443 single base substitution C A missense_variant K1328N 3984G>T UCEC-US 13 77764443 77764443 single base substitution C A missense_variant K1366N 4098G>T UCEC-US 13 77779466 77779466 single base substitution G A 5_prime_UTR_variant UCEC-US 13 77779466 77779466 single base substitution G A synonymous_variant F1218F 3654C>T UCEC-US 13 77779466 77779466 single base substitution G A synonymous_variant F1256F 3768C>T UCEC-US 13 77780922 77780922 single base substitution G A 5_prime_UTR_variant UCEC-US 13 77780922 77780922 single base substitution G A missense_variant A1114V 3341C>T UCEC-US 13 77780922 77780922 single base substitution G A missense_variant A1152V 3455C>T UCEC-US 13 77785375 77785375 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 13 77785375 77785375 single base substitution A C missense_variant F1077V 3229T>G UCEC-US 13 77785375 77785375 single base substitution A C missense_variant F1115V 3343T>G UCEC-US 13 77786162 77786162 single base substitution C T 5_prime_UTR_variant UCEC-US 13 77786162 77786162 single base substitution C T missense_variant R1026Q 3077G>A UCEC-US 13 77786162 77786162 single base substitution C T missense_variant R1064Q 3191G>A UCEC-US 13 77807290 77807290 single base substitution C T splice_donor_variant UCEC-US 13 77817953 77817953 single base substitution C T 5_prime_UTR_variant UCEC-US 13 77817953 77817953 single base substitution C T missense_variant D801N 2401G>A UCEC-US 13 77817953 77817953 single base substitution C T missense_variant D839N 2515G>A UCEC-US 13 77825385 77825385 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 13 77825385 77825385 single base substitution C A missense_variant W723L 2168G>T UCEC-US 13 77825385 77825385 single base substitution C A missense_variant W761L 2282G>T UCEC-US 13 77825420 77825420 single base substitution C A 5_prime_UTR_variant UCEC-US 13 77825420 77825420 single base substitution C A missense_variant E711D 2133G>T UCEC-US 13 77825420 77825420 single base substitution C A missense_variant E749D 2247G>T UCEC-US 13 77834691 77834691 single base substitution T G 5_prime_UTR_variant UCEC-US 13 77834691 77834691 single base substitution T G missense_variant K592T 1775A>C UCEC-US 13 77834691 77834691 single base substitution T G missense_variant K630T 1889A>C UCEC-US 13 77834697 77834697 single base substitution T G 5_prime_UTR_variant UCEC-US 13 77834697 77834697 single base substitution T G missense_variant K590T 1769A>C UCEC-US 13 77834697 77834697 single base substitution T G missense_variant K628T 1883A>C UCEC-US 13 77836212 77836212 single base substitution C T 5_prime_UTR_variant UCEC-US 13 77836212 77836212 single base substitution C T synonymous_variant A503A 1509G>A UCEC-US 13 77836212 77836212 single base substitution C T synonymous_variant A541A 1623G>A UCEC-US 13 77837813 77837813 single base substitution C T 5_prime_UTR_variant UCEC-US 13 77837813 77837813 single base substitution C T missense_variant D477N 1429G>A UCEC-US 13 77837813 77837813 single base substitution C T missense_variant D515N 1543G>A UCEC-US 13 77844161 77844161 single base substitution C A 5_prime_UTR_variant UCEC-US 13 77844161 77844161 single base substitution C A downstream_gene_variant UCEC-US 13 77844161 77844161 single base substitution C A missense_variant R371I 1112G>T UCEC-US 13 77844161 77844161 single base substitution C A missense_variant R409I 1226G>T UCEC-US 13 77844495 77844495 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 13 77844495 77844495 single base substitution A C exon_variant UCEC-US 13 77844495 77844495 single base substitution A C missense_variant F337C 1010T>G UCEC-US 13 77844495 77844495 single base substitution A C missense_variant F375C 1124T>G UCEC-US 13 77844653 77844653 single base substitution C T 5_prime_UTR_variant UCEC-US 13 77844653 77844653 single base substitution C T exon_variant UCEC-US 13 77844653 77844653 single base substitution C T synonymous_variant S284S 852G>A UCEC-US 13 77844653 77844653 single base substitution C T synonymous_variant S322S 966G>A UCEC-US 13 77862331 77862331 single base substitution C T 5_prime_UTR_variant UCEC-US 13 77862331 77862331 single base substitution C T missense_variant E149K 445G>A UCEC-US 13 77862331 77862331 single base substitution C T missense_variant E187K 559G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand CSCC-10-T COSM4479947 c.2259C>A p.V753V Substitution - coding silent 13:77251159-77251159 - CHC961T COSM4950866 c.7621C>T p.Q2541* Substitution - Nonsense 13:77126467-77126467 - YUKAT COSM5376903 c.3706G>A p.G1236R Substitution - Missense 13:77205279-77205279 - ESCC_BICR_027T COSM5443179 c.7046T>C p.L2349P Substitution - Missense 13:77146189-77146189 - CRC-31T COSM138916 c.5639G>A p.R1880Q Substitution - Missense 13:77171533-77171533 - TCGA-AC-A23H-01 COSM3826504 c.2503G>A p.E835K Substitution - Missense 5:103028202-103028202 + TCGA-BR-8680-01 COSM4048495 c.5169C>A p.F1723L Substitution - Missense 13:77177805-77177805 - PT52 COSM5939405 c.2447C>T p.S816L Substitution - Missense 5:103019805-103019805 + 587228 COSM1216061 c.9167C>T p.S3056L Substitution - Missense 13:77097873-77097873 - SNU-C4 COSM4653863 c.2171A>G p.H724R Substitution - Missense 5:103007613-103007613 + CHC1053T COSM3669356 c.1170C>A p.F390L Substitution - Missense 5:102974123-102974123 + SMS-CTR COSM4989529 c.4677C>A p.H1559Q Substitution - Missense 13:77181851-77181851 - T2940 COSM4704410 c.6838delA p.M2280fs*20 Deletion - Frameshift 13:77150913-77150913 - PD4935a COSM162705 c.5346G>A p.V1782V Substitution - coding silent 13:77176509-77176509 - XHDG34 COSM4769445 c.5548G>C p.D1850H Substitution - Missense 13:77171624-77171624 - CSCC-35-T COSM4483450 c.2587C>G p.P863A Substitution - Missense 13:77233192-77233192 - 2492721 COSM5722135 c.3259G>A p.G1087R Substitution - Missense 13:77211210-77211210 - TCGA-DJ-A1QO-01 COSM3369119 c.8085G>A p.E2695E Substitution - coding silent 13:77098955-77098955 - YURIF COSM1706860 c.5293T>A p.Y1765N Substitution - Missense 13:77176562-77176562 - PT46 COSM5928707 c.580C>T p.P194S Substitution - Missense 5:102948382-102948382 + TCGA-B5-A0K9-01 COSM948671 c.1905T>C p.S635S Substitution - coding silent 13:77257828-77257828 - TCGA-06-0214-01 COSM3409650 c.622G>C p.V208L Substitution - Missense 5:102948424-102948424 + TCGA-AP-A051-01 COSM948617 c.5077A>G p.T1693A Substitution - Missense 13:77177897-77177897 - TCGA-AX-A0J0-01 COSM948596 c.6037G>A p.E2013K Substitution - Missense 13:77166518-77166518 - TCGA-D1-A0ZZ-01 COSM948544 c.8854C>A p.R2952R Substitution - coding silent 13:77098186-77098186 - TCGA-BS-A0TC-01 COSM948662 c.2168G>T p.W723L Substitution - Missense 13:77251250-77251250 - TCGA-ER-A19S-06 COSM3469726 c.8519C>T p.P2840L Substitution - Missense 13:77098521-77098521 - CSCC-18-T COSM4512570 c.793C>T p.L265F Substitution - Missense 13:77273510-77273510 - AOCS-137-1-X COSM3943271 c.4887C>G p.V1629V Substitution - coding silent 13:77180259-77180259 - sysucc-1030T COSM5452290 c.10509G>A p.Q3503Q Substitution - coding silent 13:77088934-77088934 - TCGA-18-4083-01 COSM697323 c.5450G>C p.G1817A Substitution - Missense 13:77174398-77174398 - TCGA-CJ-5684-01 COSM469568 c.3286T>C p.Y1096H Substitution - Missense 13:77211183-77211183 - TCGA-FW-A3R5-06 COSM3885528 c.3604C>T p.H1202Y Substitution - Missense 13:77205381-77205381 - TCGA-AA-3713-01 COSM1367802 c.7029T>A p.N2343K Substitution - Missense 13:77146206-77146206 - TCGA-G4-6588-01 COSM1367763 c.8898G>A p.S2966S Substitution - coding silent 13:77098142-77098142 - TCGA-AP-A0LM-01 COSM1059274 c.2696C>T p.A899V Substitution - Missense 5:103029043-103029043 + 2492723 COSM5720358 c.1616C>T p.S539L Substitution - Missense 5:103003035-103003035 + 587342 COSM1216081 c.13805C>T p.P4602L Substitution - Missense 13:77050999-77050999 - 2492723 COSM5722135 c.3259G>A p.G1087R Substitution - Missense 13:77211210-77211210 - LS180 COSM1950172 c.4791delT p.L1599fs*19 Deletion - Frameshift 13:77181737-77181737 - TCGA-06-0745 COSM2151765 c.1597T>C p.W533R Substitution - Missense 13:77261312-77261312 - CSCC-7-T COSM4502516 c.6045C>T p.D2015D Substitution - coding silent 13:77166510-77166510 - T2269 COSM4704386 c.8390C>T p.S2797L Substitution - Missense 13:77098650-77098650 - HCC133 COSM1619283 c.1607A>G p.D536G Substitution - Missense 5:102990395-102990395 + TCGA-DI-A0WH-01 COSM948495 c.13807+2T>C p.? Unknown 13:77050995-77050995 - YUGAFFE COSM1706866 c.2587C>T p.P863S Substitution - Missense 13:77233192-77233192 - TCGA-EI-6512-01 COSM3417722 c.634+1G>A p.? Unknown 13:77278757-77278757 - TCGA-AP-A051-01 COSM948560 c.7029T>G p.N2343K Substitution - Missense 13:77146206-77146206 - TCGA-IR-A3LK-01 COSM4816600 c.4922G>A p.R1641K Substitution - Missense 13:77180224-77180224 - HCC2998 COSM1677722 c.3230T>G p.F1077C Substitution - Missense 13:77211239-77211239 - ESCC_BICR_013T COSM5439383 c.1532C>A p.P511Q Substitution - Missense 5:102990320-102990320 + TCGA-B5-A0JY-01 COSM948626 c.4848G>A p.G1616G Substitution - coding silent 13:77180298-77180298 - ESO-0123 COSM1258376 c.13693T>G p.C4565G Substitution - Missense 13:77051111-77051111 - TCGA-DM-A1D8-01 COSM1431986 c.1899C>A p.P633P Substitution - coding silent 5:103006896-103006896 + YUDEXA COSM1696010 c.2551G>A p.G851R Substitution - Missense 5:103028898-103028898 + HCT-116 COSM1677719 c.4006G>A p.V1336I Substitution - Missense 13:77190286-77190286 - CHC1742T COSM4792197 c.3605A>G p.H1202R Substitution - Missense 13:77205380-77205380 - TCGA-A8-A06P-01 COSM432563 c.9229A>G p.I3077V Substitution - Missense 13:77097811-77097811 - TCGA-BP-4331-01 COSM3360148 c.6801+1G>T p.? Unknown 13:77156057-77156057 - TCGA-AP-A053-01 COSM948632 c.4041-1G>T p.? Unknown 13:77189048-77189048 - TCGA-D3-A3MR-06 COSM3469763 c.3510A>G p.L1170L Substitution - coding silent 13:77205564-77205564 - 587222 COSM1216067 c.201T>G p.I67M Substitution - Missense 13:77296662-77296662 - HCC38 COSM1607230 c.4407A>G p.K1469K Substitution - coding silent 13:77185301-77185301 - T3147 COSM1059251 c.238C>T p.R80* Substitution - Nonsense 5:102901383-102901383 + HT115 COSM2989777 c.934T>C p.L312L Substitution - coding silent 5:102959903-102959903 + TCGA-EE-A2A1-06 COSM3469784 c.530G>A p.R177Q Substitution - Missense 13:77278862-77278862 - 05-P8014 COSM4585317 c.2508G>A p.T836T Substitution - coding silent 5:103028207-103028207 + HCC45T COSM3661293 c.259G>A p.A87T Substitution - Missense 5:102901404-102901404 + 408 COSM1219167 c.265G>A p.V89M Substitution - Missense 5:102901410-102901410 + T2225 COSM4704394 c.7891C>T p.R2631* Substitution - Nonsense 13:77125348-77125348 - ATL027 COSM5709412 c.461G>A p.G154E Substitution - Missense 5:102926603-102926603 + S02242 COSM5677129 c.13253G>C p.C4418S Substitution - Missense 13:77057056-77057056 - TCGA-D1-A0ZS-01 COSM948507 c.12437C>T p.A4146V Substitution - Missense 13:77065993-77065993 - TCGA-HT-7684-01 COSM3968652 c.2517C>G p.G839G Substitution - coding silent 13:77233262-77233262 - TCGA-FD-A3B6-01 COSM1300309 c.3064C>A p.Q1022K Substitution - Missense 13:77212040-77212040 - PT44 COSM5926519 c.2606G>A p.G869E Substitution - Missense 5:103028953-103028953 + TCGA-BT-A20Q-01 COSM416312 c.5711C>T p.S1904F Substitution - Missense 13:77169684-77169684 - C70 COSM4619421 c.3618G>C p.W1206C Substitution - Missense 13:77205367-77205367 - PCSI_0476_Pa_P_526 COSM5031343 c.5338G>C p.D1780H Substitution - Missense 13:77176517-77176517 - SW620 COSM1671785 c.177G>T p.L59F Substitution - Missense 5:102867360-102867360 + TCGA-B5-A11U-01 COSM1059255 c.779G>A p.R260Q Substitution - Missense 5:102949956-102949956 + 522_T COSM3955741 c.3149-3A>G p.? Unknown 13:77211323-77211323 - Pat_06_A COSM5017659 c.1137_1139delAGA p.E383delE Deletion - In frame 5:102961204-102961206 + PT55 COSM5942550 c.2755G>A p.E919K Substitution - Missense 13:77224521-77224521 - sysucc-1038T COSM200007 c.2120G>A p.R707Q Substitution - Missense 5:103007562-103007562 + TCGA-AX-A0J0-01 COSM948653 c.3077G>A p.R1026Q Substitution - Missense 13:77212027-77212027 - HCC45 COSM3661293 c.259G>A p.A87T Substitution - Missense 5:102901404-102901404 + LAU63 COSM235002 c.3892C>A p.R1298R Substitution - coding silent 13:77191743-77191743 - HCC5 COSM3661295 c.1480G>A p.G494R Substitution - Missense 5:102974433-102974433 + I2L-P7-Tumor-Organoid COSM5362269 c.5782-2A>G p.? Unknown 13:77168648-77168648 - 2492709 COSM5717255 c.1309C>T p.R437* Substitution - Nonsense 5:102974262-102974262 + ESCC_62 COSM1949742 c.11744T>C p.M3915T Substitution - Missense 13:77070677-77070677 - TCGA-06-2564 COSM2152936 c.9C>G p.G3G Substitution - coding silent 5:102866204-102866204 + TCGA-BP-4770-01 COSM481719 c.2669A>G p.E890G Substitution - Missense 5:103029016-103029016 + TCGA-A8-A09G-01 COSM448390 c.2049C>T p.F683F Substitution - coding silent 5:103007491-103007491 + TCGA-D5-6928-01 COSM1431974 c.561C>A p.H187Q Substitution - Missense 5:102946871-102946871 + YUDEXA COSM1696008 c.1507G>A p.D503N Substitution - Missense 5:102990295-102990295 + YUNEKI COSM5376885 c.11028T>G p.D3676E Substitution - Missense 13:77081888-77081888 - N-Thy004 COSM5095296 c.2327G>A p.R776H Substitution - Missense 5:103009862-103009862 + TCGA-EE-A3AA-06 COSM3469754 c.5540G>A p.S1847N Substitution - Missense 13:77171632-77171632 - CHC1753T COSM4952523 c.1659A>T p.P553P Substitution - coding silent 5:103003078-103003078 + 35M COSM5581765 c.7706C>T p.P2569L Substitution - Missense 13:77126382-77126382 - TCGA-39-5019-01 COSM697326 c.5694A>G p.P1898P Substitution - coding silent 13:77169701-77169701 - Case4b COSM1717339 c.9071C>G p.S3024C Substitution - Missense 13:77097969-77097969 - RK050_C COSM1629176 c.1147-1G>A p.? Unknown 13:77267938-77267938 - CHC205T COSM4407105 c.2307A>C p.I769I Substitution - coding silent 5:103009842-103009842 + TCGA-85-6561-01 COSM697338 c.7007C>A p.T2336K Substitution - Missense 13:77150744-77150744 - AOCS-149-1-7 COSM3943268 c.6169G>T p.E2057* Substitution - Nonsense 13:77166386-77166386 - HCC172T COSM3661297 c.2077C>T p.P693S Substitution - Missense 5:103007519-103007519 + TCGA-EE-A2GP-06 COSM3469734 c.7635C>T p.F2545F Substitution - coding silent 13:77126453-77126453 - ESOSCC162T COSM1171987 c.1291A>G p.I431V Substitution - Missense 13:77263955-77263955 - ESCC-F16 COSM5047205 c.2458C>T p.R820* Substitution - Nonsense 13:77243116-77243116 - TCGA-AX-A0J0-01 COSM948578 c.6367G>T p.E2123* Substitution - Nonsense 13:77164520-77164520 - CSCC-27-T COSM4496474 c.4647C>T p.L1549L Substitution - coding silent 13:77181881-77181881 - TCGA-CM-4743-01 COSM1367870 c.161delG p.G54fs*15 Deletion - Frameshift 13:77326501-77326501 - TCGA-BK-A0C9-01 COSM948644 c.3566C>G p.S1189C Substitution - Missense 13:77205508-77205508 - TCGA-IN-8663-01 COSM4048441 c.10364C>A p.P3455H Substitution - Missense 13:77090153-77090153 - TCGA-DK-A3WW-01 COSM3793381 c.6451G>C p.D2151H Substitution - Missense 13:77161938-77161938 - Gp2D COSM1950218 c.3826A>G p.K1276E Substitution - Missense 13:77191809-77191809 - CAL33 COSM1950190 c.4517A>G p.N1506S Substitution - Missense 13:77185191-77185191 - 587376 COSM1216084 c.10537C>A p.H3513N Substitution - Missense 13:77088906-77088906 - 587278 COSM1219173 c.1789G>A p.V597M Substitution - Missense 5:103005212-103005212 + BRC8 COSM5027790 c.7255G>A p.V2419I Substitution - Missense 13:77140878-77140878 - ESOSCC156T COSM313010 c.5227-3delT p.? Unknown 13:77176631-77176631 - LUAD_E00522 COSM353308 c.2039C>T p.P680L Substitution - Missense 5:103007481-103007481 + TCGA-AP-A051-01 COSM948528 c.9883C>T p.P3295S Substitution - Missense 13:77095560-77095560 - 721LT COSM4386256 c.1436A>T p.E479V Substitution - Missense 13:77263671-77263671 - TCGA-33-4538-01 COSM697293 c.1A>T p.M1L Substitution - Missense 13:77326661-77326661 - sysucc-311T COSM5478587 c.5280A>C p.L1760F Substitution - Missense 13:77176575-77176575 - 8015109 COSM3384914 c.6728G>A p.C2243Y Substitution - Missense 13:77156131-77156131 - ESCC_BICR_017T COSM5442933 c.2060A>T p.H687L Substitution - Missense 5:103007502-103007502 + 2492726 COSM5725402 c.211-1G>A p.? Unknown 5:102901355-102901355 + TCGA-IR-A3LK-01 COSM3469760 c.4917G>A p.L1639L Substitution - coding silent 13:77180229-77180229 - T368 COSM4704419 c.6048T>C p.P2016P Substitution - coding silent 13:77166507-77166507 - Pat_41_B COSM5842725 c.9067C>T p.L3023F Substitution - Missense 13:77097973-77097973 - PCSI_0473_Pa_P_526 COSM4961561 c.6656+7G>A p.? Unknown 13:77157930-77157930 - STC291 COSM5052244 c.102C>A p.A34A Substitution - coding silent 13:77326560-77326560 - SW403 COSM4216170 c.541C>A p.P181T Substitution - Missense 13:77278851-77278851 - ATL032 COSM5709414 c.913T>A p.S305T Substitution - Missense 5:102959882-102959882 + CSB1 COSM5027793 c.1569C>G p.I523M Substitution - Missense 13:77261340-77261340 - YURAY COSM5401880 c.514A>G p.S172G Substitution - Missense 5:102926656-102926656 + TCGA-BR-6706-01 COSM4126953 c.1055A>G p.K352R Substitution - Missense 5:102960024-102960024 + TCGA-46-3769-01 COSM697332 c.6344A>T p.E2115V Substitution - Missense 13:77165274-77165274 - CSCC-38-T COSM4522415 c.1161G>A p.Q387Q Substitution - coding silent 5:102961228-102961228 + CSCC-44-T COSM4537048 c.2263G>A p.G755R Substitution - Missense 13:77251155-77251155 - C008 COSM5523391 c.2656G>T p.G886* Substitution - Nonsense 5:103029003-103029003 + 61 COSM5739985 c.1753C>T p.Q585* Substitution - Nonsense 13:77260578-77260578 - TCGA-FP-8099-01 COSM4048498 c.4999G>A p.A1667T Substitution - Missense 13:77180147-77180147 - TCGA-BR-4188-01 COSM4048525 c.3342G>A p.A1114A Substitution - coding silent 13:77206786-77206786 - TCGA-BS-A0UF-01 COSM948547 c.8755T>G p.F2919V Substitution - Missense 13:77098285-77098285 - 1_PRE-TREATMENT COSM1719850 c.1852G>A p.G618R Substitution - Missense 5:103006849-103006849 + AOCS-137-3-7 COSM3943271 c.4887C>G p.V1629V Substitution - coding silent 13:77180259-77180259 - Gp2D COSM4627229 c.4926A>T p.E1642D Substitution - Missense 13:77180220-77180220 - sysucc-1135T COSM5479917 c.2826-7A>G p.? Unknown 13:77217964-77217964 - PT24_2 COSM313010 c.5227-3delT p.? Unknown 13:77176631-77176631 - HCC092T COSM5806540 c.2436C>G p.N812K Substitution - Missense 13:77243138-77243138 - TCGA-D9-A6EC-06 COSM4406307 c.3238T>A p.S1080T Substitution - Missense 13:77211231-77211231 - TCGA-D1-A16X-01 COSM948602 c.5612C>T p.A1871V Substitution - Missense 13:77171560-77171560 - TCGA-D3-A3MV-06 COSM3469738 c.7116T>C p.T2372T Substitution - coding silent 13:77144518-77144518 - TCGA-BR-4361-01 COSM4048436 c.11370+2T>C p.? Unknown 13:77078822-77078822 - HCC2998 COSM1671789 c.2599C>T p.R867* Substitution - Nonsense 5:103028946-103028946 + T578 COSM4704437 c.1363C>A p.L455I Substitution - Missense 13:77263744-77263744 - TCGA-FC-A4JI-01 COSM4393393 c.481A>G p.I161V Substitution - Missense 13:77278911-77278911 - TCGA-D1-A15X-01 COSM948620 c.5051A>G p.K1684R Substitution - Missense 13:77177923-77177923 - LUAD-S01315 COSM344257 c.1704A>T p.T568T Substitution - coding silent 13:77261205-77261205 - TCGA-EB-A4IS-01 COSM3607381 c.1982C>T p.P661L Substitution - Missense 5:103006979-103006979 + BD236T COSM5518601 c.2540-10delT p.? Unknown 5:103028877-103028877 + TCGA-BR-4370-01 COSM4048519 c.3635C>A p.S1212* Substitution - Nonsense 13:77205350-77205350 - sysucc-311T COSM196501 c.2386G>T p.E796* Substitution - Nonsense 13:77243833-77243833 - TCGA-BS-A0UV-01 COSM948695 c.445G>A p.E149K Substitution - Missense 13:77288196-77288196 - TCGA-60-2715-01 COSM697308 c.4147G>C p.E1383Q Substitution - Missense 13:77186054-77186054 - B84-Tumor COSM1747516 c.7024G>T p.E2342* Substitution - Nonsense 13:77146211-77146211 - HCC1937 COSM51110 c.4311T>C p.C1437C Substitution - coding silent 13:77185890-77185890 - TCGA-EB-A44P-01 COSM3607375 c.1469C>T p.P490L Substitution - Missense 5:102974422-102974422 + TCGA-D3-A5GU-06 COSM3469722 c.8903T>C p.F2968S Substitution - Missense 13:77098137-77098137 - TCGA-EE-A3AE-06 COSM3469757 c.5116C>T p.P1706S Substitution - Missense 13:77177858-77177858 - CHC097T COSM4790772 c.1202G>T p.R401M Substitution - Missense 5:102974155-102974155 + 1432464 COSM51621 c.6664C>T p.Q2222* Substitution - Nonsense 13:77156195-77156195 - HCC172 COSM3661297 c.2077C>T p.P693S Substitution - Missense 5:103007519-103007519 + TCGA-AY-6196-01 COSM1367873 c.111C>A p.D37E Substitution - Missense 13:77326551-77326551 - CHC1182T COSM4788698 c.396T>G p.I132M Substitution - Missense 5:102924996-102924996 + TCGA-AB-2991-03 COSM166680 c.6724C>T p.R2242C Substitution - Missense 13:77156135-77156135 - TCGA-A5-A0G9-01 COSM1059263 c.1836C>T p.G612G Substitution - coding silent 5:103006833-103006833 + TCGA-EI-6917-01 COSM3417719 c.3308G>A p.R1103Q Substitution - Missense 13:77206820-77206820 - TCGA-ER-A193-06 COSM3469751 c.5821C>T p.P1941S Substitution - Missense 13:77168607-77168607 - 587224 COSM1216064 c.542C>A p.P181Q Substitution - Missense 13:77278850-77278850 - 230 COSM3728968 c.2826-8delT p.? Unknown 13:77217965-77217965 - 587376 COSM1216087 c.8285C>A p.S2762Y Substitution - Missense 13:77098755-77098755 - 587224 COSM1219167 c.265G>A p.V89M Substitution - Missense 5:102901410-102901410 + TCGA-CM-6162-01 COSM1431998 c.2507C>T p.T836M Substitution - Missense 5:103028206-103028206 + TCGA-ER-A194-01 COSM3469778 c.1106G>A p.R369K Substitution - Missense 13:77270032-77270032 - CHC2206T COSM4956951 c.1680A>G p.A560A Substitution - coding silent 13:77261229-77261229 - HCC38T COSM1607230 c.4407A>G p.K1469K Substitution - coding silent 13:77185301-77185301 - TCGA-24-1470-01 COSM75501 c.4923A>C p.R1641S Substitution - Missense 13:77180223-77180223 - S00933 COSM313007 c.5510G>T p.G1837V Substitution - Missense 13:77174338-77174338 - DLD1 COSM1950329 c.2173C>T p.L725L Substitution - coding silent 13:77251245-77251245 - TCGA-C5-A1BQ-01 COSM4841659 c.7936C>G p.P2646A Substitution - Missense 13:77121463-77121463 - CHC1182T COSM4788698 c.396T>G p.I132M Substitution - Missense 5:102924996-102924996 + TCGA-G4-6586-01 COSM1367791 c.7876G>A p.G2626R Substitution - Missense 13:77125363-77125363 - TCGA-C8-A12Z-01 COSM432575 c.2495A>G p.H832R Substitution - Missense 13:77243079-77243079 - PCSI_0082_Pa_X COSM3381033 c.925A>T p.M309L Substitution - Missense 5:102959894-102959894 + PDA_012 COSM4998627 c.9721delT p.C3242fs*13 Deletion - Frameshift 13:77096431-77096431 - LUAD-NYU259 COSM371947 c.1407G>T p.R469S Substitution - Missense 5:102974360-102974360 + ESCC_18 COSM5626141 c.233C>T p.S78F Substitution - Missense 5:102901378-102901378 + ESO-0053 COSM1258373 c.6556C>T p.L2186F Substitution - Missense 13:77158037-77158037 - TCGA-G9-6354-01 COSM3782812 c.11981A>T p.Q3994L Substitution - Missense 13:77068641-77068641 - LC_S15 COSM1186799 c.1315G>C p.D439H Substitution - Missense 5:102974268-102974268 + 8016470 COSM3384908 c.11173G>A p.D3725N Substitution - Missense 13:77081558-77081558 - CHC1742T COSM4792197 c.3605A>G p.H1202R Substitution - Missense 13:77205380-77205380 - TCGA-BS-A0UF-01 COSM948535 c.9463C>A p.L3155I Substitution - Missense 13:77097577-77097577 - pfg122T COSM4747511 c.12476delA p.N4160fs*10 Deletion - Frameshift 13:77064697-77064697 - CSCC-49-T COSM481717 c.1516G>A p.G506R Substitution - Missense 5:102990304-102990304 + TCGA-AP-A0LM-01 COSM948623 c.4941C>A p.S1647S Substitution - coding silent 13:77180205-77180205 - CSCC-29-T COSM4468445 c.1544C>T p.S515F Substitution - Missense 5:102990332-102990332 + TCGA-AN-A046-01 COSM3814085 c.5796C>A p.V1932V Substitution - coding silent 13:77168632-77168632 - TCGA-BS-A0UV-01 COSM948581 c.6345+2T>C p.? Unknown 13:77165271-77165271 - TCGA-B9-A5W9-01 COSM3987457 c.7285A>G p.K2429E Substitution - Missense 13:77140848-77140848 - BD186T COSM5501227 c.3409G>C p.E1137Q Substitution - Missense 13:77206719-77206719 - pfg008T COSM1642547 c.1292delA p.K433fs*32 Deletion - Frameshift 5:102974245-102974245 + 2492722 COSM5720358 c.1616C>T p.S539L Substitution - Missense 5:103003035-103003035 + PR-00-1165 COSM246351 c.129T>C p.L43L Substitution - coding silent 5:102867312-102867312 + TCGA-BR-6452-01 COSM4048543 c.745G>A p.A249T Substitution - Missense 13:77273558-77273558 - TCGA-D8-A1JA-01 COSM3814091 c.3532G>C p.E1178Q Substitution - Missense 13:77205542-77205542 - YUOMEGA COSM5376892 c.8095A>G p.K2699E Substitution - Missense 13:77098945-77098945 - HT115 COSM2989817 c.1733T>G p.F578C Substitution - Missense 5:103005156-103005156 + PT49 COSM5936012 c.11909C>T p.A3970V Substitution - Missense 13:77068713-77068713 - sysucc-2215T COSM5765655 c.670C>T p.R224* Substitution - Nonsense 13:77273633-77273633 - 8036161 COSM3384911 c.7075C>T p.P2359S Substitution - Missense 13:77144559-77144559 - S0045 COSM5882443 c.1542C>A p.Y514* Substitution - Nonsense 13:77261367-77261367 - TCGA-DB-5281-01 COSM3968649 c.7398T>G p.I2466M Substitution - Missense 13:77140053-77140053 - U2940 COSM5621310 c.6817G>A p.V2273I Substitution - Missense 13:77150934-77150934 - C086 COSM5536445 c.1114C>T p.P372S Substitution - Missense 5:102961181-102961181 + sysucc-1317T COSM5450042 c.335C>A p.P112H Substitution - Missense 5:102914000-102914000 + YUDUTY COSM1300301 c.10966C>T p.L3656F Substitution - Missense 13:77081950-77081950 - 4537_T COSM3946708 c.1731-1G>T p.? Unknown 5:103005153-103005153 + 426 COSM4432845 c.13398delA p.A4468fs*2 Deletion - Frameshift 13:77055693-77055693 - EOPC-018_tumor COSM5950369 c.747A>T p.R249S Substitution - Missense 5:102949924-102949924 + PTC-7C COSM4147771 c.6519T>G p.G2173G Substitution - coding silent 13:77158074-77158074 - HDC90 COSM4637468 c.264C>T p.F88F Substitution - coding silent 5:102901409-102901409 + BL14 COSM3728176 c.4C>T p.P2S Substitution - Missense 13:77326658-77326658 - CHC1053T COSM3669356 c.1170C>A p.F390L Substitution - Missense 5:102974123-102974123 + TCGA-D1-A0ZQ-01 COSM948599 c.5741T>C p.I1914T Substitution - Missense 13:77169654-77169654 - TCGA-CG-4442-01 COSM4048477 c.7105A>G p.N2369D Substitution - Missense 13:77144529-77144529 - ESO-224 COSM1258390 c.9426G>A p.Q3142Q Substitution - coding silent 13:77097614-77097614 - TCGA-D5-6928-01 COSM1367760 c.9237A>G p.K3079K Substitution - coding silent 13:77097803-77097803 - ccRCC-71 COSM1662948 c.6340G>C p.D2114H Substitution - Missense 13:77165278-77165278 - TCGA-FR-A3YO-06 COSM3607367 c.581C>T p.P194L Substitution - Missense 5:102948383-102948383 + C99 COSM4620335 c.3412C>G p.L1138V Substitution - Missense 13:77206716-77206716 - TCGA-CD-5801-01 COSM4048474 c.7256T>C p.V2419A Substitution - Missense 13:77140877-77140877 - TCGA-BR-6566-01 COSM4048489 c.6594A>G p.E2198E Substitution - coding silent 13:77157999-77157999 - sysucc-311T COSM5478591 c.279G>T p.E93D Substitution - Missense 13:77288362-77288362 - TCGA-BS-A0UF-01 COSM948665 c.2133G>T p.E711D Substitution - Missense 13:77251285-77251285 - Case4c COSM1717339 c.9071C>G p.S3024C Substitution - Missense 13:77097969-77097969 - KYSE110 COSM5049491 c.2746G>C p.V916L Substitution - Missense 13:77224530-77224530 - TCGA-EV-5902-01 COSM3987460 c.2659A>G p.K887E Substitution - Missense 13:77225519-77225519 - TCGA-EJ-5525-01 COSM1128348 c.7089G>A p.M2363I Substitution - Missense 13:77144545-77144545 - 1517_PT COSM1949683 c.13185C>T p.F4395F Substitution - coding silent 13:77058248-77058248 - LUAD-B02515 COSM336028 c.11738A>G p.E3913G Substitution - Missense 13:77070683-77070683 - CSCC-44-T COSM1367767 c.8897C>T p.S2966L Substitution - Missense 13:77098143-77098143 - TCGA-HT-8106-01 COSM3968655 c.282T>A p.N94K Substitution - Missense 13:77288359-77288359 - 587332 COSM1216075 c.6050A>G p.Q2017R Substitution - Missense 13:77166505-77166505 - TCGA-HU-A4GU-01 COSM4048483 c.6922A>G p.M2308V Substitution - Missense 13:77150829-77150829 - pfg122T COSM4757822 c.8656G>C p.V2886L Substitution - Missense 13:77098384-77098384 - 700T COSM4963747 c.7771G>A p.V2591I Substitution - Missense 13:77125468-77125468 - PT49 COSM5935006 c.448G>A p.G150R Substitution - Missense 5:102926590-102926590 + BD72T COSM5513002 c.7114A>G p.T2372A Substitution - Missense 13:77144520-77144520 - TCGA-AP-A0LM-01 COSM948550 c.8125C>T p.R2709C Substitution - Missense 13:77098915-77098915 - SNU-175 COSM1950242 c.3281C>A p.P1094H Substitution - Missense 13:77211188-77211188 - TCGA-CM-5864-01 COSM1367795 c.7768G>T p.E2590* Substitution - Nonsense 13:77126320-77126320 - TCGA-06-0745-01 COSM2151765 c.1597T>C p.W533R Substitution - Missense 13:77261312-77261312 - HCT15 COSM2989797 c.1331C>T p.A444V Substitution - Missense 5:102974284-102974284 + 3765_T COSM3955734 c.8319A>G p.E2773E Substitution - coding silent 13:77098721-77098721 - 226 COSM4425821 c.4131C>T p.V1377V Substitution - coding silent 13:77188957-77188957 - TCGA-EE-A3AA-06 COSM3607362 c.430C>T p.R144W Substitution - Missense 5:102925030-102925030 + TCGA-CA-6718-01 COSM1431976 c.693C>A p.V231V Substitution - coding silent 5:102949586-102949586 + TCGA-AP-A059-01 COSM948557 c.7048C>T p.R2350C Substitution - Missense 13:77146187-77146187 - 437 COSM4434148 c.2796G>T p.G932G Substitution - coding silent 13:77224480-77224480 - TCGA-FS-A1ZK-06 COSM3469772 c.2420C>T p.P807L Substitution - Missense 13:77243154-77243154 - TCGA-EB-A551-01 COSM3607387 c.2108G>A p.R703Q Substitution - Missense 5:103007550-103007550 + Pat_41_B COSM5842738 c.2267G>A p.G756E Substitution - Missense 13:77251151-77251151 - SNUH_G26_S1 COSM3999127 c.6358T>C p.L2120L Substitution - coding silent 13:77164529-77164529 - TCGA-DD-A1EA-01 COSM4920142 c.124T>A p.C42S Substitution - Missense 5:102867307-102867307 + 9113_T COSM5040757 c.835A>C p.S279R Substitution - Missense 5:102950750-102950750 + AA1924 COSM4168492 c.4827G>T p.Q1609H Substitution - Missense 13:77181701-77181701 - ESO-859 COSM1239512 c.2862T>C p.P954P Substitution - coding silent 13:77217921-77217921 - PD10014a COSM5769910 c.6484-4A>G p.? Unknown 13:77158113-77158113 - 61 COSM5739982 c.4607A>G p.D1536G Substitution - Missense 13:77181921-77181921 - PD18748a COSM5771016 c.4106T>C p.L1369S Substitution - Missense 13:77188982-77188982 - 5_PRE-TREATMENT COSM1642547 c.1292delA p.K433fs*32 Deletion - Frameshift 5:102974245-102974245 + TCGA-06-0649 COSM2151455 c.4966G>T p.G1656* Substitution - Nonsense 13:77180180-77180180 - CHC097T COSM4790772 c.1202G>T p.R401M Substitution - Missense 5:102974155-102974155 + 169 COSM3729590 c.3858_3860delCCT p.L1287delL Deletion - In frame 13:77191775-77191777 - TCGA-FW-A3R5-06 COSM3885531 c.2673C>T p.Y891Y Substitution - coding silent 13:77225505-77225505 - ICGC_0044 COSM218441 c.11926T>C p.C3976R Substitution - Missense 13:77068696-77068696 - TCGA-BS-A0UF-01 COSM948575 c.6508C>A p.L2170I Substitution - Missense 13:77158085-77158085 - Case4d COSM1717339 c.9071C>G p.S3024C Substitution - Missense 13:77097969-77097969 - TCGA-BR-8078-01 COSM1059251 c.238C>T p.R80* Substitution - Nonsense 5:102901383-102901383 + Gp5D COSM1192803 c.1124delA p.K375fs*4 Deletion - Frameshift 13:77270014-77270014 - TCGA-AA-3510-01 COSM1367814 c.5557T>G p.L1853V Substitution - Missense 13:77171615-77171615 - TCGA-BR-8487-01 COSM4126948 c.327C>T p.C109C Substitution - coding silent 5:102913992-102913992 + 24 COSM4777792 c.11519_11520insA p.S3840fs*19 Insertion - Frameshift 13:77077238-77077239 - S00936 COSM313010 c.5227-3delT p.? Unknown 13:77176631-77176631 - RK261_C01 COSM4778295 c.9859A>G p.R3287G Substitution - Missense 13:77095584-77095584 - HX19T COSM1607236 c.3460G>A p.A1154T Substitution - Missense 13:77206668-77206668 - ESO-114 COSM1258384 c.3598G>C p.E1200Q Substitution - Missense 13:77205476-77205476 - 394 COSM3722650 c.4993C>T p.L1665L Substitution - coding silent 13:77180153-77180153 - LP6007548-DNA_A01 COSM5952365 c.2286C>T p.S762S Substitution - coding silent 13:77243933-77243933 - S00832 COSM5660802 c.3558G>T p.K1186N Substitution - Missense 13:77205516-77205516 - TCGA-CG-5730-01 COSM4048528 c.3193C>T p.L1065F Substitution - Missense 13:77211276-77211276 - TCGA-ER-A194-01 COSM1059267 c.2291C>T p.S764F Substitution - Missense 5:103009826-103009826 + TCGA-FW-A3R5-06 COSM3469690 c.12018C>T p.L4006L Substitution - coding silent 13:77068604-77068604 - S02382 COSM5697790 c.3883G>T p.A1295S Substitution - Missense 13:77191752-77191752 - GHE0776 COSM4704374 c.8855G>A p.R2952Q Substitution - Missense 13:77098185-77098185 - TCGA-ER-A19P-06 COSM3469748 c.5892C>A p.T1964T Substitution - coding silent 13:77168536-77168536 - SH-1537 COSM5018015 c.728G>T p.C243F Substitution - Missense 13:77273575-77273575 - 587376 COSM1216091 c.3829T>C p.Y1277H Substitution - Missense 13:77191806-77191806 - Pat_41_B COSM5842719 c.9766_9767insT p.G3256fs*9 Insertion - Frameshift 13:77096385-77096386 - TCGA-51-4080-01 COSM697311 c.4297C>T p.R1433C Substitution - Missense 13:77185904-77185904 - TCGA-33-4566-01 COSM697302 c.1643C>G p.S548* Substitution - Nonsense 13:77261266-77261266 - Pat_63_B COSM5842722 c.9415G>A p.A3139T Substitution - Missense 13:77097625-77097625 - 19 COSM5746435 c.946T>C p.Y316H Substitution - Missense 5:102959915-102959915 + 2293776 COSM4607581 c.2448C>A p.H816Q Substitution - Missense 13:77243126-77243126 - TCGA-CK-5916-01 COSM1950305 c.2480G>A p.R827H Substitution - Missense 13:77243094-77243094 - TCGA-AP-A054-01 COSM948635 c.3996T>C p.N1332N Substitution - coding silent 13:77190296-77190296 - CT-TC COSM4989529 c.4677C>A p.H1559Q Substitution - Missense 13:77181851-77181851 - PCSI_0007_Pa_P COSM216307 c.8339G>A p.R2780Q Substitution - Missense 13:77098701-77098701 - BN42T COSM1607236 c.3460G>A p.A1154T Substitution - Missense 13:77206668-77206668 - LS174T COSM1950067 c.6278A>G p.D2093G Substitution - Missense 13:77165340-77165340 - BD114T COSM1059274 c.2696C>T p.A899V Substitution - Missense 5:103029043-103029043 + TCGA-AM-5820-01 COSM3760849 c.1688A>G p.D563G Substitution - Missense 5:103003107-103003107 + tumor_4108992 COSM5949764 c.10358T>G p.I3453S Substitution - Missense 13:77090159-77090159 - 585208 COSM325881 c.2736C>A p.H912Q Substitution - Missense 13:77225442-77225442 - TCGA-FT-A3EE-01 COSM3793387 c.5317G>A p.D1773N Substitution - Missense 13:77176538-77176538 - TCGA-BT-A2LB-01 COSM3793390 c.528A>G p.T176T Substitution - coding silent 13:77278864-77278864 - KPOPBR-03-T COSM5965126 c.2270T>C p.I757T Substitution - Missense 13:77243949-77243949 - BRC39 COSM5027787 c.11562G>A p.Q3854Q Substitution - coding silent 13:77077196-77077196 - ESCC_25 COSM5626636 c.3172G>A p.E1058K Substitution - Missense 13:77211297-77211297 - pfg008T COSM1642547 c.1292delA p.K433fs*32 Deletion - Frameshift 5:102974245-102974245 + C135 COSM1192803 c.1124delA p.K375fs*4 Deletion - Frameshift 13:77270014-77270014 - BN41 COSM1607233 c.3602-7A>G p.? Unknown 13:77205390-77205390 - TCGA-EE-A3JD-06 COSM1367864 c.462C>T p.P154P Substitution - coding silent 13:77288179-77288179 - 251 COSM1741866 c.351T>G p.S117R Substitution - Missense 5:102914016-102914016 + TCGA-CD-A4MI-01 COSM4048466 c.8554G>T p.E2852* Substitution - Nonsense 13:77098486-77098486 - TCGA-AN-A046-01 COSM3826496 c.184C>T p.R62C Substitution - Missense 5:102867367-102867367 + T3527 COSM4710925 c.2379G>T p.V793V Substitution - coding silent 5:103017381-103017381 + TCGA-AX-A05Z-01 COSM1059259 c.1184C>T p.S395F Substitution - Missense 5:102974137-102974137 + PT50 COSM5937606 c.7189+8C>T p.? Unknown 13:77144437-77144437 - TCGA-EB-A41A-01 COSM3469718 c.8970C>T p.A2990A Substitution - coding silent 13:77098070-77098070 - 1_RESISTANT COSM1719850 c.1852G>A p.G618R Substitution - Missense 5:103006849-103006849 + HCC109T COSM5816762 c.13824G>T p.K4608N Substitution - Missense 13:77045477-77045477 - TCGA-EE-A2GR-06 COSM3469704 c.10731A>G p.E3577E Substitution - coding silent 13:77087514-77087514 - T1764 COSM4704443 c.725C>T p.A242V Substitution - Missense 13:77273578-77273578 - 587376 COSM1219171 c.2584C>T p.R862C Substitution - Missense 5:103028931-103028931 + TCGA-EE-A2MS-06 COSM3607365 c.538G>A p.D180N Substitution - Missense 5:102946848-102946848 + TCGA-A6-6780-01 COSM1431984 c.1291_1292insA p.D434fs*6 Insertion - Frameshift 5:102974244-102974245 + C547 COSM4442375 c.2708G>A p.R903Q Substitution - Missense 13:77225470-77225470 - Pat_06_A COSM5842735 c.5430delC p.T1811fs*8 Deletion - Frameshift 13:77174418-77174418 - TCGA-AX-A0J0-01 COSM948608 c.5317G>T p.D1773Y Substitution - Missense 13:77176538-77176538 - TCGA-A6-6653-01 COSM1367817 c.5382C>T p.R1794R Substitution - coding silent 13:77174466-77174466 - TCGA-AX-A05Z-01 COSM948584 c.6270G>T p.V2090V Substitution - coding silent 13:77165348-77165348 - TCGA-EI-6513-01 COSM3417716 c.5417A>T p.D1806V Substitution - Missense 13:77174431-77174431 - RK184_C01 COSM1633865 c.724+6A>T p.? Unknown 5:102949623-102949623 + TCGA-C5-A1BI-01 COSM4841505 c.468G>A p.E156E Substitution - coding silent 5:102926610-102926610 + T1154 COSM1642547 c.1292delA p.K433fs*32 Deletion - Frameshift 5:102974245-102974245 + T2269 COSM4704390 c.8345C>T p.S2782L Substitution - Missense 13:77098695-77098695 - 11M COSM5576838 c.8518C>T p.P2840S Substitution - Missense 13:77098522-77098522 - T207 COSM4704440 c.1102A>C p.I368L Substitution - Missense 13:77270036-77270036 - TCGA-A8-A085-01 COSM432578 c.428C>G p.S143* Substitution - Nonsense 13:77288213-77288213 - TCGA-AP-A059-01 COSM948563 c.6943T>C p.S2315P Substitution - Missense 13:77150808-77150808 - LUAD_E00522 COSM352497 c.3812G>T p.C1271F Substitution - Missense 13:77194162-77194162 - T3152 COSM4704422 c.5681-3_5681-2insT p.? Unknown 13:77169716-77169717 - 2492721 COSM5720358 c.1616C>T p.S539L Substitution - Missense 5:103003035-103003035 + LUAD-F00057 COSM339481 c.1909G>T p.A637S Substitution - Missense 5:103006906-103006906 + LUAD-B00416 COSM330910 c.10813G>A p.A3605T Substitution - Missense 13:77083141-77083141 - TCGA-D3-A3ML-06 COSM3469781 c.1012C>T p.L338F Substitution - Missense 13:77270358-77270358 - pfg019T COSM1639381 c.9841-10delT p.? Unknown 13:77095612-77095612 - TCGA-EE-A2GC-06 COSM3469715 c.9269C>T p.P3090L Substitution - Missense 13:77097771-77097771 - BD10T COSM5514555 c.8182G>T p.A2728S Substitution - Missense 13:77098858-77098858 - DLD1 COSM4622860 c.9180T>C p.N3060N Substitution - coding silent 13:77097860-77097860 - TCGA-A6-6780-01 COSM1431978 c.780G>A p.R260R Substitution - coding silent 5:102949957-102949957 + GC4_T COSM150859 c.2826-6delA p.? Unknown 13:77217963-77217963 - T3446 COSM4704363 c.13529G>A p.C4510Y Substitution - Missense 13:77055562-77055562 - YUAKER COSM1696004 c.347G>A p.G116E Substitution - Missense 5:102914012-102914012 + TCGA-IA-A40U-01 COSM3993876 c.214G>A p.D72N Substitution - Missense 5:102901359-102901359 + U2940 COSM5621316 c.769A>C p.T257P Substitution - Missense 13:77273534-77273534 - RK014_C01 COSM1629165 c.12410T>C p.I4137T Substitution - Missense 13:77066020-77066020 - TCGA-AC-A23H-01 COSM3814088 c.3984G>C p.K1328N Substitution - Missense 13:77190308-77190308 - 01-P8014 COSM4576003 c.10779A>G p.R3593R Substitution - coding silent 13:77083175-77083175 - 16 COSM1949742 c.11744T>C p.M3915T Substitution - Missense 13:77070677-77070677 - TCGA-D3-A51T-06 COSM3607377 c.1547G>A p.G516E Substitution - Missense 5:102990335-102990335 + TCGA-EK-A2RJ-01 COSM4832088 c.2503G>A p.E835K Substitution - Missense 13:77243071-77243071 - TCGA-B5-A0JY-01 COSM1059253 c.413G>T p.R138I Substitution - Missense 5:102925013-102925013 + HT115 COSM2989809 c.1602C>A p.V534V Substitution - coding silent 5:102990390-102990390 + TCGA-AN-A046-01 COSM3814062 c.9813C>T p.L3271L Substitution - coding silent 13:77096339-77096339 - LUAD-YINHD COSM348866 c.4680G>T p.T1560T Substitution - coding silent 13:77181848-77181848 - RK278_C01 COSM4943304 c.1045A>G p.I349V Substitution - Missense 13:77270325-77270325 - 2492710 COSM5717757 c.4611C>T p.I1537I Substitution - coding silent 13:77181917-77181917 - HCT8 COSM4633858 c.2401G>T p.D801Y Substitution - Missense 13:77243818-77243818 - TCGA-AA-3492-01 COSM1367753 c.10893C>T p.P3631P Substitution - coding silent 13:77083061-77083061 - TCGA-B5-A11E-01 COSM1059267 c.2291C>T p.S764F Substitution - Missense 5:103009826-103009826 + HX16T COSM1619279 c.569G>A p.R190H Substitution - Missense 5:102946879-102946879 + STC246 COSM5052238 c.12093A>G p.E4031E Substitution - coding silent 13:77067829-77067829 - TCGA-60-2698-01 COSM697317 c.4459C>T p.Q1487* Substitution - Nonsense 13:77185249-77185249 - PR-04-194 COSM246349 c.301G>T p.V101F Substitution - Missense 5:102913966-102913966 + TCGA-AA-3510-01 COSM1431988 c.2038C>T p.P680S Substitution - Missense 5:103007480-103007480 + PTC_449 COSM5960105 c.586A>G p.I196V Substitution - Missense 5:102948388-102948388 + T578 COSM4704434 c.2371C>A p.L791I Substitution - Missense 13:77243848-77243848 - HCC18T COSM1607239 c.2530G>T p.A844S Substitution - Missense 13:77233249-77233249 - B52 COSM1756825 c.2543T>C p.F848S Substitution - Missense 13:77233236-77233236 - ccRCC-58 COSM1659634 c.954delA p.E320fs*30 Deletion - Frameshift 13:77270416-77270416 - TCGA-BR-8591-01 COSM4048513 c.4102A>G p.I1368V Substitution - Missense 13:77188986-77188986 - LOVO COSM4614135 c.8446delA p.S2816fs*39 Deletion - Frameshift 13:77098594-77098594 - TCGA-46-3769-01 COSM735181 c.2499A>T p.K833N Substitution - Missense 5:103028198-103028198 + LUAD_E00522 COSM352500 c.480+1G>T p.? Unknown 13:77288160-77288160 - 064 COSM1741250 c.1698C>G p.F566L Substitution - Missense 13:77261211-77261211 - HCT15 COSM1950163 c.4861C>A p.R1621S Substitution - Missense 13:77180285-77180285 - TCGA-EE-A2GC-06 COSM3469744 c.6732T>C p.G2244G Substitution - coding silent 13:77156127-77156127 - TCGA-D3-A5GU-06 COSM3469766 c.2978C>T p.P993L Substitution - Missense 13:77212126-77212126 - CSCC-20-T COSM4572862 c.8775T>C p.G2925G Substitution - coding silent 13:77098265-77098265 - S00933 COSM313007 c.5510G>T p.G1837V Substitution - Missense 13:77174338-77174338 - STC297 COSM1219167 c.265G>A p.V89M Substitution - Missense 5:102901410-102901410 + TCGA-HU-A4G8-01 COSM3469685 c.12620C>T p.S4207F Substitution - Missense 13:77062636-77062636 - 216 COSM4424641 c.6233A>C p.E2078A Substitution - Missense 13:77165385-77165385 - T3724 COSM4704413 c.6266A>G p.Y2089C Substitution - Missense 13:77165352-77165352 - cSCCP4 COSM138916 c.5639G>A p.R1880Q Substitution - Missense 13:77171533-77171533 - Gp2D COSM4627225 c.8915G>A p.G2972E Substitution - Missense 13:77098125-77098125 - TCGA-HU-A4GQ-01 COSM4048433 c.11584C>T p.L3862L Substitution - coding silent 13:77077174-77077174 - TCGA-22-1011-01 COSM735183 c.1300G>C p.D434H Substitution - Missense 5:102974253-102974253 + PD24209a COSM5781039 c.1743A>T p.P581P Substitution - coding silent 5:103005166-103005166 + I2L-P6-Tumor-Biopsy COSM5362213 c.5109C>T p.N1703N Substitution - coding silent 13:77177865-77177865 - CSCC-45-T COSM1300301 c.10966C>T p.L3656F Substitution - Missense 13:77081950-77081950 - BN41T COSM1607233 c.3602-7A>G p.? Unknown 13:77205390-77205390 - TCGA-AC-A23H-01 COSM3814069 c.8154G>C p.K2718N Substitution - Missense 13:77098886-77098886 - ESCC_28 COSM5627306 c.573G>T p.L191L Substitution - coding silent 13:77278819-77278819 - ccRCC-71 COSM1662945 c.6341A>T p.D2114V Substitution - Missense 13:77165277-77165277 - TCGA-AP-A056-01 COSM948500 c.13529G>T p.C4510F Substitution - Missense 13:77055562-77055562 - CHC2052T COSM4789999 c.5182G>A p.G1728R Substitution - Missense 13:77177792-77177792 - RK111_C01 COSM3744203 c.6796A>G p.M2266V Substitution - Missense 13:77156063-77156063 - HCC6 COSM1619281 c.980T>A p.M327K Substitution - Missense 5:102959949-102959949 + HCC6T COSM1619281 c.980T>A p.M327K Substitution - Missense 5:102959949-102959949 + 3N39-VS-3T39 COSM4981543 c.902T>A p.I301N Substitution - Missense 5:102950817-102950817 + HCC099T COSM5816679 c.3133A>G p.S1045G Substitution - Missense 13:77211971-77211971 - TCGA-BS-A0UF-01 COSM948659 c.2401G>A p.D801N Substitution - Missense 13:77243818-77243818 - PT42 COSM5925759 c.4961C>T p.T1654I Substitution - Missense 13:77180185-77180185 - CHEWS014 COSM4576006 c.6636A>C p.S2212S Substitution - coding silent 13:77157957-77157957 - 169 COSM3728968 c.2826-8delT p.? Unknown 13:77217965-77217965 - TCGA-BR-4370-01 COSM4048534 c.2516-2A>G p.? Unknown 13:77233265-77233265 - T155 COSM1176830 c.11144G>A p.S3715N Substitution - Missense 13:77081587-77081587 - Pat_26_A COSM5866991 c.2273G>A p.G758E Substitution - Missense 5:103009808-103009808 + TCGA-EE-A3AC-06 COSM3469709 c.9357C>T p.P3119P Substitution - coding silent 13:77097683-77097683 - PT17_1 COSM3728968 c.2826-8delT p.? Unknown 13:77217965-77217965 - TCGA-AA-3663-01 COSM5827418 c.5227-5_5227-3delTTT p.? Unknown 13:77176631-77176633 - T207 COSM1192803 c.1124delA p.K375fs*4 Deletion - Frameshift 13:77270014-77270014 - TCGA-CD-8529-01 COSM4048540 c.1750C>T p.R584W Substitution - Missense 13:77260581-77260581 - pfg181T COSM4757839 c.692G>A p.S231N Substitution - Missense 13:77273611-77273611 - T3610 COSM4704374 c.8855G>A p.R2952Q Substitution - Missense 13:77098185-77098185 - TCGA-BR-4361-01 COSM4048522 c.3420A>G p.L1140L Substitution - coding silent 13:77206708-77206708 - WA16 COSM237136 c.1059C>T p.Y353Y Substitution - coding silent 13:77270311-77270311 - LS411 COSM1950317 c.2330C>T p.A777V Substitution - Missense 13:77243889-77243889 - TCGA-BK-A0C9-01 COSM948641 c.3654C>T p.F1218F Substitution - coding silent 13:77205331-77205331 - 2492724 COSM5725402 c.211-1G>A p.? Unknown 5:102901355-102901355 + TCGA-AA-3858-01 COSM272037 c.5752A>T p.I1918L Substitution - Missense 13:77169643-77169643 - EGC3 COSM1432002 c.2700C>T p.L900L Substitution - coding silent 5:103029047-103029047 + Gp5D COSM2989839 c.2208T>C p.Y736Y Substitution - coding silent 5:103007650-103007650 + ESCC_68 COSM5634002 c.1838C>G p.P613R Substitution - Missense 5:103006835-103006835 + TCGA-BR-4184-01 COSM1059251 c.238C>T p.R80* Substitution - Nonsense 5:102901383-102901383 + TCGA-EE-A2A2-06 COSM3469741 c.6826T>A p.S2276T Substitution - Missense 13:77150925-77150925 - TCGA-ER-A19P-06 COSM3469775 c.1669C>T p.L557F Substitution - Missense 13:77261240-77261240 - TCGA-AP-A0LF-01 COSM948541 c.9273G>A p.L3091L Substitution - coding silent 13:77097767-77097767 - HCC105 COSM1607242 c.2246G>A p.R749Q Substitution - Missense 13:77251172-77251172 - PT16_1 COSM5898272 c.2204C>T p.S735L Substitution - Missense 5:103007646-103007646 + GC2_T COSM147702 c.3825A>C p.E1275D Substitution - Missense 13:77191810-77191810 - TCGA-B5-A0JS-01 COSM948668 c.1937C>A p.T646N Substitution - Missense 13:77257796-77257796 - TCGA-G4-6586-01 COSM1192803 c.1124delA p.K375fs*4 Deletion - Frameshift 13:77270014-77270014 - TCGA-43-3920-01 COSM697350 c.8223G>A p.L2741L Substitution - coding silent 13:77098817-77098817 - HCC2998 COSM1950388 c.838A>G p.T280A Substitution - Missense 13:77270532-77270532 - BK0042 COSM4187317 c.9480_9481delTG p.C3160fs*1 Deletion - Frameshift 13:77097559-77097560 - NCI-H1395 COSM24421 c.3610_3610GG>TT p.G1204L Substitution - Missense 12M COSM948590 c.6177G>A p.K2059K Substitution - coding silent 13:77166378-77166378 - TCGA-AA-A010-01 COSM283690 c.1303C>A p.L435I Substitution - Missense 5:102974256-102974256 + TCGA-B0-5109-01 COSM469571 c.2474G>C p.R825P Substitution - Missense 13:77243100-77243100 - TCGA-GC-A3I6-01 COSM1300301 c.10966C>T p.L3656F Substitution - Missense 13:77081950-77081950 - TCGA-EE-A2A6-06 COSM3469685 c.12620C>T p.S4207F Substitution - Missense 13:77062636-77062636 - TCGA-EK-A2RJ-01 COSM4831959 c.2506G>A p.E836K Substitution - Missense 13:77243068-77243068 - TCGA-B5-A0JY-01 COSM948674 c.1775A>C p.K592T Substitution - Missense 13:77260556-77260556 - BD233T COSM5508969 c.2826-9T>C p.? Unknown 13:77217966-77217966 - ESO-175 COSM1258387 c.1508C>T p.A503V Substitution - Missense 13:77262078-77262078 - TCGA-D1-A17Q-01 COSM1059265 c.2180T>C p.F727S Substitution - Missense 5:103007622-103007622 + I2L-P6-Tumor-Organoid COSM5362213 c.5109C>T p.N1703N Substitution - coding silent 13:77177865-77177865 - TCGA-D3-A5GO-06 COSM3607369 c.735A>G p.V245V Substitution - coding silent 5:102949912-102949912 + TCGA-AP-A0LM-01 COSM948650 c.3229T>G p.F1077V Substitution - Missense 13:77211240-77211240 - 2492722 COSM5722135 c.3259G>A p.G1087R Substitution - Missense 13:77211210-77211210 - T2269 COSM4704425 c.5491G>A p.G1831S Substitution - Missense 13:77174357-77174357 - TCGA-BR-4184-01 COSM4048531 c.2616G>A p.K872K Substitution - coding silent 13:77233163-77233163 - TCGA-AA-3492-01 COSM1367864 c.462C>T p.P154P Substitution - coding silent 13:77288179-77288179 - EC109 COSM5049345 c.2128G>C p.D710H Substitution - Missense 13:77251290-77251290 - TCGA-BS-A0UF-01 COSM1059270 c.2455A>G p.K819E Substitution - Missense 5:103019813-103019813 + HCC074T COSM5810297 c.1190T>A p.L397Q Substitution - Missense 5:102974143-102974143 + AML50 COSM166680 c.6724C>T p.R2242C Substitution - Missense 13:77156135-77156135 - XPA23PT COSM1580101 c.1279G>T p.A427S Substitution - Missense 5:102974232-102974232 + cSCCP1 COSM135633 c.785C>T p.S262F Substitution - Missense 13:77273518-77273518 - RMS110_ COSM4987208 c.1300G>A p.D434N Substitution - Missense 5:102974253-102974253 + SNU-C4 COSM4652437 c.4243C>T p.L1415F Substitution - Missense 13:77185958-77185958 - HCC086T COSM5813055 c.4051A>T p.S1351C Substitution - Missense 13:77189037-77189037 - TCGA-D3-A3MV-06 COSM3607360 c.164C>T p.S55L Substitution - Missense 5:102867347-102867347 + TCGA-EE-A182-06 COSM3469695 c.11416C>T p.L3806F Substitution - Missense 13:77077342-77077342 - TCGA-BR-8368-01 COSM4048459 c.9008A>G p.H3003R Substitution - Missense 13:77098032-77098032 - TCGA-FS-A1ZW-06 COSM3607373 c.1442C>T p.P481L Substitution - Missense 5:102974395-102974395 + CHC961T COSM4950866 c.7621C>T p.Q2541* Substitution - Nonsense 13:77126467-77126467 - YUROC COSM5376896 c.7631C>T p.P2544L Substitution - Missense 13:77126457-77126457 - PD11748a COSM5767441 c.11717C>T p.T3906I Substitution - Missense 13:77070704-77070704 - sysucc-1370T COSM5470196 c.2569G>A p.A857T Substitution - Missense 13:77233210-77233210 - 428 COSM2989736 c.145G>A p.V49I Substitution - Missense 5:102867328-102867328 + Gp2D COSM1192803 c.1124delA p.K375fs*4 Deletion - Frameshift 13:77270014-77270014 - MEL-JWCI-WGS-34 COSM1167586 c.9148_9154delAGACATT p.R3050fs*2 Deletion - Frameshift 13:77097886-77097892 - CHC2206T COSM4956951 c.1680A>G p.A560A Substitution - coding silent 13:77261229-77261229 - PR-2661 COSM245847 c.10866C>G p.T3622T Substitution - coding silent 13:77083088-77083088 - BD236T COSM313010 c.5227-3delT p.? Unknown 13:77176631-77176631 - ESCC_123 COSM5640861 c.5972A>T p.Y1991F Substitution - Missense 13:77168456-77168456 - TCGA-B5-A11E-01 COSM1059245 c.166G>T p.D56Y Substitution - Missense 5:102867349-102867349 + TCGA-EP-A2KB-01 COSM4921422 c.212C>A p.S71Y Substitution - Missense 5:102901357-102901357 + 587380 COSM1216078 c.4396T>A p.L1466M Substitution - Missense 13:77185312-77185312 - YUSMI COSM5376888 c.8933T>G p.L2978* Substitution - Nonsense 13:77098107-77098107 - PT36 COSM5916327 c.319C>T p.P107S Substitution - Missense 13:77288322-77288322 - TCGA-AP-A056-01 COSM948554 c.7381G>T p.G2461* Substitution - Nonsense 13:77140070-77140070 - ESCC-D2 COSM5045780 c.2161G>C p.E721Q Substitution - Missense 5:103007603-103007603 + TCGA-BR-8368-01 COSM4048507 c.4668T>A p.A1556A Substitution - coding silent 13:77181860-77181860 - CRC-19T COSM5481145 c.7073+10G>A p.? Unknown 13:77146152-77146152 - ATL028 COSM5704763 c.3784G>T p.A1262S Substitution - Missense 13:77194190-77194190 - LUAD_E00522 COSM352494 c.6677A>G p.Y2226C Substitution - Missense 13:77156182-77156182 - T2269 COSM4704382 c.8482C>T p.R2828W Substitution - Missense 13:77098558-77098558 - CHC2052T COSM4789999 c.5182G>A p.G1728R Substitution - Missense 13:77177792-77177792 - TCGA-EW-A1PC-01 COSM3826501 c.2433A>C p.K811N Substitution - Missense 5:103019791-103019791 + TCGA-BR-7851-01 COSM4048480 c.7049G>A p.R2350H Substitution - Missense 13:77146186-77146186 - TCGA-BS-A0UJ-01 COSM948593 c.6100A>C p.R2034R Substitution - coding silent 13:77166455-77166455 - TCGA-D5-6930-01 COSM1431990 c.2326C>T p.R776C Substitution - Missense 5:103009861-103009861 + CSCC-52-T COSM4566907 c.4943_4944CC>TT p.S1648F Substitution - Missense 13:77180202-77180203 - DLD1 COSM4622857 c.9194C>T p.A3065V Substitution - Missense 13:77097846-77097846 - ESCC_13 COSM5625122 c.7152C>G p.L2384L Substitution - coding silent 13:77144482-77144482 - LUAD-B02477 COSM335805 c.3627T>A p.S1209S Substitution - coding silent 13:77205358-77205358 - Case4a COSM1717339 c.9071C>G p.S3024C Substitution - Missense 13:77097969-77097969 - CSCC-11-T COSM4510714 c.8348C>T p.S2783F Substitution - Missense 13:77098692-77098692 - Au10 COSM5594931 c.8843C>T p.P2948L Substitution - Missense 13:77098197-77098197 - SS6003317 COSM3980078 c.413T>C p.V138A Substitution - Missense 13:77288228-77288228 - TCGA-BR-4370-01 COSM4048470 c.8530C>T p.R2844C Substitution - Missense 13:77098510-77098510 - 01-P8014 COSM4576009 c.2184C>T p.C728C Substitution - coding silent 13:77251234-77251234 - YUFERY COSM5401884 c.1444C>T p.P482S Substitution - Missense 5:102974397-102974397 + RMH008-R2 COSM4411443 c.5497A>C p.N1833H Substitution - Missense 13:77174351-77174351 - LS174T COSM1949646 c.13921delT p.*4642fs? Deletion - Frameshift 13:77045380-77045380 - TCGA-66-2734-01 COSM697344 c.7786G>A p.G2596R Substitution - Missense 13:77125453-77125453 - TCGA-AX-A05Z-01 COSM948683 c.1429G>A p.D477N Substitution - Missense 13:77263678-77263678 - PT37 COSM5920619 c.2419C>T p.P807S Substitution - Missense 13:77243155-77243155 - GHE0645 COSM5714678 c.1834G>T p.G612C Substitution - Missense 5:103006831-103006831 + HCC058T COSM5805040 c.736A>T p.S246C Substitution - Missense 5:102949913-102949913 + CRC-32T COSM5460665 c.2817C>G p.V939V Substitution - coding silent 13:77224459-77224459 - TCGA-AC-A23H-01 COSM3814078 c.7918G>C p.D2640H Substitution - Missense 13:77121481-77121481 - 1432465 COSM51621 c.6664C>T p.Q2222* Substitution - Nonsense 13:77156195-77156195 - TCGA-D1-A17R-01 COSM948566 c.6850_6852delCAA p.Q2284delQ Deletion - In frame 13:77150899-77150901 - TCGA-A5-A0VP-01 COSM1059251 c.238C>T p.R80* Substitution - Nonsense 5:102901383-102901383 + CHC2029T COSM4793033 c.781A>C p.I261L Substitution - Missense 13:77273522-77273522 - STC263 COSM5060557 c.950A>G p.Y317C Substitution - Missense 5:102959919-102959919 + MOLT-4 COSM948557 c.7048C>T p.R2350C Substitution - Missense 13:77146187-77146187 - ccRCC-59 COSM1659731 c.7409A>G p.H2470R Substitution - Missense 13:77139332-77139332 - SNU-175 COSM1950284 c.2689C>T p.R897* Substitution - Nonsense 13:77225489-77225489 - LIM2551 COSM4644624 c.759A>G p.G253G Substitution - coding silent 5:102949936-102949936 + TCGA-EE-A2A5-06 COSM3469712 c.9350C>T p.P3117L Substitution - Missense 13:77097690-77097690 - TCGA-BR-6452-01 COSM4048456 c.9220A>T p.M3074L Substitution - Missense 13:77097820-77097820 - B52-Tumor COSM1756825 c.2543T>C p.F848S Substitution - Missense 13:77233236-77233236 - TCGA-A3-3372-01 COSM1135511 c.1670T>A p.L557H Substitution - Missense 13:77261239-77261239 - TCGA-C8-A1HK-01 COSM1486192 c.2333A>G p.H778R Substitution - Missense 5:103017335-103017335 + ICGC_0030 COSM1158932 c.4797T>G p.L1599L Substitution - coding silent 13:77181731-77181731 - ESCC_BICR_003T COSM5442649 c.1697T>G p.F566C Substitution - Missense 13:77261212-77261212 - 3N02-VS-3T02 COSM4978432 c.11591T>G p.V3864G Substitution - Missense 13:77077167-77077167 - HCC105T COSM1607242 c.2246G>A p.R749Q Substitution - Missense 13:77251172-77251172 - HCT116 COSM1677719 c.4006G>A p.V1336I Substitution - Missense 13:77190286-77190286 - ESCC_BICR_017T COSM5442930 c.2037G>T p.L679L Substitution - coding silent 5:103007479-103007479 + 9642_PT COSM5756545 c.2456A>G p.K819R Substitution - Missense 5:103019814-103019814 + TCGA-BS-A0UF-01 COSM948689 c.1010T>G p.F337C Substitution - Missense 13:77270360-77270360 - CHC1192T COSM4803610 c.11238C>G p.T3746T Substitution - coding silent 13:77081493-77081493 - TCGA-D5-6930-01 COSM1367779 c.8407C>T p.R2803C Substitution - Missense 13:77098633-77098633 - NCI-H2126 COSM24419 c.3864A>T p.Q1288H Substitution - Missense 13:77191771-77191771 - TCGA-EE-A3J5-06 COSM3469760 c.4917G>A p.L1639L Substitution - coding silent 13:77180229-77180229 - CHC1201T COSM4801687 c.7088T>C p.M2363T Substitution - Missense 13:77144546-77144546 - CHC794T COSM4949505 c.5600A>T p.N1867I Substitution - Missense 13:77171572-77171572 - SWE-8 COSM1178702 c.7656G>A p.M2552I Substitution - Missense 13:77126432-77126432 - TCGA-D8-A1JU-01 COSM1367817 c.5382C>T p.R1794R Substitution - coding silent 13:77174466-77174466 - TCGA-AP-A051-01 COSM1059247 c.173C>T p.A58V Substitution - Missense 5:102867356-102867356 + HCT116 COSM4632061 c.7534G>A p.V2512I Substitution - Missense 13:77139207-77139207 - TCGA-AA-A010-01 COSM283692 c.2439A>G p.E813E Substitution - coding silent 5:103019797-103019797 + TCGA-AP-A051-01 COSM948605 c.5381G>A p.R1794H Substitution - Missense 13:77174467-77174467 - TCGA-CF-A1HS-01 COSM416309 c.2261C>G p.P754R Substitution - Missense 13:77251157-77251157 - PT42 COSM5925756 c.5358G>A p.K1786K Substitution - coding silent 13:77176497-77176497 - 587376 COSM1219169 c.1655G>A p.G552E Substitution - Missense 5:103003074-103003074 + RK006_C02 COSM1633867 c.1681G>T p.V561F Substitution - Missense 5:103003100-103003100 + TCGA-B7-5818-01 COSM4048492 c.5619T>A p.S1873S Substitution - coding silent 13:77171553-77171553 - TCGA-43-6770-01 COSM735185 c.963G>T p.K321N Substitution - Missense 5:102959932-102959932 + SNU-C2B COSM1949665 c.13542delT p.F4515fs*76 Deletion - Frameshift 13:77051910-77051910 - KYSE180 COSM1950094 c.5773A>T p.I1925F Substitution - Missense 13:77169622-77169622 - BN42 COSM1607236 c.3460G>A p.A1154T Substitution - Missense 13:77206668-77206668 - SNU-C2B COSM2989799 c.1474C>T p.H492Y Substitution - Missense 5:102974427-102974427 + I2L-P25-Tumor-Organoid COSM5362194 c.9200A>G p.H3067R Substitution - Missense 13:77097840-77097840 - HCC157T COSM3661291 c.105C>T p.T35T Substitution - coding silent 5:102867288-102867288 + TCGA-EE-A3J4-06 COSM3918419 c.2535T>C p.F845F Substitution - coding silent 5:103028234-103028234 + TCGA-CM-4743-01 COSM1367843 c.2954T>C p.L985P Substitution - Missense 13:77212150-77212150 - TCGA-G2-A3IE-01 COSM1300306 c.7359G>A p.Q2453Q Substitution - coding silent 13:77140092-77140092 - 5_RESISTANT COSM1724927 c.1075-5_1075-4insT p.? Unknown 13:77270067-77270068 - LS174T COSM1950172 c.4791delT p.L1599fs*19 Deletion - Frameshift 13:77181737-77181737 - LUAD_E01166 COSM390754 c.3134G>A p.S1045N Substitution - Missense 13:77211970-77211970 - PT21_2 COSM3728968 c.2826-8delT p.? Unknown 13:77217965-77217965 - 2334189 COSM322459 c.2077C>G p.P693A Substitution - Missense 5:103007519-103007519 + TCGA-13-0885-01 COSM75502 c.2800C>G p.L934V Substitution - Missense 13:77224476-77224476 - sysucc-834T COSM5485669 c.2826-10T>G p.? Unknown 13:77217967-77217967 - TCGA-AO-A03M-01 COSM3814065 c.8627C>T p.S2876F Substitution - Missense 13:77098413-77098413 - BD245T COSM5519980 c.2250T>A p.F750L Substitution - Missense 5:103009785-103009785 + 2521259 COSM5890780 c.7450A>T p.I2484L Substitution - Missense 13:77139291-77139291 - HCC18 COSM1607239 c.2530G>T p.A844S Substitution - Missense 13:77233249-77233249 - CLL138 COSM1289919 c.3235G>A p.D1079N Substitution - Missense 13:77211234-77211234 - DLD1 COSM4622863 c.592C>A p.Q198K Substitution - Missense 13:77278800-77278800 - HCC118T COSM5813735 c.8780A>G p.N2927S Substitution - Missense 13:77098260-77098260 - B84-Tumor COSM1756822 c.5908G>A p.E1970K Substitution - Missense 13:77168520-77168520 - ESCC_29 COSM5627553 c.1194A>G p.L398L Substitution - coding silent 5:102974147-102974147 + 16246 COSM5613696 c.3409G>T p.E1137* Substitution - Nonsense 13:77206719-77206719 - TCGA-EE-A2ML-06 COSM3885518 c.9058C>T p.H3020Y Substitution - Missense 13:77097982-77097982 - TCGA-F4-6856-01 COSM1367840 c.2999C>T p.A1000V Substitution - Missense 13:77212105-77212105 - LUAD-CHTN-MAD06-00668 COSM360055 c.2230G>T p.V744L Substitution - Missense 5:103009765-103009765 + CSCC-20-T COSM4507862 c.645C>T p.F215F Substitution - coding silent 13:77273658-77273658 - BD246T COSM5496121 c.2437G>C p.E813Q Substitution - Missense 5:103019795-103019795 + TCGA-BS-A0UF-01 COSM948692 c.852G>A p.S284S Substitution - coding silent 13:77270518-77270518 - LC_S12 COSM1188730 c.2160G>A p.M720I Substitution - Missense 13:77251258-77251258 - T3670 COSM4710923 c.1006G>C p.D336H Substitution - Missense 5:102959975-102959975 + CHC1085T COSM4788664 c.1172A>G p.N391S Substitution - Missense 13:77267912-77267912 - TCGA-A6-6780-01 COSM1367834 c.3595T>G p.F1199V Substitution - Missense 13:77205479-77205479 - TCGA-39-5024-01 COSM697353 c.8688A>G p.E2896E Substitution - coding silent 13:77098352-77098352 - Pat_16_A COSM1367734 c.12140delC p.P4048fs*26 Deletion - Frameshift 13:77067782-77067782 - TCGA-CA-6718-01 COSM1431980 c.827T>G p.V276G Substitution - Missense 5:102950742-102950742 + Gp2D COSM4576006 c.6636A>C p.S2212S Substitution - coding silent 13:77157957-77157957 - TCGA-AX-A05Z-01 COSM948590 c.6177G>A p.K2059K Substitution - coding silent 13:77166378-77166378 - TCGA-BR-8591-01 COSM4048516 c.3661G>A p.D1221N Substitution - Missense 13:77205324-77205324 - pfg057T COSM1642547 c.1292delA p.K433fs*32 Deletion - Frameshift 5:102974245-102974245 + TCGA-AA-3688-01 COSM268235 c.403G>A p.A135T Substitution - Missense 5:102925003-102925003 + CSCC-57-T COSM4545993 c.3793G>A p.D1265N Substitution - Missense 13:77194181-77194181 - 2334201 COSM321843 c.3569A>G p.K1190R Substitution - Missense 13:77205505-77205505 - TCGA-A6-6653-01 COSM1431982 c.1050C>T p.P350P Substitution - coding silent 5:102960019-102960019 + TCGA-B5-A11E-01 COSM948525 c.10595G>A p.C3532Y Substitution - Missense 13:77088848-77088848 - PCSI0007 COSM216307 c.8339G>A p.R2780Q Substitution - Missense 13:77098701-77098701 - 193 COSM1741702 c.1318-5C>T p.? Unknown 13:77263794-77263794 - 8013142 COSM1158932 c.4797T>G p.L1599L Substitution - coding silent 13:77181731-77181731 - YUMOKI COSM1216061 c.9167C>T p.S3056L Substitution - Missense 13:77097873-77097873 - H1155 COSM1195415 c.12992C>T p.S4331F Substitution - Missense 13:77059557-77059557 - CRC-06T COSM5456407 c.1099C>T p.R367C Substitution - Missense 13:77270039-77270039 - TCGA-B5-A11E-01 COSM948587 c.6183T>G p.F2061L Substitution - Missense 13:77166372-77166372 - Pat_41_B COSM5277108 c.6317G>A p.G2106E Substitution - Missense 13:77165301-77165301 - TCGA-EE-A181-06 COSM3607390 c.2124C>T p.I708I Substitution - coding silent 5:103007566-103007566 + TCGA-HU-A4GN-01 COSM4126951 c.791A>C p.Q264P Substitution - Missense 5:102949968-102949968 + TCGA-AX-A0J0-01 COSM948538 c.9277G>T p.E3093* Substitution - Nonsense 13:77097763-77097763 - TCGA-AX-A0J0-01 COSM1059261 c.1293A>C p.Q431H Substitution - Missense 5:102974246-102974246 + S02299 COSM5690189 c.3156A>G p.V1052V Substitution - coding silent 13:77211313-77211313 - TCGA-AX-A0J0-01 COSM948629 c.4250A>G p.D1417G Substitution - Missense 13:77185951-77185951 - TCGA-BR-7703-01 COSM4048501 c.4944C>A p.S1648S Substitution - coding silent 13:77180202-77180202 - CHC1753T COSM4952523 c.1659A>T p.P553P Substitution - coding silent 5:103003078-103003078 + TCGA-GN-A26C-01 COSM3607384 c.1995C>T p.F665F Substitution - coding silent 5:103006992-103006992 + cSCCP2 COSM137606 c.7066C>T p.P2356S Substitution - Missense 13:77146169-77146169 - ESO-105 COSM1258379 c.3593G>C p.R1198T Substitution - Missense 13:77205481-77205481 - B84 COSM1747516 c.7024G>T p.E2342* Substitution - Nonsense 13:77146211-77146211 - TCGA-B0-4691-01 COSM3360145 c.9963A>G p.A3321A Substitution - coding silent 13:77095480-77095480 - 53M COSM5594931 c.8843C>T p.P2948L Substitution - Missense 13:77098197-77098197 - LUAD-S01478 COSM399674 c.4827G>C p.Q1609H Substitution - Missense 13:77181701-77181701 - 76629543 COSM1582186 c.4277C>A p.T1426N Substitution - Missense 13:77185924-77185924 - CHC303T COSM4950536 c.7153T>A p.Y2385N Substitution - Missense 13:77144481-77144481 - YURUS COSM1696006 c.1084C>T p.H362Y Substitution - Missense 5:102960053-102960053 + SH-0622 COSM5017659 c.1137_1139delAGA p.E383delE Deletion - In frame 5:102961204-102961206 + CRC-02T COSM5455336 c.1483+4C>T p.? Unknown 5:102974440-102974440 + HCC2998 COSM1677722 c.3230T>G p.F1077C Substitution - Missense 13:77211239-77211239 - TCGA-BT-A3PJ-01 COSM3793384 c.5683G>A p.D1895N Substitution - Missense 13:77169712-77169712 - TCGA-AX-A0J0-01 COSM948656 c.2623+1G>A p.? Unknown 13:77233155-77233155 - TCGA-36-2552-01 COSM1322822 c.13710T>C p.V4570V Substitution - coding silent 13:77051094-77051094 - PCSI_0090_Pa_X COSM3376589 c.2029C>T p.R677* Substitution - Nonsense 13:77257704-77257704 - TCGA-CM-5349-01 COSM1432002 c.2700C>T p.L900L Substitution - coding silent 5:103029047-103029047 + 09-131 COSM305398 c.6082C>T p.R2028C Substitution - Missense 13:77166473-77166473 - BD143T COSM948500 c.13529G>T p.C4510F Substitution - Missense 13:77055562-77055562 - D3 COSM5006694 c.1229A>T p.Y410F Substitution - Missense 5:102974182-102974182 + 2492720 COSM5722135 c.3259G>A p.G1087R Substitution - Missense 13:77211210-77211210 - HCC2998 COSM1949858 c.8964T>C p.S2988S Substitution - coding silent 13:77098076-77098076 - TCGA-G4-6294-01 COSM3688777 c.5685T>A p.D1895E Substitution - Missense 13:77169710-77169710 - 600 COSM3722930 c.2000C>A p.T667K Substitution - Missense 5:103006997-103006997 + TCGA-FC-A6HD-01 COSM3671303 c.3883G>A p.A1295T Substitution - Missense 13:77191752-77191752 - CPCG0331-F1 COSM4881073 c.5782-5A>G p.? Unknown 13:77168651-77168651 - TCGA-66-2785-01 COSM697347 c.8002G>C p.D2668H Substitution - Missense 13:77121397-77121397 - CR007 COSM4994646 c.7946G>A p.S2649N Substitution - Missense 13:77121453-77121453 - TCGA-AN-A046-01 COSM3814094 c.2920G>A p.V974I Substitution - Missense 13:77217863-77217863 - TCGA-AP-A0LM-01 COSM948677 c.1769A>C p.K590T Substitution - Missense 13:77260562-77260562 - NOKSI COSM4595455 c.1028C>T p.P343L Substitution - Missense 5:102959997-102959997 + TCGA-EE-A2MJ-06 COSM3885521 c.8036G>A p.G2679E Substitution - Missense 13:77099004-77099004 - CSCC-27-T COSM4500370 c.5527C>T p.L1843F Substitution - Missense 13:77174321-77174321 - U2940 COSM5621313 c.3601A>T p.S1201C Substitution - Missense 13:77205473-77205473 - TCGA-37-4135-01 COSM697320 c.5433A>T p.T1811T Substitution - coding silent 13:77174415-77174415 - YUMOOK COSM1706863 c.4430A>T p.H1477L Substitution - Missense 13:77185278-77185278 - TCGA-FS-A4FC-06 COSM3607379 c.1617G>A p.S539S Substitution - coding silent 5:103003036-103003036 + 2293782 COSM4609100 c.1910C>A p.A637D Substitution - Missense 5:103006907-103006907 + TCGA-CM-5861-01 COSM1367722 c.13323+2T>C p.? Unknown 13:77056984-77056984 - 2492709 COSM5717757 c.4611C>T p.I1537I Substitution - coding silent 13:77181917-77181917 - SW480 COSM4655636 c.4448A>G p.D1483G Substitution - Missense 13:77185260-77185260 - Pat_11_A COSM1950160 c.4861C>T p.R1621C Substitution - Missense 13:77180285-77180285 - HN_62237 COSM124586 c.8806G>A p.A2936T Substitution - Missense 13:77098234-77098234 - B84 COSM1756822 c.5908G>A p.E1970K Substitution - Missense 13:77168520-77168520 - 2492710 COSM5717255 c.1309C>T p.R437* Substitution - Nonsense 5:102974262-102974262 + MO_1202 COSM5572077 c.3872G>A p.W1291* Substitution - Nonsense 13:77191763-77191763 - LUAD-F00089 COSM339605 c.8256C>T p.P2752P Substitution - coding silent 13:77098784-77098784 - T1760 COSM4704378 c.8818G>C p.D2940H Substitution - Missense 13:77098222-77098222 - sysucc-880T COSM5462345 c.8725A>G p.T2909A Substitution - Missense 13:77098315-77098315 - SN12C COSM1671787 c.743A>G p.Y248C Substitution - Missense 5:102949920-102949920 + LS180 COSM1949646 c.13921delT p.*4642fs? Deletion - Frameshift 13:77045380-77045380 - Pat_26_B COSM5866991 c.2273G>A p.G758E Substitution - Missense 5:103009808-103009808 + 2521243 COSM5886421 c.1430C>T p.S477L Substitution - Missense 5:102974383-102974383 + TCGA-B0-5707-01 COSM481717 c.1516G>A p.G506R Substitution - Missense 5:102990304-102990304 + T3658 COSM1431984 c.1291_1292insA p.D434fs*6 Insertion - Frameshift 5:102974244-102974245 + ESCC_158 COSM5646638 c.5301G>A p.T1767T Substitution - coding silent 13:77176554-77176554 - TCGA-AN-A046-01 COSM3814082 c.6991C>T p.R2331* Substitution - Nonsense 13:77150760-77150760 - LP6005409-DNA_F01 COSM5036297 c.10085+7A>G p.? Unknown 13:77095351-77095351 - 587238 COSM1216058 c.2885G>A p.S962N Substitution - Missense 13:77217898-77217898 - CHC303T COSM4950536 c.7153T>A p.Y2385N Substitution - Missense 13:77144481-77144481 - 151-02-8TD COSM5416197 c.2982T>C p.Y994Y Substitution - coding silent 13:77212122-77212122 - 1517_CLM COSM1949683 c.13185C>T p.F4395F Substitution - coding silent 13:77058248-77058248 - P-Thy019 COSM5095381 c.553T>G p.S185A Substitution - Missense 5:102946863-102946863 + YUOMEGA COSM5376906 c.428C>T p.S143L Substitution - Missense 13:77288213-77288213 - TCGA-AP-A059-01 COSM948680 c.1509G>A p.A503A Substitution - coding silent 13:77262077-77262077 - HCC5T COSM3661295 c.1480G>A p.G494R Substitution - Missense 5:102974433-102974433 + RK165_C01 COSM1633869 c.1787A>G p.D596G Substitution - Missense 5:103005210-103005210 + 12T COSM109119 c.9036T>C p.A3012A Substitution - coding silent 13:77098004-77098004 - STC246 COSM5052241 c.4525A>G p.T1509A Substitution - Missense 13:77185183-77185183 - RK067_C01 COSM1629173 c.2949A>G p.G983G Substitution - coding silent 13:77212155-77212155 - TCGA-D1-A17Q-01 COSM948653 c.3077G>A p.R1026Q Substitution - Missense 13:77212027-77212027 - TCGA-AP-A0LM-01 COSM948611 c.5292G>A p.T1764T Substitution - coding silent 13:77176563-77176563 - TCGA-D1-A101-01 COSM948647 c.3341C>T p.A1114V Substitution - Missense 13:77206787-77206787 - T155 COSM1177234 c.2513C>A p.S838* Substitution - Nonsense 5:103028212-103028212 + TCGA-GD-A2C5-01 COSM1300312 c.2251G>A p.D751N Substitution - Missense 13:77251167-77251167 - OV207 COSM252627 c.5635G>A p.V1879I Substitution - Missense 13:77171537-77171537 - 96T COSM107554 c.8049A>G p.T2683T Substitution - coding silent 13:77098991-77098991 - CHC2029T COSM4793033 c.781A>C p.I261L Substitution - Missense 13:77273522-77273522 - TCGA-AM-5820-01 COSM3688780 c.3548C>T p.A1183V Substitution - Missense 13:77205526-77205526 - CHC1085T COSM4788664 c.1172A>G p.N391S Substitution - Missense 13:77267912-77267912 - 1432466 COSM51621 c.6664C>T p.Q2222* Substitution - Nonsense 13:77156195-77156195 - MZ1-PC COSM24423 c.1883C>T p.A628V Substitution - Missense 13:77260448-77260448 - PD14453a COSM5799994 c.7308G>C p.K2436N Substitution - Missense 13:77140143-77140143 - PT37 COSM5918719 c.874G>A p.G292S Substitution - Missense 5:102950789-102950789 + CH-109-T2 COSM5650649 c.12941G>C p.S4314T Substitution - Missense 13:77059608-77059608 - Gp5D COSM1950218 c.3826A>G p.K1276E Substitution - Missense 13:77191809-77191809 - ESO-887 COSM1258370 c.1903+8_1903+18delAATAAAAAGTT p.? Unknown 13:77260410-77260420 - TCGA-AA-3510-01 COSM1367767 c.8897C>T p.S2966L Substitution - Missense 13:77098143-77098143 - TCGA-BH-A0AW-01 COSM448387 c.239G>C p.R80P Substitution - Missense 5:102901384-102901384 + RK100_C01 COSM1633871 c.2571_2574delTTTC p.F858fs*>47 Deletion - Frameshift 5:103028918-103028921 + TCGA-FW-A3R5-06 COSM3918417 c.1264C>T p.L422L Substitution - coding silent 5:102974217-102974217 + CHC794T COSM4949505 c.5600A>T p.N1867I Substitution - Missense 13:77171572-77171572 - LUAD-CHTN-MAD06-00678 COSM360790 c.8215G>T p.A2739S Substitution - Missense 13:77098825-77098825 - TCGA-DJ-A3VB-01 COSM3369126 c.4048A>G p.T1350A Substitution - Missense 13:77189040-77189040 - S00944 COSM5664057 c.99G>A p.R33R Substitution - coding silent 13:77326563-77326563 - WA14 COSM240778 c.4758T>A p.S1586R Substitution - Missense 13:77181770-77181770 - LS411 COSM1950201 c.4051A>G p.S1351G Substitution - Missense 13:77189037-77189037 - TCGA-56-6545-01 COSM697329 c.6099C>G p.V2033V Substitution - coding silent 13:77166456-77166456 - ESCC_BICR_031T COSM5441042 c.7447A>T p.T2483S Substitution - Missense 13:77139294-77139294 - 587338 COSM1216070 c.5902C>T p.Q1968* Substitution - Nonsense 13:77168526-77168526 - 07-P1079 COSM4576012 c.175C>T p.H59Y Substitution - Missense 13:77326487-77326487 - BD190T COSM5517791 c.3352G>A p.D1118N Substitution - Missense 13:77206776-77206776 - Pat_53_B COSM5842716 c.10816G>A p.G3606R Substitution - Missense 13:77083138-77083138 - sysucc-1370T COSM5471934 c.4G>T p.A2S Substitution - Missense 5:102866199-102866199 + HCC2998 COSM1671789 c.2599C>T p.R867* Substitution - Nonsense 5:103028946-103028946 + TCGA-BG-A0M2-01 COSM1059249 c.211-1G>T p.? Unknown 5:102901355-102901355 + C391 COSM4441627 c.3850C>T p.P1284S Substitution - Missense 13:77191785-77191785 - J90_T COSM3955738 c.6475G>T p.A2159S Substitution - Missense 13:77161914-77161914 - LUAD_E00623 COSM354438 c.912G>T p.T304T Substitution - coding silent 5:102959881-102959881 + CHC1192T COSM4803610 c.11238C>G p.T3746T Substitution - coding silent 13:77081493-77081493 - LUAD-D02085 COSM363253 c.10234A>G p.N3412D Substitution - Missense 13:77093184-77093184 - PT45 COSM2989825 c.2107C>T p.R703W Substitution - Missense 5:103007549-103007549 + TCGA-HU-A4G8-01 COSM4126955 c.1564A>G p.K522E Substitution - Missense 5:102990352-102990352 + TCGA-AA-A00N-01 COSM276196 c.424G>A p.E142K Substitution - Missense 13:77288217-77288217 - TCGA-D7-6820-01 COSM4048450 c.9416C>T p.A3139V Substitution - Missense 13:77097624-77097624 - TCGA-ET-A3DV-01 COSM3369123 c.6147T>A p.H2049Q Substitution - Missense 13:77166408-77166408 - Case4e COSM1717339 c.9071C>G p.S3024C Substitution - Missense 13:77097969-77097969 - TCGA-AN-A046-01 COSM948596 c.6037G>A p.E2013K Substitution - Missense 13:77166518-77166518 - TCGA-AR-A251-01 COSM1477317 c.9352C>G p.L3118V Substitution - Missense 13:77097688-77097688 - N691T COSM236170 c.4652C>A p.A1551E Substitution - Missense 13:77181876-77181876 - TCGA-39-5024-01 COSM697296 c.188+1G>A p.? Unknown 13:77326473-77326473 - TCGA-AA-3713-01 COSM1367867 c.215A>G p.K72R Substitution - Missense 13:77296648-77296648 - Pat_28_B COSM5842732 c.6553G>A p.A2185T Substitution - Missense 13:77158040-77158040 - TCGA-P4-A5E6-01 COSM3993878 c.698C>T p.A233V Substitution - Missense 5:102949591-102949591 + HCC133T COSM1619283 c.1607A>G p.D536G Substitution - Missense 5:102990395-102990395 + ccRCC-58 COSM1665619 c.957delA p.E320fs*30 Deletion - Frameshift 13:77270413-77270413 - TCGA-G4-6309-01 COSM1367837 c.3226A>T p.T1076S Substitution - Missense 13:77211243-77211243 - HCT15 COSM2989831 c.2117G>A p.G706D Substitution - Missense 5:103007559-103007559 + BD127T COSM1950284 c.2689C>T p.R897* Substitution - Nonsense 13:77225489-77225489 - TCGA-AN-A046-01 COSM3814097 c.1486C>A p.L496I Substitution - Missense 13:77262100-77262100 - SH-0622 COSM5017361 c.8890_8891insA p.S2966fs*39 Insertion - Frameshift 13:77098149-77098150 - T3091 COSM4704406 c.7639C>T p.R2547* Substitution - Nonsense 13:77126449-77126449 - Pat_63_B COSM5842728 c.7819G>A p.V2607I Substitution - Missense 13:77125420-77125420 - TCGA-A6-6140-01 COSM1059251 c.238C>T p.R80* Substitution - Nonsense 5:102901383-102901383 + TCGA-FS-A1ZC-06 COSM3607371 c.1397C>T p.S466F Substitution - Missense 5:102974350-102974350 + 585208 COSM325878 c.7402G>T p.E2468* Substitution - Nonsense 13:77140049-77140049 - TCGA-AP-A059-01 COSM948614 c.5123C>T p.A1708V Substitution - Missense 13:77177851-77177851 - HCT15 COSM1950329 c.2173C>T p.L725L Substitution - coding silent 13:77251245-77251245 - TCGA-CG-4442-01 COSM4048462 c.8694C>T p.C2898C Substitution - coding silent 13:77098346-77098346 - YUKIL COSM1706869 c.1838C>T p.S613F Substitution - Missense 13:77260493-77260493 - TCGA-AA-3713-01 COSM1367858 c.1817C>T p.A606V Substitution - Missense 13:77260514-77260514 - BZ01 COSM5757664 c.8432A>G p.N2811S Substitution - Missense 13:77098608-77098608 - T3064 COSM4704431 c.2479C>T p.R827C Substitution - Missense 13:77243095-77243095 - CRC-19T COSM5481148 c.1388T>C p.L463P Substitution - Missense 13:77263719-77263719 - YUOTHO COSM1059259 c.1184C>T p.S395F Substitution - Missense 5:102974137-102974137 + TCGA-AG-A002-01 COSM262189 c.1315G>T p.D439Y Substitution - Missense 13:77263931-77263931 - TCGA-AN-A046-01 COSM3826498 c.2149G>T p.E717* Substitution - Nonsense 5:103007591-103007591 + TCGA-D1-A17Q-01 COSM948569 c.6837A>C p.K2279N Substitution - Missense 13:77150914-77150914 - TCGA-63-5128-01 COSM697365 c.11738A>C p.E3913A Substitution - Missense 13:77070683-77070683 - ESOSCC155T COSM1171984 c.6736C>T p.P2246S Substitution - Missense 13:77156123-77156123 - 2492720 COSM5720358 c.1616C>T p.S539L Substitution - Missense 5:103003035-103003035 + BK0043 COSM4187540 c.2009A>T p.N670I Substitution - Missense 13:77257724-77257724 - ESCC_11 COSM5624259 c.2895G>T p.T965T Substitution - coding silent 13:77217888-77217888 - HCC157 COSM3661291 c.105C>T p.T35T Substitution - coding silent 5:102867288-102867288 + AA1924 COSM4168495 c.4827+1G>T p.? Unknown 13:77181700-77181700 - TCGA-06-0649 COSM2151458 c.4967G>C p.G1656A Substitution - Missense 13:77180179-77180179 - TCGA-EI-6882-01 COSM5078981 c.9506delA p.K3170fs*26 Deletion - Frameshift 13:77097534-77097534 - TCGA-G4-6628-01 COSM1431992 c.2348A>G p.H783R Substitution - Missense 5:103017350-103017350 + TCGA-BR-4257-01 COSM330910 c.10813G>A p.A3605T Substitution - Missense 13:77083141-77083141 - ACINAR26 COSM1732745 c.1014C>G p.F338L Substitution - Missense 5:102959983-102959983 + TCGA-66-2781-01 COSM697314 c.4314A>T p.E1438D Substitution - Missense 13:77185887-77185887 - TCGA-BR-7716-01 COSM4048486 c.6810G>T p.V2270V Substitution - coding silent 13:77150941-77150941 - YUPAER COSM5401882 c.914C>T p.S305F Substitution - Missense 5:102959883-102959883 + TCGA-A6-5661-01 COSM1367737 c.12104G>A p.S4035N Substitution - Missense 13:77067818-77067818 - 405 COSM4430017 c.3076C>T p.R1026* Substitution - Nonsense 13:77212028-77212028 - TCGA-BR-8680-01 COSM4048537 c.2499A>C p.R833S Substitution - Missense 13:77243075-77243075 - TCGA-CG-4442-01 COSM4048549 c.143A>T p.N48I Substitution - Missense 13:77326519-77326519 - TCGA-18-3410-01 COSM697358 c.10039G>T p.E3347* Substitution - Nonsense 13:77095404-77095404 - TCGA-AA-A00N-01 COSM276587 c.908G>A p.G303D Substitution - Missense 5:102959877-102959877 + CHC1201T COSM4801687 c.7088T>C p.M2363T Substitution - Missense 13:77144546-77144546 - ITNET_0700_T COSM4963747 c.7771G>A p.V2591I Substitution - Missense 13:77125468-77125468 - TCGA-K4-A3WU-01 COSM3793377 c.8434C>G p.L2812V Substitution - Missense 13:77098606-77098606 - TCGA-18-3406-01 COSM697299 c.937A>T p.M313L Substitution - Missense 13:77270433-77270433 - T613 COSM4704428 c.4298G>A p.R1433H Substitution - Missense 13:77185903-77185903 - Gp5D COSM1949874 c.8818delG p.D2940fs*5 Deletion - Frameshift 13:77098222-77098222 - TCGA-13-1403-01 COSM75500 c.6125G>C p.G2042A Substitution - Missense 13:77166430-77166430 - TCGA-HU-A4G8-01 COSM2989763 c.599A>G p.Y200C Substitution - Missense 5:102948401-102948401 + T207 COSM4704398 c.7846G>A p.E2616K Substitution - Missense 13:77125393-77125393 - 8013294 COSM218441 c.11926T>C p.C3976R Substitution - Missense 13:77068696-77068696 - TCGA-AZ-4315-01 COSM1367744 c.11784A>C p.L3928F Substitution - Missense 13:77070637-77070637 - TCGA-AG-4008-01 COSM289543 c.1582T>A p.F528I Substitution - Missense 5:102990370-102990370 + TCGA-CG-5726-01 COSM4048546 c.332A>G p.N111S Substitution - Missense 13:77288309-77288309 - TCGA-BF-A1PX-01 COSM4905441 c.8618C>T p.S2873F Substitution - Missense 13:77098422-77098422 - T2932 COSM1192803 c.1124delA p.K375fs*4 Deletion - Frameshift 13:77270014-77270014 - P07-360 COSM242570 c.1990G>T p.V664L Substitution - Missense 13:77257743-77257743 - TCGA-FS-A1ZZ-06 COSM3469690 c.12018C>T p.L4006L Substitution - coding silent 13:77068604-77068604 - TCGA-HU-A4G9-01 COSM4048504 c.4736G>A p.R1579Q Substitution - Missense 13:77181792-77181792 - pfg092T COSM4759543 c.349A>C p.S117R Substitution - Missense 5:102914014-102914014 + 16617 COSM5617242 c.269-7G>C p.? Unknown 5:102913927-102913927 + CRC-06T COSM5456403 c.8854C>T p.R2952* Substitution - Nonsense 13:77098186-77098186 - 585208 COSM325884 c.1743-5G>T p.? Unknown 13:77260593-77260593 - TCGA-66-2758-01 COSM697335 c.6973A>G p.M2325V Substitution - Missense 13:77150778-77150778 - SNUH_G76_S1 COSM4418434 c.4378A>G p.I1460V Substitution - Missense 13:77185330-77185330 - sysucc-882T COSM5447086 c.2826-9T>G p.? Unknown 13:77217966-77217966 - CSCC-37-T COSM4493840 c.421C>T p.P141S Substitution - Missense 5:102925021-102925021 + TCGA-33-4582-01 COSM697341 c.7294A>C p.K2432Q Substitution - Missense 13:77140157-77140157 - TCGA-F4-6703-01 COSM3688783 c.2396C>A p.P799H Substitution - Missense 13:77243823-77243823 - T368 COSM4704416 c.6238C>T p.L2080F Substitution - Missense 13:77165380-77165380 - HCC063T COSM5812744 c.605T>A p.M202K Substitution - Missense 5:102948407-102948407 + TCGA-C5-A1M8-01 COSM4837323 c.1894G>A p.D632N Substitution - Missense 13:77260437-77260437 - TCGA-Q1-A73O-01 COSM4835315 c.1175C>T p.S392L Substitution - Missense 5:102974128-102974128 + TCGA-EE-A2MJ-06 COSM3469730 c.8480C>T p.P2827L Substitution - Missense 13:77098560-77098560 - NB-2058 COSM1286409 c.13577G>A p.G4526E Substitution - Missense 13:77051875-77051875 - PCSI_0082_Pa_P_526 COSM3381033 c.925A>T p.M309L Substitution - Missense 5:102959894-102959894 + SE4 COSM1165954 c.719A>C p.H240P Substitution - Missense 5:102949612-102949612 + PDA_045 COSM5000458 c.3501G>T p.M1167I Substitution - Missense 13:77205573-77205573 - RKO COSM1950154 c.4979G>A p.S1660N Substitution - Missense 13:77180167-77180167 - TCGA-13-0889-01 COSM78119 c.7928C>T p.S2643F Substitution - Missense 13:77121471-77121471 - HCT116 COSM1950148 c.5167T>C p.F1723L Substitution - Missense 13:77177807-77177807 - TCGA-AX-A0J0-01 COSM948510 c.12353G>A p.R4118Q Substitution - Missense 13:77066077-77066077 - RK050_C01 COSM1629176 c.1147-1G>A p.? Unknown 13:77267938-77267938 - TCGA-DA-A3F8-06 COSM1706866 c.2587C>T p.P863S Substitution - Missense 13:77233192-77233192 - ESCC_10 COSM5623806 c.4713G>A p.A1571A Substitution - coding silent 13:77181815-77181815 - HN_62686 COSM125106 c.1201A>T p.R401W Substitution - Missense 5:102974154-102974154 + S01873 COSM5701878 c.2701_2702GA>TT p.E901L Substitution - Missense 13:77225476-77225477 - TCGA-AZ-6598-01 COSM5827415 c.5227-4_5227-3delTT p.? Unknown 13:77176631-77176632 - 8048316 COSM3384905 c.12977G>A p.S4326N Substitution - Missense 13:77059572-77059572 - 2492708 COSM5717255 c.1309C>T p.R437* Substitution - Nonsense 5:102974262-102974262 + LS180 COSM1950067 c.6278A>G p.D2093G Substitution - Missense 13:77165340-77165340 - 40M COSM5586117 c.1898C>T p.P633L Substitution - Missense 5:103006895-103006895 + TCGA-39-5036-01 COSM697372 c.13447A>G p.I4483V Substitution - Missense 13:77055644-77055644 - PT46 COSM166680 c.6724C>T p.R2242C Substitution - Missense 13:77156135-77156135 - TCGA-AD-6964-01 COSM1367799 c.7593C>T p.C2531C Substitution - coding silent 13:77126495-77126495 - T2944 COSM1642547 c.1292delA p.K433fs*32 Deletion - Frameshift 5:102974245-102974245 + CSCC-20-T COSM4554412 c.6090G>C p.L2030F Substitution - Missense 13:77166465-77166465 - TCGA-BR-8589-01 COSM4048510 c.4534T>C p.F1512L Substitution - Missense 13:77185174-77185174 - TCGA-AO-A03M-01 COSM3814073 c.8045C>G p.S2682* Substitution - Nonsense 13:77098995-77098995 - TCGA-AZ-6601-01 COSM1367855 c.1989G>T p.E663D Substitution - Missense 13:77257744-77257744 - T207 COSM4704402 c.7800A>G p.Q2600Q Substitution - coding silent 13:77125439-77125439 - TCGA-DD-A3A7-01 COSM4916208 c.6122A>G p.Y2041C Substitution - Missense 13:77166433-77166433 - TCGA-UB-A7MB-01 COSM4931610 c.917G>A p.G306D Substitution - Missense 13:77270453-77270453 - PCSI_0007_Pa_X COSM216307 c.8339G>A p.R2780Q Substitution - Missense 13:77098701-77098701 - ESO-601 COSM1258393 c.6221T>G p.L2074W Substitution - Missense 13:77166334-77166334 - 24T COSM107434 c.8890G>A p.E2964K Substitution - Missense 13:77098150-77098150 - LUAD-YINHD COSM348869 c.3861G>A p.L1287L Substitution - coding silent 13:77191774-77191774 - TCGA-AA-3966-01 COSM272976 c.5932A>G p.T1978A Substitution - Missense 13:77168496-77168496 - TCGA-AX-A0J0-01 COSM1059257 c.1091-1G>T p.? Unknown 5:102961157-102961157 + TCGA-MI-A75E-01 COSM4939726 c.5326G>T p.E1776* Substitution - Nonsense 13:77176529-77176529 - 2497780 COSM5750957 c.110C>A p.P37Q Substitution - Missense 5:102867293-102867293 + 2492708 COSM5717757 c.4611C>T p.I1537I Substitution - coding silent 13:77181917-77181917 - CSCC-4-T COSM3469751 c.5821C>T p.P1941S Substitution - Missense 13:77168607-77168607 - YUPLA COSM5376900 c.7465C>T p.P2489S Substitution - Missense 13:77139276-77139276 - 408 COSM4430530 c.791A>G p.Q264R Substitution - Missense 5:102949968-102949968 + TCGA-B5-A11E-01 COSM948572 c.6657-1G>T p.? Unknown 13:77156203-77156203 - 214 COSM4424363 c.2076G>A p.V692V Substitution - coding silent 5:103007518-103007518 + PT42 COSM5925753 c.2152C>T p.P718S Substitution - Missense 13:77251266-77251266 - SW948 COSM1949804 c.9803A>C p.E3268A Substitution - Missense 13:77096349-77096349 - TCGA-FW-A3R5-06 COSM3885525 c.5529C>T p.L1843L Substitution - coding silent 13:77174319-77174319 - Pat_59_A COSM5017659 c.1137_1139delAGA p.E383delE Deletion - In frame 5:102961204-102961206 + RK006_C02 COSM1629170 c.7458G>A p.K2486K Substitution - coding silent 13:77139283-77139283 - PDA_108 COSM313010 c.5227-3delT p.? Unknown 13:77176631-77176631 - TCGA-AZ-4315-01 COSM1367852 c.2757A>C p.E919D Substitution - Missense 13:77224519-77224519 - SW948 COSM1950215 c.3848A>G p.E1283G Substitution - Missense 13:77191787-77191787 - TCGA-EE-A2MU-06 COSM3469680 c.13855G>T p.V4619F Substitution - Missense 13:77045446-77045446 - H166 COSM5043700 c.4013C>T p.A1338V Substitution - Missense 13:77190279-77190279 - TCGA-EE-A20C-06 COSM3469769 c.2675C>T p.P892L Substitution - Missense 13:77225503-77225503 - TCGA-D3-A5GU-06 COSM166680 c.6724C>T p.R2242C Substitution - Missense 13:77156135-77156135 - TCGA-CD-5802-01 COSM4048453 c.9336G>A p.M3112I Substitution - Missense 13:77097704-77097704 - 2293776 COSM4607584 c.836C>A p.P279Q Substitution - Missense 13:77270534-77270534 - TCGA-BS-A0UV-01 COSM948686 c.1112G>T p.R371I Substitution - Missense 13:77270026-77270026 - sysucc-311T COSM5478583 c.8752G>T p.E2918* Substitution - Nonsense 13:77098288-77098288 - 2492725 COSM5725402 c.211-1G>A p.? Unknown 5:102901355-102901355 + 3N23-VS-3T23 COSM4979620 c.427A>T p.T143S Substitution - Missense 5:102925027-102925027 + TCGA-AX-A05Z-01 COSM948638 c.3984G>T p.K1328N Substitution - Missense 13:77190308-77190308 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.369430 5q14-q21 170270 2442108|CGAP|BC018127|A/G|non-coding||3390|Validated; 2424852|dbSNP|BC018127|A/C|coding|Asp413Glu|1611|Candidate Hs.591218;Hs.591221 13q22 610392

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AACTTTTTATT - IntronicDeletion . c.2017+8_2017+18delAATAAAAAGTT 13 77834545 ESCA AATGTCT - Frameshift p.R3088Hfs*2 c.9262_9268delAGACATT 13 77672021 CM A C Missense p.C4603G c.13807T>G 13 77625246 ESCA A C Missense p.I2504M c.7512T>G 13 77714188 LGG A C Missense p.L2112W c.6335T>G 13 77740469 ESCA A C Missense p.L3580R c.10739T>G 13 77661755 CM A C Synonymous p.L1637L c.4911T>G 13 77755866 PAAD A G IntronicSNV . c.4445-12T>C 13 77759524 CLL A G IntronicSNV . c.4445-27T>C 13 77759539 STAD A G IntronicSNV . c.7303+24T>C 13 77718556 CLL A G Missense p.F3184S c.9551T>C 13 77671738 CM A G Missense p.F4014L c.12040T>C 13 77642831 PAAD A G Missense p.F4527L c.13579T>C 13 77629761 RCCC A G Missense p.I1812T c.5435T>C 13 77750669 MM A G Missense p.I1952T c.5855T>C 13 77743789 UCEC A G Missense p.L3948P c.11843T>C 13 77644827 BRCA A G Missense p.L513P c.1538T>C 13 77837818 CLL A G Missense p.M3952T c.11855T>C 13 77644815 BRCA A G Missense p.S4166P c.12496T>C 13 77640183 LUAD A G Missense p.V3510A c.10529T>C 13 77663163 CM A G Missense p.V4234A c.12701T>C 13 77636804 CM A G Missense p.W571R c.1711T>C 13 77835447 GBM A G Missense p.Y1134H c.3400T>C 13 77785318 RCCC A G Synonymous p.D1611D c.4833T>C 13 77755944 LUAD A G Synonymous p.G2282G c.6846T>C 13 77730262 CM A G Synonymous p.N1370N c.4110T>C 13 77764431 UCEC A G Synonymous p.P992P c.2976T>C 13 77792056 ESCA A G Synonymous p.T1061T c.3183T>C 13 77786170 BRCA A G Synonymous p.T2410T c.7230T>C 13 77718653 CM A G Synonymous p.Y1032Y c.3096T>C 13 77786257 CLL A - IntronicDeletion . c.10726-123delT 13 77661891 STAD A - IntronicDeletion . c.4444+18delT 13 77759988 STAD A - IntronicDeletion . c.5341-3delT 13 77750766 SCLC A - IntronicDeletion . c.9955-10delT 13 77669747 STAD - A Nonsense p.D4622*fs*1 c.13863dupT 13 77625190 HNSC A T Missense p.C4455S c.13363T>A 13 77631195 BRCA A T Missense p.C4544S c.13630T>A 13 77629710 UCEC A T Missense p.H2087Q c.6261T>A 13 77740543 THCA A T Missense p.L595H c.1784T>A 13 77835374 RCCC A T Missense p.S2314T c.6940T>A 13 77725060 CM A T Synonymous p.I199I c.597T>A 13 77853044 STAD A T Synonymous p.S1911S c.5733T>A 13 77745688 STAD C A 3-UTRSNV . c.14034+94G>T 13 77619422 CM C A Missense p.D2948Y c.8842G>T 13 77672447 HNSC C A Missense p.D3385Y c.10153G>T 13 77669539 LUSC C A Missense p.G1875V c.5624G>T 13 77748473 SCLC C A Missense p.G3643V c.10928G>T 13 77657275 ESCA C A Missense p.G4398V c.13193G>T 13 77632489 LUAD C A Missense p.M3327I c.9981G>T 13 77669711 LUAD C A Missense p.Q4170H c.12510G>T 13 77640169 SCLC C A Missense p.R3475I c.10424G>T 13 77664342 PRAD C A Missense p.V4657F c.13969G>T 13 77619581 CM C A Missense p.W1330C c.3990G>T 13 77765894 LUAD C A Missense p.W4248C c.12744G>T 13 77636761 BRCA C A Missense p.W761L c.2282G>T 13 77825385 UCEC C A Nonsense p.E1175* c.3523G>T 13 77780854 NSCLC C A Nonsense p.E2506* c.7516G>T 13 77714184 SCLC C A SpliceAcceptorSNV . c.1853-1G>T 13 77834728 SCLC C A SpliceAcceptorSNV . c.4155-1G>T 13 77763183 UCEC C A SpliceDonorSNV . c.6915+1G>T 13 77730192 RCCC C A Synonymous p.A58A c.174G>T 13 77900737 LUAD - C Frameshift p.V4607Gfs*12 c.13819dupG 13 77625234 HNSC C G Missense p.D4236H c.12706G>C 13 77636799 STAD C G Missense p.E1421Q c.4261G>C 13 77760189 LUSC C G Missense p.E1511Q c.4531G>C 13 77759426 HNSC C G Missense p.E2654Q c.7960G>C 13 77699528 HNSC C G Missense p.E3305Q c.9913G>C 13 77670488 LUSC C G Missense p.E3339Q c.10015G>C 13 77669677 LUAD C G Missense p.E3554Q c.10660G>C 13 77663032 LUAD C G Missense p.G1484A c.4451G>C 13 77759506 LUAD C G Missense p.G1855A c.5564G>C 13 77748533 LUSC C G Missense p.G2080A c.6239G>C 13 77740565 OV C G Missense p.G3245R c.9733G>C 13 77671556 HNSC C G Missense p.L3515F c.10545G>C 13 77663147 BRCA C G Missense p.M4429I c.13287G>C 13 77632395 BRCA C G Missense p.M4507I c.13521G>C 13 77629819 OV C G Missense p.R1236T c.3707G>C 13 77779616 ESCA C G Missense p.R863P c.2588G>C 13 77817235 RCCC C G Synonymous p.L1467L c.4401G>C 13 77760049 LUAD C G Synonymous p.T1003T c.3009G>C 13 77792023 CM C T Missense p.A1333T c.3997G>A 13 77765887 PRAD C T Missense p.A2974T c.8920G>A 13 77672369 HNSC C T Missense p.D1117N c.3349G>A 13 77785369 CLL C T Missense p.D1933N c.5797G>A 13 77743847 BLCA C T Missense p.D364N c.1090G>A 13 77844529 CM C T Missense p.D4004N c.12010G>A 13 77642861 CLL C T Missense p.D789N c.2365G>A 13 77825302 BLCA C T Missense p.E1775K c.5323G>A 13 77751900 HNSC C T Missense p.E3895K c.11683G>A 13 77651324 HNSC C T Missense p.E4366K c.13096G>A 13 77633702 HNSC C T Missense p.G2634R c.7900G>A 13 77699588 LUSC C T Missense p.G2717E c.8150G>A 13 77673139 CM C T Missense p.G3643R c.10927G>A 13 77657276 STAD C T Missense p.G4079R c.12235G>A 13 77641936 CM C T Missense p.G4317D c.12950G>A 13 77635390 CM C T Missense p.M2401I c.7203G>A 13 77718680 PRAD C T Missense p.M3150I c.9450G>A 13 77671839 STAD C T Missense p.M4019I c.12057G>A 13 77642814 CM C T Missense p.R1832H c.5495G>A 13 77748602 BRCA C T Missense p.R1884K c.5651G>A 13 77748446 LUAD C T Missense p.R215Q c.644G>A 13 77852997 CM C T Missense p.R2818Q c.8453G>A 13 77672836 PAAD C T Missense p.R3218K c.9653G>A 13 77671636 UCEC C T Missense p.R3803Q c.11408G>A 13 77655572 LUAD C T Missense p.R407K c.1220G>A 13 77844167 CM C T Missense p.R4564Q c.13691G>A 13 77626010 NB C T Missense p.S1885N c.5654G>A 13 77745767 CM C T Missense p.V2457I c.7369G>A 13 77715013 BRCA C T Missense p.V4136M c.12406G>A 13 77641765 UCEC C T SpliceDonorSNV . c.302+1G>A 13 77900608 LUSC C T Synonymous p.A1152A c.3456G>A 13 77780921 STAD C T Synonymous p.A1705A c.5115G>A 13 77754280 BRCA C T Synonymous p.E2733E c.8199G>A 13 77673090 THCA C T Synonymous p.K2523K c.7569G>A 13 77713421 BRCA C T Synonymous p.K2524K c.7572G>A 13 77713418 HC C T Synonymous p.L1677L c.5031G>A 13 77754364 CM C T Synonymous p.L2779L c.8337G>A 13 77672952 LUSC C T Synonymous p.L3129L c.9387G>A 13 77671902 UCEC C T Synonymous p.Q2491Q c.7473G>A 13 77714227 BLCA C T Synonymous p.Q3180Q c.9540G>A 13 77671749 ESCA C T Synonymous p.R3892R c.11676G>A 13 77651331 BRCA C T Synonymous p.V1820V c.5460G>A 13 77750644 BRCA G A IntronicSNV . c.8140+3010C>T 13 77692498 CM G A Missense p.A1152V c.3455C>T 13 77780922 UCEC G A Missense p.A2477V c.7430C>T 13 77714270 STAD G A Missense p.A3177V c.9530C>T 13 77671759 STAD G A Missense p.A3568V c.10703C>T 13 77662989 HNSC G A Missense p.A4184V c.12551C>T 13 77640128 UCEC G A Missense p.A4369V c.13106C>T 13 77633692 CM G A Missense p.A541V c.1622C>T 13 77836213 ESCA G A Missense p.H2426Y c.7276C>T 13 77718607 CM G A Missense p.H3058Y c.9172C>T 13 77672117 CM G A Missense p.H3694Y c.11080C>T 13 77656085 BLCA G A Missense p.L1103F c.3307C>T 13 77785411 STAD G A Missense p.L2224F c.6670C>T 13 77732172 ESCA G A Missense p.L376F c.1126C>T 13 77844493 CM G A Missense p.L3805F c.11413C>T 13 77655567 CM G A Missense p.L4436F c.13306C>T 13 77632376 HNSC G A Missense p.L595F c.1783C>T 13 77835375 CM G A Missense p.P1744S c.5230C>T 13 77751993 CM G A Missense p.P1979S c.5935C>T 13 77742742 CM G A Missense p.P2758S c.8272C>T 13 77673017 CM G A Missense p.P2865L c.8594C>T 13 77672695 CM G A Missense p.P2878L c.8633C>T 13 77672656 CM G A Missense p.P3128L c.9383C>T 13 77671906 CM G A Missense p.P3155L c.9464C>T 13 77671825 CM G A Missense p.P3518L c.10553C>T 13 77663139 STAD G A Missense p.P3668L c.11003C>T 13 77657200 CM G A Missense p.P3844S c.11530C>T 13 77651477 CM G A Missense p.P4631L c.13892C>T 13 77625161 CM G A Missense p.P845L c.2534C>T 13 77817289 CM G A Missense p.P901S c.2701C>T 13 77807327 CM G A Missense p.P930L c.2789C>T 13 77799638 CM G A Missense p.R1471C c.4411C>T 13 77760039 LUSC G A Missense p.R2280C c.6838C>T 13 77730270 AML G A Missense p.R2882C c.8644C>T 13 77672645 STAD G A Missense p.R3978C c.11932C>T 13 77642939 CM G A Missense p.R4456W c.13366C>T 13 77631192 BRCA G A Missense p.S1629L c.4886C>T 13 77755891 LUAD G A Missense p.S1942F c.5825C>T 13 77743819 BLCA G A Missense p.S2681F c.8042C>T 13 77695606 OV G A Missense p.S2769F c.8306C>T 13 77672983 CM G A Missense p.S2774F c.8321C>T 13 77672968 CM G A Missense p.S2911F c.8732C>T 13 77672557 CM G A Missense p.S3433L c.10298C>T 13 77667369 HNSC G A Missense p.S3661L c.10982C>T 13 77657221 LUSC G A Missense p.S3885L c.11654C>T 13 77651353 CM G A Missense p.S4245L c.12734C>T 13 77636771 CM G A Missense p.S586L c.1757C>T 13 77835401 HNSC G A Missense p.T1353I c.4058C>T 13 77765826 CM G A Nonsense p.Q3883* c.11647C>T 13 77651360 BRCA G A Synonymous p.C4397C c.13191C>T 13 77632491 STAD G A Synonymous p.F1256F c.3768C>T 13 77779466 UCEC G A Synonymous p.F2583F c.7749C>T 13 77700588 CM G A Synonymous p.F4044F c.12132C>T 13 77642739 CM G A Synonymous p.F4149F c.12447C>T 13 77641724 CM G A Synonymous p.H4411H c.13233C>T 13 77632449 BRCA G A Synonymous p.I4091I c.12273C>T 13 77641898 LUSC G A Synonymous p.L4225L c.12675C>T 13 77636830 LUSC G A Synonymous p.P192P c.576C>T 13 77862314 CM G A Synonymous p.P3157P c.9471C>T 13 77671818 CM G A Synonymous p.R1832R c.5496C>T 13 77748601 BRCA G A Synonymous p.S3802S c.11406C>T 13 77655574 CM G A Synonymous p.V3319V c.9957C>T 13 77669735 BLCA G C Missense p.A4221G c.12662C>G 13 77638760 OV G C Missense p.C3680W c.11040C>G 13 77656125 BRCA G C Missense p.I561M c.1683C>G 13 77835475 BRCA G C Missense p.L3156V c.9466C>G 13 77671823 BRCA G C Missense p.L972V c.2914C>G 13 77798611 OV G C Missense p.P4348A c.13042C>G 13 77633756 HNSC G C Missense p.P792R c.2375C>G 13 77825292 BLCA G C Missense p.Q315E c.943C>G 13 77847609 LUAD G C Missense p.S1998W c.5993C>G 13 77742684 HNSC G C Nonsense p.S181* c.542C>G 13 77862348 BRCA G C Synonymous p.G877G c.2631C>G 13 77807397 LGG G C Synonymous p.V2071V c.6213C>G 13 77740591 LUSC G C Synonymous p.V2457V c.7371C>G 13 77715011 HNSC G C Synonymous p.V3984V c.11952C>G 13 77642919 BLCA G T Missense p.F3902L c.11706C>A 13 77651301 UCEC G T Missense p.H950Q c.2850C>A 13 77799577 SCLC G T Missense p.Q1060K c.3178C>A 13 77786175 BLCA G T Missense p.Q4257K c.12769C>A 13 77636736 ESCA G T Missense p.T2374K c.7121C>A 13 77724879 LUSC G T Nonsense p.C4454* c.13362C>A 13 77631196 CM G T Nonsense p.S1250* c.3749C>A 13 77779485 STAD G T Synonymous p.R2990R c.8968C>A 13 77672321 UCEC G T Synonymous p.T2002T c.6006C>A 13 77742671 CM T A Missense p.E1476D c.4428A>T 13 77760022 LUSC T A Missense p.E2153V c.6458A>T 13 77739409 LUSC T A Missense p.I1956L c.5866A>T 13 77743778 COREAD T A Missense p.I2504F c.7510A>T 13 77714190 LUAD T A Missense p.K2778M c.8333A>T 13 77672956 BRCA T A Missense p.M351L c.1051A>T 13 77844568 LUSC T A Missense p.M39L c.115A>T 13 77900796 LUSC T A Missense p.Y4032F c.12095A>T 13 77642776 PRAD T A Synonymous p.L3564L c.10692A>T 13 77663000 LUAD T A Synonymous p.P2042P c.6126A>T 13 77740678 ALL T A Synonymous p.T1849T c.5547A>T 13 77748550 LUSC T C IntronicSNV . c.1432-11A>G 13 77837935 STAD T C Missense p.D3466G c.10397A>G 13 77664369 COREAD T C Missense p.E2399G c.7196A>G 13 77718687 CM T C Missense p.H3401R c.10202A>G 13 77667465 BLCA T C Missense p.H870R c.2609A>G 13 77817214 BRCA T C Missense p.I199V c.595A>G 13 77853046 PRAD T C Missense p.I3115V c.9343A>G 13 77671946 BRCA T C Missense p.I3175V c.9523A>G 13 77671766 LUAD T C Missense p.I4449V c.13345A>G 13 77631213 LUAD T C Missense p.K1228R c.3683A>G 13 77779640 SCLC T C Missense p.M2363V c.7087A>G 13 77724913 LUSC T C Missense p.M4108V c.12322A>G 13 77641849 COREAD T C Missense p.N2849S c.8546A>G 13 77672743 HNSC T C Missense p.T4521A c.13561A>G 13 77629779 LUSC T C Missense p.Y1032C c.3095A>G 13 77786258 LUAD T C Missense p.Y4568C c.13703A>G 13 77625998 HNSC T C SpliceAcceptorSNV . c.2630-2A>G 13 77807400 STAD T C Synonymous p.E2934E c.8802A>G 13 77672487 LUSC T C Synonymous p.E3359E c.10077A>G 13 77669615 RCCC T C Synonymous p.E3615E c.10845A>G 13 77661649 CM T C Synonymous p.G1021G c.3063A>G 13 77786290 HC T C Synonymous p.L1208L c.3624A>G 13 77779699 CM T C Synonymous p.L3649L c.10947A>G 13 77657256 LUSC T C Synonymous p.P1936P c.5808A>G 13 77743836 LUSC T C Synonymous p.R4548R c.13644A>G 13 77629696 NB T C Synonymous p.T214T c.642A>G 13 77852999 BLCA T - Frameshift p.K2470Nfs*23 c.7410delA 13 77714290 RCCC T - Frameshift p.M2318Cfs*20 c.6952delA 13 77725048 STAD T G Missense p.E3715D c.11145A>C 13 77656020 LUAD T G Missense p.H3951P c.11852A>C 13 77644818 LUSC T G Missense p.K1224Q c.3670A>C 13 77779653 LUAD T G Missense p.K2470Q c.7408A>C 13 77714292 LUSC T G Missense p.R1679S c.5037A>C 13 77754358 OV TTG - InFrameDeletion p.Q2322delQ c.6964_6966delCAA 13 77725034 UCEC A C Synonymous p.S892S c.2676A>C 5 102361025 LUAD A - Frameshift p.K433Rfs*32 c.1298delA 5 102309949 STAD AG - Frameshift p.K855Tfs*45 c.2562_2563delGA 5 102360910 GBM A G IntronicSNV . c.210+6241A>G 5 102209338 HC A G Missense p.H778R c.2333A>G 5 102353039 BRCA A G Missense p.K352R c.1055A>G 5 102295728 STAD A G SpliceAcceptorSNV . c.644-2A>G 5 102285239 LUAD A G Synonymous p.G155G c.465A>G 5 102262311 CM - A IntronicInsertion . c.2331+1235dupA 5 102346800 ESCA A T Missense p.K902N c.2706A>T 5 102363902 LUSC A T Missense p.R401W c.1201A>T 5 102309858 HNSC - ATTTTT IntronicInsertion . c.1163-4669_1163-4668insATTTTT 5 102305151 CLL - CA IntronicInsertion . c.2331+1513_2331+1514insCA 5 102347083 CM C A IntronicSNV . c.268+5066C>A 5 102242183 CLL C A Missense p.S182Y c.545C>A 5 102282559 CM C A Synonymous p.T802T c.2406C>A 5 102353112 STAD C G IntronicSNV . c.269-1096C>G 5 102248542 CLL C G Missense p.P693A c.2077C>G 5 102343223 SCLC C T Missense p.P481L c.1442C>T 5 102310099 CM C T Missense p.P678L c.2033C>T 5 102343179 CM C T Missense p.P865S c.2593C>T 5 102360942 UCEC C T Missense p.R144W c.430C>T 5 102260734 CM C T Missense p.R888W c.2662C>T 5 102361011 CM C T Missense p.S466F c.1397C>T 5 102310054 CM C T Missense p.S55L c.164C>T 5 102203051 CM C T Missense p.S660L c.1979C>T 5 102342680 HNSC C T Missense p.S764F c.2291C>T 5 102345530 CM C T Nonsense p.R80* c.238C>T 5 102237087 UCEC C T Synonymous p.F665F c.1995C>T 5 102342696 CM C T Synonymous p.G612G c.1836C>T 5 102342537 UCEC C T Synonymous p.I708I c.2124C>T 5 102343270 CM C T Synonymous p.S395S c.1185C>T 5 102309842 CM G A Missense p.A135T c.403G>A 5 102260707 COREAD G A Missense p.D180N c.538G>A 5 102282552 CM G A Missense p.E85K c.253G>A 5 102237102 CM G A Missense p.G506R c.1516G>A 5 102326008 RCCC G A Missense p.R260Q c.779G>A 5 102285660 UCEC G A Missense p.R707Q c.2120G>A 5 102343266 COREAD G C IntronicSNV . c.269-7G>C 5 102249631 NSCLC G C Missense p.D434H c.1300G>C 5 102309957 LUSC G C Missense p.E852D c.2556G>C 5 102360905 BRCA G C Missense p.G388R c.1162G>C 5 102296933 HNSC G C Missense p.G506A c.1517G>C 5 102326009 LUAD G C Missense p.R80P c.239G>C 5 102237088 BRCA G C Missense p.R915T c.2744G>C 5 102363940 HNSC G C Missense p.V208L c.622G>C 5 102284128 GBM G T Missense p.D122Y c.364G>T 5 102260668 LUAD G T Missense p.G281C c.841G>T 5 102286460 HNSC G T Missense p.G675V c.2024G>T 5 102343170 LUAD G T Missense p.K321N c.963G>T 5 102295636 LUSC G T Missense p.V561F c.1681G>T 5 102338804 HC G T Synonymous p.R707R c.2121G>T 5 102343267 HNSC T A IntronicSNV . c.1484-18T>A 5 102325958 HC T A Missense p.F528I c.1582T>A 5 102326074 COREAD T C Synonymous p.F914F c.2742T>C 5 102363938 CM T - IntronicDeletion . c.2015-10delT 5 102343144 STAD T - IntronicDeletion . c.906-9delT 5 102295563 STAD TTTC - Frameshift p.N926Tfs*55 c.2777_2780delATTT 5 102364621 HC