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 23906646 23906646 + Missense_Mutation SNP T T A TCGA-OR-A5JD-01A-11D-A29I-10 TCGA-OR-A5JD-10B-01D-A29L-10 g.chr13:23906646T>A c.11369A>T c.(11368-11370)cAg>cTg p.Q3790L ACC 13 23912220 23912220 + Missense_Mutation SNP G G T TCGA-OR-A5JW-01A-11D-A29I-10 TCGA-OR-A5JW-10A-01D-A29L-10 g.chr13:23912220G>T c.5795C>A c.(5794-5796)gCc>gAc p.A1932D BLCA 13 23904689 23904689 + Silent SNP G G T TCGA-K4-A3WS-01A-11D-A22Z-08 TCGA-K4-A3WS-10A-01D-A22Z-08 g.chr13:23904689G>T c.13326C>A c.(13324-13326)ggC>ggA p.G4442G BLCA 13 23904719 23904719 + Missense_Mutation SNP G G C TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr13:23904719G>C c.13296C>G c.(13294-13296)ttC>ttG p.F4432L BLCA 13 23904747 23904747 + Missense_Mutation SNP G G A TCGA-XF-AAMZ-01A-11D-A42E-08 TCGA-XF-AAMZ-10A-01D-A42H-08 g.chr13:23904747G>A c.13268C>T c.(13267-13269)tCa>tTa p.S4423L BLCA 13 23904867 23904867 + Nonsense_Mutation SNP G G C TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr13:23904867G>C c.13148C>G c.(13147-13149)tCa>tGa p.S4383* BLCA 13 23905173 23905173 + Missense_Mutation SNP G G C TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr13:23905173G>C c.12842C>G c.(12841-12843)tCt>tGt p.S4281C BLCA 13 23905175 23905175 + Missense_Mutation SNP G G C TCGA-FD-A3B8-01A-31D-A20D-08 TCGA-FD-A3B8-10A-01D-A20D-08 g.chr13:23905175G>C c.12840C>G c.(12838-12840)ttC>ttG p.F4280L BLCA 13 23905211 23905211 + Silent SNP G G A TCGA-FD-A6TE-01A-12D-A339-08 TCGA-FD-A6TE-10A-21D-A339-08 g.chr13:23905211G>A c.12804C>T c.(12802-12804)ttC>ttT p.F4268F BLCA 13 23905453 23905453 + Missense_Mutation SNP C C T TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr13:23905453C>T c.12562G>A c.(12562-12564)Gct>Act p.A4188T BLCA 13 23905561 23905561 + Missense_Mutation SNP C C T TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr13:23905561C>T c.12454G>A c.(12454-12456)Gaa>Aaa p.E4152K BLCA 13 23906197 23906197 + Missense_Mutation SNP C C T TCGA-XF-A9SU-01A-31D-A391-08 TCGA-XF-A9SU-10A-01D-A394-08 g.chr13:23906197C>T c.11818G>A c.(11818-11820)Gtg>Atg p.V3940M BLCA 13 23906234 23906234 + Silent SNP C C T TCGA-FT-A61P-01A-11D-A30E-08 TCGA-FT-A61P-10A-01D-A30H-08 g.chr13:23906234C>T c.11781G>A c.(11779-11781)gcG>gcA p.A3927A BLCA 13 23906256 23906256 + Missense_Mutation SNP C C G TCGA-BT-A20W-01A-21D-A14W-08 TCGA-BT-A20W-11A-11D-A14W-08 g.chr13:23906256C>G c.11759G>C c.(11758-11760)aGc>aCc p.S3920T BLCA 13 23906504 23906504 + Silent SNP C C T TCGA-ZF-A9RF-01A-11D-A38G-08 TCGA-ZF-A9RF-10A-01D-A38J-08 g.chr13:23906504C>T c.11511G>A c.(11509-11511)caG>caA p.Q3837Q BLCA 13 23906653 23906653 + Missense_Mutation SNP G G A TCGA-DK-A2I6-01A-12D-A18F-08 TCGA-DK-A2I6-10A-01D-A18F-08 g.chr13:23906653G>A c.11362C>T c.(11362-11364)Cgt>Tgt p.R3788C BLCA 13 23906980 23906980 + Missense_Mutation SNP G G C TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr13:23906980G>C c.11035C>G c.(11035-11037)Ctt>Gtt p.L3679V BLCA 13 23907010 23907010 + Missense_Mutation SNP G G C TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr13:23907010G>C c.11005C>G c.(11005-11007)Caa>Gaa p.Q3669E BLCA 13 23907016 23907016 + Missense_Mutation SNP G G A TCGA-DK-AA6L-01A-11D-A391-08 TCGA-DK-AA6L-10A-01D-A394-08 g.chr13:23907016G>A c.10999C>T c.(10999-11001)Cat>Tat p.H3667Y BLCA 13 23907016 23907016 + Missense_Mutation SNP G G A TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr13:23907016G>A c.10999C>T c.(10999-11001)Cat>Tat p.H3667Y BLCA 13 23907320 23907320 + Silent SNP T T C TCGA-K4-A6FZ-01A-11D-A31L-08 TCGA-K4-A6FZ-10A-01D-A31J-08 g.chr13:23907320T>C c.10695A>G c.(10693-10695)aaA>aaG p.K3565K BLCA 13 23907631 23907631 + Missense_Mutation SNP G G T TCGA-FD-A5BR-01A-11D-A26M-08 TCGA-FD-A5BR-10A-01D-A26K-08 g.chr13:23907631G>T c.10384C>A c.(10384-10386)Cta>Ata p.L3462I BLCA 13 23907978 23907978 + Missense_Mutation SNP G G T TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr13:23907978G>T c.10037C>A c.(10036-10038)cCt>cAt p.P3346H BLCA 13 23908464 23908464 + Missense_Mutation SNP C C T TCGA-GC-A3BM-01A-11D-A22Z-08 TCGA-GC-A3BM-10A-01D-A22Z-08 g.chr13:23908464C>T c.9551G>A c.(9550-9552)cGc>cAc p.R3184H BLCA 13 23908850 23908850 + Silent SNP G G C TCGA-XF-AAMQ-01A-11D-A42E-08 TCGA-XF-AAMQ-10A-01D-A42H-08 g.chr13:23908850G>C c.9165C>G c.(9163-9165)gtC>gtG p.V3055V BLCA 13 23908972 23908972 + Missense_Mutation SNP T T A TCGA-XF-A9SG-01A-12D-A42E-08 TCGA-XF-A9SG-10A-01D-A42H-08 g.chr13:23908972T>A c.9043A>T c.(9043-9045)Atc>Ttc p.I3015F BLCA 13 23909107 23909107 + Missense_Mutation SNP G G C TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr13:23909107G>C c.8908C>G c.(8908-8910)Cta>Gta p.L2970V BLCA 13 23909322 23909322 + Missense_Mutation SNP C C T TCGA-R3-A69X-01A-22D-A30E-08 TCGA-R3-A69X-10A-01D-A30H-08 g.chr13:23909322C>T c.8693G>A c.(8692-8694)cGt>cAt p.R2898H BLCA 13 23909330 23909330 + Silent SNP G G A TCGA-DK-A3IS-01A-21D-A21A-08 TCGA-DK-A3IS-10A-01D-A21A-08 g.chr13:23909330G>A c.8685C>T c.(8683-8685)aaC>aaT p.N2895N BLCA 13 23909550 23909550 + Missense_Mutation SNP T T C TCGA-CU-A0YN-01A-21D-A10S-08 TCGA-CU-A0YN-11A-11D-A10S-08 g.chr13:23909550T>C c.8465A>G c.(8464-8466)aAt>aGt p.N2822S BLCA 13 23909599 23909599 + Missense_Mutation SNP T T C TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chr13:23909599T>C c.8416A>G c.(8416-8418)Atg>Gtg p.M2806V BLCA 13 23909987 23909987 + Silent SNP T T A TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr13:23909987T>A c.8028A>T c.(8026-8028)acA>acT p.T2676T BLCA 13 23910518 23910518 + Silent SNP G G T TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr13:23910518G>T c.7497C>A c.(7495-7497)gtC>gtA p.V2499V BLCA 13 23911384 23911384 + Missense_Mutation SNP G G C TCGA-CU-A72E-01A-12D-A339-08 TCGA-CU-A72E-10A-01D-A339-08 g.chr13:23911384G>C c.6631C>G c.(6631-6633)Caa>Gaa p.Q2211E BLCA 13 23912230 23912230 + Missense_Mutation SNP G G A TCGA-DK-AA75-01A-11D-A391-08 TCGA-DK-AA75-10A-01D-A394-08 g.chr13:23912230G>A c.5785C>T c.(5785-5787)Cgg>Tgg p.R1929W BLCA 13 23912527 23912527 + Silent SNP G G A TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr13:23912527G>A c.5488C>T c.(5488-5490)Ctg>Ttg p.L1830L BLCA 13 23912678 23912678 + Silent SNP C C G TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr13:23912678C>G c.5337G>C c.(5335-5337)tcG>tcC p.S1779S BLCA 13 23913064 23913064 + Missense_Mutation SNP G G C TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr13:23913064G>C c.4951C>G c.(4951-4953)Caa>Gaa p.Q1651E BLCA 13 23913751 23913751 + Missense_Mutation SNP C C T TCGA-2F-A9KT-01A-11D-A38G-08 TCGA-2F-A9KT-10A-01D-A38J-08 g.chr13:23913751C>T c.4264G>A c.(4264-4266)Gtg>Atg p.V1422M BLCA 13 23913766 23913766 + Missense_Mutation SNP C C T TCGA-GV-A40E-01A-12D-A23M-08 TCGA-GV-A40E-10A-01D-A23K-08 g.chr13:23913766C>T c.4249G>A c.(4249-4251)Gaa>Aaa p.E1417K BLCA 13 23913994 23913994 + Missense_Mutation SNP G G A TCGA-ZF-A9RF-01A-11D-A38G-08 TCGA-ZF-A9RF-10A-01D-A38J-08 g.chr13:23913994G>A c.4021C>T c.(4021-4023)Ctc>Ttc p.L1341F BLCA 13 23914228 23914228 + Missense_Mutation SNP G G C TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr13:23914228G>C c.3787C>G c.(3787-3789)Cta>Gta p.L1263V BLCA 13 23914231 23914231 + Missense_Mutation SNP G G C TCGA-CF-A47V-01A-11D-A23U-08 TCGA-CF-A47V-10A-01D-A23U-08 g.chr13:23914231G>C c.3784C>G c.(3784-3786)Cat>Gat p.H1262D BLCA 13 23914486 23914486 + Missense_Mutation SNP G G C TCGA-E5-A4TZ-01A-11D-A31L-08 TCGA-E5-A4TZ-10B-01D-A31J-08 g.chr13:23914486G>C c.3529C>G c.(3529-3531)Ctc>Gtc p.L1177V BLCA 13 23914840 23914840 + Missense_Mutation SNP C C G TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr13:23914840C>G c.3175G>C c.(3175-3177)Gaa>Caa p.E1059Q BLCA 13 23914843 23914843 + Missense_Mutation SNP T T A TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr13:23914843T>A c.3172A>T c.(3172-3174)Ata>Tta p.I1058L BLCA 13 23914858 23914858 + Missense_Mutation SNP G G T TCGA-FD-A6TI-01A-11D-A32B-08 TCGA-FD-A6TI-10A-01D-A329-08 g.chr13:23914858G>T c.3157C>A c.(3157-3159)Ctc>Atc p.L1053I BLCA 13 23914933 23914933 + Missense_Mutation SNP G G C TCGA-XF-A9SP-01A-11D-A391-08 TCGA-XF-A9SP-10A-01D-A394-08 g.chr13:23914933G>C c.3082C>G c.(3082-3084)Cca>Gca p.P1028A BLCA 13 23915006 23915006 + Missense_Mutation SNP A A C TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr13:23915006A>C c.3009T>G c.(3007-3009)ttT>ttG p.F1003L BLCA 13 23915126 23915126 + Silent SNP A A G TCGA-CF-A1HS-01A-11D-A13W-08 TCGA-CF-A1HS-10A-01D-A13W-08 g.chr13:23915126A>G c.2889T>C c.(2887-2889)tcT>tcC p.S963S BLCA 13 23915196 23915196 + Missense_Mutation SNP G G C TCGA-KQ-A41O-01A-12D-A34U-08 TCGA-KQ-A41O-10D-01D-A34X-08 g.chr13:23915196G>C c.2819C>G c.(2818-2820)tCt>tGt p.S940C BLCA 13 23915245 23915246 + In_Frame_Ins INS - - TTC TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chr13:23915245_23915246insTTC c.2769_2770insGAA c.(2767-2772)gaattg>gaaGAAttg p.923_924insE BLCA 13 23915753 23915753 + Silent SNP G G A TCGA-DK-A3IS-01A-21D-A21A-08 TCGA-DK-A3IS-10A-01D-A21A-08 g.chr13:23915753G>A c.2262C>T c.(2260-2262)ttC>ttT p.F754F BLCA 13 23929191 23929191 + Missense_Mutation SNP C C G TCGA-FJ-A3ZF-01A-11D-A23M-08 TCGA-FJ-A3ZF-10A-01D-A23K-08 g.chr13:23929191C>G c.1560G>C c.(1558-1560)aaG>aaC p.K520N BLCA 13 23929791 23929791 + Silent SNP G G A TCGA-BL-A0C8-01A-11D-A10S-08 TCGA-BL-A0C8-10A-01D-A10S-08 g.chr13:23929791G>A c.960C>T c.(958-960)gtC>gtT p.V320V BLCA 13 23930039 23930039 + Missense_Mutation SNP T T C TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr13:23930039T>C c.712A>G c.(712-714)Aaa>Gaa p.K238E BLCA 13 23930096 23930096 + Nonsense_Mutation SNP G G A TCGA-BT-A20N-01A-11D-A14W-08 TCGA-BT-A20N-11A-11D-A14W-08 g.chr13:23930096G>A c.655C>T c.(655-657)Caa>Taa p.Q219* BRCA 13 23904867 23904867 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr13:23904867G>A c.13148C>T c.(13147-13149)tCa>tTa p.S4383L BRCA 13 23905513 23905513 + Silent SNP G G A TCGA-BH-A18U-01A-21D-A12B-09 TCGA-BH-A18U-11A-23D-A12B-09 g.chr13:23905513G>A c.12502C>T c.(12502-12504)Ctg>Ttg p.L4168L BRCA 13 23905703 23905703 + Missense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:23905703C>A c.12312G>T c.(12310-12312)atG>atT p.M4104I BRCA 13 23906002 23906002 + Missense_Mutation SNP G G A TCGA-A8-A09I-01A-22W-A050-09 TCGA-A8-A09I-10A-01W-A055-09 g.chr13:23906002G>A c.12013C>T c.(12013-12015)Ctc>Ttc p.L4005F BRCA 13 23907076 23907076 + Nonsense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:23907076C>A c.10939G>T c.(10939-10941)Gaa>Taa p.E3647* BRCA 13 23907634 23907634 + Nonsense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:23907634C>A c.10381G>T c.(10381-10383)Gaa>Taa p.E3461* BRCA 13 23907783 23907783 + Missense_Mutation SNP G G A TCGA-AR-A251-01A-12D-A167-09 TCGA-AR-A251-10A-01D-A167-09 g.chr13:23907783G>A c.10232C>T c.(10231-10233)cCg>cTg p.P3411L BRCA 13 23907808 23907808 + Missense_Mutation SNP C C T TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr13:23907808C>T c.10207G>A c.(10207-10209)Gat>Aat p.D3403N BRCA 13 23908825 23908825 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:23908825C>T c.9190G>A c.(9190-9192)Gaa>Aaa p.E3064K BRCA 13 23909425 23909425 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:23909425G>T c.8590C>A c.(8590-8592)Ccc>Acc p.P2864T BRCA 13 23909580 23909580 + Missense_Mutation SNP T T G TCGA-GM-A2DH-01A-11D-A17W-09 TCGA-GM-A2DH-10C-01D-A17W-09 g.chr13:23909580T>G c.8435A>C c.(8434-8436)gAa>gCa p.E2812A BRCA 13 23909753 23909753 + Missense_Mutation SNP C C A TCGA-B6-A0X4-01A-11D-A10G-09 TCGA-B6-A0X4-10A-01D-A10G-09 g.chr13:23909753C>A c.8262G>T c.(8260-8262)aaG>aaT p.K2754N BRCA 13 23909883 23909883 + Missense_Mutation SNP G G A TCGA-D8-A1J8-01A-11D-A13L-09 TCGA-D8-A1J8-10A-01D-A13O-09 g.chr13:23909883G>A c.8132C>T c.(8131-8133)tCg>tTg p.S2711L BRCA 13 23910010 23910010 + Missense_Mutation SNP C C A TCGA-A8-A06N-01A-11W-A019-09 TCGA-A8-A06N-10A-01W-A021-09 g.chr13:23910010C>A c.8005G>T c.(8005-8007)Gat>Tat p.D2669Y BRCA 13 23910337 23910337 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr13:23910337C>G c.7678G>C c.(7678-7680)Gaa>Caa p.E2560Q BRCA 13 23910500 23910500 + Silent SNP G G A TCGA-GM-A2DO-01A-11D-A19Y-09 TCGA-GM-A2DO-10D-01D-A18P-09 g.chr13:23910500G>A c.7515C>T c.(7513-7515)gcC>gcT p.A2505A BRCA 13 23910597 23910597 + Missense_Mutation SNP C C G TCGA-BH-A0B7-01A-12D-A10Y-09 TCGA-BH-A0B7-10A-01D-A110-09 g.chr13:23910597C>G c.7418G>C c.(7417-7419)tGg>tCg p.W2473S BRCA 13 23911264 23911264 + Missense_Mutation SNP G G C TCGA-A8-A095-01A-11W-A019-09 TCGA-A8-A095-10A-01W-A021-09 g.chr13:23911264G>C c.6751C>G c.(6751-6753)Caa>Gaa p.Q2251E BRCA 13 23911546 23911546 + Missense_Mutation SNP C C A TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr13:23911546C>A c.6469G>T c.(6469-6471)Gat>Tat p.D2157Y BRCA 13 23911836 23911836 + Missense_Mutation SNP A A G TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr13:23911836A>G c.6179T>C c.(6178-6180)gTg>gCg p.V2060A BRCA 13 23912087 23912087 + Silent SNP G G C TCGA-E2-A1LH-01A-11D-A14G-09 TCGA-E2-A1LH-11A-22D-A14G-09 g.chr13:23912087G>C c.5928C>G c.(5926-5928)acC>acG p.T1976T BRCA 13 23912580 23912580 + Missense_Mutation SNP G G C TCGA-A8-A096-01A-11W-A019-09 TCGA-A8-A096-10A-01W-A021-09 g.chr13:23912580G>C c.5435C>G c.(5434-5436)aCa>aGa p.T1812R BRCA 13 23912644 23912644 + Missense_Mutation SNP C C T TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr13:23912644C>T c.5371G>A c.(5371-5373)Gct>Act p.A1791T BRCA 13 23913541 23913541 + Nonsense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:23913541C>A c.4474G>T c.(4474-4476)Gaa>Taa p.E1492* BRCA 13 23913912 23913912 + Missense_Mutation SNP C C T TCGA-E2-A1LS-01A-12D-A159-09 TCGA-E2-A1LS-11A-32W-A16L-09 g.chr13:23913912C>T c.4103G>A c.(4102-4104)aGc>aAc p.S1368N BRCA 13 23913916 23913916 + Missense_Mutation SNP A A G TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr13:23913916A>G c.4099T>C c.(4099-4101)Tat>Cat p.Y1367H BRCA 13 23914806 23914806 + Missense_Mutation SNP C C T TCGA-MS-A51U-01A-31D-A25Q-09 TCGA-MS-A51U-10A-01D-A25Q-09 g.chr13:23914806C>T c.3209G>A c.(3208-3210)gGa>gAa p.G1070E BRCA 13 23915127 23915127 + Missense_Mutation SNP G G C TCGA-D8-A1JC-01A-11D-A13L-09 TCGA-D8-A1JC-10A-01D-A13O-09 g.chr13:23915127G>C c.2888C>G c.(2887-2889)tCt>tGt p.S963C BRCA 13 23915403 23915403 + Missense_Mutation SNP G G A TCGA-B6-A40C-01A-11D-A23C-09 TCGA-B6-A40C-10A-01D-A23C-09 g.chr13:23915403G>A c.2612C>T c.(2611-2613)cCa>cTa p.P871L BRCA 13 23915510 23915510 + Missense_Mutation SNP C C G TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr13:23915510C>G c.2505G>C c.(2503-2505)caG>caC p.Q835H BRCA 13 23927962 23927962 + Missense_Mutation SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr13:23927962T>G c.2147A>C c.(2146-2148)cAc>cCc p.H716P BRCA 13 23928978 23928978 + Silent SNP G G C TCGA-BH-A2L8-01A-11D-A18P-09 TCGA-BH-A2L8-10A-01D-A18P-09 g.chr13:23928978G>C c.1773C>G c.(1771-1773)ctC>ctG p.L591L BRCA 13 23929123 23929123 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr13:23929123A>C c.1628T>G c.(1627-1629)gTg>gGg p.V543G BRCA 13 23929666 23929666 + Frame_Shift_Del DEL T T - TCGA-A8-A09A-01A-11W-A019-09 TCGA-A8-A09A-10A-01W-A062-09 g.chr13:23929666delT c.1085delA c.(1084-1086)aagfs p.K362fs BRCA 13 23930148 23930148 + Splice_Site SNP T T G TCGA-BH-A0H6-01A-21W-A071-09 TCGA-BH-A0H6-10A-01W-A071-09 g.chr13:23930148T>G c.e7-2 CESC 13 23905671 23905671 + Missense_Mutation SNP G G C TCGA-DG-A2KK-01A-11D-A17W-09 TCGA-DG-A2KK-10A-01D-A17W-09 g.chr13:23905671G>C c.12344C>G c.(12343-12345)tCt>tGt p.S4115C CESC 13 23907093 23907093 + Missense_Mutation SNP G G C TCGA-C5-A1BQ-01C-11D-A20U-09 TCGA-C5-A1BQ-10A-01D-A20U-09 g.chr13:23907093G>C c.10922C>G c.(10921-10923)tCt>tGt p.S3641C CESC 13 23907900 23907900 + Missense_Mutation SNP G G A TCGA-UC-A7PF-01A-11D-A351-09 TCGA-UC-A7PF-11A-31D-A351-09 g.chr13:23907900G>A c.10115C>T c.(10114-10116)tCa>tTa p.S3372L CESC 13 23908103 23908103 + Silent SNP G G C TCGA-DG-A2KL-01A-11D-A17W-09 TCGA-DG-A2KL-10A-01D-A17W-09 g.chr13:23908103G>C c.9912C>G c.(9910-9912)ctC>ctG p.L3304L CESC 13 23909371 23909371 + Missense_Mutation SNP G G A TCGA-Q1-A73Q-01A-21D-A32I-09 TCGA-Q1-A73Q-10B-01D-A32I-09 g.chr13:23909371G>A c.8644C>T c.(8644-8646)Cat>Tat p.H2882Y CESC 13 23911873 23911873 + Missense_Mutation SNP C C T TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr13:23911873C>T c.6142G>A c.(6142-6144)Gaa>Aaa p.E2048K CESC 13 23913856 23913856 + Missense_Mutation SNP G G A TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr13:23913856G>A c.4159C>T c.(4159-4161)Cct>Tct p.P1387S CESC 13 23914001 23914001 + Silent SNP C C T TCGA-FU-A40J-01A-11D-A243-09 TCGA-FU-A40J-10A-01D-A243-09 g.chr13:23914001C>T c.4014G>A c.(4012-4014)aaG>aaA p.K1338K CHOL 13 23911856 23911856 + Missense_Mutation SNP C C A TCGA-3X-AAVC-01A-21D-A417-09 TCGA-3X-AAVC-10A-01D-A41A-09 g.chr13:23911856C>A c.6159G>T c.(6157-6159)gaG>gaT p.E2053D COAD 13 23904641 23904641 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23904641G>T c.13374C>A c.(13372-13374)ttC>ttA p.F4458L COAD 13 23904719 23904719 + Missense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr13:23904719G>T c.13296C>A c.(13294-13296)ttC>ttA p.F4432L COAD 13 23904749 23904750 + Frame_Shift_Ins INS - - G TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr13:23904749_23904750insG c.13265_13266insC c.(13264-13266)cctfs p.P4422fs COAD 13 23904795 23904795 + Missense_Mutation SNP C C A TCGA-AD-6963-01A-11D-1924-10 TCGA-AD-6963-10A-01D-1924-10 g.chr13:23904795C>A c.13220G>T c.(13219-13221)aGc>aTc p.S4407I COAD 13 23904818 23904818 + Silent SNP A A G TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr13:23904818A>G c.13197T>C c.(13195-13197)acT>acC p.T4399T COAD 13 23904819 23904819 + Missense_Mutation SNP G G T TCGA-F4-6459-01A-11D-1771-10 TCGA-F4-6459-10A-01D-1771-10 g.chr13:23904819G>T c.13196C>A c.(13195-13197)aCt>aAt p.T4399N COAD 13 23904858 23904858 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:23904858C>T c.13157G>A c.(13156-13158)cGa>cAa p.R4386Q COAD 13 23905345 23905345 + Missense_Mutation SNP T T A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr13:23905345T>A c.12670A>T c.(12670-12672)Ata>Tta p.I4224L COAD 13 23905382 23905382 + Missense_Mutation SNP T T G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr13:23905382T>G c.12633A>C c.(12631-12633)gaA>gaC p.E4211D COAD 13 23905530 23905530 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr13:23905530G>A c.12485C>T c.(12484-12486)gCt>gTt p.A4162V COAD 13 23905662 23905662 + Nonsense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:23905662G>T c.12353C>A c.(12352-12354)tCa>tAa p.S4118* COAD 13 23906034 23906034 + Missense_Mutation SNP G G A TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr13:23906034G>A c.11981C>T c.(11980-11982)gCg>gTg p.A3994V COAD 13 23906239 23906239 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23906239C>T c.11776G>A c.(11776-11778)Gat>Aat p.D3926N COAD 13 23906348 23906348 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr13:23906348C>A c.11667G>T c.(11665-11667)caG>caT p.Q3889H COAD 13 23906754 23906754 + Missense_Mutation SNP T T A TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr13:23906754T>A c.11261A>T c.(11260-11262)aAc>aTc p.N3754I COAD 13 23906768 23906768 + Silent SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:23906768G>A c.11247C>T c.(11245-11247)atC>atT p.I3749I COAD 13 23906936 23906936 + Missense_Mutation SNP T T A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:23906936T>A c.11079A>T c.(11077-11079)caA>caT p.Q3693H COAD 13 23907076 23907076 + Nonsense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:23907076C>A c.10939G>T c.(10939-10941)Gaa>Taa p.E3647* COAD 13 23907183 23907183 + Missense_Mutation SNP G G T TCGA-A6-2677-01A-01W-0831-10 TCGA-A6-2677-10A-01W-0831-10 g.chr13:23907183G>T c.10832C>A c.(10831-10833)gCt>gAt p.A3611D COAD 13 23907441 23907441 + Missense_Mutation SNP A A G TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr13:23907441A>G c.10574T>C c.(10573-10575)tTg>tCg p.L3525S COAD 13 23907634 23907634 + Nonsense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:23907634C>A c.10381G>T c.(10381-10383)Gaa>Taa p.E3461* COAD 13 23907687 23907687 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:23907687T>G c.10328A>C c.(10327-10329)aAa>aCa p.K3443T COAD 13 23907689 23907689 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23907689C>A c.10326G>T c.(10324-10326)gaG>gaT p.E3442D COAD 13 23907736 23907736 + Missense_Mutation SNP C C T TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr13:23907736C>T c.10279G>A c.(10279-10281)Gga>Aga p.G3427R COAD 13 23907796 23907796 + Missense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:23907796G>T c.10219C>A c.(10219-10221)Cta>Ata p.L3407I COAD 13 23908186 23908186 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:23908186C>A c.9829G>T c.(9829-9831)Gac>Tac p.D3277Y COAD 13 23908265 23908265 + Silent SNP A A G TCGA-AA-3848-01A-01W-0900-09 TCGA-AA-3848-10A-01W-0900-09 g.chr13:23908265A>G c.9750T>C c.(9748-9750)ttT>ttC p.F3250F COAD 13 23908466 23908466 + Silent SNP G G T TCGA-D5-6922-01A-11D-1924-10 TCGA-D5-6922-10A-01D-1924-10 g.chr13:23908466G>T c.9549C>A c.(9547-9549)tcC>tcA p.S3183S COAD 13 23908710 23908710 + Frame_Shift_Del DEL A A - TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr13:23908710delA c.9305delT c.(9304-9306)ttafs p.L3102fs COAD 13 23908778 23908778 + Silent SNP A A C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr13:23908778A>C c.9237T>G c.(9235-9237)ctT>ctG p.L3079L COAD 13 23908825 23908825 + Nonsense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:23908825C>A c.9190G>T c.(9190-9192)Gaa>Taa p.E3064* COAD 13 23909213 23909213 + Silent SNP G G A TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr13:23909213G>A c.8802C>T c.(8800-8802)ttC>ttT p.F2934F COAD 13 23909215 23909215 + Missense_Mutation SNP A A T TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr13:23909215A>T c.8800T>A c.(8800-8802)Ttc>Atc p.F2934I COAD 13 23909222 23909222 + Frame_Shift_Del DEL T T - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr13:23909222delT c.8793delA c.(8791-8793)aaafs p.K2931fs COAD 13 23909298 23909298 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:23909298C>T c.8717G>A c.(8716-8718)cGa>cAa p.R2906Q COAD 13 23909360 23909360 + Silent SNP G G A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr13:23909360G>A c.8655C>T c.(8653-8655)ggC>ggT p.G2885G COAD 13 23909377 23909377 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr13:23909377G>A c.8638C>T c.(8638-8640)Cca>Tca p.P2880S COAD 13 23909402 23909403 + Frame_Shift_Ins INS - - A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr13:23909402_23909403insA c.8612_8613insT c.(8611-8613)ttgfs p.L2871fs COAD 13 23909753 23909753 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:23909753C>A c.8262G>T c.(8260-8262)aaG>aaT p.K2754N COAD 13 23909772 23909772 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:23909772G>T c.8243C>A c.(8242-8244)tCt>tAt p.S2748Y COAD 13 23909780 23909780 + Missense_Mutation SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr13:23909780T>G c.8235A>C c.(8233-8235)gaA>gaC p.E2745D COAD 13 23909874 23909874 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:23909874G>A c.8141C>T c.(8140-8142)tCg>tTg p.S2714L COAD 13 23910042 23910042 + Missense_Mutation SNP G G T TCGA-AA-3986-01A-02W-0995-10 TCGA-AA-3986-10A-01W-0999-10 g.chr13:23910042G>T c.7973C>A c.(7972-7974)gCc>gAc p.A2658D COAD 13 23910255 23910255 + Missense_Mutation SNP G G A TCGA-AA-3972-01A-01W-0995-10 TCGA-AA-3972-10A-01W-0999-10 g.chr13:23910255G>A c.7760C>T c.(7759-7761)gCa>gTa p.A2587V COAD 13 23910439 23910439 + Nonsense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr13:23910439C>A c.7576G>T c.(7576-7578)Gaa>Taa p.E2526* COAD 13 23910661 23910661 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23910661A>C c.7354T>G c.(7354-7356)Tta>Gta p.L2452V COAD 13 23910787 23910787 + Nonsense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:23910787C>A c.7228G>T c.(7228-7230)Gaa>Taa p.E2410* COAD 13 23910866 23910866 + Silent SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr13:23910866G>A c.7149C>T c.(7147-7149)cgC>cgT p.R2383R COAD 13 23911139 23911139 + Silent SNP C C A TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr13:23911139C>A c.6876G>T c.(6874-6876)ctG>ctT p.L2292L COAD 13 23911376 23911376 + Silent SNP G G A TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr13:23911376G>A c.6639C>T c.(6637-6639)atC>atT p.I2213I COAD 13 23911439 23911439 + Silent SNP G G A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr13:23911439G>A c.6576C>T c.(6574-6576)atC>atT p.I2192I COAD 13 23911439 23911439 + Silent SNP G G T TCGA-AD-6890-01A-11D-1924-10 TCGA-AD-6890-10A-01D-1924-10 g.chr13:23911439G>T c.6576C>A c.(6574-6576)atC>atA p.I2192I COAD 13 23911439 23911439 + Silent SNP G G T TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr13:23911439G>T c.6576C>A c.(6574-6576)atC>atA p.I2192I COAD 13 23911439 23911439 + Silent SNP G G T TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr13:23911439G>T c.6576C>A c.(6574-6576)atC>atA p.I2192I COAD 13 23911441 23911441 + Missense_Mutation SNP T T C TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr13:23911441T>C c.6574A>G c.(6574-6576)Atc>Gtc p.I2192V COAD 13 23911660 23911660 + Nonsense_Mutation SNP G G A TCGA-AA-3695-01A-01W-0900-09 TCGA-AA-3695-10A-01W-0900-09 g.chr13:23911660G>A c.6355C>T c.(6355-6357)Cga>Tga p.R2119* COAD 13 23911709 23911709 + Missense_Mutation SNP C C A TCGA-DM-A28G-01A-11D-A16V-10 TCGA-DM-A28G-10A-01D-A16V-10 g.chr13:23911709C>A c.6306G>T c.(6304-6306)ttG>ttT p.L2102F COAD 13 23911741 23911741 + Missense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:23911741G>T c.6274C>A c.(6274-6276)Ctt>Att p.L2092I COAD 13 23911828 23911829 + Frame_Shift_Ins INS - - A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr13:23911828_23911829insA c.6186_6187insT c.(6184-6189)tttccafs p.P2063fs COAD 13 23911842 23911843 + Frame_Shift_Ins INS - - A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr13:23911842_23911843insA c.6172_6173insT c.(6172-6174)tctfs p.S2058fs COAD 13 23911949 23911949 + Silent SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:23911949T>C c.6066A>G c.(6064-6066)aaA>aaG p.K2022K COAD 13 23911996 23911996 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:23911996C>A c.6019G>T c.(6019-6021)Gca>Tca p.A2007S COAD 13 23912173 23912173 + Missense_Mutation SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr13:23912173C>T c.5842G>A c.(5842-5844)Gat>Aat p.D1948N COAD 13 23912323 23912323 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23912323C>A c.5692G>T c.(5692-5694)Gaa>Taa p.E1898* COAD 13 23912372 23912372 + Silent SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:23912372G>T c.5643C>A c.(5641-5643)ggC>ggA p.G1881G COAD 13 23912630 23912630 + Missense_Mutation SNP C C T TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr13:23912630C>T c.5385G>A c.(5383-5385)atG>atA p.M1795I COAD 13 23912631 23912631 + Missense_Mutation SNP A A G TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr13:23912631A>G c.5384T>C c.(5383-5385)aTg>aCg p.M1795T COAD 13 23912632 23912632 + Missense_Mutation SNP T T C TCGA-DM-A285-01A-11D-A16V-10 TCGA-DM-A285-10A-01D-A16V-10 g.chr13:23912632T>C c.5383A>G c.(5383-5385)Atg>Gtg p.M1795V COAD 13 23912947 23912947 + Missense_Mutation SNP C C T TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr13:23912947C>T c.5068G>A c.(5068-5070)Gta>Ata p.V1690I COAD 13 23913388 23913388 + Nonsense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:23913388C>A c.4627G>T c.(4627-4629)Gaa>Taa p.E1543* COAD 13 23913555 23913555 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:23913555T>G c.4460A>C c.(4459-4461)gAt>gCt p.D1487A COAD 13 23913577 23913577 + Nonsense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:23913577C>A c.4438G>T c.(4438-4440)Gaa>Taa p.E1480* COAD 13 23913826 23913826 + Missense_Mutation SNP C C T TCGA-AA-3867-01A-01W-0995-10 TCGA-AA-3867-10A-01W-0995-10 g.chr13:23913826C>T c.4189G>A c.(4189-4191)Gaa>Aaa p.E1397K COAD 13 23914120 23914120 + Missense_Mutation SNP C C A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr13:23914120C>A c.3895G>T c.(3895-3897)Gac>Tac p.D1299Y COAD 13 23914152 23914152 + Missense_Mutation SNP G G A TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr13:23914152G>A c.3863C>T c.(3862-3864)gCc>gTc p.A1288V COAD 13 23914962 23914962 + Missense_Mutation SNP T T C TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr13:23914962T>C c.3053A>G c.(3052-3054)gAg>gGg p.E1018G COAD 13 23914962 23914962 + Missense_Mutation SNP T T C TCGA-AZ-6606-01A-11D-1835-10 TCGA-AZ-6606-11A-01D-1835-10 g.chr13:23914962T>C c.3053A>G c.(3052-3054)gAg>gGg p.E1018G COAD 13 23915439 23915439 + Missense_Mutation SNP A A G TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr13:23915439A>G c.2576T>C c.(2575-2577)aTa>aCa p.I859T COAD 13 23915453 23915453 + Frame_Shift_Del DEL T T - TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr13:23915453delT c.2562delA c.(2560-2562)aaafs p.K854fs COAD 13 23915582 23915582 + Silent SNP A A G TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr13:23915582A>G c.2433T>C c.(2431-2433)ggT>ggC p.G811G COAD 13 23915617 23915617 + Missense_Mutation SNP T T A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr13:23915617T>A c.2398A>T c.(2398-2400)Atg>Ttg p.M800L COAD 13 23915778 23915778 + Missense_Mutation SNP A A G TCGA-AZ-4681-01A-01D-1408-10 TCGA-AZ-4681-10A-01D-1408-10 g.chr13:23915778A>G c.2237T>C c.(2236-2238)cTt>cCt p.L746P COAD 13 23915783 23915783 + Silent SNP T T G TCGA-AZ-4681-01A-01D-1408-10 TCGA-AZ-4681-10A-01D-1408-10 g.chr13:23915783T>G c.2232A>C c.(2230-2232)gcA>gcC p.A744A COAD 13 23928841 23928841 + Missense_Mutation SNP T T G TCGA-AA-3542-01A-02W-0831-10 TCGA-AA-3542-10A-01W-0831-10 g.chr13:23928841T>G c.1910A>C c.(1909-1911)aAg>aCg p.K637T COAD 13 23929264 23929264 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr13:23929264A>G c.1487T>C c.(1486-1488)cTt>cCt p.L496P COAD 13 23929431 23929431 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23929431G>T c.1320C>A c.(1318-1320)ttC>ttA p.F440L COAD 13 23929713 23929713 + Silent SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:23929713C>T c.1038G>A c.(1036-1038)ccG>ccA p.P346P COAD 13 23929924 23929924 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:23929924C>T c.827G>A c.(826-828)cGc>cAc p.R276H COAD 13 23929925 23929925 + Missense_Mutation SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr13:23929925G>A c.826C>T c.(826-828)Cgc>Tgc p.R276C COAD 13 23929928 23929928 + Missense_Mutation SNP G G T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr13:23929928G>T c.823C>A c.(823-825)Ctt>Att p.L275I COAD 13 23932517 23932517 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr13:23932517G>A c.561C>T c.(559-561)gtC>gtT p.V187V COAD 13 23932526 23932526 + Silent SNP A A G TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr13:23932526A>G c.552T>C c.(550-552)ccT>ccC p.P184P COAD 13 23932552 23932552 + Missense_Mutation SNP C C T TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr13:23932552C>T c.526G>A c.(526-528)Gca>Aca p.A176T COAD 13 23942607 23942607 + Silent SNP C C T TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr13:23942607C>T c.279G>A c.(277-279)acG>acA p.T93T COAD 13 23949321 23949321 + Silent SNP T T C TCGA-D5-6534-01A-21D-1924-10 TCGA-D5-6534-10A-01D-1924-10 g.chr13:23949321T>C c.108A>G c.(106-108)gaA>gaG p.E36E COADREAD 13 23904434 23904434 + Missense_Mutation SNP T T G TCGA-AG-3893-01A-01W-1073-09 TCGA-AG-3893-10A-01W-1073-09 g.chr13:23904434T>G c.13581A>C c.(13579-13581)gaA>gaC p.E4527D COADREAD 13 23904641 23904641 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23904641G>T c.13374C>A c.(13372-13374)ttC>ttA p.F4458L COADREAD 13 23904719 23904719 + Missense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr13:23904719G>T c.13296C>A c.(13294-13296)ttC>ttA p.F4432L COADREAD 13 23904749 23904750 + Frame_Shift_Ins INS - - G TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr13:23904749_23904750insG c.13265_13266insC c.(13264-13266)cctfs p.P4422fs COADREAD 13 23904795 23904795 + Missense_Mutation SNP C C A TCGA-AD-6963-01A-11D-1924-10 TCGA-AD-6963-10A-01D-1924-10 g.chr13:23904795C>A c.13220G>T c.(13219-13221)aGc>aTc p.S4407I COADREAD 13 23904818 23904818 + Silent SNP A A G TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr13:23904818A>G c.13197T>C c.(13195-13197)acT>acC p.T4399T COADREAD 13 23904819 23904819 + Missense_Mutation SNP G G T TCGA-F4-6459-01A-11D-1771-10 TCGA-F4-6459-10A-01D-1771-10 g.chr13:23904819G>T c.13196C>A c.(13195-13197)aCt>aAt p.T4399N COADREAD 13 23904858 23904858 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:23904858C>T c.13157G>A c.(13156-13158)cGa>cAa p.R4386Q COADREAD 13 23905110 23905110 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23905110G>T c.12905C>A c.(12904-12906)tCt>tAt p.S4302Y COADREAD 13 23905345 23905345 + Missense_Mutation SNP T T A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr13:23905345T>A c.12670A>T c.(12670-12672)Ata>Tta p.I4224L COADREAD 13 23905348 23905348 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23905348T>G c.12667A>C c.(12667-12669)Aag>Cag p.K4223Q COADREAD 13 23905382 23905382 + Missense_Mutation SNP T T G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr13:23905382T>G c.12633A>C c.(12631-12633)gaA>gaC p.E4211D COADREAD 13 23905530 23905530 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr13:23905530G>A c.12485C>T c.(12484-12486)gCt>gTt p.A4162V COADREAD 13 23905662 23905662 + Nonsense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:23905662G>T c.12353C>A c.(12352-12354)tCa>tAa p.S4118* COADREAD 13 23906034 23906034 + Missense_Mutation SNP G G A TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr13:23906034G>A c.11981C>T c.(11980-11982)gCg>gTg p.A3994V COADREAD 13 23906239 23906239 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23906239C>T c.11776G>A c.(11776-11778)Gat>Aat p.D3926N COADREAD 13 23906348 23906348 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr13:23906348C>A c.11667G>T c.(11665-11667)caG>caT p.Q3889H COADREAD 13 23906754 23906754 + Missense_Mutation SNP T T A TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr13:23906754T>A c.11261A>T c.(11260-11262)aAc>aTc p.N3754I COADREAD 13 23906768 23906768 + Silent SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:23906768G>A c.11247C>T c.(11245-11247)atC>atT p.I3749I COADREAD 13 23906936 23906936 + Missense_Mutation SNP T T A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:23906936T>A c.11079A>T c.(11077-11079)caA>caT p.Q3693H COADREAD 13 23907021 23907021 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23907021C>A c.10994G>T c.(10993-10995)aGa>aTa p.R3665I COADREAD 13 23907076 23907076 + Nonsense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:23907076C>A c.10939G>T c.(10939-10941)Gaa>Taa p.E3647* COADREAD 13 23907090 23907090 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23907090C>A c.10925G>T c.(10924-10926)gGa>gTa p.G3642V COADREAD 13 23907183 23907183 + Missense_Mutation SNP G G T TCGA-A6-2677-01A-01W-0831-10 TCGA-A6-2677-10A-01W-0831-10 g.chr13:23907183G>T c.10832C>A c.(10831-10833)gCt>gAt p.A3611D COADREAD 13 23907441 23907441 + Missense_Mutation SNP A A G TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr13:23907441A>G c.10574T>C c.(10573-10575)tTg>tCg p.L3525S COADREAD 13 23907566 23907566 + Silent SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23907566T>G c.10449A>C c.(10447-10449)ccA>ccC p.P3483P COADREAD 13 23907634 23907634 + Nonsense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:23907634C>A c.10381G>T c.(10381-10383)Gaa>Taa p.E3461* COADREAD 13 23907687 23907687 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:23907687T>G c.10328A>C c.(10327-10329)aAa>aCa p.K3443T COADREAD 13 23907689 23907689 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23907689C>A c.10326G>T c.(10324-10326)gaG>gaT p.E3442D COADREAD 13 23907736 23907736 + Missense_Mutation SNP C C T TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr13:23907736C>T c.10279G>A c.(10279-10281)Gga>Aga p.G3427R COADREAD 13 23907796 23907796 + Missense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:23907796G>T c.10219C>A c.(10219-10221)Cta>Ata p.L3407I COADREAD 13 23908186 23908186 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:23908186C>A c.9829G>T c.(9829-9831)Gac>Tac p.D3277Y COADREAD 13 23908265 23908265 + Silent SNP A A G TCGA-AA-3848-01A-01W-0900-09 TCGA-AA-3848-10A-01W-0900-09 g.chr13:23908265A>G c.9750T>C c.(9748-9750)ttT>ttC p.F3250F COADREAD 13 23908466 23908466 + Silent SNP G G T TCGA-D5-6922-01A-11D-1924-10 TCGA-D5-6922-10A-01D-1924-10 g.chr13:23908466G>T c.9549C>A c.(9547-9549)tcC>tcA p.S3183S COADREAD 13 23908582 23908582 + Nonsense_Mutation SNP C C A TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr13:23908582C>A c.9433G>T c.(9433-9435)Gaa>Taa p.E3145* COADREAD 13 23908710 23908710 + Frame_Shift_Del DEL A A - TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr13:23908710delA c.9305delT c.(9304-9306)ttafs p.L3102fs COADREAD 13 23908736 23908736 + Silent SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23908736C>A c.9279G>T c.(9277-9279)gtG>gtT p.V3093V COADREAD 13 23908778 23908778 + Silent SNP A A C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr13:23908778A>C c.9237T>G c.(9235-9237)ctT>ctG p.L3079L COADREAD 13 23908825 23908825 + Nonsense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:23908825C>A c.9190G>T c.(9190-9192)Gaa>Taa p.E3064* COADREAD 13 23908898 23908898 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23908898T>G c.9117A>C c.(9115-9117)aaA>aaC p.K3039N COADREAD 13 23908918 23908918 + Missense_Mutation SNP C C A TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr13:23908918C>A c.9097G>T c.(9097-9099)Gat>Tat p.D3033Y COADREAD 13 23908973 23908973 + Nonsense_Mutation SNP C C T TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr13:23908973C>T c.9042G>A c.(9040-9042)tgG>tgA p.W3014* COADREAD 13 23909113 23909113 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23909113G>T c.8902C>A c.(8902-8904)Ctt>Att p.L2968I COADREAD 13 23909213 23909213 + Silent SNP G G A TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr13:23909213G>A c.8802C>T c.(8800-8802)ttC>ttT p.F2934F COADREAD 13 23909215 23909215 + Missense_Mutation SNP A A T TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr13:23909215A>T c.8800T>A c.(8800-8802)Ttc>Atc p.F2934I COADREAD 13 23909222 23909222 + Frame_Shift_Del DEL T T - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr13:23909222delT c.8793delA c.(8791-8793)aaafs p.K2931fs COADREAD 13 23909298 23909298 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:23909298C>T c.8717G>A c.(8716-8718)cGa>cAa p.R2906Q COADREAD 13 23909360 23909360 + Silent SNP G G A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr13:23909360G>A c.8655C>T c.(8653-8655)ggC>ggT p.G2885G COADREAD 13 23909377 23909377 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr13:23909377G>A c.8638C>T c.(8638-8640)Cca>Tca p.P2880S COADREAD 13 23909402 23909403 + Frame_Shift_Ins INS - - A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr13:23909402_23909403insA c.8612_8613insT c.(8611-8613)ttgfs p.L2871fs COADREAD 13 23909694 23909694 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23909694C>A c.8321G>T c.(8320-8322)aGa>aTa p.R2774I COADREAD 13 23909753 23909753 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:23909753C>A c.8262G>T c.(8260-8262)aaG>aaT p.K2754N COADREAD 13 23909772 23909772 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:23909772G>T c.8243C>A c.(8242-8244)tCt>tAt p.S2748Y COADREAD 13 23909780 23909780 + Missense_Mutation SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr13:23909780T>G c.8235A>C c.(8233-8235)gaA>gaC p.E2745D COADREAD 13 23909874 23909874 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:23909874G>A c.8141C>T c.(8140-8142)tCg>tTg p.S2714L COADREAD 13 23910042 23910042 + Missense_Mutation SNP G G T TCGA-AA-3986-01A-02W-0995-10 TCGA-AA-3986-10A-01W-0999-10 g.chr13:23910042G>T c.7973C>A c.(7972-7974)gCc>gAc p.A2658D COADREAD 13 23910255 23910255 + Missense_Mutation SNP G G A TCGA-AA-3972-01A-01W-0995-10 TCGA-AA-3972-10A-01W-0999-10 g.chr13:23910255G>A c.7760C>T c.(7759-7761)gCa>gTa p.A2587V COADREAD 13 23910439 23910439 + Nonsense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr13:23910439C>A c.7576G>T c.(7576-7578)Gaa>Taa p.E2526* COADREAD 13 23910661 23910661 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23910661A>C c.7354T>G c.(7354-7356)Tta>Gta p.L2452V COADREAD 13 23910682 23910682 + Nonsense_Mutation SNP C C A TCGA-AG-4005-01A-01W-1073-09 TCGA-AG-4005-10A-01W-1073-09 g.chr13:23910682C>A c.7333G>T c.(7333-7335)Gag>Tag p.E2445* COADREAD 13 23910787 23910787 + Nonsense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:23910787C>A c.7228G>T c.(7228-7230)Gaa>Taa p.E2410* COADREAD 13 23910866 23910866 + Silent SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr13:23910866G>A c.7149C>T c.(7147-7149)cgC>cgT p.R2383R COADREAD 13 23911139 23911139 + Silent SNP C C A TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr13:23911139C>A c.6876G>T c.(6874-6876)ctG>ctT p.L2292L COADREAD 13 23911196 23911196 + Silent SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23911196T>G c.6819A>C c.(6817-6819)tcA>tcC p.S2273S COADREAD 13 23911376 23911376 + Silent SNP G G A TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr13:23911376G>A c.6639C>T c.(6637-6639)atC>atT p.I2213I COADREAD 13 23911439 23911439 + Silent SNP G G A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr13:23911439G>A c.6576C>T c.(6574-6576)atC>atT p.I2192I COADREAD 13 23911439 23911439 + Silent SNP G G T TCGA-AD-6890-01A-11D-1924-10 TCGA-AD-6890-10A-01D-1924-10 g.chr13:23911439G>T c.6576C>A c.(6574-6576)atC>atA p.I2192I COADREAD 13 23911439 23911439 + Silent SNP G G T TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr13:23911439G>T c.6576C>A c.(6574-6576)atC>atA p.I2192I COADREAD 13 23911439 23911439 + Silent SNP G G T TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr13:23911439G>T c.6576C>A c.(6574-6576)atC>atA p.I2192I COADREAD 13 23911441 23911441 + Missense_Mutation SNP T T C TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr13:23911441T>C c.6574A>G c.(6574-6576)Atc>Gtc p.I2192V COADREAD 13 23911660 23911660 + Nonsense_Mutation SNP G G A TCGA-AA-3695-01A-01W-0900-09 TCGA-AA-3695-10A-01W-0900-09 g.chr13:23911660G>A c.6355C>T c.(6355-6357)Cga>Tga p.R2119* COADREAD 13 23911709 23911709 + Missense_Mutation SNP C C A TCGA-DM-A28G-01A-11D-A16V-10 TCGA-DM-A28G-10A-01D-A16V-10 g.chr13:23911709C>A c.6306G>T c.(6304-6306)ttG>ttT p.L2102F COADREAD 13 23911741 23911741 + Missense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:23911741G>T c.6274C>A c.(6274-6276)Ctt>Att p.L2092I COADREAD 13 23911828 23911829 + Frame_Shift_Ins INS - - A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr13:23911828_23911829insA c.6186_6187insT c.(6184-6189)tttccafs p.P2063fs COADREAD 13 23911842 23911843 + Frame_Shift_Ins INS - - A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr13:23911842_23911843insA c.6172_6173insT c.(6172-6174)tctfs p.S2058fs COADREAD 13 23911949 23911949 + Silent SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:23911949T>C c.6066A>G c.(6064-6066)aaA>aaG p.K2022K COADREAD 13 23911996 23911996 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:23911996C>A c.6019G>T c.(6019-6021)Gca>Tca p.A2007S COADREAD 13 23912013 23912013 + Missense_Mutation SNP C C A TCGA-AG-4001-01A-02W-1073-09 TCGA-AG-4001-10A-01W-1073-09 g.chr13:23912013C>A c.6002G>T c.(6001-6003)aGa>aTa p.R2001I COADREAD 13 23912173 23912173 + Missense_Mutation SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr13:23912173C>T c.5842G>A c.(5842-5844)Gat>Aat p.D1948N COADREAD 13 23912323 23912323 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23912323C>A c.5692G>T c.(5692-5694)Gaa>Taa p.E1898* COADREAD 13 23912372 23912372 + Silent SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:23912372G>T c.5643C>A c.(5641-5643)ggC>ggA p.G1881G COADREAD 13 23912630 23912630 + Missense_Mutation SNP C C T TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr13:23912630C>T c.5385G>A c.(5383-5385)atG>atA p.M1795I COADREAD 13 23912631 23912631 + Missense_Mutation SNP A A G TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr13:23912631A>G c.5384T>C c.(5383-5385)aTg>aCg p.M1795T COADREAD 13 23912632 23912632 + Missense_Mutation SNP T T C TCGA-DM-A285-01A-11D-A16V-10 TCGA-DM-A285-10A-01D-A16V-10 g.chr13:23912632T>C c.5383A>G c.(5383-5385)Atg>Gtg p.M1795V COADREAD 13 23912947 23912947 + Missense_Mutation SNP C C T TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr13:23912947C>T c.5068G>A c.(5068-5070)Gta>Ata p.V1690I COADREAD 13 23913102 23913102 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23913102C>T c.4913G>A c.(4912-4914)aGc>aAc p.S1638N COADREAD 13 23913388 23913388 + Nonsense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr13:23913388C>A c.4627G>T c.(4627-4629)Gaa>Taa p.E1543* COADREAD 13 23913434 23913434 + Silent SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23913434A>G c.4581T>C c.(4579-4581)aaT>aaC p.N1527N COADREAD 13 23913555 23913555 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:23913555T>G c.4460A>C c.(4459-4461)gAt>gCt p.D1487A COADREAD 13 23913577 23913577 + Nonsense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:23913577C>A c.4438G>T c.(4438-4440)Gaa>Taa p.E1480* COADREAD 13 23913600 23913600 + Missense_Mutation SNP G G T TCGA-CI-6621-01A-11D-1826-10 TCGA-CI-6621-10A-01D-1826-10 g.chr13:23913600G>T c.4415C>A c.(4414-4416)cCt>cAt p.P1472H COADREAD 13 23913826 23913826 + Missense_Mutation SNP C C T TCGA-AA-3867-01A-01W-0995-10 TCGA-AA-3867-10A-01W-0995-10 g.chr13:23913826C>T c.4189G>A c.(4189-4191)Gaa>Aaa p.E1397K COADREAD 13 23914120 23914120 + Missense_Mutation SNP C C A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr13:23914120C>A c.3895G>T c.(3895-3897)Gac>Tac p.D1299Y COADREAD 13 23914152 23914152 + Missense_Mutation SNP G G A TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr13:23914152G>A c.3863C>T c.(3862-3864)gCc>gTc p.A1288V COADREAD 13 23914615 23914615 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23914615C>T c.3400G>A c.(3400-3402)Gtt>Att p.V1134I COADREAD 13 23914699 23914699 + Missense_Mutation SNP C C A TCGA-AG-4015-01A-01W-1073-09 TCGA-AG-4015-10A-01W-1073-09 g.chr13:23914699C>A c.3316G>T c.(3316-3318)Gtg>Ttg p.V1106L COADREAD 13 23914840 23914840 + Missense_Mutation SNP C C G TCGA-AG-A00H-01A-01W-A00E-09 TCGA-AG-A00H-10A-01W-A00E-09 g.chr13:23914840C>G c.3175G>C c.(3175-3177)Gaa>Caa p.E1059Q COADREAD 13 23914962 23914962 + Missense_Mutation SNP T T C TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr13:23914962T>C c.3053A>G c.(3052-3054)gAg>gGg p.E1018G COADREAD 13 23914962 23914962 + Missense_Mutation SNP T T C TCGA-AZ-6606-01A-11D-1835-10 TCGA-AZ-6606-11A-01D-1835-10 g.chr13:23914962T>C c.3053A>G c.(3052-3054)gAg>gGg p.E1018G COADREAD 13 23915071 23915071 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23915071T>G c.2944A>C c.(2944-2946)Aaa>Caa p.K982Q COADREAD 13 23915439 23915439 + Missense_Mutation SNP A A G TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr13:23915439A>G c.2576T>C c.(2575-2577)aTa>aCa p.I859T COADREAD 13 23915453 23915453 + Frame_Shift_Del DEL T T - TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr13:23915453delT c.2562delA c.(2560-2562)aaafs p.K854fs COADREAD 13 23915582 23915582 + Silent SNP A A G TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr13:23915582A>G c.2433T>C c.(2431-2433)ggT>ggC p.G811G COADREAD 13 23915617 23915617 + Missense_Mutation SNP T T A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr13:23915617T>A c.2398A>T c.(2398-2400)Atg>Ttg p.M800L COADREAD 13 23915778 23915778 + Missense_Mutation SNP A A G TCGA-AZ-4681-01A-01D-1408-10 TCGA-AZ-4681-10A-01D-1408-10 g.chr13:23915778A>G c.2237T>C c.(2236-2238)cTt>cCt p.L746P COADREAD 13 23915783 23915783 + Silent SNP T T G TCGA-AZ-4681-01A-01D-1408-10 TCGA-AZ-4681-10A-01D-1408-10 g.chr13:23915783T>G c.2232A>C c.(2230-2232)gcA>gcC p.A744A COADREAD 13 23928841 23928841 + Missense_Mutation SNP T T G TCGA-AA-3542-01A-02W-0831-10 TCGA-AA-3542-10A-01W-0831-10 g.chr13:23928841T>G c.1910A>C c.(1909-1911)aAg>aCg p.K637T COADREAD 13 23929264 23929264 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr13:23929264A>G c.1487T>C c.(1486-1488)cTt>cCt p.L496P COADREAD 13 23929431 23929431 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:23929431G>T c.1320C>A c.(1318-1320)ttC>ttA p.F440L COADREAD 13 23929713 23929713 + Silent SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:23929713C>T c.1038G>A c.(1036-1038)ccG>ccA p.P346P COADREAD 13 23929770 23929770 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23929770C>A c.981G>T c.(979-981)gaG>gaT p.E327D COADREAD 13 23929924 23929924 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:23929924C>T c.827G>A c.(826-828)cGc>cAc p.R276H COADREAD 13 23929925 23929925 + Missense_Mutation SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr13:23929925G>A c.826C>T c.(826-828)Cgc>Tgc p.R276C COADREAD 13 23929928 23929928 + Missense_Mutation SNP G G T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr13:23929928G>T c.823C>A c.(823-825)Ctt>Att p.L275I COADREAD 13 23932517 23932517 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr13:23932517G>A c.561C>T c.(559-561)gtC>gtT p.V187V COADREAD 13 23932526 23932526 + Silent SNP A A G TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr13:23932526A>G c.552T>C c.(550-552)ccT>ccC p.P184P COADREAD 13 23932552 23932552 + Missense_Mutation SNP C C T TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr13:23932552C>T c.526G>A c.(526-528)Gca>Aca p.A176T COADREAD 13 23932592 23932592 + Silent SNP C C T TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr13:23932592C>T c.486G>A c.(484-486)gcG>gcA p.A162A COADREAD 13 23942607 23942607 + Silent SNP C C T TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr13:23942607C>T c.279G>A c.(277-279)acG>acA p.T93T COADREAD 13 23949321 23949321 + Silent SNP T T C TCGA-D5-6534-01A-21D-1924-10 TCGA-D5-6534-10A-01D-1924-10 g.chr13:23949321T>C c.108A>G c.(106-108)gaA>gaG p.E36E DLBC 13 23904298 23904298 + Missense_Mutation SNP T T G TCGA-GR-7353-01A-11D-2210-10 TCGA-GR-7353-10A-01D-2210-10 g.chr13:23904298T>G c.13717A>C c.(13717-13719)Aat>Cat p.N4573H DLBC 13 23905481 23905481 + Silent SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr13:23905481C>T c.12534G>A c.(12532-12534)ccG>ccA p.P4178P DLBC 13 23907902 23907902 + Silent SNP A A C TCGA-FA-8693-01A-11D-2397-10 TCGA-FA-8693-10A-01D-2397-10 g.chr13:23907902A>C c.10113T>G c.(10111-10113)acT>acG p.T3371T DLBC 13 23908091 23908091 + Silent SNP G G A TCGA-GS-A9U3-01A-11D-A38X-10 TCGA-GS-A9U3-10A-01D-A38X-10 g.chr13:23908091G>A c.9924C>T c.(9922-9924)caC>caT p.H3308H DLBC 13 23908805 23908805 + Silent SNP A A G TCGA-FF-8042-01A-11D-2210-10 TCGA-FF-8042-10A-01D-2210-10 g.chr13:23908805A>G c.9210T>C c.(9208-9210)gtT>gtC p.V3070V DLBC 13 23910850 23910850 + Missense_Mutation SNP C C T TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr13:23910850C>T c.7165G>A c.(7165-7167)Gtg>Atg p.V2389M DLBC 13 23913163 23913163 + Missense_Mutation SNP A A G TCGA-RQ-AAAT-01A-11D-A38X-10 TCGA-RQ-AAAT-10A-01D-A38X-10 g.chr13:23913163A>G c.4852T>C c.(4852-4854)Ttc>Ctc p.F1618L DLBC 13 23914286 23914286 + Silent SNP T T C TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr13:23914286T>C c.3729A>G c.(3727-3729)gaA>gaG p.E1243E DLBC 13 23915089 23915089 + Missense_Mutation SNP G G T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr13:23915089G>T c.2926C>A c.(2926-2928)Cgt>Agt p.R976S DLBC 13 23929189 23929189 + Missense_Mutation SNP C C G TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr13:23929189C>G c.1562G>C c.(1561-1563)aGc>aCc p.S521T ESCA 13 23904431 23904431 + Silent SNP A A C TCGA-L5-A43E-01A-11D-A247-09 TCGA-L5-A43E-10A-01D-A247-09 g.chr13:23904431A>C c.13584T>G c.(13582-13584)gcT>gcG p.A4528A ESCA 13 23904549 23904549 + Missense_Mutation SNP T T C TCGA-L5-A8NS-01A-12D-A37C-09 TCGA-L5-A8NS-11A-11D-A37F-09 g.chr13:23904549T>C c.13466A>G c.(13465-13467)gAc>gGc p.D4489G ESCA 13 23905608 23905608 + Missense_Mutation SNP A A C TCGA-JY-A6FH-01A-11D-A33E-09 TCGA-JY-A6FH-10A-01D-A33H-09 g.chr13:23905608A>C c.12407T>G c.(12406-12408)cTt>cGt p.L4136R ESCA 13 23905799 23905799 + Silent SNP A A C TCGA-L5-A4OG-01A-11D-A27G-09 TCGA-L5-A4OG-11A-12D-A27G-09 g.chr13:23905799A>C c.12216T>G c.(12214-12216)acT>acG p.T4072T ESCA 13 23906661 23906661 + Missense_Mutation SNP C C T TCGA-JY-A93F-01A-21D-A37C-09 TCGA-JY-A93F-10A-01D-A37F-09 g.chr13:23906661C>T c.11354G>A c.(11353-11355)aGg>aAg p.R3785K ESCA 13 23906779 23906779 + Missense_Mutation SNP C C G TCGA-L5-A43I-01A-11D-A247-09 TCGA-L5-A43I-11A-11D-A247-09 g.chr13:23906779C>G c.11236G>C c.(11236-11238)Gat>Cat p.D3746H ESCA 13 23908710 23908710 + Nonsense_Mutation SNP A A T TCGA-ZR-A9CJ-01B-11D-A387-09 TCGA-ZR-A9CJ-10A-01D-A38A-09 g.chr13:23908710A>T c.9305T>A c.(9304-9306)tTa>tAa p.L3102* ESCA 13 23909409 23909409 + Missense_Mutation SNP C C G TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr13:23909409C>G c.8606G>C c.(8605-8607)tGt>tCt p.C2869S ESCA 13 23910851 23910851 + Silent SNP G G T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr13:23910851G>T c.7164C>A c.(7162-7164)acC>acA p.T2388T ESCA 13 23910865 23910865 + Missense_Mutation SNP C C T TCGA-S8-A6BV-01A-21D-A31U-09 TCGA-S8-A6BV-10A-01D-A31U-09 g.chr13:23910865C>T c.7150G>A c.(7150-7152)Gaa>Aaa p.E2384K ESCA 13 23911144 23911144 + Missense_Mutation SNP C C A TCGA-L5-A4OP-01A-11D-A27G-09 TCGA-L5-A4OP-11A-11D-A27G-09 g.chr13:23911144C>A c.6871G>T c.(6871-6873)Gat>Tat p.D2291Y ESCA 13 23911207 23911207 + Missense_Mutation SNP C C T TCGA-VR-A8EU-01A-11D-A36J-09 TCGA-VR-A8EU-10A-01D-A36M-09 g.chr13:23911207C>T c.6808G>A c.(6808-6810)Ggt>Agt p.G2270S ESCA 13 23911518 23911518 + Missense_Mutation SNP C C T TCGA-LN-A7HY-01A-12D-A351-09 TCGA-LN-A7HY-10A-01D-A351-09 g.chr13:23911518C>T c.6497G>A c.(6496-6498)cGt>cAt p.R2166H ESCA 13 23912160 23912160 + Missense_Mutation SNP A A C TCGA-2H-A9GI-01A-11D-A37C-09 TCGA-2H-A9GI-11A-11D-A37F-09 g.chr13:23912160A>C c.5855T>G c.(5854-5856)gTt>gGt p.V1952G ESCA 13 23912397 23912397 + Missense_Mutation SNP T T C TCGA-LN-A49R-01A-11D-A247-09 TCGA-LN-A49R-10A-01D-A247-09 g.chr13:23912397T>C c.5618A>G c.(5617-5619)tAt>tGt p.Y1873C ESCA 13 23912853 23912853 + Missense_Mutation SNP G G T TCGA-IG-A6QS-01A-12D-A33E-09 TCGA-IG-A6QS-10B-01D-A33H-09 g.chr13:23912853G>T c.5162C>A c.(5161-5163)tCc>tAc p.S1721Y ESCA 13 23913508 23913508 + Missense_Mutation SNP T T C TCGA-LN-A49M-01A-21D-A27G-09 TCGA-LN-A49M-10A-01D-A27G-09 g.chr13:23913508T>C c.4507A>G c.(4507-4509)Atg>Gtg p.M1503V ESCA 13 23914586 23914586 + Missense_Mutation SNP T T A TCGA-LN-A4MR-01A-11D-A28B-09 TCGA-LN-A4MR-10A-01D-A28E-09 g.chr13:23914586T>A c.3429A>T c.(3427-3429)caA>caT p.Q1143H ESCA 13 23915230 23915230 + Missense_Mutation SNP G G A TCGA-VR-A8Q7-01A-11D-A37C-09 TCGA-VR-A8Q7-10A-01D-A37F-09 g.chr13:23915230G>A c.2785C>T c.(2785-2787)Cgc>Tgc p.R929C ESCA 13 23915309 23915309 + Silent SNP G G C TCGA-Z6-A9VB-01A-21D-A37C-09 TCGA-Z6-A9VB-10A-01D-A37F-09 g.chr13:23915309G>C c.2706C>G c.(2704-2706)gcC>gcG p.A902A ESCA 13 23915370 23915370 + Missense_Mutation SNP T T G TCGA-L5-A8NW-01A-11D-A37C-09 TCGA-L5-A8NW-11A-11D-A37F-09 g.chr13:23915370T>G c.2645A>C c.(2644-2646)aAg>aCg p.K882T GBM 13 23908157 23908157 + Missense_Mutation SNP A A C TCGA-06-6390-01A-11D-1696-08 TCGA-06-6390-10A-01D-1696-08 g.chr13:23908157A>C c.9858T>G c.(9856-9858)ttT>ttG p.F3286L GBM 13 23908788 23908788 + Missense_Mutation SNP G G T TCGA-27-1833-01A-01W-0643-08 TCGA-27-1833-10A-01W-0644-08 g.chr13:23908788G>T c.9227C>A c.(9226-9228)aCt>aAt p.T3076N GBM 13 23911703 23911703 + Silent SNP C C T TCGA-28-5216-01A-01D-1486-08 TCGA-28-5216-10A-01D-1486-08 g.chr13:23911703C>T c.6312G>A c.(6310-6312)ggG>ggA p.G2104G GBM 13 23912431 23912431 + Missense_Mutation SNP T T C TCGA-06-0128-01A-01D-1490-08 TCGA-06-0128-10A-01D-1490-08 g.chr13:23912431T>C c.5584A>G c.(5584-5586)Aca>Gca p.T1862A GBM 13 23913301 23913301 + Missense_Mutation SNP T T C TCGA-76-6286-01A-11D-1845-08 TCGA-76-6286-10A-01D-1845-08 g.chr13:23913301T>C c.4714A>G c.(4714-4716)Att>Gtt p.I1572V GBM 13 23928995 23928995 + Missense_Mutation SNP A A G TCGA-06-0141-01A-01D-1490-08 TCGA-06-0141-10A-01D-1490-08 g.chr13:23928995A>G c.1756T>C c.(1756-1758)Tac>Cac p.Y586H GBM 13 23942617 23942617 + Missense_Mutation SNP C C A TCGA-28-5213-01A-01D-1486-08 TCGA-28-5213-10A-01D-1486-08 g.chr13:23942617C>A c.269G>T c.(268-270)gGt>gTt p.G90V GBMLGG 13 23905037 23905037 + Missense_Mutation SNP T T G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23905037T>G c.12978A>C c.(12976-12978)aaA>aaC p.K4326N GBMLGG 13 23905914 23905914 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23905914G>T c.12101C>A c.(12100-12102)gCc>gAc p.A4034D GBMLGG 13 23906959 23906959 + Nonsense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23906959G>A c.11056C>T c.(11056-11058)Cag>Tag p.Q3686* GBMLGG 13 23907741 23907741 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23907741T>C c.10274A>G c.(10273-10275)aAa>aGa p.K3425R GBMLGG 13 23907744 23907744 + Missense_Mutation SNP C C T TCGA-DU-7006-01A-11D-2024-08 TCGA-DU-7006-10A-01D-2024-08 g.chr13:23907744C>T c.10271G>A c.(10270-10272)gGa>gAa p.G3424E GBMLGG 13 23908157 23908157 + Missense_Mutation SNP A A C TCGA-06-6390-01A-11D-1696-08 TCGA-06-6390-10A-01D-1696-08 g.chr13:23908157A>C c.9858T>G c.(9856-9858)ttT>ttG p.F3286L GBMLGG 13 23908606 23908606 + Missense_Mutation SNP C C T TCGA-HT-7691-01A-11D-2253-08 TCGA-HT-7691-10A-01D-2253-08 g.chr13:23908606C>T c.9409G>A c.(9409-9411)Gat>Aat p.D3137N GBMLGG 13 23908788 23908788 + Missense_Mutation SNP G G T TCGA-27-1833-01A-01W-0643-08 TCGA-27-1833-10A-01W-0644-08 g.chr13:23908788G>T c.9227C>A c.(9226-9228)aCt>aAt p.T3076N GBMLGG 13 23909491 23909491 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23909491T>C c.8524A>G c.(8524-8526)Aac>Gac p.N2842D GBMLGG 13 23909715 23909715 + Missense_Mutation SNP C C T TCGA-VW-A7QS-01A-12D-A33T-08 TCGA-VW-A7QS-10A-02D-A33W-08 g.chr13:23909715C>T c.8300G>A c.(8299-8301)gGc>gAc p.G2767D GBMLGG 13 23911012 23911012 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23911012T>C c.7003A>G c.(7003-7005)Atg>Gtg p.M2335V GBMLGG 13 23911318 23911318 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23911318T>C c.6697A>G c.(6697-6699)Agt>Ggt p.S2233G GBMLGG 13 23911703 23911703 + Silent SNP C C T TCGA-28-5216-01A-01D-1486-08 TCGA-28-5216-10A-01D-1486-08 g.chr13:23911703C>T c.6312G>A c.(6310-6312)ggG>ggA p.G2104G GBMLGG 13 23912410 23912410 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23912410C>A c.5605G>T c.(5605-5607)Gag>Tag p.E1869* GBMLGG 13 23912431 23912431 + Missense_Mutation SNP T T C TCGA-06-0128-01A-01D-1490-08 TCGA-06-0128-10A-01D-1490-08 g.chr13:23912431T>C c.5584A>G c.(5584-5586)Aca>Gca p.T1862A GBMLGG 13 23912848 23912848 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23912848C>T c.5167G>A c.(5167-5169)Gca>Aca p.A1723T GBMLGG 13 23913301 23913301 + Missense_Mutation SNP T T C TCGA-76-6286-01A-11D-1845-08 TCGA-76-6286-10A-01D-1845-08 g.chr13:23913301T>C c.4714A>G c.(4714-4716)Att>Gtt p.I1572V GBMLGG 13 23914982 23914982 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23914982C>T c.3033G>A c.(3031-3033)caG>caA p.Q1011Q GBMLGG 13 23915088 23915088 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23915088C>T c.2927G>A c.(2926-2928)cGt>cAt p.R976H GBMLGG 13 23928995 23928995 + Missense_Mutation SNP A A G TCGA-06-0141-01A-01D-1490-08 TCGA-06-0141-10A-01D-1490-08 g.chr13:23928995A>G c.1756T>C c.(1756-1758)Tac>Cac p.Y586H GBMLGG 13 23929924 23929924 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23929924C>T c.827G>A c.(826-828)cGc>cAc p.R276H GBMLGG 13 23942617 23942617 + Missense_Mutation SNP C C A TCGA-28-5213-01A-01D-1486-08 TCGA-28-5213-10A-01D-1486-08 g.chr13:23942617C>A c.269G>T c.(268-270)gGt>gTt p.G90V HNSC 13 23904625 23904625 + Missense_Mutation SNP C C T TCGA-T2-A6WX-01A-12D-A34J-08 TCGA-T2-A6WX-10B-01D-A34M-08 g.chr13:23904625C>T c.13390G>A c.(13390-13392)Gac>Aac p.D4464N HNSC 13 23905170 23905170 + Missense_Mutation SNP C C G TCGA-CQ-5332-01A-01D-1683-08 TCGA-CQ-5332-10A-01D-1683-08 g.chr13:23905170C>G c.12845G>C c.(12844-12846)gGt>gCt p.G4282A HNSC 13 23905610 23905610 + Missense_Mutation SNP T T A TCGA-IQ-A6SH-01A-12D-A34J-08 TCGA-IQ-A6SH-10A-01D-A34M-08 g.chr13:23905610T>A c.12405A>T c.(12403-12405)aaA>aaT p.K4135N HNSC 13 23905802 23905802 + Silent SNP T T C TCGA-CN-6997-01A-11D-2012-08 TCGA-CN-6997-10A-01D-2013-08 g.chr13:23905802T>C c.12213A>G c.(12211-12213)gaA>gaG p.E4071E HNSC 13 23905822 23905822 + Missense_Mutation SNP T T A TCGA-CQ-7072-01A-21D-A30E-08 TCGA-CQ-7072-10A-01D-A30H-08 g.chr13:23905822T>A c.12193A>T c.(12193-12195)Att>Ttt p.I4065F HNSC 13 23906082 23906082 + Missense_Mutation SNP A A C TCGA-CR-6493-01A-11D-1870-08 TCGA-CR-6493-10A-01D-1870-08 g.chr13:23906082A>C c.11933T>G c.(11932-11934)cTt>cGt p.L3978R HNSC 13 23906234 23906234 + Silent SNP C C T TCGA-WA-A7GZ-01A-11D-A34J-08 TCGA-WA-A7GZ-10A-01D-A34M-08 g.chr13:23906234C>T c.11781G>A c.(11779-11781)gcG>gcA p.A3927A HNSC 13 23906424 23906424 + Missense_Mutation SNP G G C TCGA-BB-4223-01A-01D-1434-08 TCGA-BB-4223-10A-01D-1434-08 g.chr13:23906424G>C c.11591C>G c.(11590-11592)tCt>tGt p.S3864C HNSC 13 23906534 23906534 + Silent SNP C C T TCGA-CN-6018-01A-11D-1683-08 TCGA-CN-6018-10A-01D-1683-08 g.chr13:23906534C>T c.11481G>A c.(11479-11481)aaG>aaA p.K3827K HNSC 13 23907553 23907553 + Missense_Mutation SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr13:23907553G>A c.10462C>T c.(10462-10464)Ctc>Ttc p.L3488F HNSC 13 23908832 23908832 + Silent SNP G G C TCGA-CQ-7063-01A-11D-2394-08 TCGA-CQ-7063-10A-01D-2394-08 g.chr13:23908832G>C c.9183C>G c.(9181-9183)ctC>ctG p.L3061L HNSC 13 23909221 23909221 + Missense_Mutation SNP G G A TCGA-QK-A6IJ-01A-11D-A31L-08 TCGA-QK-A6IJ-10A-01D-A31J-08 g.chr13:23909221G>A c.8794C>T c.(8794-8796)Cgg>Tgg p.R2932W HNSC 13 23909308 23909308 + Missense_Mutation SNP C C A TCGA-CN-6992-01A-11D-1912-08 TCGA-CN-6992-10A-01D-1912-08 g.chr13:23909308C>A c.8707G>T c.(8707-8709)Gtt>Ttt p.V2903F HNSC 13 23909724 23909724 + Missense_Mutation SNP G G A TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr13:23909724G>A c.8291C>T c.(8290-8292)tCa>tTa p.S2764L HNSC 13 23910945 23910945 + Missense_Mutation SNP T T A TCGA-CV-6933-01A-11D-1912-08 TCGA-CV-6933-10A-01D-1912-08 g.chr13:23910945T>A c.7070A>T c.(7069-7071)gAa>gTa p.E2357V HNSC 13 23911360 23911360 + Missense_Mutation SNP G G C TCGA-CV-A463-01A-11D-A25Y-08 TCGA-CV-A463-10A-01D-A25Y-08 g.chr13:23911360G>C c.6655C>G c.(6655-6657)Ctg>Gtg p.L2219V HNSC 13 23911462 23911462 + Missense_Mutation SNP T T C TCGA-P3-A6T5-01A-11D-A34J-08 TCGA-P3-A6T5-10A-01D-A34M-08 g.chr13:23911462T>C c.6553A>G c.(6553-6555)Agt>Ggt p.S2185G HNSC 13 23912107 23912107 + Nonsense_Mutation SNP C C A TCGA-F7-A50J-01A-21D-A28R-08 TCGA-F7-A50J-10A-01D-A28U-08 g.chr13:23912107C>A c.5908G>T c.(5908-5910)Gga>Tga p.G1970* HNSC 13 23912713 23912713 + Missense_Mutation SNP G G C TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr13:23912713G>C c.5302C>G c.(5302-5304)Cac>Gac p.H1768D HNSC 13 23913048 23913048 + Missense_Mutation SNP A A C TCGA-CV-7095-01A-21D-2012-08 TCGA-CV-7095-10A-01D-2013-08 g.chr13:23913048A>C c.4967T>G c.(4966-4968)gTg>gGg p.V1656G HNSC 13 23913425 23913425 + Silent SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr13:23913425G>A c.4590C>T c.(4588-4590)ttC>ttT p.F1530F HNSC 13 23913992 23913992 + Silent SNP G G C TCGA-CR-6484-01A-11D-1870-08 TCGA-CR-6484-10A-01D-1870-08 g.chr13:23913992G>C c.4023C>G c.(4021-4023)ctC>ctG p.L1341L HNSC 13 23914846 23914846 + Missense_Mutation SNP C C G TCGA-IQ-7632-01A-11D-2078-08 TCGA-IQ-7632-10A-01D-2078-08 g.chr13:23914846C>G c.3169G>C c.(3169-3171)Gat>Cat p.D1057H HNSC 13 23915282 23915282 + Silent SNP G G A TCGA-D6-A6ES-01A-12D-A31L-08 TCGA-D6-A6ES-10A-01D-A31J-08 g.chr13:23915282G>A c.2733C>T c.(2731-2733)acC>acT p.T911T HNSC 13 23915744 23915744 + Silent SNP G G C TCGA-CQ-5332-01A-01D-1683-08 TCGA-CQ-5332-10A-01D-1683-08 g.chr13:23915744G>C c.2271C>G c.(2269-2271)ggC>ggG p.G757G HNSC 13 23929020 23929020 + Silent SNP G G A TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chr13:23929020G>A c.1731C>T c.(1729-1731)ttC>ttT p.F577F HNSC 13 23929166 23929166 + Missense_Mutation SNP C C T TCGA-CV-A6JN-01A-11D-A31L-08 TCGA-CV-A6JN-10A-01D-A31J-08 g.chr13:23929166C>T c.1585G>A c.(1585-1587)Gat>Aat p.D529N HNSC 13 23930133 23930133 + Silent SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr13:23930133G>A c.618C>T c.(616-618)atC>atT p.I206I HNSC 13 23932595 23932595 + Silent SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr13:23932595G>A c.483C>T c.(481-483)aaC>aaT p.N161N HNSC 13 23939316 23939316 + Missense_Mutation SNP G G A TCGA-BA-A6DB-01A-11D-A30E-08 TCGA-BA-A6DB-10A-01D-A30H-08 g.chr13:23939316G>A c.446C>T c.(445-447)gCg>gTg p.A149V HNSC 13 23942586 23942586 + Silent SNP G G C TCGA-BA-7269-01A-11D-2012-08 TCGA-BA-7269-10A-01D-2013-08 g.chr13:23942586G>C c.300C>G c.(298-300)ctC>ctG p.L100L HNSC 13 23945292 23945292 + Missense_Mutation SNP T T A TCGA-CX-7086-01A-11D-2078-08 TCGA-CX-7086-10D-01D-2078-08 g.chr13:23945292T>A c.184A>T c.(184-186)Atc>Ttc p.I62F KICH 13 23915268 23915268 + Missense_Mutation SNP T T G TCGA-KM-8443-01A-11D-2310-10 TCGA-KM-8443-10A-01D-2311-10 g.chr13:23915268T>G c.2747A>C c.(2746-2748)aAa>aCa p.K916T KIPAN 13 23904812 23904812 + Missense_Mutation SNP C C A TCGA-CJ-5686-01A-11D-1669-08 TCGA-CJ-5686-11A-01D-1669-08 g.chr13:23904812C>A c.13203G>T c.(13201-13203)tgG>tgT p.W4401C KIPAN 13 23906370 23906371 + Frame_Shift_Ins INS - - A TCGA-HE-A5NI-01A-11D-A26P-10 TCGA-HE-A5NI-10A-01D-A26P-10 g.chr13:23906370_23906371insA c.11644_11645insT c.(11644-11646)tctfs p.S3882fs KIPAN 13 23906942 23906942 + Silent SNP G G A TCGA-DV-5566-01A-01D-1534-10 TCGA-DV-5566-10A-01D-1535-10 g.chr13:23906942G>A c.11073C>T c.(11071-11073)ttC>ttT p.F3691F KIPAN 13 23906994 23906994 + Missense_Mutation SNP T T C TCGA-BQ-7053-01A-11D-1961-08 TCGA-BQ-7053-11A-01D-1961-08 g.chr13:23906994T>C c.11021A>G c.(11020-11022)aAt>aGt p.N3674S KIPAN 13 23907922 23907922 + Missense_Mutation SNP G G C TCGA-B0-5709-01A-11D-1534-10 TCGA-B0-5709-11A-01D-1534-10 g.chr13:23907922G>C c.10093C>G c.(10093-10095)Cta>Gta p.L3365V KIPAN 13 23909168 23909168 + Silent SNP A A G TCGA-P4-AAVL-01A-11D-A42J-10 TCGA-P4-AAVL-11A-11D-A42M-10 g.chr13:23909168A>G c.8847T>C c.(8845-8847)atT>atC p.I2949I KIPAN 13 23909182 23909182 + Missense_Mutation SNP G G T TCGA-BP-5168-01A-01D-1421-08 TCGA-BP-5168-11A-01D-1421-08 g.chr13:23909182G>T c.8833C>A c.(8833-8835)Cag>Aag p.Q2945K KIPAN 13 23909472 23909472 + Missense_Mutation SNP A A T TCGA-EV-5901-01A-11D-1589-08 TCGA-EV-5901-10A-01D-1589-08 g.chr13:23909472A>T c.8543T>A c.(8542-8544)tTc>tAc p.F2848Y KIPAN 13 23914058 23914059 + Missense_Mutation DNP CT CT GG TCGA-B8-4620-01A-02D-1386-10 TCGA-B8-4620-10A-01D-1251-10 g.chr13:23914058_23914059CT>GG c.3956_3957AG>CC c.(3955-3957)aAG>aCC p.K1319T KIPAN 13 23915268 23915268 + Missense_Mutation SNP T T G TCGA-KM-8443-01A-11D-2310-10 TCGA-KM-8443-10A-01D-2311-10 g.chr13:23915268T>G c.2747A>C c.(2746-2748)aAa>aCa p.K916T KIPAN 13 23915483 23915483 + Silent SNP T T G TCGA-B8-5549-01A-01D-1534-10 TCGA-B8-5549-10A-01D-1535-10 g.chr13:23915483T>G c.2532A>C c.(2530-2532)gtA>gtC p.V844V KIPAN 13 23929405 23929405 + Missense_Mutation SNP G G C TCGA-5P-A9KE-01A-11D-A42J-10 TCGA-5P-A9KE-10A-01D-A42M-10 g.chr13:23929405G>C c.1346C>G c.(1345-1347)cCt>cGt p.P449R KIRC 13 23904812 23904812 + Missense_Mutation SNP C C A TCGA-CJ-5686-01A-11D-1669-08 TCGA-CJ-5686-11A-01D-1669-08 g.chr13:23904812C>A c.13203G>T c.(13201-13203)tgG>tgT p.W4401C KIRC 13 23906942 23906942 + Silent SNP G G A TCGA-DV-5566-01A-01D-1534-10 TCGA-DV-5566-10A-01D-1535-10 g.chr13:23906942G>A c.11073C>T c.(11071-11073)ttC>ttT p.F3691F KIRC 13 23907922 23907922 + Missense_Mutation SNP G G C TCGA-B0-5709-01A-11D-1534-10 TCGA-B0-5709-11A-01D-1534-10 g.chr13:23907922G>C c.10093C>G c.(10093-10095)Cta>Gta p.L3365V KIRC 13 23909182 23909182 + Missense_Mutation SNP G G T TCGA-BP-5168-01A-01D-1421-08 TCGA-BP-5168-11A-01D-1421-08 g.chr13:23909182G>T c.8833C>A c.(8833-8835)Cag>Aag p.Q2945K KIRC 13 23914058 23914059 + Missense_Mutation DNP CT CT GG TCGA-B8-4620-01A-02D-1386-10 TCGA-B8-4620-10A-01D-1251-10 g.chr13:23914058_23914059CT>GG c.3956_3957AG>CC c.(3955-3957)aAG>aCC p.K1319T KIRC 13 23915483 23915483 + Silent SNP T T G TCGA-B8-5549-01A-01D-1534-10 TCGA-B8-5549-10A-01D-1535-10 g.chr13:23915483T>G c.2532A>C c.(2530-2532)gtA>gtC p.V844V KIRP 13 23906370 23906371 + Frame_Shift_Ins INS - - A TCGA-HE-A5NI-01A-11D-A26P-10 TCGA-HE-A5NI-10A-01D-A26P-10 g.chr13:23906370_23906371insA c.11644_11645insT c.(11644-11646)tctfs p.S3882fs KIRP 13 23906994 23906994 + Missense_Mutation SNP T T C TCGA-BQ-7053-01A-11D-1961-08 TCGA-BQ-7053-11A-01D-1961-08 g.chr13:23906994T>C c.11021A>G c.(11020-11022)aAt>aGt p.N3674S KIRP 13 23909168 23909168 + Silent SNP A A G TCGA-P4-AAVL-01A-11D-A42J-10 TCGA-P4-AAVL-11A-11D-A42M-10 g.chr13:23909168A>G c.8847T>C c.(8845-8847)atT>atC p.I2949I KIRP 13 23909472 23909472 + Missense_Mutation SNP A A T TCGA-EV-5901-01A-11D-1589-08 TCGA-EV-5901-10A-01D-1589-08 g.chr13:23909472A>T c.8543T>A c.(8542-8544)tTc>tAc p.F2848Y KIRP 13 23929405 23929405 + Missense_Mutation SNP G G C TCGA-5P-A9KE-01A-11D-A42J-10 TCGA-5P-A9KE-10A-01D-A42M-10 g.chr13:23929405G>C c.1346C>G c.(1345-1347)cCt>cGt p.P449R LAML 13 23928871 23928871 + Missense_Mutation SNP G G A TCGA-AB-2877-03A-01W-0732-08 TCGA-AB-2877-11A-01W-0732-08 g.chr13:23928871G>A c.1880C>T c.(1879-1881)aCg>aTg p.T627M LGG 13 23905037 23905037 + Missense_Mutation SNP T T G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23905037T>G c.12978A>C c.(12976-12978)aaA>aaC p.K4326N LGG 13 23905914 23905914 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23905914G>T c.12101C>A c.(12100-12102)gCc>gAc p.A4034D LGG 13 23906959 23906959 + Nonsense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23906959G>A c.11056C>T c.(11056-11058)Cag>Tag p.Q3686* LGG 13 23907741 23907741 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23907741T>C c.10274A>G c.(10273-10275)aAa>aGa p.K3425R LGG 13 23907744 23907744 + Missense_Mutation SNP C C T TCGA-DU-7006-01A-11D-2024-08 TCGA-DU-7006-10A-01D-2024-08 g.chr13:23907744C>T c.10271G>A c.(10270-10272)gGa>gAa p.G3424E LGG 13 23908606 23908606 + Missense_Mutation SNP C C T TCGA-HT-7691-01A-11D-2253-08 TCGA-HT-7691-10A-01D-2253-08 g.chr13:23908606C>T c.9409G>A c.(9409-9411)Gat>Aat p.D3137N LGG 13 23909491 23909491 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23909491T>C c.8524A>G c.(8524-8526)Aac>Gac p.N2842D LGG 13 23909715 23909715 + Missense_Mutation SNP C C T TCGA-VW-A7QS-01A-12D-A33T-08 TCGA-VW-A7QS-10A-02D-A33W-08 g.chr13:23909715C>T c.8300G>A c.(8299-8301)gGc>gAc p.G2767D LGG 13 23911012 23911012 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23911012T>C c.7003A>G c.(7003-7005)Atg>Gtg p.M2335V LGG 13 23911318 23911318 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23911318T>C c.6697A>G c.(6697-6699)Agt>Ggt p.S2233G LGG 13 23912410 23912410 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23912410C>A c.5605G>T c.(5605-5607)Gag>Tag p.E1869* LGG 13 23912848 23912848 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23912848C>T c.5167G>A c.(5167-5169)Gca>Aca p.A1723T LGG 13 23914982 23914982 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23914982C>T c.3033G>A c.(3031-3033)caG>caA p.Q1011Q LGG 13 23915088 23915088 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23915088C>T c.2927G>A c.(2926-2928)cGt>cAt p.R976H LGG 13 23929924 23929924 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:23929924C>T c.827G>A c.(826-828)cGc>cAc p.R276H LIHC 13 23904756 23904756 + Missense_Mutation SNP C C A TCGA-DD-A114-01A-11D-A12Z-10 TCGA-DD-A114-10A-01D-A12Z-10 g.chr13:23904756C>A c.13259G>T c.(13258-13260)tGc>tTc p.C4420F LIHC 13 23905027 23905027 + Missense_Mutation SNP T T C TCGA-BC-A10U-01A-11D-A12Z-10 TCGA-BC-A10U-11A-11D-A12Z-10 g.chr13:23905027T>C c.12988A>G c.(12988-12990)Agg>Ggg p.R4330G LIHC 13 23905055 23905055 + Silent SNP A A G TCGA-MI-A75G-01A-11D-A32G-10 TCGA-MI-A75G-10A-01D-A32G-10 g.chr13:23905055A>G c.12960T>C c.(12958-12960)ctT>ctC p.L4320L LIHC 13 23905368 23905368 + Missense_Mutation SNP T T C TCGA-MI-A75G-01A-11D-A32G-10 TCGA-MI-A75G-10A-01D-A32G-10 g.chr13:23905368T>C c.12647A>G c.(12646-12648)gAc>gGc p.D4216G LIHC 13 23906630 23906630 + Silent SNP A A G TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr13:23906630A>G c.11385T>C c.(11383-11385)gcT>gcC p.A3795A LIHC 13 23907171 23907171 + Missense_Mutation SNP T T G TCGA-G3-AAUZ-01A-11D-A382-10 TCGA-G3-AAUZ-10A-01D-A385-10 g.chr13:23907171T>G c.10844A>C c.(10843-10845)aAc>aCc p.N3615T LIHC 13 23907453 23907453 + Missense_Mutation SNP A A G TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr13:23907453A>G c.10562T>C c.(10561-10563)cTg>cCg p.L3521P LIHC 13 23907796 23907796 + Silent SNP G G A TCGA-DD-A4NF-01A-11D-A27I-10 TCGA-DD-A4NF-10A-01D-A27I-10 g.chr13:23907796G>A c.10219C>T c.(10219-10221)Cta>Tta p.L3407L LIHC 13 23908202 23908202 + Silent SNP A A G TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr13:23908202A>G c.9813T>C c.(9811-9813)gtT>gtC p.V3271V LIHC 13 23909572 23909572 + Missense_Mutation SNP G G T TCGA-DD-AADF-01A-11D-A40R-10 TCGA-DD-AADF-10A-01D-A40U-10 g.chr13:23909572G>T c.8443C>A c.(8443-8445)Ctt>Att p.L2815I LIHC 13 23909599 23909599 + Missense_Mutation SNP T T C TCGA-DD-AACU-01A-11D-A40R-10 TCGA-DD-AACU-10A-01D-A40U-10 g.chr13:23909599T>C c.8416A>G c.(8416-8418)Atg>Gtg p.M2806V LIHC 13 23909684 23909684 + Missense_Mutation SNP C C A TCGA-DD-AAE7-01A-11D-A40R-10 TCGA-DD-AAE7-10A-01D-A40U-10 g.chr13:23909684C>A c.8331G>T c.(8329-8331)agG>agT p.R2777S LIHC 13 23909856 23909856 + Missense_Mutation SNP T T C TCGA-CC-A3MA-01A-11D-A20W-10 TCGA-CC-A3MA-10A-01D-A20W-10 g.chr13:23909856T>C c.8159A>G c.(8158-8160)gAc>gGc p.D2720G LIHC 13 23910455 23910455 + Silent SNP T T G TCGA-G3-A7M5-01A-11D-A33Q-10 TCGA-G3-A7M5-10A-01D-A33Q-10 g.chr13:23910455T>G c.7560A>C c.(7558-7560)acA>acC p.T2520T LIHC 13 23910913 23910913 + Missense_Mutation SNP C C A TCGA-2Y-A9H4-01A-11D-A382-10 TCGA-2Y-A9H4-10A-01D-A385-10 g.chr13:23910913C>A c.7102G>T c.(7102-7104)Gca>Tca p.A2368S LIHC 13 23910918 23910918 + Missense_Mutation SNP T T C TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chr13:23910918T>C c.7097A>G c.(7096-7098)gAg>gGg p.E2366G LIHC 13 23911630 23911630 + Missense_Mutation SNP C C T TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr13:23911630C>T c.6385G>A c.(6385-6387)Ggg>Agg p.G2129R LIHC 13 23911712 23911712 + Silent SNP G G T TCGA-MI-A75E-01A-11D-A32G-10 TCGA-MI-A75E-10A-01D-A32G-10 g.chr13:23911712G>T c.6303C>A c.(6301-6303)tcC>tcA p.S2101S LIHC 13 23912521 23912521 + Missense_Mutation SNP A A T TCGA-DD-A4ND-01A-11D-A25V-10 TCGA-DD-A4ND-11A-11D-A25V-10 g.chr13:23912521A>T c.5494T>A c.(5494-5496)Ttt>Att p.F1832I LIHC 13 23915617 23915617 + Missense_Mutation SNP T T C TCGA-CC-A3MB-01A-11D-A20W-10 TCGA-CC-A3MB-10A-01D-A20W-10 g.chr13:23915617T>C c.2398A>G c.(2398-2400)Atg>Gtg p.M800V LIHC 13 23929049 23929049 + Missense_Mutation SNP C C A TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr13:23929049C>A c.1702G>T c.(1702-1704)Gac>Tac p.D568Y LIHC 13 23929324 23929324 + Missense_Mutation SNP C C T TCGA-DD-AACT-01A-11D-A40R-10 TCGA-DD-AACT-10A-01D-A40U-10 g.chr13:23929324C>T c.1427G>A c.(1426-1428)aGc>aAc p.S476N LUAD 13 23904603 23904603 + Missense_Mutation SNP T T A TCGA-53-7626-01A-12D-2063-08 TCGA-53-7626-10A-01D-2063-08 g.chr13:23904603T>A c.13412A>T c.(13411-13413)gAg>gTg p.E4471V LUAD 13 23904722 23904722 + Silent SNP C C T TCGA-49-4514-01A-21D-1855-08 TCGA-49-4514-11A-01D-1855-08 g.chr13:23904722C>T c.13293G>A c.(13291-13293)agG>agA p.R4431R LUAD 13 23905025 23905025 + Missense_Mutation SNP C C A TCGA-95-A4VP-01A-21D-A25L-08 TCGA-95-A4VP-10A-01D-A25L-08 g.chr13:23905025C>A c.12990G>T c.(12988-12990)agG>agT p.R4330S LUAD 13 23905303 23905303 + Missense_Mutation SNP T T A TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr13:23905303T>A c.12712A>T c.(12712-12714)Agc>Tgc p.S4238C LUAD 13 23905531 23905531 + Missense_Mutation SNP C C A TCGA-MN-A4N1-01A-11D-A24P-08 TCGA-MN-A4N1-10A-01D-A24P-08 g.chr13:23905531C>A c.12484G>T c.(12484-12486)Gct>Tct p.A4162S LUAD 13 23905743 23905743 + Nonsense_Mutation SNP G G C TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr13:23905743G>C c.12272C>G c.(12271-12273)tCa>tGa p.S4091* LUAD 13 23906171 23906171 + Missense_Mutation SNP C C G TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr13:23906171C>G c.11844G>C c.(11842-11844)caG>caC p.Q3948H LUAD 13 23906719 23906719 + Missense_Mutation SNP C C A TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chr13:23906719C>A c.11296G>T c.(11296-11298)Gta>Tta p.V3766L LUAD 13 23906879 23906879 + Silent SNP T T A TCGA-86-8674-01A-21D-2393-08 TCGA-86-8674-10A-01D-2393-08 g.chr13:23906879T>A c.11136A>T c.(11134-11136)acA>acT p.T3712T LUAD 13 23907231 23907231 + Missense_Mutation SNP A A C TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr13:23907231A>C c.10784T>G c.(10783-10785)cTt>cGt p.L3595R LUAD 13 23907731 23907731 + Silent SNP T T A TCGA-73-4666-01A-01D-1265-08 TCGA-73-4666-11A-01D-1265-08 g.chr13:23907731T>A c.10284A>T c.(10282-10284)acA>acT p.T3428T LUAD 13 23907941 23907941 + Silent SNP G G A TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr13:23907941G>A c.10074C>T c.(10072-10074)ccC>ccT p.P3358P LUAD 13 23908500 23908500 + Missense_Mutation SNP T T C TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr13:23908500T>C c.9515A>G c.(9514-9516)aAg>aGg p.K3172R LUAD 13 23908556 23908556 + Missense_Mutation SNP C C A TCGA-86-8359-01A-11D-2323-08 TCGA-86-8359-10A-01D-2323-08 g.chr13:23908556C>A c.9459G>T c.(9457-9459)ttG>ttT p.L3153F LUAD 13 23909100 23909100 + Missense_Mutation SNP G G T TCGA-44-7672-01A-11D-2063-08 TCGA-44-7672-10A-01D-2063-08 g.chr13:23909100G>T c.8915C>A c.(8914-8916)cCa>cAa p.P2972Q LUAD 13 23909311 23909311 + Nonsense_Mutation SNP C C A TCGA-69-7973-01A-11D-2184-08 TCGA-69-7973-10A-01D-2184-08 g.chr13:23909311C>A c.8704G>T c.(8704-8706)Gga>Tga p.G2902* LUAD 13 23909353 23909353 + Missense_Mutation SNP C C T TCGA-69-7763-01A-11D-2167-08 TCGA-69-7763-10A-01D-2167-08 g.chr13:23909353C>T c.8662G>A c.(8662-8664)Gca>Aca p.A2888T LUAD 13 23909383 23909383 + Missense_Mutation SNP C C A TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr13:23909383C>A c.8632G>T c.(8632-8634)Ggg>Tgg p.G2878W LUAD 13 23910183 23910183 + Missense_Mutation SNP G G T TCGA-17-Z011-01A-01W-0746-08 TCGA-17-Z011-11A-01W-0746-08 g.chr13:23910183G>T c.7832C>A c.(7831-7833)aCg>aAg p.T2611K LUAD 13 23910525 23910525 + Missense_Mutation SNP C C A TCGA-05-5428-01A-01D-1625-08 TCGA-05-5428-10A-01D-1625-08 g.chr13:23910525C>A c.7490G>T c.(7489-7491)gGa>gTa p.G2497V LUAD 13 23910594 23910594 + Missense_Mutation SNP A A T TCGA-55-6978-01A-11D-1945-08 TCGA-55-6978-11A-01D-1945-08 g.chr13:23910594A>T c.7421T>A c.(7420-7422)aTa>aAa p.I2474K LUAD 13 23912106 23912106 + Missense_Mutation SNP C C T TCGA-55-A48X-01A-11D-A24D-08 TCGA-55-A48X-10A-01D-A24F-08 g.chr13:23912106C>T c.5909G>A c.(5908-5910)gGa>gAa p.G1970E LUAD 13 23912692 23912692 + Missense_Mutation SNP C C A TCGA-17-Z007-01A-01W-0746-08 TCGA-17-Z007-11A-01W-0746-08 g.chr13:23912692C>A c.5323G>T c.(5323-5325)Gct>Tct p.A1775S LUAD 13 23912745 23912745 + Missense_Mutation SNP G G A TCGA-78-8660-01A-11D-2393-08 TCGA-78-8660-10A-01D-2393-08 g.chr13:23912745G>A c.5270C>T c.(5269-5271)tCt>tTt p.S1757F LUAD 13 23913291 23913291 + Missense_Mutation SNP C C G TCGA-55-7910-01A-11D-2167-08 TCGA-55-7910-11A-01D-2167-08 g.chr13:23913291C>G c.4724G>C c.(4723-4725)cGg>cCg p.R1575P LUAD 13 23913317 23913317 + Silent SNP G G A TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr13:23913317G>A c.4698C>T c.(4696-4698)atC>atT p.I1566I LUAD 13 23913373 23913373 + Nonsense_Mutation SNP C C A TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chr13:23913373C>A c.4642G>T c.(4642-4644)Gga>Tga p.G1548* LUAD 13 23913458 23913458 + Silent SNP T T C TCGA-44-8119-01A-11D-2238-08 TCGA-44-8119-10A-01D-2238-08 g.chr13:23913458T>C c.4557A>G c.(4555-4557)ggA>ggG p.G1519G LUAD 13 23913577 23913577 + Nonsense_Mutation SNP C C A TCGA-78-7156-01A-11D-2036-08 TCGA-78-7156-10A-01D-2036-08 g.chr13:23913577C>A c.4438G>T c.(4438-4440)Gaa>Taa p.E1480* LUAD 13 23913627 23913627 + Missense_Mutation SNP C C A TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr13:23913627C>A c.4388G>T c.(4387-4389)aGa>aTa p.R1463I LUAD 13 23913868 23913868 + Missense_Mutation SNP G G C TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr13:23913868G>C c.4147C>G c.(4147-4149)Cat>Gat p.H1383D LUAD 13 23914212 23914212 + Missense_Mutation SNP T T A TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr13:23914212T>A c.3803A>T c.(3802-3804)gAt>gTt p.D1268V LUAD 13 23914776 23914776 + Nonsense_Mutation SNP G G T TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr13:23914776G>T c.3239C>A c.(3238-3240)tCa>tAa p.S1080* LUAD 13 23915047 23915047 + Missense_Mutation SNP T T A TCGA-17-Z015-01A-01W-0746-08 TCGA-17-Z015-11A-01W-0746-08 g.chr13:23915047T>A c.2968A>T c.(2968-2970)Agc>Tgc p.S990C LUAD 13 23915110 23915110 + Missense_Mutation SNP T T A TCGA-50-5931-01A-11D-1753-08 TCGA-50-5931-11A-01D-1753-08 g.chr13:23915110T>A c.2905A>T c.(2905-2907)Agt>Tgt p.S969C LUAD 13 23915178 23915178 + Missense_Mutation SNP C C A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr13:23915178C>A c.2837G>T c.(2836-2838)gGt>gTt p.G946V LUAD 13 23915239 23915239 + Missense_Mutation SNP T T G TCGA-69-8255-01A-11D-2284-08 TCGA-69-8255-10A-01D-2284-08 g.chr13:23915239T>G c.2776A>C c.(2776-2778)Ata>Cta p.I926L LUAD 13 23915308 23915308 + Silent SNP G G A TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr13:23915308G>A c.2707C>T c.(2707-2709)Ctg>Ttg p.L903L LUAD 13 23915638 23915638 + Missense_Mutation SNP C C A TCGA-55-8511-01A-11D-2393-08 TCGA-55-8511-10A-01D-2393-08 g.chr13:23915638C>A c.2377G>T c.(2377-2379)Gat>Tat p.D793Y LUAD 13 23915735 23915735 + Missense_Mutation SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr13:23915735C>A c.2280G>T c.(2278-2280)ttG>ttT p.L760F LUAD 13 23928789 23928789 + Silent SNP C C A TCGA-55-8511-01A-11D-2393-08 TCGA-55-8511-10A-01D-2393-08 g.chr13:23928789C>A c.1962G>T c.(1960-1962)gtG>gtT p.V654V LUAD 13 23929457 23929457 + Missense_Mutation SNP C C T TCGA-55-8097-01A-11D-2238-08 TCGA-55-8097-10A-01D-2238-08 g.chr13:23929457C>T c.1294G>A c.(1294-1296)Gaa>Aaa p.E432K LUAD 13 23929924 23929924 + Missense_Mutation SNP C C T TCGA-73-4668-01A-01D-1265-08 TCGA-73-4668-11A-01D-1265-08 g.chr13:23929924C>T c.827G>A c.(826-828)cGc>cAc p.R276H LUSC 13 23905162 23905162 + Missense_Mutation SNP T T A TCGA-63-6202-01A-11D-1817-08 TCGA-63-6202-10A-01D-1817-08 g.chr13:23905162T>A c.12853A>T c.(12853-12855)Agc>Tgc p.S4285C LUSC 13 23906110 23906110 + Missense_Mutation SNP G G A TCGA-46-3768-01A-01D-0983-08 TCGA-46-3768-10A-01D-0983-08 g.chr13:23906110G>A c.11905C>T c.(11905-11907)Ctt>Ttt p.L3969F LUSC 13 23906130 23906130 + Missense_Mutation SNP A A G TCGA-66-2791-01A-01D-0983-08 TCGA-66-2791-11A-01D-0983-08 g.chr13:23906130A>G c.11885T>C c.(11884-11886)aTa>aCa p.I3962T LUSC 13 23906282 23906282 + Missense_Mutation SNP G G T TCGA-18-4086-01A-01D-1352-08 TCGA-18-4086-11A-01D-1352-08 g.chr13:23906282G>T c.11733C>A c.(11731-11733)agC>agA p.S3911R LUSC 13 23908856 23908856 + Missense_Mutation SNP C C A TCGA-34-5236-01A-21D-1817-08 TCGA-34-5236-10A-01D-1817-08 g.chr13:23908856C>A c.9159G>T c.(9157-9159)gaG>gaT p.E3053D LUSC 13 23909099 23909099 + Silent SNP T T A TCGA-18-3421-01A-01D-0983-08 TCGA-18-3421-11A-01D-0983-08 g.chr13:23909099T>A c.8916A>T c.(8914-8916)ccA>ccT p.P2972P LUSC 13 23909195 23909195 + Silent SNP T T C TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr13:23909195T>C c.8820A>G c.(8818-8820)acA>acG p.T2940T LUSC 13 23911629 23911629 + Missense_Mutation SNP C C A TCGA-66-2767-01A-01D-1522-08 TCGA-66-2767-11A-01D-1522-08 g.chr13:23911629C>A c.6386G>T c.(6385-6387)gGg>gTg p.G2129V LUSC 13 23912025 23912025 + Missense_Mutation SNP G G C TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr13:23912025G>C c.5990C>G c.(5989-5991)tCt>tGt p.S1997C LUSC 13 23912373 23912373 + Missense_Mutation SNP C C G TCGA-22-4591-01A-01D-1267-08 TCGA-22-4591-11A-01D-1267-08 g.chr13:23912373C>G c.5642G>C c.(5641-5643)gGc>gCc p.G1881A LUSC 13 23912516 23912516 + Silent SNP G G T TCGA-37-3789-01A-01D-0983-08 TCGA-37-3789-10A-01D-0983-08 g.chr13:23912516G>T c.5499C>A c.(5497-5499)tcC>tcA p.S1833S LUSC 13 23913541 23913541 + Missense_Mutation SNP C C G TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr13:23913541C>G c.4474G>C c.(4474-4476)Gaa>Caa p.E1492Q LUSC 13 23914497 23914497 + Missense_Mutation SNP C C G TCGA-66-2755-01A-01D-1522-08 TCGA-66-2755-11A-01D-1522-08 g.chr13:23914497C>G c.3518G>C c.(3517-3519)tGg>tCg p.W1173S LUSC 13 23915054 23915054 + Missense_Mutation SNP C C G TCGA-66-2781-01A-01D-1522-08 TCGA-66-2781-11A-01D-1522-08 g.chr13:23915054C>G c.2961G>C c.(2959-2961)aaG>aaC p.K987N LUSC 13 23915357 23915357 + Missense_Mutation SNP C C G TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr13:23915357C>G c.2658G>C c.(2656-2658)caG>caC p.Q886H LUSC 13 23928866 23928866 + Missense_Mutation SNP C C T TCGA-22-4593-01A-21D-1817-08 TCGA-22-4593-11A-01D-1817-08 g.chr13:23928866C>T c.1885G>A c.(1885-1887)Gcg>Acg p.A629T LUSC 13 23928927 23928927 + Silent SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr13:23928927C>T c.1824G>A c.(1822-1824)gtG>gtA p.V608V LUSC 13 23929364 23929365 + Missense_Mutation DNP GA GA AT TCGA-33-4532-01A-01D-1267-08 TCGA-33-4532-11A-01D-1267-08 g.chr13:23929364_23929365GA>AT c.1386_1387TC>AT c.(1384-1389)gtTCac>gtATac p.H463Y LUSC 13 23929996 23929996 + Missense_Mutation SNP C C A TCGA-22-4613-01A-01D-1441-08 TCGA-22-4613-11A-01D-1441-08 g.chr13:23929996C>A c.755G>T c.(754-756)gGc>gTc p.G252V OV 13 23904819 23904819 + Missense_Mutation SNP G G C TCGA-36-1576-01A-01W-0615-10 TCGA-36-1576-10A-01W-0615-10 g.chr13:23904819G>C c.13196C>G c.(13195-13197)aCt>aGt p.T4399S OV 13 23910712 23910712 + Missense_Mutation SNP G G C TCGA-25-1318-01A-01W-0490-10 TCGA-25-1318-10A-01W-0490-10 g.chr13:23910712G>C c.7303C>G c.(7303-7305)Ctc>Gtc p.L2435V OV 13 23911439 23911439 + Silent SNP G G A TCGA-13-0751-01A-01D-0446-08 TCGA-13-0751-10A-01D-0446-08 g.chr13:23911439G>A c.6576C>T c.(6574-6576)atC>atT p.I2192I OV 13 23912946 23912946 + Missense_Mutation SNP A A T TCGA-13-0904-01A-02W-0420-08 TCGA-13-0904-10A-01D-0399-08 g.chr13:23912946A>T c.5069T>A c.(5068-5070)gTa>gAa p.V1690E OV 13 23913133 23913133 + Nonsense_Mutation SNP G G A TCGA-24-1469-01A-01W-0553-09 TCGA-24-1469-10A-01W-0553-09 g.chr13:23913133G>A c.4882C>T c.(4882-4884)Cag>Tag p.Q1628* OV 13 23913870 23913870 + Missense_Mutation SNP T T C TCGA-23-1022-01A-02W-0488-09 TCGA-23-1022-10A-01W-0488-09 g.chr13:23913870T>C c.4145A>G c.(4144-4146)cAt>cGt p.H1382R OV 13 23914961 23914961 + Missense_Mutation SNP C C G TCGA-13-1510-01A-02D-0472-08 TCGA-13-1510-10A-01W-0546-08 g.chr13:23914961C>G c.3054G>C c.(3052-3054)gaG>gaC p.E1018D PAAD 13 23904672 23904672 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23904672C>T c.13343G>A c.(13342-13344)cGc>cAc p.R4448H PAAD 13 23905023 23905023 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23905023C>T c.12992G>A c.(12991-12993)cGg>cAg p.R4331Q PAAD 13 23905812 23905812 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23905812C>A c.12203G>T c.(12202-12204)aGc>aTc p.S4068I PAAD 13 23910147 23910147 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23910147C>A c.7868G>T c.(7867-7869)gGa>gTa p.G2623V PAAD 13 23910739 23910739 + Nonsense_Mutation SNP G G A TCGA-FZ-5921-01A-11D-1609-08 TCGA-FZ-5921-11A-01D-1609-08 g.chr13:23910739G>A c.7276C>T c.(7276-7278)Cga>Tga p.R2426* PAAD 13 23910802 23910802 + Nonsense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23910802C>A c.7213G>T c.(7213-7215)Gaa>Taa p.E2405* PAAD 13 23911291 23911291 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23911291C>T c.6724G>A c.(6724-6726)Gca>Aca p.A2242T PAAD 13 23911703 23911703 + Silent SNP C C T TCGA-IB-AAUV-01A-11D-A38G-08 TCGA-IB-AAUV-10A-01D-A38J-08 g.chr13:23911703C>T c.6312G>A c.(6310-6312)ggG>ggA p.G2104G PAAD 13 23912096 23912096 + Missense_Mutation SNP T T G TCGA-2L-AAQJ-01A-12D-A397-08 TCGA-2L-AAQJ-11A-11D-A39A-08 g.chr13:23912096T>G c.5919A>C c.(5917-5919)aaA>aaC p.K1973N PAAD 13 23912282 23912282 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23912282C>T c.5733G>A c.(5731-5733)acG>acA p.T1911T PAAD 13 23912863 23912864 + Frame_Shift_Ins INS - - T TCGA-FB-AAPP-01A-12D-A40W-08 TCGA-FB-AAPP-11A-11D-A40W-08 g.chr13:23912863_23912864insT c.5151_5152insA c.(5149-5154)aaatccfs p.S1718fs PAAD 13 23915088 23915088 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23915088C>T c.2927G>A c.(2926-2928)cGt>cAt p.R976H PAAD 13 23929330 23929330 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23929330C>T c.1421G>A c.(1420-1422)cGc>cAc p.R474H PAAD 13 23929587 23929587 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23929587C>A c.1164G>T c.(1162-1164)caG>caT p.Q388H PAAD 13 23929960 23929960 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23929960C>T c.791G>A c.(790-792)gGc>gAc p.G264D PAAD 13 23932601 23932601 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:23932601G>A c.477C>T c.(475-477)taC>taT p.Y159Y PCPG 13 23906391 23906391 + Missense_Mutation SNP C C A TCGA-QT-A5XO-01A-11D-A35D-08 TCGA-QT-A5XO-10A-01D-A35B-08 g.chr13:23906391C>A c.11624G>T c.(11623-11625)cGt>cTt p.R3875L PCPG 13 23909416 23909416 + Missense_Mutation SNP C C A TCGA-W2-A7HF-01A-11D-A35I-08 TCGA-W2-A7HF-10C-01D-A35G-08 g.chr13:23909416C>A c.8599G>T c.(8599-8601)Gcc>Tcc p.A2867S PRAD 13 23905654 23905654 + Missense_Mutation SNP T T G TCGA-EJ-A6RC-01A-11D-A32B-08 TCGA-EJ-A6RC-10A-01D-A329-08 g.chr13:23905654T>G c.12361A>C c.(12361-12363)Att>Ctt p.I4121L PRAD 13 23906843 23906852 + Frame_Shift_Del DEL AAGGTCACTA AAGGTCACTA - TCGA-EJ-A7NJ-01A-22D-A34U-08 TCGA-EJ-A7NJ-10A-01D-A34X-08 g.chr13:23906843_23906852delAAGGTCACTA c.11163_11172delTAGTGACCTT c.(11161-11172)ggtagtgaccttfs p.GSDL3721fs PRAD 13 23909565 23909565 + Missense_Mutation SNP G G A TCGA-J9-A52C-01A-11D-A26M-08 TCGA-J9-A52C-10A-01D-A26K-08 g.chr13:23909565G>A c.8450C>T c.(8449-8451)aCg>aTg p.T2817M PRAD 13 23909827 23909827 + Missense_Mutation SNP G G T TCGA-XJ-A9DX-01A-11D-A377-08 TCGA-XJ-A9DX-10A-01D-A37A-08 g.chr13:23909827G>T c.8188C>A c.(8188-8190)Ctg>Atg p.L2730M PRAD 13 23909862 23909862 + Missense_Mutation SNP G G C TCGA-EJ-5519-01A-01D-1576-08 TCGA-EJ-5519-10A-01D-1577-08 g.chr13:23909862G>C c.8153C>G c.(8152-8154)gCa>gGa p.A2718G PRAD 13 23911843 23911843 + Frame_Shift_Del DEL A A - TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr13:23911843delA c.6172delT c.(6172-6174)tctfs p.S2058fs PRAD 13 23912044 23912044 + Missense_Mutation SNP C C T TCGA-XK-AAJP-01A-11D-A41K-08 TCGA-XK-AAJP-10A-01D-A41N-08 g.chr13:23912044C>T c.5971G>A c.(5971-5973)Gta>Ata p.V1991I PRAD 13 23912525 23912525 + Silent SNP C C T TCGA-EJ-A46F-01A-31D-A257-08 TCGA-EJ-A46F-10A-01D-A25A-08 g.chr13:23912525C>T c.5490G>A c.(5488-5490)ctG>ctA p.L1830L PRAD 13 23912565 23912565 + Missense_Mutation SNP G G A TCGA-KK-A59Z-01A-12D-A26M-08 TCGA-KK-A59Z-11A-11D-A26K-08 g.chr13:23912565G>A c.5450C>T c.(5449-5451)aCg>aTg p.T1817M PRAD 13 23913031 23913033 + In_Frame_Del DEL TAC TAC - TCGA-J9-A52C-01A-11D-A26M-08 TCGA-J9-A52C-10A-01D-A26K-08 g.chr13:23913031_23913033delTAC c.4982_4984delGTA c.(4981-4986)agtacg>acg p.S1661del PRAD 13 23914964 23914967 + Frame_Shift_Del DEL AAGG AAGG - TCGA-KK-A59Z-01A-12D-A26M-08 TCGA-KK-A59Z-11A-11D-A26K-08 g.chr13:23914964_23914967delAAGG c.3048_3051delCCTT c.(3046-3051)gtccttfs p.VL1016fs PRAD 13 23914995 23914995 + Missense_Mutation SNP T T A TCGA-ZG-A8QY-01A-11D-A377-08 TCGA-ZG-A8QY-10A-01D-A37A-08 g.chr13:23914995T>A c.3020A>T c.(3019-3021)gAa>gTa p.E1007V PRAD 13 23929388 23929388 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr13:23929388C>T c.1363G>A c.(1363-1365)Gaa>Aaa p.E455K READ 13 23904434 23904434 + Missense_Mutation SNP T T G TCGA-AG-3893-01A-01W-1073-09 TCGA-AG-3893-10A-01W-1073-09 g.chr13:23904434T>G c.13581A>C c.(13579-13581)gaA>gaC p.E4527D READ 13 23905110 23905110 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23905110G>T c.12905C>A c.(12904-12906)tCt>tAt p.S4302Y READ 13 23905348 23905348 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23905348T>G c.12667A>C c.(12667-12669)Aag>Cag p.K4223Q READ 13 23907021 23907021 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23907021C>A c.10994G>T c.(10993-10995)aGa>aTa p.R3665I READ 13 23907090 23907090 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23907090C>A c.10925G>T c.(10924-10926)gGa>gTa p.G3642V READ 13 23907566 23907566 + Silent SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23907566T>G c.10449A>C c.(10447-10449)ccA>ccC p.P3483P READ 13 23908582 23908582 + Nonsense_Mutation SNP C C A TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr13:23908582C>A c.9433G>T c.(9433-9435)Gaa>Taa p.E3145* READ 13 23908736 23908736 + Silent SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23908736C>A c.9279G>T c.(9277-9279)gtG>gtT p.V3093V READ 13 23908898 23908898 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23908898T>G c.9117A>C c.(9115-9117)aaA>aaC p.K3039N READ 13 23908918 23908918 + Missense_Mutation SNP C C A TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr13:23908918C>A c.9097G>T c.(9097-9099)Gat>Tat p.D3033Y READ 13 23908973 23908973 + Nonsense_Mutation SNP C C T TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr13:23908973C>T c.9042G>A c.(9040-9042)tgG>tgA p.W3014* READ 13 23909113 23909113 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23909113G>T c.8902C>A c.(8902-8904)Ctt>Att p.L2968I READ 13 23909694 23909694 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23909694C>A c.8321G>T c.(8320-8322)aGa>aTa p.R2774I READ 13 23910682 23910682 + Nonsense_Mutation SNP C C A TCGA-AG-4005-01A-01W-1073-09 TCGA-AG-4005-10A-01W-1073-09 g.chr13:23910682C>A c.7333G>T c.(7333-7335)Gag>Tag p.E2445* READ 13 23911196 23911196 + Silent SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23911196T>G c.6819A>C c.(6817-6819)tcA>tcC p.S2273S READ 13 23912013 23912013 + Missense_Mutation SNP C C A TCGA-AG-4001-01A-02W-1073-09 TCGA-AG-4001-10A-01W-1073-09 g.chr13:23912013C>A c.6002G>T c.(6001-6003)aGa>aTa p.R2001I READ 13 23913102 23913102 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23913102C>T c.4913G>A c.(4912-4914)aGc>aAc p.S1638N READ 13 23913434 23913434 + Silent SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23913434A>G c.4581T>C c.(4579-4581)aaT>aaC p.N1527N READ 13 23913600 23913600 + Missense_Mutation SNP G G T TCGA-CI-6621-01A-11D-1826-10 TCGA-CI-6621-10A-01D-1826-10 g.chr13:23913600G>T c.4415C>A c.(4414-4416)cCt>cAt p.P1472H READ 13 23914615 23914615 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23914615C>T c.3400G>A c.(3400-3402)Gtt>Att p.V1134I READ 13 23914699 23914699 + Missense_Mutation SNP C C A TCGA-AG-4015-01A-01W-1073-09 TCGA-AG-4015-10A-01W-1073-09 g.chr13:23914699C>A c.3316G>T c.(3316-3318)Gtg>Ttg p.V1106L READ 13 23914840 23914840 + Missense_Mutation SNP C C G TCGA-AG-A00H-01A-01W-A00E-09 TCGA-AG-A00H-10A-01W-A00E-09 g.chr13:23914840C>G c.3175G>C c.(3175-3177)Gaa>Caa p.E1059Q READ 13 23915071 23915071 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23915071T>G c.2944A>C c.(2944-2946)Aaa>Caa p.K982Q READ 13 23929770 23929770 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:23929770C>A c.981G>T c.(979-981)gaG>gaT p.E327D READ 13 23932592 23932592 + Silent SNP C C T TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr13:23932592C>T c.486G>A c.(484-486)gcG>gcA p.A162A SARC 13 23906926 23906926 + Missense_Mutation SNP G G C TCGA-FX-A76Y-01A-11D-A351-09 TCGA-FX-A76Y-10A-01D-A351-09 g.chr13:23906926G>C c.11089C>G c.(11089-11091)Ctc>Gtc p.L3697V SARC 13 23909098 23909098 + Missense_Mutation SNP C C T TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr13:23909098C>T c.8917G>A c.(8917-8919)Gat>Aat p.D2973N SARC 13 23910319 23910319 + Missense_Mutation SNP C C T TCGA-3B-A9HQ-01A-11D-A387-09 TCGA-3B-A9HQ-10A-01D-A38A-09 g.chr13:23910319C>T c.7696G>A c.(7696-7698)Gat>Aat p.D2566N SARC 13 23910564 23910564 + Missense_Mutation SNP C C A TCGA-IE-A3OV-01A-11D-A228-09 TCGA-IE-A3OV-11A-22D-A22A-09 g.chr13:23910564C>A c.7451G>T c.(7450-7452)tGt>tTt p.C2484F SARC 13 23912516 23912516 + Silent SNP G G A TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr13:23912516G>A c.5499C>T c.(5497-5499)tcC>tcT p.S1833S SKCM 13 23904351 23904351 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr13:23904351T>G c.13664A>C c.(13663-13665)gAg>gCg p.E4555A SKCM 13 23904401 23904401 + Silent SNP G G A TCGA-D3-A5GS-06A-11D-A27K-08 TCGA-D3-A5GS-10A-01D-A27N-08 g.chr13:23904401G>A c.13614C>T c.(13612-13614)taC>taT p.Y4538Y SKCM 13 23904967 23904967 + Missense_Mutation SNP C C T TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr13:23904967C>T c.13048G>A c.(13048-13050)Gaa>Aaa p.E4350K SKCM 13 23905402 23905402 + Missense_Mutation SNP T T C TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr13:23905402T>C c.12613A>G c.(12613-12615)Att>Gtt p.I4205V SKCM 13 23905533 23905533 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr13:23905533G>A c.12482C>T c.(12481-12483)cCt>cTt p.P4161L SKCM 13 23905568 23905568 + Silent SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr13:23905568T>C c.12447A>G c.(12445-12447)tcA>tcG p.S4149S SKCM 13 23906647 23906647 + Nonsense_Mutation SNP G G A TCGA-EE-A2GU-06A-11D-A196-08 TCGA-EE-A2GU-10A-01D-A198-08 g.chr13:23906647G>A c.11368C>T c.(11368-11370)Cag>Tag p.Q3790* SKCM 13 23906653 23906653 + Missense_Mutation SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr13:23906653G>A c.11362C>T c.(11362-11364)Cgt>Tgt p.R3788C SKCM 13 23906653 23906653 + Missense_Mutation SNP G G A TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr13:23906653G>A c.11362C>T c.(11362-11364)Cgt>Tgt p.R3788C SKCM 13 23906876 23906876 + Silent SNP G G A TCGA-EE-A2GL-06A-11D-A196-08 TCGA-EE-A2GL-10A-01D-A198-08 g.chr13:23906876G>A c.11139C>T c.(11137-11139)ccC>ccT p.P3713P SKCM 13 23906980 23906980 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr13:23906980G>A c.11035C>T c.(11035-11037)Ctt>Ttt p.L3679F SKCM 13 23907016 23907016 + Missense_Mutation SNP G G A TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chr13:23907016G>A c.10999C>T c.(10999-11001)Cat>Tat p.H3667Y SKCM 13 23907292 23907292 + Missense_Mutation SNP G G A TCGA-EE-A2MN-06A-11D-A197-08 TCGA-EE-A2MN-10A-01D-A199-08 g.chr13:23907292G>A c.10723C>T c.(10723-10725)Cat>Tat p.H3575Y SKCM 13 23907395 23907395 + Silent SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr13:23907395G>A c.10620C>T c.(10618-10620)ttC>ttT p.F3540F SKCM 13 23907707 23907707 + Silent SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr13:23907707G>A c.10308C>T c.(10306-10308)atC>atT p.I3436I SKCM 13 23907771 23907771 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr13:23907771G>A c.10244C>T c.(10243-10245)tCc>tTc p.S3415F SKCM 13 23907842 23907842 + Missense_Mutation SNP G G T TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr13:23907842G>T c.10173C>A c.(10171-10173)ttC>ttA p.F3391L SKCM 13 23907979 23907979 + Missense_Mutation SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr13:23907979G>A c.10036C>T c.(10036-10038)Cct>Tct p.P3346S SKCM 13 23908108 23908108 + Missense_Mutation SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr13:23908108G>A c.9907C>T c.(9907-9909)Cct>Tct p.P3303S SKCM 13 23908129 23908129 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr13:23908129G>A c.9886C>T c.(9886-9888)Cct>Tct p.P3296S SKCM 13 23908553 23908553 + Silent SNP G G A TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr13:23908553G>A c.9462C>T c.(9460-9462)ccC>ccT p.P3154P SKCM 13 23908710 23908710 + Nonsense_Mutation SNP A A T TCGA-DA-A3F5-06A-11D-A20D-08 TCGA-DA-A3F5-10A-01D-A20D-08 g.chr13:23908710A>T c.9305T>A c.(9304-9306)tTa>tAa p.L3102* SKCM 13 23908832 23908832 + Silent SNP G G A TCGA-GN-A262-06A-11D-A196-08 TCGA-GN-A262-10A-01D-A198-08 g.chr13:23908832G>A c.9183C>T c.(9181-9183)ctC>ctT p.L3061L SKCM 13 23908923 23908941 + Frame_Shift_Del DEL AGTAAATTGTCAAAAAATG AGTAAATTGTCAAAAAATG - TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr13:23908923_23908941delAGTAAATTGTCAAAAAATG c.9074_9092delCATTTTTTGACAATTTACT c.(9073-9093)ccattttttgacaatttactafs p.PFFDNLL3025fs SKCM 13 23909019 23909019 + Missense_Mutation SNP G G A TCGA-EE-A29B-06A-11D-A197-08 TCGA-EE-A29B-10A-01D-A199-08 g.chr13:23909019G>A c.8996C>T c.(8995-8997)cCa>cTa p.P2999L SKCM 13 23909099 23909099 + Silent SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr13:23909099T>G c.8916A>C c.(8914-8916)ccA>ccC p.P2972P SKCM 13 23909148 23909148 + Frame_Shift_Del DEL A A - TCGA-EE-A29Q-06A-11D-A197-08 TCGA-EE-A29Q-10A-01D-A199-08 g.chr13:23909148delA c.8867delT c.(8866-8868)ttafs p.L2956fs SKCM 13 23909470 23909470 + Missense_Mutation SNP G G A TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr13:23909470G>A c.8545C>T c.(8545-8547)Cca>Tca p.P2849S SKCM 13 23909674 23909674 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr13:23909674G>A c.8341C>T c.(8341-8343)Cat>Tat p.H2781Y SKCM 13 23909874 23909874 + Missense_Mutation SNP G G A TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr13:23909874G>A c.8141C>T c.(8140-8142)tCg>tTg p.S2714L SKCM 13 23910492 23910492 + Missense_Mutation SNP C C T TCGA-FS-A1ZS-06A-12D-A197-08 TCGA-FS-A1ZS-10A-01D-A199-08 g.chr13:23910492C>T c.7523G>A c.(7522-7524)aGa>aAa p.R2508K SKCM 13 23910621 23910621 + Missense_Mutation SNP G G A TCGA-FS-A1ZC-06A-11D-A197-08 TCGA-FS-A1ZC-10A-01D-A199-08 g.chr13:23910621G>A c.7394C>T c.(7393-7395)tCg>tTg p.S2465L SKCM 13 23910790 23910790 + Nonsense_Mutation SNP G G A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr13:23910790G>A c.7225C>T c.(7225-7227)Caa>Taa p.Q2409* SKCM 13 23911201 23911201 + Missense_Mutation SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr13:23911201C>T c.6814G>A c.(6814-6816)Ggt>Agt p.G2272S SKCM 13 23911333 23911333 + Missense_Mutation SNP C C A TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr13:23911333C>A c.6682G>T c.(6682-6684)Gac>Tac p.D2228Y SKCM 13 23911669 23911669 + Missense_Mutation SNP G G A TCGA-DA-A1IA-06A-11D-A196-08 TCGA-DA-A1IA-10A-01D-A198-08 g.chr13:23911669G>A c.6346C>T c.(6346-6348)Ccc>Tcc p.P2116S SKCM 13 23911699 23911699 + Missense_Mutation SNP G G A TCGA-EE-A2MG-06A-11D-A197-08 TCGA-EE-A2MG-10A-01D-A199-08 g.chr13:23911699G>A c.6316C>T c.(6316-6318)Cct>Tct p.P2106S SKCM 13 23911713 23911713 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr13:23911713G>A c.6302C>T c.(6301-6303)tCc>tTc p.S2101F SKCM 13 23911734 23911734 + Missense_Mutation SNP A A G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr13:23911734A>G c.6281T>C c.(6280-6282)gTt>gCt p.V2094A SKCM 13 23911927 23911927 + Missense_Mutation SNP G G A TCGA-FS-A4FD-06A-11D-A25O-08 TCGA-FS-A4FD-10B-01D-A25O-08 g.chr13:23911927G>A c.6088C>T c.(6088-6090)Cct>Tct p.P2030S SKCM 13 23912516 23912516 + Silent SNP G G A TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr13:23912516G>A c.5499C>T c.(5497-5499)tcC>tcT p.S1833S SKCM 13 23912636 23912636 + Missense_Mutation SNP A A C TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr13:23912636A>C c.5379T>G c.(5377-5379)ttT>ttG p.F1793L SKCM 13 23912862 23912862 + Missense_Mutation SNP G G A TCGA-EE-A2GU-06A-11D-A196-08 TCGA-EE-A2GU-10A-01D-A198-08 g.chr13:23912862G>A c.5153C>T c.(5152-5154)tCc>tTc p.S1718F SKCM 13 23912862 23912862 + Missense_Mutation SNP G G A TCGA-EE-A2M6-06A-12D-A197-08 TCGA-EE-A2M6-10A-01D-A199-08 g.chr13:23912862G>A c.5153C>T c.(5152-5154)tCc>tTc p.S1718F SKCM 13 23912862 23912862 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr13:23912862G>A c.5153C>T c.(5152-5154)tCc>tTc p.S1718F SKCM 13 23912907 23912907 + Missense_Mutation SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr13:23912907G>A c.5108C>T c.(5107-5109)aCc>aTc p.T1703I SKCM 13 23913172 23913172 + Missense_Mutation SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr13:23913172G>A c.4843C>T c.(4843-4845)Cct>Tct p.P1615S SKCM 13 23913568 23913568 + Nonsense_Mutation SNP G G A TCGA-D9-A6EA-06A-11D-A30X-08 TCGA-D9-A6EA-10A-01D-A30X-08 g.chr13:23913568G>A c.4447C>T c.(4447-4449)Caa>Taa p.Q1483* SKCM 13 23913632 23913632 + Silent SNP A A C TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr13:23913632A>C c.4383T>G c.(4381-4383)acT>acG p.T1461T SKCM 13 23913792 23913792 + Missense_Mutation SNP A A G TCGA-D3-A2JA-06A-11D-A196-08 TCGA-D3-A2JA-10A-01D-A198-08 g.chr13:23913792A>G c.4223T>C c.(4222-4224)cTt>cCt p.L1408P SKCM 13 23913876 23913876 + Missense_Mutation SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr13:23913876G>A c.4139C>T c.(4138-4140)cCt>cTt p.P1380L SKCM 13 23914341 23914341 + Missense_Mutation SNP A A G TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr13:23914341A>G c.3674T>C c.(3673-3675)tTa>tCa p.L1225S SKCM 13 23914626 23914626 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr13:23914626G>A c.3389C>T c.(3388-3390)aCc>aTc p.T1130I SKCM 13 23914670 23914670 + Silent SNP G G A TCGA-D3-A51J-06A-11D-A25O-08 TCGA-D3-A51J-10A-01D-A25O-08 g.chr13:23914670G>A c.3345C>T c.(3343-3345)gtC>gtT p.V1115V SKCM 13 23914933 23914933 + Missense_Mutation SNP G G A TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chr13:23914933G>A c.3082C>T c.(3082-3084)Cca>Tca p.P1028S SKCM 13 23915199 23915199 + Missense_Mutation SNP G G A TCGA-EE-A2MT-06A-11D-A197-08 TCGA-EE-A2MT-10A-01D-A199-08 g.chr13:23915199G>A c.2816C>T c.(2815-2817)tCc>tTc p.S939F SKCM 13 23915199 23915199 + Missense_Mutation SNP G G A TCGA-FS-A1ZE-06A-11D-A197-08 TCGA-FS-A1ZE-10A-01D-A199-08 g.chr13:23915199G>A c.2816C>T c.(2815-2817)tCc>tTc p.S939F SKCM 13 23915199 23915199 + Missense_Mutation SNP G G A TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr13:23915199G>A c.2816C>T c.(2815-2817)tCc>tTc p.S939F SKCM 13 23915461 23915461 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr13:23915461G>A c.2554C>T c.(2554-2556)Ctt>Ttt p.L852F SKCM 13 23915544 23915544 + Missense_Mutation SNP G G A TCGA-D3-A2JP-06A-11D-A19A-08 TCGA-D3-A2JP-10A-01D-A19A-08 g.chr13:23915544G>A c.2471C>T c.(2470-2472)tCg>tTg p.S824L SKCM 13 23915544 23915544 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr13:23915544G>A c.2471C>T c.(2470-2472)tCg>tTg p.S824L SKCM 13 23928006 23928006 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr13:23928006G>A c.2103C>T c.(2101-2103)ttC>ttT p.F701F SKCM 13 23928011 23928011 + Missense_Mutation SNP G G A TCGA-ER-A19G-06A-11D-A196-08 TCGA-ER-A19G-10A-01D-A198-08 g.chr13:23928011G>A c.2098C>T c.(2098-2100)Ctt>Ttt p.L700F SKCM 13 23928867 23928867 + Silent SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr13:23928867G>A c.1884C>T c.(1882-1884)ccC>ccT p.P628P SKCM 13 23929328 23929328 + Missense_Mutation SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr13:23929328T>C c.1423A>G c.(1423-1425)Agg>Ggg p.R475G SKCM 13 23929371 23929371 + Silent SNP G G A TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr13:23929371G>A c.1380C>T c.(1378-1380)ctC>ctT p.L460L SKCM 13 23932610 23932610 + Silent SNP G G A TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr13:23932610G>A c.468C>T c.(466-468)ctC>ctT p.L156L

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 23904263 23904263 single base substitution C T 3_prime_UTR_variant BLCA-CN 13 23904263 23904263 single base substitution C T intron_variant BLCA-CN 13 23906160 23906160 single base substitution C A intron_variant BLCA-CN 13 23906160 23906160 single base substitution C A missense_variant G3202V 9605G>T BLCA-CN 13 23906160 23906160 single base substitution C A missense_variant G3952V 11855G>T BLCA-CN 13 23910100 23910100 single base substitution T A intron_variant BLCA-CN 13 23910100 23910100 single base substitution T A missense_variant I1889F 5665A>T BLCA-CN 13 23910100 23910100 single base substitution T A missense_variant I2639F 7915A>T BLCA-CN 13 23911606 23911606 single base substitution G C intron_variant BLCA-CN 13 23911606 23911606 single base substitution G C missense_variant Q1387E 4159C>G BLCA-CN 13 23911606 23911606 single base substitution G C missense_variant Q2137E 6409C>G BLCA-CN 13 23912400 23912400 single base substitution C A intron_variant BLCA-CN 13 23912400 23912400 single base substitution C A missense_variant C1122F 3365G>T BLCA-CN 13 23912400 23912400 single base substitution C A missense_variant C1872F 5615G>T BLCA-CN 13 23929393 23929393 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant BLCA-CN 13 23929393 23929393 single base substitution C A missense_variant G352V 1055G>T BLCA-CN 13 23929393 23929393 single base substitution C A missense_variant G453V 1358G>T BLCA-CN 13 23929393 23929393 single base substitution C A missense_variant G77V 230G>T BLCA-CN 13 23929393 23929393 single base substitution C A upstream_gene_variant BLCA-CN 13 23932478 23932478 single base substitution T G 5_prime_UTR_variant BLCA-CN 13 23932478 23932478 single base substitution T G synonymous_variant I200I 600A>C BLCA-CN 13 23932478 23932478 single base substitution T G synonymous_variant I99I 297A>C BLCA-CN 13 23932478 23932478 single base substitution T G upstream_gene_variant BLCA-US 13 23904689 23904689 single base substitution G T intron_variant BLCA-US 13 23904689 23904689 single base substitution G T synonymous_variant G3692G 11076C>A BLCA-US 13 23904689 23904689 single base substitution G T synonymous_variant G4442G 13326C>A BLCA-US 13 23904719 23904719 single base substitution G C intron_variant BLCA-US 13 23904719 23904719 single base substitution G C missense_variant F3682L 11046C>G BLCA-US 13 23904719 23904719 single base substitution G C missense_variant F4432L 13296C>G BLCA-US 13 23904867 23904867 single base substitution G C intron_variant BLCA-US 13 23904867 23904867 single base substitution G C stop_gained S3633* 10898C>G BLCA-US 13 23904867 23904867 single base substitution G C stop_gained S4383* 13148C>G BLCA-US 13 23905173 23905173 single base substitution G C intron_variant BLCA-US 13 23905173 23905173 single base substitution G C missense_variant S3531C 10592C>G BLCA-US 13 23905173 23905173 single base substitution G C missense_variant S4281C 12842C>G BLCA-US 13 23905175 23905175 single base substitution G C intron_variant BLCA-US 13 23905175 23905175 single base substitution G C missense_variant F3530L 10590C>G BLCA-US 13 23905175 23905175 single base substitution G C missense_variant F4280L 12840C>G BLCA-US 13 23906256 23906256 single base substitution C G intron_variant BLCA-US 13 23906256 23906256 single base substitution C G missense_variant S3170T 9509G>C BLCA-US 13 23906256 23906256 single base substitution C G missense_variant S3920T 11759G>C BLCA-US 13 23906653 23906653 single base substitution G A intron_variant BLCA-US 13 23906653 23906653 single base substitution G A missense_variant R3038C 9112C>T BLCA-US 13 23906653 23906653 single base substitution G A missense_variant R3788C 11362C>T BLCA-US 13 23907016 23907016 single base substitution G A intron_variant BLCA-US 13 23907016 23907016 single base substitution G A missense_variant H2917Y 8749C>T BLCA-US 13 23907016 23907016 single base substitution G A missense_variant H3667Y 10999C>T BLCA-US 13 23908464 23908464 single base substitution C T intron_variant BLCA-US 13 23908464 23908464 single base substitution C T missense_variant R2434H 7301G>A BLCA-US 13 23908464 23908464 single base substitution C T missense_variant R3184H 9551G>A BLCA-US 13 23909330 23909330 single base substitution G A intron_variant BLCA-US 13 23909330 23909330 single base substitution G A synonymous_variant N2145N 6435C>T BLCA-US 13 23909330 23909330 single base substitution G A synonymous_variant N2895N 8685C>T BLCA-US 13 23909550 23909550 single base substitution T C intron_variant BLCA-US 13 23909550 23909550 single base substitution T C missense_variant N2072S 6215A>G BLCA-US 13 23909550 23909550 single base substitution T C missense_variant N2822S 8465A>G BLCA-US 13 23913064 23913064 single base substitution G C intron_variant BLCA-US 13 23913064 23913064 single base substitution G C missense_variant Q1651E 4951C>G BLCA-US 13 23913064 23913064 single base substitution G C missense_variant Q901E 2701C>G BLCA-US 13 23913766 23913766 single base substitution C T intron_variant BLCA-US 13 23913766 23913766 single base substitution C T missense_variant E1417K 4249G>A BLCA-US 13 23913766 23913766 single base substitution C T missense_variant E667K 1999G>A BLCA-US 13 23914840 23914840 single base substitution C G intron_variant BLCA-US 13 23914840 23914840 single base substitution C G missense_variant E1059Q 3175G>C BLCA-US 13 23914840 23914840 single base substitution C G missense_variant E309Q 925G>C BLCA-US 13 23915126 23915126 single base substitution A G intron_variant BLCA-US 13 23915126 23915126 single base substitution A G synonymous_variant S213S 639T>C BLCA-US 13 23915126 23915126 single base substitution A G synonymous_variant S963S 2889T>C BLCA-US 13 23915245 23915245 insertion of <=200bp - TTC intron_variant BLCA-US 13 23915245 23915245 insertion of <=200bp - TTC stop_gained L174*M BLCA-US 13 23915245 23915245 insertion of <=200bp - TTC stop_gained L924*M BLCA-US 13 23915753 23915753 single base substitution G A intron_variant BLCA-US 13 23915753 23915753 single base substitution G A synonymous_variant F4F 12C>T BLCA-US 13 23915753 23915753 single base substitution G A synonymous_variant F653F 1959C>T BLCA-US 13 23915753 23915753 single base substitution G A synonymous_variant F754F 2262C>T BLCA-US 13 23929191 23929191 single base substitution C G 5_prime_UTR_variant BLCA-US 13 23929191 23929191 single base substitution C G missense_variant K144N 432G>C BLCA-US 13 23929191 23929191 single base substitution C G missense_variant K419N 1257G>C BLCA-US 13 23929191 23929191 single base substitution C G missense_variant K520N 1560G>C BLCA-US 13 23929191 23929191 single base substitution C G upstream_gene_variant BLCA-US 13 23929791 23929791 single base substitution G A 5_prime_UTR_variant BLCA-US 13 23929791 23929791 single base substitution G A synonymous_variant V219V 657C>T BLCA-US 13 23929791 23929791 single base substitution G A synonymous_variant V320V 960C>T BLCA-US 13 23929791 23929791 single base substitution G A upstream_gene_variant BLCA-US 13 23930039 23930039 single base substitution T C 5_prime_UTR_variant BLCA-US 13 23930039 23930039 single base substitution T C missense_variant K137E 409A>G BLCA-US 13 23930039 23930039 single base substitution T C missense_variant K238E 712A>G BLCA-US 13 23930039 23930039 single base substitution T C upstream_gene_variant BLCA-US 13 23930096 23930096 single base substitution G A 5_prime_UTR_variant BLCA-US 13 23930096 23930096 single base substitution G A stop_gained Q118* 352C>T BLCA-US 13 23930096 23930096 single base substitution G A stop_gained Q219* 655C>T BLCA-US 13 23930096 23930096 single base substitution G A upstream_gene_variant BOCA-UK 13 23906870 23906870 single base substitution G A intron_variant BOCA-UK 13 23906870 23906870 single base substitution G A synonymous_variant S2965S 8895C>T BOCA-UK 13 23906870 23906870 single base substitution G A synonymous_variant S3715S 11145C>T BRCA-EU 13 23900383 23900383 single base substitution G A downstream_gene_variant BRCA-EU 13 23902776 23902776 single base substitution A C downstream_gene_variant BRCA-EU 13 23903642 23903642 deletion of <=200bp A - 3_prime_UTR_variant BRCA-EU 13 23903642 23903642 deletion of <=200bp A - intron_variant BRCA-EU 13 23904639 23904639 single base substitution G C intron_variant BRCA-EU 13 23904639 23904639 single base substitution G C stop_gained S3709* 11126C>G BRCA-EU 13 23904639 23904639 single base substitution G C stop_gained S4459* 13376C>G BRCA-EU 13 23905992 23905992 single base substitution G C intron_variant BRCA-EU 13 23905992 23905992 single base substitution G C missense_variant S3258C 9773C>G BRCA-EU 13 23905992 23905992 single base substitution G C missense_variant S4008C 12023C>G BRCA-EU 13 23906346 23906346 single base substitution T A intron_variant BRCA-EU 13 23906346 23906346 single base substitution T A missense_variant N3140I 9419A>T BRCA-EU 13 23906346 23906346 single base substitution T A missense_variant N3890I 11669A>T BRCA-EU 13 23906895 23906895 single base substitution A G intron_variant BRCA-EU 13 23906895 23906895 single base substitution A G missense_variant L2957P 8870T>C BRCA-EU 13 23906895 23906895 single base substitution A G missense_variant L3707P 11120T>C BRCA-EU 13 23908656 23908656 single base substitution C T intron_variant BRCA-EU 13 23908656 23908656 single base substitution C T missense_variant R2370H 7109G>A BRCA-EU 13 23908656 23908656 single base substitution C T missense_variant R3120H 9359G>A BRCA-EU 13 23910025 23910025 single base substitution C T intron_variant BRCA-EU 13 23910025 23910025 single base substitution C T missense_variant G1914R 5740G>A BRCA-EU 13 23910025 23910025 single base substitution C T missense_variant G2664R 7990G>A BRCA-EU 13 23910179 23910179 single base substitution T C intron_variant BRCA-EU 13 23910179 23910179 single base substitution T C synonymous_variant K1862K 5586A>G BRCA-EU 13 23910179 23910179 single base substitution T C synonymous_variant K2612K 7836A>G BRCA-EU 13 23912362 23912362 single base substitution G T intron_variant BRCA-EU 13 23912362 23912362 single base substitution G T missense_variant H1135N 3403C>A BRCA-EU 13 23912362 23912362 single base substitution G T missense_variant H1885N 5653C>A BRCA-EU 13 23912905 23912905 single base substitution T G intron_variant BRCA-EU 13 23912905 23912905 single base substitution T G missense_variant N1704H 5110A>C BRCA-EU 13 23912905 23912905 single base substitution T G missense_variant N954H 2860A>C BRCA-EU 13 23913356 23913356 deletion of <=200bp A - frameshift_variant V1553 BRCA-EU 13 23913356 23913356 deletion of <=200bp A - frameshift_variant V803 BRCA-EU 13 23913356 23913356 deletion of <=200bp A - intron_variant BRCA-EU 13 23913430 23913430 single base substitution G A intron_variant BRCA-EU 13 23913430 23913430 single base substitution G A stop_gained Q1529* 4585C>T BRCA-EU 13 23913430 23913430 single base substitution G A stop_gained Q779* 2335C>T BRCA-EU 13 23913919 23913919 single base substitution G A intron_variant BRCA-EU 13 23913919 23913919 single base substitution G A synonymous_variant L1366L 4096C>T BRCA-EU 13 23913919 23913919 single base substitution G A synonymous_variant L616L 1846C>T BRCA-EU 13 23915601 23915601 single base substitution C T intron_variant BRCA-EU 13 23915601 23915601 single base substitution C T missense_variant R55K 164G>A BRCA-EU 13 23915601 23915601 single base substitution C T missense_variant R704K 2111G>A BRCA-EU 13 23915601 23915601 single base substitution C T missense_variant R805K 2414G>A BRCA-EU 13 23915659 23915659 single base substitution G C intron_variant BRCA-EU 13 23915659 23915659 single base substitution G C missense_variant L36V 106C>G BRCA-EU 13 23915659 23915659 single base substitution G C missense_variant L685V 2053C>G BRCA-EU 13 23915659 23915659 single base substitution G C missense_variant L786V 2356C>G BRCA-EU 13 23916541 23916541 single base substitution T G intron_variant BRCA-EU 13 23918697 23918697 single base substitution T C intron_variant BRCA-EU 13 23919362 23919362 single base substitution A C intron_variant BRCA-EU 13 23919458 23919458 single base substitution A C intron_variant BRCA-EU 13 23920560 23920560 deletion of <=200bp G - intron_variant BRCA-EU 13 23921754 23921754 single base substitution A C intron_variant BRCA-EU 13 23921901 23921901 single base substitution C A intron_variant BRCA-EU 13 23921907 23921907 single base substitution T G intron_variant BRCA-EU 13 23921913 23921913 single base substitution A T intron_variant BRCA-EU 13 23922835 23922835 single base substitution G C intron_variant BRCA-EU 13 23924112 23924112 single base substitution G A downstream_gene_variant BRCA-EU 13 23924112 23924112 single base substitution G A intron_variant BRCA-EU 13 23924350 23924350 single base substitution G A downstream_gene_variant BRCA-EU 13 23924350 23924350 single base substitution G A intron_variant BRCA-EU 13 23925303 23925303 single base substitution C G downstream_gene_variant BRCA-EU 13 23925303 23925303 single base substitution C G intron_variant BRCA-EU 13 23925891 23925891 single base substitution G C downstream_gene_variant BRCA-EU 13 23925891 23925891 single base substitution G C intron_variant BRCA-EU 13 23926782 23926782 deletion of <=200bp A - downstream_gene_variant BRCA-EU 13 23926782 23926782 deletion of <=200bp A - intron_variant BRCA-EU 13 23927272 23927272 single base substitution A G downstream_gene_variant BRCA-EU 13 23927272 23927272 single base substitution A G intron_variant BRCA-EU 13 23927277 23927277 single base substitution G A downstream_gene_variant BRCA-EU 13 23927277 23927277 single base substitution G A intron_variant BRCA-EU 13 23927999 23927999 single base substitution G A 5_prime_UTR_variant BRCA-EU 13 23927999 23927999 single base substitution G A exon_variant BRCA-EU 13 23927999 23927999 single base substitution G A missense_variant L328F 982C>T BRCA-EU 13 23927999 23927999 single base substitution G A missense_variant L603F 1807C>T BRCA-EU 13 23927999 23927999 single base substitution G A missense_variant L704F 2110C>T BRCA-EU 13 23928150 23928150 single base substitution A C intron_variant BRCA-EU 13 23928793 23928793 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 13 23928793 23928793 single base substitution A T exon_variant BRCA-EU 13 23928793 23928793 single base substitution A T missense_variant F277Y 830T>A BRCA-EU 13 23928793 23928793 single base substitution A T missense_variant F552Y 1655T>A BRCA-EU 13 23928793 23928793 single base substitution A T missense_variant F653Y 1958T>A BRCA-EU 13 23928907 23928907 single base substitution G T 5_prime_UTR_variant BRCA-EU 13 23928907 23928907 single base substitution G T exon_variant BRCA-EU 13 23928907 23928907 single base substitution G T missense_variant T239K 716C>A BRCA-EU 13 23928907 23928907 single base substitution G T missense_variant T514K 1541C>A BRCA-EU 13 23928907 23928907 single base substitution G T missense_variant T615K 1844C>A BRCA-EU 13 23934935 23934935 single base substitution C T intron_variant BRCA-EU 13 23936823 23936823 single base substitution C T intron_variant BRCA-EU 13 23937196 23937196 single base substitution C G intron_variant BRCA-EU 13 23940214 23940214 single base substitution G C intron_variant BRCA-EU 13 23941925 23941925 single base substitution G A intron_variant BRCA-EU 13 23941987 23941987 single base substitution C T intron_variant BRCA-EU 13 23942482 23942482 single base substitution A G intron_variant BRCA-EU 13 23943172 23943172 deletion of <=200bp A - intron_variant BRCA-EU 13 23943172 23943172 deletion of <=200bp A - upstream_gene_variant BRCA-EU 13 23946445 23946445 single base substitution C G intron_variant BRCA-EU 13 23946445 23946445 single base substitution C G upstream_gene_variant BRCA-EU 13 23947642 23947642 single base substitution C T intron_variant BRCA-EU 13 23948834 23948834 single base substitution G C intron_variant BRCA-EU 13 23949744 23949744 single base substitution A T intron_variant BRCA-EU 13 23949744 23949744 single base substitution A T upstream_gene_variant BRCA-EU 13 23950404 23950404 single base substitution G A intron_variant BRCA-EU 13 23950404 23950404 single base substitution G A upstream_gene_variant BRCA-EU 13 23950841 23950841 single base substitution G T intron_variant BRCA-EU 13 23950841 23950841 single base substitution G T upstream_gene_variant BRCA-EU 13 23951439 23951439 single base substitution A G intron_variant BRCA-EU 13 23951439 23951439 single base substitution A G upstream_gene_variant BRCA-EU 13 23953577 23953577 single base substitution T C intron_variant BRCA-EU 13 23953577 23953577 single base substitution T C upstream_gene_variant BRCA-EU 13 23953809 23953809 single base substitution G A intron_variant BRCA-EU 13 23953809 23953809 single base substitution G A upstream_gene_variant BRCA-EU 13 23953918 23953918 single base substitution G A intron_variant BRCA-EU 13 23953918 23953918 single base substitution G A upstream_gene_variant BRCA-EU 13 23956052 23956052 single base substitution G A intron_variant BRCA-EU 13 23958083 23958083 single base substitution C G intron_variant BRCA-EU 13 23959335 23959335 single base substitution G T intron_variant BRCA-EU 13 23960366 23960366 single base substitution C G intron_variant BRCA-EU 13 23960992 23960992 single base substitution G C intron_variant BRCA-EU 13 23961555 23961555 single base substitution C A intron_variant BRCA-EU 13 23964224 23964224 single base substitution A C intron_variant BRCA-EU 13 23964344 23964344 single base substitution G A intron_variant BRCA-EU 13 23964961 23964961 single base substitution C T intron_variant BRCA-EU 13 23965698 23965698 single base substitution A C intron_variant BRCA-EU 13 23966294 23966294 single base substitution G A intron_variant BRCA-EU 13 23967190 23967190 single base substitution G T intron_variant BRCA-EU 13 23967256 23967256 single base substitution G T intron_variant BRCA-EU 13 23968257 23968257 single base substitution C T intron_variant BRCA-EU 13 23968621 23968621 single base substitution G C intron_variant BRCA-EU 13 23968870 23968870 single base substitution T G intron_variant BRCA-EU 13 23968949 23968949 single base substitution G A intron_variant BRCA-EU 13 23973352 23973352 single base substitution T A intron_variant BRCA-EU 13 23973430 23973430 single base substitution G C intron_variant BRCA-EU 13 23976415 23976415 single base substitution C T intron_variant BRCA-EU 13 23977160 23977160 deletion of <=200bp A - intron_variant BRCA-EU 13 23977824 23977824 insertion of <=200bp - A intron_variant BRCA-EU 13 23978501 23978501 single base substitution A T intron_variant BRCA-EU 13 23979228 23979228 single base substitution C T intron_variant BRCA-EU 13 23979847 23979848 deletion of <=200bp AC - intron_variant BRCA-EU 13 23981361 23981361 single base substitution G A intron_variant BRCA-EU 13 23982329 23982329 single base substitution A G intron_variant BRCA-EU 13 23982704 23982704 single base substitution G C intron_variant BRCA-EU 13 23982871 23982871 single base substitution G A intron_variant BRCA-EU 13 23983335 23983335 single base substitution A T intron_variant BRCA-EU 13 23983476 23983476 single base substitution G A intron_variant BRCA-EU 13 23983883 23983883 single base substitution C T intron_variant BRCA-EU 13 23984277 23984277 single base substitution G A intron_variant BRCA-EU 13 23984282 23984282 single base substitution A G intron_variant BRCA-EU 13 23984658 23984658 single base substitution G C intron_variant BRCA-EU 13 23989248 23989248 single base substitution G A intron_variant BRCA-EU 13 23989248 23989248 single base substitution G A upstream_gene_variant BRCA-EU 13 23989382 23989382 single base substitution G T intron_variant BRCA-EU 13 23989382 23989382 single base substitution G T upstream_gene_variant BRCA-EU 13 23989559 23989559 single base substitution T G intron_variant BRCA-EU 13 23989559 23989559 single base substitution T G upstream_gene_variant BRCA-EU 13 23989986 23989986 single base substitution G T intron_variant BRCA-EU 13 23989986 23989986 single base substitution G T upstream_gene_variant BRCA-EU 13 23990173 23990173 single base substitution C G intron_variant BRCA-EU 13 23990173 23990173 single base substitution C G upstream_gene_variant BRCA-EU 13 23991413 23991413 single base substitution G C intron_variant BRCA-EU 13 23991585 23991585 single base substitution G C intron_variant BRCA-EU 13 23991930 23991930 single base substitution G C intron_variant BRCA-EU 13 23992190 23992190 single base substitution A C intron_variant BRCA-EU 13 23993014 23993014 single base substitution G A intron_variant BRCA-EU 13 23999162 23999162 single base substitution G T intron_variant BRCA-EU 13 24000672 24000672 single base substitution G A intron_variant BRCA-EU 13 24000826 24000826 single base substitution G C intron_variant BRCA-EU 13 24003289 24003289 single base substitution G C intron_variant BRCA-EU 13 24003304 24003304 single base substitution G C intron_variant BRCA-EU 13 24003570 24003570 single base substitution C T intron_variant BRCA-EU 13 24006805 24006807 deletion of <=200bp TTA - intron_variant BRCA-EU 13 24007085 24007085 deletion of <=200bp A - intron_variant BRCA-EU 13 24008341 24008341 single base substitution C T upstream_gene_variant BRCA-EU 13 24010526 24010526 single base substitution G T upstream_gene_variant BRCA-EU 13 24010843 24010843 single base substitution G C upstream_gene_variant BRCA-FR 13 23904639 23904639 single base substitution G C intron_variant BRCA-FR 13 23904639 23904639 single base substitution G C stop_gained S3709* 11126C>G BRCA-FR 13 23904639 23904639 single base substitution G C stop_gained S4459* 13376C>G BRCA-FR 13 23905992 23905992 single base substitution G C intron_variant BRCA-FR 13 23905992 23905992 single base substitution G C missense_variant S3258C 9773C>G BRCA-FR 13 23905992 23905992 single base substitution G C missense_variant S4008C 12023C>G BRCA-FR 13 23928150 23928150 single base substitution A C intron_variant BRCA-FR 13 23952823 23952823 single base substitution C T intron_variant BRCA-FR 13 23952823 23952823 single base substitution C T upstream_gene_variant BRCA-FR 13 23953809 23953809 single base substitution G A intron_variant BRCA-FR 13 23953809 23953809 single base substitution G A upstream_gene_variant BRCA-FR 13 23966294 23966294 single base substitution G A intron_variant BRCA-FR 13 23968257 23968257 single base substitution C T intron_variant BRCA-FR 13 23991413 23991413 single base substitution G C intron_variant BRCA-FR 13 24001153 24001153 single base substitution G A intron_variant BRCA-KR 13 23905461 23905461 single base substitution A C intron_variant BRCA-KR 13 23905461 23905461 single base substitution A C missense_variant L3435R 10304T>G BRCA-KR 13 23905461 23905461 single base substitution A C missense_variant L4185R 12554T>G BRCA-KR 13 23906440 23906440 single base substitution G A intron_variant BRCA-KR 13 23906440 23906440 single base substitution G A missense_variant R3109C 9325C>T BRCA-KR 13 23906440 23906440 single base substitution G A missense_variant R3859C 11575C>T BRCA-KR 13 23911754 23911754 single base substitution C T intron_variant BRCA-KR 13 23911754 23911754 single base substitution C T synonymous_variant E1337E 4011G>A BRCA-KR 13 23911754 23911754 single base substitution C T synonymous_variant E2087E 6261G>A BRCA-UK 13 23910751 23910751 single base substitution G A intron_variant BRCA-UK 13 23910751 23910751 single base substitution G A stop_gained Q1672* 5014C>T BRCA-UK 13 23910751 23910751 single base substitution G A stop_gained Q2422* 7264C>T BRCA-UK 13 23947716 23947716 single base substitution A G intron_variant BRCA-UK 13 23981361 23981361 single base substitution G A intron_variant BRCA-UK 13 23984277 23984277 single base substitution G A intron_variant BRCA-UK 13 23984282 23984282 single base substitution A G intron_variant BRCA-UK 13 23991930 23991930 single base substitution G C intron_variant BRCA-UK 13 24003289 24003289 single base substitution G C intron_variant BRCA-US 13 23898666 23898666 single base substitution C T downstream_gene_variant BRCA-US 13 23904867 23904867 single base substitution G A intron_variant BRCA-US 13 23904867 23904867 single base substitution G A missense_variant S3633L 10898C>T BRCA-US 13 23904867 23904867 single base substitution G A missense_variant S4383L 13148C>T BRCA-US 13 23905513 23905513 single base substitution G A intron_variant BRCA-US 13 23905513 23905513 single base substitution G A synonymous_variant L3418L 10252C>T BRCA-US 13 23905513 23905513 single base substitution G A synonymous_variant L4168L 12502C>T BRCA-US 13 23905703 23905703 single base substitution C A intron_variant BRCA-US 13 23905703 23905703 single base substitution C A missense_variant M3354I 10062G>T BRCA-US 13 23905703 23905703 single base substitution C A missense_variant M4104I 12312G>T BRCA-US 13 23906002 23906002 single base substitution G A intron_variant BRCA-US 13 23906002 23906002 single base substitution G A missense_variant L3255F 9763C>T BRCA-US 13 23906002 23906002 single base substitution G A missense_variant L4005F 12013C>T BRCA-US 13 23907076 23907076 single base substitution C A intron_variant BRCA-US 13 23907076 23907076 single base substitution C A stop_gained E2897* 8689G>T BRCA-US 13 23907076 23907076 single base substitution C A stop_gained E3647* 10939G>T BRCA-US 13 23907634 23907634 single base substitution C A intron_variant BRCA-US 13 23907634 23907634 single base substitution C A stop_gained E2711* 8131G>T BRCA-US 13 23907634 23907634 single base substitution C A stop_gained E3461* 10381G>T BRCA-US 13 23907783 23907783 single base substitution G A intron_variant BRCA-US 13 23907783 23907783 single base substitution G A missense_variant P2661L 7982C>T BRCA-US 13 23907783 23907783 single base substitution G A missense_variant P3411L 10232C>T BRCA-US 13 23907808 23907808 single base substitution C T intron_variant BRCA-US 13 23907808 23907808 single base substitution C T missense_variant D2653N 7957G>A BRCA-US 13 23907808 23907808 single base substitution C T missense_variant D3403N 10207G>A BRCA-US 13 23908825 23908825 single base substitution C T intron_variant BRCA-US 13 23908825 23908825 single base substitution C T missense_variant E2314K 6940G>A BRCA-US 13 23908825 23908825 single base substitution C T missense_variant E3064K 9190G>A BRCA-US 13 23909425 23909425 single base substitution G T intron_variant BRCA-US 13 23909425 23909425 single base substitution G T missense_variant P2114T 6340C>A BRCA-US 13 23909425 23909425 single base substitution G T missense_variant P2864T 8590C>A BRCA-US 13 23909580 23909580 single base substitution T G intron_variant BRCA-US 13 23909580 23909580 single base substitution T G missense_variant E2062A 6185A>C BRCA-US 13 23909580 23909580 single base substitution T G missense_variant E2812A 8435A>C BRCA-US 13 23909753 23909753 single base substitution C A intron_variant BRCA-US 13 23909753 23909753 single base substitution C A missense_variant K2004N 6012G>T BRCA-US 13 23909753 23909753 single base substitution C A missense_variant K2754N 8262G>T BRCA-US 13 23909883 23909883 single base substitution G A intron_variant BRCA-US 13 23909883 23909883 single base substitution G A missense_variant S1961L 5882C>T BRCA-US 13 23909883 23909883 single base substitution G A missense_variant S2711L 8132C>T BRCA-US 13 23910337 23910337 single base substitution C G intron_variant BRCA-US 13 23910337 23910337 single base substitution C G missense_variant E1810Q 5428G>C BRCA-US 13 23910337 23910337 single base substitution C G missense_variant E2560Q 7678G>C BRCA-US 13 23910500 23910500 single base substitution G A intron_variant BRCA-US 13 23910500 23910500 single base substitution G A synonymous_variant A1755A 5265C>T BRCA-US 13 23910500 23910500 single base substitution G A synonymous_variant A2505A 7515C>T BRCA-US 13 23910597 23910597 single base substitution C G intron_variant BRCA-US 13 23910597 23910597 single base substitution C G missense_variant W1723S 5168G>C BRCA-US 13 23910597 23910597 single base substitution C G missense_variant W2473S 7418G>C BRCA-US 13 23911264 23911264 single base substitution G C intron_variant BRCA-US 13 23911264 23911264 single base substitution G C missense_variant Q1501E 4501C>G BRCA-US 13 23911264 23911264 single base substitution G C missense_variant Q2251E 6751C>G BRCA-US 13 23911546 23911546 single base substitution C A intron_variant BRCA-US 13 23911546 23911546 single base substitution C A missense_variant D1407Y 4219G>T BRCA-US 13 23911546 23911546 single base substitution C A missense_variant D2157Y 6469G>T BRCA-US 13 23911836 23911836 single base substitution A G intron_variant BRCA-US 13 23911836 23911836 single base substitution A G missense_variant V1310A 3929T>C BRCA-US 13 23911836 23911836 single base substitution A G missense_variant V2060A 6179T>C BRCA-US 13 23912580 23912580 single base substitution G C intron_variant BRCA-US 13 23912580 23912580 single base substitution G C missense_variant T1062R 3185C>G BRCA-US 13 23912580 23912580 single base substitution G C missense_variant T1812R 5435C>G BRCA-US 13 23912644 23912644 single base substitution C T intron_variant BRCA-US 13 23912644 23912644 single base substitution C T missense_variant A1041T 3121G>A BRCA-US 13 23912644 23912644 single base substitution C T missense_variant A1791T 5371G>A BRCA-US 13 23913541 23913541 single base substitution C A intron_variant BRCA-US 13 23913541 23913541 single base substitution C A stop_gained E1492* 4474G>T BRCA-US 13 23913541 23913541 single base substitution C A stop_gained E742* 2224G>T BRCA-US 13 23913912 23913912 single base substitution C T intron_variant BRCA-US 13 23913912 23913912 single base substitution C T missense_variant S1368N 4103G>A BRCA-US 13 23913912 23913912 single base substitution C T missense_variant S618N 1853G>A BRCA-US 13 23913916 23913916 single base substitution A G intron_variant BRCA-US 13 23913916 23913916 single base substitution A G missense_variant Y1367H 4099T>C BRCA-US 13 23913916 23913916 single base substitution A G missense_variant Y617H 1849T>C BRCA-US 13 23914806 23914806 single base substitution C T intron_variant BRCA-US 13 23914806 23914806 single base substitution C T missense_variant G1070E 3209G>A BRCA-US 13 23914806 23914806 single base substitution C T missense_variant G320E 959G>A BRCA-US 13 23915127 23915127 single base substitution G C intron_variant BRCA-US 13 23915127 23915127 single base substitution G C missense_variant S213C 638C>G BRCA-US 13 23915127 23915127 single base substitution G C missense_variant S963C 2888C>G BRCA-US 13 23915403 23915403 single base substitution G A intron_variant BRCA-US 13 23915403 23915403 single base substitution G A missense_variant P121L 362C>T BRCA-US 13 23915403 23915403 single base substitution G A missense_variant P871L 2612C>T BRCA-US 13 23915510 23915510 single base substitution C G intron_variant BRCA-US 13 23915510 23915510 single base substitution C G missense_variant Q835H 2505G>C BRCA-US 13 23915510 23915510 single base substitution C G missense_variant Q85H 255G>C BRCA-US 13 23927962 23927962 single base substitution T G 5_prime_UTR_variant BRCA-US 13 23927962 23927962 single base substitution T G exon_variant BRCA-US 13 23927962 23927962 single base substitution T G missense_variant H340P 1019A>C BRCA-US 13 23927962 23927962 single base substitution T G missense_variant H615P 1844A>C BRCA-US 13 23927962 23927962 single base substitution T G missense_variant H716P 2147A>C BRCA-US 13 23928978 23928978 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 13 23928978 23928978 single base substitution G C exon_variant BRCA-US 13 23928978 23928978 single base substitution G C synonymous_variant L215L 645C>G BRCA-US 13 23928978 23928978 single base substitution G C synonymous_variant L490L 1470C>G BRCA-US 13 23928978 23928978 single base substitution G C synonymous_variant L591L 1773C>G BRCA-US 13 23929123 23929123 single base substitution A C 5_prime_UTR_variant BRCA-US 13 23929123 23929123 single base substitution A C missense_variant V167G 500T>G BRCA-US 13 23929123 23929123 single base substitution A C missense_variant V442G 1325T>G BRCA-US 13 23929123 23929123 single base substitution A C missense_variant V543G 1628T>G BRCA-US 13 23929123 23929123 single base substitution A C upstream_gene_variant BRCA-US 13 23929666 23929666 deletion of <=200bp T - 5_prime_UTR_variant BRCA-US 13 23929666 23929666 deletion of <=200bp T - frameshift_variant K261 BRCA-US 13 23929666 23929666 deletion of <=200bp T - frameshift_variant K362 BRCA-US 13 23929666 23929666 deletion of <=200bp T - upstream_gene_variant BRCA-US 13 23930148 23930148 single base substitution T G splice_acceptor_variant BRCA-US 13 23930148 23930148 single base substitution T G upstream_gene_variant BTCA-JP 13 23905434 23905434 single base substitution T A intron_variant BTCA-JP 13 23905434 23905434 single base substitution T A missense_variant Y3444F 10331A>T BTCA-JP 13 23905434 23905434 single base substitution T A missense_variant Y4194F 12581A>T BTCA-JP 13 23906392 23906392 single base substitution G A intron_variant BTCA-JP 13 23906392 23906392 single base substitution G A missense_variant R3125C 9373C>T BTCA-JP 13 23906392 23906392 single base substitution G A missense_variant R3875C 11623C>T BTCA-JP 13 23907911 23907911 single base substitution C A intron_variant BTCA-JP 13 23907911 23907911 single base substitution C A missense_variant M2618I 7854G>T BTCA-JP 13 23907911 23907911 single base substitution C A missense_variant M3368I 10104G>T BTCA-JP 13 23908468 23908468 single base substitution A G intron_variant BTCA-JP 13 23908468 23908468 single base substitution A G missense_variant S2433P 7297T>C BTCA-JP 13 23908468 23908468 single base substitution A G missense_variant S3183P 9547T>C BTCA-JP 13 23908773 23908773 single base substitution T C intron_variant BTCA-JP 13 23908773 23908773 single base substitution T C missense_variant H2331R 6992A>G BTCA-JP 13 23908773 23908773 single base substitution T C missense_variant H3081R 9242A>G BTCA-JP 13 23909025 23909025 single base substitution C T intron_variant BTCA-JP 13 23909025 23909025 single base substitution C T missense_variant R2247Q 6740G>A BTCA-JP 13 23909025 23909025 single base substitution C T missense_variant R2997Q 8990G>A BTCA-JP 13 23910545 23910545 single base substitution C A intron_variant BTCA-JP 13 23910545 23910545 single base substitution C A missense_variant R1740S 5220G>T BTCA-JP 13 23910545 23910545 single base substitution C A missense_variant R2490S 7470G>T BTCA-JP 13 23911225 23911225 single base substitution T C intron_variant BTCA-JP 13 23911225 23911225 single base substitution T C missense_variant N1514D 4540A>G BTCA-JP 13 23911225 23911225 single base substitution T C missense_variant N2264D 6790A>G BTCA-JP 13 23911900 23911900 single base substitution C T intron_variant BTCA-JP 13 23911900 23911900 single base substitution C T missense_variant E1289K 3865G>A BTCA-JP 13 23911900 23911900 single base substitution C T missense_variant E2039K 6115G>A BTCA-JP 13 23912864 23912864 insertion of <=200bp - T frameshift_variant K1717K? BTCA-JP 13 23912864 23912864 insertion of <=200bp - T frameshift_variant K967K? BTCA-JP 13 23912864 23912864 insertion of <=200bp - T intron_variant BTCA-JP 13 23913082 23913082 single base substitution G A intron_variant BTCA-JP 13 23913082 23913082 single base substitution G A stop_gained R1645* 4933C>T BTCA-JP 13 23913082 23913082 single base substitution G A stop_gained R895* 2683C>T BTCA-JP 13 23913988 23913988 deletion of <=200bp T - frameshift_variant S1343 BTCA-JP 13 23913988 23913988 deletion of <=200bp T - frameshift_variant S593 BTCA-JP 13 23913988 23913988 deletion of <=200bp T - intron_variant BTCA-JP 13 23914575 23914575 single base substitution C T intron_variant BTCA-JP 13 23914575 23914575 single base substitution C T missense_variant G1147E 3440G>A BTCA-JP 13 23914575 23914575 single base substitution C T missense_variant G397E 1190G>A BTCA-JP 13 23914687 23914687 deletion of <=200bp T - frameshift_variant I1110 BTCA-JP 13 23914687 23914687 deletion of <=200bp T - frameshift_variant I360 BTCA-JP 13 23914687 23914687 deletion of <=200bp T - intron_variant BTCA-JP 13 23914762 23914762 single base substitution G C intron_variant BTCA-JP 13 23914762 23914762 single base substitution G C missense_variant H1085D 3253C>G BTCA-JP 13 23914762 23914762 single base substitution G C missense_variant H335D 1003C>G BTCA-JP 13 23927937 23927937 single base substitution A G 5_prime_UTR_variant BTCA-JP 13 23927937 23927937 single base substitution A G exon_variant BTCA-JP 13 23927937 23927937 single base substitution A G synonymous_variant A348A 1044T>C BTCA-JP 13 23927937 23927937 single base substitution A G synonymous_variant A623A 1869T>C BTCA-JP 13 23927937 23927937 single base substitution A G synonymous_variant A724A 2172T>C BTCA-JP 13 23929793 23929793 single base substitution C G 5_prime_UTR_variant BTCA-JP 13 23929793 23929793 single base substitution C G missense_variant V219L 655G>C BTCA-JP 13 23929793 23929793 single base substitution C G missense_variant V320L 958G>C BTCA-JP 13 23929793 23929793 single base substitution C G upstream_gene_variant BTCA-JP 13 23949332 23949332 single base substitution C T 5_prime_UTR_variant BTCA-JP 13 23949332 23949332 single base substitution C T missense_variant D33N 97G>A BTCA-JP 13 23985503 23985503 deletion of <=200bp A - 5_prime_UTR_variant CESC-US 13 23898522 23898522 single base substitution G A downstream_gene_variant CESC-US 13 23905671 23905671 single base substitution G C intron_variant CESC-US 13 23905671 23905671 single base substitution G C missense_variant S3365C 10094C>G CESC-US 13 23905671 23905671 single base substitution G C missense_variant S4115C 12344C>G CESC-US 13 23907093 23907093 single base substitution G C intron_variant CESC-US 13 23907093 23907093 single base substitution G C missense_variant S2891C 8672C>G CESC-US 13 23907093 23907093 single base substitution G C missense_variant S3641C 10922C>G CESC-US 13 23907900 23907900 single base substitution G A intron_variant CESC-US 13 23907900 23907900 single base substitution G A missense_variant S2622L 7865C>T CESC-US 13 23907900 23907900 single base substitution G A missense_variant S3372L 10115C>T CESC-US 13 23908103 23908103 single base substitution G C intron_variant CESC-US 13 23908103 23908103 single base substitution G C synonymous_variant L2554L 7662C>G CESC-US 13 23908103 23908103 single base substitution G C synonymous_variant L3304L 9912C>G CESC-US 13 23909371 23909371 single base substitution G A intron_variant CESC-US 13 23909371 23909371 single base substitution G A missense_variant H2132Y 6394C>T CESC-US 13 23909371 23909371 single base substitution G A missense_variant H2882Y 8644C>T CESC-US 13 23911873 23911873 single base substitution C T intron_variant CESC-US 13 23911873 23911873 single base substitution C T missense_variant E1298K 3892G>A CESC-US 13 23911873 23911873 single base substitution C T missense_variant E2048K 6142G>A CESC-US 13 23913856 23913856 single base substitution G A intron_variant CESC-US 13 23913856 23913856 single base substitution G A missense_variant P1387S 4159C>T CESC-US 13 23913856 23913856 single base substitution G A missense_variant P637S 1909C>T CESC-US 13 23914001 23914001 single base substitution C T intron_variant CESC-US 13 23914001 23914001 single base substitution C T synonymous_variant K1338K 4014G>A CESC-US 13 23914001 23914001 single base substitution C T synonymous_variant K588K 1764G>A CLLE-ES 13 23933864 23933864 single base substitution A G intron_variant CLLE-ES 13 23933864 23933864 single base substitution A G upstream_gene_variant CLLE-ES 13 23947580 23947580 single base substitution G A intron_variant CLLE-ES 13 23947580 23947580 single base substitution G A upstream_gene_variant CLLE-ES 13 23955773 23955773 single base substitution G A intron_variant CLLE-ES 13 23960936 23960936 single base substitution G A intron_variant CLLE-ES 13 23965773 23965773 single base substitution G A intron_variant CLLE-ES 13 23976482 23976482 single base substitution A G intron_variant CLLE-ES 13 23977594 23977594 single base substitution A G intron_variant CLLE-ES 13 23983675 23983675 single base substitution C T intron_variant CLLE-ES 13 23988704 23988704 single base substitution A T intron_variant CLLE-ES 13 23988704 23988704 single base substitution A T upstream_gene_variant CLLE-ES 13 24002168 24002168 single base substitution C T intron_variant COAD-US 13 23904795 23904795 single base substitution C A intron_variant COAD-US 13 23904795 23904795 single base substitution C A missense_variant S3657I 10970G>T COAD-US 13 23904795 23904795 single base substitution C A missense_variant S4407I 13220G>T COAD-US 13 23905382 23905382 single base substitution T G intron_variant COAD-US 13 23905382 23905382 single base substitution T G missense_variant E3461D 10383A>C COAD-US 13 23905382 23905382 single base substitution T G missense_variant E4211D 12633A>C COAD-US 13 23905662 23905662 single base substitution G T intron_variant COAD-US 13 23905662 23905662 single base substitution G T stop_gained S3368* 10103C>A COAD-US 13 23905662 23905662 single base substitution G T stop_gained S4118* 12353C>A COAD-US 13 23906034 23906034 single base substitution G A intron_variant COAD-US 13 23906034 23906034 single base substitution G A missense_variant A3244V 9731C>T COAD-US 13 23906034 23906034 single base substitution G A missense_variant A3994V 11981C>T COAD-US 13 23906754 23906754 single base substitution T A intron_variant COAD-US 13 23906754 23906754 single base substitution T A missense_variant N3004I 9011A>T COAD-US 13 23906754 23906754 single base substitution T A missense_variant N3754I 11261A>T COAD-US 13 23906768 23906768 single base substitution G A intron_variant COAD-US 13 23906768 23906768 single base substitution G A synonymous_variant I2999I 8997C>T COAD-US 13 23906768 23906768 single base substitution G A synonymous_variant I3749I 11247C>T COAD-US 13 23906936 23906936 single base substitution T A intron_variant COAD-US 13 23906936 23906936 single base substitution T A missense_variant Q2943H 8829A>T COAD-US 13 23906936 23906936 single base substitution T A missense_variant Q3693H 11079A>T COAD-US 13 23906965 23906965 single base substitution C T intron_variant COAD-US 13 23906965 23906965 single base substitution C T missense_variant G2934R 8800G>A COAD-US 13 23906965 23906965 single base substitution C T missense_variant G3684R 11050G>A COAD-US 13 23907076 23907076 single base substitution C A intron_variant COAD-US 13 23907076 23907076 single base substitution C A stop_gained E2897* 8689G>T COAD-US 13 23907076 23907076 single base substitution C A stop_gained E3647* 10939G>T COAD-US 13 23907441 23907441 single base substitution A G intron_variant COAD-US 13 23907441 23907441 single base substitution A G missense_variant L2775S 8324T>C COAD-US 13 23907441 23907441 single base substitution A G missense_variant L3525S 10574T>C COAD-US 13 23907634 23907634 single base substitution C A intron_variant COAD-US 13 23907634 23907634 single base substitution C A stop_gained E2711* 8131G>T COAD-US 13 23907634 23907634 single base substitution C A stop_gained E3461* 10381G>T COAD-US 13 23907687 23907687 single base substitution T G intron_variant COAD-US 13 23907687 23907687 single base substitution T G missense_variant K2693T 8078A>C COAD-US 13 23907687 23907687 single base substitution T G missense_variant K3443T 10328A>C COAD-US 13 23907736 23907736 single base substitution C T intron_variant COAD-US 13 23907736 23907736 single base substitution C T missense_variant G2677R 8029G>A COAD-US 13 23907736 23907736 single base substitution C T missense_variant G3427R 10279G>A COAD-US 13 23907796 23907796 single base substitution G T intron_variant COAD-US 13 23907796 23907796 single base substitution G T missense_variant L2657I 7969C>A COAD-US 13 23907796 23907796 single base substitution G T missense_variant L3407I 10219C>A COAD-US 13 23908825 23908825 single base substitution C A intron_variant COAD-US 13 23908825 23908825 single base substitution C A stop_gained E2314* 6940G>T COAD-US 13 23908825 23908825 single base substitution C A stop_gained E3064* 9190G>T COAD-US 13 23909222 23909222 deletion of <=200bp T - frameshift_variant K2181 COAD-US 13 23909222 23909222 deletion of <=200bp T - frameshift_variant K2931 COAD-US 13 23909222 23909222 deletion of <=200bp T - intron_variant COAD-US 13 23909298 23909298 single base substitution C T intron_variant COAD-US 13 23909298 23909298 single base substitution C T missense_variant R2156Q 6467G>A COAD-US 13 23909298 23909298 single base substitution C T missense_variant R2906Q 8717G>A COAD-US 13 23909360 23909360 single base substitution G A intron_variant COAD-US 13 23909360 23909360 single base substitution G A synonymous_variant G2135G 6405C>T COAD-US 13 23909360 23909360 single base substitution G A synonymous_variant G2885G 8655C>T COAD-US 13 23909377 23909377 single base substitution G A intron_variant COAD-US 13 23909377 23909377 single base substitution G A missense_variant P2130S 6388C>T COAD-US 13 23909377 23909377 single base substitution G A missense_variant P2880S 8638C>T COAD-US 13 23909402 23909402 insertion of <=200bp - A frameshift_variant L2121L? COAD-US 13 23909402 23909402 insertion of <=200bp - A frameshift_variant L2871L? COAD-US 13 23909402 23909402 insertion of <=200bp - A intron_variant COAD-US 13 23909753 23909753 single base substitution C A intron_variant COAD-US 13 23909753 23909753 single base substitution C A missense_variant K2004N 6012G>T COAD-US 13 23909753 23909753 single base substitution C A missense_variant K2754N 8262G>T COAD-US 13 23909772 23909772 single base substitution G T intron_variant COAD-US 13 23909772 23909772 single base substitution G T missense_variant S1998Y 5993C>A COAD-US 13 23909772 23909772 single base substitution G T missense_variant S2748Y 8243C>A COAD-US 13 23909874 23909874 single base substitution G A intron_variant COAD-US 13 23909874 23909874 single base substitution G A missense_variant S1964L 5891C>T COAD-US 13 23909874 23909874 single base substitution G A missense_variant S2714L 8141C>T COAD-US 13 23910866 23910866 single base substitution G A intron_variant COAD-US 13 23910866 23910866 single base substitution G A synonymous_variant R1633R 4899C>T COAD-US 13 23910866 23910866 single base substitution G A synonymous_variant R2383R 7149C>T COAD-US 13 23911139 23911139 single base substitution C A intron_variant COAD-US 13 23911139 23911139 single base substitution C A synonymous_variant L1542L 4626G>T COAD-US 13 23911139 23911139 single base substitution C A synonymous_variant L2292L 6876G>T COAD-US 13 23911709 23911709 single base substitution C A intron_variant COAD-US 13 23911709 23911709 single base substitution C A missense_variant L1352F 4056G>T COAD-US 13 23911709 23911709 single base substitution C A missense_variant L2102F 6306G>T COAD-US 13 23911741 23911741 single base substitution G T intron_variant COAD-US 13 23911741 23911741 single base substitution G T missense_variant L1342I 4024C>A COAD-US 13 23911741 23911741 single base substitution G T missense_variant L2092I 6274C>A COAD-US 13 23911828 23911828 insertion of <=200bp - A frameshift_variant P1313L? COAD-US 13 23911828 23911828 insertion of <=200bp - A frameshift_variant P2063L? COAD-US 13 23911828 23911828 insertion of <=200bp - A intron_variant COAD-US 13 23911842 23911842 insertion of <=200bp - A frameshift_variant S1308S? COAD-US 13 23911842 23911842 insertion of <=200bp - A frameshift_variant S2058S? COAD-US 13 23911842 23911842 insertion of <=200bp - A intron_variant COAD-US 13 23911931 23911931 single base substitution T A intron_variant COAD-US 13 23911931 23911931 single base substitution T A missense_variant E1278D 3834A>T COAD-US 13 23911931 23911931 single base substitution T A missense_variant E2028D 6084A>T COAD-US 13 23911949 23911949 single base substitution T C intron_variant COAD-US 13 23911949 23911949 single base substitution T C synonymous_variant K1272K 3816A>G COAD-US 13 23911949 23911949 single base substitution T C synonymous_variant K2022K 6066A>G COAD-US 13 23911996 23911996 single base substitution C A intron_variant COAD-US 13 23911996 23911996 single base substitution C A missense_variant A1257S 3769G>T COAD-US 13 23911996 23911996 single base substitution C A missense_variant A2007S 6019G>T COAD-US 13 23912372 23912372 single base substitution G T intron_variant COAD-US 13 23912372 23912372 single base substitution G T synonymous_variant G1131G 3393C>A COAD-US 13 23912372 23912372 single base substitution G T synonymous_variant G1881G 5643C>A COAD-US 13 23912864 23912864 deletion of <=200bp T - frameshift_variant K1717 COAD-US 13 23912864 23912864 deletion of <=200bp T - frameshift_variant K967 COAD-US 13 23912864 23912864 deletion of <=200bp T - intron_variant COAD-US 13 23913388 23913388 single base substitution C A intron_variant COAD-US 13 23913388 23913388 single base substitution C A stop_gained E1543* 4627G>T COAD-US 13 23913388 23913388 single base substitution C A stop_gained E793* 2377G>T COAD-US 13 23913555 23913555 single base substitution T G intron_variant COAD-US 13 23913555 23913555 single base substitution T G missense_variant D1487A 4460A>C COAD-US 13 23913555 23913555 single base substitution T G missense_variant D737A 2210A>C COAD-US 13 23914152 23914152 single base substitution G A intron_variant COAD-US 13 23914152 23914152 single base substitution G A missense_variant A1288V 3863C>T COAD-US 13 23914152 23914152 single base substitution G A missense_variant A538V 1613C>T COAD-US 13 23915439 23915439 single base substitution A G intron_variant COAD-US 13 23915439 23915439 single base substitution A G missense_variant I109T 326T>C COAD-US 13 23915439 23915439 single base substitution A G missense_variant I859T 2576T>C COAD-US 13 23915453 23915453 deletion of <=200bp T - frameshift_variant K104 COAD-US 13 23915453 23915453 deletion of <=200bp T - frameshift_variant K854 COAD-US 13 23915453 23915453 deletion of <=200bp T - intron_variant COAD-US 13 23929095 23929095 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant COAD-US 13 23929095 23929095 single base substitution T C synonymous_variant L176L 528A>G COAD-US 13 23929095 23929095 single base substitution T C synonymous_variant L451L 1353A>G COAD-US 13 23929095 23929095 single base substitution T C synonymous_variant L552L 1656A>G COAD-US 13 23929095 23929095 single base substitution T C upstream_gene_variant COAD-US 13 23929264 23929264 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant COAD-US 13 23929264 23929264 single base substitution A G missense_variant L120P 359T>C COAD-US 13 23929264 23929264 single base substitution A G missense_variant L395P 1184T>C COAD-US 13 23929264 23929264 single base substitution A G missense_variant L496P 1487T>C COAD-US 13 23929264 23929264 single base substitution A G upstream_gene_variant COAD-US 13 23930055 23930055 single base substitution A T 5_prime_UTR_variant COAD-US 13 23930055 23930055 single base substitution A T missense_variant N131K 393T>A COAD-US 13 23930055 23930055 single base substitution A T missense_variant N232K 696T>A COAD-US 13 23930055 23930055 single base substitution A T upstream_gene_variant COAD-US 13 23932517 23932517 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 13 23932517 23932517 single base substitution G A synonymous_variant V187V 561C>T COAD-US 13 23932517 23932517 single base substitution G A synonymous_variant V86V 258C>T COAD-US 13 23932517 23932517 single base substitution G A upstream_gene_variant COAD-US 13 23942607 23942607 single base substitution C T 5_prime_UTR_variant COAD-US 13 23942607 23942607 single base substitution C T synonymous_variant T93T 279G>A COAD-US 13 23942607 23942607 single base substitution C T upstream_gene_variant COAD-US 13 23945307 23945307 insertion of <=200bp - A intron_variant COAD-US 13 23945307 23945307 insertion of <=200bp - A splice_region_variant COAD-US 13 23945307 23945307 insertion of <=200bp - A upstream_gene_variant COAD-US 13 23945308 23945308 deletion of <=200bp A - intron_variant COAD-US 13 23945308 23945308 deletion of <=200bp A - splice_region_variant COAD-US 13 23945308 23945308 deletion of <=200bp A - upstream_gene_variant COCA-CN 13 23905102 23905102 single base substitution C A intron_variant COCA-CN 13 23905102 23905102 single base substitution C A stop_gained E3555* 10663G>T COCA-CN 13 23905102 23905102 single base substitution C A stop_gained E4305* 12913G>T COCA-CN 13 23905111 23905111 single base substitution A C intron_variant COCA-CN 13 23905111 23905111 single base substitution A C missense_variant S3552A 10654T>G COCA-CN 13 23905111 23905111 single base substitution A C missense_variant S4302A 12904T>G COCA-CN 13 23906234 23906234 single base substitution C T intron_variant COCA-CN 13 23906234 23906234 single base substitution C T synonymous_variant A3177A 9531G>A COCA-CN 13 23906234 23906234 single base substitution C T synonymous_variant A3927A 11781G>A COCA-CN 13 23906239 23906239 single base substitution C T intron_variant COCA-CN 13 23906239 23906239 single base substitution C T missense_variant D3176N 9526G>A COCA-CN 13 23906239 23906239 single base substitution C T missense_variant D3926N 11776G>A COCA-CN 13 23906590 23906590 single base substitution C A intron_variant COCA-CN 13 23906590 23906590 single base substitution C A stop_gained E3059* 9175G>T COCA-CN 13 23906590 23906590 single base substitution C A stop_gained E3809* 11425G>T COCA-CN 13 23906723 23906723 single base substitution T G intron_variant COCA-CN 13 23906723 23906723 single base substitution T G missense_variant E3014D 9042A>C COCA-CN 13 23906723 23906723 single base substitution T G missense_variant E3764D 11292A>C COCA-CN 13 23906738 23906738 single base substitution C T intron_variant COCA-CN 13 23906738 23906738 single base substitution C T synonymous_variant T3009T 9027G>A COCA-CN 13 23906738 23906738 single base substitution C T synonymous_variant T3759T 11277G>A COCA-CN 13 23907043 23907043 single base substitution G A intron_variant COCA-CN 13 23907043 23907043 single base substitution G A missense_variant R2908W 8722C>T COCA-CN 13 23907043 23907043 single base substitution G A missense_variant R3658W 10972C>T COCA-CN 13 23907078 23907078 single base substitution T G intron_variant COCA-CN 13 23907078 23907078 single base substitution T G missense_variant K2896T 8687A>C COCA-CN 13 23907078 23907078 single base substitution T G missense_variant K3646T 10937A>C COCA-CN 13 23907674 23907674 single base substitution T C intron_variant COCA-CN 13 23907674 23907674 single base substitution T C synonymous_variant S2697S 8091A>G COCA-CN 13 23907674 23907674 single base substitution T C synonymous_variant S3447S 10341A>G COCA-CN 13 23907724 23907724 single base substitution C T intron_variant COCA-CN 13 23907724 23907724 single base substitution C T missense_variant V2681I 8041G>A COCA-CN 13 23907724 23907724 single base substitution C T missense_variant V3431I 10291G>A COCA-CN 13 23908237 23908237 single base substitution C A intron_variant COCA-CN 13 23908237 23908237 single base substitution C A missense_variant D2510Y 7528G>T COCA-CN 13 23908237 23908237 single base substitution C A missense_variant D3260Y 9778G>T COCA-CN 13 23911010 23911010 single base substitution C T intron_variant COCA-CN 13 23911010 23911010 single base substitution C T missense_variant M1585I 4755G>A COCA-CN 13 23911010 23911010 single base substitution C T missense_variant M2335I 7005G>A COCA-CN 13 23911431 23911431 single base substitution T C intron_variant COCA-CN 13 23911431 23911431 single base substitution T C missense_variant K1445R 4334A>G COCA-CN 13 23911431 23911431 single base substitution T C missense_variant K2195R 6584A>G COCA-CN 13 23911856 23911856 single base substitution C A intron_variant COCA-CN 13 23911856 23911856 single base substitution C A missense_variant E1303D 3909G>T COCA-CN 13 23911856 23911856 single base substitution C A missense_variant E2053D 6159G>T COCA-CN 13 23912095 23912095 single base substitution C A intron_variant COCA-CN 13 23912095 23912095 single base substitution C A stop_gained E1224* 3670G>T COCA-CN 13 23912095 23912095 single base substitution C A stop_gained E1974* 5920G>T COCA-CN 13 23912798 23912798 single base substitution C A intron_variant COCA-CN 13 23912798 23912798 single base substitution C A missense_variant M1739I 5217G>T COCA-CN 13 23912798 23912798 single base substitution C A missense_variant M989I 2967G>T COCA-CN 13 23913032 23913032 single base substitution A G intron_variant COCA-CN 13 23913032 23913032 single base substitution A G synonymous_variant S1661S 4983T>C COCA-CN 13 23913032 23913032 single base substitution A G synonymous_variant S911S 2733T>C COCA-CN 13 23913069 23913069 single base substitution C A intron_variant COCA-CN 13 23913069 23913069 single base substitution C A missense_variant R1649I 4946G>T COCA-CN 13 23913069 23913069 single base substitution C A missense_variant R899I 2696G>T COCA-CN 13 23913516 23913516 single base substitution C T intron_variant COCA-CN 13 23913516 23913516 single base substitution C T missense_variant R1500K 4499G>A COCA-CN 13 23913516 23913516 single base substitution C T missense_variant R750K 2249G>A COCA-CN 13 23913643 23913643 single base substitution C A intron_variant COCA-CN 13 23913643 23913643 single base substitution C A stop_gained E1458* 4372G>T COCA-CN 13 23913643 23913643 single base substitution C A stop_gained E708* 2122G>T COCA-CN 13 23914583 23914583 single base substitution T C intron_variant COCA-CN 13 23914583 23914583 single base substitution T C synonymous_variant S1144S 3432A>G COCA-CN 13 23914583 23914583 single base substitution T C synonymous_variant S394S 1182A>G COCA-CN 13 23915248 23915248 single base substitution C A intron_variant COCA-CN 13 23915248 23915248 single base substitution C A stop_gained E173* 517G>T COCA-CN 13 23915248 23915248 single base substitution C A stop_gained E923* 2767G>T COCA-CN 13 23915496 23915496 single base substitution A C intron_variant COCA-CN 13 23915496 23915496 single base substitution A C stop_gained L840* 2519T>G COCA-CN 13 23915496 23915496 single base substitution A C stop_gained L90* 269T>G COCA-CN 13 23915762 23915762 single base substitution C A intron_variant COCA-CN 13 23915762 23915762 single base substitution C A missense_variant M650I 1950G>T COCA-CN 13 23915762 23915762 single base substitution C A missense_variant M751I 2253G>T COCA-CN 13 23915762 23915762 single base substitution C A start_lost M1I 3G>T COCA-CN 13 23915776 23915776 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 13 23915776 23915776 single base substitution T C intron_variant COCA-CN 13 23915776 23915776 single base substitution T C missense_variant I646V 1936A>G COCA-CN 13 23915776 23915776 single base substitution T C missense_variant I747V 2239A>G COCA-CN 13 23928089 23928089 single base substitution T C intron_variant COCA-CN 13 23928982 23928982 single base substitution A G 5_prime_UTR_variant COCA-CN 13 23928982 23928982 single base substitution A G exon_variant COCA-CN 13 23928982 23928982 single base substitution A G missense_variant V214A 641T>C COCA-CN 13 23928982 23928982 single base substitution A G missense_variant V489A 1466T>C COCA-CN 13 23928982 23928982 single base substitution A G missense_variant V590A 1769T>C COCA-CN 13 23929330 23929330 single base substitution C T 5_prime_UTR_variant COCA-CN 13 23929330 23929330 single base substitution C T missense_variant R373H 1118G>A COCA-CN 13 23929330 23929330 single base substitution C T missense_variant R474H 1421G>A COCA-CN 13 23929330 23929330 single base substitution C T missense_variant R98H 293G>A COCA-CN 13 23929330 23929330 single base substitution C T upstream_gene_variant COCA-CN 13 23929331 23929331 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 13 23929331 23929331 single base substitution G A missense_variant R373C 1117C>T COCA-CN 13 23929331 23929331 single base substitution G A missense_variant R474C 1420C>T COCA-CN 13 23929331 23929331 single base substitution G A missense_variant R98C 292C>T COCA-CN 13 23929331 23929331 single base substitution G A upstream_gene_variant COCA-CN 13 23945089 23945089 single base substitution C T intron_variant COCA-CN 13 23945089 23945089 single base substitution C T upstream_gene_variant COCA-CN 13 23945167 23945167 single base substitution C A intron_variant COCA-CN 13 23945167 23945167 single base substitution C A upstream_gene_variant COCA-CN 13 23949399 23949399 single base substitution C T 5_prime_UTR_variant COCA-CN 13 23949399 23949399 single base substitution C T synonymous_variant P10P 30G>A COCA-CN 13 23984539 23984539 single base substitution A T intron_variant COCA-CN 13 23985516 23985516 single base substitution T G 5_prime_UTR_variant COCA-CN 13 23985542 23985542 single base substitution C A 5_prime_UTR_variant COCA-CN 13 23993107 23993107 single base substitution G A intron_variant EOPC-DE 13 24001973 24001973 single base substitution C A intron_variant ESAD-UK 13 23899177 23899177 single base substitution A C downstream_gene_variant ESAD-UK 13 23900758 23900758 single base substitution A C downstream_gene_variant ESAD-UK 13 23900997 23900997 single base substitution T G downstream_gene_variant ESAD-UK 13 23901081 23901081 single base substitution G A downstream_gene_variant ESAD-UK 13 23901238 23901238 single base substitution C T downstream_gene_variant ESAD-UK 13 23902332 23902332 single base substitution G T downstream_gene_variant ESAD-UK 13 23902367 23902367 single base substitution T G downstream_gene_variant ESAD-UK 13 23903046 23903046 single base substitution A T 3_prime_UTR_variant ESAD-UK 13 23903650 23903650 single base substitution A T 3_prime_UTR_variant ESAD-UK 13 23903650 23903650 single base substitution A T intron_variant ESAD-UK 13 23903688 23903688 single base substitution A C 3_prime_UTR_variant ESAD-UK 13 23903688 23903688 single base substitution A C intron_variant ESAD-UK 13 23903814 23903814 single base substitution C T 3_prime_UTR_variant ESAD-UK 13 23903814 23903814 single base substitution C T intron_variant ESAD-UK 13 23904255 23904255 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 13 23904255 23904255 deletion of <=200bp T - intron_variant ESAD-UK 13 23904305 23904305 deletion of <=200bp T - frameshift_variant K3820 ESAD-UK 13 23904305 23904305 deletion of <=200bp T - frameshift_variant K4570 ESAD-UK 13 23904305 23904305 deletion of <=200bp T - intron_variant ESAD-UK 13 23904762 23904762 single base substitution T C intron_variant ESAD-UK 13 23904762 23904762 single base substitution T C missense_variant E3668G 11003A>G ESAD-UK 13 23904762 23904762 single base substitution T C missense_variant E4418G 13253A>G ESAD-UK 13 23905151 23905151 single base substitution A C intron_variant ESAD-UK 13 23905151 23905151 single base substitution A C synonymous_variant T3538T 10614T>G ESAD-UK 13 23905151 23905151 single base substitution A C synonymous_variant T4288T 12864T>G ESAD-UK 13 23905608 23905608 single base substitution A C intron_variant ESAD-UK 13 23905608 23905608 single base substitution A C missense_variant L3386R 10157T>G ESAD-UK 13 23905608 23905608 single base substitution A C missense_variant L4136R 12407T>G ESAD-UK 13 23905608 23905608 single base substitution A G intron_variant ESAD-UK 13 23905608 23905608 single base substitution A G missense_variant L3386P 10157T>C ESAD-UK 13 23905608 23905608 single base substitution A G missense_variant L4136P 12407T>C ESAD-UK 13 23906164 23906164 single base substitution A T intron_variant ESAD-UK 13 23906164 23906164 single base substitution A T missense_variant L3201I 9601T>A ESAD-UK 13 23906164 23906164 single base substitution A T missense_variant L3951I 11851T>A ESAD-UK 13 23907199 23907199 single base substitution C T intron_variant ESAD-UK 13 23907199 23907199 single base substitution C T missense_variant E2856K 8566G>A ESAD-UK 13 23907199 23907199 single base substitution C T missense_variant E3606K 10816G>A ESAD-UK 13 23907902 23907902 single base substitution A C intron_variant ESAD-UK 13 23907902 23907902 single base substitution A C synonymous_variant T2621T 7863T>G ESAD-UK 13 23907902 23907902 single base substitution A C synonymous_variant T3371T 10113T>G ESAD-UK 13 23908327 23908327 single base substitution T G intron_variant ESAD-UK 13 23908327 23908327 single base substitution T G missense_variant S2480R 7438A>C ESAD-UK 13 23908327 23908327 single base substitution T G missense_variant S3230R 9688A>C ESAD-UK 13 23908419 23908419 single base substitution A G intron_variant ESAD-UK 13 23908419 23908419 single base substitution A G missense_variant I2449T 7346T>C ESAD-UK 13 23908419 23908419 single base substitution A G missense_variant I3199T 9596T>C ESAD-UK 13 23908500 23908500 single base substitution T G intron_variant ESAD-UK 13 23908500 23908500 single base substitution T G missense_variant K2422T 7265A>C ESAD-UK 13 23908500 23908500 single base substitution T G missense_variant K3172T 9515A>C ESAD-UK 13 23908583 23908583 single base substitution T G intron_variant ESAD-UK 13 23908583 23908583 single base substitution T G missense_variant E2394D 7182A>C ESAD-UK 13 23908583 23908583 single base substitution T G missense_variant E3144D 9432A>C ESAD-UK 13 23908823 23908823 single base substitution T C intron_variant ESAD-UK 13 23908823 23908823 single base substitution T C synonymous_variant E2314E 6942A>G ESAD-UK 13 23908823 23908823 single base substitution T C synonymous_variant E3064E 9192A>G ESAD-UK 13 23911286 23911286 single base substitution A G intron_variant ESAD-UK 13 23911286 23911286 single base substitution A G synonymous_variant T1493T 4479T>C ESAD-UK 13 23911286 23911286 single base substitution A G synonymous_variant T2243T 6729T>C ESAD-UK 13 23912523 23912523 single base substitution T G intron_variant ESAD-UK 13 23912523 23912523 single base substitution T G missense_variant K1081T 3242A>C ESAD-UK 13 23912523 23912523 single base substitution T G missense_variant K1831T 5492A>C ESAD-UK 13 23912749 23912749 single base substitution A G intron_variant ESAD-UK 13 23912749 23912749 single base substitution A G missense_variant S1006P 3016T>C ESAD-UK 13 23912749 23912749 single base substitution A G missense_variant S1756P 5266T>C ESAD-UK 13 23913438 23913438 single base substitution T C intron_variant ESAD-UK 13 23913438 23913438 single base substitution T C missense_variant N1526S 4577A>G ESAD-UK 13 23913438 23913438 single base substitution T C missense_variant N776S 2327A>G ESAD-UK 13 23913454 23913454 single base substitution C G intron_variant ESAD-UK 13 23913454 23913454 single base substitution C G missense_variant A1521P 4561G>C ESAD-UK 13 23913454 23913454 single base substitution C G missense_variant A771P 2311G>C ESAD-UK 13 23913803 23913803 single base substitution T C intron_variant ESAD-UK 13 23913803 23913803 single base substitution T C synonymous_variant K1404K 4212A>G ESAD-UK 13 23913803 23913803 single base substitution T C synonymous_variant K654K 1962A>G ESAD-UK 13 23913846 23913846 single base substitution A C intron_variant ESAD-UK 13 23913846 23913846 single base substitution A C missense_variant L1390R 4169T>G ESAD-UK 13 23913846 23913846 single base substitution A C missense_variant L640R 1919T>G ESAD-UK 13 23914342 23914342 single base substitution A C intron_variant ESAD-UK 13 23914342 23914342 single base substitution A C missense_variant L1225V 3673T>G ESAD-UK 13 23914342 23914342 single base substitution A C missense_variant L475V 1423T>G ESAD-UK 13 23915133 23915133 single base substitution C T intron_variant ESAD-UK 13 23915133 23915133 single base substitution C T missense_variant R211Q 632G>A ESAD-UK 13 23915133 23915133 single base substitution C T missense_variant R961Q 2882G>A ESAD-UK 13 23916573 23916573 single base substitution A G intron_variant ESAD-UK 13 23918127 23918127 single base substitution C T intron_variant ESAD-UK 13 23918318 23918318 deletion of <=200bp A - intron_variant ESAD-UK 13 23918837 23918837 single base substitution A G intron_variant ESAD-UK 13 23919404 23919404 single base substitution A G intron_variant ESAD-UK 13 23919608 23919608 single base substitution T G intron_variant ESAD-UK 13 23919640 23919640 single base substitution T G intron_variant ESAD-UK 13 23921233 23921233 single base substitution A T intron_variant ESAD-UK 13 23925153 23925153 single base substitution C T downstream_gene_variant ESAD-UK 13 23925153 23925153 single base substitution C T intron_variant ESAD-UK 13 23925663 23925663 single base substitution T C downstream_gene_variant ESAD-UK 13 23925663 23925663 single base substitution T C intron_variant ESAD-UK 13 23925895 23925895 single base substitution C G downstream_gene_variant ESAD-UK 13 23925895 23925895 single base substitution C G intron_variant ESAD-UK 13 23927009 23927009 single base substitution C A downstream_gene_variant ESAD-UK 13 23927009 23927009 single base substitution C A intron_variant ESAD-UK 13 23927010 23927010 single base substitution T G downstream_gene_variant ESAD-UK 13 23927010 23927010 single base substitution T G intron_variant ESAD-UK 13 23927351 23927351 single base substitution G A downstream_gene_variant ESAD-UK 13 23927351 23927351 single base substitution G A intron_variant ESAD-UK 13 23928295 23928295 single base substitution T C intron_variant ESAD-UK 13 23931398 23931398 single base substitution A G intron_variant ESAD-UK 13 23931398 23931398 single base substitution A G upstream_gene_variant ESAD-UK 13 23931452 23931452 single base substitution C T intron_variant ESAD-UK 13 23931452 23931452 single base substitution C T upstream_gene_variant ESAD-UK 13 23938437 23938437 single base substitution C A intron_variant ESAD-UK 13 23940276 23940276 single base substitution T G intron_variant ESAD-UK 13 23940519 23940519 single base substitution A C intron_variant ESAD-UK 13 23941335 23941335 single base substitution T G intron_variant ESAD-UK 13 23941632 23941632 single base substitution C A intron_variant ESAD-UK 13 23941825 23941825 single base substitution C T intron_variant ESAD-UK 13 23941952 23941952 single base substitution C A intron_variant ESAD-UK 13 23943497 23943497 single base substitution A T intron_variant ESAD-UK 13 23943497 23943497 single base substitution A T upstream_gene_variant ESAD-UK 13 23943850 23943850 single base substitution A C intron_variant ESAD-UK 13 23943850 23943850 single base substitution A C upstream_gene_variant ESAD-UK 13 23943862 23943862 single base substitution T C intron_variant ESAD-UK 13 23943862 23943862 single base substitution T C upstream_gene_variant ESAD-UK 13 23945011 23945011 single base substitution A C intron_variant ESAD-UK 13 23945011 23945011 single base substitution A C upstream_gene_variant ESAD-UK 13 23945802 23945802 single base substitution A G intron_variant ESAD-UK 13 23945802 23945802 single base substitution A G upstream_gene_variant ESAD-UK 13 23947854 23947854 single base substitution G A intron_variant ESAD-UK 13 23950646 23950646 deletion of <=200bp A - intron_variant ESAD-UK 13 23950646 23950646 deletion of <=200bp A - upstream_gene_variant ESAD-UK 13 23952211 23952211 deletion of <=200bp T - intron_variant ESAD-UK 13 23952211 23952211 deletion of <=200bp T - upstream_gene_variant ESAD-UK 13 23952375 23952375 single base substitution G A intron_variant ESAD-UK 13 23952375 23952375 single base substitution G A upstream_gene_variant ESAD-UK 13 23952434 23952434 single base substitution A G intron_variant ESAD-UK 13 23952434 23952434 single base substitution A G upstream_gene_variant ESAD-UK 13 23953024 23953024 single base substitution T A intron_variant ESAD-UK 13 23953024 23953024 single base substitution T A upstream_gene_variant ESAD-UK 13 23953753 23953753 single base substitution C A intron_variant ESAD-UK 13 23953753 23953753 single base substitution C A upstream_gene_variant ESAD-UK 13 23953813 23953813 single base substitution T A intron_variant ESAD-UK 13 23953813 23953813 single base substitution T A upstream_gene_variant ESAD-UK 13 23954788 23954788 single base substitution G A intron_variant ESAD-UK 13 23955104 23955104 single base substitution T C intron_variant ESAD-UK 13 23955429 23955429 single base substitution G C intron_variant ESAD-UK 13 23956928 23956928 single base substitution G T intron_variant ESAD-UK 13 23958179 23958179 single base substitution A C intron_variant ESAD-UK 13 23958276 23958276 single base substitution G A intron_variant ESAD-UK 13 23958295 23958295 single base substitution C T intron_variant ESAD-UK 13 23958633 23958633 single base substitution T A intron_variant ESAD-UK 13 23958908 23958908 deletion of <=200bp T - intron_variant ESAD-UK 13 23959602 23959602 single base substitution G A intron_variant ESAD-UK 13 23959749 23959749 single base substitution G A intron_variant ESAD-UK 13 23959871 23959871 single base substitution C T intron_variant ESAD-UK 13 23962390 23962390 single base substitution G A intron_variant ESAD-UK 13 23962802 23962802 single base substitution A C intron_variant ESAD-UK 13 23963555 23963555 single base substitution T C intron_variant ESAD-UK 13 23964376 23964376 single base substitution A G intron_variant ESAD-UK 13 23964539 23964539 single base substitution T G intron_variant ESAD-UK 13 23965157 23965157 single base substitution C T intron_variant ESAD-UK 13 23965599 23965599 single base substitution A C intron_variant ESAD-UK 13 23966804 23966804 single base substitution A C intron_variant ESAD-UK 13 23966836 23966836 single base substitution A C intron_variant ESAD-UK 13 23967026 23967026 single base substitution A G intron_variant ESAD-UK 13 23967212 23967212 single base substitution C T intron_variant ESAD-UK 13 23967602 23967602 single base substitution C T intron_variant ESAD-UK 13 23967728 23967728 single base substitution T G intron_variant ESAD-UK 13 23968326 23968326 single base substitution A G intron_variant ESAD-UK 13 23971272 23971272 single base substitution A C intron_variant ESAD-UK 13 23972057 23972057 single base substitution G A intron_variant ESAD-UK 13 23974088 23974088 single base substitution T C intron_variant ESAD-UK 13 23974446 23974446 single base substitution T G intron_variant ESAD-UK 13 23975186 23975186 single base substitution T A intron_variant ESAD-UK 13 23975194 23975194 single base substitution T C intron_variant ESAD-UK 13 23975281 23975281 single base substitution T C intron_variant ESAD-UK 13 23975287 23975287 single base substitution C A intron_variant ESAD-UK 13 23975621 23975621 single base substitution T G intron_variant ESAD-UK 13 23976051 23976051 single base substitution G T intron_variant ESAD-UK 13 23976889 23976889 single base substitution A C intron_variant ESAD-UK 13 23977725 23977725 single base substitution C A intron_variant ESAD-UK 13 23978246 23978246 single base substitution A T intron_variant ESAD-UK 13 23978489 23978489 single base substitution A G intron_variant ESAD-UK 13 23979848 23979848 single base substitution C A intron_variant ESAD-UK 13 23979942 23979942 single base substitution G T intron_variant ESAD-UK 13 23980135 23980135 single base substitution A G intron_variant ESAD-UK 13 23981677 23981677 single base substitution A G intron_variant ESAD-UK 13 23983101 23983101 insertion of <=200bp - A intron_variant ESAD-UK 13 23984193 23984193 insertion of <=200bp - A intron_variant ESAD-UK 13 23984625 23984625 single base substitution A C intron_variant ESAD-UK 13 23987242 23987242 single base substitution G C intron_variant ESAD-UK 13 23987242 23987242 single base substitution G C upstream_gene_variant ESAD-UK 13 23987413 23987413 single base substitution G C intron_variant ESAD-UK 13 23987413 23987413 single base substitution G C upstream_gene_variant ESAD-UK 13 23987906 23987906 single base substitution A C intron_variant ESAD-UK 13 23987906 23987906 single base substitution A C upstream_gene_variant ESAD-UK 13 23987908 23987908 single base substitution C A intron_variant ESAD-UK 13 23987908 23987908 single base substitution C A upstream_gene_variant ESAD-UK 13 23988979 23988979 single base substitution C A intron_variant ESAD-UK 13 23988979 23988979 single base substitution C A upstream_gene_variant ESAD-UK 13 23989735 23989735 single base substitution C A intron_variant ESAD-UK 13 23989735 23989735 single base substitution C A upstream_gene_variant ESAD-UK 13 23989833 23989833 single base substitution T A intron_variant ESAD-UK 13 23989833 23989833 single base substitution T A upstream_gene_variant ESAD-UK 13 23990969 23990969 single base substitution G A intron_variant ESAD-UK 13 23991363 23991363 insertion of <=200bp - G intron_variant ESAD-UK 13 23992052 23992052 single base substitution A G intron_variant ESAD-UK 13 23993667 23993667 single base substitution G A intron_variant ESAD-UK 13 23994491 23994491 single base substitution A C intron_variant ESAD-UK 13 23995685 23995685 single base substitution C T intron_variant ESAD-UK 13 23997437 23997437 single base substitution G A intron_variant ESAD-UK 13 23998589 23998589 single base substitution G A intron_variant ESAD-UK 13 23999656 23999656 single base substitution C A intron_variant ESAD-UK 13 23999974 23999974 single base substitution C T intron_variant ESAD-UK 13 24001693 24001693 single base substitution C T intron_variant ESAD-UK 13 24002009 24002009 single base substitution G A intron_variant ESAD-UK 13 24003003 24003003 single base substitution A G intron_variant ESAD-UK 13 24003946 24003946 single base substitution G A intron_variant ESAD-UK 13 24004178 24004178 single base substitution C T intron_variant ESAD-UK 13 24004563 24004563 single base substitution A C intron_variant ESAD-UK 13 24005828 24005828 single base substitution G T intron_variant ESAD-UK 13 24006154 24006154 single base substitution C G intron_variant ESAD-UK 13 24007192 24007192 single base substitution A C intron_variant ESAD-UK 13 24009444 24009444 single base substitution G T upstream_gene_variant ESAD-UK 13 24010056 24010056 single base substitution C T upstream_gene_variant ESAD-UK 13 24010294 24010294 single base substitution T C upstream_gene_variant ESAD-UK 13 24010661 24010661 single base substitution A C upstream_gene_variant ESAD-UK 13 24010662 24010662 single base substitution C T upstream_gene_variant ESAD-UK 13 24012046 24012046 single base substitution T G upstream_gene_variant ESCA-CN 13 23903651 23903651 single base substitution T A 3_prime_UTR_variant ESCA-CN 13 23903651 23903651 single base substitution T A intron_variant ESCA-CN 13 23904320 23904320 single base substitution G A intron_variant ESCA-CN 13 23904320 23904320 single base substitution G A synonymous_variant A3815A 11445C>T ESCA-CN 13 23904320 23904320 single base substitution G A synonymous_variant A4565A 13695C>T ESCA-CN 13 23906785 23906785 single base substitution G A intron_variant ESCA-CN 13 23906785 23906785 single base substitution G A missense_variant P2994S 8980C>T ESCA-CN 13 23906785 23906785 single base substitution G A missense_variant P3744S 11230C>T ESCA-CN 13 23908872 23908872 single base substitution C T intron_variant ESCA-CN 13 23908872 23908872 single base substitution C T missense_variant R2298H 6893G>A ESCA-CN 13 23908872 23908872 single base substitution C T missense_variant R3048H 9143G>A ESCA-CN 13 23909116 23909116 single base substitution G A intron_variant ESCA-CN 13 23909116 23909116 single base substitution G A missense_variant R2217C 6649C>T ESCA-CN 13 23909116 23909116 single base substitution G A missense_variant R2967C 8899C>T ESCA-CN 13 23909201 23909201 single base substitution A G intron_variant ESCA-CN 13 23909201 23909201 single base substitution A G synonymous_variant D2188D 6564T>C ESCA-CN 13 23909201 23909201 single base substitution A G synonymous_variant D2938D 8814T>C ESCA-CN 13 23910607 23910607 single base substitution C T intron_variant ESCA-CN 13 23910607 23910607 single base substitution C T missense_variant D1720N 5158G>A ESCA-CN 13 23910607 23910607 single base substitution C T missense_variant D2470N 7408G>A ESCA-CN 13 23911197 23911197 single base substitution G A intron_variant ESCA-CN 13 23911197 23911197 single base substitution G A missense_variant S1523L 4568C>T ESCA-CN 13 23911197 23911197 single base substitution G A missense_variant S2273L 6818C>T ESCA-CN 13 23913303 23913303 single base substitution A T intron_variant ESCA-CN 13 23913303 23913303 single base substitution A T missense_variant I1571N 4712T>A ESCA-CN 13 23913303 23913303 single base substitution A T missense_variant I821N 2462T>A ESCA-CN 13 23914869 23914869 single base substitution G A intron_variant ESCA-CN 13 23914869 23914869 single base substitution G A missense_variant S1049L 3146C>T ESCA-CN 13 23914869 23914869 single base substitution G A missense_variant S299L 896C>T ESCA-CN 13 23942548 23942548 single base substitution A G 5_prime_UTR_variant ESCA-CN 13 23942548 23942548 single base substitution A G missense_variant I113T 338T>C ESCA-CN 13 23942548 23942548 single base substitution A G missense_variant I12T 35T>C GBM-US 13 23908788 23908788 single base substitution G T intron_variant GBM-US 13 23908788 23908788 single base substitution G T missense_variant T2326N 6977C>A GBM-US 13 23908788 23908788 single base substitution G T missense_variant T3076N 9227C>A GBM-US 13 23911703 23911703 single base substitution C T intron_variant GBM-US 13 23911703 23911703 single base substitution C T synonymous_variant G1354G 4062G>A GBM-US 13 23911703 23911703 single base substitution C T synonymous_variant G2104G 6312G>A GBM-US 13 23912431 23912431 single base substitution T C intron_variant GBM-US 13 23912431 23912431 single base substitution T C missense_variant T1112A 3334A>G GBM-US 13 23912431 23912431 single base substitution T C missense_variant T1862A 5584A>G GBM-US 13 23913301 23913301 single base substitution T C intron_variant GBM-US 13 23913301 23913301 single base substitution T C missense_variant I1572V 4714A>G GBM-US 13 23913301 23913301 single base substitution T C missense_variant I822V 2464A>G GBM-US 13 23914687 23914687 deletion of <=200bp T - frameshift_variant I1110 GBM-US 13 23914687 23914687 deletion of <=200bp T - frameshift_variant I360 GBM-US 13 23914687 23914687 deletion of <=200bp T - intron_variant GBM-US 13 23928995 23928995 single base substitution A G 5_prime_UTR_variant GBM-US 13 23928995 23928995 single base substitution A G exon_variant GBM-US 13 23928995 23928995 single base substitution A G missense_variant Y210H 628T>C GBM-US 13 23928995 23928995 single base substitution A G missense_variant Y485H 1453T>C GBM-US 13 23928995 23928995 single base substitution A G missense_variant Y586H 1756T>C GBM-US 13 23942617 23942617 single base substitution C A 5_prime_UTR_variant GBM-US 13 23942617 23942617 single base substitution C A missense_variant G90V 269G>T GBM-US 13 23942617 23942617 single base substitution C A upstream_gene_variant KIRC-US 13 23904812 23904812 single base substitution C A intron_variant KIRC-US 13 23904812 23904812 single base substitution C A missense_variant W3651C 10953G>T KIRC-US 13 23904812 23904812 single base substitution C A missense_variant W4401C 13203G>T KIRC-US 13 23906942 23906942 single base substitution G A intron_variant KIRC-US 13 23906942 23906942 single base substitution G A synonymous_variant F2941F 8823C>T KIRC-US 13 23906942 23906942 single base substitution G A synonymous_variant F3691F 11073C>T KIRC-US 13 23907922 23907922 single base substitution G C intron_variant KIRC-US 13 23907922 23907922 single base substitution G C missense_variant L2615V 7843C>G KIRC-US 13 23907922 23907922 single base substitution G C missense_variant L3365V 10093C>G KIRC-US 13 23909182 23909182 single base substitution G T intron_variant KIRC-US 13 23909182 23909182 single base substitution G T missense_variant Q2195K 6583C>A KIRC-US 13 23909182 23909182 single base substitution G T missense_variant Q2945K 8833C>A KIRC-US 13 23912564 23912564 single base substitution C T intron_variant KIRC-US 13 23912564 23912564 single base substitution C T synonymous_variant T1067T 3201G>A KIRC-US 13 23912564 23912564 single base substitution C T synonymous_variant T1817T 5451G>A KIRC-US 13 23914058 23914058 single base substitution C G intron_variant KIRC-US 13 23914058 23914058 single base substitution C G missense_variant K1319N 3957G>C KIRC-US 13 23914058 23914058 single base substitution C G missense_variant K569N 1707G>C KIRC-US 13 23914059 23914059 single base substitution T G intron_variant KIRC-US 13 23914059 23914059 single base substitution T G missense_variant K1319T 3956A>C KIRC-US 13 23914059 23914059 single base substitution T G missense_variant K569T 1706A>C KIRC-US 13 23915483 23915483 single base substitution T G intron_variant KIRC-US 13 23915483 23915483 single base substitution T G synonymous_variant V844V 2532A>C KIRC-US 13 23915483 23915483 single base substitution T G synonymous_variant V94V 282A>C KIRP-US 13 23906370 23906370 insertion of <=200bp - A frameshift_variant S3132S? KIRP-US 13 23906370 23906370 insertion of <=200bp - A frameshift_variant S3882S? KIRP-US 13 23906370 23906370 insertion of <=200bp - A intron_variant KIRP-US 13 23906994 23906994 single base substitution T C intron_variant KIRP-US 13 23906994 23906994 single base substitution T C missense_variant N2924S 8771A>G KIRP-US 13 23906994 23906994 single base substitution T C missense_variant N3674S 11021A>G KIRP-US 13 23909472 23909472 single base substitution A T intron_variant KIRP-US 13 23909472 23909472 single base substitution A T missense_variant F2098Y 6293T>A KIRP-US 13 23909472 23909472 single base substitution A T missense_variant F2848Y 8543T>A LAML-CN 13 23910893 23910893 single base substitution C A intron_variant LAML-CN 13 23910893 23910893 single base substitution C A missense_variant L1624F 4872G>T LAML-CN 13 23910893 23910893 single base substitution C A missense_variant L2374F 7122G>T LAML-KR 13 23898489 23898489 single base substitution T C downstream_gene_variant LAML-KR 13 23908034 23908034 single base substitution A G intron_variant LAML-KR 13 23908034 23908034 single base substitution A G synonymous_variant A2577A 7731T>C LAML-KR 13 23908034 23908034 single base substitution A G synonymous_variant A3327A 9981T>C LAML-KR 13 23937265 23937265 single base substitution C T intron_variant LAML-KR 13 23937271 23937271 single base substitution T C intron_variant LAML-KR 13 23937586 23937586 single base substitution G A intron_variant LAML-KR 13 23985391 23985391 single base substitution T C 5_prime_UTR_variant LGG-US 13 23907744 23907744 single base substitution C T intron_variant LGG-US 13 23907744 23907744 single base substitution C T missense_variant G2674E 8021G>A LGG-US 13 23907744 23907744 single base substitution C T missense_variant G3424E 10271G>A LGG-US 13 23908606 23908606 single base substitution C T intron_variant LGG-US 13 23908606 23908606 single base substitution C T missense_variant D2387N 7159G>A LGG-US 13 23908606 23908606 single base substitution C T missense_variant D3137N 9409G>A LGG-US 13 23914687 23914687 deletion of <=200bp T - frameshift_variant I1110 LGG-US 13 23914687 23914687 deletion of <=200bp T - frameshift_variant I360 LGG-US 13 23914687 23914687 deletion of <=200bp T - intron_variant LICA-CN 13 23905207 23905207 single base substitution T A intron_variant LICA-CN 13 23905207 23905207 single base substitution T A missense_variant T3520S 10558A>T LICA-CN 13 23905207 23905207 single base substitution T A missense_variant T4270S 12808A>T LICA-CN 13 23906659 23906659 single base substitution C T intron_variant LICA-CN 13 23906659 23906659 single base substitution C T missense_variant E3036K 9106G>A LICA-CN 13 23906659 23906659 single base substitution C T missense_variant E3786K 11356G>A LICA-CN 13 23906696 23906696 single base substitution T A intron_variant LICA-CN 13 23906696 23906696 single base substitution T A missense_variant L3023F 9069A>T LICA-CN 13 23906696 23906696 single base substitution T A missense_variant L3773F 11319A>T LICA-CN 13 23909614 23909614 single base substitution G T intron_variant LICA-CN 13 23909614 23909614 single base substitution G T missense_variant Q2051K 6151C>A LICA-CN 13 23909614 23909614 single base substitution G T missense_variant Q2801K 8401C>A LICA-CN 13 23929091 23929091 single base substitution T C 5_prime_UTR_variant LICA-CN 13 23929091 23929091 single base substitution T C missense_variant S178G 532A>G LICA-CN 13 23929091 23929091 single base substitution T C missense_variant S453G 1357A>G LICA-CN 13 23929091 23929091 single base substitution T C missense_variant S554G 1660A>G LICA-CN 13 23929091 23929091 single base substitution T C upstream_gene_variant LICA-CN 13 23929368 23929368 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant LICA-CN 13 23929368 23929368 single base substitution T A synonymous_variant P360P 1080A>T LICA-CN 13 23929368 23929368 single base substitution T A synonymous_variant P461P 1383A>T LICA-CN 13 23929368 23929368 single base substitution T A synonymous_variant P85P 255A>T LICA-CN 13 23929368 23929368 single base substitution T A upstream_gene_variant LICA-FR 13 23899191 23899191 single base substitution G T downstream_gene_variant LICA-FR 13 23905062 23905062 single base substitution C T intron_variant LICA-FR 13 23905062 23905062 single base substitution C T stop_gained W3568* 10703G>A LICA-FR 13 23905062 23905062 single base substitution C T stop_gained W4318* 12953G>A LICA-FR 13 23906155 23906155 single base substitution C T intron_variant LICA-FR 13 23906155 23906155 single base substitution C T missense_variant D3204N 9610G>A LICA-FR 13 23906155 23906155 single base substitution C T missense_variant D3954N 11860G>A LICA-FR 13 23910541 23910541 single base substitution C A intron_variant LICA-FR 13 23910541 23910541 single base substitution C A missense_variant V1742L 5224G>T LICA-FR 13 23910541 23910541 single base substitution C A missense_variant V2492L 7474G>T LICA-FR 13 23910542 23910542 single base substitution T A intron_variant LICA-FR 13 23910542 23910542 single base substitution T A missense_variant E1741D 5223A>T LICA-FR 13 23910542 23910542 single base substitution T A missense_variant E2491D 7473A>T LICA-FR 13 23911098 23911098 single base substitution T C intron_variant LICA-FR 13 23911098 23911098 single base substitution T C missense_variant D1556G 4667A>G LICA-FR 13 23911098 23911098 single base substitution T C missense_variant D2306G 6917A>G LICA-FR 13 23912040 23912040 single base substitution C T intron_variant LICA-FR 13 23912040 23912040 single base substitution C T missense_variant R1242K 3725G>A LICA-FR 13 23912040 23912040 single base substitution C T missense_variant R1992K 5975G>A LICA-FR 13 23914892 23914892 single base substitution C A intron_variant LICA-FR 13 23914892 23914892 single base substitution C A missense_variant Q1041H 3123G>T LICA-FR 13 23914892 23914892 single base substitution C A missense_variant Q291H 873G>T LICA-FR 13 23926048 23926048 single base substitution T G downstream_gene_variant LICA-FR 13 23926048 23926048 single base substitution T G intron_variant LICA-FR 13 23929173 23929173 single base substitution C A 5_prime_UTR_variant LICA-FR 13 23929173 23929173 single base substitution C A missense_variant L150F 450G>T LICA-FR 13 23929173 23929173 single base substitution C A missense_variant L425F 1275G>T LICA-FR 13 23929173 23929173 single base substitution C A missense_variant L526F 1578G>T LICA-FR 13 23929173 23929173 single base substitution C A upstream_gene_variant LICA-FR 13 23929960 23929960 single base substitution C T 5_prime_UTR_variant LICA-FR 13 23929960 23929960 single base substitution C T missense_variant G163D 488G>A LICA-FR 13 23929960 23929960 single base substitution C T missense_variant G264D 791G>A LICA-FR 13 23929960 23929960 single base substitution C T upstream_gene_variant LICA-FR 13 23945251 23945251 single base substitution A G intron_variant LICA-FR 13 23945251 23945251 single base substitution A G synonymous_variant F75F 225T>C LICA-FR 13 23945251 23945251 single base substitution A G upstream_gene_variant LICA-FR 13 23951508 23951508 single base substitution G T intron_variant LICA-FR 13 23951508 23951508 single base substitution G T upstream_gene_variant LICA-FR 13 23955713 23955713 single base substitution T A intron_variant LICA-FR 13 23965776 23965776 single base substitution A G intron_variant LICA-FR 13 23967047 23967047 single base substitution G A intron_variant LICA-FR 13 23968810 23968810 single base substitution T C intron_variant LICA-FR 13 23977329 23977329 single base substitution A T intron_variant LICA-FR 13 24012222 24012222 single base substitution T A upstream_gene_variant LIHC-US 13 23898515 23898515 single base substitution T A downstream_gene_variant LIHC-US 13 23904756 23904756 single base substitution C A intron_variant LIHC-US 13 23904756 23904756 single base substitution C A missense_variant C3670F 11009G>T LIHC-US 13 23904756 23904756 single base substitution C A missense_variant C4420F 13259G>T LIHC-US 13 23905027 23905027 single base substitution T C intron_variant LIHC-US 13 23905027 23905027 single base substitution T C missense_variant R3580G 10738A>G LIHC-US 13 23905027 23905027 single base substitution T C missense_variant R4330G 12988A>G LIHC-US 13 23905055 23905055 single base substitution A G intron_variant LIHC-US 13 23905055 23905055 single base substitution A G synonymous_variant L3570L 10710T>C LIHC-US 13 23905055 23905055 single base substitution A G synonymous_variant L4320L 12960T>C LIHC-US 13 23905368 23905368 single base substitution T C intron_variant LIHC-US 13 23905368 23905368 single base substitution T C missense_variant D3466G 10397A>G LIHC-US 13 23905368 23905368 single base substitution T C missense_variant D4216G 12647A>G LIHC-US 13 23906630 23906630 single base substitution A G intron_variant LIHC-US 13 23906630 23906630 single base substitution A G synonymous_variant A3045A 9135T>C LIHC-US 13 23906630 23906630 single base substitution A G synonymous_variant A3795A 11385T>C LIHC-US 13 23907796 23907796 single base substitution G A intron_variant LIHC-US 13 23907796 23907796 single base substitution G A synonymous_variant L2657L 7969C>T LIHC-US 13 23907796 23907796 single base substitution G A synonymous_variant L3407L 10219C>T LIHC-US 13 23908202 23908202 single base substitution A G intron_variant LIHC-US 13 23908202 23908202 single base substitution A G synonymous_variant V2521V 7563T>C LIHC-US 13 23908202 23908202 single base substitution A G synonymous_variant V3271V 9813T>C LIHC-US 13 23909856 23909856 single base substitution T C intron_variant LIHC-US 13 23909856 23909856 single base substitution T C missense_variant D1970G 5909A>G LIHC-US 13 23909856 23909856 single base substitution T C missense_variant D2720G 8159A>G LIHC-US 13 23910455 23910455 single base substitution T G intron_variant LIHC-US 13 23910455 23910455 single base substitution T G synonymous_variant T1770T 5310A>C LIHC-US 13 23910455 23910455 single base substitution T G synonymous_variant T2520T 7560A>C LIHC-US 13 23911609 23911609 single base substitution T A intron_variant LIHC-US 13 23911609 23911609 single base substitution T A missense_variant T1386S 4156A>T LIHC-US 13 23911609 23911609 single base substitution T A missense_variant T2136S 6406A>T LIHC-US 13 23911630 23911630 single base substitution C T intron_variant LIHC-US 13 23911630 23911630 single base substitution C T missense_variant G1379R 4135G>A LIHC-US 13 23911630 23911630 single base substitution C T missense_variant G2129R 6385G>A LIHC-US 13 23911712 23911712 single base substitution G T intron_variant LIHC-US 13 23911712 23911712 single base substitution G T synonymous_variant S1351S 4053C>A LIHC-US 13 23911712 23911712 single base substitution G T synonymous_variant S2101S 6303C>A LIHC-US 13 23912521 23912521 single base substitution A T intron_variant LIHC-US 13 23912521 23912521 single base substitution A T missense_variant F1082I 3244T>A LIHC-US 13 23912521 23912521 single base substitution A T missense_variant F1832I 5494T>A LIHC-US 13 23915816 23915816 single base substitution A G 5_prime_UTR_variant LIHC-US 13 23915816 23915816 single base substitution A G intron_variant LIHC-US 13 23915816 23915816 single base substitution A G synonymous_variant T632T 1896T>C LIHC-US 13 23915816 23915816 single base substitution A G synonymous_variant T733T 2199T>C LIHC-US 13 23929049 23929049 single base substitution C A 5_prime_UTR_variant LIHC-US 13 23929049 23929049 single base substitution C A missense_variant D192Y 574G>T LIHC-US 13 23929049 23929049 single base substitution C A missense_variant D467Y 1399G>T LIHC-US 13 23929049 23929049 single base substitution C A missense_variant D568Y 1702G>T LIHC-US 13 23929049 23929049 single base substitution C A upstream_gene_variant LINC-JP 13 23905974 23905974 single base substitution C T intron_variant LINC-JP 13 23905974 23905974 single base substitution C T missense_variant G3264E 9791G>A LINC-JP 13 23905974 23905974 single base substitution C T missense_variant G4014E 12041G>A LINC-JP 13 23906661 23906661 single base substitution C T intron_variant LINC-JP 13 23906661 23906661 single base substitution C T missense_variant R3035K 9104G>A LINC-JP 13 23906661 23906661 single base substitution C T missense_variant R3785K 11354G>A LINC-JP 13 23907735 23907735 single base substitution C A intron_variant LINC-JP 13 23907735 23907735 single base substitution C A missense_variant G2677V 8030G>T LINC-JP 13 23907735 23907735 single base substitution C A missense_variant G3427V 10280G>T LINC-JP 13 23908048 23908048 single base substitution C T intron_variant LINC-JP 13 23908048 23908048 single base substitution C T missense_variant A2573T 7717G>A LINC-JP 13 23908048 23908048 single base substitution C T missense_variant A3323T 9967G>A LINC-JP 13 23908773 23908773 single base substitution T C intron_variant LINC-JP 13 23908773 23908773 single base substitution T C missense_variant H2331R 6992A>G LINC-JP 13 23908773 23908773 single base substitution T C missense_variant H3081R 9242A>G LINC-JP 13 23909025 23909025 single base substitution C T intron_variant LINC-JP 13 23909025 23909025 single base substitution C T missense_variant R2247Q 6740G>A LINC-JP 13 23909025 23909025 single base substitution C T missense_variant R2997Q 8990G>A LINC-JP 13 23909386 23909386 single base substitution T A intron_variant LINC-JP 13 23909386 23909386 single base substitution T A missense_variant T2127S 6379A>T LINC-JP 13 23909386 23909386 single base substitution T A missense_variant T2877S 8629A>T LINC-JP 13 23911538 23911538 single base substitution T A intron_variant LINC-JP 13 23911538 23911538 single base substitution T A missense_variant L1409F 4227A>T LINC-JP 13 23911538 23911538 single base substitution T A missense_variant L2159F 6477A>T LINC-JP 13 23912431 23912431 single base substitution T C intron_variant LINC-JP 13 23912431 23912431 single base substitution T C missense_variant T1112A 3334A>G LINC-JP 13 23912431 23912431 single base substitution T C missense_variant T1862A 5584A>G LINC-JP 13 23913706 23913706 single base substitution G A intron_variant LINC-JP 13 23913706 23913706 single base substitution G A missense_variant P1437S 4309C>T LINC-JP 13 23913706 23913706 single base substitution G A missense_variant P687S 2059C>T LINC-JP 13 23915795 23915795 single base substitution T C 5_prime_UTR_variant LINC-JP 13 23915795 23915795 single base substitution T C intron_variant LINC-JP 13 23915795 23915795 single base substitution T C synonymous_variant P639P 1917A>G LINC-JP 13 23915795 23915795 single base substitution T C synonymous_variant P740P 2220A>G LINC-JP 13 23923942 23923942 single base substitution T A downstream_gene_variant LINC-JP 13 23923942 23923942 single base substitution T A intron_variant LINC-JP 13 23930108 23930108 single base substitution G A 5_prime_UTR_variant LINC-JP 13 23930108 23930108 single base substitution G A synonymous_variant L114L 340C>T LINC-JP 13 23930108 23930108 single base substitution G A synonymous_variant L215L 643C>T LINC-JP 13 23930108 23930108 single base substitution G A upstream_gene_variant LINC-JP 13 23948051 23948051 single base substitution G A intron_variant LINC-JP 13 23949008 23949008 single base substitution T C intron_variant LINC-JP 13 23950441 23950441 single base substitution T G intron_variant LINC-JP 13 23950441 23950441 single base substitution T G upstream_gene_variant LINC-JP 13 23950478 23950478 single base substitution A G intron_variant LINC-JP 13 23950478 23950478 single base substitution A G upstream_gene_variant LINC-JP 13 23961776 23961776 single base substitution T A intron_variant LINC-JP 13 23962379 23962379 single base substitution A G intron_variant LINC-JP 13 23962380 23962380 single base substitution G A intron_variant LINC-JP 13 23963195 23963195 single base substitution A T intron_variant LINC-JP 13 23967605 23967605 single base substitution T A intron_variant LINC-JP 13 23971056 23971056 single base substitution G T intron_variant LINC-JP 13 23978659 23978659 single base substitution G T intron_variant LINC-JP 13 23978660 23978660 single base substitution G T intron_variant LINC-JP 13 23985092 23985092 single base substitution C T intron_variant LINC-JP 13 23992224 23992224 single base substitution G C intron_variant LINC-JP 13 23992660 23992660 single base substitution A T intron_variant LINC-JP 13 23992661 23992661 single base substitution C A intron_variant LINC-JP 13 23997583 23997583 single base substitution T A intron_variant LINC-JP 13 23999142 23999142 single base substitution G A intron_variant LINC-JP 13 24002210 24002210 single base substitution A G intron_variant LINC-JP 13 24006072 24006072 single base substitution T C intron_variant LINC-JP 13 24010938 24010938 single base substitution G A upstream_gene_variant LIRI-JP 13 23898205 23898205 single base substitution A G downstream_gene_variant LIRI-JP 13 23899161 23899161 single base substitution T C downstream_gene_variant LIRI-JP 13 23900108 23900108 single base substitution A G downstream_gene_variant LIRI-JP 13 23900541 23900541 single base substitution C A downstream_gene_variant LIRI-JP 13 23900547 23900547 single base substitution T A downstream_gene_variant LIRI-JP 13 23901809 23901809 single base substitution T A downstream_gene_variant LIRI-JP 13 23902453 23902453 single base substitution C T downstream_gene_variant LIRI-JP 13 23903281 23903281 single base substitution G C 3_prime_UTR_variant LIRI-JP 13 23903823 23903823 single base substitution G C 3_prime_UTR_variant LIRI-JP 13 23903823 23903823 single base substitution G C intron_variant LIRI-JP 13 23904755 23904755 single base substitution G A intron_variant LIRI-JP 13 23904755 23904755 single base substitution G A synonymous_variant C3670C 11010C>T LIRI-JP 13 23904755 23904755 single base substitution G A synonymous_variant C4420C 13260C>T LIRI-JP 13 23905810 23905810 single base substitution T C intron_variant LIRI-JP 13 23905810 23905810 single base substitution T C missense_variant R3319G 9955A>G LIRI-JP 13 23905810 23905810 single base substitution T C missense_variant R4069G 12205A>G LIRI-JP 13 23907184 23907184 single base substitution C T intron_variant LIRI-JP 13 23907184 23907184 single base substitution C T missense_variant A2861T 8581G>A LIRI-JP 13 23907184 23907184 single base substitution C T missense_variant A3611T 10831G>A LIRI-JP 13 23907841 23907841 single base substitution T A intron_variant LIRI-JP 13 23907841 23907841 single base substitution T A missense_variant N2642Y 7924A>T LIRI-JP 13 23907841 23907841 single base substitution T A missense_variant N3392Y 10174A>T LIRI-JP 13 23908006 23908006 single base substitution T C intron_variant LIRI-JP 13 23908006 23908006 single base substitution T C missense_variant I2587V 7759A>G LIRI-JP 13 23908006 23908006 single base substitution T C missense_variant I3337V 10009A>G LIRI-JP 13 23910342 23910342 single base substitution G A intron_variant LIRI-JP 13 23910342 23910342 single base substitution G A missense_variant A1808V 5423C>T LIRI-JP 13 23910342 23910342 single base substitution G A missense_variant A2558V 7673C>T LIRI-JP 13 23913026 23913026 single base substitution G T intron_variant LIRI-JP 13 23913026 23913026 single base substitution G T stop_gained C1663* 4989C>A LIRI-JP 13 23913026 23913026 single base substitution G T stop_gained C913* 2739C>A LIRI-JP 13 23913354 23913354 single base substitution C T intron_variant LIRI-JP 13 23913354 23913354 single base substitution C T missense_variant G1554E 4661G>A LIRI-JP 13 23913354 23913354 single base substitution C T missense_variant G804E 2411G>A LIRI-JP 13 23914539 23914539 single base substitution G C intron_variant LIRI-JP 13 23914539 23914539 single base substitution G C missense_variant A1159G 3476C>G LIRI-JP 13 23914539 23914539 single base substitution G C missense_variant A409G 1226C>G LIRI-JP 13 23915277 23915277 single base substitution C A intron_variant LIRI-JP 13 23915277 23915277 single base substitution C A missense_variant S163I 488G>T LIRI-JP 13 23915277 23915277 single base substitution C A missense_variant S913I 2738G>T LIRI-JP 13 23916321 23916321 single base substitution A G intron_variant LIRI-JP 13 23919124 23919124 single base substitution T C intron_variant LIRI-JP 13 23921031 23921031 single base substitution T A intron_variant LIRI-JP 13 23924910 23924910 single base substitution C G downstream_gene_variant LIRI-JP 13 23924910 23924910 single base substitution C G intron_variant LIRI-JP 13 23925257 23925257 single base substitution G T downstream_gene_variant LIRI-JP 13 23925257 23925257 single base substitution G T intron_variant LIRI-JP 13 23925688 23925688 single base substitution T C downstream_gene_variant LIRI-JP 13 23925688 23925688 single base substitution T C intron_variant LIRI-JP 13 23926303 23926303 single base substitution G A downstream_gene_variant LIRI-JP 13 23926303 23926303 single base substitution G A intron_variant LIRI-JP 13 23927999 23927999 single base substitution G A 5_prime_UTR_variant LIRI-JP 13 23927999 23927999 single base substitution G A exon_variant LIRI-JP 13 23927999 23927999 single base substitution G A missense_variant L328F 982C>T LIRI-JP 13 23927999 23927999 single base substitution G A missense_variant L603F 1807C>T LIRI-JP 13 23927999 23927999 single base substitution G A missense_variant L704F 2110C>T LIRI-JP 13 23929592 23929592 single base substitution C T 5_prime_UTR_variant LIRI-JP 13 23929592 23929592 single base substitution C T missense_variant A11T 31G>A LIRI-JP 13 23929592 23929592 single base substitution C T missense_variant A286T 856G>A LIRI-JP 13 23929592 23929592 single base substitution C T missense_variant A387T 1159G>A LIRI-JP 13 23929592 23929592 single base substitution C T upstream_gene_variant LIRI-JP 13 23930146 23930146 single base substitution T C missense_variant D101G 302A>G LIRI-JP 13 23930146 23930146 single base substitution T C missense_variant D202G 605A>G LIRI-JP 13 23930146 23930146 single base substitution T C splice_region_variant LIRI-JP 13 23930146 23930146 single base substitution T C upstream_gene_variant LIRI-JP 13 23931090 23931090 single base substitution C T intron_variant LIRI-JP 13 23931090 23931090 single base substitution C T upstream_gene_variant LIRI-JP 13 23933093 23933093 single base substitution T G intron_variant LIRI-JP 13 23933093 23933093 single base substitution T G upstream_gene_variant LIRI-JP 13 23936322 23936322 single base substitution A C intron_variant LIRI-JP 13 23936687 23936687 single base substitution G A intron_variant LIRI-JP 13 23938961 23938961 single base substitution C T intron_variant LIRI-JP 13 23938982 23938982 single base substitution T C intron_variant LIRI-JP 13 23942824 23942824 single base substitution A G intron_variant LIRI-JP 13 23942824 23942824 single base substitution A G upstream_gene_variant LIRI-JP 13 23943018 23943018 single base substitution T G intron_variant LIRI-JP 13 23943018 23943018 single base substitution T G upstream_gene_variant LIRI-JP 13 23944298 23944298 single base substitution C T intron_variant LIRI-JP 13 23944298 23944298 single base substitution C T upstream_gene_variant LIRI-JP 13 23947579 23947579 single base substitution C A intron_variant LIRI-JP 13 23947579 23947579 single base substitution C A upstream_gene_variant LIRI-JP 13 23950390 23950390 single base substitution T C intron_variant LIRI-JP 13 23950390 23950390 single base substitution T C upstream_gene_variant LIRI-JP 13 23950742 23950742 single base substitution G C intron_variant LIRI-JP 13 23950742 23950742 single base substitution G C upstream_gene_variant LIRI-JP 13 23951373 23951373 single base substitution C T intron_variant LIRI-JP 13 23951373 23951373 single base substitution C T upstream_gene_variant LIRI-JP 13 23952830 23952830 single base substitution C A intron_variant LIRI-JP 13 23952830 23952830 single base substitution C A upstream_gene_variant LIRI-JP 13 23955042 23955042 single base substitution G T intron_variant LIRI-JP 13 23956426 23956426 single base substitution G T intron_variant LIRI-JP 13 23956880 23956880 single base substitution G C intron_variant LIRI-JP 13 23957210 23957210 single base substitution G A intron_variant LIRI-JP 13 23957381 23957381 single base substitution C T intron_variant LIRI-JP 13 23957651 23957651 single base substitution T G intron_variant LIRI-JP 13 23958311 23958311 single base substitution C A intron_variant LIRI-JP 13 23958535 23958535 single base substitution A G intron_variant LIRI-JP 13 23958706 23958706 single base substitution T C intron_variant LIRI-JP 13 23960169 23960169 single base substitution G A intron_variant LIRI-JP 13 23961509 23961509 single base substitution G T intron_variant LIRI-JP 13 23962284 23962284 single base substitution A G intron_variant LIRI-JP 13 23962586 23962586 single base substitution A G intron_variant LIRI-JP 13 23963206 23963206 single base substitution A G intron_variant LIRI-JP 13 23963666 23963666 single base substitution C A intron_variant LIRI-JP 13 23964381 23964381 single base substitution A T intron_variant LIRI-JP 13 23965579 23965579 single base substitution A G intron_variant LIRI-JP 13 23965842 23965842 single base substitution A T intron_variant LIRI-JP 13 23965851 23965851 single base substitution T A intron_variant LIRI-JP 13 23967232 23967232 single base substitution C A intron_variant LIRI-JP 13 23967404 23967404 single base substitution T A intron_variant LIRI-JP 13 23970803 23970803 single base substitution A G intron_variant LIRI-JP 13 23971103 23971103 single base substitution T C intron_variant LIRI-JP 13 23971377 23971377 single base substitution T G intron_variant LIRI-JP 13 23971404 23971404 single base substitution G A intron_variant LIRI-JP 13 23971751 23971751 single base substitution C A intron_variant LIRI-JP 13 23971935 23971935 single base substitution G T intron_variant LIRI-JP 13 23972613 23972613 single base substitution C A intron_variant LIRI-JP 13 23973115 23973115 single base substitution G C intron_variant LIRI-JP 13 23973814 23973814 single base substitution G A intron_variant LIRI-JP 13 23974851 23974851 single base substitution G A intron_variant LIRI-JP 13 23976099 23976099 single base substitution A G intron_variant LIRI-JP 13 23977822 23977822 single base substitution T C intron_variant LIRI-JP 13 23979054 23979054 single base substitution C A intron_variant LIRI-JP 13 23979308 23979308 single base substitution G C intron_variant LIRI-JP 13 23979490 23979490 single base substitution T G intron_variant LIRI-JP 13 23980215 23980215 single base substitution G C intron_variant LIRI-JP 13 23980992 23980992 single base substitution G A intron_variant LIRI-JP 13 23981067 23981067 single base substitution T C intron_variant LIRI-JP 13 23984511 23984511 single base substitution A G intron_variant LIRI-JP 13 23986022 23986022 single base substitution A G intron_variant LIRI-JP 13 23986022 23986022 single base substitution A G upstream_gene_variant LIRI-JP 13 23986520 23986520 single base substitution G A intron_variant LIRI-JP 13 23986520 23986520 single base substitution G A upstream_gene_variant LIRI-JP 13 23988229 23988229 single base substitution G T intron_variant LIRI-JP 13 23988229 23988229 single base substitution G T upstream_gene_variant LIRI-JP 13 23988536 23988536 single base substitution A G intron_variant LIRI-JP 13 23988536 23988536 single base substitution A G upstream_gene_variant LIRI-JP 13 23992364 23992364 single base substitution A C intron_variant LIRI-JP 13 23992640 23992640 single base substitution A G intron_variant LIRI-JP 13 23992773 23992773 single base substitution T C intron_variant LIRI-JP 13 23993417 23993417 single base substitution G T intron_variant LIRI-JP 13 23998341 23998341 single base substitution T C intron_variant LIRI-JP 13 23998501 23998501 single base substitution C A intron_variant LIRI-JP 13 23998600 23998600 single base substitution G T intron_variant LIRI-JP 13 23998773 23998773 single base substitution T C intron_variant LIRI-JP 13 23999371 23999371 single base substitution T C intron_variant LIRI-JP 13 23999623 23999623 single base substitution A T intron_variant LIRI-JP 13 23999635 23999635 single base substitution G T intron_variant LIRI-JP 13 24001046 24001046 single base substitution A G intron_variant LIRI-JP 13 24002265 24002265 single base substitution G C intron_variant LIRI-JP 13 24003408 24003408 single base substitution A G intron_variant LIRI-JP 13 24005136 24005136 single base substitution G T intron_variant LIRI-JP 13 24005639 24005639 single base substitution A T intron_variant LIRI-JP 13 24006268 24006268 single base substitution G T intron_variant LIRI-JP 13 24006994 24006994 single base substitution A G intron_variant LIRI-JP 13 24007254 24007254 single base substitution C T intron_variant LIRI-JP 13 24008101 24008101 single base substitution A G upstream_gene_variant LIRI-JP 13 24008474 24008474 single base substitution G T upstream_gene_variant LIRI-JP 13 24008517 24008517 single base substitution A G upstream_gene_variant LIRI-JP 13 24009623 24009623 single base substitution A C upstream_gene_variant LIRI-JP 13 24010900 24010900 single base substitution A G upstream_gene_variant LIRI-JP 13 24012383 24012383 single base substitution G A upstream_gene_variant LIRI-JP 13 24012561 24012561 single base substitution T C upstream_gene_variant LIRI-JP 13 24012634 24012634 single base substitution T C upstream_gene_variant LUSC-CN 13 23906834 23906834 single base substitution T C intron_variant LUSC-CN 13 23906834 23906834 single base substitution T C synonymous_variant Q2977Q 8931A>G LUSC-CN 13 23906834 23906834 single base substitution T C synonymous_variant Q3727Q 11181A>G LUSC-KR 13 23898489 23898489 single base substitution T C downstream_gene_variant LUSC-KR 13 23898816 23898816 single base substitution T A downstream_gene_variant LUSC-KR 13 23899185 23899185 single base substitution A G downstream_gene_variant LUSC-KR 13 23899799 23899799 single base substitution A C downstream_gene_variant LUSC-KR 13 23900238 23900238 single base substitution A G downstream_gene_variant LUSC-KR 13 23907759 23907759 single base substitution C T intron_variant LUSC-KR 13 23907759 23907759 single base substitution C T missense_variant R2669H 8006G>A LUSC-KR 13 23907759 23907759 single base substitution C T missense_variant R3419H 10256G>A LUSC-KR 13 23907818 23907818 single base substitution C A intron_variant LUSC-KR 13 23907818 23907818 single base substitution C A missense_variant M2649I 7947G>T LUSC-KR 13 23907818 23907818 single base substitution C A missense_variant M3399I 10197G>T LUSC-KR 13 23913423 23913423 single base substitution G A intron_variant LUSC-KR 13 23913423 23913423 single base substitution G A missense_variant S1531L 4592C>T LUSC-KR 13 23913423 23913423 single base substitution G A missense_variant S781L 2342C>T LUSC-KR 13 23914231 23914231 single base substitution G T intron_variant LUSC-KR 13 23914231 23914231 single base substitution G T missense_variant H1262N 3784C>A LUSC-KR 13 23914231 23914231 single base substitution G T missense_variant H512N 1534C>A LUSC-KR 13 23917934 23917934 single base substitution C A intron_variant LUSC-KR 13 23918761 23918761 single base substitution T C intron_variant LUSC-KR 13 23919177 23919177 single base substitution G A intron_variant LUSC-KR 13 23932525 23932525 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 13 23932525 23932525 single base substitution G A synonymous_variant L185L 553C>T LUSC-KR 13 23932525 23932525 single base substitution G A synonymous_variant L84L 250C>T LUSC-KR 13 23932525 23932525 single base substitution G A upstream_gene_variant LUSC-KR 13 23943273 23943273 single base substitution G C intron_variant LUSC-KR 13 23943273 23943273 single base substitution G C upstream_gene_variant LUSC-KR 13 23945433 23945433 single base substitution T C intron_variant LUSC-KR 13 23945433 23945433 single base substitution T C upstream_gene_variant LUSC-KR 13 23947655 23947655 single base substitution G A intron_variant LUSC-KR 13 23951478 23951478 single base substitution C G intron_variant LUSC-KR 13 23951478 23951478 single base substitution C G upstream_gene_variant LUSC-KR 13 23956970 23956970 single base substitution G T intron_variant LUSC-KR 13 23957545 23957545 single base substitution C A intron_variant LUSC-KR 13 23963863 23963863 single base substitution C A intron_variant LUSC-KR 13 23964039 23964039 single base substitution T C intron_variant LUSC-KR 13 23968876 23968876 single base substitution C T intron_variant LUSC-KR 13 23969285 23969285 single base substitution G A intron_variant LUSC-KR 13 23970094 23970094 single base substitution A G intron_variant LUSC-KR 13 23972540 23972540 single base substitution G T intron_variant LUSC-KR 13 23976914 23976914 single base substitution A T intron_variant LUSC-KR 13 23978929 23978929 single base substitution G A intron_variant LUSC-KR 13 23980845 23980845 single base substitution T C intron_variant LUSC-KR 13 23981267 23981267 single base substitution G T intron_variant LUSC-KR 13 23981483 23981483 single base substitution G A intron_variant LUSC-KR 13 23981626 23981626 single base substitution C A intron_variant LUSC-KR 13 23983812 23983812 single base substitution T A intron_variant LUSC-KR 13 23986267 23986267 single base substitution G A intron_variant LUSC-KR 13 23986267 23986267 single base substitution G A upstream_gene_variant LUSC-KR 13 23988335 23988335 single base substitution C A intron_variant LUSC-KR 13 23988335 23988335 single base substitution C A upstream_gene_variant LUSC-KR 13 23998229 23998229 single base substitution T C intron_variant LUSC-KR 13 24000177 24000177 single base substitution G A intron_variant LUSC-KR 13 24000518 24000518 single base substitution G A intron_variant LUSC-KR 13 24004248 24004248 single base substitution G A intron_variant LUSC-KR 13 24007084 24007084 single base substitution G C intron_variant LUSC-US 13 23898647 23898647 single base substitution C T downstream_gene_variant LUSC-US 13 23905162 23905162 single base substitution T A intron_variant LUSC-US 13 23905162 23905162 single base substitution T A missense_variant S3535C 10603A>T LUSC-US 13 23905162 23905162 single base substitution T A missense_variant S4285C 12853A>T LUSC-US 13 23906110 23906110 single base substitution G A intron_variant LUSC-US 13 23906110 23906110 single base substitution G A missense_variant L3219F 9655C>T LUSC-US 13 23906110 23906110 single base substitution G A missense_variant L3969F 11905C>T LUSC-US 13 23906130 23906130 single base substitution A G intron_variant LUSC-US 13 23906130 23906130 single base substitution A G missense_variant I3212T 9635T>C LUSC-US 13 23906130 23906130 single base substitution A G missense_variant I3962T 11885T>C LUSC-US 13 23906282 23906282 single base substitution G T intron_variant LUSC-US 13 23906282 23906282 single base substitution G T missense_variant S3161R 9483C>A LUSC-US 13 23906282 23906282 single base substitution G T missense_variant S3911R 11733C>A LUSC-US 13 23908856 23908856 single base substitution C A intron_variant LUSC-US 13 23908856 23908856 single base substitution C A missense_variant E2303D 6909G>T LUSC-US 13 23908856 23908856 single base substitution C A missense_variant E3053D 9159G>T LUSC-US 13 23909099 23909099 single base substitution T A intron_variant LUSC-US 13 23909099 23909099 single base substitution T A synonymous_variant P2222P 6666A>T LUSC-US 13 23909099 23909099 single base substitution T A synonymous_variant P2972P 8916A>T LUSC-US 13 23909195 23909195 single base substitution T C intron_variant LUSC-US 13 23909195 23909195 single base substitution T C synonymous_variant T2190T 6570A>G LUSC-US 13 23909195 23909195 single base substitution T C synonymous_variant T2940T 8820A>G LUSC-US 13 23911629 23911629 single base substitution C A intron_variant LUSC-US 13 23911629 23911629 single base substitution C A missense_variant G1379V 4136G>T LUSC-US 13 23911629 23911629 single base substitution C A missense_variant G2129V 6386G>T LUSC-US 13 23912025 23912025 single base substitution G C intron_variant LUSC-US 13 23912025 23912025 single base substitution G C missense_variant S1247C 3740C>G LUSC-US 13 23912025 23912025 single base substitution G C missense_variant S1997C 5990C>G LUSC-US 13 23912373 23912373 single base substitution C G intron_variant LUSC-US 13 23912373 23912373 single base substitution C G missense_variant G1131A 3392G>C LUSC-US 13 23912373 23912373 single base substitution C G missense_variant G1881A 5642G>C LUSC-US 13 23912516 23912516 single base substitution G T intron_variant LUSC-US 13 23912516 23912516 single base substitution G T synonymous_variant S1083S 3249C>A LUSC-US 13 23912516 23912516 single base substitution G T synonymous_variant S1833S 5499C>A LUSC-US 13 23913541 23913541 single base substitution C G intron_variant LUSC-US 13 23913541 23913541 single base substitution C G missense_variant E1492Q 4474G>C LUSC-US 13 23913541 23913541 single base substitution C G missense_variant E742Q 2224G>C LUSC-US 13 23914497 23914497 single base substitution C G intron_variant LUSC-US 13 23914497 23914497 single base substitution C G missense_variant W1173S 3518G>C LUSC-US 13 23914497 23914497 single base substitution C G missense_variant W423S 1268G>C LUSC-US 13 23915054 23915054 single base substitution C G intron_variant LUSC-US 13 23915054 23915054 single base substitution C G missense_variant K237N 711G>C LUSC-US 13 23915054 23915054 single base substitution C G missense_variant K987N 2961G>C LUSC-US 13 23915357 23915357 single base substitution C G intron_variant LUSC-US 13 23915357 23915357 single base substitution C G missense_variant Q136H 408G>C LUSC-US 13 23915357 23915357 single base substitution C G missense_variant Q886H 2658G>C LUSC-US 13 23928866 23928866 single base substitution C T 5_prime_UTR_variant LUSC-US 13 23928866 23928866 single base substitution C T exon_variant LUSC-US 13 23928866 23928866 single base substitution C T missense_variant A253T 757G>A LUSC-US 13 23928866 23928866 single base substitution C T missense_variant A528T 1582G>A LUSC-US 13 23928866 23928866 single base substitution C T missense_variant A629T 1885G>A LUSC-US 13 23928927 23928927 single base substitution C T 5_prime_UTR_variant LUSC-US 13 23928927 23928927 single base substitution C T exon_variant LUSC-US 13 23928927 23928927 single base substitution C T synonymous_variant V232V 696G>A LUSC-US 13 23928927 23928927 single base substitution C T synonymous_variant V507V 1521G>A LUSC-US 13 23928927 23928927 single base substitution C T synonymous_variant V608V 1824G>A LUSC-US 13 23929364 23929364 single base substitution G A 5_prime_UTR_variant LUSC-US 13 23929364 23929364 single base substitution G A missense_variant H362Y 1084C>T LUSC-US 13 23929364 23929364 single base substitution G A missense_variant H463Y 1387C>T LUSC-US 13 23929364 23929364 single base substitution G A missense_variant H87Y 259C>T LUSC-US 13 23929364 23929364 single base substitution G A upstream_gene_variant LUSC-US 13 23929365 23929365 single base substitution A T 5_prime_UTR_variant LUSC-US 13 23929365 23929365 single base substitution A T synonymous_variant V361V 1083T>A LUSC-US 13 23929365 23929365 single base substitution A T synonymous_variant V462V 1386T>A LUSC-US 13 23929365 23929365 single base substitution A T synonymous_variant V86V 258T>A LUSC-US 13 23929365 23929365 single base substitution A T upstream_gene_variant LUSC-US 13 23929996 23929996 single base substitution C A 5_prime_UTR_variant LUSC-US 13 23929996 23929996 single base substitution C A missense_variant G151V 452G>T LUSC-US 13 23929996 23929996 single base substitution C A missense_variant G252V 755G>T LUSC-US 13 23929996 23929996 single base substitution C A upstream_gene_variant MALY-DE 13 23898098 23898098 single base substitution T C downstream_gene_variant MALY-DE 13 23899746 23899746 single base substitution G A downstream_gene_variant MALY-DE 13 23923511 23923511 single base substitution G T downstream_gene_variant MALY-DE 13 23923511 23923511 single base substitution G T intron_variant MALY-DE 13 23933668 23933668 single base substitution T C intron_variant MALY-DE 13 23933668 23933668 single base substitution T C upstream_gene_variant MALY-DE 13 23934431 23934431 single base substitution T G intron_variant MALY-DE 13 23934431 23934431 single base substitution T G upstream_gene_variant MALY-DE 13 23946349 23946349 single base substitution C A intron_variant MALY-DE 13 23946349 23946349 single base substitution C A upstream_gene_variant MALY-DE 13 23953145 23953145 single base substitution C A intron_variant MALY-DE 13 23953145 23953145 single base substitution C A upstream_gene_variant MALY-DE 13 23956303 23956303 insertion of <=200bp - T intron_variant MALY-DE 13 23956811 23956811 single base substitution T G intron_variant MALY-DE 13 23959926 23959926 single base substitution A C intron_variant MALY-DE 13 23968257 23968257 single base substitution C T intron_variant MALY-DE 13 23973018 23973018 deletion of <=200bp A - intron_variant MALY-DE 13 23978295 23978295 single base substitution C A intron_variant MALY-DE 13 23979838 23979838 deletion of <=200bp A - intron_variant MALY-DE 13 23991120 23991120 single base substitution C G intron_variant MALY-DE 13 24001770 24001770 single base substitution C A intron_variant MALY-DE 13 24003465 24003465 single base substitution T A intron_variant MALY-DE 13 24004947 24004947 single base substitution A C intron_variant MALY-DE 13 24005155 24005155 single base substitution G C intron_variant MALY-DE 13 24008532 24008532 single base substitution C T upstream_gene_variant MELA-AU 13 23898030 23898030 single base substitution G A downstream_gene_variant MELA-AU 13 23898050 23898050 single base substitution G A downstream_gene_variant MELA-AU 13 23898061 23898061 single base substitution G A downstream_gene_variant MELA-AU 13 23898235 23898236 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 13 23898438 23898438 single base substitution G A downstream_gene_variant MELA-AU 13 23898478 23898478 single base substitution C G downstream_gene_variant MELA-AU 13 23898591 23898591 single base substitution G A downstream_gene_variant MELA-AU 13 23898635 23898635 single base substitution C T downstream_gene_variant MELA-AU 13 23898726 23898726 single base substitution C A downstream_gene_variant MELA-AU 13 23898808 23898808 single base substitution A T downstream_gene_variant MELA-AU 13 23899234 23899234 single base substitution G A downstream_gene_variant MELA-AU 13 23899504 23899504 single base substitution C T downstream_gene_variant MELA-AU 13 23899671 23899671 single base substitution G T downstream_gene_variant MELA-AU 13 23900449 23900449 single base substitution G A downstream_gene_variant MELA-AU 13 23900524 23900524 single base substitution C A downstream_gene_variant MELA-AU 13 23900952 23900952 single base substitution A G downstream_gene_variant MELA-AU 13 23901334 23901334 single base substitution C T downstream_gene_variant MELA-AU 13 23901385 23901385 single base substitution G A downstream_gene_variant MELA-AU 13 23901413 23901413 single base substitution C T downstream_gene_variant MELA-AU 13 23901424 23901424 single base substitution G A downstream_gene_variant MELA-AU 13 23901823 23901823 single base substitution C T downstream_gene_variant MELA-AU 13 23902050 23902050 single base substitution G T downstream_gene_variant MELA-AU 13 23902286 23902286 single base substitution A C downstream_gene_variant MELA-AU 13 23902623 23902623 single base substitution G C downstream_gene_variant MELA-AU 13 23902668 23902668 single base substitution G A downstream_gene_variant MELA-AU 13 23902850 23902850 single base substitution G A downstream_gene_variant MELA-AU 13 23902900 23902900 single base substitution A T downstream_gene_variant MELA-AU 13 23903085 23903086 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 13 23903325 23903325 single base substitution T A 3_prime_UTR_variant MELA-AU 13 23903327 23903327 single base substitution T C 3_prime_UTR_variant MELA-AU 13 23906163 23906163 deletion of <=200bp A - frameshift_variant L3201 MELA-AU 13 23906163 23906163 deletion of <=200bp A - frameshift_variant L3951 MELA-AU 13 23906163 23906163 deletion of <=200bp A - intron_variant MELA-AU 13 23906653 23906653 single base substitution G A intron_variant MELA-AU 13 23906653 23906653 single base substitution G A missense_variant R3038C 9112C>T MELA-AU 13 23906653 23906653 single base substitution G A missense_variant R3788C 11362C>T MELA-AU 13 23907031 23907031 single base substitution C T intron_variant MELA-AU 13 23907031 23907031 single base substitution C T missense_variant E2912K 8734G>A MELA-AU 13 23907031 23907031 single base substitution C T missense_variant E3662K 10984G>A MELA-AU 13 23907273 23907273 single base substitution G A intron_variant MELA-AU 13 23907273 23907273 single base substitution G A missense_variant S2831F 8492C>T MELA-AU 13 23907273 23907273 single base substitution G A missense_variant S3581F 10742C>T MELA-AU 13 23907292 23907292 single base substitution G A intron_variant MELA-AU 13 23907292 23907292 single base substitution G A missense_variant H2825Y 8473C>T MELA-AU 13 23907292 23907292 single base substitution G A missense_variant H3575Y 10723C>T MELA-AU 13 23907590 23907590 single base substitution C T intron_variant MELA-AU 13 23907590 23907590 single base substitution C T synonymous_variant E2725E 8175G>A MELA-AU 13 23907590 23907590 single base substitution C T synonymous_variant E3475E 10425G>A MELA-AU 13 23908108 23908108 single base substitution G A intron_variant MELA-AU 13 23908108 23908108 single base substitution G A missense_variant P2553S 7657C>T MELA-AU 13 23908108 23908108 single base substitution G A missense_variant P3303S 9907C>T MELA-AU 13 23908728 23908728 single base substitution G A intron_variant MELA-AU 13 23908728 23908728 single base substitution G A missense_variant A2346V 7037C>T MELA-AU 13 23908728 23908728 single base substitution G A missense_variant A3096V 9287C>T MELA-AU 13 23909116 23909116 single base substitution G A intron_variant MELA-AU 13 23909116 23909116 single base substitution G A missense_variant R2217C 6649C>T MELA-AU 13 23909116 23909116 single base substitution G A missense_variant R2967C 8899C>T MELA-AU 13 23909492 23909492 single base substitution C A intron_variant MELA-AU 13 23909492 23909492 single base substitution C A missense_variant K2091N 6273G>T MELA-AU 13 23909492 23909492 single base substitution C A missense_variant K2841N 8523G>T MELA-AU 13 23910042 23910042 single base substitution G A intron_variant MELA-AU 13 23910042 23910042 single base substitution G A missense_variant A1908V 5723C>T MELA-AU 13 23910042 23910042 single base substitution G A missense_variant A2658V 7973C>T MELA-AU 13 23910124 23910124 single base substitution G A intron_variant MELA-AU 13 23910124 23910124 single base substitution G A missense_variant H1881Y 5641C>T MELA-AU 13 23910124 23910124 single base substitution G A missense_variant H2631Y 7891C>T MELA-AU 13 23910471 23910471 single base substitution A T intron_variant MELA-AU 13 23910471 23910471 single base substitution A T missense_variant F1765Y 5294T>A MELA-AU 13 23910471 23910471 single base substitution A T missense_variant F2515Y 7544T>A MELA-AU 13 23910790 23910790 single base substitution G A intron_variant MELA-AU 13 23910790 23910790 single base substitution G A stop_gained Q1659* 4975C>T MELA-AU 13 23910790 23910790 single base substitution G A stop_gained Q2409* 7225C>T MELA-AU 13 23911622 23911622 single base substitution G A intron_variant MELA-AU 13 23911622 23911622 single base substitution G A synonymous_variant F1381F 4143C>T MELA-AU 13 23911622 23911622 single base substitution G A synonymous_variant F2131F 6393C>T MELA-AU 13 23911699 23911699 single base substitution G A intron_variant MELA-AU 13 23911699 23911699 single base substitution G A missense_variant P1356S 4066C>T MELA-AU 13 23911699 23911699 single base substitution G A missense_variant P2106S 6316C>T MELA-AU 13 23911738 23911738 single base substitution G A intron_variant MELA-AU 13 23911738 23911738 single base substitution G A missense_variant R1343C 4027C>T MELA-AU 13 23911738 23911738 single base substitution G A missense_variant R2093C 6277C>T MELA-AU 13 23911743 23911743 single base substitution A G intron_variant MELA-AU 13 23911743 23911743 single base substitution A G missense_variant V1341A 4022T>C MELA-AU 13 23911743 23911743 single base substitution A G missense_variant V2091A 6272T>C MELA-AU 13 23911748 23911748 single base substitution C T intron_variant MELA-AU 13 23911748 23911748 single base substitution C T synonymous_variant S1339S 4017G>A MELA-AU 13 23911748 23911748 single base substitution C T synonymous_variant S2089S 6267G>A MELA-AU 13 23911927 23911927 single base substitution G A intron_variant MELA-AU 13 23911927 23911927 single base substitution G A missense_variant P1280S 3838C>T MELA-AU 13 23911927 23911927 single base substitution G A missense_variant P2030S 6088C>T MELA-AU 13 23912234 23912234 single base substitution G A intron_variant MELA-AU 13 23912234 23912234 single base substitution G A synonymous_variant V1177V 3531C>T MELA-AU 13 23912234 23912234 single base substitution G A synonymous_variant V1927V 5781C>T MELA-AU 13 23912391 23912391 single base substitution G A intron_variant MELA-AU 13 23912391 23912391 single base substitution G A missense_variant P1125L 3374C>T MELA-AU 13 23912391 23912391 single base substitution G A missense_variant P1875L 5624C>T MELA-AU 13 23912447 23912447 single base substitution G A intron_variant MELA-AU 13 23912447 23912447 single base substitution G A synonymous_variant I1106I 3318C>T MELA-AU 13 23912447 23912447 single base substitution G A synonymous_variant I1856I 5568C>T MELA-AU 13 23912862 23912862 single base substitution G A intron_variant MELA-AU 13 23912862 23912862 single base substitution G A missense_variant S1718F 5153C>T MELA-AU 13 23912862 23912862 single base substitution G A missense_variant S968F 2903C>T MELA-AU 13 23913031 23913033 deletion of <=200bp TAC - disruptive_inframe_deletion ST1661T MELA-AU 13 23913031 23913033 deletion of <=200bp TAC - disruptive_inframe_deletion ST911T MELA-AU 13 23913031 23913033 deletion of <=200bp TAC - intron_variant MELA-AU 13 23913632 23913632 single base substitution A C intron_variant MELA-AU 13 23913632 23913632 single base substitution A C synonymous_variant T1461T 4383T>G MELA-AU 13 23913632 23913632 single base substitution A C synonymous_variant T711T 2133T>G MELA-AU 13 23913705 23913705 single base substitution G A intron_variant MELA-AU 13 23913705 23913705 single base substitution G A missense_variant P1437L 4310C>T MELA-AU 13 23913705 23913705 single base substitution G A missense_variant P687L 2060C>T MELA-AU 13 23914073 23914073 single base substitution G A intron_variant MELA-AU 13 23914073 23914073 single base substitution G A synonymous_variant F1314F 3942C>T MELA-AU 13 23914073 23914073 single base substitution G A synonymous_variant F564F 1692C>T MELA-AU 13 23914110 23914110 single base substitution G A intron_variant MELA-AU 13 23914110 23914110 single base substitution G A missense_variant P1302L 3905C>T MELA-AU 13 23914110 23914110 single base substitution G A missense_variant P552L 1655C>T MELA-AU 13 23914271 23914271 single base substitution G A intron_variant MELA-AU 13 23914271 23914271 single base substitution G A synonymous_variant F1248F 3744C>T MELA-AU 13 23914271 23914271 single base substitution G A synonymous_variant F498F 1494C>T MELA-AU 13 23914757 23914757 single base substitution G A intron_variant MELA-AU 13 23914757 23914757 single base substitution G A synonymous_variant S1086S 3258C>T MELA-AU 13 23914757 23914757 single base substitution G A synonymous_variant S336S 1008C>T MELA-AU 13 23914848 23914848 single base substitution G A intron_variant MELA-AU 13 23914848 23914848 single base substitution G A missense_variant P1056L 3167C>T MELA-AU 13 23914848 23914848 single base substitution G A missense_variant P306L 917C>T MELA-AU 13 23915678 23915678 single base substitution A G intron_variant MELA-AU 13 23915678 23915678 single base substitution A G synonymous_variant L29L 87T>C MELA-AU 13 23915678 23915678 single base substitution A G synonymous_variant L678L 2034T>C MELA-AU 13 23915678 23915678 single base substitution A G synonymous_variant L779L 2337T>C MELA-AU 13 23915912 23915912 single base substitution G A intron_variant MELA-AU 13 23915950 23915950 single base substitution G A intron_variant MELA-AU 13 23916093 23916093 deletion of <=200bp T - intron_variant MELA-AU 13 23916157 23916157 single base substitution A G intron_variant MELA-AU 13 23916503 23916503 single base substitution G A intron_variant MELA-AU 13 23916588 23916588 single base substitution C T intron_variant MELA-AU 13 23916637 23916637 single base substitution G A intron_variant MELA-AU 13 23917265 23917265 single base substitution C T intron_variant MELA-AU 13 23917446 23917446 single base substitution C T intron_variant MELA-AU 13 23917452 23917452 single base substitution G A intron_variant MELA-AU 13 23917608 23917608 single base substitution G A intron_variant MELA-AU 13 23917749 23917749 single base substitution G A intron_variant MELA-AU 13 23918128 23918128 single base substitution G A intron_variant MELA-AU 13 23919312 23919312 single base substitution G A intron_variant MELA-AU 13 23919492 23919492 single base substitution C T intron_variant MELA-AU 13 23919997 23919997 single base substitution G A intron_variant MELA-AU 13 23920160 23920160 single base substitution G A intron_variant MELA-AU 13 23920474 23920474 single base substitution G A intron_variant MELA-AU 13 23921342 23921342 single base substitution A T intron_variant MELA-AU 13 23921934 23921934 deletion of <=200bp C - intron_variant MELA-AU 13 23921959 23921959 single base substitution G A intron_variant MELA-AU 13 23922115 23922115 single base substitution G A intron_variant MELA-AU 13 23922746 23922746 single base substitution G A intron_variant MELA-AU 13 23923466 23923466 single base substitution G A downstream_gene_variant MELA-AU 13 23923466 23923466 single base substitution G A intron_variant MELA-AU 13 23923467 23923467 single base substitution G A downstream_gene_variant MELA-AU 13 23923467 23923467 single base substitution G A intron_variant MELA-AU 13 23923913 23923913 single base substitution G A downstream_gene_variant MELA-AU 13 23923913 23923913 single base substitution G A intron_variant MELA-AU 13 23924036 23924036 single base substitution G A downstream_gene_variant MELA-AU 13 23924036 23924036 single base substitution G A intron_variant MELA-AU 13 23924479 23924479 single base substitution G A downstream_gene_variant MELA-AU 13 23924479 23924479 single base substitution G A intron_variant MELA-AU 13 23924518 23924518 single base substitution G A downstream_gene_variant MELA-AU 13 23924518 23924518 single base substitution G A intron_variant MELA-AU 13 23925036 23925036 single base substitution G A downstream_gene_variant MELA-AU 13 23925036 23925036 single base substitution G A intron_variant MELA-AU 13 23925271 23925271 single base substitution G A downstream_gene_variant MELA-AU 13 23925271 23925271 single base substitution G A intron_variant MELA-AU 13 23925386 23925386 single base substitution G A downstream_gene_variant MELA-AU 13 23925386 23925386 single base substitution G A intron_variant MELA-AU 13 23925563 23925563 single base substitution G A downstream_gene_variant MELA-AU 13 23925563 23925563 single base substitution G A intron_variant MELA-AU 13 23925579 23925579 single base substitution G A downstream_gene_variant MELA-AU 13 23925579 23925579 single base substitution G A intron_variant MELA-AU 13 23926178 23926178 single base substitution G A downstream_gene_variant MELA-AU 13 23926178 23926178 single base substitution G A intron_variant MELA-AU 13 23926857 23926857 single base substitution G A downstream_gene_variant MELA-AU 13 23926857 23926857 single base substitution G A intron_variant MELA-AU 13 23927715 23927715 single base substitution G A downstream_gene_variant MELA-AU 13 23927715 23927715 single base substitution G A intron_variant MELA-AU 13 23927879 23927879 single base substitution A G exon_variant MELA-AU 13 23927879 23927879 single base substitution A G intron_variant MELA-AU 13 23928615 23928615 single base substitution G A intron_variant MELA-AU 13 23928767 23928767 single base substitution C T 5_prime_UTR_variant MELA-AU 13 23928767 23928767 single base substitution C T exon_variant MELA-AU 13 23928767 23928767 single base substitution C T missense_variant E286K 856G>A MELA-AU 13 23928767 23928767 single base substitution C T missense_variant E561K 1681G>A MELA-AU 13 23928767 23928767 single base substitution C T missense_variant E662K 1984G>A MELA-AU 13 23928800 23928800 single base substitution G A 5_prime_UTR_variant MELA-AU 13 23928800 23928800 single base substitution G A exon_variant MELA-AU 13 23928800 23928800 single base substitution G A synonymous_variant L275L 823C>T MELA-AU 13 23928800 23928800 single base substitution G A synonymous_variant L550L 1648C>T MELA-AU 13 23928800 23928800 single base substitution G A synonymous_variant L651L 1951C>T MELA-AU 13 23930076 23930076 single base substitution A T 5_prime_UTR_variant MELA-AU 13 23930076 23930076 single base substitution A T missense_variant H124Q 372T>A MELA-AU 13 23930076 23930076 single base substitution A T missense_variant H225Q 675T>A MELA-AU 13 23930076 23930076 single base substitution A T upstream_gene_variant MELA-AU 13 23930081 23930081 single base substitution G A 5_prime_UTR_variant MELA-AU 13 23930081 23930081 single base substitution G A missense_variant P123S 367C>T MELA-AU 13 23930081 23930081 single base substitution G A missense_variant P224S 670C>T MELA-AU 13 23930081 23930081 single base substitution G A upstream_gene_variant MELA-AU 13 23931154 23931154 single base substitution G A intron_variant MELA-AU 13 23931154 23931154 single base substitution G A upstream_gene_variant MELA-AU 13 23931816 23931816 single base substitution C G intron_variant MELA-AU 13 23931816 23931816 single base substitution C G upstream_gene_variant MELA-AU 13 23931906 23931906 single base substitution G A intron_variant MELA-AU 13 23931906 23931906 single base substitution G A upstream_gene_variant MELA-AU 13 23933350 23933350 single base substitution G A intron_variant MELA-AU 13 23933350 23933350 single base substitution G A upstream_gene_variant MELA-AU 13 23933949 23933949 single base substitution C T intron_variant MELA-AU 13 23933949 23933949 single base substitution C T upstream_gene_variant MELA-AU 13 23934640 23934640 single base substitution G A intron_variant MELA-AU 13 23934709 23934709 single base substitution G A intron_variant MELA-AU 13 23934987 23934988 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 23935265 23935265 single base substitution G A intron_variant MELA-AU 13 23935779 23935779 single base substitution G A intron_variant MELA-AU 13 23935927 23935927 single base substitution G A intron_variant MELA-AU 13 23935994 23935994 single base substitution G A intron_variant MELA-AU 13 23937172 23937172 single base substitution C T intron_variant MELA-AU 13 23937912 23937912 single base substitution G A intron_variant MELA-AU 13 23937925 23937925 single base substitution T C intron_variant MELA-AU 13 23938235 23938235 single base substitution G A intron_variant MELA-AU 13 23938554 23938554 single base substitution G A intron_variant MELA-AU 13 23938634 23938634 single base substitution G A intron_variant MELA-AU 13 23939180 23939180 single base substitution G A intron_variant MELA-AU 13 23939970 23939970 single base substitution G A intron_variant MELA-AU 13 23940327 23940327 single base substitution C A intron_variant MELA-AU 13 23941868 23941868 single base substitution G A intron_variant MELA-AU 13 23942662 23942662 single base substitution A T intron_variant MELA-AU 13 23942662 23942662 single base substitution A T upstream_gene_variant MELA-AU 13 23943498 23943498 single base substitution G A intron_variant MELA-AU 13 23943498 23943498 single base substitution G A upstream_gene_variant MELA-AU 13 23943933 23943933 single base substitution C T intron_variant MELA-AU 13 23943933 23943933 single base substitution C T upstream_gene_variant MELA-AU 13 23944016 23944016 single base substitution G A intron_variant MELA-AU 13 23944016 23944016 single base substitution G A upstream_gene_variant MELA-AU 13 23944061 23944061 single base substitution G A intron_variant MELA-AU 13 23944061 23944061 single base substitution G A upstream_gene_variant MELA-AU 13 23944374 23944374 single base substitution G A intron_variant MELA-AU 13 23944374 23944374 single base substitution G A upstream_gene_variant MELA-AU 13 23944886 23944886 single base substitution G A intron_variant MELA-AU 13 23944886 23944886 single base substitution G A upstream_gene_variant MELA-AU 13 23946409 23946409 single base substitution G A intron_variant MELA-AU 13 23946409 23946409 single base substitution G A upstream_gene_variant MELA-AU 13 23947840 23947840 single base substitution G T intron_variant MELA-AU 13 23949811 23949811 single base substitution G A intron_variant MELA-AU 13 23949811 23949811 single base substitution G A upstream_gene_variant MELA-AU 13 23949889 23949889 single base substitution C T intron_variant MELA-AU 13 23949889 23949889 single base substitution C T upstream_gene_variant MELA-AU 13 23951091 23951091 single base substitution A G intron_variant MELA-AU 13 23951091 23951091 single base substitution A G upstream_gene_variant MELA-AU 13 23951127 23951127 single base substitution C T intron_variant MELA-AU 13 23951127 23951127 single base substitution C T upstream_gene_variant MELA-AU 13 23951258 23951258 single base substitution G A intron_variant MELA-AU 13 23951258 23951258 single base substitution G A upstream_gene_variant MELA-AU 13 23951336 23951336 single base substitution G A intron_variant MELA-AU 13 23951336 23951336 single base substitution G A upstream_gene_variant MELA-AU 13 23951484 23951484 single base substitution C T intron_variant MELA-AU 13 23951484 23951484 single base substitution C T upstream_gene_variant MELA-AU 13 23951512 23951512 single base substitution G A intron_variant MELA-AU 13 23951512 23951512 single base substitution G A upstream_gene_variant MELA-AU 13 23951520 23951520 single base substitution G A intron_variant MELA-AU 13 23951520 23951520 single base substitution G A upstream_gene_variant MELA-AU 13 23952066 23952066 single base substitution G A intron_variant MELA-AU 13 23952066 23952066 single base substitution G A upstream_gene_variant MELA-AU 13 23952366 23952366 single base substitution T C intron_variant MELA-AU 13 23952366 23952366 single base substitution T C upstream_gene_variant MELA-AU 13 23953006 23953006 single base substitution G A intron_variant MELA-AU 13 23953006 23953006 single base substitution G A upstream_gene_variant MELA-AU 13 23953082 23953082 single base substitution G A intron_variant MELA-AU 13 23953082 23953082 single base substitution G A upstream_gene_variant MELA-AU 13 23953274 23953274 single base substitution G C intron_variant MELA-AU 13 23953274 23953274 single base substitution G C upstream_gene_variant MELA-AU 13 23953412 23953412 single base substitution C T intron_variant MELA-AU 13 23953412 23953412 single base substitution C T upstream_gene_variant MELA-AU 13 23954059 23954059 single base substitution G A intron_variant MELA-AU 13 23954059 23954059 single base substitution G A upstream_gene_variant MELA-AU 13 23954180 23954180 single base substitution C T intron_variant MELA-AU 13 23954180 23954180 single base substitution C T upstream_gene_variant MELA-AU 13 23954921 23954921 single base substitution C T intron_variant MELA-AU 13 23955119 23955119 single base substitution C T intron_variant MELA-AU 13 23955128 23955128 single base substitution G A intron_variant MELA-AU 13 23955341 23955341 single base substitution G A intron_variant MELA-AU 13 23955491 23955491 single base substitution G A intron_variant MELA-AU 13 23955989 23955989 single base substitution G A intron_variant MELA-AU 13 23956062 23956062 single base substitution C T intron_variant MELA-AU 13 23956485 23956485 single base substitution G A intron_variant MELA-AU 13 23956708 23956708 single base substitution G A intron_variant MELA-AU 13 23957259 23957259 single base substitution T C intron_variant MELA-AU 13 23957646 23957646 single base substitution C T intron_variant MELA-AU 13 23957841 23957841 single base substitution G A intron_variant MELA-AU 13 23958011 23958011 single base substitution C T intron_variant MELA-AU 13 23958150 23958150 single base substitution A G intron_variant MELA-AU 13 23958763 23958763 single base substitution G A intron_variant MELA-AU 13 23958811 23958811 single base substitution G A intron_variant MELA-AU 13 23959541 23959541 single base substitution C T intron_variant MELA-AU 13 23960392 23960392 single base substitution C T intron_variant MELA-AU 13 23960405 23960405 single base substitution C T intron_variant MELA-AU 13 23960748 23960748 single base substitution C T intron_variant MELA-AU 13 23961272 23961272 single base substitution G A intron_variant MELA-AU 13 23961279 23961279 single base substitution G A intron_variant MELA-AU 13 23961368 23961368 single base substitution G A intron_variant MELA-AU 13 23961555 23961555 single base substitution C T intron_variant MELA-AU 13 23961705 23961705 single base substitution G A intron_variant MELA-AU 13 23962163 23962163 single base substitution G A intron_variant MELA-AU 13 23962320 23962320 single base substitution G A intron_variant MELA-AU 13 23962331 23962331 single base substitution G A intron_variant MELA-AU 13 23962405 23962405 single base substitution G A intron_variant MELA-AU 13 23962420 23962420 single base substitution C T intron_variant MELA-AU 13 23962547 23962547 single base substitution A G intron_variant MELA-AU 13 23962561 23962561 single base substitution G A intron_variant MELA-AU 13 23962647 23962647 single base substitution T C intron_variant MELA-AU 13 23962895 23962895 single base substitution G A intron_variant MELA-AU 13 23963203 23963203 single base substitution A T intron_variant MELA-AU 13 23963572 23963572 single base substitution G A intron_variant MELA-AU 13 23963734 23963734 single base substitution C T intron_variant MELA-AU 13 23963793 23963793 single base substitution G A intron_variant MELA-AU 13 23964081 23964081 single base substitution G A intron_variant MELA-AU 13 23964389 23964391 deletion of <=200bp GGT - intron_variant MELA-AU 13 23964439 23964439 single base substitution C T intron_variant MELA-AU 13 23965027 23965027 single base substitution C T intron_variant MELA-AU 13 23965260 23965260 single base substitution G A intron_variant MELA-AU 13 23965492 23965492 single base substitution C T intron_variant MELA-AU 13 23965498 23965498 single base substitution C T intron_variant MELA-AU 13 23965570 23965570 single base substitution G A intron_variant MELA-AU 13 23965614 23965614 single base substitution G A intron_variant MELA-AU 13 23965754 23965755 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 23966015 23966015 single base substitution C T intron_variant MELA-AU 13 23966146 23966146 single base substitution G A intron_variant MELA-AU 13 23966210 23966210 single base substitution G A intron_variant MELA-AU 13 23966265 23966265 single base substitution G A intron_variant MELA-AU 13 23966303 23966303 single base substitution C T intron_variant MELA-AU 13 23966344 23966344 single base substitution C T intron_variant MELA-AU 13 23966472 23966472 single base substitution C T intron_variant MELA-AU 13 23966888 23966888 single base substitution G A intron_variant MELA-AU 13 23966990 23966990 single base substitution C T intron_variant MELA-AU 13 23967228 23967228 single base substitution C T intron_variant MELA-AU 13 23967472 23967472 single base substitution G A intron_variant MELA-AU 13 23967485 23967485 single base substitution G A intron_variant MELA-AU 13 23967511 23967511 single base substitution C T intron_variant MELA-AU 13 23967644 23967644 single base substitution C T intron_variant MELA-AU 13 23967890 23967890 single base substitution C T intron_variant MELA-AU 13 23967963 23967963 single base substitution G A intron_variant MELA-AU 13 23967984 23967984 single base substitution C T intron_variant MELA-AU 13 23968156 23968157 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 13 23968240 23968240 single base substitution G A intron_variant MELA-AU 13 23968479 23968479 single base substitution G A intron_variant MELA-AU 13 23968594 23968594 single base substitution C T intron_variant MELA-AU 13 23968595 23968595 single base substitution C T intron_variant MELA-AU 13 23968747 23968747 single base substitution C T intron_variant MELA-AU 13 23968877 23968877 single base substitution C T intron_variant MELA-AU 13 23968923 23968923 single base substitution G A intron_variant MELA-AU 13 23968952 23968952 single base substitution C A intron_variant MELA-AU 13 23969139 23969139 single base substitution C T intron_variant MELA-AU 13 23969166 23969166 single base substitution G A intron_variant MELA-AU 13 23969403 23969403 single base substitution C T intron_variant MELA-AU 13 23969512 23969512 single base substitution G A intron_variant MELA-AU 13 23969590 23969590 single base substitution C T intron_variant MELA-AU 13 23969624 23969624 single base substitution C T intron_variant MELA-AU 13 23969654 23969654 single base substitution A C intron_variant MELA-AU 13 23970131 23970131 single base substitution G A intron_variant MELA-AU 13 23970255 23970255 single base substitution G A intron_variant MELA-AU 13 23970338 23970338 single base substitution C T intron_variant MELA-AU 13 23970386 23970386 single base substitution C T intron_variant MELA-AU 13 23970948 23970958 deletion of <=200bp AATATGTCTGC - intron_variant MELA-AU 13 23971403 23971403 single base substitution G A intron_variant MELA-AU 13 23971412 23971412 single base substitution G A intron_variant MELA-AU 13 23972078 23972078 single base substitution C T intron_variant MELA-AU 13 23972079 23972079 single base substitution C T intron_variant MELA-AU 13 23972288 23972288 single base substitution C T intron_variant MELA-AU 13 23972318 23972318 single base substitution G A intron_variant MELA-AU 13 23972430 23972430 single base substitution G A intron_variant MELA-AU 13 23972582 23972582 single base substitution A T intron_variant MELA-AU 13 23972668 23972668 single base substitution C T intron_variant MELA-AU 13 23972766 23972766 single base substitution T G intron_variant MELA-AU 13 23972828 23972828 single base substitution G A intron_variant MELA-AU 13 23972829 23972829 single base substitution G A intron_variant MELA-AU 13 23973206 23973206 single base substitution G A intron_variant MELA-AU 13 23973631 23973631 single base substitution T G intron_variant MELA-AU 13 23974195 23974195 single base substitution T C intron_variant MELA-AU 13 23974342 23974342 single base substitution G A intron_variant MELA-AU 13 23974343 23974343 single base substitution G A intron_variant MELA-AU 13 23974529 23974529 single base substitution C T intron_variant MELA-AU 13 23975050 23975050 single base substitution C T intron_variant MELA-AU 13 23975197 23975197 single base substitution G A intron_variant MELA-AU 13 23975339 23975339 single base substitution C T intron_variant MELA-AU 13 23975449 23975449 single base substitution G A intron_variant MELA-AU 13 23975512 23975512 single base substitution A T intron_variant MELA-AU 13 23975563 23975563 single base substitution C T intron_variant MELA-AU 13 23975568 23975568 single base substitution C T intron_variant MELA-AU 13 23975580 23975580 single base substitution C T intron_variant MELA-AU 13 23975758 23975758 single base substitution G A intron_variant MELA-AU 13 23975926 23975926 single base substitution G A intron_variant MELA-AU 13 23975942 23975942 single base substitution C T intron_variant MELA-AU 13 23976252 23976252 single base substitution G A intron_variant MELA-AU 13 23976266 23976266 single base substitution G C intron_variant MELA-AU 13 23976365 23976365 single base substitution G A intron_variant MELA-AU 13 23976838 23976838 single base substitution G A intron_variant MELA-AU 13 23977224 23977224 single base substitution G A intron_variant MELA-AU 13 23977431 23977431 single base substitution G A intron_variant MELA-AU 13 23977589 23977589 single base substitution G A intron_variant MELA-AU 13 23977848 23977848 single base substitution G A intron_variant MELA-AU 13 23978022 23978022 single base substitution G A intron_variant MELA-AU 13 23978213 23978213 single base substitution C T intron_variant MELA-AU 13 23978614 23978614 single base substitution G A intron_variant MELA-AU 13 23978753 23978753 single base substitution G A intron_variant MELA-AU 13 23978901 23978901 single base substitution T C intron_variant MELA-AU 13 23979458 23979458 single base substitution C T intron_variant MELA-AU 13 23979480 23979480 single base substitution G A intron_variant MELA-AU 13 23979596 23979596 single base substitution G A intron_variant MELA-AU 13 23979837 23979837 single base substitution G A intron_variant MELA-AU 13 23980080 23980080 single base substitution G A intron_variant MELA-AU 13 23980160 23980160 single base substitution C T intron_variant MELA-AU 13 23980194 23980194 single base substitution C T intron_variant MELA-AU 13 23980208 23980208 single base substitution G A intron_variant MELA-AU 13 23980269 23980269 single base substitution C T intron_variant MELA-AU 13 23980292 23980292 single base substitution G A intron_variant MELA-AU 13 23980493 23980493 single base substitution G A intron_variant MELA-AU 13 23980527 23980527 single base substitution G A intron_variant MELA-AU 13 23980535 23980535 single base substitution G A intron_variant MELA-AU 13 23981276 23981276 single base substitution A G intron_variant MELA-AU 13 23981362 23981362 single base substitution G A intron_variant MELA-AU 13 23982003 23982003 single base substitution G A intron_variant MELA-AU 13 23982075 23982075 single base substitution T A intron_variant MELA-AU 13 23982318 23982318 single base substitution C T intron_variant MELA-AU 13 23982525 23982525 single base substitution C T intron_variant MELA-AU 13 23982867 23982867 single base substitution G A intron_variant MELA-AU 13 23982900 23982900 single base substitution C T intron_variant MELA-AU 13 23983223 23983223 single base substitution C T intron_variant MELA-AU 13 23983255 23983255 single base substitution G A intron_variant MELA-AU 13 23983352 23983352 single base substitution C T intron_variant MELA-AU 13 23983416 23983416 single base substitution G A intron_variant MELA-AU 13 23983419 23983419 single base substitution C T intron_variant MELA-AU 13 23983586 23983586 single base substitution C T intron_variant MELA-AU 13 23983592 23983592 single base substitution T C intron_variant MELA-AU 13 23985213 23985213 single base substitution C T intron_variant MELA-AU 13 23985231 23985231 single base substitution G A intron_variant MELA-AU 13 23985663 23985663 single base substitution G A 5_prime_UTR_variant MELA-AU 13 23985663 23985663 single base substitution G A upstream_gene_variant MELA-AU 13 23985751 23985751 single base substitution G A 5_prime_UTR_variant MELA-AU 13 23985751 23985751 single base substitution G A upstream_gene_variant MELA-AU 13 23985753 23985753 single base substitution G A 5_prime_UTR_variant MELA-AU 13 23985753 23985753 single base substitution G A upstream_gene_variant MELA-AU 13 23985864 23985865 multiple base substitution (>=2bp and <=200bp) CC TT 5_prime_UTR_variant MELA-AU 13 23985864 23985865 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 13 23985886 23985886 single base substitution G A splice_region_variant MELA-AU 13 23985886 23985886 single base substitution G A upstream_gene_variant MELA-AU 13 23986108 23986108 single base substitution A C intron_variant MELA-AU 13 23986108 23986108 single base substitution A C upstream_gene_variant MELA-AU 13 23986134 23986134 single base substitution C T intron_variant MELA-AU 13 23986134 23986134 single base substitution C T upstream_gene_variant MELA-AU 13 23986224 23986224 single base substitution C T intron_variant MELA-AU 13 23986224 23986224 single base substitution C T upstream_gene_variant MELA-AU 13 23986321 23986321 single base substitution C T intron_variant MELA-AU 13 23986321 23986321 single base substitution C T upstream_gene_variant MELA-AU 13 23986352 23986352 single base substitution C T intron_variant MELA-AU 13 23986352 23986352 single base substitution C T upstream_gene_variant MELA-AU 13 23986479 23986479 single base substitution G A intron_variant MELA-AU 13 23986479 23986479 single base substitution G A upstream_gene_variant MELA-AU 13 23986643 23986643 single base substitution C T intron_variant MELA-AU 13 23986643 23986643 single base substitution C T upstream_gene_variant MELA-AU 13 23986646 23986646 single base substitution G A intron_variant MELA-AU 13 23986646 23986646 single base substitution G A upstream_gene_variant MELA-AU 13 23986824 23986824 single base substitution G A intron_variant MELA-AU 13 23986824 23986824 single base substitution G A upstream_gene_variant MELA-AU 13 23986854 23986854 single base substitution C T intron_variant MELA-AU 13 23986854 23986854 single base substitution C T upstream_gene_variant MELA-AU 13 23986947 23986947 single base substitution G A intron_variant MELA-AU 13 23986947 23986947 single base substitution G A upstream_gene_variant MELA-AU 13 23986964 23986964 single base substitution A G intron_variant MELA-AU 13 23986964 23986964 single base substitution A G upstream_gene_variant MELA-AU 13 23987308 23987308 single base substitution G A intron_variant MELA-AU 13 23987308 23987308 single base substitution G A upstream_gene_variant MELA-AU 13 23987833 23987833 single base substitution C T intron_variant MELA-AU 13 23987833 23987833 single base substitution C T upstream_gene_variant MELA-AU 13 23988437 23988437 single base substitution C T intron_variant MELA-AU 13 23988437 23988437 single base substitution C T upstream_gene_variant MELA-AU 13 23988672 23988672 single base substitution T G intron_variant MELA-AU 13 23988672 23988672 single base substitution T G upstream_gene_variant MELA-AU 13 23988940 23988940 single base substitution G A intron_variant MELA-AU 13 23988940 23988940 single base substitution G A upstream_gene_variant MELA-AU 13 23988979 23988979 single base substitution C T intron_variant MELA-AU 13 23988979 23988979 single base substitution C T upstream_gene_variant MELA-AU 13 23989065 23989065 single base substitution G A intron_variant MELA-AU 13 23989065 23989065 single base substitution G A upstream_gene_variant MELA-AU 13 23989291 23989291 single base substitution C T intron_variant MELA-AU 13 23989291 23989291 single base substitution C T upstream_gene_variant MELA-AU 13 23989553 23989553 single base substitution G A intron_variant MELA-AU 13 23989553 23989553 single base substitution G A upstream_gene_variant MELA-AU 13 23989718 23989718 single base substitution G A intron_variant MELA-AU 13 23989718 23989718 single base substitution G A upstream_gene_variant MELA-AU 13 23990414 23990414 single base substitution C T intron_variant MELA-AU 13 23990414 23990414 single base substitution C T upstream_gene_variant MELA-AU 13 23990426 23990426 single base substitution G A intron_variant MELA-AU 13 23990426 23990426 single base substitution G A upstream_gene_variant MELA-AU 13 23990427 23990427 single base substitution G A intron_variant MELA-AU 13 23990427 23990427 single base substitution G A upstream_gene_variant MELA-AU 13 23991289 23991289 single base substitution G A intron_variant MELA-AU 13 23991319 23991319 single base substitution A T intron_variant MELA-AU 13 23991379 23991379 single base substitution T C intron_variant MELA-AU 13 23991466 23991466 single base substitution A G intron_variant MELA-AU 13 23991726 23991726 single base substitution G A intron_variant MELA-AU 13 23992174 23992174 single base substitution C T intron_variant MELA-AU 13 23992182 23992182 single base substitution G A intron_variant MELA-AU 13 23992950 23992950 single base substitution T A intron_variant MELA-AU 13 23992963 23992963 single base substitution T A intron_variant MELA-AU 13 23993037 23993038 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 23993042 23993042 single base substitution G A intron_variant MELA-AU 13 23993061 23993061 single base substitution C T intron_variant MELA-AU 13 23993072 23993072 single base substitution G A intron_variant MELA-AU 13 23993225 23993225 single base substitution G A intron_variant MELA-AU 13 23993476 23993476 single base substitution G A intron_variant MELA-AU 13 23993493 23993493 single base substitution C T intron_variant MELA-AU 13 23993630 23993630 single base substitution C T intron_variant MELA-AU 13 23993868 23993868 single base substitution C T intron_variant MELA-AU 13 23994067 23994067 single base substitution C T intron_variant MELA-AU 13 23994073 23994073 single base substitution G A intron_variant MELA-AU 13 23994333 23994333 single base substitution G A intron_variant MELA-AU 13 23994483 23994483 single base substitution G A intron_variant MELA-AU 13 23994743 23994743 single base substitution G A intron_variant MELA-AU 13 23994797 23994797 single base substitution G A intron_variant MELA-AU 13 23994859 23994859 single base substitution C T intron_variant MELA-AU 13 23995000 23995001 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 23995018 23995018 single base substitution G A intron_variant MELA-AU 13 23995036 23995036 single base substitution G A intron_variant MELA-AU 13 23995042 23995042 single base substitution G A intron_variant MELA-AU 13 23995725 23995725 single base substitution C T intron_variant MELA-AU 13 23995921 23995921 single base substitution G A intron_variant MELA-AU 13 23996219 23996220 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 13 23996315 23996315 single base substitution C T intron_variant MELA-AU 13 23996935 23996935 single base substitution A G intron_variant MELA-AU 13 23998718 23998718 single base substitution T C intron_variant MELA-AU 13 23999068 23999068 single base substitution C T intron_variant MELA-AU 13 23999257 23999257 single base substitution T G intron_variant MELA-AU 13 23999319 23999319 single base substitution C T intron_variant MELA-AU 13 23999438 23999438 single base substitution G A intron_variant MELA-AU 13 23999533 23999533 single base substitution G T intron_variant MELA-AU 13 23999538 23999538 single base substitution C T intron_variant MELA-AU 13 23999715 23999715 single base substitution C T intron_variant MELA-AU 13 23999813 23999813 single base substitution G A intron_variant MELA-AU 13 23999823 23999823 single base substitution A T intron_variant MELA-AU 13 23999950 23999950 single base substitution C T intron_variant MELA-AU 13 24000034 24000034 single base substitution G A intron_variant MELA-AU 13 24000152 24000152 single base substitution G A intron_variant MELA-AU 13 24000198 24000198 single base substitution G A intron_variant MELA-AU 13 24000636 24000636 single base substitution C T intron_variant MELA-AU 13 24001156 24001156 single base substitution G A intron_variant MELA-AU 13 24001233 24001233 single base substitution C T intron_variant MELA-AU 13 24001670 24001670 single base substitution G A intron_variant MELA-AU 13 24001749 24001749 single base substitution G A intron_variant MELA-AU 13 24002004 24002004 single base substitution G A intron_variant MELA-AU 13 24002882 24002882 single base substitution C T intron_variant MELA-AU 13 24003375 24003375 single base substitution G A intron_variant MELA-AU 13 24003388 24003388 single base substitution C T intron_variant MELA-AU 13 24003532 24003532 single base substitution C T intron_variant MELA-AU 13 24003747 24003747 single base substitution C T intron_variant MELA-AU 13 24003964 24003964 single base substitution T A intron_variant MELA-AU 13 24004277 24004278 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 13 24004280 24004280 single base substitution G A intron_variant MELA-AU 13 24004694 24004694 single base substitution G A intron_variant MELA-AU 13 24005031 24005031 single base substitution G A intron_variant MELA-AU 13 24005140 24005140 single base substitution C T intron_variant MELA-AU 13 24005164 24005164 single base substitution T C intron_variant MELA-AU 13 24005358 24005358 single base substitution G A intron_variant MELA-AU 13 24005457 24005457 single base substitution C T intron_variant MELA-AU 13 24005501 24005501 single base substitution C T intron_variant MELA-AU 13 24005759 24005759 single base substitution G A intron_variant MELA-AU 13 24006293 24006293 single base substitution G A intron_variant MELA-AU 13 24006446 24006446 single base substitution G A intron_variant MELA-AU 13 24006986 24006986 single base substitution G A intron_variant MELA-AU 13 24007038 24007038 single base substitution A G intron_variant MELA-AU 13 24007640 24007640 single base substitution C T intron_variant MELA-AU 13 24007683 24007683 single base substitution G A intron_variant MELA-AU 13 24007856 24007856 single base substitution C T upstream_gene_variant MELA-AU 13 24008594 24008594 single base substitution C T upstream_gene_variant MELA-AU 13 24008850 24008850 single base substitution C T upstream_gene_variant MELA-AU 13 24009113 24009113 single base substitution G A upstream_gene_variant MELA-AU 13 24010102 24010102 single base substitution T G upstream_gene_variant MELA-AU 13 24011081 24011082 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 13 24011274 24011274 single base substitution G A upstream_gene_variant MELA-AU 13 24011490 24011490 single base substitution G A upstream_gene_variant MELA-AU 13 24011695 24011695 single base substitution C T upstream_gene_variant MELA-AU 13 24011856 24011856 single base substitution T A upstream_gene_variant MELA-AU 13 24011892 24011892 single base substitution C T upstream_gene_variant MELA-AU 13 24012045 24012045 single base substitution C T upstream_gene_variant MELA-AU 13 24012089 24012089 single base substitution C T upstream_gene_variant MELA-AU 13 24012291 24012291 single base substitution C T upstream_gene_variant MELA-AU 13 24012686 24012686 single base substitution A C upstream_gene_variant ORCA-IN 13 23904421 23904421 single base substitution C T intron_variant ORCA-IN 13 23904421 23904421 single base substitution C T missense_variant D3782N 11344G>A ORCA-IN 13 23904421 23904421 single base substitution C T missense_variant D4532N 13594G>A ORCA-IN 13 23906298 23906298 single base substitution G A intron_variant ORCA-IN 13 23906298 23906298 single base substitution G A missense_variant A3156V 9467C>T ORCA-IN 13 23906298 23906298 single base substitution G A missense_variant A3906V 11717C>T ORCA-IN 13 23913992 23913992 single base substitution G C intron_variant ORCA-IN 13 23913992 23913992 single base substitution G C synonymous_variant L1341L 4023C>G ORCA-IN 13 23913992 23913992 single base substitution G C synonymous_variant L591L 1773C>G ORCA-IN 13 23917758 23917758 single base substitution G T intron_variant ORCA-IN 13 23919080 23919080 single base substitution G C intron_variant ORCA-IN 13 23929133 23929133 single base substitution T C 5_prime_UTR_variant ORCA-IN 13 23929133 23929133 single base substitution T C missense_variant K164E 490A>G ORCA-IN 13 23929133 23929133 single base substitution T C missense_variant K439E 1315A>G ORCA-IN 13 23929133 23929133 single base substitution T C missense_variant K540E 1618A>G ORCA-IN 13 23929133 23929133 single base substitution T C upstream_gene_variant ORCA-IN 13 23954274 23954274 single base substitution G T intron_variant ORCA-IN 13 23954274 23954274 single base substitution G T upstream_gene_variant ORCA-IN 13 23958375 23958375 single base substitution G A intron_variant OV-AU 13 23902569 23902569 single base substitution G A downstream_gene_variant OV-AU 13 23906275 23906275 single base substitution C A intron_variant OV-AU 13 23906275 23906275 single base substitution C A missense_variant G3164C 9490G>T OV-AU 13 23906275 23906275 single base substitution C A missense_variant G3914C 11740G>T OV-AU 13 23908246 23908246 single base substitution C T intron_variant OV-AU 13 23908246 23908246 single base substitution C T missense_variant V2507M 7519G>A OV-AU 13 23908246 23908246 single base substitution C T missense_variant V3257M 9769G>A OV-AU 13 23910218 23910218 single base substitution A G intron_variant OV-AU 13 23910218 23910218 single base substitution A G synonymous_variant D1849D 5547T>C OV-AU 13 23910218 23910218 single base substitution A G synonymous_variant D2599D 7797T>C OV-AU 13 23915155 23915155 single base substitution C T intron_variant OV-AU 13 23915155 23915155 single base substitution C T missense_variant A204T 610G>A OV-AU 13 23915155 23915155 single base substitution C T missense_variant A954T 2860G>A OV-AU 13 23917608 23917608 single base substitution G A intron_variant OV-AU 13 23919973 23919973 single base substitution C A intron_variant OV-AU 13 23927255 23927255 single base substitution G A downstream_gene_variant OV-AU 13 23927255 23927255 single base substitution G A intron_variant OV-AU 13 23933793 23933793 single base substitution T C intron_variant OV-AU 13 23933793 23933793 single base substitution T C upstream_gene_variant OV-AU 13 23942255 23942255 single base substitution G T intron_variant OV-AU 13 23944314 23944314 single base substitution C G intron_variant OV-AU 13 23944314 23944314 single base substitution C G upstream_gene_variant OV-AU 13 23949589 23949589 single base substitution G C 5_prime_UTR_variant OV-AU 13 23949589 23949589 single base substitution G C intron_variant OV-AU 13 23956212 23956212 single base substitution G A intron_variant OV-AU 13 23961296 23961296 single base substitution G A intron_variant OV-AU 13 23964769 23964769 single base substitution C A intron_variant OV-AU 13 23974138 23974138 single base substitution G A intron_variant OV-AU 13 23985219 23985219 single base substitution G A intron_variant OV-AU 13 23986329 23986329 single base substitution T A intron_variant OV-AU 13 23986329 23986329 single base substitution T A upstream_gene_variant OV-AU 13 24000330 24000330 single base substitution A C intron_variant OV-AU 13 24002575 24002575 single base substitution A T intron_variant OV-AU 13 24012605 24012605 single base substitution G C upstream_gene_variant OV-US 13 23913133 23913133 single base substitution G A intron_variant OV-US 13 23913133 23913133 single base substitution G A stop_gained Q1628* 4882C>T OV-US 13 23913133 23913133 single base substitution G A stop_gained Q878* 2632C>T OV-US 13 23913870 23913870 single base substitution T C intron_variant OV-US 13 23913870 23913870 single base substitution T C missense_variant H1382R 4145A>G OV-US 13 23913870 23913870 single base substitution T C missense_variant H632R 1895A>G PACA-AU 13 23901767 23901767 single base substitution G A downstream_gene_variant PACA-AU 13 23903651 23903651 single base substitution T A 3_prime_UTR_variant PACA-AU 13 23903651 23903651 single base substitution T A intron_variant PACA-AU 13 23904859 23904859 single base substitution G A intron_variant PACA-AU 13 23904859 23904859 single base substitution G A stop_gained R3636* 10906C>T PACA-AU 13 23904859 23904859 single base substitution G A stop_gained R4386* 13156C>T PACA-AU 13 23906392 23906392 single base substitution G A intron_variant PACA-AU 13 23906392 23906392 single base substitution G A missense_variant R3125C 9373C>T PACA-AU 13 23906392 23906392 single base substitution G A missense_variant R3875C 11623C>T PACA-AU 13 23906739 23906739 single base substitution G A intron_variant PACA-AU 13 23906739 23906739 single base substitution G A missense_variant T3009M 9026C>T PACA-AU 13 23906739 23906739 single base substitution G A missense_variant T3759M 11276C>T PACA-AU 13 23908500 23908500 single base substitution T G intron_variant PACA-AU 13 23908500 23908500 single base substitution T G missense_variant K2422T 7265A>C PACA-AU 13 23908500 23908500 single base substitution T G missense_variant K3172T 9515A>C PACA-AU 13 23909538 23909538 single base substitution A T intron_variant PACA-AU 13 23909538 23909538 single base substitution A T missense_variant F2076Y 6227T>A PACA-AU 13 23909538 23909538 single base substitution A T missense_variant F2826Y 8477T>A PACA-AU 13 23909874 23909874 single base substitution G A intron_variant PACA-AU 13 23909874 23909874 single base substitution G A missense_variant S1964L 5891C>T PACA-AU 13 23909874 23909874 single base substitution G A missense_variant S2714L 8141C>T PACA-AU 13 23914837 23914837 single base substitution C T intron_variant PACA-AU 13 23914837 23914837 single base substitution C T missense_variant V1060I 3178G>A PACA-AU 13 23914837 23914837 single base substitution C T missense_variant V310I 928G>A PACA-AU 13 23915142 23915142 single base substitution G C intron_variant PACA-AU 13 23915142 23915142 single base substitution G C missense_variant A208G 623C>G PACA-AU 13 23915142 23915142 single base substitution G C missense_variant A958G 2873C>G PACA-AU 13 23915698 23915698 single base substitution G A intron_variant PACA-AU 13 23915698 23915698 single base substitution G A missense_variant H23Y 67C>T PACA-AU 13 23915698 23915698 single base substitution G A missense_variant H672Y 2014C>T PACA-AU 13 23915698 23915698 single base substitution G A missense_variant H773Y 2317C>T PACA-AU 13 23918528 23918529 deletion of <=200bp AC - intron_variant PACA-AU 13 23924742 23924742 single base substitution C T downstream_gene_variant PACA-AU 13 23924742 23924742 single base substitution C T intron_variant PACA-AU 13 23928926 23928926 deletion of <=200bp C - 5_prime_UTR_variant PACA-AU 13 23928926 23928926 deletion of <=200bp C - exon_variant PACA-AU 13 23928926 23928926 deletion of <=200bp C - frameshift_variant D233 PACA-AU 13 23928926 23928926 deletion of <=200bp C - frameshift_variant D508 PACA-AU 13 23928926 23928926 deletion of <=200bp C - frameshift_variant D609 PACA-AU 13 23941516 23941516 single base substitution T C intron_variant PACA-AU 13 23944604 23944604 single base substitution A C intron_variant PACA-AU 13 23944604 23944604 single base substitution A C upstream_gene_variant PACA-AU 13 23945178 23945178 single base substitution C A intron_variant PACA-AU 13 23945178 23945178 single base substitution C A upstream_gene_variant PACA-AU 13 23945510 23945510 single base substitution C T intron_variant PACA-AU 13 23945510 23945510 single base substitution C T upstream_gene_variant PACA-AU 13 23947853 23947853 single base substitution C T intron_variant PACA-AU 13 23949463 23949463 single base substitution G A intron_variant PACA-AU 13 23951910 23951910 single base substitution G A intron_variant PACA-AU 13 23951910 23951910 single base substitution G A upstream_gene_variant PACA-AU 13 23952181 23952181 single base substitution G A intron_variant PACA-AU 13 23952181 23952181 single base substitution G A upstream_gene_variant PACA-AU 13 23954434 23954434 single base substitution C A intron_variant PACA-AU 13 23954434 23954434 single base substitution C A upstream_gene_variant PACA-AU 13 23956314 23956314 single base substitution A G intron_variant PACA-AU 13 23957660 23957660 single base substitution C T intron_variant PACA-AU 13 23957851 23957851 single base substitution A C intron_variant PACA-AU 13 23960711 23960711 single base substitution A G intron_variant PACA-AU 13 23961404 23961404 single base substitution C G intron_variant PACA-AU 13 23961467 23961467 single base substitution G A intron_variant PACA-AU 13 23966184 23966184 single base substitution T A intron_variant PACA-AU 13 23972863 23972863 single base substitution G C intron_variant PACA-AU 13 23975986 23975986 single base substitution T C intron_variant PACA-AU 13 23976058 23976058 single base substitution G A intron_variant PACA-AU 13 23984685 23984685 single base substitution C T intron_variant PACA-AU 13 23985409 23985409 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant PACA-AU 13 23985423 23985423 single base substitution C T 5_prime_UTR_variant PACA-AU 13 23986170 23986170 single base substitution G A intron_variant PACA-AU 13 23986170 23986170 single base substitution G A upstream_gene_variant PACA-AU 13 23986171 23986171 single base substitution C T intron_variant PACA-AU 13 23986171 23986171 single base substitution C T upstream_gene_variant PACA-AU 13 24005179 24005179 single base substitution T C intron_variant PACA-AU 13 24009378 24009378 single base substitution C T upstream_gene_variant PACA-AU 13 24009832 24009832 single base substitution C T upstream_gene_variant PACA-AU 13 24010727 24010727 single base substitution A G upstream_gene_variant PACA-AU 13 24011759 24011759 single base substitution G A upstream_gene_variant PACA-CA 13 23898887 23898887 single base substitution G T downstream_gene_variant PACA-CA 13 23901418 23901418 single base substitution C T downstream_gene_variant PACA-CA 13 23903289 23903289 single base substitution A C 3_prime_UTR_variant PACA-CA 13 23905372 23905372 single base substitution C A intron_variant PACA-CA 13 23905372 23905372 single base substitution C A missense_variant A3465S 10393G>T PACA-CA 13 23905372 23905372 single base substitution C A missense_variant A4215S 12643G>T PACA-CA 13 23905591 23905591 single base substitution T A intron_variant PACA-CA 13 23905591 23905591 single base substitution T A stop_gained K3392* 10174A>T PACA-CA 13 23905591 23905591 single base substitution T A stop_gained K4142* 12424A>T PACA-CA 13 23906548 23906548 single base substitution G T intron_variant PACA-CA 13 23906548 23906548 single base substitution G T missense_variant P3073T 9217C>A PACA-CA 13 23906548 23906548 single base substitution G T missense_variant P3823T 11467C>A PACA-CA 13 23908138 23908138 single base substitution G T intron_variant PACA-CA 13 23908138 23908138 single base substitution G T missense_variant L2543I 7627C>A PACA-CA 13 23908138 23908138 single base substitution G T missense_variant L3293I 9877C>A PACA-CA 13 23908806 23908806 single base substitution A C intron_variant PACA-CA 13 23908806 23908806 single base substitution A C missense_variant V2320G 6959T>G PACA-CA 13 23908806 23908806 single base substitution A C missense_variant V3070G 9209T>G PACA-CA 13 23908911 23908911 single base substitution A G intron_variant PACA-CA 13 23908911 23908911 single base substitution A G missense_variant L2285S 6854T>C PACA-CA 13 23908911 23908911 single base substitution A G missense_variant L3035S 9104T>C PACA-CA 13 23909094 23909094 single base substitution A G intron_variant PACA-CA 13 23909094 23909094 single base substitution A G missense_variant L2224S 6671T>C PACA-CA 13 23909094 23909094 single base substitution A G missense_variant L2974S 8921T>C PACA-CA 13 23909329 23909329 single base substitution G T intron_variant PACA-CA 13 23909329 23909329 single base substitution G T missense_variant L2146M 6436C>A PACA-CA 13 23909329 23909329 single base substitution G T missense_variant L2896M 8686C>A PACA-CA 13 23911243 23911243 single base substitution G T intron_variant PACA-CA 13 23911243 23911243 single base substitution G T missense_variant Q1508K 4522C>A PACA-CA 13 23911243 23911243 single base substitution G T missense_variant Q2258K 6772C>A PACA-CA 13 23912386 23912386 single base substitution G A intron_variant PACA-CA 13 23912386 23912386 single base substitution G A stop_gained R1127* 3379C>T PACA-CA 13 23912386 23912386 single base substitution G A stop_gained R1877* 5629C>T PACA-CA 13 23914149 23914149 single base substitution T C intron_variant PACA-CA 13 23914149 23914149 single base substitution T C missense_variant Q1289R 3866A>G PACA-CA 13 23914149 23914149 single base substitution T C missense_variant Q539R 1616A>G PACA-CA 13 23915092 23915092 single base substitution T C intron_variant PACA-CA 13 23915092 23915092 single base substitution T C missense_variant I225V 673A>G PACA-CA 13 23915092 23915092 single base substitution T C missense_variant I975V 2923A>G PACA-CA 13 23919576 23919576 single base substitution G A intron_variant PACA-CA 13 23921230 23921230 single base substitution A C intron_variant PACA-CA 13 23923881 23923881 single base substitution G T downstream_gene_variant PACA-CA 13 23923881 23923881 single base substitution G T intron_variant PACA-CA 13 23927572 23927572 single base substitution T C downstream_gene_variant PACA-CA 13 23927572 23927572 single base substitution T C intron_variant PACA-CA 13 23927736 23927736 single base substitution T C downstream_gene_variant PACA-CA 13 23927736 23927736 single base substitution T C intron_variant PACA-CA 13 23928867 23928867 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant PACA-CA 13 23928867 23928867 single base substitution G A exon_variant PACA-CA 13 23928867 23928867 single base substitution G A synonymous_variant P252P 756C>T PACA-CA 13 23928867 23928867 single base substitution G A synonymous_variant P527P 1581C>T PACA-CA 13 23928867 23928867 single base substitution G A synonymous_variant P628P 1884C>T PACA-CA 13 23933024 23933024 single base substitution A C intron_variant PACA-CA 13 23933024 23933024 single base substitution A C upstream_gene_variant PACA-CA 13 23939736 23939736 single base substitution A G intron_variant PACA-CA 13 23939757 23939757 single base substitution C A intron_variant PACA-CA 13 23939857 23939857 single base substitution A G intron_variant PACA-CA 13 23945680 23945680 insertion of <=200bp - A intron_variant PACA-CA 13 23945680 23945680 insertion of <=200bp - A upstream_gene_variant PACA-CA 13 23948108 23948108 single base substitution C T intron_variant PACA-CA 13 23949082 23949082 single base substitution A T intron_variant PACA-CA 13 23952307 23952324 deletion of <=200bp TTTTGAGTCTACTGGTCA - intron_variant PACA-CA 13 23952307 23952324 deletion of <=200bp TTTTGAGTCTACTGGTCA - upstream_gene_variant PACA-CA 13 23952664 23952664 single base substitution C A intron_variant PACA-CA 13 23952664 23952664 single base substitution C A upstream_gene_variant PACA-CA 13 23953344 23953344 single base substitution T A intron_variant PACA-CA 13 23953344 23953344 single base substitution T A upstream_gene_variant PACA-CA 13 23954274 23954274 insertion of <=200bp - TGTGTT intron_variant PACA-CA 13 23954274 23954274 insertion of <=200bp - TGTGTT upstream_gene_variant PACA-CA 13 23957821 23957821 insertion of <=200bp - C intron_variant PACA-CA 13 23958381 23958381 single base substitution G A intron_variant PACA-CA 13 23958384 23958384 single base substitution G C intron_variant PACA-CA 13 23958913 23958913 single base substitution T G intron_variant PACA-CA 13 23959216 23959216 single base substitution C T intron_variant PACA-CA 13 23959259 23959259 single base substitution C T intron_variant PACA-CA 13 23964078 23964078 single base substitution T C intron_variant PACA-CA 13 23965703 23965703 single base substitution G A intron_variant PACA-CA 13 23969070 23969070 single base substitution G A intron_variant PACA-CA 13 23975144 23975144 single base substitution A C intron_variant PACA-CA 13 23975956 23975956 single base substitution A G intron_variant PACA-CA 13 23975991 23975991 single base substitution T C intron_variant PACA-CA 13 23976887 23976887 single base substitution T G intron_variant PACA-CA 13 23976896 23976896 single base substitution T C intron_variant PACA-CA 13 23977054 23977054 single base substitution C T intron_variant PACA-CA 13 23977861 23977861 insertion of <=200bp - T intron_variant PACA-CA 13 23980759 23980759 single base substitution G A intron_variant PACA-CA 13 23982875 23982875 single base substitution C T intron_variant PACA-CA 13 23982892 23982892 single base substitution C T intron_variant PACA-CA 13 23983800 23983800 single base substitution A G intron_variant PACA-CA 13 23984151 23984151 single base substitution T A intron_variant PACA-CA 13 23986065 23986065 single base substitution G C intron_variant PACA-CA 13 23986065 23986065 single base substitution G C upstream_gene_variant PACA-CA 13 23986070 23986070 single base substitution G C intron_variant PACA-CA 13 23986070 23986070 single base substitution G C upstream_gene_variant PACA-CA 13 23987878 23987878 single base substitution G C intron_variant PACA-CA 13 23987878 23987878 single base substitution G C upstream_gene_variant PACA-CA 13 23988368 23988368 single base substitution G A intron_variant PACA-CA 13 23988368 23988368 single base substitution G A upstream_gene_variant PACA-CA 13 23990355 23990355 single base substitution A C intron_variant PACA-CA 13 23990355 23990355 single base substitution A C upstream_gene_variant PACA-CA 13 23997912 23997912 single base substitution C T intron_variant PACA-CA 13 24002210 24002210 single base substitution A G intron_variant PACA-CA 13 24003422 24003422 single base substitution G C intron_variant PACA-CA 13 24008532 24008532 single base substitution C T upstream_gene_variant PACA-CA 13 24008877 24008877 single base substitution C T upstream_gene_variant PACA-CA 13 24009832 24009832 single base substitution C T upstream_gene_variant PACA-CA 13 24010891 24010891 single base substitution A C upstream_gene_variant PACA-CA 13 24012752 24012752 single base substitution C T upstream_gene_variant PAEN-AU 13 23933976 23933976 single base substitution C A intron_variant PAEN-AU 13 23933976 23933976 single base substitution C A upstream_gene_variant PAEN-AU 13 23962618 23962619 deletion of <=200bp GT - intron_variant PAEN-IT 13 23953770 23953770 single base substitution C T intron_variant PAEN-IT 13 23953770 23953770 single base substitution C T upstream_gene_variant PAEN-IT 13 23980506 23980506 single base substitution C G intron_variant PAEN-IT 13 23982352 23982352 single base substitution G A intron_variant PBCA-DE 13 23900386 23900386 single base substitution A G downstream_gene_variant PBCA-DE 13 23904255 23904255 insertion of <=200bp - T 3_prime_UTR_variant PBCA-DE 13 23904255 23904255 insertion of <=200bp - T intron_variant PBCA-DE 13 23915623 23915623 deletion of <=200bp C - frameshift_variant D48 PBCA-DE 13 23915623 23915623 deletion of <=200bp C - frameshift_variant D697 PBCA-DE 13 23915623 23915623 deletion of <=200bp C - frameshift_variant D798 PBCA-DE 13 23915623 23915623 deletion of <=200bp C - intron_variant PBCA-DE 13 23923313 23923313 single base substitution A G downstream_gene_variant PBCA-DE 13 23923313 23923313 single base substitution A G intron_variant PBCA-DE 13 23924913 23924913 single base substitution C T downstream_gene_variant PBCA-DE 13 23924913 23924913 single base substitution C T intron_variant PBCA-DE 13 23931671 23931671 single base substitution G A intron_variant PBCA-DE 13 23931671 23931671 single base substitution G A upstream_gene_variant PBCA-DE 13 23933840 23933840 single base substitution T A intron_variant PBCA-DE 13 23933840 23933840 single base substitution T A upstream_gene_variant PBCA-DE 13 23940640 23940640 single base substitution A G intron_variant PBCA-DE 13 23941767 23941767 deletion of <=200bp C - intron_variant PBCA-DE 13 23961862 23961862 single base substitution A G intron_variant PBCA-DE 13 23963328 23963328 insertion of <=200bp - TG intron_variant PBCA-DE 13 23968919 23968919 single base substitution G A intron_variant PBCA-DE 13 23974168 23974168 single base substitution T C intron_variant PBCA-DE 13 23984020 23984020 single base substitution A G intron_variant PBCA-DE 13 24002435 24002435 single base substitution C T intron_variant PRAD-CA 13 23923432 23923432 single base substitution G A downstream_gene_variant PRAD-CA 13 23923432 23923432 single base substitution G A intron_variant PRAD-CA 13 23940309 23940309 single base substitution C T intron_variant PRAD-CA 13 23976144 23976144 single base substitution C T intron_variant PRAD-CA 13 23978136 23978136 single base substitution T C intron_variant PRAD-CA 13 23987417 23987417 single base substitution G A intron_variant PRAD-CA 13 23987417 23987417 single base substitution G A upstream_gene_variant PRAD-CA 13 23993846 23993846 single base substitution G A intron_variant PRAD-CA 13 24004977 24004977 single base substitution T A intron_variant PRAD-UK 13 23900415 23900415 single base substitution G A downstream_gene_variant PRAD-UK 13 23902444 23902444 single base substitution T C downstream_gene_variant PRAD-UK 13 23902478 23902478 single base substitution G C downstream_gene_variant PRAD-UK 13 23902540 23902540 single base substitution A G downstream_gene_variant PRAD-UK 13 23921133 23921133 single base substitution G C intron_variant PRAD-UK 13 23924591 23924591 single base substitution C T downstream_gene_variant PRAD-UK 13 23924591 23924591 single base substitution C T intron_variant PRAD-UK 13 23928429 23928429 deletion of <=200bp G - intron_variant PRAD-UK 13 23936881 23936881 single base substitution C T intron_variant PRAD-UK 13 23954944 23954944 single base substitution G A intron_variant PRAD-UK 13 23957368 23957368 single base substitution C T intron_variant PRAD-UK 13 23958440 23958440 single base substitution T G intron_variant PRAD-UK 13 23963163 23963163 single base substitution G A intron_variant PRAD-UK 13 23970254 23970254 deletion of <=200bp G - intron_variant PRAD-UK 13 23975812 23975812 single base substitution T C intron_variant PRAD-UK 13 23976724 23976724 single base substitution G T intron_variant PRAD-UK 13 23983813 23983813 single base substitution A T intron_variant PRAD-UK 13 24000965 24000965 single base substitution T C intron_variant PRAD-US 13 23909565 23909565 single base substitution G A intron_variant PRAD-US 13 23909565 23909565 single base substitution G A missense_variant T2067M 6200C>T PRAD-US 13 23909565 23909565 single base substitution G A missense_variant T2817M 8450C>T PRAD-US 13 23909862 23909862 single base substitution G C intron_variant PRAD-US 13 23909862 23909862 single base substitution G C missense_variant A1968G 5903C>G PRAD-US 13 23909862 23909862 single base substitution G C missense_variant A2718G 8153C>G PRAD-US 13 23911843 23911843 deletion of <=200bp A - frameshift_variant S1308 PRAD-US 13 23911843 23911843 deletion of <=200bp A - frameshift_variant S2058 PRAD-US 13 23911843 23911843 deletion of <=200bp A - intron_variant PRAD-US 13 23912525 23912525 single base substitution C T intron_variant PRAD-US 13 23912525 23912525 single base substitution C T synonymous_variant L1080L 3240G>A PRAD-US 13 23912525 23912525 single base substitution C T synonymous_variant L1830L 5490G>A PRAD-US 13 23912565 23912565 single base substitution G A intron_variant PRAD-US 13 23912565 23912565 single base substitution G A missense_variant T1067M 3200C>T PRAD-US 13 23912565 23912565 single base substitution G A missense_variant T1817M 5450C>T PRAD-US 13 23913031 23913033 deletion of <=200bp TAC - disruptive_inframe_deletion ST1661T PRAD-US 13 23913031 23913033 deletion of <=200bp TAC - disruptive_inframe_deletion ST911T PRAD-US 13 23913031 23913033 deletion of <=200bp TAC - intron_variant PRAD-US 13 23914687 23914687 deletion of <=200bp T - frameshift_variant I1110 PRAD-US 13 23914687 23914687 deletion of <=200bp T - frameshift_variant I360 PRAD-US 13 23914687 23914687 deletion of <=200bp T - intron_variant PRAD-US 13 23914964 23914967 deletion of <=200bp AAGG - frameshift_variant VL1016 PRAD-US 13 23914964 23914967 deletion of <=200bp AAGG - frameshift_variant VL266 PRAD-US 13 23914964 23914967 deletion of <=200bp AAGG - intron_variant READ-US 13 23898591 23898591 single base substitution G A downstream_gene_variant READ-US 13 23904498 23904498 single base substitution G A intron_variant READ-US 13 23904498 23904498 single base substitution G A missense_variant A3756V 11267C>T READ-US 13 23904498 23904498 single base substitution G A missense_variant A4506V 13517C>T READ-US 13 23904661 23904661 single base substitution T G intron_variant READ-US 13 23904661 23904661 single base substitution T G synonymous_variant R3702R 11104A>C READ-US 13 23904661 23904661 single base substitution T G synonymous_variant R4452R 13354A>C READ-US 13 23904749 23904749 single base substitution A C intron_variant READ-US 13 23904749 23904749 single base substitution A C synonymous_variant P3672P 11016T>G READ-US 13 23904749 23904749 single base substitution A C synonymous_variant P4422P 13266T>G READ-US 13 23904858 23904858 single base substitution C T intron_variant READ-US 13 23904858 23904858 single base substitution C T missense_variant R3636Q 10907G>A READ-US 13 23904858 23904858 single base substitution C T missense_variant R4386Q 13157G>A READ-US 13 23905041 23905041 single base substitution C T intron_variant READ-US 13 23905041 23905041 single base substitution C T missense_variant R3575Q 10724G>A READ-US 13 23905041 23905041 single base substitution C T missense_variant R4325Q 12974G>A READ-US 13 23905194 23905194 single base substitution C A intron_variant READ-US 13 23905194 23905194 single base substitution C A missense_variant R3524I 10571G>T READ-US 13 23905194 23905194 single base substitution C A missense_variant R4274I 12821G>T READ-US 13 23905746 23905746 single base substitution T A intron_variant READ-US 13 23905746 23905746 single base substitution T A missense_variant H3340L 10019A>T READ-US 13 23905746 23905746 single base substitution T A missense_variant H4090L 12269A>T READ-US 13 23906077 23906077 single base substitution C A intron_variant READ-US 13 23906077 23906077 single base substitution C A stop_gained E3230* 9688G>T READ-US 13 23906077 23906077 single base substitution C A stop_gained E3980* 11938G>T READ-US 13 23906144 23906144 single base substitution A C intron_variant READ-US 13 23906144 23906144 single base substitution A C missense_variant F3207L 9621T>G READ-US 13 23906144 23906144 single base substitution A C missense_variant F3957L 11871T>G READ-US 13 23906738 23906738 single base substitution C T intron_variant READ-US 13 23906738 23906738 single base substitution C T synonymous_variant T3009T 9027G>A READ-US 13 23906738 23906738 single base substitution C T synonymous_variant T3759T 11277G>A READ-US 13 23907118 23907118 single base substitution A C intron_variant READ-US 13 23907118 23907118 single base substitution A C missense_variant F2883V 8647T>G READ-US 13 23907118 23907118 single base substitution A C missense_variant F3633V 10897T>G READ-US 13 23907517 23907517 single base substitution G A intron_variant READ-US 13 23907517 23907517 single base substitution G A missense_variant L2750F 8248C>T READ-US 13 23907517 23907517 single base substitution G A missense_variant L3500F 10498C>T READ-US 13 23908506 23908506 single base substitution C T intron_variant READ-US 13 23908506 23908506 single base substitution C T missense_variant R2420Q 7259G>A READ-US 13 23908506 23908506 single base substitution C T missense_variant R3170Q 9509G>A READ-US 13 23908582 23908582 single base substitution C A intron_variant READ-US 13 23908582 23908582 single base substitution C A stop_gained E2395* 7183G>T READ-US 13 23908582 23908582 single base substitution C A stop_gained E3145* 9433G>T READ-US 13 23908918 23908918 single base substitution C A intron_variant READ-US 13 23908918 23908918 single base substitution C A missense_variant D2283Y 6847G>T READ-US 13 23908918 23908918 single base substitution C A missense_variant D3033Y 9097G>T READ-US 13 23908973 23908973 single base substitution C T intron_variant READ-US 13 23908973 23908973 single base substitution C T stop_gained W2264* 6792G>A READ-US 13 23908973 23908973 single base substitution C T stop_gained W3014* 9042G>A READ-US 13 23909298 23909298 single base substitution C T intron_variant READ-US 13 23909298 23909298 single base substitution C T missense_variant R2156Q 6467G>A READ-US 13 23909298 23909298 single base substitution C T missense_variant R2906Q 8717G>A READ-US 13 23909929 23909929 single base substitution T G intron_variant READ-US 13 23909929 23909929 single base substitution T G missense_variant T1946P 5836A>C READ-US 13 23909929 23909929 single base substitution T G missense_variant T2696P 8086A>C READ-US 13 23910182 23910182 single base substitution C T intron_variant READ-US 13 23910182 23910182 single base substitution C T synonymous_variant T1861T 5583G>A READ-US 13 23910182 23910182 single base substitution C T synonymous_variant T2611T 7833G>A READ-US 13 23911438 23911438 single base substitution C T intron_variant READ-US 13 23911438 23911438 single base substitution C T missense_variant D1443N 4327G>A READ-US 13 23911438 23911438 single base substitution C T missense_variant D2193N 6577G>A READ-US 13 23911821 23911821 single base substitution A T intron_variant READ-US 13 23911821 23911821 single base substitution A T missense_variant I1315N 3944T>A READ-US 13 23911821 23911821 single base substitution A T missense_variant I2065N 6194T>A READ-US 13 23913399 23913399 single base substitution G A intron_variant READ-US 13 23913399 23913399 single base substitution G A missense_variant T1539I 4616C>T READ-US 13 23913399 23913399 single base substitution G A missense_variant T789I 2366C>T READ-US 13 23913600 23913600 single base substitution G T intron_variant READ-US 13 23913600 23913600 single base substitution G T missense_variant P1472H 4415C>A READ-US 13 23913600 23913600 single base substitution G T missense_variant P722H 2165C>A READ-US 13 23914209 23914209 single base substitution G T intron_variant READ-US 13 23914209 23914209 single base substitution G T missense_variant S1269Y 3806C>A READ-US 13 23914209 23914209 single base substitution G T missense_variant S519Y 1556C>A READ-US 13 23928014 23928014 single base substitution A G missense_variant S323P 967T>C READ-US 13 23928014 23928014 single base substitution A G missense_variant S598P 1792T>C READ-US 13 23928014 23928014 single base substitution A G missense_variant S699P 2095T>C READ-US 13 23928014 23928014 single base substitution A G splice_region_variant READ-US 13 23932592 23932592 single base substitution C T 5_prime_UTR_variant READ-US 13 23932592 23932592 single base substitution C T synonymous_variant A162A 486G>A READ-US 13 23932592 23932592 single base substitution C T synonymous_variant A61A 183G>A READ-US 13 23932592 23932592 single base substitution C T upstream_gene_variant READ-US 13 23985364 23985364 single base substitution C A missense_variant E5D 15G>T RECA-EU 13 23903769 23903769 single base substitution A T 3_prime_UTR_variant RECA-EU 13 23903769 23903769 single base substitution A T intron_variant RECA-EU 13 23907738 23907738 single base substitution A G intron_variant RECA-EU 13 23907738 23907738 single base substitution A G missense_variant F2676S 8027T>C RECA-EU 13 23907738 23907738 single base substitution A G missense_variant F3426S 10277T>C RECA-EU 13 23934236 23934236 single base substitution G C intron_variant RECA-EU 13 23934236 23934236 single base substitution G C upstream_gene_variant RECA-EU 13 23936404 23936404 single base substitution A T intron_variant RECA-EU 13 23943071 23943071 single base substitution C A intron_variant RECA-EU 13 23943071 23943071 single base substitution C A upstream_gene_variant RECA-EU 13 23943145 23943145 single base substitution T A intron_variant RECA-EU 13 23943145 23943145 single base substitution T A upstream_gene_variant RECA-EU 13 23950410 23950410 single base substitution G T intron_variant RECA-EU 13 23950410 23950410 single base substitution G T upstream_gene_variant RECA-EU 13 23956329 23956329 single base substitution G A intron_variant RECA-EU 13 23960163 23960163 single base substitution C T intron_variant RECA-EU 13 23960226 23960226 single base substitution C T intron_variant RECA-EU 13 23973591 23973591 single base substitution G A intron_variant RECA-EU 13 23974745 23974745 single base substitution G T intron_variant RECA-EU 13 23974918 23974918 single base substitution A T intron_variant RECA-EU 13 23977653 23977653 single base substitution C A intron_variant RECA-EU 13 23989275 23989275 single base substitution A C intron_variant RECA-EU 13 23989275 23989275 single base substitution A C upstream_gene_variant RECA-EU 13 23989784 23989784 single base substitution C A intron_variant RECA-EU 13 23989784 23989784 single base substitution C A upstream_gene_variant RECA-EU 13 24000670 24000670 single base substitution T C intron_variant SKCA-BR 13 23899234 23899234 single base substitution G A downstream_gene_variant SKCA-BR 13 23909019 23909019 single base substitution G A intron_variant SKCA-BR 13 23909019 23909019 single base substitution G A missense_variant P2249L 6746C>T SKCA-BR 13 23909019 23909019 single base substitution G A missense_variant P2999L 8996C>T SKCA-BR 13 23909133 23909133 single base substitution G A intron_variant SKCA-BR 13 23909133 23909133 single base substitution G A missense_variant S2211L 6632C>T SKCA-BR 13 23909133 23909133 single base substitution G A missense_variant S2961L 8882C>T SKCA-BR 13 23914738 23914738 single base substitution T C intron_variant SKCA-BR 13 23914738 23914738 single base substitution T C missense_variant K1093E 3277A>G SKCA-BR 13 23914738 23914738 single base substitution T C missense_variant K343E 1027A>G SKCA-BR 13 23915919 23915920 deletion of <=200bp CT - intron_variant SKCA-BR 13 23917822 23917822 single base substitution C A intron_variant SKCA-BR 13 23918299 23918299 single base substitution G A intron_variant SKCA-BR 13 23920553 23920553 single base substitution G A intron_variant SKCA-BR 13 23925840 23925840 single base substitution T C downstream_gene_variant SKCA-BR 13 23925840 23925840 single base substitution T C intron_variant SKCA-BR 13 23927823 23927823 single base substitution G A downstream_gene_variant SKCA-BR 13 23927823 23927823 single base substitution G A intron_variant SKCA-BR 13 23928588 23928588 single base substitution G A intron_variant SKCA-BR 13 23930055 23930055 single base substitution A T 5_prime_UTR_variant SKCA-BR 13 23930055 23930055 single base substitution A T missense_variant N131K 393T>A SKCA-BR 13 23930055 23930055 single base substitution A T missense_variant N232K 696T>A SKCA-BR 13 23930055 23930055 single base substitution A T upstream_gene_variant SKCA-BR 13 23934309 23934309 single base substitution C T intron_variant SKCA-BR 13 23934309 23934309 single base substitution C T upstream_gene_variant SKCA-BR 13 23935356 23935356 single base substitution A T intron_variant SKCA-BR 13 23938052 23938052 single base substitution G A intron_variant SKCA-BR 13 23938570 23938570 single base substitution C G intron_variant SKCA-BR 13 23942194 23942194 single base substitution G A intron_variant SKCA-BR 13 23947190 23947190 single base substitution A C intron_variant SKCA-BR 13 23947190 23947190 single base substitution A C upstream_gene_variant SKCA-BR 13 23948086 23948086 single base substitution T G intron_variant SKCA-BR 13 23949522 23949522 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant SKCA-BR 13 23949522 23949522 single base substitution T C intron_variant SKCA-BR 13 23953083 23953083 single base substitution G A intron_variant SKCA-BR 13 23953083 23953083 single base substitution G A upstream_gene_variant SKCA-BR 13 23953362 23953362 single base substitution C T intron_variant SKCA-BR 13 23953362 23953362 single base substitution C T upstream_gene_variant SKCA-BR 13 23953677 23953677 single base substitution C T intron_variant SKCA-BR 13 23953677 23953677 single base substitution C T upstream_gene_variant SKCA-BR 13 23954274 23954274 insertion of <=200bp - GTGTGTT intron_variant SKCA-BR 13 23954274 23954274 insertion of <=200bp - GTGTGTT upstream_gene_variant SKCA-BR 13 23954280 23954280 single base substitution G T intron_variant SKCA-BR 13 23954280 23954280 single base substitution G T upstream_gene_variant SKCA-BR 13 23958926 23958926 single base substitution C T intron_variant SKCA-BR 13 23960217 23960217 single base substitution A T intron_variant SKCA-BR 13 23960475 23960475 single base substitution C T intron_variant SKCA-BR 13 23960530 23960530 single base substitution C T intron_variant SKCA-BR 13 23961322 23961322 single base substitution G A intron_variant SKCA-BR 13 23961854 23961854 single base substitution T C intron_variant SKCA-BR 13 23961865 23961865 single base substitution G A intron_variant SKCA-BR 13 23962647 23962647 single base substitution T C intron_variant SKCA-BR 13 23964763 23964763 single base substitution C T intron_variant SKCA-BR 13 23965231 23965231 single base substitution G A intron_variant SKCA-BR 13 23967239 23967239 single base substitution G A intron_variant SKCA-BR 13 23968261 23968262 deletion of <=200bp AT - intron_variant SKCA-BR 13 23969285 23969285 single base substitution G A intron_variant SKCA-BR 13 23973388 23973388 single base substitution T C intron_variant SKCA-BR 13 23973986 23973986 single base substitution A C intron_variant SKCA-BR 13 23974013 23974013 single base substitution A C intron_variant SKCA-BR 13 23975096 23975096 single base substitution C T intron_variant SKCA-BR 13 23975843 23975843 single base substitution C T intron_variant SKCA-BR 13 23975913 23975913 single base substitution C A intron_variant SKCA-BR 13 23976046 23976046 single base substitution G A intron_variant SKCA-BR 13 23977065 23977065 single base substitution C T intron_variant SKCA-BR 13 23978679 23978679 single base substitution C T intron_variant SKCA-BR 13 23978680 23978680 single base substitution C T intron_variant SKCA-BR 13 23978761 23978761 single base substitution G A intron_variant SKCA-BR 13 23979390 23979390 single base substitution A G intron_variant SKCA-BR 13 23983527 23983527 single base substitution C T intron_variant SKCA-BR 13 23984392 23984392 single base substitution G A intron_variant SKCA-BR 13 23984791 23984791 single base substitution G A intron_variant SKCA-BR 13 23985753 23985753 single base substitution G A 5_prime_UTR_variant SKCA-BR 13 23985753 23985753 single base substitution G A upstream_gene_variant SKCA-BR 13 23986451 23986451 single base substitution C T intron_variant SKCA-BR 13 23986451 23986451 single base substitution C T upstream_gene_variant SKCA-BR 13 23987252 23987252 single base substitution G T intron_variant SKCA-BR 13 23987252 23987252 single base substitution G T upstream_gene_variant SKCA-BR 13 23990435 23990435 single base substitution G A intron_variant SKCA-BR 13 23990435 23990435 single base substitution G A upstream_gene_variant SKCA-BR 13 23991289 23991289 single base substitution G A intron_variant SKCA-BR 13 23995390 23995390 single base substitution G A intron_variant SKCA-BR 13 23995401 23995401 single base substitution G A intron_variant SKCA-BR 13 23995499 23995499 single base substitution C T intron_variant SKCA-BR 13 23998680 23998681 deletion of <=200bp GA - intron_variant SKCA-BR 13 24001362 24001362 single base substitution T C intron_variant SKCA-BR 13 24001941 24001941 single base substitution T C intron_variant SKCA-BR 13 24005083 24005083 single base substitution G A intron_variant SKCA-BR 13 24006239 24006239 single base substitution G C intron_variant SKCA-BR 13 24007152 24007152 single base substitution C T intron_variant SKCA-BR 13 24009113 24009113 single base substitution G A upstream_gene_variant SKCA-BR 13 24009720 24009720 single base substitution C T upstream_gene_variant SKCA-BR 13 24010946 24010946 single base substitution G A upstream_gene_variant SKCM-US 13 23904351 23904351 single base substitution T G intron_variant SKCM-US 13 23904351 23904351 single base substitution T G missense_variant E3805A 11414A>C SKCM-US 13 23904351 23904351 single base substitution T G missense_variant E4555A 13664A>C SKCM-US 13 23904401 23904401 single base substitution G A intron_variant SKCM-US 13 23904401 23904401 single base substitution G A synonymous_variant Y3788Y 11364C>T SKCM-US 13 23904401 23904401 single base substitution G A synonymous_variant Y4538Y 13614C>T SKCM-US 13 23904564 23904564 single base substitution G A intron_variant SKCM-US 13 23904564 23904564 single base substitution G A missense_variant A3734V 11201C>T SKCM-US 13 23904564 23904564 single base substitution G A missense_variant A4484V 13451C>T SKCM-US 13 23904967 23904967 single base substitution C T intron_variant SKCM-US 13 23904967 23904967 single base substitution C T missense_variant E3600K 10798G>A SKCM-US 13 23904967 23904967 single base substitution C T missense_variant E4350K 13048G>A SKCM-US 13 23905402 23905402 single base substitution T C intron_variant SKCM-US 13 23905402 23905402 single base substitution T C missense_variant I3455V 10363A>G SKCM-US 13 23905402 23905402 single base substitution T C missense_variant I4205V 12613A>G SKCM-US 13 23905533 23905533 single base substitution G A intron_variant SKCM-US 13 23905533 23905533 single base substitution G A missense_variant P3411L 10232C>T SKCM-US 13 23905533 23905533 single base substitution G A missense_variant P4161L 12482C>T SKCM-US 13 23905568 23905568 single base substitution T C intron_variant SKCM-US 13 23905568 23905568 single base substitution T C synonymous_variant S3399S 10197A>G SKCM-US 13 23905568 23905568 single base substitution T C synonymous_variant S4149S 12447A>G SKCM-US 13 23906647 23906647 single base substitution G A intron_variant SKCM-US 13 23906647 23906647 single base substitution G A stop_gained Q3040* 9118C>T SKCM-US 13 23906647 23906647 single base substitution G A stop_gained Q3790* 11368C>T SKCM-US 13 23906653 23906653 single base substitution G A intron_variant SKCM-US 13 23906653 23906653 single base substitution G A missense_variant R3038C 9112C>T SKCM-US 13 23906653 23906653 single base substitution G A missense_variant R3788C 11362C>T SKCM-US 13 23906876 23906876 single base substitution G A intron_variant SKCM-US 13 23906876 23906876 single base substitution G A synonymous_variant P2963P 8889C>T SKCM-US 13 23906876 23906876 single base substitution G A synonymous_variant P3713P 11139C>T SKCM-US 13 23906980 23906980 single base substitution G A intron_variant SKCM-US 13 23906980 23906980 single base substitution G A missense_variant L2929F 8785C>T SKCM-US 13 23906980 23906980 single base substitution G A missense_variant L3679F 11035C>T SKCM-US 13 23907016 23907016 single base substitution G A intron_variant SKCM-US 13 23907016 23907016 single base substitution G A missense_variant H2917Y 8749C>T SKCM-US 13 23907016 23907016 single base substitution G A missense_variant H3667Y 10999C>T SKCM-US 13 23907292 23907292 single base substitution G A intron_variant SKCM-US 13 23907292 23907292 single base substitution G A missense_variant H2825Y 8473C>T SKCM-US 13 23907292 23907292 single base substitution G A missense_variant H3575Y 10723C>T SKCM-US 13 23907395 23907395 single base substitution G A intron_variant SKCM-US 13 23907395 23907395 single base substitution G A synonymous_variant F2790F 8370C>T SKCM-US 13 23907395 23907395 single base substitution G A synonymous_variant F3540F 10620C>T SKCM-US 13 23907707 23907707 single base substitution G A intron_variant SKCM-US 13 23907707 23907707 single base substitution G A synonymous_variant I2686I 8058C>T SKCM-US 13 23907707 23907707 single base substitution G A synonymous_variant I3436I 10308C>T SKCM-US 13 23907771 23907771 single base substitution G A intron_variant SKCM-US 13 23907771 23907771 single base substitution G A missense_variant S2665F 7994C>T SKCM-US 13 23907771 23907771 single base substitution G A missense_variant S3415F 10244C>T SKCM-US 13 23907842 23907842 single base substitution G T intron_variant SKCM-US 13 23907842 23907842 single base substitution G T missense_variant F2641L 7923C>A SKCM-US 13 23907842 23907842 single base substitution G T missense_variant F3391L 10173C>A SKCM-US 13 23907979 23907979 single base substitution G A intron_variant SKCM-US 13 23907979 23907979 single base substitution G A missense_variant P2596S 7786C>T SKCM-US 13 23907979 23907979 single base substitution G A missense_variant P3346S 10036C>T SKCM-US 13 23908108 23908108 single base substitution G A intron_variant SKCM-US 13 23908108 23908108 single base substitution G A missense_variant P2553S 7657C>T SKCM-US 13 23908108 23908108 single base substitution G A missense_variant P3303S 9907C>T SKCM-US 13 23908129 23908129 single base substitution G A intron_variant SKCM-US 13 23908129 23908129 single base substitution G A missense_variant P2546S 7636C>T SKCM-US 13 23908129 23908129 single base substitution G A missense_variant P3296S 9886C>T SKCM-US 13 23908553 23908553 single base substitution G A intron_variant SKCM-US 13 23908553 23908553 single base substitution G A synonymous_variant P2404P 7212C>T SKCM-US 13 23908553 23908553 single base substitution G A synonymous_variant P3154P 9462C>T SKCM-US 13 23908710 23908710 single base substitution A T intron_variant SKCM-US 13 23908710 23908710 single base substitution A T stop_gained L2352* 7055T>A SKCM-US 13 23908710 23908710 single base substitution A T stop_gained L3102* 9305T>A SKCM-US 13 23908832 23908832 single base substitution G A intron_variant SKCM-US 13 23908832 23908832 single base substitution G A synonymous_variant L2311L 6933C>T SKCM-US 13 23908832 23908832 single base substitution G A synonymous_variant L3061L 9183C>T SKCM-US 13 23908923 23908941 deletion of <=200bp AGTAAATTGTCAAAAAATG - frameshift_variant PFFDNLL2275 SKCM-US 13 23908923 23908941 deletion of <=200bp AGTAAATTGTCAAAAAATG - frameshift_variant PFFDNLL3025 SKCM-US 13 23908923 23908941 deletion of <=200bp AGTAAATTGTCAAAAAATG - intron_variant SKCM-US 13 23909019 23909019 single base substitution G A intron_variant SKCM-US 13 23909019 23909019 single base substitution G A missense_variant P2249L 6746C>T SKCM-US 13 23909019 23909019 single base substitution G A missense_variant P2999L 8996C>T SKCM-US 13 23909099 23909099 single base substitution T G intron_variant SKCM-US 13 23909099 23909099 single base substitution T G synonymous_variant P2222P 6666A>C SKCM-US 13 23909099 23909099 single base substitution T G synonymous_variant P2972P 8916A>C SKCM-US 13 23909148 23909148 deletion of <=200bp A - frameshift_variant L2206 SKCM-US 13 23909148 23909148 deletion of <=200bp A - frameshift_variant L2956 SKCM-US 13 23909148 23909148 deletion of <=200bp A - intron_variant SKCM-US 13 23909470 23909470 single base substitution G A intron_variant SKCM-US 13 23909470 23909470 single base substitution G A missense_variant P2099S 6295C>T SKCM-US 13 23909470 23909470 single base substitution G A missense_variant P2849S 8545C>T SKCM-US 13 23909674 23909674 single base substitution G A intron_variant SKCM-US 13 23909674 23909674 single base substitution G A missense_variant H2031Y 6091C>T SKCM-US 13 23909674 23909674 single base substitution G A missense_variant H2781Y 8341C>T SKCM-US 13 23909874 23909874 single base substitution G A intron_variant SKCM-US 13 23909874 23909874 single base substitution G A missense_variant S1964L 5891C>T SKCM-US 13 23909874 23909874 single base substitution G A missense_variant S2714L 8141C>T SKCM-US 13 23910492 23910492 single base substitution C T intron_variant SKCM-US 13 23910492 23910492 single base substitution C T missense_variant R1758K 5273G>A SKCM-US 13 23910492 23910492 single base substitution C T missense_variant R2508K 7523G>A SKCM-US 13 23910621 23910621 single base substitution G A intron_variant SKCM-US 13 23910621 23910621 single base substitution G A missense_variant S1715L 5144C>T SKCM-US 13 23910621 23910621 single base substitution G A missense_variant S2465L 7394C>T SKCM-US 13 23910790 23910790 single base substitution G A intron_variant SKCM-US 13 23910790 23910790 single base substitution G A stop_gained Q1659* 4975C>T SKCM-US 13 23910790 23910790 single base substitution G A stop_gained Q2409* 7225C>T SKCM-US 13 23910909 23910909 single base substitution G A intron_variant SKCM-US 13 23910909 23910909 single base substitution G A missense_variant P1619L 4856C>T SKCM-US 13 23910909 23910909 single base substitution G A missense_variant P2369L 7106C>T SKCM-US 13 23910931 23910931 single base substitution G A intron_variant SKCM-US 13 23910931 23910931 single base substitution G A missense_variant H1612Y 4834C>T SKCM-US 13 23910931 23910931 single base substitution G A missense_variant H2362Y 7084C>T SKCM-US 13 23911201 23911201 single base substitution C T intron_variant SKCM-US 13 23911201 23911201 single base substitution C T missense_variant G1522S 4564G>A SKCM-US 13 23911201 23911201 single base substitution C T missense_variant G2272S 6814G>A SKCM-US 13 23911333 23911333 single base substitution C A intron_variant SKCM-US 13 23911333 23911333 single base substitution C A missense_variant D1478Y 4432G>T SKCM-US 13 23911333 23911333 single base substitution C A missense_variant D2228Y 6682G>T SKCM-US 13 23911669 23911669 single base substitution G A intron_variant SKCM-US 13 23911669 23911669 single base substitution G A missense_variant P1366S 4096C>T SKCM-US 13 23911669 23911669 single base substitution G A missense_variant P2116S 6346C>T SKCM-US 13 23911699 23911699 single base substitution G A intron_variant SKCM-US 13 23911699 23911699 single base substitution G A missense_variant P1356S 4066C>T SKCM-US 13 23911699 23911699 single base substitution G A missense_variant P2106S 6316C>T SKCM-US 13 23911713 23911713 single base substitution G A intron_variant SKCM-US 13 23911713 23911713 single base substitution G A missense_variant S1351F 4052C>T SKCM-US 13 23911713 23911713 single base substitution G A missense_variant S2101F 6302C>T SKCM-US 13 23911734 23911734 single base substitution A G intron_variant SKCM-US 13 23911734 23911734 single base substitution A G missense_variant V1344A 4031T>C SKCM-US 13 23911734 23911734 single base substitution A G missense_variant V2094A 6281T>C SKCM-US 13 23911927 23911927 single base substitution G A intron_variant SKCM-US 13 23911927 23911927 single base substitution G A missense_variant P1280S 3838C>T SKCM-US 13 23911927 23911927 single base substitution G A missense_variant P2030S 6088C>T SKCM-US 13 23912516 23912516 single base substitution G A intron_variant SKCM-US 13 23912516 23912516 single base substitution G A synonymous_variant S1083S 3249C>T SKCM-US 13 23912516 23912516 single base substitution G A synonymous_variant S1833S 5499C>T SKCM-US 13 23912519 23912519 single base substitution A C intron_variant SKCM-US 13 23912519 23912519 single base substitution A C missense_variant F1082L 3246T>G SKCM-US 13 23912519 23912519 single base substitution A C missense_variant F1832L 5496T>G SKCM-US 13 23912636 23912636 single base substitution A C intron_variant SKCM-US 13 23912636 23912636 single base substitution A C missense_variant F1043L 3129T>G SKCM-US 13 23912636 23912636 single base substitution A C missense_variant F1793L 5379T>G SKCM-US 13 23912862 23912862 single base substitution G A intron_variant SKCM-US 13 23912862 23912862 single base substitution G A missense_variant S1718F 5153C>T SKCM-US 13 23912862 23912862 single base substitution G A missense_variant S968F 2903C>T SKCM-US 13 23912907 23912907 single base substitution G A intron_variant SKCM-US 13 23912907 23912907 single base substitution G A missense_variant T1703I 5108C>T SKCM-US 13 23912907 23912907 single base substitution G A missense_variant T953I 2858C>T SKCM-US 13 23913172 23913172 single base substitution G A intron_variant SKCM-US 13 23913172 23913172 single base substitution G A missense_variant P1615S 4843C>T SKCM-US 13 23913172 23913172 single base substitution G A missense_variant P865S 2593C>T SKCM-US 13 23913568 23913568 single base substitution G A intron_variant SKCM-US 13 23913568 23913568 single base substitution G A stop_gained Q1483* 4447C>T SKCM-US 13 23913568 23913568 single base substitution G A stop_gained Q733* 2197C>T SKCM-US 13 23913632 23913632 single base substitution A C intron_variant SKCM-US 13 23913632 23913632 single base substitution A C synonymous_variant T1461T 4383T>G SKCM-US 13 23913632 23913632 single base substitution A C synonymous_variant T711T 2133T>G SKCM-US 13 23913792 23913792 single base substitution A G intron_variant SKCM-US 13 23913792 23913792 single base substitution A G missense_variant L1408P 4223T>C SKCM-US 13 23913792 23913792 single base substitution A G missense_variant L658P 1973T>C SKCM-US 13 23913856 23913856 single base substitution G A intron_variant SKCM-US 13 23913856 23913856 single base substitution G A missense_variant P1387S 4159C>T SKCM-US 13 23913856 23913856 single base substitution G A missense_variant P637S 1909C>T SKCM-US 13 23913876 23913876 single base substitution G A intron_variant SKCM-US 13 23913876 23913876 single base substitution G A missense_variant P1380L 4139C>T SKCM-US 13 23913876 23913876 single base substitution G A missense_variant P630L 1889C>T SKCM-US 13 23914341 23914341 single base substitution A G intron_variant SKCM-US 13 23914341 23914341 single base substitution A G missense_variant L1225S 3674T>C SKCM-US 13 23914341 23914341 single base substitution A G missense_variant L475S 1424T>C SKCM-US 13 23914626 23914626 single base substitution G A intron_variant SKCM-US 13 23914626 23914626 single base substitution G A missense_variant T1130I 3389C>T SKCM-US 13 23914626 23914626 single base substitution G A missense_variant T380I 1139C>T SKCM-US 13 23914670 23914670 single base substitution G A intron_variant SKCM-US 13 23914670 23914670 single base substitution G A synonymous_variant V1115V 3345C>T SKCM-US 13 23914670 23914670 single base substitution G A synonymous_variant V365V 1095C>T SKCM-US 13 23914933 23914933 single base substitution G A intron_variant SKCM-US 13 23914933 23914933 single base substitution G A missense_variant P1028S 3082C>T SKCM-US 13 23914933 23914933 single base substitution G A missense_variant P278S 832C>T SKCM-US 13 23915199 23915199 single base substitution G A intron_variant SKCM-US 13 23915199 23915199 single base substitution G A missense_variant S189F 566C>T SKCM-US 13 23915199 23915199 single base substitution G A missense_variant S939F 2816C>T SKCM-US 13 23915461 23915461 single base substitution G A intron_variant SKCM-US 13 23915461 23915461 single base substitution G A missense_variant L102F 304C>T SKCM-US 13 23915461 23915461 single base substitution G A missense_variant L852F 2554C>T SKCM-US 13 23915544 23915544 single base substitution G A intron_variant SKCM-US 13 23915544 23915544 single base substitution G A missense_variant S74L 221C>T SKCM-US 13 23915544 23915544 single base substitution G A missense_variant S824L 2471C>T SKCM-US 13 23928006 23928006 single base substitution G A 5_prime_UTR_variant SKCM-US 13 23928006 23928006 single base substitution G A exon_variant SKCM-US 13 23928006 23928006 single base substitution G A synonymous_variant F325F 975C>T SKCM-US 13 23928006 23928006 single base substitution G A synonymous_variant F600F 1800C>T SKCM-US 13 23928006 23928006 single base substitution G A synonymous_variant F701F 2103C>T SKCM-US 13 23928011 23928011 single base substitution G A 5_prime_UTR_variant SKCM-US 13 23928011 23928011 single base substitution G A exon_variant SKCM-US 13 23928011 23928011 single base substitution G A missense_variant L324F 970C>T SKCM-US 13 23928011 23928011 single base substitution G A missense_variant L599F 1795C>T SKCM-US 13 23928011 23928011 single base substitution G A missense_variant L700F 2098C>T SKCM-US 13 23928772 23928772 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 13 23928772 23928772 single base substitution T C exon_variant SKCM-US 13 23928772 23928772 single base substitution T C missense_variant Y284C 851A>G SKCM-US 13 23928772 23928772 single base substitution T C missense_variant Y559C 1676A>G SKCM-US 13 23928772 23928772 single base substitution T C missense_variant Y660C 1979A>G SKCM-US 13 23928867 23928867 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 13 23928867 23928867 single base substitution G A exon_variant SKCM-US 13 23928867 23928867 single base substitution G A synonymous_variant P252P 756C>T SKCM-US 13 23928867 23928867 single base substitution G A synonymous_variant P527P 1581C>T SKCM-US 13 23928867 23928867 single base substitution G A synonymous_variant P628P 1884C>T SKCM-US 13 23928945 23928945 single base substitution G A 5_prime_UTR_variant SKCM-US 13 23928945 23928945 single base substitution G A exon_variant SKCM-US 13 23928945 23928945 single base substitution G A synonymous_variant A226A 678C>T SKCM-US 13 23928945 23928945 single base substitution G A synonymous_variant A501A 1503C>T SKCM-US 13 23928945 23928945 single base substitution G A synonymous_variant A602A 1806C>T SKCM-US 13 23929328 23929328 single base substitution T C 5_prime_UTR_variant SKCM-US 13 23929328 23929328 single base substitution T C missense_variant R374G 1120A>G SKCM-US 13 23929328 23929328 single base substitution T C missense_variant R475G 1423A>G SKCM-US 13 23929328 23929328 single base substitution T C missense_variant R99G 295A>G SKCM-US 13 23929328 23929328 single base substitution T C upstream_gene_variant SKCM-US 13 23929371 23929371 single base substitution G A 5_prime_UTR_variant SKCM-US 13 23929371 23929371 single base substitution G A synonymous_variant L359L 1077C>T SKCM-US 13 23929371 23929371 single base substitution G A synonymous_variant L460L 1380C>T SKCM-US 13 23929371 23929371 single base substitution G A synonymous_variant L84L 252C>T SKCM-US 13 23929371 23929371 single base substitution G A upstream_gene_variant SKCM-US 13 23929489 23929489 single base substitution C T 5_prime_UTR_variant SKCM-US 13 23929489 23929489 single base substitution C T missense_variant G320E 959G>A SKCM-US 13 23929489 23929489 single base substitution C T missense_variant G421E 1262G>A SKCM-US 13 23929489 23929489 single base substitution C T missense_variant G45E 134G>A SKCM-US 13 23929489 23929489 single base substitution C T upstream_gene_variant SKCM-US 13 23932610 23932610 single base substitution G A 5_prime_UTR_variant SKCM-US 13 23932610 23932610 single base substitution G A synonymous_variant L156L 468C>T SKCM-US 13 23932610 23932610 single base substitution G A synonymous_variant L55L 165C>T SKCM-US 13 23932610 23932610 single base substitution G A upstream_gene_variant SKCM-US 13 23939335 23939335 single base substitution G A 5_prime_UTR_variant SKCM-US 13 23939335 23939335 single base substitution G A missense_variant L143F 427C>T SKCM-US 13 23939335 23939335 single base substitution G A missense_variant L42F 124C>T STAD-US 13 23904309 23904309 single base substitution A G intron_variant STAD-US 13 23904309 23904309 single base substitution A G missense_variant I3819T 11456T>C STAD-US 13 23904309 23904309 single base substitution A G missense_variant I4569T 13706T>C STAD-US 13 23904580 23904580 single base substitution G T intron_variant STAD-US 13 23904580 23904580 single base substitution G T missense_variant L3729I 11185C>A STAD-US 13 23904580 23904580 single base substitution G T missense_variant L4479I 13435C>A STAD-US 13 23905041 23905041 single base substitution C T intron_variant STAD-US 13 23905041 23905041 single base substitution C T missense_variant R3575Q 10724G>A STAD-US 13 23905041 23905041 single base substitution C T missense_variant R4325Q 12974G>A STAD-US 13 23905080 23905080 single base substitution G T intron_variant STAD-US 13 23905080 23905080 single base substitution G T missense_variant S3562Y 10685C>A STAD-US 13 23905080 23905080 single base substitution G T missense_variant S4312Y 12935C>A STAD-US 13 23905122 23905122 single base substitution A C intron_variant STAD-US 13 23905122 23905122 single base substitution A C missense_variant L3548R 10643T>G STAD-US 13 23905122 23905122 single base substitution A C missense_variant L4298R 12893T>G STAD-US 13 23905184 23905184 single base substitution A G intron_variant STAD-US 13 23905184 23905184 single base substitution A G synonymous_variant P3527P 10581T>C STAD-US 13 23905184 23905184 single base substitution A G synonymous_variant P4277P 12831T>C STAD-US 13 23905203 23905203 deletion of <=200bp G - frameshift_variant P3521 STAD-US 13 23905203 23905203 deletion of <=200bp G - frameshift_variant P4271 STAD-US 13 23905203 23905203 deletion of <=200bp G - intron_variant STAD-US 13 23905259 23905259 single base substitution A G intron_variant STAD-US 13 23905259 23905259 single base substitution A G synonymous_variant S3502S 10506T>C STAD-US 13 23905259 23905259 single base substitution A G synonymous_variant S4252S 12756T>C STAD-US 13 23905608 23905608 single base substitution A C intron_variant STAD-US 13 23905608 23905608 single base substitution A C missense_variant L3386R 10157T>G STAD-US 13 23905608 23905608 single base substitution A C missense_variant L4136R 12407T>G STAD-US 13 23905616 23905616 single base substitution A G intron_variant STAD-US 13 23905616 23905616 single base substitution A G synonymous_variant G3383G 10149T>C STAD-US 13 23905616 23905616 single base substitution A G synonymous_variant G4133G 12399T>C STAD-US 13 23906034 23906034 single base substitution G A intron_variant STAD-US 13 23906034 23906034 single base substitution G A missense_variant A3244V 9731C>T STAD-US 13 23906034 23906034 single base substitution G A missense_variant A3994V 11981C>T STAD-US 13 23906234 23906234 single base substitution C T intron_variant STAD-US 13 23906234 23906234 single base substitution C T synonymous_variant A3177A 9531G>A STAD-US 13 23906234 23906234 single base substitution C T synonymous_variant A3927A 11781G>A STAD-US 13 23906235 23906235 single base substitution G A intron_variant STAD-US 13 23906235 23906235 single base substitution G A missense_variant A3177V 9530C>T STAD-US 13 23906235 23906235 single base substitution G A missense_variant A3927V 11780C>T STAD-US 13 23906297 23906297 single base substitution C T intron_variant STAD-US 13 23906297 23906297 single base substitution C T synonymous_variant A3156A 9468G>A STAD-US 13 23906297 23906297 single base substitution C T synonymous_variant A3906A 11718G>A STAD-US 13 23906308 23906308 single base substitution G A intron_variant STAD-US 13 23906308 23906308 single base substitution G A stop_gained R3153* 9457C>T STAD-US 13 23906308 23906308 single base substitution G A stop_gained R3903* 11707C>T STAD-US 13 23906391 23906391 single base substitution C T intron_variant STAD-US 13 23906391 23906391 single base substitution C T missense_variant R3125H 9374G>A STAD-US 13 23906391 23906391 single base substitution C T missense_variant R3875H 11624G>A STAD-US 13 23906662 23906662 deletion of <=200bp T - frameshift_variant R3035 STAD-US 13 23906662 23906662 deletion of <=200bp T - frameshift_variant R3785 STAD-US 13 23906662 23906662 deletion of <=200bp T - intron_variant STAD-US 13 23906689 23906704 deletion of <=200bp TGCTCCTTAAGACTTT - frameshift_variant KVLRSI3021 STAD-US 13 23906689 23906704 deletion of <=200bp TGCTCCTTAAGACTTT - frameshift_variant KVLRSI3771 STAD-US 13 23906689 23906704 deletion of <=200bp TGCTCCTTAAGACTTT - intron_variant STAD-US 13 23906840 23906840 single base substitution A G intron_variant STAD-US 13 23906840 23906840 single base substitution A G synonymous_variant G2975G 8925T>C STAD-US 13 23906840 23906840 single base substitution A G synonymous_variant G3725G 11175T>C STAD-US 13 23907108 23907108 single base substitution C T intron_variant STAD-US 13 23907108 23907108 single base substitution C T missense_variant R2886Q 8657G>A STAD-US 13 23907108 23907108 single base substitution C T missense_variant R3636Q 10907G>A STAD-US 13 23907231 23907231 single base substitution A G intron_variant STAD-US 13 23907231 23907231 single base substitution A G missense_variant L2845P 8534T>C STAD-US 13 23907231 23907231 single base substitution A G missense_variant L3595P 10784T>C STAD-US 13 23907309 23907309 single base substitution A C intron_variant STAD-US 13 23907309 23907309 single base substitution A C missense_variant L2819R 8456T>G STAD-US 13 23907309 23907309 single base substitution A C missense_variant L3569R 10706T>G STAD-US 13 23907444 23907444 single base substitution A G intron_variant STAD-US 13 23907444 23907444 single base substitution A G missense_variant L2774S 8321T>C STAD-US 13 23907444 23907444 single base substitution A G missense_variant L3524S 10571T>C STAD-US 13 23907766 23907766 single base substitution T G intron_variant STAD-US 13 23907766 23907766 single base substitution T G missense_variant S2667R 7999A>C STAD-US 13 23907766 23907766 single base substitution T G missense_variant S3417R 10249A>C STAD-US 13 23907855 23907855 single base substitution A C intron_variant STAD-US 13 23907855 23907855 single base substitution A C missense_variant L2637R 7910T>G STAD-US 13 23907855 23907855 single base substitution A C missense_variant L3387R 10160T>G STAD-US 13 23907994 23907994 single base substitution C A intron_variant STAD-US 13 23907994 23907994 single base substitution C A missense_variant D2591Y 7771G>T STAD-US 13 23907994 23907994 single base substitution C A missense_variant D3341Y 10021G>T STAD-US 13 23908017 23908017 single base substitution G T intron_variant STAD-US 13 23908017 23908017 single base substitution G T missense_variant A2583D 7748C>A STAD-US 13 23908017 23908017 single base substitution G T missense_variant A3333D 9998C>A STAD-US 13 23908236 23908238 deletion of <=200bp TCT - disruptive_inframe_deletion ED2509D STAD-US 13 23908236 23908238 deletion of <=200bp TCT - disruptive_inframe_deletion ED3259D STAD-US 13 23908236 23908238 deletion of <=200bp TCT - intron_variant STAD-US 13 23908271 23908271 single base substitution C T intron_variant STAD-US 13 23908271 23908271 single base substitution C T stop_gained W2498* 7494G>A STAD-US 13 23908271 23908271 single base substitution C T stop_gained W3248* 9744G>A STAD-US 13 23908498 23908498 single base substitution A C intron_variant STAD-US 13 23908498 23908498 single base substitution A C missense_variant F2423V 7267T>G STAD-US 13 23908498 23908498 single base substitution A C missense_variant F3173V 9517T>G STAD-US 13 23908500 23908500 single base substitution T G intron_variant STAD-US 13 23908500 23908500 single base substitution T G missense_variant K2422T 7265A>C STAD-US 13 23908500 23908500 single base substitution T G missense_variant K3172T 9515A>C STAD-US 13 23908520 23908520 single base substitution A C intron_variant STAD-US 13 23908520 23908520 single base substitution A C synonymous_variant T2415T 7245T>G STAD-US 13 23908520 23908520 single base substitution A C synonymous_variant T3165T 9495T>G STAD-US 13 23908827 23908827 single base substitution A G intron_variant STAD-US 13 23908827 23908827 single base substitution A G missense_variant L2313S 6938T>C STAD-US 13 23908827 23908827 single base substitution A G missense_variant L3063S 9188T>C STAD-US 13 23908934 23908934 deletion of <=200bp A - frameshift_variant F2277 STAD-US 13 23908934 23908934 deletion of <=200bp A - frameshift_variant F3027 STAD-US 13 23908934 23908934 deletion of <=200bp A - intron_variant STAD-US 13 23909044 23909044 single base substitution G A intron_variant STAD-US 13 23909044 23909044 single base substitution G A missense_variant R2241C 6721C>T STAD-US 13 23909044 23909044 single base substitution G A missense_variant R2991C 8971C>T STAD-US 13 23909096 23909096 single base substitution A C intron_variant STAD-US 13 23909096 23909096 single base substitution A C missense_variant D2223E 6669T>G STAD-US 13 23909096 23909096 single base substitution A C missense_variant D2973E 8919T>G STAD-US 13 23909127 23909127 deletion of <=200bp A - frameshift_variant F2213 STAD-US 13 23909127 23909127 deletion of <=200bp A - frameshift_variant F2963 STAD-US 13 23909127 23909127 deletion of <=200bp A - intron_variant STAD-US 13 23909640 23909640 single base substitution C A intron_variant STAD-US 13 23909640 23909640 single base substitution C A missense_variant R2042M 6125G>T STAD-US 13 23909640 23909640 single base substitution C A missense_variant R2792M 8375G>T STAD-US 13 23909908 23909908 single base substitution G A intron_variant STAD-US 13 23909908 23909908 single base substitution G A missense_variant R1953C 5857C>T STAD-US 13 23909908 23909908 single base substitution G A missense_variant R2703C 8107C>T STAD-US 13 23909914 23909914 single base substitution G A intron_variant STAD-US 13 23909914 23909914 single base substitution G A missense_variant P1951S 5851C>T STAD-US 13 23909914 23909914 single base substitution G A missense_variant P2701S 8101C>T STAD-US 13 23910025 23910025 single base substitution C T intron_variant STAD-US 13 23910025 23910025 single base substitution C T missense_variant G1914R 5740G>A STAD-US 13 23910025 23910025 single base substitution C T missense_variant G2664R 7990G>A STAD-US 13 23910322 23910322 single base substitution A G intron_variant STAD-US 13 23910322 23910322 single base substitution A G missense_variant F1815L 5443T>C STAD-US 13 23910322 23910322 single base substitution A G missense_variant F2565L 7693T>C STAD-US 13 23910752 23910752 single base substitution A C intron_variant STAD-US 13 23910752 23910752 single base substitution A C missense_variant F1671L 5013T>G STAD-US 13 23910752 23910752 single base substitution A C missense_variant F2421L 7263T>G STAD-US 13 23910913 23910913 single base substitution C T intron_variant STAD-US 13 23910913 23910913 single base substitution C T missense_variant A1618T 4852G>A STAD-US 13 23910913 23910913 single base substitution C T missense_variant A2368T 7102G>A STAD-US 13 23911305 23911305 single base substitution T C intron_variant STAD-US 13 23911305 23911305 single base substitution T C missense_variant E1487G 4460A>G STAD-US 13 23911305 23911305 single base substitution T C missense_variant E2237G 6710A>G STAD-US 13 23911396 23911396 single base substitution C T intron_variant STAD-US 13 23911396 23911396 single base substitution C T missense_variant A1457T 4369G>A STAD-US 13 23911396 23911396 single base substitution C T missense_variant A2207T 6619G>A STAD-US 13 23911438 23911438 single base substitution C T intron_variant STAD-US 13 23911438 23911438 single base substitution C T missense_variant D1443N 4327G>A STAD-US 13 23911438 23911438 single base substitution C T missense_variant D2193N 6577G>A STAD-US 13 23911667 23911667 single base substitution G A intron_variant STAD-US 13 23911667 23911667 single base substitution G A synonymous_variant P1366P 4098C>T STAD-US 13 23911667 23911667 single base substitution G A synonymous_variant P2116P 6348C>T STAD-US 13 23911721 23911721 single base substitution A C intron_variant STAD-US 13 23911721 23911721 single base substitution A C missense_variant I1348M 4044T>G STAD-US 13 23911721 23911721 single base substitution A C missense_variant I2098M 6294T>G STAD-US 13 23911749 23911749 single base substitution G A intron_variant STAD-US 13 23911749 23911749 single base substitution G A missense_variant S1339L 4016C>T STAD-US 13 23911749 23911749 single base substitution G A missense_variant S2089L 6266C>T STAD-US 13 23911829 23911829 insertion of <=200bp - A frameshift_variant F1312F? STAD-US 13 23911829 23911829 insertion of <=200bp - A frameshift_variant F2062F? STAD-US 13 23911829 23911829 insertion of <=200bp - A intron_variant STAD-US 13 23911843 23911843 deletion of <=200bp A - frameshift_variant S1308 STAD-US 13 23911843 23911843 deletion of <=200bp A - frameshift_variant S2058 STAD-US 13 23911843 23911843 deletion of <=200bp A - intron_variant STAD-US 13 23911920 23911920 single base substitution G A intron_variant STAD-US 13 23911920 23911920 single base substitution G A missense_variant S1282L 3845C>T STAD-US 13 23911920 23911920 single base substitution G A missense_variant S2032L 6095C>T STAD-US 13 23911987 23911987 single base substitution T C intron_variant STAD-US 13 23911987 23911987 single base substitution T C missense_variant K1260E 3778A>G STAD-US 13 23911987 23911987 single base substitution T C missense_variant K2010E 6028A>G STAD-US 13 23912055 23912055 single base substitution G A intron_variant STAD-US 13 23912055 23912055 single base substitution G A missense_variant S1237F 3710C>T STAD-US 13 23912055 23912055 single base substitution G A missense_variant S1987F 5960C>T STAD-US 13 23912295 23912295 single base substitution C T intron_variant STAD-US 13 23912295 23912295 single base substitution C T missense_variant R1157Q 3470G>A STAD-US 13 23912295 23912295 single base substitution C T missense_variant R1907Q 5720G>A STAD-US 13 23912948 23912948 single base substitution A G intron_variant STAD-US 13 23912948 23912948 single base substitution A G synonymous_variant S1689S 5067T>C STAD-US 13 23912948 23912948 single base substitution A G synonymous_variant S939S 2817T>C STAD-US 13 23913082 23913082 single base substitution G A intron_variant STAD-US 13 23913082 23913082 single base substitution G A stop_gained R1645* 4933C>T STAD-US 13 23913082 23913082 single base substitution G A stop_gained R895* 2683C>T STAD-US 13 23913665 23913665 single base substitution T A intron_variant STAD-US 13 23913665 23913665 single base substitution T A synonymous_variant G1450G 4350A>T STAD-US 13 23913665 23913665 single base substitution T A synonymous_variant G700G 2100A>T STAD-US 13 23913780 23913780 single base substitution A G intron_variant STAD-US 13 23913780 23913780 single base substitution A G missense_variant L1412P 4235T>C STAD-US 13 23913780 23913780 single base substitution A G missense_variant L662P 1985T>C STAD-US 13 23914670 23914670 single base substitution G A intron_variant STAD-US 13 23914670 23914670 single base substitution G A synonymous_variant V1115V 3345C>T STAD-US 13 23914670 23914670 single base substitution G A synonymous_variant V365V 1095C>T STAD-US 13 23914771 23914771 single base substitution C T intron_variant STAD-US 13 23914771 23914771 single base substitution C T missense_variant D1082N 3244G>A STAD-US 13 23914771 23914771 single base substitution C T missense_variant D332N 994G>A STAD-US 13 23914780 23914780 single base substitution T C intron_variant STAD-US 13 23914780 23914780 single base substitution T C missense_variant T1079A 3235A>G STAD-US 13 23914780 23914780 single base substitution T C missense_variant T329A 985A>G STAD-US 13 23914825 23914825 single base substitution G A intron_variant STAD-US 13 23914825 23914825 single base substitution G A missense_variant L1064F 3190C>T STAD-US 13 23914825 23914825 single base substitution G A missense_variant L314F 940C>T STAD-US 13 23915417 23915417 deletion of <=200bp T - frameshift_variant K116 STAD-US 13 23915417 23915417 deletion of <=200bp T - frameshift_variant K866 STAD-US 13 23915417 23915417 deletion of <=200bp T - intron_variant STAD-US 13 23915457 23915457 single base substitution T G intron_variant STAD-US 13 23915457 23915457 single base substitution T G missense_variant K103T 308A>C STAD-US 13 23915457 23915457 single base substitution T G missense_variant K853T 2558A>C STAD-US 13 23915477 23915477 deletion of <=200bp T - frameshift_variant K846 STAD-US 13 23915477 23915477 deletion of <=200bp T - frameshift_variant K96 STAD-US 13 23915477 23915477 deletion of <=200bp T - intron_variant STAD-US 13 23915664 23915664 single base substitution T G intron_variant STAD-US 13 23915664 23915664 single base substitution T G missense_variant K34T 101A>C STAD-US 13 23915664 23915664 single base substitution T G missense_variant K683T 2048A>C STAD-US 13 23915664 23915664 single base substitution T G missense_variant K784T 2351A>C STAD-US 13 23928673 23928673 single base substitution G A 5_prime_UTR_variant STAD-US 13 23928673 23928673 single base substitution G A exon_variant STAD-US 13 23928673 23928673 single base substitution G A missense_variant S317L 950C>T STAD-US 13 23928673 23928673 single base substitution G A missense_variant S592L 1775C>T STAD-US 13 23928673 23928673 single base substitution G A missense_variant S693L 2078C>T STAD-US 13 23928948 23928948 single base substitution A G 5_prime_UTR_variant STAD-US 13 23928948 23928948 single base substitution A G exon_variant STAD-US 13 23928948 23928948 single base substitution A G synonymous_variant I225I 675T>C STAD-US 13 23928948 23928948 single base substitution A G synonymous_variant I500I 1500T>C STAD-US 13 23928948 23928948 single base substitution A G synonymous_variant I601I 1803T>C STAD-US 13 23928962 23928962 single base substitution A C 5_prime_UTR_variant STAD-US 13 23928962 23928962 single base substitution A C exon_variant STAD-US 13 23928962 23928962 single base substitution A C missense_variant S221A 661T>G STAD-US 13 23928962 23928962 single base substitution A C missense_variant S496A 1486T>G STAD-US 13 23928962 23928962 single base substitution A C missense_variant S597A 1789T>G STAD-US 13 23929289 23929289 single base substitution G A 5_prime_UTR_variant STAD-US 13 23929289 23929289 single base substitution G A missense_variant P112S 334C>T STAD-US 13 23929289 23929289 single base substitution G A missense_variant P387S 1159C>T STAD-US 13 23929289 23929289 single base substitution G A missense_variant P488S 1462C>T STAD-US 13 23929289 23929289 single base substitution G A upstream_gene_variant STAD-US 13 23929463 23929463 single base substitution C A 5_prime_UTR_variant STAD-US 13 23929463 23929463 single base substitution C A missense_variant D329Y 985G>T STAD-US 13 23929463 23929463 single base substitution C A missense_variant D430Y 1288G>T STAD-US 13 23929463 23929463 single base substitution C A missense_variant D54Y 160G>T STAD-US 13 23929463 23929463 single base substitution C A upstream_gene_variant STAD-US 13 23929574 23929574 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant STAD-US 13 23929574 23929574 single base substitution A G synonymous_variant L17L 49T>C STAD-US 13 23929574 23929574 single base substitution A G synonymous_variant L292L 874T>C STAD-US 13 23929574 23929574 single base substitution A G synonymous_variant L393L 1177T>C STAD-US 13 23929574 23929574 single base substitution A G upstream_gene_variant STAD-US 13 23929676 23929676 single base substitution A G 5_prime_UTR_variant STAD-US 13 23929676 23929676 single base substitution A G missense_variant Y258H 772T>C STAD-US 13 23929676 23929676 single base substitution A G missense_variant Y359H 1075T>C STAD-US 13 23929676 23929676 single base substitution A G upstream_gene_variant STAD-US 13 23930063 23930063 single base substitution A G 5_prime_UTR_variant STAD-US 13 23930063 23930063 single base substitution A G missense_variant C129R 385T>C STAD-US 13 23930063 23930063 single base substitution A G missense_variant C230R 688T>C STAD-US 13 23930063 23930063 single base substitution A G upstream_gene_variant STAD-US 13 23932488 23932488 single base substitution A G 5_prime_UTR_variant STAD-US 13 23932488 23932488 single base substitution A G missense_variant V197A 590T>C STAD-US 13 23932488 23932488 single base substitution A G missense_variant V96A 287T>C STAD-US 13 23932488 23932488 single base substitution A G upstream_gene_variant STAD-US 13 23942607 23942607 single base substitution C T 5_prime_UTR_variant STAD-US 13 23942607 23942607 single base substitution C T synonymous_variant T93T 279G>A STAD-US 13 23942607 23942607 single base substitution C T upstream_gene_variant STAD-US 13 23942624 23942624 single base substitution G A splice_region_variant STAD-US 13 23942624 23942624 single base substitution G A stop_gained R88* 262C>T STAD-US 13 23942624 23942624 single base substitution G A upstream_gene_variant THCA-SA 13 23898975 23898975 single base substitution T C downstream_gene_variant THCA-SA 13 23903791 23903791 single base substitution A G 3_prime_UTR_variant THCA-SA 13 23903791 23903791 single base substitution A G intron_variant THCA-SA 13 23908034 23908034 single base substitution A G intron_variant THCA-SA 13 23908034 23908034 single base substitution A G synonymous_variant A2577A 7731T>C THCA-SA 13 23908034 23908034 single base substitution A G synonymous_variant A3327A 9981T>C THCA-SA 13 23912283 23912283 single base substitution G A intron_variant THCA-SA 13 23912283 23912283 single base substitution G A missense_variant T1161M 3482C>T THCA-SA 13 23912283 23912283 single base substitution G A missense_variant T1911M 5732C>T THCA-SA 13 23912864 23912864 deletion of <=200bp T - frameshift_variant K1717 THCA-SA 13 23912864 23912864 deletion of <=200bp T - frameshift_variant K967 THCA-SA 13 23912864 23912864 deletion of <=200bp T - intron_variant THCA-SA 13 23915239 23915239 single base substitution T C intron_variant THCA-SA 13 23915239 23915239 single base substitution T C missense_variant I176V 526A>G THCA-SA 13 23915239 23915239 single base substitution T C missense_variant I926V 2776A>G THCA-SA 13 23929747 23929747 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant THCA-SA 13 23929747 23929747 single base substitution G A missense_variant S234L 701C>T THCA-SA 13 23929747 23929747 single base substitution G A missense_variant S335L 1004C>T THCA-SA 13 23929747 23929747 single base substitution G A upstream_gene_variant THCA-US 13 23904954 23904954 single base substitution T A intron_variant THCA-US 13 23904954 23904954 single base substitution T A missense_variant H3604L 10811A>T THCA-US 13 23904954 23904954 single base substitution T A missense_variant H4354L 13061A>T THCA-US 13 23909544 23909544 single base substitution G A intron_variant THCA-US 13 23909544 23909544 single base substitution G A missense_variant S2074L 6221C>T THCA-US 13 23909544 23909544 single base substitution G A missense_variant S2824L 8471C>T UCEC-US 13 23898584 23898584 single base substitution C T downstream_gene_variant UCEC-US 13 23904403 23904403 single base substitution A G intron_variant UCEC-US 13 23904403 23904403 single base substitution A G missense_variant Y3788H 11362T>C UCEC-US 13 23904403 23904403 single base substitution A G missense_variant Y4538H 13612T>C UCEC-US 13 23904941 23904941 single base substitution T G intron_variant UCEC-US 13 23904941 23904941 single base substitution T G missense_variant E3608D 10824A>C UCEC-US 13 23904941 23904941 single base substitution T G missense_variant E4358D 13074A>C UCEC-US 13 23904986 23904986 single base substitution C A intron_variant UCEC-US 13 23904986 23904986 single base substitution C A missense_variant E3593D 10779G>T UCEC-US 13 23904986 23904986 single base substitution C A missense_variant E4343D 13029G>T UCEC-US 13 23905090 23905090 single base substitution C A intron_variant UCEC-US 13 23905090 23905090 single base substitution C A stop_gained E3559* 10675G>T UCEC-US 13 23905090 23905090 single base substitution C A stop_gained E4309* 12925G>T UCEC-US 13 23905534 23905534 single base substitution G T intron_variant UCEC-US 13 23905534 23905534 single base substitution G T missense_variant P3411T 10231C>A UCEC-US 13 23905534 23905534 single base substitution G T missense_variant P4161T 12481C>A UCEC-US 13 23905590 23905590 single base substitution T G intron_variant UCEC-US 13 23905590 23905590 single base substitution T G missense_variant K3392T 10175A>C UCEC-US 13 23905590 23905590 single base substitution T G missense_variant K4142T 12425A>C UCEC-US 13 23905732 23905732 single base substitution C A intron_variant UCEC-US 13 23905732 23905732 single base substitution C A missense_variant D3345Y 10033G>T UCEC-US 13 23905732 23905732 single base substitution C A missense_variant D4095Y 12283G>T UCEC-US 13 23905768 23905768 single base substitution C T intron_variant UCEC-US 13 23905768 23905768 single base substitution C T missense_variant V3333I 9997G>A UCEC-US 13 23905768 23905768 single base substitution C T missense_variant V4083I 12247G>A UCEC-US 13 23906196 23906196 single base substitution A G intron_variant UCEC-US 13 23906196 23906196 single base substitution A G missense_variant V3190A 9569T>C UCEC-US 13 23906196 23906196 single base substitution A G missense_variant V3940A 11819T>C UCEC-US 13 23906234 23906234 single base substitution C T intron_variant UCEC-US 13 23906234 23906234 single base substitution C T synonymous_variant A3177A 9531G>A UCEC-US 13 23906234 23906234 single base substitution C T synonymous_variant A3927A 11781G>A UCEC-US 13 23906318 23906318 single base substitution G A intron_variant UCEC-US 13 23906318 23906318 single base substitution G A synonymous_variant L3149L 9447C>T UCEC-US 13 23906318 23906318 single base substitution G A synonymous_variant L3899L 11697C>T UCEC-US 13 23906479 23906479 single base substitution C A intron_variant UCEC-US 13 23906479 23906479 single base substitution C A missense_variant D3096Y 9286G>T UCEC-US 13 23906479 23906479 single base substitution C A missense_variant D3846Y 11536G>T UCEC-US 13 23907076 23907076 single base substitution C A intron_variant UCEC-US 13 23907076 23907076 single base substitution C A stop_gained E2897* 8689G>T UCEC-US 13 23907076 23907076 single base substitution C A stop_gained E3647* 10939G>T UCEC-US 13 23907160 23907160 single base substitution C A intron_variant UCEC-US 13 23907160 23907160 single base substitution C A stop_gained E2869* 8605G>T UCEC-US 13 23907160 23907160 single base substitution C A stop_gained E3619* 10855G>T UCEC-US 13 23907160 23907160 single base substitution C T intron_variant UCEC-US 13 23907160 23907160 single base substitution C T missense_variant E2869K 8605G>A UCEC-US 13 23907160 23907160 single base substitution C T missense_variant E3619K 10855G>A UCEC-US 13 23907329 23907329 single base substitution G T intron_variant UCEC-US 13 23907329 23907329 single base substitution G T missense_variant F2812L 8436C>A UCEC-US 13 23907329 23907329 single base substitution G T missense_variant F3562L 10686C>A UCEC-US 13 23907634 23907634 single base substitution C A intron_variant UCEC-US 13 23907634 23907634 single base substitution C A stop_gained E2711* 8131G>T UCEC-US 13 23907634 23907634 single base substitution C A stop_gained E3461* 10381G>T UCEC-US 13 23907648 23907648 single base substitution T G intron_variant UCEC-US 13 23907648 23907648 single base substitution T G missense_variant K2706T 8117A>C UCEC-US 13 23907648 23907648 single base substitution T G missense_variant K3456T 10367A>C UCEC-US 13 23907742 23907742 single base substitution T G intron_variant UCEC-US 13 23907742 23907742 single base substitution T G missense_variant K2675Q 8023A>C UCEC-US 13 23907742 23907742 single base substitution T G missense_variant K3425Q 10273A>C UCEC-US 13 23907744 23907744 single base substitution C A intron_variant UCEC-US 13 23907744 23907744 single base substitution C A missense_variant G2674V 8021G>T UCEC-US 13 23907744 23907744 single base substitution C A missense_variant G3424V 10271G>T UCEC-US 13 23907759 23907759 single base substitution C T intron_variant UCEC-US 13 23907759 23907759 single base substitution C T missense_variant R2669H 8006G>A UCEC-US 13 23907759 23907759 single base substitution C T missense_variant R3419H 10256G>A UCEC-US 13 23908270 23908270 single base substitution G A intron_variant UCEC-US 13 23908270 23908270 single base substitution G A missense_variant H2499Y 7495C>T UCEC-US 13 23908270 23908270 single base substitution G A missense_variant H3249Y 9745C>T UCEC-US 13 23908277 23908277 single base substitution A G intron_variant UCEC-US 13 23908277 23908277 single base substitution A G synonymous_variant N2496N 7488T>C UCEC-US 13 23908277 23908277 single base substitution A G synonymous_variant N3246N 9738T>C UCEC-US 13 23908582 23908582 single base substitution C A intron_variant UCEC-US 13 23908582 23908582 single base substitution C A stop_gained E2395* 7183G>T UCEC-US 13 23908582 23908582 single base substitution C A stop_gained E3145* 9433G>T UCEC-US 13 23908764 23908764 single base substitution A G intron_variant UCEC-US 13 23908764 23908764 single base substitution A G missense_variant I2334T 7001T>C UCEC-US 13 23908764 23908764 single base substitution A G missense_variant I3084T 9251T>C UCEC-US 13 23908825 23908825 single base substitution C T intron_variant UCEC-US 13 23908825 23908825 single base substitution C T missense_variant E2314K 6940G>A UCEC-US 13 23908825 23908825 single base substitution C T missense_variant E3064K 9190G>A UCEC-US 13 23909043 23909043 single base substitution C T intron_variant UCEC-US 13 23909043 23909043 single base substitution C T missense_variant R2241H 6722G>A UCEC-US 13 23909043 23909043 single base substitution C T missense_variant R2991H 8972G>A UCEC-US 13 23909101 23909101 single base substitution G A intron_variant UCEC-US 13 23909101 23909101 single base substitution G A missense_variant P2222S 6664C>T UCEC-US 13 23909101 23909101 single base substitution G A missense_variant P2972S 8914C>T UCEC-US 13 23909141 23909141 single base substitution C T intron_variant UCEC-US 13 23909141 23909141 single base substitution C T synonymous_variant K2208K 6624G>A UCEC-US 13 23909141 23909141 single base substitution C T synonymous_variant K2958K 8874G>A UCEC-US 13 23909144 23909144 single base substitution C A intron_variant UCEC-US 13 23909144 23909144 single base substitution C A missense_variant K2207N 6621G>T UCEC-US 13 23909144 23909144 single base substitution C A missense_variant K2957N 8871G>T UCEC-US 13 23909298 23909298 single base substitution C T intron_variant UCEC-US 13 23909298 23909298 single base substitution C T missense_variant R2156Q 6467G>A UCEC-US 13 23909298 23909298 single base substitution C T missense_variant R2906Q 8717G>A UCEC-US 13 23909322 23909322 single base substitution C T intron_variant UCEC-US 13 23909322 23909322 single base substitution C T missense_variant R2148H 6443G>A UCEC-US 13 23909322 23909322 single base substitution C T missense_variant R2898H 8693G>A UCEC-US 13 23909492 23909492 single base substitution C A intron_variant UCEC-US 13 23909492 23909492 single base substitution C A missense_variant K2091N 6273G>T UCEC-US 13 23909492 23909492 single base substitution C A missense_variant K2841N 8523G>T UCEC-US 13 23909873 23909873 single base substitution C T intron_variant UCEC-US 13 23909873 23909873 single base substitution C T synonymous_variant S1964S 5892G>A UCEC-US 13 23909873 23909873 single base substitution C T synonymous_variant S2714S 8142G>A UCEC-US 13 23909977 23909977 single base substitution C A intron_variant UCEC-US 13 23909977 23909977 single base substitution C A missense_variant D1930Y 5788G>T UCEC-US 13 23909977 23909977 single base substitution C A missense_variant D2680Y 8038G>T UCEC-US 13 23910132 23910132 single base substitution G T intron_variant UCEC-US 13 23910132 23910132 single base substitution G T missense_variant S1878Y 5633C>A UCEC-US 13 23910132 23910132 single base substitution G T missense_variant S2628Y 7883C>A UCEC-US 13 23910435 23910435 single base substitution T G intron_variant UCEC-US 13 23910435 23910435 single base substitution T G missense_variant K1777T 5330A>C UCEC-US 13 23910435 23910435 single base substitution T G missense_variant K2527T 7580A>C UCEC-US 13 23910738 23910738 single base substitution C T intron_variant UCEC-US 13 23910738 23910738 single base substitution C T missense_variant R1676Q 5027G>A UCEC-US 13 23910738 23910738 single base substitution C T missense_variant R2426Q 7277G>A UCEC-US 13 23910760 23910760 single base substitution C T intron_variant UCEC-US 13 23910760 23910760 single base substitution C T missense_variant E1669K 5005G>A UCEC-US 13 23910760 23910760 single base substitution C T missense_variant E2419K 7255G>A UCEC-US 13 23910763 23910763 single base substitution C A intron_variant UCEC-US 13 23910763 23910763 single base substitution C A stop_gained E1668* 5002G>T UCEC-US 13 23910763 23910763 single base substitution C A stop_gained E2418* 7252G>T UCEC-US 13 23910865 23910865 single base substitution C T intron_variant UCEC-US 13 23910865 23910865 single base substitution C T missense_variant E1634K 4900G>A UCEC-US 13 23910865 23910865 single base substitution C T missense_variant E2384K 7150G>A UCEC-US 13 23911014 23911014 single base substitution T G intron_variant UCEC-US 13 23911014 23911014 single base substitution T G missense_variant K1584T 4751A>C UCEC-US 13 23911014 23911014 single base substitution T G missense_variant K2334T 7001A>C UCEC-US 13 23911305 23911305 single base substitution T G intron_variant UCEC-US 13 23911305 23911305 single base substitution T G missense_variant E1487A 4460A>C UCEC-US 13 23911305 23911305 single base substitution T G missense_variant E2237A 6710A>C UCEC-US 13 23911306 23911306 single base substitution C T intron_variant UCEC-US 13 23911306 23911306 single base substitution C T missense_variant E1487K 4459G>A UCEC-US 13 23911306 23911306 single base substitution C T missense_variant E2237K 6709G>A UCEC-US 13 23911432 23911432 single base substitution T G intron_variant UCEC-US 13 23911432 23911432 single base substitution T G missense_variant K1445Q 4333A>C UCEC-US 13 23911432 23911432 single base substitution T G missense_variant K2195Q 6583A>C UCEC-US 13 23911549 23911549 single base substitution C A intron_variant UCEC-US 13 23911549 23911549 single base substitution C A missense_variant D1406Y 4216G>T UCEC-US 13 23911549 23911549 single base substitution C A missense_variant D2156Y 6466G>T UCEC-US 13 23911754 23911754 single base substitution C T intron_variant UCEC-US 13 23911754 23911754 single base substitution C T synonymous_variant E1337E 4011G>A UCEC-US 13 23911754 23911754 single base substitution C T synonymous_variant E2087E 6261G>A UCEC-US 13 23911784 23911784 single base substitution C A intron_variant UCEC-US 13 23911784 23911784 single base substitution C A missense_variant M1327I 3981G>T UCEC-US 13 23911784 23911784 single base substitution C A missense_variant M2077I 6231G>T UCEC-US 13 23911922 23911922 single base substitution A C intron_variant UCEC-US 13 23911922 23911922 single base substitution A C synonymous_variant S1281S 3843T>G UCEC-US 13 23911922 23911922 single base substitution A C synonymous_variant S2031S 6093T>G UCEC-US 13 23912155 23912155 single base substitution C A intron_variant UCEC-US 13 23912155 23912155 single base substitution C A missense_variant D1204Y 3610G>T UCEC-US 13 23912155 23912155 single base substitution C A missense_variant D1954Y 5860G>T UCEC-US 13 23912290 23912290 single base substitution T C intron_variant UCEC-US 13 23912290 23912290 single base substitution T C missense_variant N1159D 3475A>G UCEC-US 13 23912290 23912290 single base substitution T C missense_variant N1909D 5725A>G UCEC-US 13 23912295 23912295 single base substitution C T intron_variant UCEC-US 13 23912295 23912295 single base substitution C T missense_variant R1157Q 3470G>A UCEC-US 13 23912295 23912295 single base substitution C T missense_variant R1907Q 5720G>A UCEC-US 13 23912323 23912323 single base substitution C A intron_variant UCEC-US 13 23912323 23912323 single base substitution C A stop_gained E1148* 3442G>T UCEC-US 13 23912323 23912323 single base substitution C A stop_gained E1898* 5692G>T UCEC-US 13 23912385 23912385 single base substitution C T intron_variant UCEC-US 13 23912385 23912385 single base substitution C T missense_variant R1127Q 3380G>A UCEC-US 13 23912385 23912385 single base substitution C T missense_variant R1877Q 5630G>A UCEC-US 13 23912488 23912488 single base substitution G T intron_variant UCEC-US 13 23912488 23912488 single base substitution G T missense_variant L1093M 3277C>A UCEC-US 13 23912488 23912488 single base substitution G T missense_variant L1843M 5527C>A UCEC-US 13 23912622 23912622 single base substitution G T intron_variant UCEC-US 13 23912622 23912622 single base substitution G T missense_variant S1048Y 3143C>A UCEC-US 13 23912622 23912622 single base substitution G T missense_variant S1798Y 5393C>A UCEC-US 13 23912751 23912751 single base substitution T G intron_variant UCEC-US 13 23912751 23912751 single base substitution T G missense_variant K1005T 3014A>C UCEC-US 13 23912751 23912751 single base substitution T G missense_variant K1755T 5264A>C UCEC-US 13 23912892 23912892 single base substitution G A intron_variant UCEC-US 13 23912892 23912892 single base substitution G A missense_variant A1708V 5123C>T UCEC-US 13 23912892 23912892 single base substitution G A missense_variant A958V 2873C>T UCEC-US 13 23912936 23912936 single base substitution C T intron_variant UCEC-US 13 23912936 23912936 single base substitution C T missense_variant M1693I 5079G>A UCEC-US 13 23912936 23912936 single base substitution C T missense_variant M943I 2829G>A UCEC-US 13 23913043 23913043 single base substitution C T intron_variant UCEC-US 13 23913043 23913043 single base substitution C T missense_variant E1658K 4972G>A UCEC-US 13 23913043 23913043 single base substitution C T missense_variant E908K 2722G>A UCEC-US 13 23913275 23913275 single base substitution C T intron_variant UCEC-US 13 23913275 23913275 single base substitution C T missense_variant M1580I 4740G>A UCEC-US 13 23913275 23913275 single base substitution C T missense_variant M830I 2490G>A UCEC-US 13 23913425 23913425 single base substitution G T intron_variant UCEC-US 13 23913425 23913425 single base substitution G T missense_variant F1530L 4590C>A UCEC-US 13 23913425 23913425 single base substitution G T missense_variant F780L 2340C>A UCEC-US 13 23913541 23913541 single base substitution C A intron_variant UCEC-US 13 23913541 23913541 single base substitution C A stop_gained E1492* 4474G>T UCEC-US 13 23913541 23913541 single base substitution C A stop_gained E742* 2224G>T UCEC-US 13 23913641 23913641 single base substitution C A intron_variant UCEC-US 13 23913641 23913641 single base substitution C A missense_variant E1458D 4374G>T UCEC-US 13 23913641 23913641 single base substitution C A missense_variant E708D 2124G>T UCEC-US 13 23913700 23913700 single base substitution G T intron_variant UCEC-US 13 23913700 23913700 single base substitution G T missense_variant L1439I 4315C>A UCEC-US 13 23913700 23913700 single base substitution G T missense_variant L689I 2065C>A UCEC-US 13 23913743 23913743 single base substitution C T intron_variant UCEC-US 13 23913743 23913743 single base substitution C T synonymous_variant E1424E 4272G>A UCEC-US 13 23913743 23913743 single base substitution C T synonymous_variant E674E 2022G>A UCEC-US 13 23913964 23913964 single base substitution C A intron_variant UCEC-US 13 23913964 23913964 single base substitution C A stop_gained E1351* 4051G>T UCEC-US 13 23913964 23913964 single base substitution C A stop_gained E601* 1801G>T UCEC-US 13 23914067 23914067 single base substitution T G intron_variant UCEC-US 13 23914067 23914067 single base substitution T G missense_variant Q1316H 3948A>C UCEC-US 13 23914067 23914067 single base substitution T G missense_variant Q566H 1698A>C UCEC-US 13 23914717 23914717 single base substitution C A intron_variant UCEC-US 13 23914717 23914717 single base substitution C A stop_gained E1100* 3298G>T UCEC-US 13 23914717 23914717 single base substitution C A stop_gained E350* 1048G>T UCEC-US 13 23914732 23914732 single base substitution C T intron_variant UCEC-US 13 23914732 23914732 single base substitution C T missense_variant E1095K 3283G>A UCEC-US 13 23914732 23914732 single base substitution C T missense_variant E345K 1033G>A UCEC-US 13 23914939 23914939 single base substitution C A intron_variant UCEC-US 13 23914939 23914939 single base substitution C A stop_gained E1026* 3076G>T UCEC-US 13 23914939 23914939 single base substitution C A stop_gained E276* 826G>T UCEC-US 13 23915089 23915089 single base substitution G A intron_variant UCEC-US 13 23915089 23915089 single base substitution G A missense_variant R226C 676C>T UCEC-US 13 23915089 23915089 single base substitution G A missense_variant R976C 2926C>T UCEC-US 13 23915229 23915229 single base substitution C T intron_variant UCEC-US 13 23915229 23915229 single base substitution C T missense_variant R179H 536G>A UCEC-US 13 23915229 23915229 single base substitution C T missense_variant R929H 2786G>A UCEC-US 13 23915259 23915259 single base substitution C A intron_variant UCEC-US 13 23915259 23915259 single base substitution C A missense_variant R169I 506G>T UCEC-US 13 23915259 23915259 single base substitution C A missense_variant R919I 2756G>T UCEC-US 13 23915307 23915307 single base substitution A G intron_variant UCEC-US 13 23915307 23915307 single base substitution A G missense_variant L153P 458T>C UCEC-US 13 23915307 23915307 single base substitution A G missense_variant L903P 2708T>C UCEC-US 13 23915333 23915333 single base substitution C T intron_variant UCEC-US 13 23915333 23915333 single base substitution C T synonymous_variant S144S 432G>A UCEC-US 13 23915333 23915333 single base substitution C T synonymous_variant S894S 2682G>A UCEC-US 13 23915369 23915369 single base substitution C A intron_variant UCEC-US 13 23915369 23915369 single base substitution C A missense_variant K132N 396G>T UCEC-US 13 23915369 23915369 single base substitution C A missense_variant K882N 2646G>T UCEC-US 13 23915421 23915421 single base substitution T G intron_variant UCEC-US 13 23915421 23915421 single base substitution T G missense_variant K115T 344A>C UCEC-US 13 23915421 23915421 single base substitution T G missense_variant K865T 2594A>C UCEC-US 13 23915703 23915703 single base substitution C A intron_variant UCEC-US 13 23915703 23915703 single base substitution C A missense_variant R21I 62G>T UCEC-US 13 23915703 23915703 single base substitution C A missense_variant R670I 2009G>T UCEC-US 13 23915703 23915703 single base substitution C A missense_variant R771I 2312G>T UCEC-US 13 23928797 23928797 single base substitution C A 5_prime_UTR_variant UCEC-US 13 23928797 23928797 single base substitution C A exon_variant UCEC-US 13 23928797 23928797 single base substitution C A stop_gained E276* 826G>T UCEC-US 13 23928797 23928797 single base substitution C A stop_gained E551* 1651G>T UCEC-US 13 23928797 23928797 single base substitution C A stop_gained E652* 1954G>T UCEC-US 13 23929248 23929248 single base substitution G A 5_prime_UTR_variant UCEC-US 13 23929248 23929248 single base substitution G A synonymous_variant V125V 375C>T UCEC-US 13 23929248 23929248 single base substitution G A synonymous_variant V400V 1200C>T UCEC-US 13 23929248 23929248 single base substitution G A synonymous_variant V501V 1503C>T UCEC-US 13 23929248 23929248 single base substitution G A upstream_gene_variant UCEC-US 13 23929566 23929566 single base substitution A G 5_prime_UTR_variant UCEC-US 13 23929566 23929566 single base substitution A G synonymous_variant C19C 57T>C UCEC-US 13 23929566 23929566 single base substitution A G synonymous_variant C294C 882T>C UCEC-US 13 23929566 23929566 single base substitution A G synonymous_variant C395C 1185T>C UCEC-US 13 23929566 23929566 single base substitution A G upstream_gene_variant UCEC-US 13 23929628 23929628 single base substitution C A 5_prime_UTR_variant UCEC-US 13 23929628 23929628 single base substitution C A missense_variant V274L 820G>T UCEC-US 13 23929628 23929628 single base substitution C A missense_variant V375L 1123G>T UCEC-US 13 23929628 23929628 single base substitution C A upstream_gene_variant UCEC-US 13 23929663 23929663 single base substitution G A 5_prime_UTR_variant UCEC-US 13 23929663 23929663 single base substitution G A missense_variant T262I 785C>T UCEC-US 13 23929663 23929663 single base substitution G A missense_variant T363I 1088C>T UCEC-US 13 23929663 23929663 single base substitution G A upstream_gene_variant UCEC-US 13 23929681 23929681 single base substitution C A 5_prime_UTR_variant UCEC-US 13 23929681 23929681 single base substitution C A missense_variant S256I 767G>T UCEC-US 13 23929681 23929681 single base substitution C A missense_variant S357I 1070G>T UCEC-US 13 23929681 23929681 single base substitution C A upstream_gene_variant UCEC-US 13 23929682 23929682 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 13 23929682 23929682 single base substitution T A missense_variant S256C 766A>T UCEC-US 13 23929682 23929682 single base substitution T A missense_variant S357C 1069A>T UCEC-US 13 23929682 23929682 single base substitution T A upstream_gene_variant UCEC-US 13 23929831 23929831 single base substitution A G 5_prime_UTR_variant UCEC-US 13 23929831 23929831 single base substitution A G missense_variant L206P 617T>C UCEC-US 13 23929831 23929831 single base substitution A G missense_variant L307P 920T>C UCEC-US 13 23929831 23929831 single base substitution A G upstream_gene_variant UCEC-US 13 23929833 23929833 single base substitution C T 5_prime_UTR_variant UCEC-US 13 23929833 23929833 single base substitution C T synonymous_variant V205V 615G>A UCEC-US 13 23929833 23929833 single base substitution C T synonymous_variant V306V 918G>A UCEC-US 13 23929833 23929833 single base substitution C T upstream_gene_variant UCEC-US 13 23929960 23929960 single base substitution C T 5_prime_UTR_variant UCEC-US 13 23929960 23929960 single base substitution C T missense_variant G163D 488G>A UCEC-US 13 23929960 23929960 single base substitution C T missense_variant G264D 791G>A UCEC-US 13 23929960 23929960 single base substitution C T upstream_gene_variant UCEC-US 13 23929962 23929962 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 13 23929962 23929962 single base substitution G A synonymous_variant N162N 486C>T UCEC-US 13 23929962 23929962 single base substitution G A synonymous_variant N263N 789C>T UCEC-US 13 23929962 23929962 single base substitution G A upstream_gene_variant UCEC-US 13 23930115 23930115 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 13 23930115 23930115 single base substitution G A synonymous_variant I111I 333C>T UCEC-US 13 23930115 23930115 single base substitution G A synonymous_variant I212I 636C>T UCEC-US 13 23930115 23930115 single base substitution G A upstream_gene_variant UCEC-US 13 23932558 23932558 single base substitution C A 5_prime_UTR_variant UCEC-US 13 23932558 23932558 single base substitution C A stop_gained E174* 520G>T UCEC-US 13 23932558 23932558 single base substitution C A stop_gained E73* 217G>T UCEC-US 13 23932558 23932558 single base substitution C A upstream_gene_variant UCEC-US 13 23939315 23939315 single base substitution C T 5_prime_UTR_variant UCEC-US 13 23939315 23939315 single base substitution C T synonymous_variant A149A 447G>A UCEC-US 13 23939315 23939315 single base substitution C T synonymous_variant A48A 144G>A UCEC-US 13 23945280 23945280 single base substitution C T intron_variant UCEC-US 13 23945280 23945280 single base substitution C T missense_variant D66N 196G>A UCEC-US 13 23945280 23945280 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 8035113 COSM3384770 c.8036T>A p.F2679Y Substitution - Missense 13:23335399-23335399 - CHC2200T COSM4953065 c.7032A>T p.E2344D Substitution - Missense 13:23336403-23336403 - TCGA-DY-A0XA-01 COSM1562340 c.45G>A p.A15A Substitution - coding silent 13:23358453-23358453 - PD4203a COSM164153 c.6823C>T p.Q2275* Substitution - Nonsense 13:23336612-23336612 - TCGA-CZ-5454-01 COSM469248 c.11418A>G p.K3806K Substitution - coding silent 13:23332017-23332017 - J46_T COSM946013 c.9815G>A p.R3272H Substitution - Missense 13:23333620-23333620 - P03-2345 COSM247164 c.13247G>T p.C4416F Substitution - Missense 13:23330188-23330188 - TCGA-CA-6718-01 COSM1365927 c.5578G>T p.A1860S Substitution - Missense 13:23337857-23337857 - D28 COSM5545732 c.4420T>A p.F1474I Substitution - Missense 13:23339015-23339015 - SC_9017 COSM5558073 c.12449A>C p.K4150T Substitution - Missense 13:23330986-23330986 - TCGA-BF-A1PX-01 COSM4905014 c.13010C>T p.A4337V Substitution - Missense 13:23330425-23330425 - TCGA-AA-A00N-01 COSM277154 c.597G>A p.P199P Substitution - coding silent 13:23355574-23355574 - TCGA-B5-A0JY-01 COSM946067 c.2485C>T p.R829C Substitution - Missense 13:23340950-23340950 - ESO-122 COSM1264794 c.4045T>G p.L1349V Substitution - Missense 13:23339390-23339390 - ESCC_164 COSM5648176 c.3269C>T p.S1090L Substitution - Missense 13:23340166-23340166 - Pa10X COSM84209 c.3108A>T p.P1036P Substitution - coding silent 13:23340327-23340327 - MSK-PCa7_organoid COSM5423893 c.3381A>C p.K1127N Substitution - Missense 13:23340054-23340054 - TCGA-AA-A00N-01 COSM277155 c.386G>A p.R129H Substitution - Missense 13:23355785-23355785 - TCGA-AA-3510-01 COSM1365880 c.9778C>A p.L3260I Substitution - Missense 13:23333657-23333657 - TCGA-BT-A20W-01 COSM416412 c.11318G>C p.S3773T Substitution - Missense 13:23332117-23332117 - J30_T COSM3955445 c.9756G>T p.M3252I Substitution - Missense 13:23333679-23333679 - TCGA-AZ-4315-01 COSM946009 c.9940G>T p.E3314* Substitution - Nonsense 13:23333495-23333495 - TCGA-AX-A063-01 COSM946001 c.11378T>C p.V3793A Substitution - Missense 13:23332057-23332057 - TCGA-DD-A114-01 COSM4925454 c.12818G>T p.C4273F Substitution - Missense 13:23330617-23330617 - TCGA-D5-6927-01 COSM1365923 c.5731_5732insT p.S1911fs*2 Insertion - Frameshift 13:23337703-23337704 - RK111_C01 COSM3744095 c.4548C>A p.C1516* Substitution - Nonsense 13:23338887-23338887 - COLO201 COSM1677531 c.5188C>T p.R1730* Substitution - Nonsense 13:23338247-23338247 - TCGA-GN-A266-06 COSM1706527 c.7900C>T p.H2634Y Substitution - Missense 13:23335535-23335535 - 42T COSM3711016 c.13153G>A p.D4385N Substitution - Missense 13:23330282-23330282 - TCGA-AN-A046-01 COSM3813575 c.8149C>A p.P2717T Substitution - Missense 13:23335286-23335286 - TCGA-B7-5818-01 COSM4046527 c.8747T>C p.L2916S Substitution - Missense 13:23334688-23334688 - TCGA-D1-A103-01 COSM946011 c.9832A>C p.K3278Q Substitution - Missense 13:23333603-23333603 - TCGA-B5-A0K6-01 COSM946027 c.7701G>A p.S2567S Substitution - coding silent 13:23335734-23335734 - I2L-P24Ta-Tumor-Biopsy COSM5362174 c.7952C>A p.P2651Q Substitution - Missense 13:23335483-23335483 - TCGA-EE-A3JD-06 COSM4395904 c.5861C>T p.S1954F Substitution - Missense 13:23337574-23337574 - CSCC-27-T COSM4493952 c.3803C>T p.S1268F Substitution - Missense 13:23339632-23339632 - TCGA-EP-A2KA-01 COSM4917164 c.9372T>C p.V3124V Substitution - coding silent 13:23334063-23334063 - H1155 COSM1195252 c.1955A>T p.E652V Substitution - Missense 13:23341480-23341480 - SW1417 COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - PCSI_0083_Pa_P COSM3376512 c.8245C>A p.L2749M Substitution - Missense 13:23335190-23335190 - TCGA-B5-A11E-01 COSM946024 c.8276G>A p.R2759Q Substitution - Missense 13:23335159-23335159 - sysucc-1028T COSM5468924 c.12463T>G p.S4155A Substitution - Missense 13:23330972-23330972 - YUOMEGA COSM5376525 c.3501C>T p.F1167F Substitution - coding silent 13:23339934-23339934 - TCGA-BR-4361-01 COSM4046571 c.2794A>G p.T932A Substitution - Missense 13:23340641-23340641 - TCGA-HU-A4GC-01 COSM4046487 c.12452T>G p.L4151R Substitution - Missense 13:23330983-23330983 - HT-29 COSM1677541 c.785C>T p.S262F Substitution - Missense 13:23355386-23355386 - 2492721 COSM5722099 c.8947C>T p.H2983Y Substitution - Missense 13:23334488-23334488 - 1517_PT COSM5754057 c.8678delA p.N2893fs*12 Deletion - Frameshift 13:23334757-23334757 - CSCC-29-T COSM4521142 c.10542G>A p.A3514A Substitution - coding silent 13:23332893-23332893 - TCGA-ER-A193-06 COSM3467696 c.9867C>T p.I3289I Substitution - coding silent 13:23333568-23333568 - TCGA-AZ-4315-01 COSM1365876 c.9887A>C p.K3296T Substitution - Missense 13:23333548-23333548 - SNU-175 COSM2266257 c.5259G>A p.W1753* Substitution - Nonsense 13:23338176-23338176 - TCGA-F5-6814-01 COSM3417453 c.9068G>A p.R3023Q Substitution - Missense 13:23334367-23334367 - pfg043T COSM4751284 c.2318T>G p.I773S Substitution - Missense 13:23341117-23341117 - CoCM-1 COSM4620981 c.10454T>C p.I3485T Substitution - Missense 13:23332981-23332981 - CHC2200T COSM4953065 c.7032A>T p.E2344D Substitution - Missense 13:23336403-23336403 - PT38 COSM5923051 c.9593T>C p.V3198A Substitution - Missense 13:23333842-23333842 - TCGA-CA-6717-01 COSM1365862 c.11912C>A p.S3971* Substitution - Nonsense 13:23331523-23331523 - CHC2200T COSM4952980 c.7033G>T p.V2345L Substitution - Missense 13:23336402-23336402 - LUAD-S01381 COSM398452 c.400C>A p.Q134K Substitution - Missense 13:23355771-23355771 - TCGA-D9-A1JW-06 COSM3467702 c.9595C>T p.P3199S Substitution - Missense 13:23333840-23333840 - TCGA-MS-A51U-01 COSM3813591 c.2768G>A p.G923E Substitution - Missense 13:23340667-23340667 - HCT8 COSM2266191 c.6662C>T p.A2221V Substitution - Missense 13:23336773-23336773 - SNU-C2B COSM2266438 c.374G>A p.R125H Substitution - Missense 13:23355797-23355797 - P07-684 COSM247165 c.1589T>C p.V530A Substitution - Missense 13:23354582-23354582 - TCGA-AX-A05Z-01 COSM946058 c.4033G>T p.E1345* Substitution - Nonsense 13:23339402-23339402 - TCGA-A5-A0VQ-01 COSM946070 c.2267T>C p.L756P Substitution - Missense 13:23341168-23341168 - PTC_448 COSM946082 c.563C>T p.S188L Substitution - Missense 13:23355608-23355608 - TCGA-EB-A3XC-01 COSM3467732 c.5055T>G p.F1685L Substitution - Missense 13:23338380-23338380 - TCGA-EE-A2MS-06 COSM1706521 c.12041C>T p.P4014L Substitution - Missense 13:23331394-23331394 - TCGA-A8-A095-01 COSM432219 c.6310C>G p.Q2104E Substitution - Missense 13:23337125-23337125 - PT49 COSM5936028 c.6706C>T p.R2236C Substitution - Missense 13:23336729-23336729 - TCGA-EE-A2GJ-06 COSM3467746 c.3233T>C p.L1078S Substitution - Missense 13:23340202-23340202 - CSCC-7-T COSM2266102 c.9216C>T p.S3072S Substitution - coding silent 13:23334219-23334219 - LUAD-NYU669 COSM375595 c.9640A>T p.I3214F Substitution - Missense 13:23333795-23333795 - TCGA-D1-A17M-01 COSM946029 c.7553G>A p.R2518H Substitution - Missense 13:23335882-23335882 - Gp5D COSM2266361 c.2049T>C p.D683D Substitution - coding silent 13:23341386-23341386 - T3306 COSM4723426 c.3115A>G p.M1039V Substitution - Missense 13:23340320-23340320 - pfg092T COSM4751282 c.3754T>C p.C1252R Substitution - Missense 13:23339681-23339681 - HCT15 COSM2266199 c.6412C>A p.L2138I Substitution - Missense 13:23337023-23337023 - TCGA-DA-A3F5-06 COSM3467708 c.8864T>A p.L2955* Substitution - Nonsense 13:23334571-23334571 - U87 COSM2266205 c.6354C>T p.S2118S Substitution - coding silent 13:23337081-23337081 - JVM-2 COSM1740043 c.10717G>T p.E3573* Substitution - Nonsense 13:23332718-23332718 - OVCAR-5 COSM1677529 c.6055C>T p.R2019C Substitution - Missense 13:23337380-23337380 - NCI-H835 COSM2266115 c.8923C>A p.Q2975K Substitution - Missense 13:23334512-23334512 - 2492729 COSM5726143 c.5429C>T p.S1810F Substitution - Missense 13:23338006-23338006 - TCGA-BR-6852-01 COSM4046547 c.6269A>G p.E2090G Substitution - Missense 13:23337166-23337166 - LUAD-5V8LT COSM401412 c.827C>A p.A276D Substitution - Missense 13:23355344-23355344 - ESO-1733 COSM1264804 c.10315T>G p.L3439V Substitution - Missense 13:23333120-23333120 - T2269 COSM4723441 c.47T>C p.V16A Substitution - Missense 13:23358451-23358451 - PD4951a COSM5793555 c.4669A>C p.N1557H Substitution - Missense 13:23338766-23338766 - BD119T COSM5520906 c.6349A>G p.N2117D Substitution - Missense 13:23337086-23337086 - LS411 COSM2266064 c.10000C>A p.L3334I Substitution - Missense 13:23333435-23333435 - TCGA-EE-A2MS-06 COSM3467754 c.2113C>T p.L705F Substitution - Missense 13:23341322-23341322 - TCGA-BS-A0T9-01 COSM946014 c.9463C>A p.L3155I Substitution - Missense 13:23333972-23333972 - T2269 COSM4723406 c.7351G>A p.E2451K Substitution - Missense 13:23336084-23336084 - CSCC-46-T COSM2266389 c.1376G>T p.G459V Substitution - Missense 13:23354795-23354795 - TCGA-B0-5709-01 COSM469249 c.9652C>G p.L3218V Substitution - Missense 13:23333783-23333783 - HCC2998 COSM1677537 c.2094A>C p.Q698H Substitution - Missense 13:23341341-23341341 - TCGA-AG-A002-01 COSM263501 c.12464C>A p.S4155Y Substitution - Missense 13:23330971-23330971 - T3174 COSM4723418 c.4806T>C p.L1602L Substitution - coding silent 13:23338629-23338629 - 587376 COSM1224563 c.7374G>T p.Q2458H Substitution - Missense 13:23336061-23336061 - YUNIBO COSM5376527 c.1105C>T p.L369L Substitution - coding silent 13:23355066-23355066 - TCGA-EI-6882-01 COSM3417434 c.12825T>G p.P4275P Substitution - coding silent 13:23330610-23330610 - TCGA-DA-A1HY-06 COSM3467706 c.9021C>T p.P3007P Substitution - coding silent 13:23334414-23334414 - TCGA-Q1-A73Q-01 COSM4213593 c.8203C>T p.H2735Y Substitution - Missense 13:23335232-23335232 - S00827 COSM314972 c.9756G>A p.M3252I Substitution - Missense 13:23333679-23333679 - TCGA-A8-A09A-01 COSM5201258 c.644delA p.K215fs*10 Deletion - Frameshift 13:23355527-23355527 - NOKSI COSM4596349 c.3760T>C p.C1254R Substitution - Missense 13:23339675-23339675 - TCGA-B5-A11E-01 COSM945992 c.13171T>C p.Y4391H Substitution - Missense 13:23330264-23330264 - SW48 COSM4615932 c.2887_2888insA p.I963fs*2 Insertion - Frameshift 13:23340547-23340548 - HN_62421 COSM121787 c.11286C>A p.L3762L Substitution - coding silent 13:23332149-23332149 - MD-340 COSM303144 c.2914C>T p.P972S Substitution - Missense 13:23340521-23340521 - TCGA-EI-6917-01 COSM3417437 c.12533G>A p.R4178Q Substitution - Missense 13:23330902-23330902 - C547 COSM4389707 c.12715C>T p.R4239* Substitution - Nonsense 13:23330720-23330720 - T578 COSM4723424 c.3474T>C p.H1158H Substitution - coding silent 13:23339961-23339961 - SC_9047 COSM5558372 c.2651T>C p.L884P Substitution - Missense 13:23340784-23340784 - TCGA-CG-5726-01 COSM4046557 c.5654C>T p.S1885L Substitution - Missense 13:23337781-23337781 - TCGA-F1-6177-01 COSM4046551 c.5907C>T p.P1969P Substitution - coding silent 13:23337528-23337528 - TCGA-H4-A2HQ-01 COSM265244 c.2734G>C p.E912Q Substitution - Missense 13:23340701-23340701 - TCGA-B8-4620-01 COSM469255 c.3516G>C p.K1172N Substitution - Missense 13:23339919-23339919 - BD63T COSM4046563 c.4492C>T p.R1498* Substitution - Nonsense 13:23338943-23338943 - TCGA-CA-6718-01 COSM1365902 c.7802C>A p.S2601Y Substitution - Missense 13:23335633-23335633 - TCGA-AA-3542-01 COSM292084 c.1469A>C p.K490T Substitution - Missense 13:23354702-23354702 - SJHGG064_A COSM4969802 c.3506_3512delAACTATT p.Q1169fs*7 Deletion - Frameshift 13:23339923-23339929 - TCGA-39-5031-01 COSM695792 c.8379A>G p.T2793T Substitution - coding silent 13:23335056-23335056 - 90879 COSM125994 c.7232C>T p.A2411V Substitution - Missense 13:23336203-23336203 - TCGA-EE-A3AA-06 COSM233297 c.10921C>T p.R3641C Substitution - Missense 13:23332514-23332514 - TCGA-EE-A2GL-06 COSM3467692 c.10698C>T p.P3566P Substitution - coding silent 13:23332737-23332737 - BD73T COSM5499524 c.2999G>A p.G1000E Substitution - Missense 13:23340436-23340436 - Au1 COSM5597533 c.12334C>T p.P4112S Substitution - Missense 13:23331101-23331101 - GC8_T COSM147643 c.468A>G p.A156A Substitution - coding silent 13:23355703-23355703 - T3267 COSM4723430 c.2621C>A p.S874Y Substitution - Missense 13:23340814-23340814 - T2766 COSM4723414 c.5030T>C p.M1677T Substitution - Missense 13:23338405-23338405 - Pat_41_B COSM5842286 c.6506C>T p.T2169I Substitution - Missense 13:23336929-23336929 - CCC60T COSM2266135 c.8549G>A p.R2850Q Substitution - Missense 13:23334886-23334886 - TCGA-EE-A3AA-06 COSM3467740 c.3942T>G p.T1314T Substitution - coding silent 13:23339493-23339493 - TCGA-HU-A4GQ-01 COSM4046529 c.8530C>T p.R2844C Substitution - Missense 13:23334905-23334905 - GCT57 COSM5749881 c.12568C>A p.H4190N Substitution - Missense 13:23330867-23330867 - sysucc-1397T COSM5473456 c.1328T>C p.V443A Substitution - Missense 13:23354843-23354843 - TCGA-B5-A11G-01 COSM946077 c.744T>C p.C248C Substitution - coding silent 13:23355427-23355427 - ESCC_BICR_048T COSM2266131 c.8702G>A p.R2901H Substitution - Missense 13:23334733-23334733 - TCGA-EJ-5519-01 COSM1128395 c.7712C>G p.A2571G Substitution - Missense 13:23335723-23335723 - TCGA-B8-4620-01 COSM469257 c.3515A>C p.K1172T Substitution - Missense 13:23339920-23339920 - Pat_41_B COSM5842282 c.8491G>A p.V2831M Substitution - Missense 13:23334944-23334944 - TCGA-HT-7691-01 COSM3968574 c.8968G>A p.D2990N Substitution - Missense 13:23334467-23334467 - 61 COSM5739913 c.2975A>T p.H992L Substitution - Missense 13:23340460-23340460 - PCSI_0083_Pa_P COSM3376506 c.9436C>A p.L3146I Substitution - Missense 13:23333999-23333999 - TCGA-AZ-6598-01 COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - PTC_285 COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - RK308_C01 COSM3744099 c.718G>A p.A240T Substitution - Missense 13:23355453-23355453 - C709 COSM4443846 c.8554C>T p.P2852S Substitution - Missense 13:23334881-23334881 - TCGA-BR-4184-01 COSM1365864 c.11540C>T p.A3847V Substitution - Missense 13:23331895-23331895 - TCGA-AP-A051-01 COSM946020 c.8473C>T p.P2825S Substitution - Missense 13:23334962-23334962 - TCGA-AA-A00N-01 COSM277153 c.3997G>T p.E1333* Substitution - Nonsense 13:23339438-23339438 - TCGA-B5-A0K2-01 COSM946089 c.42C>T p.N14N Substitution - coding silent 13:23358456-23358456 - 1517_PT COSM1365946 c.2887delA p.I963fs*16 Deletion - Frameshift 13:23340548-23340548 - sysucc-1397T COSM5473454 c.6564G>A p.M2188I Substitution - Missense 13:23336871-23336871 - TCGA-EE-A3JB-06 COSM4898849 c.6241G>T p.D2081Y Substitution - Missense 13:23337194-23337194 - PD6749a COSM1637674 c.10704C>T p.S3568S Substitution - coding silent 13:23332731-23332731 - TCGA-BG-A0M4-01 COSM946083 c.479T>C p.L160P Substitution - Missense 13:23355692-23355692 - BCM339T COSM4802514 c.6476A>G p.D2159G Substitution - Missense 13:23336959-23336959 - TCGA-GV-A40E-01 COSM3793193 c.3808G>A p.E1270K Substitution - Missense 13:23339627-23339627 - C608 COSM4442729 c.13136T>C p.L4379S Substitution - Missense 13:23330299-23330299 - TCGA-AX-A0J0-01 COSM946063 c.3507A>C p.Q1169H Substitution - Missense 13:23339928-23339928 - HCT8 COSM2265948 c.13253C>A p.A4418D Substitution - Missense 13:23330182-23330182 - SNUH_G76_S1 COSM3753623 c.255T>A p.N85K Substitution - Missense 13:23355916-23355916 - PD11357a COSM5767113 c.8918G>A p.R2973H Substitution - Missense 13:23334517-23334517 - 063T COSM1731541 c.12415delC p.H4139fs*22 Deletion - Frameshift 13:23331020-23331020 - TCGA-EE-A2MI-06 COSM3467686 c.12607G>A p.E4203K Substitution - Missense 13:23330828-23330828 - TCGA-FJ-A3ZF-01 COSM3793195 c.1119G>C p.K373N Substitution - Missense 13:23355052-23355052 - TCGA-B5-A0JY-01 COSM946042 c.5820G>A p.E1940E Substitution - coding silent 13:23337615-23337615 - TCGA-KK-A59Z-01 COSM4876413 c.5009C>T p.T1670M Substitution - Missense 13:23338426-23338426 - U87 COSM2266203 c.6377C>A p.S2126* Substitution - Nonsense 13:23337058-23337058 - 40M COSM5586458 c.9296A>T p.N3099I Substitution - Missense 13:23334139-23334139 - TCGA-D8-A1JA-01 COSM3813573 c.9766G>A p.D3256N Substitution - Missense 13:23333669-23333669 - PCSI_0083_Pa_P COSM3376516 c.3425A>G p.Q1142R Substitution - Missense 13:23340010-23340010 - TCGA-18-4086-01 COSM695795 c.11292C>A p.S3764R Substitution - Missense 13:23332143-23332143 - TCGA-AX-A0J0-01 COSM946031 c.7139A>C p.K2380T Substitution - Missense 13:23336296-23336296 - SK-MEL-28 COSM1677525 c.7593C>G p.F2531L Substitution - Missense 13:23335842-23335842 - Gp2D COSM2266419 c.954T>C p.S318S Substitution - coding silent 13:23355217-23355217 - TCGA-AP-A0LM-01 COSM946059 c.3933G>T p.E1311D Substitution - Missense 13:23339502-23339502 - 587350 COSM1224549 c.11291G>T p.S3764I Substitution - Missense 13:23332144-23332144 - LUAD-CHTN-MAD06-00668 COSM358782 c.6858G>T p.W2286C Substitution - Missense 13:23336577-23336577 - T2269 COSM4723404 c.7799T>A p.I2600N Substitution - Missense 13:23335636-23335636 - TCGA-AG-A002-01 COSM263503 c.10553G>T p.R3518I Substitution - Missense 13:23332882-23332882 - TCGA-D3-A5GO-06 COSM3467688 c.12172A>G p.I4058V Substitution - Missense 13:23331263-23331263 - TCGA-BT-A20N-01 COSM416408 c.214C>T p.Q72* Substitution - Nonsense 13:23355957-23355957 - HN_00761 COSM125994 c.7232C>T p.A2411V Substitution - Missense 13:23336203-23336203 - TCGA-AC-A5XS-01 COSM4391199 c.6028G>T p.D2010Y Substitution - Missense 13:23337407-23337407 - T3091 COSM4723388 c.12705C>A p.T4235T Substitution - coding silent 13:23330730-23330730 - TCGA-BS-A0UF-01 COSM946066 c.2635G>T p.E879* Substitution - Nonsense 13:23340800-23340800 - HCC59 COSM3704564 c.9839G>T p.G3280V Substitution - Missense 13:23333596-23333596 - B90 COSM254921 c.5968C>G p.Q1990E Substitution - Missense 13:23337467-23337467 - TCGA-D3-A2JA-06 COSM3467742 c.3782T>C p.L1261P Substitution - Missense 13:23339653-23339653 - TCGA-FD-A3B8-01 COSM1300074 c.12399C>G p.F4133L Substitution - Missense 13:23331036-23331036 - HCC153T COSM5823207 c.1219A>G p.S407G Substitution - Missense 13:23354952-23354952 - TCGA-AX-A05Z-01 COSM946006 c.10414G>T p.E3472* Substitution - Nonsense 13:23333021-23333021 - 587376 COSM1224580 c.1099A>C p.K367Q Substitution - Missense 13:23355072-23355072 - LUAD-S00484 COSM342816 c.11952G>T p.R3984S Substitution - Missense 13:23331483-23331483 - LUAD-5V8LT COSM401410 c.10091C>A p.S3364* Substitution - Nonsense 13:23333344-23333344 - T155 COSM1177346 c.1032A>G p.L344L Substitution - coding silent 13:23355139-23355139 - HCC021T COSM5815811 c.942A>T p.P314P Substitution - coding silent 13:23355229-23355229 - HCT-15 COSM1677527 c.6516C>A p.C2172* Substitution - Nonsense 13:23336919-23336919 - T3064 COSM4723400 c.8282A>T p.D2761V Substitution - Missense 13:23335153-23335153 - TCGA-FW-A3R5-06 COSM3885091 c.10594C>T p.L3532F Substitution - Missense 13:23332841-23332841 - PT35 COSM4509418 c.7624C>T p.H2542Y Substitution - Missense 13:23335811-23335811 - PD10058a COSM3719042 c.282T>A p.S94R Substitution - Missense 13:23355889-23355889 - TCGA-AP-A059-01 COSM946044 c.5652T>G p.S1884S Substitution - coding silent 13:23337783-23337783 - S00936 COSM314974 c.8251C>T p.R2751C Substitution - Missense 13:23335184-23335184 - HX28T COSM1606925 c.3868C>T p.P1290S Substitution - Missense 13:23339567-23339567 - TCGA-CG-4441-01 COSM4046561 c.4626T>C p.S1542S Substitution - coding silent 13:23338809-23338809 - TCGA-AX-A05Z-01 COSM946055 c.4531G>A p.E1511K Substitution - Missense 13:23338904-23338904 - TCGA-FY-A3W9-01 COSM3369044 c.12620A>T p.H4207L Substitution - Missense 13:23330815-23330815 - HCT8 COSM1677527 c.6516C>A p.C2172* Substitution - Nonsense 13:23336919-23336919 - MSK-PCa7_tissue COSM5423893 c.3381A>C p.K1127N Substitution - Missense 13:23340054-23340054 - TCGA-AP-A059-01 COSM946051 c.4952C>A p.S1651Y Substitution - Missense 13:23338483-23338483 - TCGA-GM-A2DH-01 COSM3813577 c.7994A>C p.E2665A Substitution - Missense 13:23335441-23335441 - TCGA-AZ-4315-01 COSM1365929 c.5202C>A p.G1734G Substitution - coding silent 13:23338233-23338233 - TCGA-D3-A3MR-06 COSM3467714 c.8104C>T p.P2702S Substitution - Missense 13:23335331-23335331 - 2492721 COSM5722101 c.6235T>G p.S2079A Substitution - Missense 13:23337200-23337200 - SC_9038 COSM5573968 c.12742_12743insT p.Q4248fs*15 Insertion - Frameshift 13:23330692-23330693 - Pat_66_A COSM5376521 c.6353C>T p.S2118F Substitution - Missense 13:23337082-23337082 - I2L-P10-Tumor-Organoid COSM5362062 c.12084T>A p.V4028V Substitution - coding silent 13:23331351-23331351 - T578 COSM1264796 c.349G>A p.G117S Substitution - Missense 13:23355822-23355822 - PT26 COSM5905292 c.8441C>T p.S2814L Substitution - Missense 13:23334994-23334994 - TCGA-BH-A2L8-01 COSM3813597 c.1332C>G p.L444L Substitution - coding silent 13:23354839-23354839 - CSCC-47-T COSM4509418 c.7624C>T p.H2542Y Substitution - Missense 13:23335811-23335811 - TCGA-AP-A056-01 COSM946022 c.8430G>T p.K2810N Substitution - Missense 13:23335005-23335005 - T3174 COSM2265990 c.12088delT p.Y4030fs*45 Deletion - Frameshift 13:23331347-23331347 - DLD1 COSM1677527 c.6516C>A p.C2172* Substitution - Nonsense 13:23336919-23336919 - Pat_06_A COSM1513932 c.2611G>C p.E871Q Substitution - Missense 13:23340824-23340824 - P05-3829 COSM247163 c.8531G>A p.R2844H Substitution - Missense 13:23334904-23334904 - TCGA-66-2791-01 COSM695796 c.11444T>C p.I3815T Substitution - Missense 13:23331991-23331991 - TCGA-BR-4369-01 COSM1264775 c.11966T>G p.L3989R Substitution - Missense 13:23331469-23331469 - C84 COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - TCGA-BR-8680-01 COSM4046589 c.736T>C p.L246L Substitution - coding silent 13:23355435-23355435 - RK288_C01 COSM4780530 c.4220G>A p.G1407E Substitution - Missense 13:23339215-23339215 - CHC2200T COSM4953067 c.1137G>T p.L379F Substitution - Missense 13:23355034-23355034 - 3N50-VS-3T50 COSM4982962 c.6597C>T p.F2199F Substitution - coding silent 13:23336838-23336838 - TCGA-BR-4184-01 COSM4046537 c.7660C>T p.P2554S Substitution - Missense 13:23335775-23335775 - TCGA-D7-6815-01 COSM4046585 c.1021C>T p.P341S Substitution - Missense 13:23355150-23355150 - TCGA-DK-A3IS-01 COSM1300079 c.8244C>T p.N2748N Substitution - coding silent 13:23335191-23335191 - pfg016T COSM1639311 c.2090T>C p.V697A Substitution - Missense 13:23341345-23341345 - TCGA-FW-A3R5-06 COSM3467756 c.2030C>T p.S677L Substitution - Missense 13:23341405-23341405 - TCGA-EE-A2GM-06 COSM3467750 c.2641C>T p.P881S Substitution - Missense 13:23340794-23340794 - OSCC-GB_01170111 COSM5954030 c.3582C>G p.L1194L Substitution - coding silent 13:23339853-23339853 - ESCC_170 COSM5649177 c.7663C>T p.L2555F Substitution - Missense 13:23335772-23335772 - PD3226a COSM1659012 c.6353C>A p.S2118Y Substitution - Missense 13:23337082-23337082 - C086 COSM5538506 c.900C>T p.F300F Substitution - coding silent 13:23355271-23355271 - TCGA-23-1022-01 COSM76328 c.3704A>G p.H1235R Substitution - Missense 13:23339731-23339731 - TCGA-AG-A002-01 COSM263507 c.2959G>A p.V987I Substitution - Missense 13:23340476-23340476 - TCGA-CI-6621-01 COSM1562342 c.3974C>A p.P1325H Substitution - Missense 13:23339461-23339461 - Pat_40_B COSM5842274 c.13075G>A p.A4359T Substitution - Missense 13:23330360-23330360 - TCGA-B5-A11N-01 COSM946032 c.6836G>A p.R2279Q Substitution - Missense 13:23336599-23336599 - YURTHE COSM1706539 c.839C>T p.S280L Substitution - Missense 13:23355332-23355332 - B96 COSM1747366 c.917G>T p.G306V Substitution - Missense 13:23355254-23355254 - TCGA-F5-6814-01 COSM3417467 c.1654T>C p.S552P Substitution - Missense 13:23353875-23353875 - TCGA-CG-5726-01 COSM4046581 c.1362T>C p.I454I Substitution - coding silent 13:23354809-23354809 - CHC902T COSM4790372 c.5534G>A p.R1845K Substitution - Missense 13:23337901-23337901 - TCGA-ED-A7PZ-01 COSM4916983 c.5965A>T p.T1989S Substitution - Missense 13:23337470-23337470 - TCGA-22-4591-01 COSM695789 c.5201G>C p.G1734A Substitution - Missense 13:23338234-23338234 - ATL069 COSM946024 c.8276G>A p.R2759Q Substitution - Missense 13:23335159-23335159 - DLD1 COSM2266191 c.6662C>T p.A2221V Substitution - Missense 13:23336773-23336773 - HN_62601 COSM121010 c.4056G>A p.M1352I Substitution - Missense 13:23339379-23339379 - B77 COSM254920 c.7474A>T p.I2492F Substitution - Missense 13:23335961-23335961 - B2 COSM253822 c.5174G>T p.C1725F Substitution - Missense 13:23338261-23338261 - TCGA-FW-A3R5-06 COSM1706533 c.4712C>T p.S1571F Substitution - Missense 13:23338723-23338723 - TCGA-34-5236-01 COSM695794 c.8718G>T p.E2906D Substitution - Missense 13:23334717-23334717 - SE3 COSM1165808 c.9721T>A p.L3241M Substitution - Missense 13:23333714-23333714 - TCGA-AP-A056-01 COSM946035 c.6709G>A p.E2237K Substitution - Missense 13:23336726-23336726 - TCGA-AN-A046-01 COSM946058 c.4033G>T p.E1345* Substitution - Nonsense 13:23339402-23339402 - sysucc-1171T COSM5452701 c.979C>T p.R327C Substitution - Missense 13:23355192-23355192 - BD35T COSM5520209 c.7029G>T p.R2343S Substitution - Missense 13:23336406-23336406 - TCGA-F5-6814-01 COSM3417465 c.3365C>A p.S1122Y Substitution - Missense 13:23340070-23340070 - T84 COSM2266070 c.9894A>G p.T3298T Substitution - coding silent 13:23333541-23333541 - TCGA-AY-6196-01 COSM1365908 c.6708C>T p.R2236R Substitution - coding silent 13:23336727-23336727 - TCGA-BR-4368-01 COSM4046555 c.5825C>T p.S1942L Substitution - Missense 13:23337610-23337610 - TCGA-CA-6717-01 COSM1365940 c.4019A>C p.D1340A Substitution - Missense 13:23339416-23339416 - T3202 COSM1706539 c.839C>T p.S280L Substitution - Missense 13:23355332-23355332 - TCGA-AP-A0LP-01 COSM946086 c.348C>T p.N116N Substitution - coding silent 13:23355823-23355823 - LUAD-CHTN-MAD08-00104 COSM361144 c.12498G>T p.V4166V Substitution - coding silent 13:23330937-23330937 - TCGA-AX-A06H-01 COSM946082 c.563C>T p.S188L Substitution - Missense 13:23355608-23355608 - HN_62854 COSM126914 c.12737C>G p.S4246* Substitution - Nonsense 13:23330698-23330698 - TCGA-BR-6458-01 COSM4046525 c.9054T>G p.T3018T Substitution - coding silent 13:23334381-23334381 - B77-Tumor COSM254920 c.7474A>T p.I2492F Substitution - Missense 13:23335961-23335961 - PT52 COSM1706533 c.4712C>T p.S1571F Substitution - Missense 13:23338723-23338723 - B80-4-Tumor COSM1747364 c.11414G>T p.G3805V Substitution - Missense 13:23332021-23332021 - HCC2998 COSM1677533 c.4080G>T p.E1360D Substitution - Missense 13:23339355-23339355 - TCGA-D9-A4Z3-01 COSM3467762 c.1538A>G p.Y513C Substitution - Missense 13:23354633-23354633 - ESCC-201T COSM3936259 c.13254C>T p.A4418A Substitution - coding silent 13:23330181-23330181 - TCGA-EI-6917-01 COSM3417457 c.7392G>A p.T2464T Substitution - coding silent 13:23336043-23336043 - PD24307a COSM5794585 c.3655C>T p.L1219L Substitution - coding silent 13:23339780-23339780 - U87 COSM2266197 c.6444C>G p.N2148K Substitution - Missense 13:23336991-23336991 - pfg008T COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - COLO205 COSM1677531 c.5188C>T p.R1730* Substitution - Nonsense 13:23338247-23338247 - TCGA-ET-A2MY-01 COSM3369046 c.8030C>T p.S2677L Substitution - Missense 13:23335405-23335405 - sysucc-311T COSM5478471 c.4542T>C p.S1514S Substitution - coding silent 13:23338893-23338893 - CSCC-7-T COSM4568464 c.11210T>G p.L3737R Substitution - Missense 13:23332225-23332225 - 2492703 COSM5600411 c.3050C>T p.P1017L Substitution - Missense 13:23340385-23340385 - ME009T COSM223625 c.7735C>T p.L2579F Substitution - Missense 13:23335700-23335700 - HT115 COSM2265996 c.11765G>T p.R3922I Substitution - Missense 13:23331670-23331670 - TCGA-BS-A0UF-01 COSM945995 c.12484G>T p.E4162* Substitution - Nonsense 13:23330951-23330951 - PCSI_0295_Pa_P_526 COSM3753621 c.1215A>G p.L405L Substitution - coding silent 13:23354956-23354956 - pfg057T COSM4765664 c.12450_12451insA p.L4151fs*2 Insertion - Frameshift 13:23330984-23330985 - 587376 COSM946035 c.6709G>A p.E2237K Substitution - Missense 13:23336726-23336726 - HCC2998 COSM1677523 c.12299G>T p.R4100I Substitution - Missense 13:23331136-23331136 - 40M COSM5586460 c.3444C>T p.I1148I Substitution - coding silent 13:23339991-23339991 - TCGA-A6-6781-01 COSM1365899 c.8171_8172insT p.L2724fs*29 Insertion - Frameshift 13:23335263-23335264 - PCSI_0083_Pa_X COSM3376514 c.6331C>A p.Q2111K Substitution - Missense 13:23337104-23337104 - TCGA-BG-A0LX-01 COSM946039 c.6193A>T p.T2065S Substitution - Missense 13:23337242-23337242 - SNU-175 COSM2266050 c.10280delA p.N3427fs*6 Deletion - Frameshift 13:23333155-23333155 - YULAN COSM1706535 c.4346C>T p.S1449F Substitution - Missense 13:23339089-23339089 - TCGA-D9-A6EC-06 COSM4406068 c.5840T>C p.V1947A Substitution - Missense 13:23337595-23337595 - SJAMLM7015 COSM4776087 c.11394T>A p.D3798E Substitution - Missense 13:23332041-23332041 - PDA_091 COSM5003096 c.9665T>C p.V3222A Substitution - Missense 13:23333770-23333770 - TCGA-FS-A1ZQ-06 COSM1365904 c.7700C>T p.S2567L Substitution - Missense 13:23335735-23335735 - TCGA-AP-A051-01 COSM946081 c.628A>T p.S210C Substitution - Missense 13:23355543-23355543 - ACINAR09 COSM1733952 c.8351_8352insA p.R2785fs*7 Insertion - Frameshift 13:23335083-23335084 - PCSI_0083_Pa_X COSM3376506 c.9436C>A p.L3146I Substitution - Missense 13:23333999-23333999 - TCGA-BR-4361-01 COSM4046495 c.11339C>T p.A3780V Substitution - Missense 13:23332096-23332096 - TCGA-BR-8680-01 COSM4046577 c.1910A>C p.K637T Substitution - Missense 13:23341525-23341525 - HCC89T COSM1606927 c.1779A>G p.P593P Substitution - coding silent 13:23341656-23341656 - SNU-C4 COSM4615530 c.12088_12089insT p.Y4030fs*11 Insertion - Frameshift 13:23331346-23331347 - TCGA-D7-A4Z0-01 COSM3384768 c.9074A>C p.K3025T Substitution - Missense 13:23334361-23334361 - PT36 COSM5916332 c.10667C>T p.S3556F Substitution - Missense 13:23332768-23332768 - H1672 COSM314970 c.6545A>G p.Q2182R Substitution - Missense 13:23336890-23336890 - SNU-175 COSM2266450 c.70G>A p.G24S Substitution - Missense 13:23358428-23358428 - ME035T COSM227593 c.12277C>T p.L4093F Substitution - Missense 13:23331158-23331158 - PCSI_0069_Pa_X COSM3376508 c.8768T>G p.V2923G Substitution - Missense 13:23334667-23334667 - 16461 COSM5613661 c.12338C>T p.S4113F Substitution - Missense 13:23331097-23331097 - TCGA-EI-6508-01 COSM1562346 c.8656G>T p.D2886Y Substitution - Missense 13:23334779-23334779 - BB30-HNC COSM23320 c.9108C>T p.S3036S Substitution - coding silent 13:23334327-23334327 - PT38 COSM5923049 c.11756C>T p.P3919L Substitution - Missense 13:23331679-23331679 - PCSI_0083_Pa_P_526 COSM3376506 c.9436C>A p.L3146I Substitution - Missense 13:23333999-23333999 - TCGA-FU-A40J-01 COSM4843965 c.3573G>A p.K1191K Substitution - coding silent 13:23339862-23339862 - TCGA-DK-A3IS-01 COSM1300082 c.1821C>T p.F607F Substitution - coding silent 13:23341614-23341614 - ESO-0280 COSM1264775 c.11966T>G p.L3989R Substitution - Missense 13:23331469-23331469 - ESO-0459 COSM1264785 c.272A>T p.K91I Substitution - Missense 13:23355899-23355899 - Pat_73_A COSM3467702 c.9595C>T p.P3199S Substitution - Missense 13:23333840-23333840 - S02209 COSM5675146 c.4184G>T p.G1395V Substitution - Missense 13:23339251-23339251 - TCGA-DA-A1IC-06 COSM3467730 c.5058C>T p.S1686S Substitution - coding silent 13:23338377-23338377 - HCC2998 COSM946072 c.2205G>T p.K735N Substitution - Missense 13:23341230-23341230 - CR007 COSM4994555 c.11597C>T p.T3866I Substitution - Missense 13:23331838-23331838 - T3446 COSM4723398 c.8875T>C p.S2959P Substitution - Missense 13:23334560-23334560 - CSCC-31-T COSM4509996 c.382C>T p.L128F Substitution - Missense 13:23355789-23355789 - TCGA-G3-A3CJ-01 COSM4914788 c.1261G>T p.D421Y Substitution - Missense 13:23354910-23354910 - TCGA-HU-8602-01 COSM4046533 c.7934G>T p.R2645M Substitution - Missense 13:23335501-23335501 - TCGA-EI-6508-01 COSM946017 c.8992G>T p.E2998* Substitution - Nonsense 13:23334443-23334443 - TCGA-BR-4184-01 COSM4046521 c.9303G>A p.W3101* Substitution - Nonsense 13:23334132-23334132 - TCGA-ER-A194-01 COSM3467766 c.1365C>T p.A455A Substitution - coding silent 13:23354806-23354806 - 587222 COSM1224541 c.5758G>T p.E1920* Substitution - Nonsense 13:23337677-23337677 - 19 COSM1677539 c.1792C>T p.R598C Substitution - Missense 13:23341643-23341643 - HCT15 COSM2266174 c.7099T>C p.C2367R Substitution - Missense 13:23336336-23336336 - 66 COSM5743600 c.7769T>C p.L2590P Substitution - Missense 13:23335666-23335666 - YUWALI COSM1706533 c.4712C>T p.S1571F Substitution - Missense 13:23338723-23338723 - RK055_C01 COSM1629017 c.1669C>T p.L557F Substitution - Missense 13:23353860-23353860 - 8068976 COSM3772787 c.11182C>T p.R3728C Substitution - Missense 13:23332253-23332253 - PCSI_0076_Pa_P COSM3376504 c.12202G>T p.A4068S Substitution - Missense 13:23331233-23331233 - TCGA-BR-4362-01 COSM2266247 c.5519C>T p.S1840F Substitution - Missense 13:23337916-23337916 - TCGA-AG-A002-01 COSM263505 c.6378A>C p.S2126S Substitution - coding silent 13:23337057-23337057 - TCGA-AX-A05Z-01 COSM946057 c.4149C>A p.F1383L Substitution - Missense 13:23339286-23339286 - ESO-0053 COSM1264779 c.12115G>T p.V4039F Substitution - Missense 13:23331320-23331320 - AOCS-075-1-0 COSM3981962 c.11299G>T p.G3767C Substitution - Missense 13:23332136-23332136 - TCGA-AA-A00N-01 COSM277152 c.9388G>T p.D3130Y Substitution - Missense 13:23334047-23334047 - TCGA-CA-6717-01 COSM432217 c.7821G>T p.K2607N Substitution - Missense 13:23335614-23335614 - CSCC-62-T COSM4494355 c.3874C>T p.L1292F Substitution - Missense 13:23339561-23339561 - TCGA-GN-A269-01 COSM3467744 c.3718C>T p.P1240S Substitution - Missense 13:23339717-23339717 - 19 COSM5747465 c.10475T>C p.L3492S Substitution - Missense 13:23332960-23332960 - TCGA-13-0751-01 COSM80484 c.6135C>T p.I2045I Substitution - coding silent 13:23337300-23337300 - T578 COSM946064 c.2857G>T p.E953* Substitution - Nonsense 13:23340578-23340578 - TCGA-H4-A2HQ-01 COSM1300077 c.10558C>T p.H3520Y Substitution - Missense 13:23332877-23332877 - PA195 COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - COLO-205 COSM1677531 c.5188C>T p.R1730* Substitution - Nonsense 13:23338247-23338247 - 6115115 COSM5565436 c.8353C>T p.R2785W Substitution - Missense 13:23335082-23335082 - CHC892T COSM946085 c.350G>A p.G117D Substitution - Missense 13:23355821-23355821 - TCGA-AX-A0J1-01 COSM946079 c.647C>T p.T216I Substitution - Missense 13:23355524-23355524 - OSCC-GB_00420111 COSM3711016 c.13153G>A p.D4385N Substitution - Missense 13:23330282-23330282 - ME050T COSM230714 c.8139C>A p.N2713K Substitution - Missense 13:23335296-23335296 - 2492723 COSM5722099 c.8947C>T p.H2983Y Substitution - Missense 13:23334488-23334488 - MI2 COSM1165172 c.10718A>T p.E3573V Substitution - Missense 13:23332717-23332717 - YUSWI COSM1706523 c.10498G>A p.E3500K Substitution - Missense 13:23332937-23332937 - TCGA-AX-A0J1-01 COSM247163 c.8531G>A p.R2844H Substitution - Missense 13:23334904-23334904 - TCGA-AP-A059-01 COSM946053 c.4682C>T p.A1561V Substitution - Missense 13:23338753-23338753 - TCGA-BS-A0U7-01 COSM946090 c.6G>A p.A2A Substitution - coding silent 13:23365176-23365176 - CSCC-31-T COSM4492512 c.3557C>T p.S1186F Substitution - Missense 13:23339878-23339878 - PD4968a COSM5768561 c.4144C>T p.Q1382* Substitution - Nonsense 13:23339291-23339291 - PCSI_0083_Pa_P COSM3376514 c.6331C>A p.Q2111K Substitution - Missense 13:23337104-23337104 - TCGA-EI-6917-01 COSM3417461 c.5753T>A p.I1918N Substitution - Missense 13:23337682-23337682 - TCGA-CG-5726-01 COSM4046541 c.7252T>C p.F2418L Substitution - Missense 13:23336183-23336183 - TCGA-36-1576-01 COSM78441 c.12755C>G p.T4252S Substitution - Missense 13:23330680-23330680 - RK088_C01 COSM3700390 c.11764A>G p.R3922G Substitution - Missense 13:23331671-23331671 - ML_12_T_01 COSM3753623 c.255T>A p.N85K Substitution - Missense 13:23355916-23355916 - 2334192 COSM314970 c.6545A>G p.Q2182R Substitution - Missense 13:23336890-23336890 - Pat_59_B COSM5842288 c.3371G>A p.R1124K Substitution - Missense 13:23340064-23340064 - YUKAT COSM5200164 c.4808C>T p.P1603L Substitution - Missense 13:23338627-23338627 - ESO-409 COSM1264806 c.9672T>G p.T3224T Substitution - coding silent 13:23333763-23333763 - CHC902T COSM4790372 c.5534G>A p.R1845K Substitution - Missense 13:23337901-23337901 - TCGA-A6-6782-01 COSM1365878 c.9838G>A p.G3280R Substitution - Missense 13:23333597-23333597 - TCGA-F4-6570-01 COSM1365952 c.2121delA p.K707fs*2 Deletion - Frameshift 13:23341314-23341314 - HCC78T COSM1606923 c.5143A>G p.T1715A Substitution - Missense 13:23338292-23338292 - TCGA-DG-A2KL-01 COSM4851435 c.9471C>G p.L3157L Substitution - coding silent 13:23333964-23333964 - COLO678 COSM2266440 c.302C>A p.A101E Substitution - Missense 13:23355869-23355869 - 117 COSM3732867 c.2198T>C p.M733T Substitution - Missense 13:23341237-23341237 - TCGA-B5-A0JY-01 COSM946030 c.7442C>A p.S2481Y Substitution - Missense 13:23335993-23335993 - K44 COSM249642 c.7625delA p.H2542fs*50 Deletion - Frameshift 13:23335810-23335810 - TCGA-AD-6889-01 COSM1365897 c.8197C>T p.P2733S Substitution - Missense 13:23335238-23335238 - TCGA-AA-3848-01 COSM295502 c.9309T>C p.F3103F Substitution - coding silent 13:23334126-23334126 - HCC93 COSM3704568 c.6036A>T p.L2012F Substitution - Missense 13:23337399-23337399 - PCSI_0280_Pa_P_526 COSM4807660 c.11026C>A p.P3676T Substitution - Missense 13:23332409-23332409 - BD124T COSM5493079 c.1731T>C p.A577A Substitution - coding silent 13:23353798-23353798 - T36 COSM4723396 c.10832delT p.I3611fs*9 Deletion - Frameshift 13:23332603-23332603 - TCGA-13-1510-01 COSM72532 c.2613G>C p.E871D Substitution - Missense 13:23340822-23340822 - RKO COSM2266277 c.4649A>G p.Y1550C Substitution - Missense 13:23338786-23338786 - TCGA-AM-5820-01 COSM3688644 c.5643A>T p.E1881D Substitution - Missense 13:23337792-23337792 - T155 COSM1176753 c.9691A>C p.K3231Q Substitution - Missense 13:23333744-23333744 - MD-343 COSM303145 c.3043G>A p.E1015K Substitution - Missense 13:23340392-23340392 - PT16_1 COSM5898473 c.6389C>T p.A2130V Substitution - Missense 13:23337046-23337046 - GHE0609 COSM5714137 c.13022C>T p.A4341V Substitution - Missense 13:23330413-23330413 - HCT8 COSM2266174 c.7099T>C p.C2367R Substitution - Missense 13:23336336-23336336 - HCC93T COSM3704568 c.6036A>T p.L2012F Substitution - Missense 13:23337399-23337399 - TCGA-FS-A1ZC-06 COSM3467718 c.6953C>T p.S2318L Substitution - Missense 13:23336482-23336482 - TCGA-EE-A2GR-06 COSM3467738 c.4402C>T p.P1468S Substitution - Missense 13:23339033-23339033 - TCGA-DK-A1A3-01 COSM416413 c.12401C>G p.S4134C Substitution - Missense 13:23331034-23331034 - sysucc-1397T COSM2266072 c.9850G>A p.V3284I Substitution - Missense 13:23333585-23333585 - PAPNNX COSM1224568 c.5837G>A p.R1946H Substitution - Missense 13:23337598-23337598 - CRC-8 COSM304529 c.11728T>A p.L3910I Substitution - Missense 13:23331707-23331707 - TCGA-DV-5566-01 COSM3360045 c.10632C>T p.F3544F Substitution - coding silent 13:23332803-23332803 - TCGA-HU-A4GN-01 COSM4046499 c.11266C>T p.R3756* Substitution - Nonsense 13:23332169-23332169 - 61 COSM2265954 c.12902G>A p.R4301H Substitution - Missense 13:23330533-23330533 - 587278 COSM1224543 c.12844T>C p.S4282P Substitution - Missense 13:23330591-23330591 - TCGA-D1-A103-01 COSM946073 c.2153A>C p.K718T Substitution - Missense 13:23341282-23341282 - TCGA-AX-A060-01 COSM946025 c.8252G>A p.R2751H Substitution - Missense 13:23335183-23335183 - TCGA-06-0128 COSM1606923 c.5143A>G p.T1715A Substitution - Missense 13:23338292-23338292 - TCGA-EE-A2MS-06 COSM3467698 c.9803C>T p.S3268F Substitution - Missense 13:23333632-23333632 - CP66-MEL COSM23317 c.8361C>T p.F2787F Substitution - coding silent 13:23335074-23335074 - LAU63 COSM233297 c.10921C>T p.R3641C Substitution - Missense 13:23332514-23332514 - TCGA-AA-3510-01 COSM1365919 c.5833C>A p.L1945I Substitution - Missense 13:23337602-23337602 - CCK81 COSM1365946 c.2887delA p.I963fs*16 Deletion - Frameshift 13:23340548-23340548 - TCGA-BR-6452-01 COSM4046483 c.12994C>A p.L4332I Substitution - Missense 13:23330441-23330441 - DLD1 COSM2266199 c.6412C>A p.L2138I Substitution - Missense 13:23337023-23337023 - LP6008031-DNA_B01 COSM1171957 c.11966T>C p.L3989P Substitution - Missense 13:23331469-23331469 - LAU63 COSM233296 c.967C>T p.L323F Substitution - Missense 13:23355204-23355204 - PT55 COSM5942570 c.11287C>T p.P3763S Substitution - Missense 13:23332148-23332148 - CHC2200T COSM4953067 c.1137G>T p.L379F Substitution - Missense 13:23355034-23355034 - CSCC-31-T COSM4568533 c.11535T>G p.F3845L Substitution - Missense 13:23331900-23331900 - TCGA-BR-6852-01 COSM4046513 c.9808A>C p.S3270R Substitution - Missense 13:23333627-23333627 - TCGA-B5-A0JR-01 COSM946000 c.11806G>A p.V3936I Substitution - Missense 13:23331629-23331629 - 587376 COSM1224560 c.8497G>A p.A2833T Substitution - Missense 13:23334938-23334938 - YUGATOR COSM5376519 c.7709C>T p.P2570L Substitution - Missense 13:23335726-23335726 - B80-4 COSM1747364 c.11414G>T p.G3805V Substitution - Missense 13:23332021-23332021 - TCGA-D1-A16Y-01 COSM946065 c.2842G>A p.E948K Substitution - Missense 13:23340593-23340593 - TCGA-DK-A1A3-01 COSM416415 c.12855C>G p.F4285L Substitution - Missense 13:23330580-23330580 - ESO-D76 COSM946013 c.9815G>A p.R3272H Substitution - Missense 13:23333620-23333620 - HCC2998 COSM1677523 c.12299G>T p.R4100I Substitution - Missense 13:23331136-23331136 - LUAD-D01603 COSM337371 c.7201G>T p.E2401* Substitution - Nonsense 13:23336234-23336234 - 587376 COSM284762 c.11335G>A p.D3779N Substitution - Missense 13:23332100-23332100 - 8035823 COSM3384774 c.2737G>A p.V913I Substitution - Missense 13:23340698-23340698 - PCSI_0083_Pa_X COSM3376512 c.8245C>A p.L2749M Substitution - Missense 13:23335190-23335190 - CSCC-29-T COSM356007 c.1132C>T p.P378S Substitution - Missense 13:23355039-23355039 - Au2 COSM5600411 c.3050C>T p.P1017L Substitution - Missense 13:23340385-23340385 - BN17T COSM1606915 c.11600G>A p.G3867E Substitution - Missense 13:23331835-23331835 - TCGA-BR-8680-01 COSM4046497 c.11277G>A p.A3759A Substitution - coding silent 13:23332158-23332158 - TCGA-AX-A05Z-01 COSM946019 c.8749G>A p.E2917K Substitution - Missense 13:23334686-23334686 - Gp2D COSM2266241 c.5667A>G p.G1889G Substitution - coding silent 13:23337768-23337768 - PCSI_0056_Pa_X COSM3376510 c.8480T>C p.L2827S Substitution - Missense 13:23334955-23334955 - TCGA-AP-A059-01 COSM946012 c.9830G>T p.G3277V Substitution - Missense 13:23333605-23333605 - AOCS-094-6-X COSM3981966 c.7356T>C p.D2452D Substitution - coding silent 13:23336079-23336079 - TCGA-BL-A0C8-01 COSM416409 c.519C>T p.V173V Substitution - coding silent 13:23355652-23355652 - TCGA-D7-6525-01 COSM4046489 c.12390T>C p.P4130P Substitution - coding silent 13:23331045-23331045 - TCGA-BR-4361-01 COSM4046569 c.2803G>A p.D935N Substitution - Missense 13:23340632-23340632 - TCGA-EE-A2MS-06 COSM3467758 c.1662C>T p.F554F Substitution - coding silent 13:23353867-23353867 - TCGA-B5-A11E-01 COSM946047 c.5279G>A p.R1760Q Substitution - Missense 13:23338156-23338156 - ESO-0292 COSM1241699 c.1522_1531del10 p.L508fs*56 Deletion - Frameshift 13:23354640-23354649 - 27 COSM3732693 c.6509A>G p.N2170S Substitution - Missense 13:23336926-23336926 - TCGA-AG-3893-01 COSM258581 c.13140A>C p.E4380D Substitution - Missense 13:23330295-23330295 - TCGA-BR-8680-01 COSM4046549 c.6178G>A p.A2060T Substitution - Missense 13:23337257-23337257 - TCGA-G4-6586-01 COSM1365893 c.8352delA p.K2784fs*22 Deletion - Frameshift 13:23335083-23335083 - LUAD-RT-S01699 COSM378179 c.8655G>T p.Q2885H Substitution - Missense 13:23334780-23334780 - 585260 COSM323182 c.71G>T p.G24V Substitution - Missense 13:23358427-23358427 - LUAD-D01278 COSM362879 c.11473C>T p.R3825* Substitution - Nonsense 13:23331962-23331962 - sysucc-311T COSM284762 c.11335G>A p.D3779N Substitution - Missense 13:23332100-23332100 - pfg181T COSM1365946 c.2887delA p.I963fs*16 Deletion - Frameshift 13:23340548-23340548 - B2-Tumor COSM253822 c.5174G>T p.C1725F Substitution - Missense 13:23338261-23338261 - TCGA-D5-6927-01 COSM1365895 c.8214C>T p.G2738G Substitution - coding silent 13:23335221-23335221 - TCGA-ER-A193-06 COSM3467764 c.1443C>T p.P481P Substitution - coding silent 13:23354728-23354728 - Pat_41_B COSM5842276 c.12484G>A p.E4162K Substitution - Missense 13:23330951-23330951 - U87 COSM2266207 c.6353C>G p.S2118C Substitution - Missense 13:23337082-23337082 - TCGA-22-4593-01 COSM695783 c.1444G>A p.A482T Substitution - Missense 13:23354727-23354727 - TCGA-AZ-6598-01 COSM1365860 c.12192A>C p.E4064D Substitution - Missense 13:23331243-23331243 - TCGA-FS-A1ZS-06 COSM3467716 c.7082G>A p.R2361K Substitution - Missense 13:23336353-23336353 - 8035107 COSM4389707 c.12715C>T p.R4239* Substitution - Nonsense 13:23330720-23330720 - RK190_C01 COSM3744093 c.9733A>T p.N3245Y Substitution - Missense 13:23333702-23333702 - TCGA-EB-A431-01 COSM2266193 c.6643C>T p.H2215Y Substitution - Missense 13:23336792-23336792 - SJAMLM7015 COSM4776087 c.11394T>A p.D3798E Substitution - Missense 13:23332041-23332041 - RKO COSM4647696 c.189C>T p.D63D Substitution - coding silent 13:23355982-23355982 - LC_S51 COSM1188681 c.773G>T p.S258I Substitution - Missense 13:23355398-23355398 - H1672 COSM314969 c.9890G>T p.W3297L Substitution - Missense 13:23333545-23333545 - BD130T COSM5516047 c.2812C>G p.H938D Substitution - Missense 13:23340623-23340623 - RKO COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - CSCC-41-T COSM3467694 c.10282C>T p.H3428Y Substitution - Missense 13:23333153-23333153 - TCGA-AM-5821-01 COSM3753623 c.255T>A p.N85K Substitution - Missense 13:23355916-23355916 - TCGA-F5-6814-01 COSM3417449 c.10456T>G p.F3486V Substitution - Missense 13:23332979-23332979 - HCC42 COSM1606919 c.9526G>A p.A3176T Substitution - Missense 13:23333909-23333909 - LUAD-CHTN-Z4716A COSM361726 c.4436G>T p.G1479V Substitution - Missense 13:23338999-23338999 - TCGA-33-4532-01 COSM695778 c.945T>A p.V315V Substitution - coding silent 13:23355226-23355226 - 234 COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - CHEWS019 COSM4575875 c.7421A>G p.Q2474R Substitution - Missense 13:23336014-23336014 - PT08_2 COSM5376521 c.6353C>T p.S2118F Substitution - Missense 13:23337082-23337082 - BD202T COSM5501378 c.12140A>T p.Y4047F Substitution - Missense 13:23331295-23331295 - 13280 COSM5613663 c.1907G>A p.W636* Substitution - Nonsense 13:23341528-23341528 - SS6003320 COSM3980190 c.4136A>G p.N1379S Substitution - Missense 13:23339299-23339299 - Gp2D COSM1365893 c.8352delA p.K2784fs*22 Deletion - Frameshift 13:23335083-23335083 - CHC2110Tbis COSM4957670 c.11419G>A p.D3807N Substitution - Missense 13:23332016-23332016 - TCGA-66-2755-01 COSM695786 c.3077G>C p.W1026S Substitution - Missense 13:23340358-23340358 - HCT15 COSM2265948 c.13253C>A p.A4418D Substitution - Missense 13:23330182-23330182 - T3724 COSM4723412 c.6717delT p.F2239fs*6 Deletion - Frameshift 13:23336718-23336718 - 587376 COSM1224555 c.12794G>T p.R4265I Substitution - Missense 13:23330641-23330641 - S01563 COSM314975 c.4721C>T p.S1574F Substitution - Missense 13:23338714-23338714 - ESO-130 COSM1264796 c.349G>A p.G117S Substitution - Missense 13:23355822-23355822 - TCGA-B5-A0JY-01 COSM946087 c.195C>T p.I65I Substitution - coding silent 13:23355976-23355976 - 273T COSM1727309 c.7717G>C p.D2573H Substitution - Missense 13:23335718-23335718 - CHEWS010 COSM4575873 c.11262T>C p.N3754N Substitution - coding silent 13:23332173-23332173 - T3503 COSM183268 c.385C>T p.R129C Substitution - Missense 13:23355786-23355786 - sysucc-1317T COSM5448575 c.2991A>G p.S997S Substitution - coding silent 13:23340444-23340444 - SWE-42 COSM551061 c.2083G>T p.D695Y Substitution - Missense 13:23341352-23341352 - TCGA-B6-A0X4-01 COSM432217 c.7821G>T p.K2607N Substitution - Missense 13:23335614-23335614 - LUAD-NYU1219 COSM391871 c.1328_1329delTG p.V443fs*55 Deletion - Frameshift 13:23354842-23354843 - TCGA-GM-A2DO-01 COSM3813583 c.7074C>T p.A2358A Substitution - coding silent 13:23336361-23336361 - TCGA-37-3789-01 COSM695788 c.5058C>A p.S1686S Substitution - coding silent 13:23338377-23338377 - TCGA-DG-A2KK-01 COSM4828196 c.11903C>G p.S3968C Substitution - Missense 13:23331532-23331532 - NPC38F COSM4995199 c.12052C>T p.H4018Y Substitution - Missense 13:23331383-23331383 - BD6T COSM5499158 c.5674G>A p.E1892K Substitution - Missense 13:23337761-23337761 - TCGA-BS-A0UV-01 COSM946024 c.8276G>A p.R2759Q Substitution - Missense 13:23335159-23335159 - HCC2998 COSM1677535 c.4075A>G p.R1359G Substitution - Missense 13:23339360-23339360 - TCGA-B7-5816-01 COSM4046567 c.3794T>C p.L1265P Substitution - Missense 13:23339641-23339641 - TCGA-AX-A05Z-01 COSM945997 c.12040C>A p.P4014T Substitution - Missense 13:23331395-23331395 - PCSI_0083_Pa_P_526 COSM3376512 c.8245C>A p.L2749M Substitution - Missense 13:23335190-23335190 - U373 COSM5713239 c.1998_1999delAT p.V668fs*4 Deletion - Frameshift 13:23341436-23341437 - HCC42T COSM1606919 c.9526G>A p.A3176T Substitution - Missense 13:23333909-23333909 - 587376 COSM1224572 c.3900A>C p.E1300D Substitution - Missense 13:23339535-23339535 - TCGA-AX-A0J0-01 COSM945999 c.11842G>T p.D3948Y Substitution - Missense 13:23331593-23331593 - TCGA-B5-A0JR-01 COSM946018 c.8810T>C p.I2937T Substitution - Missense 13:23334625-23334625 - TCGA-AX-A05Z-01 COSM946064 c.2857G>T p.E953* Substitution - Nonsense 13:23340578-23340578 - TCGA-CG-5721-01 COSM4046595 c.149T>C p.V50A Substitution - Missense 13:23358349-23358349 - TCGA-EE-A2GC-06 COSM3467724 c.6373G>A p.G2125S Substitution - Missense 13:23337062-23337062 - ESO-118 COSM1264792 c.6835C>T p.R2279* Substitution - Nonsense 13:23336600-23336600 - HCC2998 COSM946024 c.8276G>A p.R2759Q Substitution - Missense 13:23335159-23335159 - TCGA-AA-3715-01 COSM270100 c.1957A>T p.M653L Substitution - Missense 13:23341478-23341478 - LUAD_E00565 COSM389093 c.3333C>T p.F1111F Substitution - coding silent 13:23340102-23340102 - TCGA-DD-A4NF-01 COSM4912728 c.9778C>T p.L3260L Substitution - coding silent 13:23333657-23333657 - HCC39T COSM1606921 c.8188A>T p.T2730S Substitution - Missense 13:23335247-23335247 - 8052570 COSM3384776 c.2432C>G p.A811G Substitution - Missense 13:23341003-23341003 - 587376 COSM1224568 c.5837G>A p.R1946H Substitution - Missense 13:23337598-23337598 - TCGA-AP-A056-01 COSM946040 c.6142A>C p.K2048Q Substitution - Missense 13:23337293-23337293 - pfg019T COSM1639309 c.10403A>G p.N3468S Substitution - Missense 13:23333032-23333032 - CCC5 COSM3704566 c.8801A>G p.H2934R Substitution - Missense 13:23334634-23334634 - TCGA-DD-A1E9-01 COSM4912362 c.1758T>C p.T586T Substitution - coding silent 13:23341677-23341677 - TCGA-G3-A7M5-01 COSM4942052 c.7119A>C p.T2373T Substitution - coding silent 13:23336316-23336316 - PT52 COSM5940402 c.4268C>T p.P1423L Substitution - Missense 13:23339167-23339167 - SNU-C4 COSM4615532 c.4905delT p.F1635fs*32 Deletion - Frameshift 13:23338530-23338530 - HCT15 COSM1677527 c.6516C>A p.C2172* Substitution - Nonsense 13:23336919-23336919 - TCGA-AX-A05Z-01 COSM946062 c.3610G>T p.E1204* Substitution - Nonsense 13:23339825-23339825 - TCGA-J9-A52C-01 COSM4877411 c.8009C>T p.T2670M Substitution - Missense 13:23335426-23335426 - HCC2998 COSM1677539 c.1792C>T p.R598C Substitution - Missense 13:23341643-23341643 - DLD1 COSM2266174 c.7099T>C p.C2367R Substitution - Missense 13:23336336-23336336 - CHC1040T COSM4799567 c.2682G>T p.Q894H Substitution - Missense 13:23340753-23340753 - LIM2405 COSM1365946 c.2887delA p.I963fs*16 Deletion - Frameshift 13:23340548-23340548 - sysucc-311T COSM5478475 c.1798A>G p.I600V Substitution - Missense 13:23341637-23341637 - TCGA-BR-A4QL-01 COSM4046485 c.12494C>A p.S4165Y Substitution - Missense 13:23330941-23330941 - CRC-06T COSM5456379 c.10531C>T p.R3511W Substitution - Missense 13:23332904-23332904 - T578 COSM4723428 c.2923G>T p.D975Y Substitution - Missense 13:23340512-23340512 - PAPNNX COSM5004561 c.8442G>A p.S2814S Substitution - coding silent 13:23334993-23334993 - YURAY COSM5376523 c.5884T>G p.L1962V Substitution - Missense 13:23337551-23337551 - TCGA-EE-A29B-06 COSM3467712 c.8555C>T p.P2852L Substitution - Missense 13:23334880-23334880 - TCGA-G5-6233-01 COSM3417432 c.12913A>C p.R4305R Substitution - coding silent 13:23330522-23330522 - PT17_1 COSM5899092 c.10021C>T p.L3341F Substitution - Missense 13:23333414-23333414 - TCGA-D9-A6EA-06 COSM4398275 c.4006C>T p.Q1336* Substitution - Nonsense 13:23339429-23339429 - 587226 COSM946065 c.2842G>A p.E948K Substitution - Missense 13:23340593-23340593 - GC6_T COSM147642 c.9780A>T p.L3260L Substitution - coding silent 13:23333655-23333655 - TCGA-AX-A0J1-01 COSM946076 c.1062C>T p.V354V Substitution - coding silent 13:23355109-23355109 - TCGA-DU-7006-01 COSM3968572 c.9830G>A p.G3277E Substitution - Missense 13:23333605-23333605 - TCGA-D1-A16X-01 COSM945994 c.12588G>T p.E4196D Substitution - Missense 13:23330847-23330847 - TCGA-GN-A266-06 COSM3467704 c.9445C>T p.P3149S Substitution - Missense 13:23333990-23333990 - LUAD-5V8LT COSM401408 c.12108G>T p.G4036G Substitution - coding silent 13:23331327-23331327 - S00833 COSM314973 c.12732A>G p.K4244K Substitution - coding silent 13:23330703-23330703 - TCGA-AP-A05P-01 COSM946050 c.4968G>A p.K1656K Substitution - coding silent 13:23338467-23338467 - TCGA-EE-A2MT-06 COSM3467752 c.2375C>T p.S792F Substitution - Missense 13:23341060-23341060 - YUDEXA COSM1706527 c.7900C>T p.H2634Y Substitution - Missense 13:23335535-23335535 - J87_T COSM3955449 c.3343C>A p.H1115N Substitution - Missense 13:23340092-23340092 - ESCC-015T COSM3936261 c.10789C>T p.P3597S Substitution - Missense 13:23332646-23332646 - TCGA-AX-A05Z-01 COSM946043 c.5790G>T p.M1930I Substitution - Missense 13:23337645-23337645 - TCGA-IR-A3LA-01 COSM4844365 c.5701G>A p.E1901K Substitution - Missense 13:23337734-23337734 - 587376 COSM1224576 c.2441G>A p.R814Q Substitution - Missense 13:23340994-23340994 - CCC5T COSM3704566 c.8801A>G p.H2934R Substitution - Missense 13:23334634-23334634 - OSCC-GB_00310111 COSM3718449 c.11276C>T p.A3759V Substitution - Missense 13:23332159-23332159 - TCGA-AA-3510-01 COSM1365938 c.4186G>T p.E1396* Substitution - Nonsense 13:23339249-23339249 - HCC2998 COSM1677535 c.4075A>G p.R1359G Substitution - Missense 13:23339360-23339360 - TCGA-FP-A4BF-01 COSM4046507 c.10343T>C p.L3448P Substitution - Missense 13:23333092-23333092 - 12T COSM110198 c.2666C>T p.P889L Substitution - Missense 13:23340769-23340769 - TCGA-28-5216-01 COSM3399273 c.5871G>A p.G1957G Substitution - coding silent 13:23337564-23337564 - TCGA-25-1318-01 COSM78442 c.6862C>G p.L2288V Substitution - Missense 13:23336573-23336573 - TCGA-18-3421-01 COSM695793 c.8475A>T p.P2825P Substitution - coding silent 13:23334960-23334960 - TCGA-AX-A05Z-01 COSM946074 c.1871G>T p.R624I Substitution - Missense 13:23341564-23341564 - TCGA-A6-6780-01 COSM1365921 c.5745_5746insT p.P1916fs*7 Insertion - Frameshift 13:23337689-23337690 - HCC2998 COSM2266223 c.6141G>A p.E2047E Substitution - coding silent 13:23337294-23337294 - BN17 COSM1606915 c.11600G>A p.G3867E Substitution - Missense 13:23331835-23331835 - 61 COSM5739907 c.11156G>A p.G3719D Substitution - Missense 13:23332279-23332279 - Gp5D COSM2266241 c.5667A>G p.G1889G Substitution - coding silent 13:23337768-23337768 - TCGA-DA-A1IA-06 COSM1706531 c.5905C>T p.P1969S Substitution - Missense 13:23337530-23337530 - TCGA-EE-A2M5-06 COSM3467720 c.6784C>T p.Q2262* Substitution - Nonsense 13:23336651-23336651 - CSCC-60-T COSM4568412 c.10940T>C p.V3647A Substitution - Missense 13:23332495-23332495 - HCC108 COSM1606929 c.202C>T p.L68L Substitution - coding silent 13:23355969-23355969 - 1946219 COSM96920 c.1493_1494AA>GG p.E498G Substitution - Missense 13:23354677-23354678 - B90 COSM254921 c.5968C>G p.Q1990E Substitution - Missense 13:23337467-23337467 - PD13420a COSM5790370 c.10679T>C p.L3560P Substitution - Missense 13:23332756-23332756 - TCGA-BP-5168-01 COSM469250 c.8392C>A p.Q2798K Substitution - Missense 13:23335043-23335043 - T1743 COSM4723422 c.4470C>T p.Y1490Y Substitution - coding silent 13:23338965-23338965 - TCGA-EE-A2MD-06 COSM1706525 c.9466C>T p.P3156S Substitution - Missense 13:23333969-23333969 - 2492722 COSM5722101 c.6235T>G p.S2079A Substitution - Missense 13:23337200-23337200 - I2L-P24Tb-Tumor-Organoid COSM5362174 c.7952C>A p.P2651Q Substitution - Missense 13:23335483-23335483 - TCGA-BC-A10U-01 COSM4942482 c.12547A>G p.R4183G Substitution - Missense 13:23330888-23330888 - TCGA-B8-5549-01 COSM469258 c.2091A>C p.V697V Substitution - coding silent 13:23341344-23341344 - 226 COSM3730201 c.1384G>A p.D462N Substitution - Missense 13:23354787-23354787 - C141 COSM4441432 c.8423C>A p.T2808N Substitution - Missense 13:23335012-23335012 - TCGA-EE-A2MD-06 COSM233297 c.10921C>T p.R3641C Substitution - Missense 13:23332514-23332514 - Pat_53_B COSM1365946 c.2887delA p.I963fs*16 Deletion - Frameshift 13:23340548-23340548 - 168 COSM3733062 c.1898A>G p.K633R Substitution - Missense 13:23341537-23341537 - GC_312T-GC_312N COSM4773700 c.6587C>G p.P2196R Substitution - Missense 13:23336848-23336848 - 45 COSM5734265 c.1913A>T p.N638I Substitution - Missense 13:23341522-23341522 - TCGA-CM-6674-01 COSM1365950 c.2135T>C p.I712T Substitution - Missense 13:23341300-23341300 - HCC49T COSM1606917 c.10913G>A p.R3638K Substitution - Missense 13:23332522-23332522 - TCGA-AH-6897-01 COSM3417441 c.11828A>T p.H3943L Substitution - Missense 13:23331607-23331607 - BD5T COSM3704566 c.8801A>G p.H2934R Substitution - Missense 13:23334634-23334634 - TCGA-CA-6717-01 COSM1365888 c.8749G>T p.E2917* Substitution - Nonsense 13:23334686-23334686 - BCM339T COSM4802514 c.6476A>G p.D2159G Substitution - Missense 13:23336959-23336959 - TCGA-06-6390 COSM2153437 c.9417T>G p.F3139L Substitution - Missense 13:23334018-23334018 - ESO14T COSM1171957 c.11966T>C p.L3989P Substitution - Missense 13:23331469-23331469 - TCGA-D8-A1J8-01 COSM3813579 c.7691C>T p.S2564L Substitution - Missense 13:23335744-23335744 - TCGA-F1-6177-01 COSM4046545 c.6661G>A p.A2221T Substitution - Missense 13:23336774-23336774 - TCGA-24-1469-01 COSM79275 c.4441C>T p.Q1481* Substitution - Nonsense 13:23338994-23338994 - TCGA-EE-A2GU-06 COSM1706533 c.4712C>T p.S1571F Substitution - Missense 13:23338723-23338723 - TCGA-BR-7707-01 COSM4046583 c.1348T>G p.S450A Substitution - Missense 13:23354823-23354823 - CCC60 COSM2266135 c.8549G>A p.R2850Q Substitution - Missense 13:23334886-23334886 - pfg057T COSM4765662 c.12616_12617insT p.K4206fs*6 Insertion - Frameshift 13:23330818-23330819 - Mx41 COSM32414 c.4944G>A p.M1648I Substitution - Missense 13:23338491-23338491 - TCGA-CG-5726-01 COSM4046565 c.3909A>T p.G1303G Substitution - coding silent 13:23339526-23339526 - ESCC_BICR_070T COSM5444873 c.6377C>T p.S2126L Substitution - Missense 13:23337058-23337058 - Pat_41_B COSM5842284 c.7148G>A p.S2383N Substitution - Missense 13:23336287-23336287 - 587220 COSM1224535 c.7447T>C p.Y2483H Substitution - Missense 13:23335988-23335988 - TCGA-BH-A18G-01 COSM3813587 c.4930G>A p.A1644T Substitution - Missense 13:23338505-23338505 - ESCC_164 COSM2266427 c.625A>G p.I209V Substitution - Missense 13:23355546-23355546 - ccRCC-8 COSM1665731 c.7629delT p.F2543fs*49 Deletion - Frameshift 13:23335806-23335806 - TCGA-F5-6814-01 COSM3417455 c.7645A>C p.T2549P Substitution - Missense 13:23335790-23335790 - 2521259 COSM5890786 c.7073C>T p.A2358V Substitution - Missense 13:23336362-23336362 - TCGA-D7-A4YT-01 COSM946047 c.5279G>A p.R1760Q Substitution - Missense 13:23338156-23338156 - TCGA-66-2785-01 COSM695790 c.5549C>G p.S1850C Substitution - Missense 13:23337886-23337886 - HCC24 COSM1606925 c.3868C>T p.P1290S Substitution - Missense 13:23339567-23339567 - 587332 COSM1224582 c.1450G>A p.V484M Substitution - Missense 13:23354721-23354721 - TCGA-C5-A1BQ-01 COSM2266044 c.10481C>G p.S3494C Substitution - Missense 13:23332954-23332954 - CHC892T COSM946085 c.350G>A p.G117D Substitution - Missense 13:23355821-23355821 - TCGA-06-0128-01 COSM1606923 c.5143A>G p.T1715A Substitution - Missense 13:23338292-23338292 - I2L-P19Ta-Tumor-Biopsy COSM5362111 c.1490C>A p.A497D Substitution - Missense 13:23354681-23354681 - TCGA-F5-6814-01 COSM3417430 c.13076C>T p.A4359V Substitution - Missense 13:23330359-23330359 - PCSI_0083_Pa_X COSM3376516 c.3425A>G p.Q1142R Substitution - Missense 13:23340010-23340010 - TCGA-FS-A1ZE-06 COSM3467752 c.2375C>T p.S792F Substitution - Missense 13:23341060-23341060 - TCGA-BQ-7053-01 COSM3987333 c.10580A>G p.N3527S Substitution - Missense 13:23332855-23332855 - TCGA-D9-A6EC-06 COSM4405707 c.12006A>G p.S4002S Substitution - coding silent 13:23331429-23331429 - B77 COSM254920 c.7474A>T p.I2492F Substitution - Missense 13:23335961-23335961 - AOCS-057-1-2 COSM3981964 c.9328G>A p.V3110M Substitution - Missense 13:23334107-23334107 - Pat_63_B COSM5842290 c.242G>A p.G81D Substitution - Missense 13:23355929-23355929 - CHC2110Tbis COSM4957670 c.11419G>A p.D3807N Substitution - Missense 13:23332016-23332016 - TCGA-BS-A0UV-01 COSM946048 c.5189G>A p.R1730Q Substitution - Missense 13:23338246-23338246 - TCGA-EE-A2M6-06 COSM1706533 c.4712C>T p.S1571F Substitution - Missense 13:23338723-23338723 - TCGA-76-6286-01 COSM3399275 c.4273A>G p.I1425V Substitution - Missense 13:23339162-23339162 - 3N09-VS-3T09 COSM4979180 c.12631G>A p.E4211K Substitution - Missense 13:23330804-23330804 - TCGA-D1-A176-01 COSM946023 c.8287A>T p.N2763Y Substitution - Missense 13:23335148-23335148 - LS411 COSM2265974 c.12380G>A p.R4127K Substitution - Missense 13:23331055-23331055 - TCGA-EE-A2MG-06 COSM3467726 c.5875C>T p.P1959S Substitution - Missense 13:23337560-23337560 - SNUH_G16_S1 COSM3999045 c.5826G>T p.S1942S Substitution - coding silent 13:23337609-23337609 - TCGA-A5-A0GB-01 COSM946080 c.629G>T p.S210I Substitution - Missense 13:23355542-23355542 - pfg068T COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - Pat_54_A COSM1365946 c.2887delA p.I963fs*16 Deletion - Frameshift 13:23340548-23340548 - HT115 COSM2266261 c.5023A>G p.T1675A Substitution - Missense 13:23338412-23338412 - TCGA-BR-8589-01 COSM4046531 c.8478T>G p.D2826E Substitution - Missense 13:23334957-23334957 - LIM1899 COSM4639931 c.696A>T p.L232F Substitution - Missense 13:23355475-23355475 - TCGA-B5-A0JY-01 COSM946052 c.4823A>C p.K1608T Substitution - Missense 13:23338612-23338612 - TCGA-AC-A23H-01 COSM3813569 c.12707C>T p.S4236L Substitution - Missense 13:23330728-23330728 - TCGA-BH-A0H6-01 COSM432221 c.164-2A>C p.? Unknown 13:23356009-23356009 - TCGA-AX-A05Z-01 COSM946004 c.11095G>T p.D3699Y Substitution - Missense 13:23332340-23332340 - TCGA-BS-A0UV-01 COSM946069 c.2315G>T p.R772I Substitution - Missense 13:23341120-23341120 - TCGA-EE-A3J7-06 COSM3885093 c.939C>T p.L313L Substitution - coding silent 13:23355232-23355232 - YUTRAIN COSM5376521 c.6353C>T p.S2118F Substitution - Missense 13:23337082-23337082 - TCGA-BR-8680-01 COSM946002 c.11340G>A p.A3780A Substitution - coding silent 13:23332095-23332095 - TCGA-D1-A16X-01 COSM946075 c.1513G>T p.E505* Substitution - Nonsense 13:23354658-23354658 - TCGA-CK-4950-01 COSM1365864 c.11540C>T p.A3847V Substitution - Missense 13:23331895-23331895 - TCGA-EB-A41A-01 COSM3467722 c.6665C>T p.P2222L Substitution - Missense 13:23336770-23336770 - ESCC_139 COSM5643218 c.7357G>A p.D2453N Substitution - Missense 13:23336078-23336078 - RKO COSM2266269 c.4878G>A p.R1626R Substitution - coding silent 13:23338557-23338557 - TCGA-A5-A0GP-01 COSM946045 c.5419G>T p.D1807Y Substitution - Missense 13:23338016-23338016 - KPOPBR-03-T COSM5965393 c.12113T>G p.L4038R Substitution - Missense 13:23331322-23331322 - PD18247a COSM5770903 c.1915C>G p.L639V Substitution - Missense 13:23341520-23341520 - TCGA-BS-A0UV-01 COSM946061 c.3831G>A p.E1277E Substitution - coding silent 13:23339604-23339604 - TCGA-D1-A0ZO-01 COSM946013 c.9815G>A p.R3272H Substitution - Missense 13:23333620-23333620 - U373 COSM5712657 c.11626A>G p.N3876D Substitution - Missense 13:23331809-23331809 - TCGA-EI-6508-01 COSM1562344 c.8601G>A p.W2867* Substitution - Nonsense 13:23334834-23334834 - TCGA-BR-8680-01 COSM4046517 c.9580G>T p.D3194Y Substitution - Missense 13:23333855-23333855 - T3021 COSM4723408 c.7318G>A p.A2440T Substitution - Missense 13:23336117-23336117 - TCGA-ER-A19G-06 COSM3467760 c.1657C>T p.L553F Substitution - Missense 13:23353872-23353872 - PCSI_0537_Pa_P_526 COSM5031194 c.8663T>C p.L2888S Substitution - Missense 13:23334772-23334772 - 2492720 COSM5722101 c.6235T>G p.S2079A Substitution - Missense 13:23337200-23337200 - 2492729 COSM5726145 c.864A>G p.G288G Substitution - coding silent 13:23355307-23355307 - TCGA-AP-A0LM-01 COSM946071 c.2241G>A p.S747S Substitution - coding silent 13:23341194-23341194 - OSCC-GB_01240111 COSM5954124 c.1177A>G p.K393E Substitution - Missense 13:23354994-23354994 - TCGA-33-4532-01 COSM695780 c.946C>T p.H316Y Substitution - Missense 13:23355225-23355225 - RK282_C01 COSM4964044 c.9568A>G p.I3190V Substitution - Missense 13:23333867-23333867 - HCC24T COSM1606925 c.3868C>T p.P1290S Substitution - Missense 13:23339567-23339567 - 8031133 COSM1168776 c.1876C>T p.H626Y Substitution - Missense 13:23341559-23341559 - 74 COSM4778011 c.7603C>G p.L2535V Substitution - Missense 13:23335832-23335832 - TCGA-AG-A002-01 COSM263506 c.4472G>A p.S1491N Substitution - Missense 13:23338963-23338963 - SNU-175 COSM2266084 c.9586G>A p.A3196T Substitution - Missense 13:23333849-23333849 - BD57T COSM5510669 c.9106T>C p.S3036P Substitution - Missense 13:23334329-23334329 - 2492701 COSM5600411 c.3050C>T p.P1017L Substitution - Missense 13:23340385-23340385 - DLD1 COSM2266178 c.7017T>G p.A2339A Substitution - coding silent 13:23336418-23336418 - TCGA-63-6202-01 COSM695798 c.12412A>T p.S4138C Substitution - Missense 13:23331023-23331023 - TCGA-AA-A010-01 COSM284765 c.5251G>T p.E1751* Substitution - Nonsense 13:23338184-23338184 - CSCC-29-T COSM4460327 c.11170C>T p.P3724S Substitution - Missense 13:23332265-23332265 - TCGA-AP-A059-01 COSM946054 c.4638G>A p.M1546I Substitution - Missense 13:23338797-23338797 - TCGA-B5-A11E-01 COSM946069 c.2315G>T p.R772I Substitution - Missense 13:23341120-23341120 - I2L-P7-Tumor-Organoid COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - TCGA-BR-8589-01 COSM4046543 c.6822T>G p.F2274L Substitution - Missense 13:23336613-23336613 - TCGA-F5-6814-01 COSM3417445 c.11430T>G p.F3810L Substitution - Missense 13:23332005-23332005 - TCGA-BR-8297-01 COSM4046515 c.9719T>G p.L3240R Substitution - Missense 13:23333716-23333716 - TCGA-DK-A3WW-01 COSM3793191 c.4510C>G p.Q1504E Substitution - Missense 13:23338925-23338925 - TCGA-BR-8680-01 COSM4046563 c.4492C>T p.R1498* Substitution - Nonsense 13:23338943-23338943 - CSCC-27-T COSM4046537 c.7660C>T p.P2554S Substitution - Missense 13:23335775-23335775 - TCGA-EB-A24D-01 COSM3467768 c.821G>A p.G274E Substitution - Missense 13:23355350-23355350 - HCC2998 COSM1677537 c.2094A>C p.Q698H Substitution - Missense 13:23341341-23341341 - TCGA-DD-A119-01 COSM2266231 c.5944G>A p.G1982R Substitution - Missense 13:23337491-23337491 - TCGA-D9-A6EC-06 COSM4403992 c.3698C>T p.P1233L Substitution - Missense 13:23339737-23339737 - C106 COSM4616204 c.6317T>C p.I2106T Substitution - Missense 13:23337118-23337118 - 46M COSM5565572 c.520C>T p.R174* Substitution - Nonsense 13:23355651-23355651 - TCGA-AN-A046-01 COSM946005 c.10498G>T p.E3500* Substitution - Nonsense 13:23332937-23332937 - SNUH_G76_S1 COSM3753621 c.1215A>G p.L405L Substitution - coding silent 13:23354956-23354956 - KPOPBR-14-T COSM946042 c.5820G>A p.E1940E Substitution - coding silent 13:23337615-23337615 - PT35 COSM5913525 c.3385C>T p.P1129S Substitution - Missense 13:23340050-23340050 - I2L-P19Ta-Tumor-Organoid COSM5362111 c.1490C>A p.A497D Substitution - Missense 13:23354681-23354681 - ESCC_BICR_047T COSM5430321 c.2705C>T p.S902L Substitution - Missense 13:23340730-23340730 - TCGA-B0-5695-01 COSM469254 c.3735G>T p.M1245I Substitution - Missense 13:23339700-23339700 - C086 COSM233297 c.10921C>T p.R3641C Substitution - Missense 13:23332514-23332514 - TCGA-DK-A2I6-01 COSM233297 c.10921C>T p.R3641C Substitution - Missense 13:23332514-23332514 - TCGA-AO-A128-01 COSM3813589 c.3658T>C p.Y1220H Substitution - Missense 13:23339777-23339777 - TCGA-DD-A4ND-01 COSM4935038 c.5053T>A p.F1685I Substitution - Missense 13:23338382-23338382 - TCGA-F5-6814-01 COSM3417459 c.6136G>A p.D2046N Substitution - Missense 13:23337299-23337299 - TCGA-BG-A0VX-01 COSM946038 c.6268G>A p.E2090K Substitution - Missense 13:23337167-23337167 - TCGA-EE-A2MJ-06 COSM3467734 c.4938T>G p.F1646L Substitution - Missense 13:23338497-23338497 - 587222 COSM1224539 c.6397G>T p.E2133* Substitution - Nonsense 13:23337038-23337038 - TCGA-AZ-4615-01 COSM2266042 c.10609G>A p.G3537R Substitution - Missense 13:23332826-23332826 - T2269 COSM4723402 c.7978G>T p.D2660Y Substitution - Missense 13:23335457-23335457 - TCGA-HU-A4G9-01 COSM4046493 c.11958T>C p.G3986G Substitution - coding silent 13:23331477-23331477 - S01297 COSM5667438 c.5551A>G p.I1851V Substitution - Missense 13:23337884-23337884 - TCGA-EI-6917-01 COSM946024 c.8276G>A p.R2759Q Substitution - Missense 13:23335159-23335159 - TCGA-66-2767-01 COSM695791 c.5945G>T p.G1982V Substitution - Missense 13:23337490-23337490 - 2492702 COSM5600411 c.3050C>T p.P1017L Substitution - Missense 13:23340385-23340385 - sysucc-1512T COSM5450714 c.9337G>T p.D3113Y Substitution - Missense 13:23334098-23334098 - TCGA-BS-A0TC-01 COSM945993 c.12633A>C p.E4211D Substitution - Missense 13:23330802-23330802 - TCGA-D3-A5GS-06 COSM3467684 c.13173C>T p.Y4391Y Substitution - coding silent 13:23330262-23330262 - ESO-0025 COSM1264775 c.11966T>G p.L3989R Substitution - Missense 13:23331469-23331469 - TCGA-CG-4469-01 COSM4046573 c.2749C>T p.L917F Substitution - Missense 13:23340686-23340686 - HCC108T COSM1606929 c.202C>T p.L68L Substitution - coding silent 13:23355969-23355969 - 61 COSM5739911 c.4730T>C p.L1577S Substitution - Missense 13:23338705-23338705 - TCGA-AX-A0J0-01 COSM946048 c.5189G>A p.R1730Q Substitution - Missense 13:23338246-23338246 - TCGA-BH-A0B7-01 COSM432218 c.6977G>C p.W2326S Substitution - Missense 13:23336458-23336458 - T3105 COSM1365946 c.2887delA p.I963fs*16 Deletion - Frameshift 13:23340548-23340548 - TCGA-BH-A18G-01 COSM3813585 c.5738T>C p.V1913A Substitution - Missense 13:23337697-23337697 - TCGA-AD-6963-01 COSM1365854 c.12779G>T p.S4260I Substitution - Missense 13:23330656-23330656 - HCC020T COSM5809154 c.7960C>A p.Q2654K Substitution - Missense 13:23335475-23335475 - TCGA-UC-A7PF-01 COSM4830441 c.9674C>T p.S3225L Substitution - Missense 13:23333761-23333761 - TCGA-BS-A0UF-01 COSM946017 c.8992G>T p.E2998* Substitution - Nonsense 13:23334443-23334443 - TCGA-F5-6814-01 COSM3417463 c.4175C>T p.T1392I Substitution - Missense 13:23339260-23339260 - YULOCUS COSM5376517 c.12353C>T p.P4118L Substitution - Missense 13:23331082-23331082 - 61 COSM5739909 c.7115G>A p.G2372D Substitution - Missense 13:23336320-23336320 - SNUH_G16_S1 COSM3999047 c.3747C>T p.H1249H Substitution - coding silent 13:23339688-23339688 - CSCC-31-T COSM4503899 c.209C>T p.P70L Substitution - Missense 13:23355962-23355962 - Pat_40_A COSM5842274 c.13075G>A p.A4359T Substitution - Missense 13:23330360-23330360 - T3262 COSM4723432 c.1258T>C p.C420R Substitution - Missense 13:23354913-23354913 - AA2055 COSM4168505 c.8868G>T p.M2956I Substitution - Missense 13:23334567-23334567 - TCGA-G2-A3VY-01 COSM3793197 c.271A>G p.K91E Substitution - Missense 13:23355900-23355900 - CSCC-20-T COSM4503390 c.5953C>T p.P1985S Substitution - Missense 13:23337482-23337482 - PD24216a COSM5795093 c.11228A>T p.N3743I Substitution - Missense 13:23332207-23332207 - PD12803a COSM233297 c.10921C>T p.R3641C Substitution - Missense 13:23332514-23332514 - DLD1 COSM2265948 c.13253C>A p.A4418D Substitution - Missense 13:23330182-23330182 - HCT8 COSM4633793 c.12602C>T p.A4201V Substitution - Missense 13:23330833-23330833 - YUBER COSM1706525 c.9466C>T p.P3156S Substitution - Missense 13:23333969-23333969 - SNUH_G45_S1 COSM147643 c.468A>G p.A156A Substitution - coding silent 13:23355703-23355703 - PD23554a COSM5780713 c.7395A>G p.K2465K Substitution - coding silent 13:23336040-23336040 - TCGA-BR-4362-01 COSM4046591 c.634T>C p.Y212H Substitution - Missense 13:23355537-23355537 - TCGA-BR-8680-01 COSM4046503 c.10734T>C p.G3578G Substitution - coding silent 13:23332701-23332701 - 2207 COSM5012648 c.8467C>A p.L2823I Substitution - Missense 13:23334968-23334968 - sysucc-1173T COSM5459605 c.10984G>T p.E3662* Substitution - Nonsense 13:23332451-23332451 - TCGA-BS-A0UF-01 COSM946043 c.5790G>T p.M1930I Substitution - Missense 13:23337645-23337645 - TCGA-AX-A0J1-01 COSM946084 c.477G>A p.V159V Substitution - coding silent 13:23355694-23355694 - LUAD-5V8LT COSM401409 c.10304G>T p.W3435L Substitution - Missense 13:23333131-23333131 - ESO-139 COSM1264798 c.8518G>A p.E2840K Substitution - Missense 13:23334917-23334917 - 067T COSM1730413 c.8272G>T p.V2758F Substitution - Missense 13:23335163-23335163 - UM-SCC-4 COSM4599710 c.7598A>G p.D2533G Substitution - Missense 13:23335837-23335837 - TCGA-CC-A3MA-01 COSM4942884 c.7718A>G p.D2573G Substitution - Missense 13:23335717-23335717 - HCT15 COSM2266178 c.7017T>G p.A2339A Substitution - coding silent 13:23336418-23336418 - HCC78 COSM1606923 c.5143A>G p.T1715A Substitution - Missense 13:23338292-23338292 - BD180T COSM3772787 c.11182C>T p.R3728C Substitution - Missense 13:23332253-23332253 - TCGA-FS-A4FD-06 COSM3467728 c.5647C>T p.P1883S Substitution - Missense 13:23337788-23337788 - TCGA-AG-4001-01 COSM258958 c.5561G>T p.R1854I Substitution - Missense 13:23337874-23337874 - TCGA-AG-A002-01 COSM263502 c.12226A>C p.K4076Q Substitution - Missense 13:23331209-23331209 - LUAD-S01409 COSM346378 c.5259G>T p.W1753C Substitution - Missense 13:23338176-23338176 - TCGA-CA-6718-01 COSM1365868 c.10806C>T p.I3602I Substitution - coding silent 13:23332629-23332629 - HCC2998 COSM1677539 c.1792C>T p.R598C Substitution - Missense 13:23341643-23341643 - TCGA-AP-A0LM-01 COSM946068 c.2345G>A p.R782H Substitution - Missense 13:23341090-23341090 - 8029770 COSM1365904 c.7700C>T p.S2567L Substitution - Missense 13:23335735-23335735 - UD-SCC-2 COSM4213605 c.2573C>T p.S858L Substitution - Missense 13:23340862-23340862 - TCGA-D9-A6EC-06 COSM4403699 c.982A>G p.R328G Substitution - Missense 13:23355189-23355189 - 169 COSM1365899 c.8171_8172insT p.L2724fs*29 Insertion - Frameshift 13:23335263-23335264 - cSCCP1 COSM135627 c.3160C>T p.L1054F Substitution - Missense 13:23340275-23340275 - TCGA-AP-A05J-01 COSM946028 c.7597G>T p.D2533Y Substitution - Missense 13:23335838-23335838 - Pat_41_B COSM5842278 c.11923G>A p.A3975T Substitution - Missense 13:23331512-23331512 - TCGA-AG-4015-01 COSM259203 c.2875G>T p.V959L Substitution - Missense 13:23340560-23340560 - TCGA-BR-8680-01 COSM4046575 c.2117A>C p.K706T Substitution - Missense 13:23341318-23341318 - TCGA-CJ-5686-01 COSM469246 c.12762G>T p.W4254C Substitution - Missense 13:23330673-23330673 - BD209T COSM5496339 c.9663G>T p.M3221I Substitution - Missense 13:23333772-23333772 - 587316 COSM1224537 c.9545G>A p.C3182Y Substitution - Missense 13:23333890-23333890 - YUPROST COSM1706537 c.3557C>A p.S1186Y Substitution - Missense 13:23339878-23339878 - Pat_73_B COSM3467702 c.9595C>T p.P3199S Substitution - Missense 13:23333840-23333840 - 587376 COSM946024 c.8276G>A p.R2759Q Substitution - Missense 13:23335159-23335159 - TCGA-AA-3510-01 COSM946024 c.8276G>A p.R2759Q Substitution - Missense 13:23335159-23335159 - TCGA-AA-3695-01 COSM268452 c.5914C>T p.R1972* Substitution - Nonsense 13:23337521-23337521 - TCGA-K4-A3WS-01 COSM3793187 c.12885C>A p.G4295G Substitution - coding silent 13:23330550-23330550 - Au10 COSM1706533 c.4712C>T p.S1571F Substitution - Missense 13:23338723-23338723 - TCGA-RP-A695-06 COSM4896409 c.27C>T p.L9L Substitution - coding silent 13:23358471-23358471 - HCC107T COSM5813470 c.10878A>T p.L3626F Substitution - Missense 13:23332557-23332557 - TCGA-BR-8680-01 COSM4046505 c.10466G>A p.R3489Q Substitution - Missense 13:23332969-23332969 - TCGA-FP-7916-01 COSM3467748 c.2904C>T p.V968V Substitution - coding silent 13:23340531-23340531 - TCGA-BS-A0UF-01 COSM946037 c.6269A>C p.E2090A Substitution - Missense 13:23337166-23337166 - TCGA-MI-A75G-01 COSM4940109 c.12519T>C p.L4173L Substitution - coding silent 13:23330916-23330916 - SNU-175 COSM1562340 c.45G>A p.A15A Substitution - coding silent 13:23358453-23358453 - LUAD-CHTN-MAD04-00674 COSM357830 c.11275G>A p.A3759T Substitution - Missense 13:23332160-23332160 - TCGA-A8-A09I-01 COSM432216 c.11572C>T p.L3858F Substitution - Missense 13:23331863-23331863 - T3152 COSM1365893 c.8352delA p.K2784fs*22 Deletion - Frameshift 13:23335083-23335083 - TCGA-D1-A16X-01 COSM946009 c.9940G>T p.E3314* Substitution - Nonsense 13:23333495-23333495 - TCGA-BR-8369-01 COSM4046511 c.10130T>C p.L3377S Substitution - Missense 13:23333305-23333305 - T3080 COSM4723394 c.10922G>A p.R3641H Substitution - Missense 13:23332513-23332513 - LUAD_E00703 COSM389822 c.2771C>A p.T924N Substitution - Missense 13:23340664-23340664 - ESCC_143 COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - sysucc-1173T COSM2266417 c.980G>A p.R327H Substitution - Missense 13:23355191-23355191 - PCSI_0305_Pa_P_526 COSM3786152 c.2482A>G p.I828V Substitution - Missense 13:23340953-23340953 - J90_T COSM3955447 c.4151C>T p.S1384L Substitution - Missense 13:23339284-23339284 - TCGA-13-0904-01 COSM72531 c.4628T>A p.V1543E Substitution - Missense 13:23338807-23338807 - TCGA-AC-A23H-01 COSM3813581 c.7237G>C p.E2413Q Substitution - Missense 13:23336198-23336198 - TCGA-BP-5194-01 COSM469245 c.13237G>C p.V4413L Substitution - Missense 13:23330198-23330198 - pfg008T COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - pfg143T COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - TCGA-D3-A2JP-06 COSM3467756 c.2030C>T p.S677L Substitution - Missense 13:23341405-23341405 - Pat_66_A COSM5842280 c.10891G>A p.E3631K Substitution - Missense 13:23332544-23332544 - SNU-175 COSM2266141 c.8346A>T p.L2782F Substitution - Missense 13:23335089-23335089 - 587336 COSM1224545 c.7010G>A p.C2337Y Substitution - Missense 13:23336425-23336425 - TCGA-AN-A046-01 COSM3813571 c.11871G>T p.M3957I Substitution - Missense 13:23331564-23331564 - CSCC-40-T COSM4458498 c.10440C>T p.I3480I Substitution - coding silent 13:23332995-23332995 - TCGA-AA-3510-01 COSM946005 c.10498G>T p.E3500* Substitution - Nonsense 13:23332937-23332937 - TCGA-AA-A010-01 COSM284763 c.9885G>T p.E3295D Substitution - Missense 13:23333550-23333550 - P142 COSM1737019 c.11383A>T p.M3795L Substitution - Missense 13:23332052-23332052 - TCGA-EI-6917-01 COSM277151 c.12716G>A p.R4239Q Substitution - Missense 13:23330719-23330719 - TCGA-AG-A00H-01 COSM265244 c.2734G>C p.E912Q Substitution - Missense 13:23340701-23340701 - 587376 COSM1224553 c.12811G>T p.E4271* Substitution - Nonsense 13:23330624-23330624 - ESO-0123 COSM1264781 c.617G>A p.G206E Substitution - Missense 13:23355554-23355554 - AOCS-145-1-6 COSM3981968 c.2419G>A p.A807T Substitution - Missense 13:23341016-23341016 - TCGA-EK-A3GK-01 COSM3467744 c.3718C>T p.P1240S Substitution - Missense 13:23339717-23339717 - pfg019T COSM1365946 c.2887delA p.I963fs*16 Deletion - Frameshift 13:23340548-23340548 - BD72T COSM5512966 c.3586delA p.S1196fs*18 Deletion - Frameshift 13:23339849-23339849 - YULAN COSM1706521 c.12041C>T p.P4014L Substitution - Missense 13:23331394-23331394 - ESCC-018T COSM3936263 c.4271T>A p.I1424N Substitution - Missense 13:23339164-23339164 - 2_RESISTANT COSM1722642 c.4167G>A p.V1389V Substitution - coding silent 13:23339268-23339268 - TCGA-B5-A0JY-01 COSM946033 c.6814G>A p.E2272K Substitution - Missense 13:23336621-23336621 - TCGA-CD-A4MG-01 COSM4046553 c.5853T>G p.I1951M Substitution - Missense 13:23337582-23337582 - PCSI_0083_Pa_P_526 COSM3467764 c.1443C>T p.P481P Substitution - coding silent 13:23354728-23354728 - PT48 COSM5933246 c.12584C>T p.P4195L Substitution - Missense 13:23330851-23330851 - ESO-866 COSM1264808 c.9862A>C p.S3288R Substitution - Missense 13:23333573-23333573 - CHC2200T COSM4952980 c.7033G>T p.V2345L Substitution - Missense 13:23336402-23336402 - cSCCP7 COSM139983 c.2147T>A p.L716H Substitution - Missense 13:23341288-23341288 - TCGA-AX-A0J1-01 COSM946015 c.9304C>T p.H3102Y Substitution - Missense 13:23334131-23334131 - ESO-114 COSM1264788 c.4467T>G p.P1489P Substitution - coding silent 13:23338968-23338968 - TCGA-GF-A3OT-06 COSM3467752 c.2375C>T p.S792F Substitution - Missense 13:23341060-23341060 - sysucc-311T COSM5478469 c.4776G>T p.M1592I Substitution - Missense 13:23338659-23338659 - J6_T COSM3955451 c.112C>T p.L38L Substitution - coding silent 13:23358386-23358386 - B90-Tumor COSM254921 c.5968C>G p.Q1990E Substitution - Missense 13:23337467-23337467 - B89-4-Tumor COSM1747368 c.159A>C p.I53I Substitution - coding silent 13:23358339-23358339 - 2492722 COSM5722099 c.8947C>T p.H2983Y Substitution - Missense 13:23334488-23334488 - TCGA-BS-A0UV-01 COSM946003 c.11256C>T p.L3752L Substitution - coding silent 13:23332179-23332179 - MS3 COSM1165350 c.869C>T p.T290M Substitution - Missense 13:23355302-23355302 - TCGA-AR-A251-01 COSM1477141 c.9791C>T p.P3264L Substitution - Missense 13:23333644-23333644 - TCGA-EI-6917-01 COSM3417447 c.10836G>A p.T3612T Substitution - coding silent 13:23332599-23332599 - QC2-25-T2 COSM5653335 c.4792A>T p.S1598C Substitution - Missense 13:23338643-23338643 - TCGA-EI-6917-01 COSM3417443 c.11497G>T p.E3833* Substitution - Nonsense 13:23331938-23331938 - 2521259 COSM5890788 c.5906C>T p.P1969L Substitution - Missense 13:23337529-23337529 - S00827 COSM314972 c.9756G>A p.M3252I Substitution - Missense 13:23333679-23333679 - I2L-P7-Tumor-Organoid COSM5362271 c.6303T>C p.A2101A Substitution - coding silent 13:23337132-23337132 - TCGA-CF-A1HS-01 COSM416410 c.2448T>C p.S816S Substitution - coding silent 13:23340987-23340987 - TCGA-D8-A1XQ-01 COSM3813593 c.2064G>C p.Q688H Substitution - Missense 13:23341371-23341371 - TCGA-D7-A4Z0-01 COSM4046523 c.9076T>G p.F3026V Substitution - Missense 13:23334359-23334359 - B89-4 COSM1747368 c.159A>C p.I53I Substitution - coding silent 13:23358339-23358339 - LP6005690-DNA_D01 COSM4966234 c.9155T>C p.I3052T Substitution - Missense 13:23334280-23334280 - TCGA-AG-A002-01 COSM263504 c.10008A>C p.P3336P Substitution - coding silent 13:23333427-23333427 - TCGA-AX-A05Z-01 COSM946088 c.79G>T p.E27* Substitution - Nonsense 13:23358419-23358419 - TCGA-46-3768-01 COSM695797 c.11464C>T p.L3822F Substitution - Missense 13:23331971-23331971 - TCGA-66-2759-01 COSM695787 c.4033G>C p.E1345Q Substitution - Missense 13:23339402-23339402 - TCGA-B5-A0JY-01 COSM946072 c.2205G>T p.K735N Substitution - Missense 13:23341230-23341230 - TCGA-CM-6169-01 COSM1365910 c.6435G>T p.L2145L Substitution - coding silent 13:23337000-23337000 - I2L-P19Ta-Tumor-Organoid COSM5362107 c.1200G>A p.P400P Substitution - coding silent 13:23354971-23354971 - TCGA-F5-6863-01 COSM3417451 c.10057C>T p.L3353F Substitution - Missense 13:23333378-23333378 - ESO-1145 COSM1264790 c.5414T>C p.V1805A Substitution - Missense 13:23338021-23338021 - TCGA-DK-A1A3-01 COSM416414 c.12707C>G p.S4236* Substitution - Nonsense 13:23330728-23330728 - 587376 COSM1224570 c.4044C>A p.F1348L Substitution - Missense 13:23339391-23339391 - ACINAR13 COSM1733950 c.10678C>T p.L3560F Substitution - Missense 13:23332757-23332757 - 229 COSM4426215 c.812C>T p.P271L Substitution - Missense 13:23355359-23355359 - T207 COSM4723416 c.5005A>G p.T1669A Substitution - Missense 13:23338430-23338430 - HCC077T COSM5810409 c.10915G>A p.E3639K Substitution - Missense 13:23332520-23332520 - YUGURT COSM1706533 c.4712C>T p.S1571F Substitution - Missense 13:23338723-23338723 - TCGA-D1-A16S-01 COSM945996 c.12076A>G p.M4026V Substitution - Missense 13:23331359-23331359 - ESCC_BICR_066T COSM5444566 c.6967G>A p.D2323N Substitution - Missense 13:23336468-23336468 - TCGA-BR-8680-01 COSM4046519 c.9557C>A p.A3186D Substitution - Missense 13:23333878-23333878 - TCGA-AN-A046-01 COSM946019 c.8749G>A p.E2917K Substitution - Missense 13:23334686-23334686 - TCGA-A5-A0GP-01 COSM284765 c.5251G>T p.E1751* Substitution - Nonsense 13:23338184-23338184 - T3011 COSM4723390 c.12290A>C p.K4097T Substitution - Missense 13:23331145-23331145 - SNUH_G45_S1 COSM3676574 c.2555T>C p.I852T Substitution - Missense 13:23340880-23340880 - TCGA-BR-7707-01 COSM4046491 c.12315T>C p.S4105S Substitution - coding silent 13:23331120-23331120 - TCGA-B6-A40C-01 COSM4391307 c.2171C>T p.P724L Substitution - Missense 13:23341264-23341264 - TCGA-BR-8372-01 COSM4046481 c.13265T>C p.I4422T Substitution - Missense 13:23330170-23330170 - TCGA-D3-A5GO-06 COSM3467736 c.4667C>T p.T1556I Substitution - Missense 13:23338768-23338768 - HCC89 COSM1606927 c.1779A>G p.P593P Substitution - coding silent 13:23341656-23341656 - TCGA-BS-A0TA-01 COSM946085 c.350G>A p.G117D Substitution - Missense 13:23355821-23355821 - MO_1012 COSM5565572 c.520C>T p.R174* Substitution - Nonsense 13:23355651-23355651 - TP_2054 COSM5568884 c.2053T>A p.S685T Substitution - Missense 13:23341382-23341382 - I2L-P24Tb-Tumor-Biopsy COSM5362174 c.7952C>A p.P2651Q Substitution - Missense 13:23335483-23335483 - CHC1040T COSM4799567 c.2682G>T p.Q894H Substitution - Missense 13:23340753-23340753 - sysucc-311T COSM5478473 c.4058G>A p.R1353K Substitution - Missense 13:23339377-23339377 - TCGA-D9-A6EC-06 COSM4404457 c.13223A>C p.E4408A Substitution - Missense 13:23330212-23330212 - TCGA-BP-4163-01 COSM469251 c.7594T>C p.S2532P Substitution - Missense 13:23335841-23335841 - TCGA-AA-A00N-01 COSM277151 c.12716G>A p.R4239Q Substitution - Missense 13:23330719-23330719 - TCGA-BR-8679-01 COSM4046491 c.12315T>C p.S4105S Substitution - coding silent 13:23331120-23331120 - CSCC-29-T COSM4521257 c.10582G>A p.G3528R Substitution - Missense 13:23332853-23332853 - TCGA-33-4566-01 COSM695784 c.2217G>C p.Q739H Substitution - Missense 13:23341218-23341218 - S01563 COSM314975 c.4721C>T p.S1574F Substitution - Missense 13:23338714-23338714 - TCGA-BR-8680-01 COSM3417459 c.6136G>A p.D2046N Substitution - Missense 13:23337299-23337299 - TCGA-AZ-4315-01 COSM1365904 c.7700C>T p.S2567L Substitution - Missense 13:23335735-23335735 - B099 COSM308142 c.5660A>T p.K1887I Substitution - Missense 13:23337775-23337775 - 587376 COSM1224574 c.2884A>T p.K962* Substitution - Nonsense 13:23340551-23340551 - TCGA-EV-5901-01 COSM3987335 c.8102T>A p.F2701Y Substitution - Missense 13:23335333-23335333 - AA2055 COSM4169109 c.8869A>G p.T2957A Substitution - Missense 13:23334566-23334566 - LUAD-5V8LT COSM401411 c.3143T>C p.I1048T Substitution - Missense 13:23340292-23340292 - TCGA-D8-A1JC-01 COSM1477148 c.2447C>G p.S816C Substitution - Missense 13:23340988-23340988 - Mel18 COSM1677525 c.7593C>G p.F2531L Substitution - Missense 13:23335842-23335842 - 8036078 COSM3384772 c.5059C>A p.L1687M Substitution - Missense 13:23338376-23338376 - 9113_T COSM5041458 c.9314G>C p.S3105T Substitution - Missense 13:23334121-23334121 - LUAD-B01970 COSM356007 c.1132C>T p.P378S Substitution - Missense 13:23355039-23355039 - TCGA-EE-A3JD-06 COSM4396235 c.2948C>T p.T983I Substitution - Missense 13:23340487-23340487 - TCGA-EJ-A46F-01 COSM3782788 c.5049G>A p.L1683L Substitution - coding silent 13:23338386-23338386 - TCGA-AP-A056-01 COSM945995 c.12484G>T p.E4162* Substitution - Nonsense 13:23330951-23330951 - TCGA-BS-A0TC-01 COSM946041 c.6025G>T p.D2009Y Substitution - Missense 13:23337410-23337410 - TCGA-D5-6533-01 COSM1365866 c.10820A>T p.N3607I Substitution - Missense 13:23332615-23332615 - TCGA-F5-6814-01 COSM3417439 c.12380G>T p.R4127I Substitution - Missense 13:23331055-23331055 - CH-LA6 COSM4166371 c.10740A>G p.Q3580Q Substitution - coding silent 13:23332695-23332695 - C086 COSM5538504 c.10567T>C p.Y3523H Substitution - Missense 13:23332868-23332868 - TCGA-BR-8361-01 COSM4046559 c.5587A>G p.K1863E Substitution - Missense 13:23337848-23337848 - TCGA-CD-5798-01 COSM4046539 c.7549G>A p.G2517R Substitution - Missense 13:23335886-23335886 - TCGA-A6-6781-01 COSM1365960 c.120C>T p.V40V Substitution - coding silent 13:23358378-23358378 - 2_PRE-TREATMENT COSM1722642 c.4167G>A p.V1389V Substitution - coding silent 13:23339268-23339268 - TCGA-MI-A75E-01 COSM4939826 c.5862C>A p.S1954S Substitution - coding silent 13:23337573-23337573 - TCGA-AM-5821-01 COSM3753621 c.1215A>G p.L405L Substitution - coding silent 13:23354956-23354956 - TCGA-22-4613-01 COSM695777 c.314G>T p.G105V Substitution - Missense 13:23355857-23355857 - TCGA-66-2781-01 COSM695785 c.2520G>C p.K840N Substitution - Missense 13:23340915-23340915 - TCGA-MI-A75G-01 COSM4940160 c.12206A>G p.D4069G Substitution - Missense 13:23331229-23331229 - 587234 COSM1224551 c.4604G>T p.R1535M Substitution - Missense 13:23338831-23338831 - TCGA-BR-8680-01 COSM4046535 c.7666C>T p.R2556C Substitution - Missense 13:23335769-23335769 - TCGA-D1-A103-01 COSM945998 c.11984A>C p.K3995T Substitution - Missense 13:23331451-23331451 - TCGA-A8-A0A6-01 COSM3813595 c.1706A>C p.H569P Substitution - Missense 13:23353823-23353823 - T3064 COSM4723420 c.4783_4784insT p.C1595fs*5 Insertion - Frameshift 13:23338651-23338652 - PCSI_0076_Pa_X COSM3376504 c.12202G>T p.A4068S Substitution - Missense 13:23331233-23331233 - RKO COSM4647694 c.8929A>G p.T2977A Substitution - Missense 13:23334506-23334506 - TCGA-B5-A0JY-01 COSM946008 c.10245C>A p.F3415L Substitution - Missense 13:23333190-23333190 - TCGA-AA-A010-01 COSM284762 c.11335G>A p.D3779N Substitution - Missense 13:23332100-23332100 - TCGA-D1-A17M-01 COSM946016 c.9297T>C p.N3099N Substitution - coding silent 13:23334138-23334138 - HCC4T COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - BN24T COSM1365946 c.2887delA p.I963fs*16 Deletion - Frameshift 13:23340548-23340548 - TCGA-AP-A056-01 COSM946024 c.8276G>A p.R2759Q Substitution - Missense 13:23335159-23335159 - TCGA-HU-A4H3-01 COSM4046501 c.11183G>A p.R3728H Substitution - Missense 13:23332252-23332252 - PDA_074 COSM4417840 c.10591C>G p.P3531A Substitution - Missense 13:23332844-23332844 - PT25 COSM5003096 c.9665T>C p.V3222A Substitution - Missense 13:23333770-23333770 - CCK81 COSM4611400 c.4710_4711insA p.S1571fs*20 Insertion - Frameshift 13:23338724-23338725 - TCGA-BH-A18U-01 COSM432215 c.12061C>T p.L4021L Substitution - coding silent 13:23331374-23331374 - T3446 COSM4723434 c.1221C>T p.S407S Substitution - coding silent 13:23354950-23354950 - RK053_C01 COSM3744097 c.2297G>T p.S766I Substitution - Missense 13:23341138-23341138 - RK193_C01 COSM3744089 c.12819C>T p.C4273C Substitution - coding silent 13:23330616-23330616 - ESCC-112T COSM2266137 c.8458C>T p.R2820C Substitution - Missense 13:23334977-23334977 - LUAD-F00089 COSM339599 c.6934A>C p.M2312L Substitution - Missense 13:23336501-23336501 - 587376 COSM1224578 c.2118A>T p.K706N Substitution - Missense 13:23341317-23341317 - pfg122T COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - 8057726 COSM3384768 c.9074A>C p.K3025T Substitution - Missense 13:23334361-23334361 - I2L-P19Ta-Tumor-Biopsy COSM5362107 c.1200G>A p.P400P Substitution - coding silent 13:23354971-23354971 - TCGA-AA-A010-01 COSM284764 c.6913T>G p.L2305V Substitution - Missense 13:23336522-23336522 - SW837 COSM2266170 c.7200A>G p.K2400K Substitution - coding silent 13:23336235-23336235 - TCGA-CG-5719-01 COSM4046579 c.1637C>T p.S546L Substitution - Missense 13:23354534-23354534 - Pat_60_B COSM1365946 c.2887delA p.I963fs*16 Deletion - Frameshift 13:23340548-23340548 - TCGA-BR-8487-01 COSM3417437 c.12533G>A p.R4178Q Substitution - Missense 13:23330902-23330902 - TCGA-GN-A262-06 COSM3467710 c.8742C>T p.L2914L Substitution - coding silent 13:23334693-23334693 - pfg099T COSM4751278 c.7933A>G p.R2645G Substitution - Missense 13:23335502-23335502 - PT49 COSM5936030 c.10505C>T p.S3502F Substitution - Missense 13:23332930-23332930 - YULAN COSM1706529 c.6938T>G p.L2313R Substitution - Missense 13:23336497-23336497 - 29 COSM5013942 c.12418A>T p.K4140* Substitution - Nonsense 13:23331017-23331017 - HCC2998 COSM1677533 c.4080G>T p.E1360D Substitution - Missense 13:23339355-23339355 - TCGA-DD-A119-01 COSM4919780 c.10944T>C p.A3648A Substitution - coding silent 13:23332491-23332491 - Gp5D COSM1365893 c.8352delA p.K2784fs*22 Deletion - Frameshift 13:23335083-23335083 - SNUH_G76_S1 COSM4417840 c.10591C>G p.P3531A Substitution - Missense 13:23332844-23332844 - Gp2D COSM2266361 c.2049T>C p.D683D Substitution - coding silent 13:23341386-23341386 - ESO-153 COSM1264800 c.6580T>G p.L2194V Substitution - Missense 13:23336855-23336855 - T3225 COSM4723436 c.681C>T p.H227H Substitution - coding silent 13:23355490-23355490 - CSCC-20-T COSM4549793 c.4388G>A p.R1463K Substitution - Missense 13:23339047-23339047 - RK308_C01 COSM125994 c.7232C>T p.A2411V Substitution - Missense 13:23336203-23336203 - LUAD-B02515 COSM336025 c.8116G>T p.V2706L Substitution - Missense 13:23335319-23335319 - ESO-161 COSM1264802 c.2265C>A p.A755A Substitution - coding silent 13:23341170-23341170 - 631056 COSM323183 c.5392G>C p.V1798L Substitution - Missense 13:23338043-23338043 - TCGA-AA-A010-01 COSM284766 c.879C>A p.F293L Substitution - Missense 13:23355292-23355292 - TCGA-AP-A059-01 COSM946021 c.8433G>A p.K2811K Substitution - coding silent 13:23335002-23335002 - TCGA-B0-4712-01 COSM469253 c.4178G>T p.R1393M Substitution - Missense 13:23339257-23339257 - 587332 COSM1224547 c.11860G>A p.A3954T Substitution - Missense 13:23331575-23331575 - TCGA-27-1833-01 COSM3747941 c.8786C>A p.T2929N Substitution - Missense 13:23334649-23334649 - TCGA-AN-A046-01 COSM946009 c.9940G>T p.E3314* Substitution - Nonsense 13:23333495-23333495 - PD7440a COSM2266072 c.9850G>A p.V3284I Substitution - Missense 13:23333585-23333585 - TCGA-AA-A010-01 COSM284761 c.12933C>A p.F4311L Substitution - Missense 13:23330502-23330502 - TCGA-D5-6928-01 COSM1365873 c.10133T>C p.L3378S Substitution - Missense 13:23333302-23333302 - 31T COSM3718449 c.11276C>T p.A3759V Substitution - Missense 13:23332159-23332159 - TCGA-E2-A1LS-01 COSM1477146 c.3662G>A p.S1221N Substitution - Missense 13:23339773-23339773 - YUKRIN COSM1706531 c.5905C>T p.P1969S Substitution - Missense 13:23337530-23337530 - P161 COSM1737770 c.152A>G p.Y51C Substitution - Missense 13:23358346-23358346 - 19M COSM5579502 c.12836A>G p.Q4279R Substitution - Missense 13:23330599-23330599 - TCGA-D3-A3C7-06 COSM1300077 c.10558C>T p.H3520Y Substitution - Missense 13:23332877-23332877 - LS411 COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - TCGA-06-0141-01 COSM3399277 c.1315T>C p.Y439H Substitution - Missense 13:23354856-23354856 - TCGA-BS-A0UF-01 COSM946036 c.6560A>C p.K2187T Substitution - Missense 13:23336875-23336875 - 26 COSM5748697 c.2259A>C p.K753N Substitution - Missense 13:23341176-23341176 - PD5934a COSM1629017 c.1669C>T p.L557F Substitution - Missense 13:23353860-23353860 - 600 COSM3723470 c.11509G>A p.E3837K Substitution - Missense 13:23331926-23331926 - TCGA-AP-A056-01 COSM946034 c.6811G>T p.E2271* Substitution - Nonsense 13:23336624-23336624 - T3024 COSM4723392 c.11689G>T p.G3897* Substitution - Nonsense 13:23331746-23331746 - PT13 COSM5896215 c.3719C>T p.P1240L Substitution - Missense 13:23339716-23339716 - ESO-0176 COSM1264783 c.3728T>G p.L1243R Substitution - Missense 13:23339707-23339707 - B96-Tumor COSM1747366 c.917G>T p.G306V Substitution - Missense 13:23355254-23355254 - PCSI_0521_Pa_P_526 COSM1677531 c.5188C>T p.R1730* Substitution - Nonsense 13:23338247-23338247 - HCC064T COSM5809863 c.12367A>T p.T4123S Substitution - Missense 13:23331068-23331068 - 2492723 COSM5722101 c.6235T>G p.S2079A Substitution - Missense 13:23337200-23337200 - TCGA-D1-A16X-01 COSM946026 c.8082G>T p.K2694N Substitution - Missense 13:23335353-23335353 - sysucc-1062T COSM5763272 c.2078T>G p.L693* Substitution - Nonsense 13:23341357-23341357 - S0029 COSM5882392 c.7210C>T p.Q2404* Substitution - Nonsense 13:23336225-23336225 - TCGA-AX-A0J0-01 COSM946005 c.10498G>T p.E3500* Substitution - Nonsense 13:23332937-23332937 - TCGA-AP-A059-01 COSM946056 c.4299G>A p.M1433I Substitution - Missense 13:23339136-23339136 - cSCCP1 COSM135626 c.5545G>T p.D1849Y Substitution - Missense 13:23337890-23337890 - TCGA-EE-A2GU-06 COSM3467690 c.10927C>T p.Q3643* Substitution - Nonsense 13:23332508-23332508 - TCGA-EE-A2MN-06 COSM3467694 c.10282C>T p.H3428Y Substitution - Missense 13:23333153-23333153 - 8015299 COSM4213583 c.10835C>T p.T3612M Substitution - Missense 13:23332600-23332600 - 2218461 COSM4421271 c.7715C>T p.S2572L Substitution - Missense 13:23335720-23335720 - TCGA-AP-A056-01 COSM946046 c.5284A>G p.N1762D Substitution - Missense 13:23338151-23338151 - PT52 COSM5940404 c.12862C>T p.P4288S Substitution - Missense 13:23330573-23330573 - CSCC-44-T COSM4507673 c.7092C>T p.S2364S Substitution - coding silent 13:23336343-23336343 - TCGA-AG-4005-01 COSM259015 c.6892G>T p.E2298* Substitution - Nonsense 13:23336543-23336543 - TCGA-AB-2877-03 COSM1317934 c.1439C>T p.T480M Substitution - Missense 13:23354732-23354732 - TCGA-FS-A4FC-06 COSM3467700 c.9732C>A p.F3244L Substitution - Missense 13:23333703-23333703 - C086 COSM5538508 c.2352C>T p.N784N Substitution - coding silent 13:23341083-23341083 - 2497769 COSM5750303 c.2144C>A p.P715Q Substitution - Missense 13:23341291-23341291 - C0075T COSM4152730 c.9836T>C p.F3279S Substitution - Missense 13:23333599-23333599 - PT48 COSM3467718 c.6953C>T p.S2318L Substitution - Missense 13:23336482-23336482 - PTC_448 COSM5959468 c.5291C>T p.T1764M Substitution - Missense 13:23338144-23338144 - 2492720 COSM5722099 c.8947C>T p.H2983Y Substitution - Missense 13:23334488-23334488 - TCGA-AA-3663-01 COSM1365958 c.1046T>C p.L349P Substitution - Missense 13:23355125-23355125 - Gp5D COSM2266419 c.954T>C p.S318S Substitution - coding silent 13:23355217-23355217 - TCGA-18-3409-01 COSM695781 c.1383G>A p.V461V Substitution - coding silent 13:23354788-23354788 - TCGA-DM-A1DA-01 COSM1365944 c.3422C>T p.A1141V Substitution - Missense 13:23340013-23340013 - CML051T COSM5802664 c.6681G>T p.L2227F Substitution - Missense 13:23336754-23336754 - TCGA-BS-A0UV-01 COSM946010 c.9926A>C p.K3309T Substitution - Missense 13:23333509-23333509 - ESCC_BICR_038T COSM5434518 c.8373T>C p.D2791D Substitution - coding silent 13:23335062-23335062 - TCGA-CA-6718-01 COSM1365925 c.5625A>G p.K1875K Substitution - coding silent 13:23337810-23337810 - TCGA-EQ-A4SO-01 COSM4046593 c.247T>C p.C83R Substitution - Missense 13:23355924-23355924 - PCSI_0083_Pa_P_526 COSM3376516 c.3425A>G p.Q1142R Substitution - Missense 13:23340010-23340010 - HN_62897 COSM125995 c.683T>C p.V228A Substitution - Missense 13:23355488-23355488 - TCGA-A8-A096-01 COSM432220 c.4994C>G p.T1665R Substitution - Missense 13:23338441-23338441 - TCGA-D9-A6EC-06 COSM4403455 c.8475A>C p.P2825P Substitution - coding silent 13:23334960-23334960 - TCGA-B2-5633-01 COSM469252 c.7386A>G p.K2462K Substitution - coding silent 13:23336049-23336049 - HCT15 COSM2266191 c.6662C>T p.A2221V Substitution - Missense 13:23336773-23336773 - HCC2998 COSM946024 c.8276G>A p.R2759Q Substitution - Missense 13:23335159-23335159 - T2258 COSM4723439 c.300T>A p.F100L Substitution - Missense 13:23355871-23355871 - TCGA-AP-A059-01 COSM946060 c.3874C>A p.L1292I Substitution - Missense 13:23339561-23339561 - TCGA-FS-A1ZZ-06 COSM2266054 c.10179C>T p.F3393F Substitution - coding silent 13:23333256-23333256 - I2L-P24Ta-Tumor-Organoid COSM5362174 c.7952C>A p.P2651Q Substitution - Missense 13:23335483-23335483 - 2492700 COSM5600411 c.3050C>T p.P1017L Substitution - Missense 13:23340385-23340385 - Gp2D COSM4627170 c.8492T>C p.V2831A Substitution - Missense 13:23334943-23334943 - CSCC-52-T COSM4511198 c.8163C>T p.F2721F Substitution - coding silent 13:23335272-23335272 - PT33 COSM5909347 c.811C>T p.P271S Substitution - Missense 13:23355360-23355360 - TCGA-D3-A51J-06 COSM3467748 c.2904C>T p.V968V Substitution - coding silent 13:23340531-23340531 - RK099_C01 COSM1629019 c.164A>G p.D55G Substitution - Missense 13:23356007-23356007 - RK308_C01 COSM3744091 c.10390G>A p.A3464T Substitution - Missense 13:23333045-23333045 - HCC59T COSM3704564 c.9839G>T p.G3280V Substitution - Missense 13:23333596-23333596 - TCGA-HU-A4G8-01 COSM4046587 c.847G>T p.D283Y Substitution - Missense 13:23355324-23355324 - TCGA-AX-A05Z-01 COSM946078 c.682G>T p.V228L Substitution - Missense 13:23355489-23355489 - 46M COSM5071700 c.12040C>T p.P4014S Substitution - Missense 13:23331395-23331395 - TCGA-D7-6528-01 COSM1264775 c.11966T>G p.L3989R Substitution - Missense 13:23331469-23331469 - HT55 COSM2266163 c.7593C>T p.F2531F Substitution - coding silent 13:23335842-23335842 - TCGA-A8-A0A6-01 COSM3813599 c.1187T>G p.V396G Substitution - Missense 13:23354984-23354984 - TCGA-BR-8589-01 COSM4046509 c.10265T>G p.L3422R Substitution - Missense 13:23333170-23333170 - TCGA-AP-A0LM-01 COSM946002 c.11340G>A p.A3780A Substitution - coding silent 13:23332095-23332095 - PD13416a COSM5802168 c.4218delT p.G1407fs*20 Deletion - Frameshift 13:23339217-23339217 - TCGA-BP-4342-01 COSM3360047 c.5010G>A p.T1670T Substitution - coding silent 13:23338425-23338425 - TCGA-CU-A0YN-01 COSM416411 c.8024A>G p.N2675S Substitution - Missense 13:23335411-23335411 - TCGA-BS-A0UF-01 COSM946007 c.10414G>A p.E3472K Substitution - Missense 13:23333021-23333021 - ESO-005 COSM1264777 c.1167G>A p.P389P Substitution - coding silent 13:23355004-23355004 - T3724 COSM1365946 c.2887delA p.I963fs*16 Deletion - Frameshift 13:23340548-23340548 - TCGA-GC-A3BM-01 COSM3793189 c.9110G>A p.R3037H Substitution - Missense 13:23334325-23334325 - CSCC-11-T COSM4563661 c.9406G>A p.G3136R Substitution - Missense 13:23334029-23334029 - TCGA-CA-6718-01 COSM1365870 c.10638A>T p.Q3546H Substitution - Missense 13:23332797-23332797 - HT115 COSM2266002 c.11680C>A p.L3894I Substitution - Missense 13:23331755-23331755 - WM3211 COSM3727200 c.10673C>T p.P3558L Substitution - Missense 13:23332762-23332762 - TCGA-EB-A3XC-01 COSM3467696 c.9867C>T p.I3289I Substitution - coding silent 13:23333568-23333568 - TCGA-AX-A05Z-01 COSM945999 c.11842G>T p.D3948Y Substitution - Missense 13:23331593-23331593 - HCC49 COSM1606917 c.10913G>A p.R3638K Substitution - Missense 13:23332522-23332522 - 587376 COSM1224565 c.7120G>T p.E2374* Substitution - Nonsense 13:23336315-23336315 - MO_1262 COSM5563635 c.10423C>T p.Q3475* Substitution - Nonsense 13:23333012-23333012 - KPOPBR-03-T COSM5965123 c.11134C>T p.R3712C Substitution - Missense 13:23332301-23332301 - PTC-7C COSM4147638 c.5754T>C p.I1918I Substitution - coding silent 13:23337681-23337681 - T2269 COSM4723410 c.6883G>T p.E2295* Substitution - Nonsense 13:23336552-23336552 - S00501 COSM314971 c.9261delG p.W3087fs*1 Deletion - Frameshift 13:23334174-23334174 - pfg053T COSM4751280 c.3987T>A p.D1329E Substitution - Missense 13:23339448-23339448 - T55 COSM1163669 c.4710delA p.K1570fs*8 Deletion - Frameshift 13:23338725-23338725 - 148 COSM2266113 c.9067C>T p.R3023* Substitution - Nonsense 13:23334368-23334368 - TCGA-DM-A28G-01 COSM1365917 c.5865G>T p.L1955F Substitution - Missense 13:23337570-23337570 - HCC2998 COSM2266283 c.4383G>T p.Q1461H Substitution - Missense 13:23339052-23339052 - TCGA-AX-A0J0-01 COSM946049 c.5086C>A p.L1696M Substitution - Missense 13:23338349-23338349 - CME_0001_Pa_C COSM3376510 c.8480T>C p.L2827S Substitution - Missense 13:23334955-23334955 - 587376 COSM1224558 c.10240G>T p.D3414Y Substitution - Missense 13:23333195-23333195 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.159492 13q12 604490

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAATCC - InFrameDeletion p.G1559_F1560delGF c.4675_4680delGGATTT 13 23913335 THCA AAGG - Frameshift p.L1017Rfs*17 c.3048_3051delCCTT 13 23914964 PRAD A C Missense p.F1793L c.5379T>G 13 23912636 CM A C Missense p.F3286L c.9858T>G 13 23908157 GBM A C Missense p.L1390R c.4169T>G 13 23913846 ESCA A C Missense p.L1496V c.4486T>G 13 23913529 ESCA A C Missense p.L2341V c.7021T>G 13 23910994 ESCA A C Missense p.L3586V c.10756T>G 13 23907259 ESCA A C Missense p.L3978R c.11933T>G 13 23906082 HNSC A C Missense p.L4136R c.12407T>G 13 23905608 ESCA A C Missense p.L4136R c.12407T>G 13 23905608 STAD A C Missense p.V1656G c.4967T>G 13 23913048 HNSC A C Missense p.V2168G c.6503T>G 13 23911512 CM A C Synonymous p.P1636P c.4908T>G 13 23913107 ESCA A C Synonymous p.T1461T c.4383T>G 13 23913632 CM A C Synonymous p.T3165T c.9495T>G 13 23908520 STAD A C Synonymous p.T3371T c.10113T>G 13 23907902 ESCA A - Frameshift p.L2956*fs*1 c.8867delT 13 23909148 CM A G Missense p.F2565L c.7693T>C 13 23910322 STAD A G Missense p.I3084T c.9251T>C 13 23908764 UCEC A G Missense p.I3962T c.11885T>C 13 23906130 LUSC A G Missense p.L1225S c.3674T>C 13 23914341 CM A G Missense p.L1408P c.4223T>C 13 23913792 CM A G Missense p.L1412P c.4235T>C 13 23913780 STAD A G Missense p.L307P c.920T>C 13 23929831 UCEC A G Missense p.L903P c.2708T>C 13 23915307 UCEC A G Missense p.V1952A c.5855T>C 13 23912160 ESCA A G Missense p.V375A c.1124T>C 13 23929627 HNSC A G Missense p.V3940A c.11819T>C 13 23906196 UCEC A G Missense p.V844A c.2531T>C 13 23915484 STAD A G Missense p.Y586H c.1756T>C 13 23928995 GBM A G Synonymous p.C395C c.1185T>C 13 23929566 UCEC A G Synonymous p.F3250F c.9750T>C 13 23908265 COREAD A G Synonymous p.I601I c.1803T>C 13 23928948 STAD A G Synonymous p.N3246N c.9738T>C 13 23908277 UCEC A G Synonymous p.P4277P c.12831T>C 13 23905184 STAD A G Synonymous p.S1689S c.5067T>C 13 23912948 STAD A G Synonymous p.S963S c.2889T>C 13 23915126 BLCA AGTAAATTGTCAAAAAATG - Frameshift p.P3025Hfs*21 c.9074_9092delCATTTTTTGACAATTTACT 13 23908923 CM A T Missense p.V1690E c.5069T>A 13 23912946 OV A T Nonsense p.L3102* c.9305T>A 13 23908710 CM A T Synonymous p.L1221L c.3663T>A 13 23914352 CM A T Synonymous p.P1183P c.3549A>T 13 23914466 PAAD A T Synonymous p.V462V c.1386T>A 13 23929365 LUSC C A Missense p.A1775S c.5323G>T 13 23912692 LUAD C A Missense p.D1954Y c.5860G>T 13 23912155 UCEC C A Missense p.D2156Y c.6466G>T 13 23911549 UCEC C A Missense p.D2228Y c.6682G>T 13 23911333 CM C A Missense p.D2669Y c.8005G>T 13 23910010 BRCA C A Missense p.D2680Y c.8038G>T 13 23909977 UCEC C A Missense p.D3846Y c.11536G>T 13 23906479 CM C A Missense p.D842Y c.2524G>T 13 23915491 LUAD C A Missense p.E3053D c.9159G>T 13 23908856 LUSC C A Missense p.G171V c.512G>T 13 23932566 SCLC C A Missense p.G2129V c.6386G>T 13 23911629 LUSC C A Missense p.G2497V c.7490G>T 13 23910525 LUAD C A Missense p.G252V c.755G>T 13 23929996 LUSC C A Missense p.G466V c.1397G>T 13 23929354 LUAD C A Missense p.G90V c.269G>T 13 23942617 GBM C A Missense p.K2754N c.8262G>T 13 23909753 BRCA C A Missense p.L760F c.2280G>T 13 23915735 LUAD C A Missense p.Q1852H c.5556G>T 13 23912459 STAD C A Missense p.R2001I c.6002G>T 13 23912013 COREAD C A Missense p.S357I c.1070G>T 13 23929681 UCEC C A Missense p.V1106L c.3316G>T 13 23914699 COREAD C A Missense p.V1550F c.4648G>T 13 23913367 CM C A Missense p.V2723F c.8167G>T 13 23909848 LUAD C A Missense p.V2903F c.8707G>T 13 23909308 HNSC C A Missense p.V3766L c.11296G>T 13 23906719 LUAD C A Missense p.V4186F c.12556G>T 13 23905459 ESCA C A Missense p.W4401C c.13203G>T 13 23904812 RCCC C A Nonsense p.E1898* c.5692G>T 13 23912323 UCEC C A Nonsense p.E2445* c.7333G>T 13 23910682 COREAD C A Nonsense p.E2745* c.8233G>T 13 23909782 LUAD C A Synonymous p.L2686L c.8058G>T 13 23909957 LUAD C - Frameshift p.W3234*fs*1 c.9702delG 13 23908313 SCLC C G Missense p.A629P c.1885G>C 13 23928866 STAD C G Missense p.D1057H c.3169G>C 13 23914846 HNSC C G Missense p.E1018D c.3054G>C 13 23914961 OV C G Missense p.E1059Q c.3175G>C 13 23914840 BLCA C G Missense p.E1059Q c.3175G>C 13 23914840 COREAD C G Missense p.E1492Q c.4474G>C 13 23913541 LUSC C G Missense p.G1881A c.5642G>C 13 23912373 LUSC C G Missense p.G2687R c.8059G>C 13 23909956 CM C G Missense p.G4282A c.12845G>C 13 23905170 HNSC C G Missense p.K1319N c.3957G>C 13 23914058 RCCC C G Missense p.K987N c.2961G>C 13 23915054 LUSC C G Missense p.Q1761H c.5283G>C 13 23912732 CM C G Missense p.S3920T c.11759G>C 13 23906256 BLCA C G Missense p.V1945L c.5833G>C 13 23912182 SCLC C G Missense p.W1173S c.3518G>C 13 23914497 LUSC C G Missense p.W2473S c.7418G>C 13 23910597 BRCA C T Missense p.A176T c.526G>A 13 23932552 COREAD C T Missense p.A2368T c.7102G>A 13 23910913 STAD C T Missense p.A629T c.1885G>A 13 23928866 LUSC C T Missense p.D3137N c.9409G>A 13 23908606 LGG C T Missense p.D483N c.1447G>A 13 23929304 CM C T Missense p.E1095K c.3283G>A 13 23914732 UCEC C T Missense p.E1397K c.4189G>A 13 23913826 COREAD C T Missense p.E2103K c.6307G>A 13 23911708 CM C T Missense p.E2237K c.6709G>A 13 23911306 UCEC C T Missense p.E2987K c.8959G>A 13 23909056 ESCA C T Missense p.E4350K c.13048G>A 13 23904967 CM C T Missense p.G1169S c.3505G>A 13 23914510 CM C T Missense p.G2134D c.6401G>A 13 23911614 ALL C T Missense p.G2272S c.6814G>A 13 23911201 CM C T Missense p.G264D c.791G>A 13 23929960 UCEC C T Missense p.G264S c.790G>A 13 23929961 ESCA C T Missense p.G2664R c.7990G>A 13 23910025 STAD C T Missense p.G3424E c.10271G>A 13 23907744 LGG C T Missense p.G353E c.1058G>A 13 23929693 ESCA C T Missense p.G421E c.1262G>A 13 23929489 CM C T Missense p.M1499I c.4497G>A 13 23913518 HNSC C T Missense p.M3399I c.10197G>A 13 23907818 SCLC C T Missense p.R2508K c.7523G>A 13 23910492 CM C T Missense p.R276H c.827G>A 13 23929924 LUAD C T Missense p.R2898H c.8693G>A 13 23909322 UCEC C T Missense p.R3419H c.10256G>A 13 23907759 ESCA C T Missense p.R3419H c.10256G>A 13 23907759 UCEC C T Missense p.S1368N c.4103G>A 13 23913912 BRCA C T Missense p.V4083I c.12247G>A 13 23905768 UCEC C T Nonsense p.W2229* c.6687G>A 13 23911328 CM C T Nonsense p.W783* c.2348G>A 13 23915667 NSCLC C T Synonymous p.A149A c.447G>A 13 23939315 UCEC C T Synonymous p.G2104G c.6312G>A 13 23911703 GBM C T Synonymous p.K3827K c.11481G>A 13 23906534 HNSC C T Synonymous p.L1830L c.5490G>A 13 23912525 PRAD C T Synonymous p.P536P c.1608G>A 13 23929143 ESCA C T Synonymous p.R4431R c.13293G>A 13 23904722 LUAD C T Synonymous p.S2714S c.8142G>A 13 23909873 UCEC C T Synonymous p.T1817T c.5451G>A 13 23912564 RCCC G A IntronicSNV . c.171+1678C>T 13 23947580 CLL G A Missense p.A2558V c.7673C>T 13 23910342 HNSC G A Missense p.A2587V c.7760C>T 13 23910255 COREAD G A Missense p.A3310V c.9929C>T 13 23908086 CM G A Missense p.A4484V c.13451C>T 13 23904564 CM G A Missense p.H2882Y c.8644C>T 13 23909371 CM G A Missense p.H3575Y c.10723C>T 13 23907292 CM G A Missense p.H3667Y c.10999C>T 13 23907016 BLCA G A Missense p.H3667Y c.10999C>T 13 23907016 CM G A Missense p.H463Y c.1387C>T 13 23929364 LUSC G A Missense p.H861Y c.2581C>T 13 23915434 LUAD G A Missense p.L1064F c.3190C>T 13 23914825 STAD G A Missense p.L143F c.427C>T 13 23939335 CM G A Missense p.L2191F c.6571C>T 13 23911444 CM G A Missense p.L2726F c.8176C>T 13 23909839 CM G A Missense p.L3969F c.11905C>T 13 23906110 LUSC G A Missense p.L4005F c.12013C>T 13 23906002 BRCA G A Missense p.L4240F c.12718C>T 13 23905297 CM G A Missense p.L700F c.2098C>T 13 23928011 CM G A Missense p.L704F c.2110C>T 13 23927999 HC G A Missense p.L852F c.2554C>T 13 23915461 CM G A Missense p.M1795I c.5385G>A 13 23912630 COREAD G A Missense p.P1028S c.3082C>T 13 23914933 CM G A Missense p.P1378L c.4133C>T 13 23913882 GBM G A Missense p.P1387L c.4160C>T 13 23913855 CM G A Missense p.P1387S c.4159C>T 13 23913856 CM G A Missense p.P1615S c.4843C>T 13 23913172 CM G A Missense p.P2106S c.6316C>T 13 23911699 CM G A Missense p.P2116S c.6346C>T 13 23911669 CM G A Missense p.P2849S c.8545C>T 13 23909470 CM G A Missense p.P2999L c.8996C>T 13 23909019 CM G A Missense p.P3296S c.9886C>T 13 23908129 CM G A Missense p.P3303S c.9907C>T 13 23908108 CM G A Missense p.P3346S c.10036C>T 13 23907979 CM G A Missense p.P3411L c.10232C>T 13 23907783 BRCA G A Missense p.P4161L c.12482C>T 13 23905533 CM G A Missense p.P488S c.1462C>T 13 23929289 STAD G A Missense p.R2898C c.8692C>T 13 23909323 SCLC G A Missense p.R3788C c.11362C>T 13 23906653 BLCA G A Missense p.R3788C c.11362C>T 13 23906653 CM G A Missense p.S1544F c.4631C>T 13 23913384 CM G A Missense p.S1718F c.5153C>T 13 23912862 CM G A Missense p.S1721F c.5162C>T 13 23912853 SCLC G A Missense p.S2032L c.6095C>T 13 23911920 STAD G A Missense p.S2089L c.6266C>T 13 23911749 STAD G A Missense p.S2101F c.6302C>T 13 23911713 CM G A Missense p.S2465L c.7394C>T 13 23910621 CM G A Missense p.S2714L c.8141C>T 13 23909874 CM G A Missense p.S2715F c.8144C>T 13 23909871 CM G A Missense p.S2824L c.8471C>T 13 23909544 THCA G A Missense p.S3415F c.10244C>T 13 23907771 CM G A Missense p.S4260F c.12779C>T 13 23905236 NSCLC G A Missense p.S693L c.2078C>T 13 23928673 STAD G A Missense p.S824L c.2471C>T 13 23915544 CM G A Missense p.S939F c.2816C>T 13 23915199 CM G A Missense p.T1130I c.3389C>T 13 23914626 CM G A Missense p.T1817M c.5450C>T 13 23912565 PRAD G A Missense p.T627M c.1880C>T 13 23928871 AML G A Nonsense p.Q1628* c.4882C>T 13 23913133 OV G A Nonsense p.Q219* c.655C>T 13 23930096 BLCA G A Nonsense p.Q2409* c.7225C>T 13 23910790 CM G A Nonsense p.Q2422* c.7264C>T 13 23910751 BRCA G A Nonsense p.Q2724* c.8170C>T 13 23909845 CM G A Nonsense p.Q3790* c.11368C>T 13 23906647 CM G A Nonsense p.Q4395* c.13183C>T 13 23904832 BRCA G A Nonsense p.R2119* c.6355C>T 13 23911660 COREAD G A Nonsense p.R2426* c.7276C>T 13 23910739 ESCA G A Nonsense p.R88* c.262C>T 13 23942624 STAD G A Synonymous p.A602A c.1806C>T 13 23928945 CM G A Synonymous p.F2963F c.8889C>T 13 23909126 CM G A Synonymous p.F3540F c.10620C>T 13 23907395 CM G A Synonymous p.F3562F c.10686C>T 13 23907329 CM G A Synonymous p.F3691F c.11073C>T 13 23906942 RCCC G A Synonymous p.F701F c.2103C>T 13 23928006 CM G A Synonymous p.F754F c.2262C>T 13 23915753 BLCA G A Synonymous p.I2192I c.6576C>T 13 23911439 OV G A Synonymous p.I3436I c.10308C>T 13 23907707 CM G A Synonymous p.L3061L c.9183C>T 13 23908832 CM G A Synonymous p.L4168L c.12502C>T 13 23905513 BRCA G A Synonymous p.L460L c.1380C>T 13 23929371 CM G A Synonymous p.L903L c.2707C>T 13 23915308 LUAD G A Synonymous p.N263N c.789C>T 13 23929962 UCEC G A Synonymous p.N2895N c.8685C>T 13 23909330 BLCA G A Synonymous p.P2116P c.6348C>T 13 23911667 STAD G A Synonymous p.P3154P c.9462C>T 13 23908553 CM G A Synonymous p.P3713P c.11139C>T 13 23906876 CM G A Synonymous p.P628P c.1884C>T 13 23928867 CM G A Synonymous p.S1721S c.5163C>T 13 23912852 CM G A Synonymous p.S1833S c.5499C>T 13 23912516 CM G A Synonymous p.V320V c.960C>T 13 23929791 BLCA G C Missense p.A2718G c.8153C>G 13 23909862 PRAD G C Missense p.F4280L c.12840C>G 13 23905175 BLCA G C Missense p.F4432L c.13296C>G 13 23904719 BLCA G C Missense p.H1768D c.5302C>G 13 23912713 HNSC G C Missense p.L2435V c.7303C>G 13 23910712 OV G C Missense p.L3365V c.10093C>G 13 23907922 RCCC G C Missense p.Q2251E c.6751C>G 13 23911264 BRCA G C Missense p.S3864C c.11591C>G 13 23906424 HNSC G C Missense p.S4281C c.12842C>G 13 23905173 BLCA G C Missense p.S963C c.2888C>G 13 23915127 BRCA G C Missense p.T1812R c.5435C>G 13 23912580 BRCA G C Missense p.T4399S c.13196C>G 13 23904819 OV G C Nonsense p.S4383* c.13148C>G 13 23904867 BLCA G C Nonsense p.S4393* c.13178C>G 13 23904837 HNSC G C Synonymous p.G757G c.2271C>G 13 23915744 HNSC G C Synonymous p.L100L c.300C>G 13 23942586 HNSC G C Synonymous p.L1341L c.4023C>G 13 23913992 HNSC G C Synonymous p.T1976T c.5928C>G 13 23912087 BRCA G T Missense p.A2658D c.7973C>A 13 23910042 COREAD G T Missense p.A3611D c.10832C>A 13 23907183 COREAD G T Missense p.N2860K c.8580C>A 13 23909435 CM G T Missense p.Q2945K c.8833C>A 13 23909182 RCCC G T Missense p.R2214S c.6640C>A 13 23911375 STAD G T Missense p.S3911R c.11733C>A 13 23906282 LUSC G T Missense p.T2611K c.7832C>A 13 23910183 LUAD G T Missense p.T3076N c.9227C>A 13 23908788 GBM G T Synonymous p.A902A c.2706C>A 13 23915309 ESCA G T Synonymous p.L3909L c.11727C>A 13 23906288 HNSC G T Synonymous p.S1833S c.5499C>A 13 23912516 LUSC T A Missense p.D1268V c.3803A>T 13 23914212 LUAD T A Missense p.E2357V c.7070A>T 13 23910945 HNSC T A Missense p.H4354L c.13061A>T 13 23904954 THCA T A Missense p.I62F c.184A>T 13 23945292 HNSC T A Missense p.K238I c.713A>T 13 23930038 ESCA T A Missense p.S4285C c.12853A>T 13 23905162 LUSC T A Missense p.S969C c.2905A>T 13 23915110 LUAD T A Missense p.S990C c.2968A>T 13 23915047 LUAD T A Synonymous p.G1450G c.4350A>T 13 23913665 STAD T A Synonymous p.P2972P c.8916A>T 13 23909099 LUSC T A Synonymous p.T3428T c.10284A>T 13 23907731 LUAD T C Missense p.D202G c.605A>G 13 23930146 HC T C Missense p.E2237G c.6710A>G 13 23911305 STAD T C Missense p.H1382R c.4145A>G 13 23913870 OV T C Missense p.I1572V c.4714A>G 13 23913301 GBM T C Missense p.K1174R c.3521A>G 13 23914494 COREAD T C Missense p.N2822S c.8465A>G 13 23909550 BLCA T C Missense p.N3615S c.10844A>G 13 23907171 STAD T C Missense p.N6S c.17A>G 13 23985362 ESCA T C Missense p.Q2329R c.6986A>G 13 23911029 SCLC T C Missense p.T1862A c.5584A>G 13 23912431 GBM T C Synonymous p.E4071E c.12213A>G 13 23905802 HNSC T C Synonymous p.K4391K c.13173A>G 13 23904842 SCLC T C Synonymous p.T2940T c.8820A>G 13 23909195 LUSC T C Synonymous p.T3577T c.10731A>G 13 23907284 HNSC T - Frameshift p.I1110Lfs*16 c.3328delA 13 23914687 GBM T - Frameshift p.I1110Lfs*16 c.3328delA 13 23914687 HNSC T - Frameshift p.I1110Lfs*16 c.3328delA 13 23914687 PRAD T - Frameshift p.I1110Lfs*16 c.3328delA 13 23914687 STAD T - Frameshift p.I1110Lfs*16 c.3328delA 13 23914687 THCA T - Frameshift p.K1717Nfs*8 c.5151delA 13 23912864 STAD T G Missense p.E4358D c.13074A>C 13 23904941 UCEC T G Missense p.E4527D c.13581A>C 13 23904434 COREAD T G Missense p.K1319T c.3956A>C 13 23914059 RCCC T G Missense p.K637T c.1910A>C 13 23928841 COREAD T G Missense p.S3417R c.10249A>C 13 23907766 STAD T G Missense p.S3435R c.10303A>C 13 23907712 ESCA T G SpliceAcceptorSNV . c.605-2A>C 13 23930148 BRCA T G Synonymous p.V844V c.2532A>C 13 23915483 RCCC