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 1 235904873 235904873 + Missense_Mutation SNP C C G TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr1:235904873C>G c.8207G>C c.(8206-8208)tGt>tCt p.C2736S ACC 1 235966313 235966313 + Missense_Mutation SNP C C G TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr1:235966313C>G c.3607G>C c.(3607-3609)Gaa>Caa p.E1203Q ACC 1 235972428 235972428 + Missense_Mutation SNP C C A TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr1:235972428C>A c.1690G>T c.(1690-1692)Gct>Tct p.A564S ACC 1 235973763 235973763 + Missense_Mutation SNP G G C TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr1:235973763G>C c.355C>G c.(355-357)Cag>Gag p.Q119E BLCA 1 235826288 235826288 + Silent SNP C C T TCGA-K4-A3WU-01B-11D-A23M-08 TCGA-K4-A3WU-10A-01D-A23K-08 g.chr1:235826288C>T c.11358G>A c.(11356-11358)ttG>ttA p.L3786L BLCA 1 235827817 235827817 + Missense_Mutation SNP C C G TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr1:235827817C>G c.11143G>C c.(11143-11145)Gag>Cag p.E3715Q BLCA 1 235884050 235884050 + Silent SNP G G A TCGA-BT-A42C-01A-11D-A23M-08 TCGA-BT-A42C-10A-01D-A23K-08 g.chr1:235884050G>A c.9471C>T c.(9469-9471)ttC>ttT p.F3157F BLCA 1 235884083 235884083 + Silent SNP C C T TCGA-XF-A9SG-01A-12D-A42E-08 TCGA-XF-A9SG-10A-01D-A42H-08 g.chr1:235884083C>T c.9438G>A c.(9436-9438)ttG>ttA p.L3146L BLCA 1 235884187 235884187 + Missense_Mutation SNP G G C TCGA-FT-A3EE-01A-11D-A202-08 TCGA-FT-A3EE-10A-01D-A202-08 g.chr1:235884187G>C c.9334C>G c.(9334-9336)Cac>Gac p.H3112D BLCA 1 235887452 235887452 + Nonsense_Mutation SNP G G T TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr1:235887452G>T c.9191C>A c.(9190-9192)tCa>tAa p.S3064* BLCA 1 235887453 235887453 + Missense_Mutation SNP A A T TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr1:235887453A>T c.9190T>A c.(9190-9192)Tca>Aca p.S3064T BLCA 1 235892949 235892949 + Missense_Mutation SNP C C T TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chr1:235892949C>T c.9053G>A c.(9052-9054)cGa>cAa p.R3018Q BLCA 1 235894422 235894422 + Missense_Mutation SNP C C T TCGA-DK-A3IN-01A-11D-A20D-08 TCGA-DK-A3IN-10A-01D-A20D-08 g.chr1:235894422C>T c.8857G>A c.(8857-8859)Gaa>Aaa p.E2953K BLCA 1 235904826 235904826 + Missense_Mutation SNP A A C TCGA-FT-A61P-01A-11D-A30E-08 TCGA-FT-A61P-10A-01D-A30H-08 g.chr1:235904826A>C c.8254T>G c.(8254-8256)Ttg>Gtg p.L2752V BLCA 1 235907429 235907429 + Missense_Mutation SNP C C G TCGA-FD-A3B5-01A-11D-A20D-08 TCGA-FD-A3B5-10A-01D-A20D-08 g.chr1:235907429C>G c.8001G>C c.(7999-8001)ttG>ttC p.L2667F BLCA 1 235907458 235907458 + Splice_Site SNP C C G TCGA-FD-A3B5-01A-11D-A20D-08 TCGA-FD-A3B5-10A-01D-A20D-08 g.chr1:235907458C>G c.e30-1 BLCA 1 235915462 235915462 + Missense_Mutation SNP C C T TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr1:235915462C>T c.7470G>A c.(7468-7470)atG>atA p.M2490I BLCA 1 235920623 235920623 + Silent SNP G G A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr1:235920623G>A c.7017C>T c.(7015-7017)ctC>ctT p.L2339L BLCA 1 235920751 235920751 + Missense_Mutation SNP C C T TCGA-UY-A9PH-01A-11D-A38G-08 TCGA-UY-A9PH-10A-01D-A38J-08 g.chr1:235920751C>T c.6889G>A c.(6889-6891)Gaa>Aaa p.E2297K BLCA 1 235922510 235922510 + Missense_Mutation SNP C C T TCGA-DK-A2I1-01A-11D-A17V-08 TCGA-DK-A2I1-10A-01D-A17V-08 g.chr1:235922510C>T c.6643G>A c.(6643-6645)Gat>Aat p.D2215N BLCA 1 235922785 235922785 + Missense_Mutation SNP C C T TCGA-R3-A69X-01A-22D-A30E-08 TCGA-R3-A69X-10A-01D-A30H-08 g.chr1:235922785C>T c.6368G>A c.(6367-6369)gGa>gAa p.G2123E BLCA 1 235922848 235922848 + Missense_Mutation SNP C C T TCGA-GV-A3JV-01A-11D-A21Z-08 TCGA-GV-A3JV-10B-01D-A21Z-08 g.chr1:235922848C>T c.6305G>A c.(6304-6306)cGt>cAt p.R2102H BLCA 1 235929543 235929543 + Missense_Mutation SNP C C T TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr1:235929543C>T c.5957G>A c.(5956-5958)cGa>cAa p.R1986Q BLCA 1 235940493 235940493 + Nonsense_Mutation SNP G G C TCGA-DK-AA6P-01A-11D-A391-08 TCGA-DK-AA6P-10A-01D-A394-08 g.chr1:235940493G>C c.5330C>G c.(5329-5331)tCa>tGa p.S1777* BLCA 1 235940598 235940598 + Missense_Mutation SNP G G A TCGA-UY-A78O-01A-12D-A339-08 TCGA-UY-A78O-10A-01D-A339-08 g.chr1:235940598G>A c.5225C>T c.(5224-5226)tCa>tTa p.S1742L BLCA 1 235952011 235952011 + Missense_Mutation SNP G G C TCGA-GC-A3RB-01A-12D-A21Z-08 TCGA-GC-A3RB-10A-01D-A21Z-08 g.chr1:235952011G>C c.4678C>G c.(4678-4680)Ctt>Gtt p.L1560V BLCA 1 235952067 235952067 + Missense_Mutation SNP G G A TCGA-G2-A2EK-01A-22D-A18F-08 TCGA-G2-A2EK-10A-01D-A18F-08 g.chr1:235952067G>A c.4622C>T c.(4621-4623)tCa>tTa p.S1541L BLCA 1 235952110 235952110 + Missense_Mutation SNP G G C TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr1:235952110G>C c.4579C>G c.(4579-4581)Cct>Gct p.P1527A BLCA 1 235956879 235956879 + Missense_Mutation SNP G G C TCGA-S5-AA26-01A-11D-A38G-08 TCGA-S5-AA26-10A-01D-A38J-08 g.chr1:235956879G>C c.4040C>G c.(4039-4041)tCt>tGt p.S1347C BLCA 1 235964228 235964228 + Silent SNP C C T TCGA-GV-A3QI-01A-11D-A21Z-08 TCGA-GV-A3QI-10A-01D-A21Z-08 g.chr1:235964228C>T c.3882G>A c.(3880-3882)gaG>gaA p.E1294E BLCA 1 235966211 235966211 + Missense_Mutation SNP C C T TCGA-DK-A1AG-01A-11D-A13W-08 TCGA-DK-A1AG-10A-01D-A13W-08 g.chr1:235966211C>T c.3709G>A c.(3709-3711)Gat>Aat p.D1237N BLCA 1 235967904 235967904 + Missense_Mutation SNP A A G TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr1:235967904A>G c.3455T>C c.(3454-3456)aTt>aCt p.I1152T BLCA 1 235969280 235969280 + Silent SNP T T C TCGA-E7-A6ME-01A-22D-A32B-08 TCGA-E7-A6ME-10B-01D-A329-08 g.chr1:235969280T>C c.3156A>G c.(3154-3156)ctA>ctG p.L1052L BLCA 1 235969730 235969730 + Silent SNP G G C TCGA-GC-A3YS-01A-11D-A23M-08 TCGA-GC-A3YS-10A-01D-A23K-08 g.chr1:235969730G>C c.2706C>G c.(2704-2706)ctC>ctG p.L902L BLCA 1 235969823 235969823 + Silent SNP G G A TCGA-DK-A3IU-01A-11D-A20D-08 TCGA-DK-A3IU-10A-01D-A20D-08 g.chr1:235969823G>A c.2613C>T c.(2611-2613)ctC>ctT p.L871L BLCA 1 235971786 235971786 + Missense_Mutation SNP C C A TCGA-E7-A677-01A-11D-A30E-08 TCGA-E7-A677-10A-01D-A30H-08 g.chr1:235971786C>A c.2332G>T c.(2332-2334)Gta>Tta p.V778L BLCA 1 235972029 235972029 + Nonsense_Mutation SNP G G A TCGA-BT-A20O-01A-21D-A14W-08 TCGA-BT-A20O-11A-11D-A14W-08 g.chr1:235972029G>A c.2089C>T c.(2089-2091)Cag>Tag p.Q697* BLCA 1 235972124 235972124 + Missense_Mutation SNP G G A TCGA-K4-A3WU-01B-11D-A23M-08 TCGA-K4-A3WU-10A-01D-A23K-08 g.chr1:235972124G>A c.1994C>T c.(1993-1995)tCa>tTa p.S665L BLCA 1 235972598 235972598 + Missense_Mutation SNP G G A TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr1:235972598G>A c.1520C>T c.(1519-1521)tCt>tTt p.S507F BLCA 1 235972605 235972605 + Missense_Mutation SNP C C G TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr1:235972605C>G c.1513G>C c.(1513-1515)Gaa>Caa p.E505Q BLCA 1 235972637 235972637 + Missense_Mutation SNP G G A TCGA-BT-A3PJ-01A-21D-A21Z-08 TCGA-BT-A3PJ-10A-01D-A21Z-08 g.chr1:235972637G>A c.1481C>T c.(1480-1482)tCg>tTg p.S494L BLCA 1 235972890 235972890 + Nonsense_Mutation SNP G G A TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr1:235972890G>A c.1228C>T c.(1228-1230)Cag>Tag p.Q410* BLCA 1 235973008 235973008 + Silent SNP C C T TCGA-DK-AA76-01A-11D-A391-08 TCGA-DK-AA76-10A-01D-A394-08 g.chr1:235973008C>T c.1110G>A c.(1108-1110)caG>caA p.Q370Q BLCA 1 235973317 235973317 + Silent SNP T T C TCGA-XF-AAML-01A-11D-A42E-08 TCGA-XF-AAML-10A-01D-A42H-08 g.chr1:235973317T>C c.801A>G c.(799-801)aaA>aaG p.K267K BLCA 1 235973465 235973465 + Missense_Mutation SNP G G T TCGA-DK-AA6W-01A-12D-A391-08 TCGA-DK-AA6W-10A-01D-A394-08 g.chr1:235973465G>T c.653C>A c.(652-654)gCt>gAt p.A218D BLCA 1 235973532 235973532 + Missense_Mutation SNP G G T TCGA-GU-A42R-01A-11D-A23M-08 TCGA-GU-A42R-10A-01D-A23K-08 g.chr1:235973532G>T c.586C>A c.(586-588)Cct>Act p.P196T BLCA 1 235973621 235973621 + Nonsense_Mutation SNP G G C TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chr1:235973621G>C c.497C>G c.(496-498)tCa>tGa p.S166* BLCA 1 235973651 235973651 + Missense_Mutation SNP C C G TCGA-CU-A3KJ-01A-11D-A21A-08 TCGA-CU-A3KJ-10A-01D-A21A-08 g.chr1:235973651C>G c.467G>C c.(466-468)aGa>aCa p.R156T BLCA 1 235973787 235973787 + Missense_Mutation SNP T T A TCGA-E5-A2PC-01A-11D-A202-08 TCGA-E5-A2PC-10B-01D-A202-08 g.chr1:235973787T>A c.331A>T c.(331-333)Aac>Tac p.N111Y BRCA 1 235856727 235856727 + Missense_Mutation SNP C C T TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr1:235856727C>T c.10624G>A c.(10624-10626)Gct>Act p.A3542T BRCA 1 235860498 235860498 + Silent SNP G G T TCGA-AR-A256-01A-11D-A167-09 TCGA-AR-A256-10A-01D-A167-09 g.chr1:235860498G>T c.10449C>A c.(10447-10449)gtC>gtA p.V3483V BRCA 1 235872479 235872479 + Missense_Mutation SNP T T G TCGA-A2-A04T-01A-21W-A050-09 TCGA-A2-A04T-10A-01W-A055-09 g.chr1:235872479T>G c.10055A>C c.(10054-10056)cAg>cCg p.Q3352P BRCA 1 235872544 235872544 + Silent SNP C C T TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr1:235872544C>T c.9990G>A c.(9988-9990)gcG>gcA p.A3330A BRCA 1 235872550 235872550 + Silent SNP A A C TCGA-GM-A3NW-01A-21D-A228-09 TCGA-GM-A3NW-10A-01D-A22A-09 g.chr1:235872550A>C c.9984T>G c.(9982-9984)ccT>ccG p.P3328P BRCA 1 235875443 235875443 + Missense_Mutation SNP C C G TCGA-A8-A07R-01A-21W-A050-09 TCGA-A8-A07R-10B-01D-A047-09 g.chr1:235875443C>G c.9839G>C c.(9838-9840)cGa>cCa p.R3280P BRCA 1 235884046 235884046 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr1:235884046C>T c.9475G>A c.(9475-9477)Gat>Aat p.D3159N BRCA 1 235891402 235891402 + Missense_Mutation SNP T T C TCGA-A2-A25E-01A-11D-A167-09 TCGA-A2-A25E-10A-01D-A167-09 g.chr1:235891402T>C c.9136A>G c.(9136-9138)Aat>Gat p.N3046D BRCA 1 235904748 235904748 + Missense_Mutation SNP G G C TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr1:235904748G>C c.8332C>G c.(8332-8334)Cga>Gga p.R2778G BRCA 1 235907399 235907399 + Missense_Mutation SNP C C G TCGA-E2-A1LH-01A-11D-A14G-09 TCGA-E2-A1LH-11A-22D-A14G-09 g.chr1:235907399C>G c.8031G>C c.(8029-8031)aaG>aaC p.K2677N BRCA 1 235909789 235909789 + Silent SNP G G A TCGA-BH-A0B6-01A-11D-A19Y-09 TCGA-BH-A0B6-10A-01D-A19Y-09 g.chr1:235909789G>A c.7819C>T c.(7819-7821)Ctg>Ttg p.L2607L BRCA 1 235909794 235909794 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr1:235909794G>A c.7814C>T c.(7813-7815)tCg>tTg p.S2605L BRCA 1 235916501 235916501 + Missense_Mutation SNP C C G TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chr1:235916501C>G c.7303G>C c.(7303-7305)Gag>Cag p.E2435Q BRCA 1 235922289 235922289 + Silent SNP T T A TCGA-A7-A0DA-01A-31D-A10Y-09 TCGA-A7-A0DA-10A-01D-A110-09 g.chr1:235922289T>A c.6864A>T c.(6862-6864)cgA>cgT p.R2288R BRCA 1 235922292 235922292 + Missense_Mutation SNP G G T TCGA-AC-A2FO-01A-11D-A17W-09 TCGA-AC-A2FO-11A-12D-A17W-09 g.chr1:235922292G>T c.6861C>A c.(6859-6861)aaC>aaA p.N2287K BRCA 1 235922444 235922444 + Nonsense_Mutation SNP G G A TCGA-A2-A0CR-01A-11D-A228-09 TCGA-A2-A0CR-10A-01D-A22A-09 g.chr1:235922444G>A c.6709C>T c.(6709-6711)Cag>Tag p.Q2237* BRCA 1 235926116 235926116 + Missense_Mutation SNP T T C TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr1:235926116T>C c.6157A>G c.(6157-6159)Atg>Gtg p.M2053V BRCA 1 235929455 235929455 + Missense_Mutation SNP G G T TCGA-BH-A5IZ-01A-11D-A27P-09 TCGA-BH-A5IZ-11A-13D-A27P-09 g.chr1:235929455G>T c.6045C>A c.(6043-6045)ttC>ttA p.F2015L BRCA 1 235940493 235940493 + Nonsense_Mutation SNP G G C TCGA-GM-A2DB-01A-31D-A19Y-09 TCGA-GM-A2DB-10C-01D-A18P-09 g.chr1:235940493G>C c.5330C>G c.(5329-5331)tCa>tGa p.S1777* BRCA 1 235945333 235945333 + Silent SNP A A G TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr1:235945333A>G c.4917T>C c.(4915-4917)tcT>tcC p.S1639S BRCA 1 235967816 235967816 + Silent SNP A A G TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr1:235967816A>G c.3543T>C c.(3541-3543)gcT>gcC p.A1181A BRCA 1 235969126 235969126 + Missense_Mutation SNP G G C TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr1:235969126G>C c.3310C>G c.(3310-3312)Cga>Gga p.R1104G BRCA 1 235969147 235969147 + Missense_Mutation SNP C C T TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr1:235969147C>T c.3289G>A c.(3289-3291)Gag>Aag p.E1097K BRCA 1 235969153 235969153 + Missense_Mutation SNP C C T TCGA-A2-A0CT-01A-31W-A071-09 TCGA-A2-A0CT-10A-01W-A071-09 g.chr1:235969153C>T c.3283G>A c.(3283-3285)Gaa>Aaa p.E1095K BRCA 1 235969744 235969745 + Frame_Shift_Ins INS - - G TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr1:235969744_235969745insG c.2691_2692insC c.(2689-2694)acaatafs p.I898fs BRCA 1 235969747 235969748 + Frame_Shift_Ins INS - - C TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr1:235969747_235969748insC c.2688_2689insG c.(2686-2691)aacacafs p.T897fs BRCA 1 235969927 235969927 + Missense_Mutation SNP G G A TCGA-AO-A03N-01B-11D-A10M-09 TCGA-AO-A03N-10A-01D-A10M-09 g.chr1:235969927G>A c.2509C>T c.(2509-2511)Cca>Tca p.P837S BRCA 1 235972478 235972478 + Missense_Mutation SNP C C A TCGA-OL-A66I-01A-21D-A29N-09 TCGA-OL-A66I-10A-01D-A29N-09 g.chr1:235972478C>A c.1640G>T c.(1639-1641)tGc>tTc p.C547F BRCA 1 235972815 235972815 + Nonsense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr1:235972815C>A c.1303G>T c.(1303-1305)Gaa>Taa p.E435* BRCA 1 235972931 235972931 + Missense_Mutation SNP T T C TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr1:235972931T>C c.1187A>G c.(1186-1188)cAt>cGt p.H396R BRCA 1 235973301 235973301 + Missense_Mutation SNP C C T TCGA-AO-A0JE-01A-11W-A071-09 TCGA-AO-A0JE-10A-01W-A071-09 g.chr1:235973301C>T c.817G>A c.(817-819)Gtt>Att p.V273I CESC 1 235850285 235850285 + Silent SNP G G A TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr1:235850285G>A c.10764C>T c.(10762-10764)gtC>gtT p.V3588V CESC 1 235944211 235944211 + Missense_Mutation SNP C C G TCGA-IR-A3LI-01A-11D-A20U-09 TCGA-IR-A3LI-10A-01D-A20U-09 g.chr1:235944211C>G c.5168G>C c.(5167-5169)aGa>aCa p.R1723T CESC 1 235944340 235944340 + Nonsense_Mutation SNP G G C TCGA-C5-A1MH-01A-11D-A14W-08 TCGA-C5-A1MH-10A-01D-A14W-08 g.chr1:235944340G>C c.5039C>G c.(5038-5040)tCa>tGa p.S1680* CESC 1 235952024 235952024 + Silent SNP G G T TCGA-RA-A741-01A-11D-A33O-09 TCGA-RA-A741-10B-01D-A33O-09 g.chr1:235952024G>T c.4665C>A c.(4663-4665)ccC>ccA p.P1555P CESC 1 235955247 235955247 + Missense_Mutation SNP G G A TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr1:235955247G>A c.4295C>T c.(4294-4296)tCa>tTa p.S1432L CESC 1 235964185 235964185 + Missense_Mutation SNP G G C TCGA-IR-A3LH-01A-21D-A20U-09 TCGA-IR-A3LH-10A-01D-A20U-09 g.chr1:235964185G>C c.3925C>G c.(3925-3927)Ctg>Gtg p.L1309V CESC 1 235964366 235964366 + Silent SNP G G A TCGA-IR-A3LH-01A-21D-A20U-09 TCGA-IR-A3LH-10A-01D-A20U-09 g.chr1:235964366G>A c.3744C>T c.(3742-3744)ttC>ttT p.F1248F CESC 1 235969198 235969198 + Missense_Mutation SNP C C G TCGA-FU-A23K-01A-11D-A16O-08 TCGA-FU-A23K-10A-01D-A16O-08 g.chr1:235969198C>G c.3238G>C c.(3238-3240)Gct>Cct p.A1080P CESC 1 235969573 235969573 + Missense_Mutation SNP C C G TCGA-FU-A23K-01A-11D-A16O-08 TCGA-FU-A23K-10A-01D-A16O-08 g.chr1:235969573C>G c.2863G>C c.(2863-2865)Gaa>Caa p.E955Q CESC 1 235973634 235973634 + Missense_Mutation SNP G G T TCGA-HG-A2PA-01A-11D-A20U-09 TCGA-HG-A2PA-10B-01D-A20U-09 g.chr1:235973634G>T c.484C>A c.(484-486)Cag>Aag p.Q162K CHOL 1 235827341 235827341 + Missense_Mutation SNP C C A TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr1:235827341C>A c.11210G>T c.(11209-11211)tGg>tTg p.W3737L CHOL 1 235878584 235878584 + Missense_Mutation SNP C C T TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr1:235878584C>T c.9701G>A c.(9700-9702)gGc>gAc p.G3234D CHOL 1 235972607 235972607 + Missense_Mutation SNP C C T TCGA-ZH-A8Y6-01A-11D-A417-09 TCGA-ZH-A8Y6-10A-01D-A41A-09 g.chr1:235972607C>T c.1511G>A c.(1510-1512)tGt>tAt p.C504Y COAD 1 235826347 235826347 + Missense_Mutation SNP A A G TCGA-AA-A02W-01A-01W-A00E-09 TCGA-AA-A02W-10A-01W-A00E-09 g.chr1:235826347A>G c.11299T>C c.(11299-11301)Tac>Cac p.Y3767H COAD 1 235827874 235827874 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr1:235827874C>T c.11086G>A c.(11086-11088)Gtt>Att p.V3696I COAD 1 235850345 235850345 + Silent SNP C C G TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr1:235850345C>G c.10704G>C c.(10702-10704)gtG>gtC p.V3568V COAD 1 235856654 235856654 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr1:235856654T>C c.10697A>G c.(10696-10698)tAc>tGc p.Y3566C COAD 1 235860531 235860531 + Silent SNP G G A TCGA-AD-6899-01A-11D-1924-10 TCGA-AD-6899-10A-01D-1924-10 g.chr1:235860531G>A c.10416C>T c.(10414-10416)taC>taT p.Y3472Y COAD 1 235860557 235860557 + Missense_Mutation SNP T T C TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr1:235860557T>C c.10390A>G c.(10390-10392)Ata>Gta p.I3464V COAD 1 235860568 235860568 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr1:235860568G>T c.10379C>A c.(10378-10380)cCt>cAt p.P3460H COAD 1 235884035 235884035 + Silent SNP C C T TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr1:235884035C>T c.9486G>A c.(9484-9486)caG>caA p.Q3162Q COAD 1 235884036 235884036 + Missense_Mutation SNP T T C TCGA-A6-6652-01A-11D-1771-10 TCGA-A6-6652-10A-01D-1771-10 g.chr1:235884036T>C c.9485A>G c.(9484-9486)cAg>cGg p.Q3162R COAD 1 235884036 235884036 + Missense_Mutation SNP T T C TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr1:235884036T>C c.9485A>G c.(9484-9486)cAg>cGg p.Q3162R COAD 1 235884036 235884036 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr1:235884036T>C c.9485A>G c.(9484-9486)cAg>cGg p.Q3162R COAD 1 235884037 235884037 + Nonsense_Mutation SNP G G A TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr1:235884037G>A c.9484C>T c.(9484-9486)Cag>Tag p.Q3162* COAD 1 235884060 235884060 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr1:235884060C>T c.9461G>A c.(9460-9462)gGc>gAc p.G3154D COAD 1 235884120 235884120 + Nonsense_Mutation SNP A A C TCGA-AD-6888-01A-11D-1924-10 TCGA-AD-6888-10A-01D-1924-10 g.chr1:235884120A>C c.9401T>G c.(9400-9402)tTa>tGa p.L3134* COAD 1 235884128 235884128 + Silent SNP C C G TCGA-AA-3526-01A-02W-0831-10 TCGA-AA-3526-10A-01W-0831-10 g.chr1:235884128C>G c.9393G>C c.(9391-9393)ctG>ctC p.L3131L COAD 1 235887410 235887410 + Missense_Mutation SNP C C T TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr1:235887410C>T c.9233G>A c.(9232-9234)cGt>cAt p.R3078H COAD 1 235897871 235897871 + Missense_Mutation SNP A A G TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr1:235897871A>G c.8447T>C c.(8446-8448)cTg>cCg p.L2816P COAD 1 235907315 235907315 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr1:235907315A>C c.8115T>G c.(8113-8115)atT>atG p.I2705M COAD 1 235920637 235920637 + Missense_Mutation SNP T T C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr1:235920637T>C c.7003A>G c.(7003-7005)Aca>Gca p.T2335A COAD 1 235922642 235922642 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr1:235922642C>T c.6511G>A c.(6511-6513)Gca>Aca p.A2171T COAD 1 235922694 235922694 + Silent SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr1:235922694G>A c.6459C>T c.(6457-6459)tcC>tcT p.S2153S COAD 1 235922805 235922805 + Silent SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr1:235922805C>T c.6348G>A c.(6346-6348)acG>acA p.T2116T COAD 1 235938333 235938333 + Missense_Mutation SNP T T C TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr1:235938333T>C c.5514A>G c.(5512-5514)atA>atG p.I1838M COAD 1 235938333 235938333 + Silent SNP T T G TCGA-D5-5539-01A-01D-1650-10 TCGA-D5-5539-10A-01D-1650-10 g.chr1:235938333T>G c.5514A>C c.(5512-5514)atA>atC p.I1838I COAD 1 235940533 235940533 + Missense_Mutation SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr1:235940533C>A c.5290G>T c.(5290-5292)Ggt>Tgt p.G1764C COAD 1 235944202 235944202 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr1:235944202A>C c.5177T>G c.(5176-5178)tTt>tGt p.F1726C COAD 1 235950518 235950518 + Missense_Mutation SNP A A G TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr1:235950518A>G c.4844T>C c.(4843-4845)aTa>aCa p.I1615T COAD 1 235955345 235955345 + Silent SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:235955345T>C c.4197A>G c.(4195-4197)ttA>ttG p.L1399L COAD 1 235956857 235956857 + Silent SNP A A G TCGA-AD-6548-01A-11D-1835-10 TCGA-AD-6548-10A-01D-1835-10 g.chr1:235956857A>G c.4062T>C c.(4060-4062)tgT>tgC p.C1354C COAD 1 235969113 235969113 + Missense_Mutation SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr1:235969113G>A c.3323C>T c.(3322-3324)gCc>gTc p.A1108V COAD 1 235969311 235969311 + Missense_Mutation SNP G G C TCGA-CM-6167-01A-11D-1650-10 TCGA-CM-6167-10A-01D-1650-10 g.chr1:235969311G>C c.3125C>G c.(3124-3126)gCt>gGt p.A1042G COAD 1 235969317 235969317 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr1:235969317G>T c.3119C>A c.(3118-3120)tCt>tAt p.S1040Y COAD 1 235969412 235969412 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr1:235969412C>A c.3024G>T c.(3022-3024)gaG>gaT p.E1008D COAD 1 235969521 235969521 + Missense_Mutation SNP A A G TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr1:235969521A>G c.2915T>C c.(2914-2916)aTg>aCg p.M972T COAD 1 235969825 235969825 + Missense_Mutation SNP G G A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr1:235969825G>A c.2611C>T c.(2611-2613)Ctc>Ttc p.L871F COAD 1 235969925 235969925 + Silent SNP T T C TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr1:235969925T>C c.2511A>G c.(2509-2511)ccA>ccG p.P837P COAD 1 235969925 235969925 + Silent SNP T T C TCGA-D5-5539-01A-01D-1650-10 TCGA-D5-5539-10A-01D-1650-10 g.chr1:235969925T>C c.2511A>G c.(2509-2511)ccA>ccG p.P837P COAD 1 235969998 235969998 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr1:235969998C>T c.2438G>A c.(2437-2439)cGa>cAa p.R813Q COAD 1 235969998 235969998 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:235969998C>T c.2438G>A c.(2437-2439)cGa>cAa p.R813Q COAD 1 235970023 235970023 + Missense_Mutation SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr1:235970023C>T c.2413G>A c.(2413-2415)Gaa>Aaa p.E805K COAD 1 235971896 235971896 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr1:235971896C>T c.2222G>A c.(2221-2223)aGa>aAa p.R741K COAD 1 235972015 235972015 + Silent SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr1:235972015A>G c.2103T>C c.(2101-2103)ttT>ttC p.F701F COAD 1 235972336 235972336 + Silent SNP A A G TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr1:235972336A>G c.1782T>C c.(1780-1782)ccT>ccC p.P594P COAD 1 235972337 235972337 + Missense_Mutation SNP G G T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr1:235972337G>T c.1781C>A c.(1780-1782)cCt>cAt p.P594H COAD 1 235972351 235972351 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:235972351T>G c.1767A>C c.(1765-1767)aaA>aaC p.K589N COAD 1 235972459 235972459 + Silent SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr1:235972459A>G c.1659T>C c.(1657-1659)tgT>tgC p.C553C COAD 1 235972482 235972482 + Missense_Mutation SNP G G A TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr1:235972482G>A c.1636C>T c.(1636-1638)Cgg>Tgg p.R546W COAD 1 235972592 235972592 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr1:235972592A>C c.1526T>G c.(1525-1527)tTt>tGt p.F509C COAD 1 235973040 235973040 + Missense_Mutation SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr1:235973040C>T c.1078G>A c.(1078-1080)Gct>Act p.A360T COAD 1 235973062 235973062 + Missense_Mutation SNP A A T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr1:235973062A>T c.1056T>A c.(1054-1056)aaT>aaA p.N352K COAD 1 235973133 235973133 + Nonsense_Mutation SNP G G A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr1:235973133G>A c.985C>T c.(985-987)Cga>Tga p.R329* COAD 1 235973203 235973204 + Frame_Shift_Ins INS - - T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr1:235973203_235973204insT c.914_915insA c.(913-915)aacfs p.N305fs COAD 1 235973543 235973543 + Frame_Shift_Del DEL A A - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr1:235973543delA c.575delT c.(574-576)ttafs p.L192fs COAD 1 235973559 235973559 + Missense_Mutation SNP G G T TCGA-AA-3514-01A-02W-0831-10 TCGA-AA-3514-10A-01W-0831-10 g.chr1:235973559G>T c.559C>A c.(559-561)Ctg>Atg p.L187M COADREAD 1 235826273 235826273 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:235826273G>T c.11373C>A c.(11371-11373)ttC>ttA p.F3791L COADREAD 1 235826347 235826347 + Missense_Mutation SNP A A G TCGA-AA-A02W-01A-01W-A00E-09 TCGA-AA-A02W-10A-01W-A00E-09 g.chr1:235826347A>G c.11299T>C c.(11299-11301)Tac>Cac p.Y3767H COADREAD 1 235827874 235827874 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr1:235827874C>T c.11086G>A c.(11086-11088)Gtt>Att p.V3696I COADREAD 1 235840882 235840882 + Missense_Mutation SNP T T C TCGA-F5-6702-01A-11D-1826-10 TCGA-F5-6702-10A-01D-1826-10 g.chr1:235840882T>C c.10838A>G c.(10837-10839)tAt>tGt p.Y3613C COADREAD 1 235840883 235840883 + Missense_Mutation SNP A A G TCGA-DY-A1DG-01A-11D-A152-10 TCGA-DY-A1DG-10A-01D-A152-10 g.chr1:235840883A>G c.10837T>C c.(10837-10839)Tat>Cat p.Y3613H COADREAD 1 235850291 235850291 + Silent SNP G G A TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr1:235850291G>A c.10758C>T c.(10756-10758)tgC>tgT p.C3586C COADREAD 1 235850345 235850345 + Silent SNP C C G TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr1:235850345C>G c.10704G>C c.(10702-10704)gtG>gtC p.V3568V COADREAD 1 235856654 235856654 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr1:235856654T>C c.10697A>G c.(10696-10698)tAc>tGc p.Y3566C COADREAD 1 235860531 235860531 + Silent SNP G G A TCGA-AD-6899-01A-11D-1924-10 TCGA-AD-6899-10A-01D-1924-10 g.chr1:235860531G>A c.10416C>T c.(10414-10416)taC>taT p.Y3472Y COADREAD 1 235860557 235860557 + Missense_Mutation SNP T T C TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr1:235860557T>C c.10390A>G c.(10390-10392)Ata>Gta p.I3464V COADREAD 1 235860568 235860568 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr1:235860568G>T c.10379C>A c.(10378-10380)cCt>cAt p.P3460H COADREAD 1 235884035 235884035 + Silent SNP C C T TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr1:235884035C>T c.9486G>A c.(9484-9486)caG>caA p.Q3162Q COADREAD 1 235884036 235884036 + Missense_Mutation SNP T T C TCGA-A6-6652-01A-11D-1771-10 TCGA-A6-6652-10A-01D-1771-10 g.chr1:235884036T>C c.9485A>G c.(9484-9486)cAg>cGg p.Q3162R COADREAD 1 235884036 235884036 + Missense_Mutation SNP T T C TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr1:235884036T>C c.9485A>G c.(9484-9486)cAg>cGg p.Q3162R COADREAD 1 235884036 235884036 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr1:235884036T>C c.9485A>G c.(9484-9486)cAg>cGg p.Q3162R COADREAD 1 235884037 235884037 + Nonsense_Mutation SNP G G A TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr1:235884037G>A c.9484C>T c.(9484-9486)Cag>Tag p.Q3162* COADREAD 1 235884060 235884060 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr1:235884060C>T c.9461G>A c.(9460-9462)gGc>gAc p.G3154D COADREAD 1 235884120 235884120 + Nonsense_Mutation SNP A A C TCGA-AD-6888-01A-11D-1924-10 TCGA-AD-6888-10A-01D-1924-10 g.chr1:235884120A>C c.9401T>G c.(9400-9402)tTa>tGa p.L3134* COADREAD 1 235884128 235884128 + Silent SNP C C G TCGA-AA-3526-01A-02W-0831-10 TCGA-AA-3526-10A-01W-0831-10 g.chr1:235884128C>G c.9393G>C c.(9391-9393)ctG>ctC p.L3131L COADREAD 1 235887410 235887410 + Missense_Mutation SNP C C T TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr1:235887410C>T c.9233G>A c.(9232-9234)cGt>cAt p.R3078H COADREAD 1 235897871 235897871 + Missense_Mutation SNP A A G TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr1:235897871A>G c.8447T>C c.(8446-8448)cTg>cCg p.L2816P COADREAD 1 235907315 235907315 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr1:235907315A>C c.8115T>G c.(8113-8115)atT>atG p.I2705M COADREAD 1 235920623 235920623 + Silent SNP G G A TCGA-AG-3890-01A-01W-1073-09 TCGA-AG-3890-10A-01W-1073-09 g.chr1:235920623G>A c.7017C>T c.(7015-7017)ctC>ctT p.L2339L COADREAD 1 235920637 235920637 + Missense_Mutation SNP T T C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr1:235920637T>C c.7003A>G c.(7003-7005)Aca>Gca p.T2335A COADREAD 1 235922642 235922642 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr1:235922642C>T c.6511G>A c.(6511-6513)Gca>Aca p.A2171T COADREAD 1 235922694 235922694 + Silent SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr1:235922694G>A c.6459C>T c.(6457-6459)tcC>tcT p.S2153S COADREAD 1 235922805 235922805 + Silent SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr1:235922805C>T c.6348G>A c.(6346-6348)acG>acA p.T2116T COADREAD 1 235938333 235938333 + Missense_Mutation SNP T T C TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr1:235938333T>C c.5514A>G c.(5512-5514)atA>atG p.I1838M COADREAD 1 235938333 235938333 + Silent SNP T T G TCGA-D5-5539-01A-01D-1650-10 TCGA-D5-5539-10A-01D-1650-10 g.chr1:235938333T>G c.5514A>C c.(5512-5514)atA>atC p.I1838I COADREAD 1 235938335 235938335 + Missense_Mutation SNP T T C TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr1:235938335T>C c.5512A>G c.(5512-5514)Ata>Gta p.I1838V COADREAD 1 235940533 235940533 + Missense_Mutation SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr1:235940533C>A c.5290G>T c.(5290-5292)Ggt>Tgt p.G1764C COADREAD 1 235944202 235944202 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr1:235944202A>C c.5177T>G c.(5176-5178)tTt>tGt p.F1726C COADREAD 1 235950518 235950518 + Missense_Mutation SNP A A G TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr1:235950518A>G c.4844T>C c.(4843-4845)aTa>aCa p.I1615T COADREAD 1 235955020 235955020 + Missense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr1:235955020C>A c.4522G>T c.(4522-4524)Gat>Tat p.D1508Y COADREAD 1 235955345 235955345 + Silent SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:235955345T>C c.4197A>G c.(4195-4197)ttA>ttG p.L1399L COADREAD 1 235956857 235956857 + Silent SNP A A G TCGA-AD-6548-01A-11D-1835-10 TCGA-AD-6548-10A-01D-1835-10 g.chr1:235956857A>G c.4062T>C c.(4060-4062)tgT>tgC p.C1354C COADREAD 1 235969113 235969113 + Missense_Mutation SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr1:235969113G>A c.3323C>T c.(3322-3324)gCc>gTc p.A1108V COADREAD 1 235969311 235969311 + Missense_Mutation SNP G G C TCGA-CM-6167-01A-11D-1650-10 TCGA-CM-6167-10A-01D-1650-10 g.chr1:235969311G>C c.3125C>G c.(3124-3126)gCt>gGt p.A1042G COADREAD 1 235969317 235969317 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr1:235969317G>T c.3119C>A c.(3118-3120)tCt>tAt p.S1040Y COADREAD 1 235969412 235969412 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr1:235969412C>A c.3024G>T c.(3022-3024)gaG>gaT p.E1008D COADREAD 1 235969521 235969521 + Missense_Mutation SNP A A G TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr1:235969521A>G c.2915T>C c.(2914-2916)aTg>aCg p.M972T COADREAD 1 235969825 235969825 + Missense_Mutation SNP G G A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr1:235969825G>A c.2611C>T c.(2611-2613)Ctc>Ttc p.L871F COADREAD 1 235969925 235969925 + Silent SNP T T C TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr1:235969925T>C c.2511A>G c.(2509-2511)ccA>ccG p.P837P COADREAD 1 235969925 235969925 + Silent SNP T T C TCGA-D5-5539-01A-01D-1650-10 TCGA-D5-5539-10A-01D-1650-10 g.chr1:235969925T>C c.2511A>G c.(2509-2511)ccA>ccG p.P837P COADREAD 1 235969926 235969926 + Missense_Mutation SNP G G T TCGA-F5-6464-01A-11D-1733-10 TCGA-F5-6464-10A-01D-1733-10 g.chr1:235969926G>T c.2510C>A c.(2509-2511)cCa>cAa p.P837Q COADREAD 1 235969998 235969998 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr1:235969998C>T c.2438G>A c.(2437-2439)cGa>cAa p.R813Q COADREAD 1 235969998 235969998 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:235969998C>T c.2438G>A c.(2437-2439)cGa>cAa p.R813Q COADREAD 1 235970023 235970023 + Missense_Mutation SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr1:235970023C>T c.2413G>A c.(2413-2415)Gaa>Aaa p.E805K COADREAD 1 235971896 235971896 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr1:235971896C>T c.2222G>A c.(2221-2223)aGa>aAa p.R741K COADREAD 1 235972015 235972015 + Silent SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr1:235972015A>G c.2103T>C c.(2101-2103)ttT>ttC p.F701F COADREAD 1 235972336 235972336 + Silent SNP A A G TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr1:235972336A>G c.1782T>C c.(1780-1782)ccT>ccC p.P594P COADREAD 1 235972337 235972337 + Missense_Mutation SNP G G T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr1:235972337G>T c.1781C>A c.(1780-1782)cCt>cAt p.P594H COADREAD 1 235972351 235972351 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:235972351T>G c.1767A>C c.(1765-1767)aaA>aaC p.K589N COADREAD 1 235972459 235972459 + Silent SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr1:235972459A>G c.1659T>C c.(1657-1659)tgT>tgC p.C553C COADREAD 1 235972482 235972482 + Missense_Mutation SNP G G A TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr1:235972482G>A c.1636C>T c.(1636-1638)Cgg>Tgg p.R546W COADREAD 1 235972592 235972592 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr1:235972592A>C c.1526T>G c.(1525-1527)tTt>tGt p.F509C COADREAD 1 235972610 235972610 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:235972610C>T c.1508G>A c.(1507-1509)cGa>cAa p.R503Q COADREAD 1 235972904 235972904 + Missense_Mutation SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:235972904A>G c.1214T>C c.(1213-1215)tTg>tCg p.L405S COADREAD 1 235973040 235973040 + Missense_Mutation SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr1:235973040C>T c.1078G>A c.(1078-1080)Gct>Act p.A360T COADREAD 1 235973062 235973062 + Missense_Mutation SNP A A T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr1:235973062A>T c.1056T>A c.(1054-1056)aaT>aaA p.N352K COADREAD 1 235973133 235973133 + Nonsense_Mutation SNP G G A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr1:235973133G>A c.985C>T c.(985-987)Cga>Tga p.R329* COADREAD 1 235973133 235973133 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:235973133G>A c.985C>T c.(985-987)Cga>Tga p.R329* COADREAD 1 235973203 235973204 + Frame_Shift_Ins INS - - T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr1:235973203_235973204insT c.914_915insA c.(913-915)aacfs p.N305fs COADREAD 1 235973543 235973543 + Frame_Shift_Del DEL A A - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr1:235973543delA c.575delT c.(574-576)ttafs p.L192fs COADREAD 1 235973559 235973559 + Missense_Mutation SNP G G T TCGA-AA-3514-01A-02W-0831-10 TCGA-AA-3514-10A-01W-0831-10 g.chr1:235973559G>T c.559C>A c.(559-561)Ctg>Atg p.L187M COADREAD 1 235973720 235973720 + Missense_Mutation SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:235973720A>G c.398T>C c.(397-399)gTt>gCt p.V133A DLBC 1 235887393 235887393 + Missense_Mutation SNP C C T TCGA-GR-7351-01A-11D-2210-10 TCGA-GR-7351-10A-01D-2210-10 g.chr1:235887393C>T c.9250G>A c.(9250-9252)Gat>Aat p.D3084N DLBC 1 235907279 235907279 + Splice_Site SNP A A G TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr1:235907279A>G c.8151T>C c.(8149-8151)atT>atC p.I2717I DLBC 1 235918870 235918870 + Silent SNP T T G TCGA-GR-7351-01A-11D-2210-10 TCGA-GR-7351-10A-01D-2210-10 g.chr1:235918870T>G c.7137A>C c.(7135-7137)ctA>ctC p.L2379L DLBC 1 235933535 235933535 + Missense_Mutation SNP C C G TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr1:235933535C>G c.5847G>C c.(5845-5847)caG>caC p.Q1949H DLBC 1 235955276 235955276 + Silent SNP G G T TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr1:235955276G>T c.4266C>A c.(4264-4266)gcC>gcA p.A1422A DLBC 1 235966354 235966354 + Missense_Mutation SNP G G C TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr1:235966354G>C c.3566C>G c.(3565-3567)tCt>tGt p.S1189C DLBC 1 235971802 235971802 + Silent SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr1:235971802G>A c.2316C>T c.(2314-2316)gaC>gaT p.D772D ESCA 1 235827307 235827307 + Silent SNP G G A TCGA-L5-A4OU-01A-11D-A28B-09 TCGA-L5-A4OU-11A-11D-A28E-09 g.chr1:235827307G>A c.11244C>T c.(11242-11244)ccC>ccT p.P3748P ESCA 1 235860435 235860435 + Missense_Mutation SNP G G C TCGA-VR-A8EP-01A-31D-A403-09 TCGA-VR-A8EP-10B-01D-A403-09 g.chr1:235860435G>C c.10512C>G c.(10510-10512)atC>atG p.I3504M ESCA 1 235878571 235878571 + Silent SNP G G T TCGA-JY-A6F8-01A-11D-A33E-09 TCGA-JY-A6F8-10A-01D-A33H-09 g.chr1:235878571G>T c.9714C>A c.(9712-9714)tcC>tcA p.S3238S ESCA 1 235896893 235896893 + Frame_Shift_Del DEL T T - TCGA-L5-A8NF-01A-11D-A37C-09 TCGA-L5-A8NF-11A-11D-A37F-09 g.chr1:235896893delT c.8711delA c.(8710-8712)aagfs p.K2904fs ESCA 1 235897834 235897834 + Nonsense_Mutation SNP G G T TCGA-IG-A4P3-01A-11D-A27G-09 TCGA-IG-A4P3-10A-01D-A27G-09 g.chr1:235897834G>T c.8484C>A c.(8482-8484)tgC>tgA p.C2828* ESCA 1 235897834 235897834 + Nonsense_Mutation SNP G G T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr1:235897834G>T c.8484C>A c.(8482-8484)tgC>tgA p.C2828* ESCA 1 235914600 235914600 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr1:235914600C>T c.7690G>A c.(7690-7692)Gca>Aca p.A2564T ESCA 1 235918868 235918868 + Missense_Mutation SNP G G T TCGA-L5-A4OH-01A-11D-A27G-09 TCGA-L5-A4OH-11A-11D-A27G-09 g.chr1:235918868G>T c.7139C>A c.(7138-7140)gCc>gAc p.A2380D ESCA 1 235922855 235922855 + Missense_Mutation SNP T T C TCGA-LN-A4MR-01A-11D-A28B-09 TCGA-LN-A4MR-10A-01D-A28E-09 g.chr1:235922855T>C c.6298A>G c.(6298-6300)Atg>Gtg p.M2100V ESCA 1 235972611 235972611 + Nonsense_Mutation SNP G G A TCGA-S8-A6BV-01A-21D-A31U-09 TCGA-S8-A6BV-10A-01D-A31U-09 g.chr1:235972611G>A c.1507C>T c.(1507-1509)Cga>Tga p.R503* ESCA 1 235972743 235972743 + Missense_Mutation SNP C C G TCGA-LN-A4A6-01A-11D-A27G-09 TCGA-LN-A4A6-10A-01D-A27G-09 g.chr1:235972743C>G c.1375G>C c.(1375-1377)Gat>Cat p.D459H ESCA 1 235976294 235976294 + Missense_Mutation SNP G G A TCGA-L5-A8NL-01A-12D-A37C-09 TCGA-L5-A8NL-11A-12D-A37F-09 g.chr1:235976294G>A c.260C>T c.(259-261)cCt>cTt p.P87L GBM 1 235860518 235860518 + Missense_Mutation SNP T T C TCGA-12-0619-01A-01D-1492-08 TCGA-12-0619-10A-01D-1492-08 g.chr1:235860518T>C c.10429A>G c.(10429-10431)Agt>Ggt p.S3477G GBM 1 235866229 235866229 + Nonsense_Mutation SNP G G A TCGA-12-3649-01A-01D-1495-08 TCGA-12-3649-10A-01D-1495-08 g.chr1:235866229G>A c.10192C>T c.(10192-10194)Cga>Tga p.R3398* GBM 1 235866238 235866238 + Missense_Mutation SNP C C T TCGA-14-4157-01A-01D-1353-08 TCGA-14-4157-10A-01D-1353-08 g.chr1:235866238C>T c.10183G>A c.(10183-10185)Gtt>Att p.V3395I GBM 1 235922440 235922440 + Missense_Mutation SNP C C T TCGA-26-5132-01A-01D-1486-08 TCGA-26-5132-10A-01D-1486-08 g.chr1:235922440C>T c.6713G>A c.(6712-6714)cGa>cAa p.R2238Q GBM 1 235940405 235940405 + Silent SNP G G A TCGA-06-0214-01A-02D-1491-08 TCGA-06-0214-10A-01D-1491-08 g.chr1:235940405G>A c.5418C>T c.(5416-5418)caC>caT p.H1806H GBM 1 235969724 235969724 + Silent SNP C C T TCGA-06-0168-01A-01D-1491-08 TCGA-06-0168-10A-01D-1491-08 g.chr1:235969724C>T c.2712G>A c.(2710-2712)gtG>gtA p.V904V GBM 1 235993676 235993676 + Silent SNP G G A TCGA-32-1982-01A-01D-1494-08 TCGA-32-1982-10A-01D-1494-08 g.chr1:235993676G>A c.42C>T c.(40-42)acC>acT p.T14T GBMLGG 1 235827839 235827839 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235827839G>A c.11121C>T c.(11119-11121)tcC>tcT p.S3707S GBMLGG 1 235860518 235860518 + Missense_Mutation SNP T T C TCGA-12-0619-01A-01D-1492-08 TCGA-12-0619-10A-01D-1492-08 g.chr1:235860518T>C c.10429A>G c.(10429-10431)Agt>Ggt p.S3477G GBMLGG 1 235866229 235866229 + Nonsense_Mutation SNP G G A TCGA-12-3649-01A-01D-1495-08 TCGA-12-3649-10A-01D-1495-08 g.chr1:235866229G>A c.10192C>T c.(10192-10194)Cga>Tga p.R3398* GBMLGG 1 235866238 235866238 + Missense_Mutation SNP C C T TCGA-14-4157-01A-01D-1353-08 TCGA-14-4157-10A-01D-1353-08 g.chr1:235866238C>T c.10183G>A c.(10183-10185)Gtt>Att p.V3395I GBMLGG 1 235922440 235922440 + Missense_Mutation SNP C C T TCGA-26-5132-01A-01D-1486-08 TCGA-26-5132-10A-01D-1486-08 g.chr1:235922440C>T c.6713G>A c.(6712-6714)cGa>cAa p.R2238Q GBMLGG 1 235922652 235922652 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235922652G>T c.6501C>A c.(6499-6501)agC>agA p.S2167R GBMLGG 1 235922740 235922740 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235922740G>T c.6413C>A c.(6412-6414)aCt>aAt p.T2138N GBMLGG 1 235926125 235926125 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235926125G>A c.6148C>T c.(6148-6150)Cgg>Tgg p.R2050W GBMLGG 1 235929502 235929502 + Missense_Mutation SNP G G A TCGA-QH-A6CY-01A-11D-A32B-08 TCGA-QH-A6CY-10A-01D-A329-08 g.chr1:235929502G>A c.5998C>T c.(5998-6000)Ctt>Ttt p.L2000F GBMLGG 1 235929518 235929518 + Silent SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235929518T>C c.5982A>G c.(5980-5982)aaA>aaG p.K1994K GBMLGG 1 235940405 235940405 + Silent SNP G G A TCGA-06-0214-01A-02D-1491-08 TCGA-06-0214-10A-01D-1491-08 g.chr1:235940405G>A c.5418C>T c.(5416-5418)caC>caT p.H1806H GBMLGG 1 235950608 235950608 + Missense_Mutation SNP T T C TCGA-S9-A6WH-01A-12D-A33T-08 TCGA-S9-A6WH-10A-01D-A33W-08 g.chr1:235950608T>C c.4754A>G c.(4753-4755)aAt>aGt p.N1585S GBMLGG 1 235964233 235964233 + Missense_Mutation SNP A A C TCGA-DU-7299-01A-21D-2024-08 TCGA-DU-7299-10A-01D-2024-08 g.chr1:235964233A>C c.3877T>G c.(3877-3879)Ttt>Gtt p.F1293V GBMLGG 1 235969400 235969400 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235969400C>A c.3036G>T c.(3034-3036)aaG>aaT p.K1012N GBMLGG 1 235969487 235969487 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235969487C>T c.2949G>A c.(2947-2949)agG>agA p.R983R GBMLGG 1 235969724 235969724 + Silent SNP C C T TCGA-06-0168-01A-01D-1491-08 TCGA-06-0168-10A-01D-1491-08 g.chr1:235969724C>T c.2712G>A c.(2710-2712)gtG>gtA p.V904V GBMLGG 1 235972444 235972444 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235972444C>T c.1674G>A c.(1672-1674)ttG>ttA p.L558L GBMLGG 1 235973133 235973133 + Nonsense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235973133G>A c.985C>T c.(985-987)Cga>Tga p.R329* GBMLGG 1 235993676 235993676 + Silent SNP G G A TCGA-32-1982-01A-01D-1494-08 TCGA-32-1982-10A-01D-1494-08 g.chr1:235993676G>A c.42C>T c.(40-42)acC>acT p.T14T HNSC 1 235827826 235827826 + Missense_Mutation SNP T T C TCGA-CV-6954-01A-11D-1912-08 TCGA-CV-6954-10A-01D-1912-08 g.chr1:235827826T>C c.11134A>G c.(11134-11136)Aac>Gac p.N3712D HNSC 1 235850334 235850334 + Missense_Mutation SNP G G A TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chr1:235850334G>A c.10715C>T c.(10714-10716)gCt>gTt p.A3572V HNSC 1 235860530 235860530 + Missense_Mutation SNP C C T TCGA-CX-7082-01A-11D-2012-08 TCGA-CX-7082-10A-01D-2013-08 g.chr1:235860530C>T c.10417G>A c.(10417-10419)Gtg>Atg p.V3473M HNSC 1 235866193 235866193 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr1:235866193T>C c.10228A>G c.(10228-10230)Act>Gct p.T3410A HNSC 1 235904812 235904812 + Silent SNP G G A TCGA-CV-7250-01A-11D-2012-08 TCGA-CV-7250-10A-01D-2013-08 g.chr1:235904812G>A c.8268C>T c.(8266-8268)caC>caT p.H2756H HNSC 1 235904814 235904814 + Missense_Mutation SNP G G A TCGA-CR-6478-01A-11D-1870-08 TCGA-CR-6478-10A-01D-1870-08 g.chr1:235904814G>A c.8266C>T c.(8266-8268)Cac>Tac p.H2756Y HNSC 1 235915332 235915332 + Nonsense_Mutation SNP G G A TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr1:235915332G>A c.7600C>T c.(7600-7602)Caa>Taa p.Q2534* HNSC 1 235915397 235915397 + Missense_Mutation SNP C C T TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr1:235915397C>T c.7535G>A c.(7534-7536)tGc>tAc p.C2512Y HNSC 1 235915445 235915445 + Missense_Mutation SNP A A G TCGA-CN-5373-01A-01D-1434-08 TCGA-CN-5373-10A-01D-1434-08 g.chr1:235915445A>G c.7487T>C c.(7486-7488)cTt>cCt p.L2496P HNSC 1 235922444 235922444 + Nonsense_Mutation SNP G G A TCGA-CQ-A4CD-01A-21D-A25D-08 TCGA-CQ-A4CD-10A-01D-A25E-08 g.chr1:235922444G>A c.6709C>T c.(6709-6711)Cag>Tag p.Q2237* HNSC 1 235922480 235922480 + Missense_Mutation SNP G G A TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr1:235922480G>A c.6673C>T c.(6673-6675)Cgc>Tgc p.R2225C HNSC 1 235933543 235933543 + Missense_Mutation SNP G G C TCGA-CV-A45Q-01A-11D-A24D-08 TCGA-CV-A45Q-10A-01D-A24F-08 g.chr1:235933543G>C c.5839C>G c.(5839-5841)Cac>Gac p.H1947D HNSC 1 235940477 235940477 + Silent SNP G G A TCGA-CR-7401-01A-11D-2012-08 TCGA-CR-7401-10A-01D-2013-08 g.chr1:235940477G>A c.5346C>T c.(5344-5346)agC>agT p.S1782S HNSC 1 235945231 235945231 + Missense_Mutation SNP G G T TCGA-CN-A6UY-01A-12D-A34J-08 TCGA-CN-A6UY-10B-01D-A34M-08 g.chr1:235945231G>T c.5019C>A c.(5017-5019)ttC>ttA p.F1673L HNSC 1 235952058 235952058 + Missense_Mutation SNP G G T TCGA-BA-7269-01A-11D-2012-08 TCGA-BA-7269-10A-01D-2013-08 g.chr1:235952058G>T c.4631C>A c.(4630-4632)tCc>tAc p.S1544Y HNSC 1 235964315 235964327 + Frame_Shift_Del DEL TTCCCCTTGAGTG TTCCCCTTGAGTG - TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr1:235964315_235964327delTTCCCCTTGAGTG c.3783_3795delCACTCAAGGGGAA c.(3781-3795)ctcactcaaggggaafs p.LTQGE1261fs HNSC 1 235966293 235966293 + Silent SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr1:235966293A>G c.3627T>C c.(3625-3627)tgT>tgC p.C1209C HNSC 1 235969554 235969554 + Missense_Mutation SNP G G C TCGA-F7-A622-01A-11D-A28R-08 TCGA-F7-A622-10A-01D-A28U-08 g.chr1:235969554G>C c.2882C>G c.(2881-2883)gCa>gGa p.A961G HNSC 1 235972380 235972385 + In_Frame_Del DEL TGTTAT TGTTAT - TCGA-CV-7177-01A-11D-2012-08 TCGA-CV-7177-10A-01D-2013-08 g.chr1:235972380_235972385delTGTTAT c.1733_1738delATAACA c.(1732-1740)cataacatt>ctt p.578_580HNI>L HNSC 1 235972988 235972988 + Missense_Mutation SNP C C G TCGA-BB-4223-01A-01D-1434-08 TCGA-BB-4223-10A-01D-1434-08 g.chr1:235972988C>G c.1130G>C c.(1129-1131)aGa>aCa p.R377T HNSC 1 235972999 235972999 + Silent SNP A A G TCGA-D6-6515-01A-21D-1870-08 TCGA-D6-6515-10A-01D-1870-08 g.chr1:235972999A>G c.1119T>C c.(1117-1119)ccT>ccC p.P373P HNSC 1 235973499 235973499 + Missense_Mutation SNP G G A TCGA-CQ-7068-01A-11D-2078-08 TCGA-CQ-7068-10A-01D-2078-08 g.chr1:235973499G>A c.619C>T c.(619-621)Cgc>Tgc p.R207C HNSC 1 235973763 235973763 + Missense_Mutation SNP G G T TCGA-CQ-A4C6-01A-11D-A25D-08 TCGA-CQ-A4C6-10A-01D-A25E-08 g.chr1:235973763G>T c.355C>A c.(355-357)Cag>Aag p.Q119K HNSC 1 235993528 235993528 + Nonsense_Mutation SNP G G A TCGA-P3-A6T3-01A-11D-A34J-08 TCGA-P3-A6T3-10A-01D-A34M-08 g.chr1:235993528G>A c.190C>T c.(190-192)Cag>Tag p.Q64* HNSC 1 235993708 235993708 + Missense_Mutation SNP C C T TCGA-CV-A6JO-01B-11D-A34J-08 TCGA-CV-A6JO-10A-01D-A34M-08 g.chr1:235993708C>T c.10G>A c.(10-12)Gac>Aac p.D4N KICH 1 235964396 235964396 + Splice_Site SNP C C T TCGA-KL-8343-01A-11D-2310-10 TCGA-KL-8343-11A-01D-2310-10 g.chr1:235964396C>T c.3714G>A c.(3712-3714)ggG>ggA p.G1238G KIPAN 1 235827769 235827769 + Missense_Mutation SNP C C A TCGA-MH-A857-01A-11D-A34Z-10 TCGA-MH-A857-10A-01D-A34Z-10 g.chr1:235827769C>A c.11191G>T c.(11191-11193)Gta>Tta p.V3731L KIPAN 1 235872510 235872510 + Missense_Mutation SNP G G A TCGA-HE-A5NL-01A-11D-A26P-10 TCGA-HE-A5NL-10A-01D-A26P-10 g.chr1:235872510G>A c.10024C>T c.(10024-10026)Cgg>Tgg p.R3342W KIPAN 1 235884146 235884146 + Silent SNP A A G TCGA-CZ-4865-01A-02D-1501-10 TCGA-CZ-4865-11A-01D-1501-10 g.chr1:235884146A>G c.9375T>C c.(9373-9375)taT>taC p.Y3125Y KIPAN 1 235884164 235884164 + Silent SNP G G A TCGA-MH-A55Z-01A-11D-A26P-10 TCGA-MH-A55Z-10A-01D-A26P-10 g.chr1:235884164G>A c.9357C>T c.(9355-9357)ctC>ctT p.L3119L KIPAN 1 235894212 235894212 + Missense_Mutation SNP A A C TCGA-B0-5088-01A-01D-1462-08 TCGA-B0-5088-11A-01D-1462-08 g.chr1:235894212A>C c.8979T>G c.(8977-8979)ttT>ttG p.F2993L KIPAN 1 235904811 235904811 + Missense_Mutation SNP C C T TCGA-SX-A7SL-01A-11D-A34Z-10 TCGA-SX-A7SL-10A-01D-A34Z-10 g.chr1:235904811C>T c.8269G>A c.(8269-8271)Gct>Act p.A2757T KIPAN 1 235904825 235904825 + Missense_Mutation SNP A A C TCGA-CJ-4873-01A-01D-1373-10 TCGA-CJ-4873-11A-01D-1373-10 g.chr1:235904825A>C c.8255T>G c.(8254-8256)tTg>tGg p.L2752W KIPAN 1 235907322 235907322 + Missense_Mutation SNP T T C TCGA-BP-4782-01A-02D-1421-08 TCGA-BP-4782-11A-01D-1421-08 g.chr1:235907322T>C c.8108A>G c.(8107-8109)aAa>aGa p.K2703R KIPAN 1 235918806 235918806 + Missense_Mutation SNP A A C TCGA-BP-5191-01A-01D-1429-08 TCGA-BP-5191-11A-01D-1429-08 g.chr1:235918806A>C c.7201T>G c.(7201-7203)Ttt>Gtt p.F2401V KIPAN 1 235918888 235918889 + Frame_Shift_Ins INS - - T TCGA-CJ-4640-01A-02D-1386-10 TCGA-CJ-4640-11A-01D-1251-10 g.chr1:235918888_235918889insT c.7118_7119insA c.(7117-7119)aatfs p.N2373fs KIPAN 1 235922372 235922372 + Missense_Mutation SNP G G A TCGA-A3-3322-01A-01W-0886-08 TCGA-A3-3322-11A-01D-0966-08 g.chr1:235922372G>A c.6781C>T c.(6781-6783)Cgt>Tgt p.R2261C KIPAN 1 235944201 235944201 + Frame_Shift_Del DEL A A - TCGA-BP-4976-01A-01D-1462-08 TCGA-BP-4976-11A-01D-1462-08 g.chr1:235944201delA c.5178delT c.(5176-5178)tttfs p.F1726fs KIPAN 1 235950642 235950643 + Frame_Shift_Ins INS - - T TCGA-CJ-6028-01A-11D-1669-08 TCGA-CJ-6028-11A-01D-1669-08 g.chr1:235950642_235950643insT c.4719_4720insA c.(4717-4722)aaagctfs p.A1574fs KIPAN 1 235964396 235964396 + Splice_Site SNP C C T TCGA-KL-8343-01A-11D-2310-10 TCGA-KL-8343-11A-01D-2310-10 g.chr1:235964396C>T c.3714G>A c.(3712-3714)ggG>ggA p.G1238G KIPAN 1 235969775 235969775 + Silent SNP C C T TCGA-CJ-5672-01A-11D-1534-10 TCGA-CJ-5672-11A-01D-1534-10 g.chr1:235969775C>T c.2661G>A c.(2659-2661)aaG>aaA p.K887K KIPAN 1 235969849 235969849 + Missense_Mutation SNP C C T TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr1:235969849C>T c.2587G>A c.(2587-2589)Gct>Act p.A863T KIPAN 1 235971939 235971939 + Nonsense_Mutation SNP G G A TCGA-CZ-5452-01A-01D-1501-10 TCGA-CZ-5452-11A-01D-1501-10 g.chr1:235971939G>A c.2179C>T c.(2179-2181)Cag>Tag p.Q727* KIRC 1 235884146 235884146 + Silent SNP A A G TCGA-CZ-4865-01A-02D-1501-10 TCGA-CZ-4865-11A-01D-1501-10 g.chr1:235884146A>G c.9375T>C c.(9373-9375)taT>taC p.Y3125Y KIRC 1 235894212 235894212 + Missense_Mutation SNP A A C TCGA-B0-5088-01A-01D-1462-08 TCGA-B0-5088-11A-01D-1462-08 g.chr1:235894212A>C c.8979T>G c.(8977-8979)ttT>ttG p.F2993L KIRC 1 235904825 235904825 + Missense_Mutation SNP A A C TCGA-CJ-4873-01A-01D-1373-10 TCGA-CJ-4873-11A-01D-1373-10 g.chr1:235904825A>C c.8255T>G c.(8254-8256)tTg>tGg p.L2752W KIRC 1 235907322 235907322 + Missense_Mutation SNP T T C TCGA-BP-4782-01A-02D-1421-08 TCGA-BP-4782-11A-01D-1421-08 g.chr1:235907322T>C c.8108A>G c.(8107-8109)aAa>aGa p.K2703R KIRC 1 235918806 235918806 + Missense_Mutation SNP A A C TCGA-BP-5191-01A-01D-1429-08 TCGA-BP-5191-11A-01D-1429-08 g.chr1:235918806A>C c.7201T>G c.(7201-7203)Ttt>Gtt p.F2401V KIRC 1 235918888 235918889 + Frame_Shift_Ins INS - - T TCGA-CJ-4640-01A-02D-1386-10 TCGA-CJ-4640-11A-01D-1251-10 g.chr1:235918888_235918889insT c.7118_7119insA c.(7117-7119)aatfs p.N2373fs KIRC 1 235922372 235922372 + Missense_Mutation SNP G G A TCGA-A3-3322-01A-01W-0886-08 TCGA-A3-3322-11A-01D-0966-08 g.chr1:235922372G>A c.6781C>T c.(6781-6783)Cgt>Tgt p.R2261C KIRC 1 235944201 235944201 + Frame_Shift_Del DEL A A - TCGA-BP-4976-01A-01D-1462-08 TCGA-BP-4976-11A-01D-1462-08 g.chr1:235944201delA c.5178delT c.(5176-5178)tttfs p.F1726fs KIRC 1 235950642 235950643 + Frame_Shift_Ins INS - - T TCGA-CJ-6028-01A-11D-1669-08 TCGA-CJ-6028-11A-01D-1669-08 g.chr1:235950642_235950643insT c.4719_4720insA c.(4717-4722)aaagctfs p.A1574fs KIRC 1 235969775 235969775 + Silent SNP C C T TCGA-CJ-5672-01A-11D-1534-10 TCGA-CJ-5672-11A-01D-1534-10 g.chr1:235969775C>T c.2661G>A c.(2659-2661)aaG>aaA p.K887K KIRC 1 235971939 235971939 + Nonsense_Mutation SNP G G A TCGA-CZ-5452-01A-01D-1501-10 TCGA-CZ-5452-11A-01D-1501-10 g.chr1:235971939G>A c.2179C>T c.(2179-2181)Cag>Tag p.Q727* KIRP 1 235827769 235827769 + Missense_Mutation SNP C C A TCGA-MH-A857-01A-11D-A34Z-10 TCGA-MH-A857-10A-01D-A34Z-10 g.chr1:235827769C>A c.11191G>T c.(11191-11193)Gta>Tta p.V3731L KIRP 1 235872510 235872510 + Missense_Mutation SNP G G A TCGA-HE-A5NL-01A-11D-A26P-10 TCGA-HE-A5NL-10A-01D-A26P-10 g.chr1:235872510G>A c.10024C>T c.(10024-10026)Cgg>Tgg p.R3342W KIRP 1 235884164 235884164 + Silent SNP G G A TCGA-MH-A55Z-01A-11D-A26P-10 TCGA-MH-A55Z-10A-01D-A26P-10 g.chr1:235884164G>A c.9357C>T c.(9355-9357)ctC>ctT p.L3119L KIRP 1 235904811 235904811 + Missense_Mutation SNP C C T TCGA-SX-A7SL-01A-11D-A34Z-10 TCGA-SX-A7SL-10A-01D-A34Z-10 g.chr1:235904811C>T c.8269G>A c.(8269-8271)Gct>Act p.A2757T KIRP 1 235969849 235969849 + Missense_Mutation SNP C C T TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr1:235969849C>T c.2587G>A c.(2587-2589)Gct>Act p.A863T LGG 1 235827839 235827839 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235827839G>A c.11121C>T c.(11119-11121)tcC>tcT p.S3707S LGG 1 235922652 235922652 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235922652G>T c.6501C>A c.(6499-6501)agC>agA p.S2167R LGG 1 235922740 235922740 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235922740G>T c.6413C>A c.(6412-6414)aCt>aAt p.T2138N LGG 1 235926125 235926125 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235926125G>A c.6148C>T c.(6148-6150)Cgg>Tgg p.R2050W LGG 1 235929502 235929502 + Missense_Mutation SNP G G A TCGA-QH-A6CY-01A-11D-A32B-08 TCGA-QH-A6CY-10A-01D-A329-08 g.chr1:235929502G>A c.5998C>T c.(5998-6000)Ctt>Ttt p.L2000F LGG 1 235929518 235929518 + Silent SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235929518T>C c.5982A>G c.(5980-5982)aaA>aaG p.K1994K LGG 1 235950608 235950608 + Missense_Mutation SNP T T C TCGA-S9-A6WH-01A-12D-A33T-08 TCGA-S9-A6WH-10A-01D-A33W-08 g.chr1:235950608T>C c.4754A>G c.(4753-4755)aAt>aGt p.N1585S LGG 1 235964233 235964233 + Missense_Mutation SNP A A C TCGA-DU-7299-01A-21D-2024-08 TCGA-DU-7299-10A-01D-2024-08 g.chr1:235964233A>C c.3877T>G c.(3877-3879)Ttt>Gtt p.F1293V LGG 1 235969400 235969400 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235969400C>A c.3036G>T c.(3034-3036)aaG>aaT p.K1012N LGG 1 235969487 235969487 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235969487C>T c.2949G>A c.(2947-2949)agG>agA p.R983R LGG 1 235972444 235972444 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235972444C>T c.1674G>A c.(1672-1674)ttG>ttA p.L558L LGG 1 235973133 235973133 + Nonsense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:235973133G>A c.985C>T c.(985-987)Cga>Tga p.R329* LIHC 1 235860518 235860519 + Frame_Shift_Ins INS - - G TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr1:235860518_235860519insG c.10428_10429insC c.(10426-10431)cccagtfs p.S3477fs LIHC 1 235880039 235880039 + Frame_Shift_Del DEL T T - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr1:235880039delT c.9600delA c.(9598-9600)aaafs p.K3200fs LIHC 1 235887447 235887447 + Frame_Shift_Del DEL A A - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr1:235887447delA c.9196delT c.(9196-9198)tccfs p.S3066fs LIHC 1 235892901 235892901 + Missense_Mutation SNP A A G TCGA-WX-AA44-01A-11D-A38X-10 TCGA-WX-AA44-10A-01D-A38X-10 g.chr1:235892901A>G c.9101T>C c.(9100-9102)tTa>tCa p.L3034S LIHC 1 235897870 235897870 + Silent SNP C C A TCGA-DD-AADN-01A-11D-A40R-10 TCGA-DD-AADN-10A-01D-A40U-10 g.chr1:235897870C>A c.8448G>T c.(8446-8448)ctG>ctT p.L2816L LIHC 1 235915327 235915327 + Silent SNP A A G TCGA-DD-A73B-01A-12D-A32G-10 TCGA-DD-A73B-10A-01D-A32G-10 g.chr1:235915327A>G c.7605T>C c.(7603-7605)aaT>aaC p.N2535N LIHC 1 235916449 235916451 + In_Frame_Del DEL AGA AGA - TCGA-DD-AADR-01A-11D-A40R-10 TCGA-DD-AADR-10A-01D-A40U-10 g.chr1:235916449_235916451delAGA c.7353_7355delTCT c.(7351-7356)cttctc>ctc p.2451_2452LL>L LIHC 1 235922305 235922305 + Missense_Mutation SNP T T C TCGA-BC-A10W-01A-11D-A12Z-10 TCGA-BC-A10W-11A-11D-A12Z-10 g.chr1:235922305T>C c.6848A>G c.(6847-6849)gAg>gGg p.E2283G LIHC 1 235922871 235922871 + Silent SNP T T C TCGA-DD-AAE3-01A-11D-A40R-10 TCGA-DD-AAE3-10A-01D-A40U-10 g.chr1:235922871T>C c.6282A>G c.(6280-6282)caA>caG p.Q2094Q LIHC 1 235937265 235937265 + Missense_Mutation SNP T T A TCGA-G3-A3CH-01A-11D-A22F-10 TCGA-G3-A3CH-11A-11D-A22F-10 g.chr1:235937265T>A c.5661A>T c.(5659-5661)gaA>gaT p.E1887D LIHC 1 235940366 235940366 + Silent SNP G G A TCGA-DD-A4NH-01A-11D-A27I-10 TCGA-DD-A4NH-10A-01D-A27I-10 g.chr1:235940366G>A c.5457C>T c.(5455-5457)gcC>gcT p.A1819A LIHC 1 235945311 235945311 + Missense_Mutation SNP T T C TCGA-CC-A3MB-01A-11D-A20W-10 TCGA-CC-A3MB-10A-01D-A20W-10 g.chr1:235945311T>C c.4939A>G c.(4939-4941)Atg>Gtg p.M1647V LIHC 1 235955183 235955183 + Missense_Mutation SNP T T C TCGA-DD-AACJ-01A-11D-A40R-10 TCGA-DD-AACJ-10A-01D-A40U-10 g.chr1:235955183T>C c.4359A>G c.(4357-4359)atA>atG p.I1453M LIHC 1 235955200 235955200 + Missense_Mutation SNP G G C TCGA-RC-A7S9-01A-11D-A33Q-10 TCGA-RC-A7S9-10A-02D-A33Q-10 g.chr1:235955200G>C c.4342C>G c.(4342-4344)Ctt>Gtt p.L1448V LIHC 1 235964220 235964220 + Frame_Shift_Del DEL A A - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr1:235964220delA c.3890delT c.(3889-3891)ttgfs p.L1297fs LIHC 1 235964399 235964399 + Splice_Site SNP T T A TCGA-G3-A5SJ-01A-11D-A27I-10 TCGA-G3-A5SJ-10A-01D-A27I-10 g.chr1:235964399T>A c.e9-2 LIHC 1 235973623 235973623 + Silent SNP G G T TCGA-DD-A4NQ-01A-21D-A28X-10 TCGA-DD-A4NQ-10A-01D-A28X-10 g.chr1:235973623G>T c.495C>A c.(493-495)acC>acA p.T165T LUAD 1 235826260 235826260 + Missense_Mutation SNP T T C TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr1:235826260T>C c.11386A>G c.(11386-11388)Agc>Ggc p.S3796G LUAD 1 235826344 235826344 + Missense_Mutation SNP T T C TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr1:235826344T>C c.11302A>G c.(11302-11304)Aca>Gca p.T3768A LUAD 1 235826359 235826359 + Missense_Mutation SNP C C A TCGA-55-8510-01A-11D-2393-08 TCGA-55-8510-10A-01D-2393-08 g.chr1:235826359C>A c.11287G>T c.(11287-11289)Ggc>Tgc p.G3763C LUAD 1 235827894 235827894 + Missense_Mutation SNP C C A TCGA-17-Z049-01A-01W-0746-08 TCGA-17-Z049-11A-01W-0747-08 g.chr1:235827894C>A c.11066G>T c.(11065-11067)tGg>tTg p.W3689L LUAD 1 235840794 235840794 + Silent SNP T T A TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr1:235840794T>A c.10926A>T c.(10924-10926)atA>atT p.I3642I LUAD 1 235840796 235840796 + Missense_Mutation SNP T T G TCGA-95-8039-01A-11D-2238-08 TCGA-95-8039-10A-01D-2238-08 g.chr1:235840796T>G c.10924A>C c.(10924-10926)Ata>Cta p.I3642L LUAD 1 235850271 235850271 + Missense_Mutation SNP G G T TCGA-62-8399-01A-21D-2323-08 TCGA-62-8399-10A-01D-2323-08 g.chr1:235850271G>T c.10778C>A c.(10777-10779)aCa>aAa p.T3593K LUAD 1 235850271 235850271 + Missense_Mutation SNP G G T TCGA-91-6835-01A-11D-1855-08 TCGA-91-6835-11A-01D-1855-08 g.chr1:235850271G>T c.10778C>A c.(10777-10779)aCa>aAa p.T3593K LUAD 1 235860531 235860531 + Silent SNP G G A TCGA-50-5941-01A-11D-1753-08 TCGA-50-5941-10A-01D-1753-08 g.chr1:235860531G>A c.10416C>T c.(10414-10416)taC>taT p.Y3472Y LUAD 1 235860540 235860540 + Missense_Mutation SNP C C A TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr1:235860540C>A c.10407G>T c.(10405-10407)tgG>tgT p.W3469C LUAD 1 235866047 235866047 + Splice_Site SNP C C G TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr1:235866047C>G c.10374G>C c.(10372-10374)ccG>ccC p.P3458P LUAD 1 235878548 235878548 + Missense_Mutation SNP A A G TCGA-86-8674-01A-21D-2393-08 TCGA-86-8674-10A-01D-2393-08 g.chr1:235878548A>G c.9737T>C c.(9736-9738)tTc>tCc p.F3246S LUAD 1 235878603 235878603 + Missense_Mutation SNP C C A TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chr1:235878603C>A c.9682G>T c.(9682-9684)Gtg>Ttg p.V3228L LUAD 1 235883977 235883977 + Missense_Mutation SNP C C G TCGA-44-7662-01A-11D-2063-08 TCGA-44-7662-10A-01D-2063-08 g.chr1:235883977C>G c.9544G>C c.(9544-9546)Gat>Cat p.D3182H LUAD 1 235894397 235894397 + Missense_Mutation SNP C C A TCGA-05-5425-01A-02D-1625-08 TCGA-05-5425-10A-01D-1625-08 g.chr1:235894397C>A c.8882G>T c.(8881-8883)cGt>cTt p.R2961L LUAD 1 235896917 235896917 + Missense_Mutation SNP A A T TCGA-95-7562-01A-11D-2238-08 TCGA-95-7562-10B-01D-2238-08 g.chr1:235896917A>T c.8687T>A c.(8686-8688)cTc>cAc p.L2896H LUAD 1 235897896 235897896 + Missense_Mutation SNP C C T TCGA-44-A47A-01A-21D-A24D-08 TCGA-44-A47A-10A-01D-A24F-08 g.chr1:235897896C>T c.8422G>A c.(8422-8424)Gaa>Aaa p.E2808K LUAD 1 235904858 235904858 + Missense_Mutation SNP C C G TCGA-17-Z015-01A-01W-0746-08 TCGA-17-Z015-11A-01W-0746-08 g.chr1:235904858C>G c.8222G>C c.(8221-8223)cGa>cCa p.R2741P LUAD 1 235907394 235907394 + Missense_Mutation SNP G G A TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr1:235907394G>A c.8036C>T c.(8035-8037)tCa>tTa p.S2679L LUAD 1 235909637 235909637 + Splice_Site SNP T T G TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr1:235909637T>G c.7971A>C c.(7969-7971)caA>caC p.Q2657H LUAD 1 235914598 235914598 + Silent SNP T T A TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chr1:235914598T>A c.7692A>T c.(7690-7692)gcA>gcT p.A2564A LUAD 1 235915417 235915417 + Missense_Mutation SNP T T C TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr1:235915417T>C c.7515A>G c.(7513-7515)atA>atG p.I2505M LUAD 1 235918832 235918832 + Nonsense_Mutation SNP A A T TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr1:235918832A>T c.7175T>A c.(7174-7176)tTg>tAg p.L2392* LUAD 1 235918847 235918847 + Missense_Mutation SNP C C T TCGA-91-8497-01A-11D-2393-08 TCGA-91-8497-10A-01D-2393-08 g.chr1:235918847C>T c.7160G>A c.(7159-7161)cGa>cAa p.R2387Q LUAD 1 235918893 235918893 + Nonsense_Mutation SNP T T A TCGA-44-6145-01A-11D-1753-08 TCGA-44-6145-10A-01D-1753-08 g.chr1:235918893T>A c.7114A>T c.(7114-7116)Aag>Tag p.K2372* LUAD 1 235918941 235918941 + Missense_Mutation SNP C C G TCGA-93-A4JQ-01A-11D-A24P-08 TCGA-93-A4JQ-10A-01D-A24P-08 g.chr1:235918941C>G c.7066G>C c.(7066-7068)Gat>Cat p.D2356H LUAD 1 235922575 235922575 + Frame_Shift_Del DEL C C - TCGA-05-4405-01A-21D-1855-08 TCGA-05-4405-10A-01D-1855-08 g.chr1:235922575delC c.6578delG c.(6577-6579)ggafs p.G2193fs LUAD 1 235922757 235922757 + Missense_Mutation SNP T T A TCGA-55-7913-01B-11D-2238-08 TCGA-55-7913-10A-01D-2238-08 g.chr1:235922757T>A c.6396A>T c.(6394-6396)ttA>ttT p.L2132F LUAD 1 235929473 235929473 + Missense_Mutation SNP C C G TCGA-86-A4P7-01A-11D-A24P-08 TCGA-86-A4P7-10A-01D-A24P-08 g.chr1:235929473C>G c.6027G>C c.(6025-6027)ttG>ttC p.L2009F LUAD 1 235929520 235929520 + Nonsense_Mutation SNP T T A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr1:235929520T>A c.5980A>T c.(5980-5982)Aaa>Taa p.K1994* LUAD 1 235933492 235933492 + Missense_Mutation SNP G G A TCGA-44-A47A-01A-21D-A24D-08 TCGA-44-A47A-10A-01D-A24F-08 g.chr1:235933492G>A c.5890C>T c.(5890-5892)Cat>Tat p.H1964Y LUAD 1 235937220 235937220 + Silent SNP T T C TCGA-78-7537-01A-11D-2063-08 TCGA-78-7537-10A-01D-2063-08 g.chr1:235937220T>C c.5706A>G c.(5704-5706)gtA>gtG p.V1902V LUAD 1 235938216 235938216 + Missense_Mutation SNP C C G TCGA-86-8585-01A-11D-2393-08 TCGA-86-8585-10A-01D-2393-08 g.chr1:235938216C>G c.5631G>C c.(5629-5631)ttG>ttC p.L1877F LUAD 1 235944170 235944170 + Missense_Mutation SNP A A T TCGA-44-7660-01A-11D-2063-08 TCGA-44-7660-10A-01D-2063-08 g.chr1:235944170A>T c.5209T>A c.(5209-5211)Tta>Ata p.L1737I LUAD 1 235945360 235945360 + Missense_Mutation SNP C C A TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chr1:235945360C>A c.4890G>T c.(4888-4890)atG>atT p.M1630I LUAD 1 235950500 235950500 + Splice_Site SNP C C A TCGA-55-8511-01A-11D-2393-08 TCGA-55-8511-10A-01D-2393-08 g.chr1:235950500C>A c.4862G>T c.(4861-4863)aGg>aTg p.R1621M LUAD 1 235950598 235950598 + Silent SNP G G A TCGA-49-4512-01A-21D-1855-08 TCGA-49-4512-11A-01D-1855-08 g.chr1:235950598G>A c.4764C>T c.(4762-4764)ctC>ctT p.L1588L LUAD 1 235955264 235955264 + Silent SNP C C T TCGA-69-A59K-01A-11D-A25L-08 TCGA-69-A59K-10A-01D-A25L-08 g.chr1:235955264C>T c.4278G>A c.(4276-4278)ttG>ttA p.L1426L LUAD 1 235956906 235956906 + Missense_Mutation SNP T T G TCGA-55-8299-01A-11D-2284-08 TCGA-55-8299-10B-01D-2323-08 g.chr1:235956906T>G c.4013A>C c.(4012-4014)cAg>cCg p.Q1338P LUAD 1 235967931 235967931 + Missense_Mutation SNP C C A TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr1:235967931C>A c.3428G>T c.(3427-3429)aGg>aTg p.R1143M LUAD 1 235969162 235969162 + Missense_Mutation SNP T T C TCGA-49-6767-01A-11D-1855-08 TCGA-49-6767-11A-01D-1855-08 g.chr1:235969162T>C c.3274A>G c.(3274-3276)Aca>Gca p.T1092A LUAD 1 235969330 235969330 + Missense_Mutation SNP C C T TCGA-MP-A4TA-01A-21D-A24P-08 TCGA-MP-A4TA-10A-01D-A24P-08 g.chr1:235969330C>T c.3106G>A c.(3106-3108)Gaa>Aaa p.E1036K LUAD 1 235969372 235969372 + Missense_Mutation SNP G G T TCGA-64-5778-01A-01D-1625-08 TCGA-64-5778-10A-01D-1625-08 g.chr1:235969372G>T c.3064C>A c.(3064-3066)Cag>Aag p.Q1022K LUAD 1 235969480 235969480 + Missense_Mutation SNP C C T TCGA-80-5611-01A-01D-1625-08 TCGA-80-5611-10A-01D-1625-08 g.chr1:235969480C>T c.2956G>A c.(2956-2958)Ggt>Agt p.G986S LUAD 1 235969542 235969542 + Missense_Mutation SNP G G C TCGA-91-6829-01A-21D-1855-08 TCGA-91-6829-11A-01D-1855-08 g.chr1:235969542G>C c.2894C>G c.(2893-2895)tCt>tGt p.S965C LUAD 1 235969785 235969785 + Missense_Mutation SNP T T C TCGA-50-5049-01A-01D-1625-08 TCGA-50-5049-10A-01D-1625-08 g.chr1:235969785T>C c.2651A>G c.(2650-2652)aAg>aGg p.K884R LUAD 1 235969806 235969806 + Missense_Mutation SNP C C A TCGA-05-5428-01A-01D-1625-08 TCGA-05-5428-10A-01D-1625-08 g.chr1:235969806C>A c.2630G>T c.(2629-2631)gGc>gTc p.G877V LUAD 1 235970013 235970013 + Missense_Mutation SNP C C T TCGA-17-Z020-01A-01W-0746-08 TCGA-17-Z020-11A-01W-0746-08 g.chr1:235970013C>T c.2423G>A c.(2422-2424)tGc>tAc p.C808Y LUAD 1 235971799 235971799 + Silent SNP C C G TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr1:235971799C>G c.2319G>C c.(2317-2319)gtG>gtC p.V773V LUAD 1 235972070 235972070 + Missense_Mutation SNP G G C TCGA-49-4514-01A-21D-1855-08 TCGA-49-4514-11A-01D-1855-08 g.chr1:235972070G>C c.2048C>G c.(2047-2049)tCt>tGt p.S683C LUAD 1 235972212 235972212 + Missense_Mutation SNP C C G TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chr1:235972212C>G c.1906G>C c.(1906-1908)Gct>Cct p.A636P LUAD 1 235972423 235972423 + Silent SNP G G A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr1:235972423G>A c.1695C>T c.(1693-1695)tcC>tcT p.S565S LUAD 1 235973040 235973040 + Missense_Mutation SNP C C A TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr1:235973040C>A c.1078G>T c.(1078-1080)Gct>Tct p.A360S LUAD 1 235973322 235973322 + Missense_Mutation SNP C C G TCGA-55-7913-01B-11D-2238-08 TCGA-55-7913-10A-01D-2238-08 g.chr1:235973322C>G c.796G>C c.(796-798)Gaa>Caa p.E266Q LUAD 1 235973489 235973489 + Missense_Mutation SNP G G A TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr1:235973489G>A c.629C>T c.(628-630)aCc>aTc p.T210I LUAD 1 235973558 235973558 + Missense_Mutation SNP A A G TCGA-17-Z021-01A-01W-0746-08 TCGA-17-Z021-11A-01W-0746-08 g.chr1:235973558A>G c.560T>C c.(559-561)cTg>cCg p.L187P LUAD 1 235973570 235973570 + Missense_Mutation SNP C C G TCGA-MP-A4SV-01A-11D-A24P-08 TCGA-MP-A4SV-10A-01D-A24P-08 g.chr1:235973570C>G c.548G>C c.(547-549)aGa>aCa p.R183T LUAD 1 235973688 235973688 + Missense_Mutation SNP T T C TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr1:235973688T>C c.430A>G c.(430-432)Aga>Gga p.R144G LUAD 1 235976294 235976294 + Missense_Mutation SNP G G A TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chr1:235976294G>A c.260C>T c.(259-261)cCt>cTt p.P87L LUAD 1 235993607 235993607 + Silent SNP C C A TCGA-55-8511-01A-11D-2393-08 TCGA-55-8511-10A-01D-2393-08 g.chr1:235993607C>A c.111G>T c.(109-111)acG>acT p.T37T LUSC 1 235827887 235827887 + Silent SNP C C G TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr1:235827887C>G c.11073G>C c.(11071-11073)gtG>gtC p.V3691V LUSC 1 235840490 235840490 + Splice_Site SNP T T A TCGA-18-3414-01A-01D-0983-08 TCGA-18-3414-11A-01D-0983-08 g.chr1:235840490T>A c.e50-2 LUSC 1 235860456 235860456 + Missense_Mutation SNP C C A TCGA-66-2742-01A-01D-0983-08 TCGA-66-2742-11A-01D-0983-08 g.chr1:235860456C>A c.10491G>T c.(10489-10491)caG>caT p.Q3497H LUSC 1 235866082 235866082 + Missense_Mutation SNP C C G TCGA-66-2778-01A-02D-1522-08 TCGA-66-2778-11A-01D-1522-08 g.chr1:235866082C>G c.10339G>C c.(10339-10341)Gag>Cag p.E3447Q LUSC 1 235892930 235892930 + Silent SNP T T C TCGA-85-6560-01A-11D-1817-08 TCGA-85-6560-10A-01D-1817-08 g.chr1:235892930T>C c.9072A>G c.(9070-9072)gcA>gcG p.A3024A LUSC 1 235896901 235896901 + Missense_Mutation SNP C C A TCGA-22-5482-01A-01D-1632-08 TCGA-22-5482-11A-01D-1632-08 g.chr1:235896901C>A c.8703G>T c.(8701-8703)gaG>gaT p.E2901D LUSC 1 235929511 235929511 + Missense_Mutation SNP C C A TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr1:235929511C>A c.5989G>T c.(5989-5991)Gca>Tca p.A1997S LUSC 1 235937219 235937219 + Missense_Mutation SNP C C G TCGA-37-3783-01A-01D-1267-08 TCGA-37-3783-10A-01D-1267-08 g.chr1:235937219C>G c.5707G>C c.(5707-5709)Gac>Cac p.D1903H LUSC 1 235944340 235944340 + Nonsense_Mutation SNP G G C TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr1:235944340G>C c.5039C>G c.(5038-5040)tCa>tGa p.S1680* LUSC 1 235945292 235945292 + Nonsense_Mutation SNP G G T TCGA-33-4547-01A-01D-1267-08 TCGA-33-4547-11A-01D-1267-08 g.chr1:235945292G>T c.4958C>A c.(4957-4959)tCa>tAa p.S1653* LUSC 1 235955020 235955020 + Missense_Mutation SNP C C A TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr1:235955020C>A c.4522G>T c.(4522-4524)Gat>Tat p.D1508Y LUSC 1 235967923 235967923 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr1:235967923G>A c.3436C>T c.(3436-3438)Ctt>Ttt p.L1146F LUSC 1 235969140 235969140 + Nonsense_Mutation SNP G G T TCGA-66-2795-01A-02D-0983-08 TCGA-66-2795-11A-01D-0983-08 g.chr1:235969140G>T c.3296C>A c.(3295-3297)tCa>tAa p.S1099* LUSC 1 235969541 235969541 + Silent SNP A A T TCGA-37-4135-01A-01D-1352-08 TCGA-37-4135-10A-01D-1352-08 g.chr1:235969541A>T c.2895T>A c.(2893-2895)tcT>tcA p.S965S LUSC 1 235972254 235972254 + Nonsense_Mutation SNP G G A TCGA-22-5489-01A-01D-1632-08 TCGA-22-5489-11A-01D-1632-08 g.chr1:235972254G>A c.1864C>T c.(1864-1866)Cag>Tag p.Q622* LUSC 1 235972330 235972330 + Silent SNP G G C TCGA-22-5489-01A-01D-1632-08 TCGA-22-5489-11A-01D-1632-08 g.chr1:235972330G>C c.1788C>G c.(1786-1788)ctC>ctG p.L596L LUSC 1 235972415 235972415 + Missense_Mutation SNP C C A TCGA-46-6025-01A-11D-1817-08 TCGA-46-6025-10A-01D-1817-08 g.chr1:235972415C>A c.1703G>T c.(1702-1704)aGc>aTc p.S568I LUSC 1 235973326 235973326 + Missense_Mutation SNP T T G TCGA-33-4583-01A-01D-1441-08 TCGA-33-4583-11A-01D-1441-08 g.chr1:235973326T>G c.792A>C c.(790-792)ttA>ttC p.L264F OV 1 235840882 235840882 + Missense_Mutation SNP T T C TCGA-23-2072-01A-01W-0722-08 TCGA-23-2072-10A-01W-0722-08 g.chr1:235840882T>C c.10838A>G c.(10837-10839)tAt>tGt p.Y3613C OV 1 235897870 235897870 + Silent SNP C C T TCGA-13-1411-01A-01W-0494-09 TCGA-13-1411-10A-01W-0495-09 g.chr1:235897870C>T c.8448G>A c.(8446-8448)ctG>ctA p.L2816L OV 1 235929573 235929573 + Missense_Mutation SNP T T C TCGA-61-1740-01A-01W-0639-09 TCGA-61-1740-11A-01W-0639-09 g.chr1:235929573T>C c.5927A>G c.(5926-5928)tAc>tGc p.Y1976C OV 1 235966296 235966296 + Missense_Mutation SNP C C A TCGA-23-1123-01A-01W-0488-09 TCGA-23-1123-10A-01W-0488-09 g.chr1:235966296C>A c.3624G>T c.(3622-3624)caG>caT p.Q1208H OV 1 235969927 235969927 + Missense_Mutation SNP G G A TCGA-13-0903-01A-01W-0421-09 TCGA-13-0903-10A-01W-0421-09 g.chr1:235969927G>A c.2509C>T c.(2509-2511)Cca>Tca p.P837S OV 1 235972337 235972337 + Missense_Mutation SNP G G T TCGA-25-1313-01A-01W-0492-08 TCGA-25-1313-10A-01W-0492-08 g.chr1:235972337G>T c.1781C>A c.(1780-1782)cCt>cAt p.P594H OV 1 235993636 235993636 + Missense_Mutation SNP C C T TCGA-25-1319-01A-01W-0492-08 TCGA-25-1319-10A-01W-0492-08 g.chr1:235993636C>T c.82G>A c.(82-84)Gag>Aag p.E28K PAAD 1 235826308 235826308 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:235826308G>A c.11338C>T c.(11338-11340)Cgg>Tgg p.R3780W PAAD 1 235866228 235866228 + Missense_Mutation SNP C C A TCGA-HZ-A77Q-01A-11D-A36O-08 TCGA-HZ-A77Q-10A-01D-A367-08 g.chr1:235866228C>A c.10193G>T c.(10192-10194)cGa>cTa p.R3398L PAAD 1 235909723 235909723 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:235909723C>T c.7885G>A c.(7885-7887)Gag>Aag p.E2629K PAAD 1 235944227 235944227 + Nonsense_Mutation SNP G G A TCGA-IB-A7M4-01A-11D-A36O-08 TCGA-IB-A7M4-10A-01D-A367-08 g.chr1:235944227G>A c.5152C>T c.(5152-5154)Cga>Tga p.R1718* PAAD 1 235952092 235952092 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:235952092C>T c.4597G>A c.(4597-4599)Gaa>Aaa p.E1533K PAAD 1 235955384 235955384 + Silent SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:235955384A>G c.4158T>C c.(4156-4158)gaT>gaC p.D1386D PAAD 1 235964335 235964335 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:235964335C>T c.3775G>A c.(3775-3777)Gaa>Aaa p.E1259K PAAD 1 235969949 235969949 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:235969949C>A c.2487G>T c.(2485-2487)gaG>gaT p.E829D PAAD 1 235970023 235970023 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:235970023C>T c.2413G>A c.(2413-2415)Gaa>Aaa p.E805K PAAD 1 235972089 235972089 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:235972089T>C c.2029A>G c.(2029-2031)Atc>Gtc p.I677V PAAD 1 235973135 235973135 + Missense_Mutation SNP A A C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:235973135A>C c.983T>G c.(982-984)tTt>tGt p.F328C PCPG 1 235929422 235929422 + Nonsense_Mutation SNP G G T TCGA-S7-A7WN-01A-12D-A35I-08 TCGA-S7-A7WN-10A-01D-A35G-08 g.chr1:235929422G>T c.6078C>A c.(6076-6078)taC>taA p.Y2026* PCPG 1 235940409 235940409 + Missense_Mutation SNP A A G TCGA-RW-A680-01A-11D-A35D-08 TCGA-RW-A680-10B-01D-A35B-08 g.chr1:235940409A>G c.5414T>C c.(5413-5415)cTg>cCg p.L1805P PCPG 1 235969125 235969125 + Missense_Mutation SNP C C T TCGA-RW-A67W-01A-11D-A35D-08 TCGA-RW-A67W-10A-01D-A35B-08 g.chr1:235969125C>T c.3311G>A c.(3310-3312)cGa>cAa p.R1104Q PRAD 1 235840808 235840808 + Missense_Mutation SNP C C T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 g.chr1:235840808C>T c.10912G>A c.(10912-10914)Gga>Aga p.G3638R PRAD 1 235840908 235840908 + Missense_Mutation SNP T T C TCGA-ZG-A9KY-01A-11D-A41K-08 TCGA-ZG-A9KY-10A-01D-A41N-08 g.chr1:235840908T>C c.10812A>G c.(10810-10812)atA>atG p.I3604M PRAD 1 235887435 235887435 + Missense_Mutation SNP C C T TCGA-V1-A9ZG-01A-11D-A41K-08 TCGA-V1-A9ZG-10A-01D-A41N-08 g.chr1:235887435C>T c.9208G>A c.(9208-9210)Gaa>Aaa p.E3070K PRAD 1 235922371 235922371 + Missense_Mutation SNP C C T TCGA-G9-A9S4-01A-11D-A41K-08 TCGA-G9-A9S4-10A-01D-A41N-08 g.chr1:235922371C>T c.6782G>A c.(6781-6783)cGt>cAt p.R2261H PRAD 1 235933474 235933482 + In_Frame_Del DEL AAGTCAGTA AAGTCAGTA - TCGA-XA-A8JR-01A-11D-A364-08 TCGA-XA-A8JR-10A-01D-A362-08 g.chr1:235933474_235933482delAAGTCAGTA c.5900_5908delTACTGACTT c.(5899-5910)ctactgacttgt>cgt p.1967_1970LLTC>R PRAD 1 235944227 235944227 + Nonsense_Mutation SNP G G A TCGA-V1-A8WW-01A-11D-A377-08 TCGA-V1-A8WW-10A-01D-A37A-08 g.chr1:235944227G>A c.5152C>T c.(5152-5154)Cga>Tga p.R1718* PRAD 1 235944227 235944227 + Nonsense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr1:235944227G>A c.5152C>T c.(5152-5154)Cga>Tga p.R1718* PRAD 1 235950607 235950607 + Silent SNP A A G TCGA-CH-5739-01A-11D-1576-08 TCGA-CH-5739-10A-01D-1576-08 g.chr1:235950607A>G c.4755T>C c.(4753-4755)aaT>aaC p.N1585N PRAD 1 235964219 235964220 + Frame_Shift_Ins INS - - A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr1:235964219_235964220insA c.3890_3891insT c.(3889-3891)ttgfs p.L1297fs PRAD 1 235973754 235973754 + Missense_Mutation SNP A A T TCGA-KK-A7AV-01A-11D-A32B-08 TCGA-KK-A7AV-11A-11D-A329-08 g.chr1:235973754A>T c.364T>A c.(364-366)Tta>Ata p.L122I READ 1 235826273 235826273 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:235826273G>T c.11373C>A c.(11371-11373)ttC>ttA p.F3791L READ 1 235840882 235840882 + Missense_Mutation SNP T T C TCGA-F5-6702-01A-11D-1826-10 TCGA-F5-6702-10A-01D-1826-10 g.chr1:235840882T>C c.10838A>G c.(10837-10839)tAt>tGt p.Y3613C READ 1 235840883 235840883 + Missense_Mutation SNP A A G TCGA-DY-A1DG-01A-11D-A152-10 TCGA-DY-A1DG-10A-01D-A152-10 g.chr1:235840883A>G c.10837T>C c.(10837-10839)Tat>Cat p.Y3613H READ 1 235850291 235850291 + Silent SNP G G A TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr1:235850291G>A c.10758C>T c.(10756-10758)tgC>tgT p.C3586C READ 1 235920623 235920623 + Silent SNP G G A TCGA-AG-3890-01A-01W-1073-09 TCGA-AG-3890-10A-01W-1073-09 g.chr1:235920623G>A c.7017C>T c.(7015-7017)ctC>ctT p.L2339L READ 1 235938335 235938335 + Missense_Mutation SNP T T C TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr1:235938335T>C c.5512A>G c.(5512-5514)Ata>Gta p.I1838V READ 1 235955020 235955020 + Missense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr1:235955020C>A c.4522G>T c.(4522-4524)Gat>Tat p.D1508Y READ 1 235969926 235969926 + Missense_Mutation SNP G G T TCGA-F5-6464-01A-11D-1733-10 TCGA-F5-6464-10A-01D-1733-10 g.chr1:235969926G>T c.2510C>A c.(2509-2511)cCa>cAa p.P837Q READ 1 235972610 235972610 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:235972610C>T c.1508G>A c.(1507-1509)cGa>cAa p.R503Q READ 1 235972904 235972904 + Missense_Mutation SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:235972904A>G c.1214T>C c.(1213-1215)tTg>tCg p.L405S READ 1 235973133 235973133 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:235973133G>A c.985C>T c.(985-987)Cga>Tga p.R329* READ 1 235973720 235973720 + Missense_Mutation SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:235973720A>G c.398T>C c.(397-399)gTt>gCt p.V133A SARC 1 235929492 235929492 + Missense_Mutation SNP G G A TCGA-QQ-A5VD-01A-21D-A32I-09 TCGA-QQ-A5VD-10A-01D-A32I-09 g.chr1:235929492G>A c.6008C>T c.(6007-6009)cCt>cTt p.P2003L SARC 1 235929493 235929493 + Missense_Mutation SNP G G A TCGA-QQ-A5VD-01A-21D-A32I-09 TCGA-QQ-A5VD-10A-01D-A32I-09 g.chr1:235929493G>A c.6007C>T c.(6007-6009)Cct>Tct p.P2003S SARC 1 235950617 235950617 + Nonsense_Mutation SNP G G T TCGA-IW-A3M4-01A-11D-A21Q-09 TCGA-IW-A3M4-10B-01D-A21Q-09 g.chr1:235950617G>T c.4745C>A c.(4744-4746)tCa>tAa p.S1582* SARC 1 235972736 235972736 + Missense_Mutation SNP A A G TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr1:235972736A>G c.1382T>C c.(1381-1383)gTt>gCt p.V461A SKCM 1 235827771 235827771 + Missense_Mutation SNP A A C TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr1:235827771A>C c.11189T>G c.(11188-11190)aTt>aGt p.I3730S SKCM 1 235840451 235840451 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr1:235840451G>A c.10978C>T c.(10978-10980)Cct>Tct p.P3660S SKCM 1 235860390 235860390 + Silent SNP C C T TCGA-ER-A3PL-06A-11D-A23B-08 TCGA-ER-A3PL-10A-01D-A23B-08 g.chr1:235860390C>T c.10557G>A c.(10555-10557)aaG>aaA p.K3519K SKCM 1 235860522 235860522 + Silent SNP G G A TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr1:235860522G>A c.10425C>T c.(10423-10425)tcC>tcT p.S3475S SKCM 1 235866166 235866166 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr1:235866166G>A c.10255C>T c.(10255-10257)Cat>Tat p.H3419Y SKCM 1 235866167 235866167 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr1:235866167G>A c.10254C>T c.(10252-10254)gcC>gcT p.A3418A SKCM 1 235866213 235866213 + Missense_Mutation SNP A A G TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr1:235866213A>G c.10208T>C c.(10207-10209)aTg>aCg p.M3403T SKCM 1 235884159 235884159 + Missense_Mutation SNP T T A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr1:235884159T>A c.9362A>T c.(9361-9363)aAt>aTt p.N3121I SKCM 1 235887328 235887328 + Splice_Site SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr1:235887328C>T c.9315G>A c.(9313-9315)aaG>aaA p.K3105K SKCM 1 235891379 235891379 + Silent SNP A A G TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr1:235891379A>G c.9159T>C c.(9157-9159)agT>agC p.S3053S SKCM 1 235904728 235904728 + Silent SNP G G A TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr1:235904728G>A c.8352C>T c.(8350-8352)tcC>tcT p.S2784S SKCM 1 235907411 235907411 + Silent SNP T T G TCGA-D3-A2JO-06A-11D-A196-08 TCGA-D3-A2JO-10A-01D-A198-08 g.chr1:235907411T>G c.8019A>C c.(8017-8019)gtA>gtC p.V2673V SKCM 1 235915467 235915467 + Missense_Mutation SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr1:235915467G>A c.7465C>T c.(7465-7467)Ccc>Tcc p.P2489S SKCM 1 235922487 235922487 + Silent SNP G G A TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr1:235922487G>A c.6666C>T c.(6664-6666)tcC>tcT p.S2222S SKCM 1 235929509 235929509 + Silent SNP T T C TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr1:235929509T>C c.5991A>G c.(5989-5991)gcA>gcG p.A1997A SKCM 1 235950601 235950601 + Silent SNP G G A TCGA-D3-A51J-06A-11D-A25O-08 TCGA-D3-A51J-10A-01D-A25O-08 g.chr1:235950601G>A c.4761C>T c.(4759-4761)ttC>ttT p.F1587F SKCM 1 235950643 235950643 + Silent SNP T T C TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr1:235950643T>C c.4719A>G c.(4717-4719)aaA>aaG p.K1573K SKCM 1 235955205 235955205 + Missense_Mutation SNP C C T TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chr1:235955205C>T c.4337G>A c.(4336-4338)cGg>cAg p.R1446Q SKCM 1 235955367 235955367 + Nonsense_Mutation SNP G G T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr1:235955367G>T c.4175C>A c.(4174-4176)tCa>tAa p.S1392* SKCM 1 235956850 235956850 + Missense_Mutation SNP C C T TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr1:235956850C>T c.4069G>A c.(4069-4071)Gag>Aag p.E1357K SKCM 1 235967804 235967804 + Splice_Site SNP C C T TCGA-D3-A5GR-06A-11D-A27K-08 TCGA-D3-A5GR-10A-01D-A27N-08 g.chr1:235967804C>T c.3555G>A c.(3553-3555)aaG>aaA p.K1185K SKCM 1 235969062 235969062 + Missense_Mutation SNP T T C TCGA-EE-A29B-06A-11D-A197-08 TCGA-EE-A29B-10A-01D-A199-08 g.chr1:235969062T>C c.3374A>G c.(3373-3375)gAa>gGa p.E1125G SKCM 1 235969138 235969138 + Missense_Mutation SNP G G A TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr1:235969138G>A c.3298C>T c.(3298-3300)Ctt>Ttt p.L1100F SKCM 1 235969221 235969221 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:235969221G>A c.3215C>T c.(3214-3216)tCc>tTc p.S1072F SKCM 1 235969576 235969576 + Missense_Mutation SNP G G A TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr1:235969576G>A c.2860C>T c.(2860-2862)Cct>Tct p.P954S SKCM 1 235969602 235969602 + Missense_Mutation SNP G G A TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr1:235969602G>A c.2834C>T c.(2833-2835)tCt>tTt p.S945F SKCM 1 235972340 235972340 + Missense_Mutation SNP A A G TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr1:235972340A>G c.1778T>C c.(1777-1779)aTt>aCt p.I593T SKCM 1 235972583 235972583 + Missense_Mutation SNP T T C TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr1:235972583T>C c.1535A>G c.(1534-1536)cAt>cGt p.H512R SKCM 1 235972605 235972605 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr1:235972605C>T c.1513G>A c.(1513-1515)Gaa>Aaa p.E505K SKCM 1 235972806 235972806 + Missense_Mutation SNP G G C TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr1:235972806G>C c.1312C>G c.(1312-1314)Cag>Gag p.Q438E SKCM 1 235973240 235973240 + Missense_Mutation SNP A A G TCGA-ER-A19O-06A-11D-A197-08 TCGA-ER-A19O-10A-01D-A199-08 g.chr1:235973240A>G c.878T>C c.(877-879)cTa>cCa p.L293P SKCM 1 235973317 235973317 + Silent SNP T T C TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr1:235973317T>C c.801A>G c.(799-801)aaA>aaG p.K267K SKCM 1 235973358 235973358 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr1:235973358G>A c.760C>T c.(760-762)Cca>Tca p.P254S SKCM 1 235973516 235973516 + Missense_Mutation SNP G G A TCGA-FS-A1ZM-06A-12D-A197-08 TCGA-FS-A1ZM-10A-01D-A199-08 g.chr1:235973516G>A c.602C>T c.(601-603)cCc>cTc p.P201L SKCM 1 235973692 235973692 + Missense_Mutation SNP T T G TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr1:235973692T>G c.426A>C c.(424-426)aaA>aaC p.K142N SKCM 1 235973733 235973733 + Silent SNP G G A TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr1:235973733G>A c.385C>T c.(385-387)Ctg>Ttg p.L129L SKCM 1 235973803 235973803 + Silent SNP G G A TCGA-D3-A51J-06A-11D-A25O-08 TCGA-D3-A51J-10A-01D-A25O-08 g.chr1:235973803G>A c.315C>T c.(313-315)atC>atT p.I105I SKCM 1 235973814 235973814 + Missense_Mutation SNP C C G TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr1:235973814C>G c.304G>C c.(304-306)Gca>Cca p.A102P

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 1 235945384 235945384 single base substitution C A 3_prime_UTR_variant BLCA-CN 1 235945384 235945384 single base substitution C A downstream_gene_variant BLCA-CN 1 235945384 235945384 single base substitution C A exon_variant BLCA-CN 1 235945384 235945384 single base substitution C A missense_variant K1622N 4866G>T BLCA-CN 1 235963652 235963652 single base substitution C T exon_variant BLCA-CN 1 235963652 235963652 single base substitution C T missense_variant S1325N 3974G>A BLCA-CN 1 235969457 235969457 single base substitution T G exon_variant BLCA-CN 1 235969457 235969457 single base substitution T G missense_variant L993F 2979A>C BLCA-US 1 235826288 235826288 single base substitution C T exon_variant BLCA-US 1 235826288 235826288 single base substitution C T synonymous_variant L3786L 11358G>A BLCA-US 1 235884050 235884050 single base substitution G A exon_variant BLCA-US 1 235884050 235884050 single base substitution G A synonymous_variant F3157F 9471C>T BLCA-US 1 235884187 235884187 single base substitution G C exon_variant BLCA-US 1 235884187 235884187 single base substitution G C missense_variant H3112D 9334C>G BLCA-US 1 235894422 235894422 single base substitution C T exon_variant BLCA-US 1 235894422 235894422 single base substitution C T missense_variant E2953K 8857G>A BLCA-US 1 235894422 235894422 single base substitution C T upstream_gene_variant BLCA-US 1 235907429 235907429 single base substitution C G downstream_gene_variant BLCA-US 1 235907429 235907429 single base substitution C G missense_variant L2667F 8001G>C BLCA-US 1 235907429 235907429 single base substitution C G upstream_gene_variant BLCA-US 1 235907458 235907458 single base substitution C G downstream_gene_variant BLCA-US 1 235907458 235907458 single base substitution C G splice_acceptor_variant BLCA-US 1 235907458 235907458 single base substitution C G upstream_gene_variant BLCA-US 1 235920623 235920623 single base substitution G A downstream_gene_variant BLCA-US 1 235920623 235920623 single base substitution G A synonymous_variant L2339L 7017C>T BLCA-US 1 235922510 235922510 single base substitution C T downstream_gene_variant BLCA-US 1 235922510 235922510 single base substitution C T exon_variant BLCA-US 1 235922510 235922510 single base substitution C T missense_variant D2215N 6643G>A BLCA-US 1 235922848 235922848 single base substitution C T 3_prime_UTR_variant BLCA-US 1 235922848 235922848 single base substitution C T exon_variant BLCA-US 1 235922848 235922848 single base substitution C T missense_variant R2102H 6305G>A BLCA-US 1 235929543 235929543 single base substitution C T 3_prime_UTR_variant BLCA-US 1 235929543 235929543 single base substitution C T exon_variant BLCA-US 1 235929543 235929543 single base substitution C T missense_variant R1986Q 5957G>A BLCA-US 1 235952011 235952011 single base substitution G C 3_prime_UTR_variant BLCA-US 1 235952011 235952011 single base substitution G C downstream_gene_variant BLCA-US 1 235952011 235952011 single base substitution G C exon_variant BLCA-US 1 235952011 235952011 single base substitution G C missense_variant L1560V 4678C>G BLCA-US 1 235952067 235952067 single base substitution G A 3_prime_UTR_variant BLCA-US 1 235952067 235952067 single base substitution G A downstream_gene_variant BLCA-US 1 235952067 235952067 single base substitution G A exon_variant BLCA-US 1 235952067 235952067 single base substitution G A missense_variant S1541L 4622C>T BLCA-US 1 235964228 235964228 single base substitution C T exon_variant BLCA-US 1 235964228 235964228 single base substitution C T synonymous_variant E1294E 3882G>A BLCA-US 1 235966211 235966211 single base substitution C T exon_variant BLCA-US 1 235966211 235966211 single base substitution C T missense_variant D1237N 3709G>A BLCA-US 1 235969730 235969730 single base substitution G C exon_variant BLCA-US 1 235969730 235969730 single base substitution G C synonymous_variant L902L 2706C>G BLCA-US 1 235969823 235969823 single base substitution G A exon_variant BLCA-US 1 235969823 235969823 single base substitution G A synonymous_variant L871L 2613C>T BLCA-US 1 235972029 235972029 single base substitution G A exon_variant BLCA-US 1 235972029 235972029 single base substitution G A stop_gained Q697* 2089C>T BLCA-US 1 235972124 235972124 single base substitution G A exon_variant BLCA-US 1 235972124 235972124 single base substitution G A missense_variant S665L 1994C>T BLCA-US 1 235972637 235972637 single base substitution G A exon_variant BLCA-US 1 235972637 235972637 single base substitution G A missense_variant S494L 1481C>T BLCA-US 1 235973532 235973532 single base substitution G T exon_variant BLCA-US 1 235973532 235973532 single base substitution G T missense_variant P196T 586C>A BLCA-US 1 235973651 235973651 single base substitution C G exon_variant BLCA-US 1 235973651 235973651 single base substitution C G missense_variant R156T 467G>C BLCA-US 1 235973787 235973787 single base substitution T A exon_variant BLCA-US 1 235973787 235973787 single base substitution T A missense_variant N111Y 331A>T BOCA-FR 1 235870041 235870041 single base substitution C T downstream_gene_variant BOCA-FR 1 235870041 235870041 single base substitution C T intron_variant BOCA-UK 1 235866267 235866267 single base substitution C T exon_variant BOCA-UK 1 235866267 235866267 single base substitution C T missense_variant G3385E 10154G>A BOCA-UK 1 235922440 235922440 single base substitution C T downstream_gene_variant BOCA-UK 1 235922440 235922440 single base substitution C T missense_variant R2238Q 6713G>A BRCA-EU 1 235820156 235820156 single base substitution T C downstream_gene_variant BRCA-EU 1 235820918 235820918 single base substitution C T downstream_gene_variant BRCA-EU 1 235821354 235821354 single base substitution C A downstream_gene_variant BRCA-EU 1 235822421 235822421 single base substitution T G downstream_gene_variant BRCA-EU 1 235824304 235824304 single base substitution T C downstream_gene_variant BRCA-EU 1 235826693 235826693 single base substitution G A intron_variant BRCA-EU 1 235826740 235826740 single base substitution A G intron_variant BRCA-EU 1 235829108 235829108 single base substitution C T intron_variant BRCA-EU 1 235829246 235829246 single base substitution T C intron_variant BRCA-EU 1 235829278 235829278 single base substitution A C intron_variant BRCA-EU 1 235829438 235829438 single base substitution G A intron_variant BRCA-EU 1 235830014 235830014 single base substitution A T intron_variant BRCA-EU 1 235830455 235830455 single base substitution G T intron_variant BRCA-EU 1 235833696 235833696 single base substitution C G intron_variant BRCA-EU 1 235834833 235834833 single base substitution T C intron_variant BRCA-EU 1 235836521 235836521 deletion of <=200bp T - intron_variant BRCA-EU 1 235836805 235836805 single base substitution C T intron_variant BRCA-EU 1 235836862 235836862 insertion of <=200bp - C intron_variant BRCA-EU 1 235836923 235836923 single base substitution C T intron_variant BRCA-EU 1 235837267 235837267 deletion of <=200bp C - intron_variant BRCA-EU 1 235839560 235839560 single base substitution C G intron_variant BRCA-EU 1 235839571 235839571 single base substitution C T intron_variant BRCA-EU 1 235840025 235840025 single base substitution C A intron_variant BRCA-EU 1 235842338 235842338 single base substitution T A intron_variant BRCA-EU 1 235843781 235843781 single base substitution C G intron_variant BRCA-EU 1 235843825 235843825 single base substitution C T intron_variant BRCA-EU 1 235844789 235844789 single base substitution G T intron_variant BRCA-EU 1 235846901 235846901 single base substitution T C intron_variant BRCA-EU 1 235846949 235846949 single base substitution A T intron_variant BRCA-EU 1 235847166 235847166 deletion of <=200bp G - intron_variant BRCA-EU 1 235848100 235848100 deletion of <=200bp T - intron_variant BRCA-EU 1 235849335 235849335 single base substitution A G intron_variant BRCA-EU 1 235849357 235849357 single base substitution C A intron_variant BRCA-EU 1 235849392 235849392 single base substitution C T intron_variant BRCA-EU 1 235849865 235849865 single base substitution C T intron_variant BRCA-EU 1 235850535 235850535 single base substitution T C intron_variant BRCA-EU 1 235854829 235854829 single base substitution A G intron_variant BRCA-EU 1 235855001 235855001 single base substitution T C intron_variant BRCA-EU 1 235855431 235855431 single base substitution G A intron_variant BRCA-EU 1 235856191 235856191 single base substitution C T intron_variant BRCA-EU 1 235856583 235856583 single base substitution C G intron_variant BRCA-EU 1 235857027 235857027 single base substitution C G intron_variant BRCA-EU 1 235861413 235861413 single base substitution C A intron_variant BRCA-EU 1 235861836 235861836 deletion of <=200bp T - intron_variant BRCA-EU 1 235862095 235862095 single base substitution C T intron_variant BRCA-EU 1 235862602 235862602 single base substitution T C intron_variant BRCA-EU 1 235862674 235862674 single base substitution G C intron_variant BRCA-EU 1 235863106 235863106 single base substitution G C intron_variant BRCA-EU 1 235863107 235863107 single base substitution A C intron_variant BRCA-EU 1 235864328 235864328 single base substitution G C intron_variant BRCA-EU 1 235866150 235866150 single base substitution C G exon_variant BRCA-EU 1 235866150 235866150 single base substitution C G missense_variant G3424A 10271G>C BRCA-EU 1 235866481 235866481 single base substitution A T intron_variant BRCA-EU 1 235866572 235866572 single base substitution A C intron_variant BRCA-EU 1 235866796 235866796 single base substitution G T intron_variant BRCA-EU 1 235866883 235866883 single base substitution C A intron_variant BRCA-EU 1 235867035 235867035 single base substitution C G intron_variant BRCA-EU 1 235867796 235867796 single base substitution C G downstream_gene_variant BRCA-EU 1 235867796 235867796 single base substitution C G intron_variant BRCA-EU 1 235868067 235868067 single base substitution C A downstream_gene_variant BRCA-EU 1 235868067 235868067 single base substitution C A intron_variant BRCA-EU 1 235868268 235868268 single base substitution C T downstream_gene_variant BRCA-EU 1 235868268 235868268 single base substitution C T intron_variant BRCA-EU 1 235868953 235868953 single base substitution T C downstream_gene_variant BRCA-EU 1 235868953 235868953 single base substitution T C intron_variant BRCA-EU 1 235869734 235869734 single base substitution C G downstream_gene_variant BRCA-EU 1 235869734 235869734 single base substitution C G intron_variant BRCA-EU 1 235871442 235871442 single base substitution A G downstream_gene_variant BRCA-EU 1 235871442 235871442 single base substitution A G intron_variant BRCA-EU 1 235871712 235871712 single base substitution T C downstream_gene_variant BRCA-EU 1 235871712 235871712 single base substitution T C intron_variant BRCA-EU 1 235872500 235872500 single base substitution A G downstream_gene_variant BRCA-EU 1 235872500 235872500 single base substitution A G exon_variant BRCA-EU 1 235872500 235872500 single base substitution A G missense_variant L3345P 10034T>C BRCA-EU 1 235872834 235872834 single base substitution C G downstream_gene_variant BRCA-EU 1 235872834 235872834 single base substitution C G intron_variant BRCA-EU 1 235873781 235873781 single base substitution C G downstream_gene_variant BRCA-EU 1 235873781 235873781 single base substitution C G intron_variant BRCA-EU 1 235875458 235875458 single base substitution G A downstream_gene_variant BRCA-EU 1 235875458 235875458 single base substitution G A exon_variant BRCA-EU 1 235875458 235875458 single base substitution G A missense_variant T3275I 9824C>T BRCA-EU 1 235876227 235876227 single base substitution A G downstream_gene_variant BRCA-EU 1 235876227 235876227 single base substitution A G intron_variant BRCA-EU 1 235876227 235876227 single base substitution A G upstream_gene_variant BRCA-EU 1 235876711 235876711 single base substitution G T intron_variant BRCA-EU 1 235876711 235876711 single base substitution G T upstream_gene_variant BRCA-EU 1 235877168 235877168 single base substitution C T intron_variant BRCA-EU 1 235877168 235877168 single base substitution C T upstream_gene_variant BRCA-EU 1 235877596 235877596 single base substitution C T intron_variant BRCA-EU 1 235877596 235877596 single base substitution C T upstream_gene_variant BRCA-EU 1 235879081 235879081 single base substitution G C intron_variant BRCA-EU 1 235879081 235879081 single base substitution G C upstream_gene_variant BRCA-EU 1 235879376 235879376 single base substitution A G intron_variant BRCA-EU 1 235879376 235879376 single base substitution A G upstream_gene_variant BRCA-EU 1 235879950 235879950 single base substitution C T intron_variant BRCA-EU 1 235879950 235879950 single base substitution C T upstream_gene_variant BRCA-EU 1 235881495 235881495 single base substitution T G intron_variant BRCA-EU 1 235881723 235881723 single base substitution A T intron_variant BRCA-EU 1 235882176 235882176 single base substitution T C intron_variant BRCA-EU 1 235882706 235882706 single base substitution C G intron_variant BRCA-EU 1 235883083 235883083 single base substitution C T intron_variant BRCA-EU 1 235884056 235884056 single base substitution T A exon_variant BRCA-EU 1 235884056 235884056 single base substitution T A synonymous_variant R3155R 9465A>T BRCA-EU 1 235884166 235884166 single base substitution G A exon_variant BRCA-EU 1 235884166 235884166 single base substitution G A missense_variant L3119F 9355C>T BRCA-EU 1 235884443 235884443 single base substitution C G intron_variant BRCA-EU 1 235884493 235884493 insertion of <=200bp - A intron_variant BRCA-EU 1 235886501 235886501 single base substitution G C intron_variant BRCA-EU 1 235887794 235887794 single base substitution T A intron_variant BRCA-EU 1 235888731 235888731 single base substitution C G intron_variant BRCA-EU 1 235889259 235889259 insertion of <=200bp - A intron_variant BRCA-EU 1 235890105 235890105 single base substitution G C intron_variant BRCA-EU 1 235890363 235890363 deletion of <=200bp T - intron_variant BRCA-EU 1 235890588 235890588 single base substitution A G intron_variant BRCA-EU 1 235890813 235890813 single base substitution T A intron_variant BRCA-EU 1 235891110 235891110 single base substitution G T intron_variant BRCA-EU 1 235891126 235891126 single base substitution G T intron_variant BRCA-EU 1 235891204 235891204 single base substitution G T intron_variant BRCA-EU 1 235892304 235892304 single base substitution G C intron_variant BRCA-EU 1 235892304 235892304 single base substitution G C upstream_gene_variant BRCA-EU 1 235893009 235893009 single base substitution G A intron_variant BRCA-EU 1 235893009 235893009 single base substitution G A upstream_gene_variant BRCA-EU 1 235894534 235894534 deletion of <=200bp A - intron_variant BRCA-EU 1 235894534 235894534 deletion of <=200bp A - upstream_gene_variant BRCA-EU 1 235894966 235894966 single base substitution C A intron_variant BRCA-EU 1 235894966 235894966 single base substitution C A upstream_gene_variant BRCA-EU 1 235895057 235895057 single base substitution C T intron_variant BRCA-EU 1 235895057 235895057 single base substitution C T upstream_gene_variant BRCA-EU 1 235895916 235895916 single base substitution G A intron_variant BRCA-EU 1 235895916 235895916 single base substitution G A upstream_gene_variant BRCA-EU 1 235896437 235896437 single base substitution G A downstream_gene_variant BRCA-EU 1 235896437 235896437 single base substitution G A intron_variant BRCA-EU 1 235896629 235896629 deletion of <=200bp A - downstream_gene_variant BRCA-EU 1 235896629 235896629 deletion of <=200bp A - intron_variant BRCA-EU 1 235896661 235896661 insertion of <=200bp - A downstream_gene_variant BRCA-EU 1 235896661 235896661 insertion of <=200bp - A intron_variant BRCA-EU 1 235896701 235896701 single base substitution G A downstream_gene_variant BRCA-EU 1 235896701 235896701 single base substitution G A intron_variant BRCA-EU 1 235897270 235897270 single base substitution G A downstream_gene_variant BRCA-EU 1 235897270 235897270 single base substitution G A intron_variant BRCA-EU 1 235898304 235898304 single base substitution G A downstream_gene_variant BRCA-EU 1 235898304 235898304 single base substitution G A exon_variant BRCA-EU 1 235898304 235898304 single base substitution G A intron_variant BRCA-EU 1 235898469 235898469 single base substitution G C downstream_gene_variant BRCA-EU 1 235898469 235898469 single base substitution G C exon_variant BRCA-EU 1 235898469 235898469 single base substitution G C intron_variant BRCA-EU 1 235899808 235899808 single base substitution G A downstream_gene_variant BRCA-EU 1 235899808 235899808 single base substitution G A exon_variant BRCA-EU 1 235899808 235899808 single base substitution G A intron_variant BRCA-EU 1 235899874 235899874 single base substitution G T downstream_gene_variant BRCA-EU 1 235899874 235899874 single base substitution G T exon_variant BRCA-EU 1 235899874 235899874 single base substitution G T intron_variant BRCA-EU 1 235901552 235901552 single base substitution G A exon_variant BRCA-EU 1 235901552 235901552 single base substitution G A intron_variant BRCA-EU 1 235901552 235901552 single base substitution G A upstream_gene_variant BRCA-EU 1 235902221 235902221 single base substitution G C intron_variant BRCA-EU 1 235902221 235902221 single base substitution G C upstream_gene_variant BRCA-EU 1 235903472 235903472 single base substitution C G intron_variant BRCA-EU 1 235903472 235903472 single base substitution C G upstream_gene_variant BRCA-EU 1 235904390 235904390 single base substitution C T intron_variant BRCA-EU 1 235904390 235904390 single base substitution C T upstream_gene_variant BRCA-EU 1 235905005 235905007 deletion of <=200bp AAG - downstream_gene_variant BRCA-EU 1 235905005 235905007 deletion of <=200bp AAG - intron_variant BRCA-EU 1 235905005 235905007 deletion of <=200bp AAG - upstream_gene_variant BRCA-EU 1 235907227 235907227 single base substitution C T downstream_gene_variant BRCA-EU 1 235907227 235907227 single base substitution C T intron_variant BRCA-EU 1 235907458 235907458 single base substitution C T downstream_gene_variant BRCA-EU 1 235907458 235907458 single base substitution C T splice_acceptor_variant BRCA-EU 1 235907458 235907458 single base substitution C T upstream_gene_variant BRCA-EU 1 235907664 235907664 single base substitution C T downstream_gene_variant BRCA-EU 1 235907664 235907664 single base substitution C T intron_variant BRCA-EU 1 235907664 235907664 single base substitution C T upstream_gene_variant BRCA-EU 1 235907813 235907813 single base substitution C T downstream_gene_variant BRCA-EU 1 235907813 235907813 single base substitution C T intron_variant BRCA-EU 1 235907813 235907813 single base substitution C T upstream_gene_variant BRCA-EU 1 235907907 235907907 single base substitution A G downstream_gene_variant BRCA-EU 1 235907907 235907907 single base substitution A G intron_variant BRCA-EU 1 235907907 235907907 single base substitution A G upstream_gene_variant BRCA-EU 1 235908517 235908517 deletion of <=200bp T - downstream_gene_variant BRCA-EU 1 235908517 235908517 deletion of <=200bp T - intron_variant BRCA-EU 1 235908517 235908517 deletion of <=200bp T - upstream_gene_variant BRCA-EU 1 235911086 235911086 single base substitution A T intron_variant BRCA-EU 1 235911086 235911086 single base substitution A T upstream_gene_variant BRCA-EU 1 235911151 235911151 single base substitution G C intron_variant BRCA-EU 1 235911151 235911151 single base substitution G C upstream_gene_variant BRCA-EU 1 235912197 235912197 single base substitution G A intron_variant BRCA-EU 1 235912197 235912197 single base substitution G A upstream_gene_variant BRCA-EU 1 235912663 235912663 single base substitution A G intron_variant BRCA-EU 1 235912735 235912736 deletion of <=200bp AG - intron_variant BRCA-EU 1 235914177 235914177 single base substitution G A intron_variant BRCA-EU 1 235915116 235915116 single base substitution A T intron_variant BRCA-EU 1 235916022 235916022 single base substitution T C intron_variant BRCA-EU 1 235916022 235916022 single base substitution T C upstream_gene_variant BRCA-EU 1 235916554 235916554 single base substitution C T missense_variant R2417K 7250G>A BRCA-EU 1 235916554 235916554 single base substitution C T upstream_gene_variant BRCA-EU 1 235916694 235916694 single base substitution G C intron_variant BRCA-EU 1 235916694 235916694 single base substitution G C upstream_gene_variant BRCA-EU 1 235917265 235917265 single base substitution C T intron_variant BRCA-EU 1 235917265 235917265 single base substitution C T upstream_gene_variant BRCA-EU 1 235918882 235918882 single base substitution T C downstream_gene_variant BRCA-EU 1 235918882 235918882 single base substitution T C synonymous_variant G2375G 7125A>G BRCA-EU 1 235918882 235918882 single base substitution T C upstream_gene_variant BRCA-EU 1 235919186 235919186 deletion of <=200bp T - downstream_gene_variant BRCA-EU 1 235919186 235919186 deletion of <=200bp T - intron_variant BRCA-EU 1 235919186 235919186 deletion of <=200bp T - upstream_gene_variant BRCA-EU 1 235919527 235919527 single base substitution T G downstream_gene_variant BRCA-EU 1 235919527 235919527 single base substitution T G intron_variant BRCA-EU 1 235919527 235919527 single base substitution T G upstream_gene_variant BRCA-EU 1 235920406 235920406 single base substitution C G downstream_gene_variant BRCA-EU 1 235920406 235920406 single base substitution C G intron_variant BRCA-EU 1 235920406 235920406 single base substitution C G upstream_gene_variant BRCA-EU 1 235920608 235920608 single base substitution T C downstream_gene_variant BRCA-EU 1 235920608 235920608 single base substitution T C synonymous_variant S2344S 7032A>G BRCA-EU 1 235921948 235921948 single base substitution C T downstream_gene_variant BRCA-EU 1 235921948 235921948 single base substitution C T intron_variant BRCA-EU 1 235922371 235922371 single base substitution C T downstream_gene_variant BRCA-EU 1 235922371 235922371 single base substitution C T missense_variant R2261H 6782G>A BRCA-EU 1 235923142 235923142 single base substitution C T intron_variant BRCA-EU 1 235923431 235923431 single base substitution G C intron_variant BRCA-EU 1 235923687 235923687 single base substitution C G intron_variant BRCA-EU 1 235924396 235924396 deletion of <=200bp A - intron_variant BRCA-EU 1 235924403 235924403 single base substitution A T intron_variant BRCA-EU 1 235924564 235924564 single base substitution C G intron_variant BRCA-EU 1 235924734 235924734 single base substitution C T intron_variant BRCA-EU 1 235924909 235924909 single base substitution G A intron_variant BRCA-EU 1 235925219 235925219 single base substitution C A intron_variant BRCA-EU 1 235926105 235926105 single base substitution C G 3_prime_UTR_variant BRCA-EU 1 235926105 235926105 single base substitution C G exon_variant BRCA-EU 1 235926105 235926105 single base substitution C G missense_variant R2056S 6168G>C BRCA-EU 1 235926395 235926395 single base substitution T A intron_variant BRCA-EU 1 235926484 235926484 single base substitution G A intron_variant BRCA-EU 1 235927984 235927984 single base substitution G A intron_variant BRCA-EU 1 235928224 235928224 deletion of <=200bp A - intron_variant BRCA-EU 1 235928316 235928316 single base substitution A G intron_variant BRCA-EU 1 235929791 235929791 single base substitution C A intron_variant BRCA-EU 1 235930450 235930450 single base substitution A C intron_variant BRCA-EU 1 235931499 235931499 deletion of <=200bp T - intron_variant BRCA-EU 1 235932050 235932050 single base substitution T C intron_variant BRCA-EU 1 235934455 235934455 single base substitution G C intron_variant BRCA-EU 1 235935360 235935360 insertion of <=200bp - A intron_variant BRCA-EU 1 235935932 235935932 single base substitution C G intron_variant BRCA-EU 1 235936676 235936676 single base substitution C T intron_variant BRCA-EU 1 235937339 235937339 single base substitution C T intron_variant BRCA-EU 1 235937627 235937627 single base substitution G T intron_variant BRCA-EU 1 235937801 235937801 single base substitution C T intron_variant BRCA-EU 1 235940002 235940002 single base substitution T A intron_variant BRCA-EU 1 235941133 235941133 single base substitution C G intron_variant BRCA-EU 1 235941376 235941376 single base substitution C A intron_variant BRCA-EU 1 235941598 235941598 single base substitution A G intron_variant BRCA-EU 1 235941610 235941610 single base substitution T C intron_variant BRCA-EU 1 235941738 235941738 single base substitution G A intron_variant BRCA-EU 1 235943973 235943973 single base substitution A G intron_variant BRCA-EU 1 235944793 235944793 single base substitution T A intron_variant BRCA-EU 1 235946917 235946917 single base substitution C G downstream_gene_variant BRCA-EU 1 235946917 235946917 single base substitution C G intron_variant BRCA-EU 1 235947170 235947170 single base substitution G C downstream_gene_variant BRCA-EU 1 235947170 235947170 single base substitution G C intron_variant BRCA-EU 1 235949535 235949535 single base substitution G T downstream_gene_variant BRCA-EU 1 235949535 235949535 single base substitution G T intron_variant BRCA-EU 1 235950818 235950818 single base substitution C T downstream_gene_variant BRCA-EU 1 235950818 235950818 single base substitution C T intron_variant BRCA-EU 1 235951895 235951895 single base substitution T C downstream_gene_variant BRCA-EU 1 235951895 235951895 single base substitution T C intron_variant BRCA-EU 1 235952271 235952271 single base substitution G T downstream_gene_variant BRCA-EU 1 235952271 235952271 single base substitution G T intron_variant BRCA-EU 1 235952271 235952271 single base substitution G T upstream_gene_variant BRCA-EU 1 235952567 235952567 deletion of <=200bp A - downstream_gene_variant BRCA-EU 1 235952567 235952567 deletion of <=200bp A - intron_variant BRCA-EU 1 235952567 235952567 deletion of <=200bp A - upstream_gene_variant BRCA-EU 1 235952756 235952756 single base substitution C T downstream_gene_variant BRCA-EU 1 235952756 235952756 single base substitution C T intron_variant BRCA-EU 1 235952756 235952756 single base substitution C T upstream_gene_variant BRCA-EU 1 235953648 235953653 deletion of <=200bp CTTCCT - downstream_gene_variant BRCA-EU 1 235953648 235953653 deletion of <=200bp CTTCCT - intron_variant BRCA-EU 1 235953648 235953653 deletion of <=200bp CTTCCT - upstream_gene_variant BRCA-EU 1 235955186 235955186 single base substitution G C exon_variant BRCA-EU 1 235955186 235955186 single base substitution G C intron_variant BRCA-EU 1 235955186 235955186 single base substitution G C missense_variant H1452Q 4356C>G BRCA-EU 1 235955186 235955186 single base substitution G C upstream_gene_variant BRCA-EU 1 235956062 235956062 single base substitution C A intron_variant BRCA-EU 1 235956062 235956062 single base substitution C A upstream_gene_variant BRCA-EU 1 235956567 235956567 single base substitution G A intron_variant BRCA-EU 1 235956567 235956567 single base substitution G A upstream_gene_variant BRCA-EU 1 235956591 235956591 single base substitution T C intron_variant BRCA-EU 1 235956591 235956591 single base substitution T C upstream_gene_variant BRCA-EU 1 235956672 235956672 single base substitution T C intron_variant BRCA-EU 1 235956672 235956672 single base substitution T C upstream_gene_variant BRCA-EU 1 235957094 235957094 single base substitution C G intron_variant BRCA-EU 1 235957094 235957094 single base substitution C G upstream_gene_variant BRCA-EU 1 235957703 235957703 single base substitution A G intron_variant BRCA-EU 1 235957857 235957857 single base substitution T A intron_variant BRCA-EU 1 235960724 235960724 single base substitution C T intron_variant BRCA-EU 1 235962351 235962351 single base substitution C G intron_variant BRCA-EU 1 235964373 235964373 single base substitution T C exon_variant BRCA-EU 1 235964373 235964373 single base substitution T C missense_variant E1246G 3737A>G BRCA-EU 1 235964526 235964526 single base substitution C A intron_variant BRCA-EU 1 235964716 235964716 insertion of <=200bp - C intron_variant BRCA-EU 1 235968189 235968189 single base substitution C T intron_variant BRCA-EU 1 235968287 235968287 single base substitution C G intron_variant BRCA-EU 1 235969288 235969288 single base substitution A T exon_variant BRCA-EU 1 235969288 235969288 single base substitution A T missense_variant S1050T 3148T>A BRCA-EU 1 235969662 235969662 single base substitution T A exon_variant BRCA-EU 1 235969662 235969662 single base substitution T A missense_variant D925V 2774A>T BRCA-EU 1 235971409 235971409 single base substitution G A intron_variant BRCA-EU 1 235971428 235971428 single base substitution C G intron_variant BRCA-EU 1 235971578 235971578 single base substitution T C intron_variant BRCA-EU 1 235971864 235971864 single base substitution G C exon_variant BRCA-EU 1 235971864 235971864 single base substitution G C missense_variant L752V 2254C>G BRCA-EU 1 235971988 235971988 single base substitution C T exon_variant BRCA-EU 1 235971988 235971988 single base substitution C T synonymous_variant Q710Q 2130G>A BRCA-EU 1 235973476 235973476 single base substitution A C exon_variant BRCA-EU 1 235973476 235973476 single base substitution A C synonymous_variant T214T 642T>G BRCA-EU 1 235973990 235973998 deletion of <=200bp CTGGGTTAC - intron_variant BRCA-EU 1 235975664 235975664 single base substitution T C intron_variant BRCA-EU 1 235975679 235975679 single base substitution C T intron_variant BRCA-EU 1 235976282 235976282 single base substitution T C exon_variant BRCA-EU 1 235976282 235976282 single base substitution T C missense_variant E91G 272A>G BRCA-EU 1 235977159 235977159 single base substitution G A intron_variant BRCA-EU 1 235977690 235977690 single base substitution G A intron_variant BRCA-EU 1 235979161 235979161 single base substitution G A intron_variant BRCA-EU 1 235980296 235980296 single base substitution T G intron_variant BRCA-EU 1 235981181 235981181 single base substitution T A intron_variant BRCA-EU 1 235981634 235981634 single base substitution C T intron_variant BRCA-EU 1 235982199 235982199 single base substitution G A intron_variant BRCA-EU 1 235983983 235983983 single base substitution C G intron_variant BRCA-EU 1 235984264 235984264 single base substitution G A intron_variant BRCA-EU 1 235985051 235985051 single base substitution G C intron_variant BRCA-EU 1 235985291 235985291 single base substitution C G intron_variant BRCA-EU 1 235985439 235985439 single base substitution A T intron_variant BRCA-EU 1 235985649 235985649 single base substitution T C intron_variant BRCA-EU 1 235987360 235987360 single base substitution T C downstream_gene_variant BRCA-EU 1 235987360 235987360 single base substitution T C intron_variant BRCA-EU 1 235987465 235987465 single base substitution A G downstream_gene_variant BRCA-EU 1 235987465 235987465 single base substitution A G intron_variant BRCA-EU 1 235988633 235988633 single base substitution T A downstream_gene_variant BRCA-EU 1 235988633 235988633 single base substitution T A intron_variant BRCA-EU 1 235988933 235988933 single base substitution G C downstream_gene_variant BRCA-EU 1 235988933 235988933 single base substitution G C intron_variant BRCA-EU 1 235990030 235990030 single base substitution G A downstream_gene_variant BRCA-EU 1 235990030 235990030 single base substitution G A intron_variant BRCA-EU 1 235990405 235990405 single base substitution T A downstream_gene_variant BRCA-EU 1 235990405 235990405 single base substitution T A intron_variant BRCA-EU 1 235990407 235990407 single base substitution T A downstream_gene_variant BRCA-EU 1 235990407 235990407 single base substitution T A intron_variant BRCA-EU 1 235990525 235990525 single base substitution C T downstream_gene_variant BRCA-EU 1 235990525 235990525 single base substitution C T intron_variant BRCA-EU 1 235990570 235990570 single base substitution G A downstream_gene_variant BRCA-EU 1 235990570 235990570 single base substitution G A intron_variant BRCA-EU 1 235991392 235991392 single base substitution G C downstream_gene_variant BRCA-EU 1 235991392 235991392 single base substitution G C intron_variant BRCA-EU 1 235991903 235991903 single base substitution A G downstream_gene_variant BRCA-EU 1 235991903 235991903 single base substitution A G intron_variant BRCA-EU 1 235991926 235991926 single base substitution A G downstream_gene_variant BRCA-EU 1 235991926 235991926 single base substitution A G intron_variant BRCA-EU 1 235993154 235993154 single base substitution C T exon_variant BRCA-EU 1 235993154 235993154 single base substitution C T intron_variant BRCA-EU 1 235993390 235993390 deletion of <=200bp T - exon_variant BRCA-EU 1 235993390 235993390 deletion of <=200bp T - intron_variant BRCA-EU 1 235993398 235993398 single base substitution T C exon_variant BRCA-EU 1 235993398 235993398 single base substitution T C intron_variant BRCA-EU 1 235993484 235993484 single base substitution T C exon_variant BRCA-EU 1 235993484 235993484 single base substitution T C intron_variant BRCA-EU 1 235994520 235994520 single base substitution C G intron_variant BRCA-EU 1 235995198 235995199 deletion of <=200bp TT - intron_variant BRCA-EU 1 235995899 235995899 single base substitution C G intron_variant BRCA-EU 1 235996004 235996004 single base substitution C G intron_variant BRCA-EU 1 235996362 235996362 single base substitution C A intron_variant BRCA-EU 1 235996516 235996516 single base substitution C G intron_variant BRCA-EU 1 235996806 235996806 single base substitution G A intron_variant BRCA-EU 1 235996972 235996972 deletion of <=200bp A - intron_variant BRCA-EU 1 235996972 235996972 deletion of <=200bp A - splice_region_variant BRCA-EU 1 235997460 235997460 single base substitution T G intron_variant BRCA-EU 1 235997712 235997712 deletion of <=200bp A - intron_variant BRCA-EU 1 235997795 235997795 single base substitution C G intron_variant BRCA-EU 1 235998566 235998566 single base substitution A T intron_variant BRCA-EU 1 236000181 236000181 single base substitution C G intron_variant BRCA-EU 1 236000632 236000632 single base substitution T A intron_variant BRCA-EU 1 236001167 236001167 deletion of <=200bp A - intron_variant BRCA-EU 1 236002152 236002152 single base substitution G A intron_variant BRCA-EU 1 236008075 236008077 deletion of <=200bp GGG - intron_variant BRCA-EU 1 236009005 236009005 single base substitution G A intron_variant BRCA-EU 1 236009140 236009140 single base substitution C T intron_variant BRCA-EU 1 236009261 236009261 single base substitution C T intron_variant BRCA-EU 1 236010590 236010590 single base substitution G T intron_variant BRCA-EU 1 236010827 236010827 single base substitution T C intron_variant BRCA-EU 1 236011205 236011205 single base substitution G C intron_variant BRCA-EU 1 236011865 236011865 single base substitution A G intron_variant BRCA-EU 1 236012013 236012013 single base substitution G T intron_variant BRCA-EU 1 236012149 236012149 single base substitution G C intron_variant BRCA-EU 1 236012189 236012189 deletion of <=200bp A - intron_variant BRCA-EU 1 236012189 236012189 insertion of <=200bp - A intron_variant BRCA-EU 1 236014178 236014178 single base substitution G C intron_variant BRCA-EU 1 236014221 236014221 single base substitution C T intron_variant BRCA-EU 1 236015723 236015723 single base substitution C T intron_variant BRCA-EU 1 236016528 236016528 single base substitution G C intron_variant BRCA-EU 1 236018143 236018143 single base substitution A G intron_variant BRCA-EU 1 236019136 236019136 single base substitution G A intron_variant BRCA-EU 1 236019755 236019755 single base substitution C A intron_variant BRCA-EU 1 236020789 236020789 single base substitution G C intron_variant BRCA-EU 1 236021894 236021894 single base substitution C G intron_variant BRCA-EU 1 236023304 236023304 single base substitution C G intron_variant BRCA-EU 1 236024327 236024327 single base substitution T G intron_variant BRCA-EU 1 236026517 236026517 single base substitution C A intron_variant BRCA-EU 1 236026602 236026602 single base substitution G C intron_variant BRCA-EU 1 236027716 236027716 single base substitution G A intron_variant BRCA-EU 1 236027925 236027925 single base substitution G C intron_variant BRCA-EU 1 236028059 236028059 single base substitution C T intron_variant BRCA-EU 1 236028793 236028793 single base substitution A G intron_variant BRCA-EU 1 236030407 236030407 single base substitution G A intron_variant BRCA-EU 1 236030407 236030407 single base substitution G A upstream_gene_variant BRCA-EU 1 236032246 236032246 single base substitution C G intron_variant BRCA-EU 1 236032246 236032246 single base substitution C G upstream_gene_variant BRCA-EU 1 236032506 236032506 single base substitution C T intron_variant BRCA-EU 1 236032506 236032506 single base substitution C T upstream_gene_variant BRCA-EU 1 236032755 236032755 single base substitution G T intron_variant BRCA-EU 1 236032755 236032755 single base substitution G T upstream_gene_variant BRCA-EU 1 236032759 236032759 single base substitution G C intron_variant BRCA-EU 1 236032759 236032759 single base substitution G C upstream_gene_variant BRCA-EU 1 236032894 236032894 single base substitution A T intron_variant BRCA-EU 1 236032894 236032894 single base substitution A T upstream_gene_variant BRCA-EU 1 236033387 236033387 single base substitution G A intron_variant BRCA-EU 1 236033387 236033387 single base substitution G A upstream_gene_variant BRCA-EU 1 236033929 236033929 single base substitution T C intron_variant BRCA-EU 1 236033929 236033929 single base substitution T C upstream_gene_variant BRCA-EU 1 236035692 236035692 single base substitution A T intron_variant BRCA-EU 1 236035803 236035803 single base substitution C A intron_variant BRCA-EU 1 236036040 236036040 single base substitution C T intron_variant BRCA-EU 1 236036490 236036490 single base substitution A G intron_variant BRCA-EU 1 236036731 236036731 single base substitution A G intron_variant BRCA-EU 1 236037259 236037259 single base substitution G A intron_variant BRCA-EU 1 236037654 236037654 single base substitution G A intron_variant BRCA-EU 1 236038555 236038555 single base substitution A C intron_variant BRCA-EU 1 236039171 236039171 single base substitution A C intron_variant BRCA-EU 1 236039663 236039663 deletion of <=200bp A - intron_variant BRCA-EU 1 236039786 236039786 single base substitution G A intron_variant BRCA-EU 1 236041603 236041603 single base substitution G C intron_variant BRCA-EU 1 236042047 236042047 single base substitution T A intron_variant BRCA-EU 1 236042048 236042048 single base substitution G T intron_variant BRCA-EU 1 236042301 236042301 single base substitution C T intron_variant BRCA-EU 1 236042404 236042404 single base substitution C G intron_variant BRCA-EU 1 236042412 236042412 single base substitution C T intron_variant BRCA-EU 1 236042477 236042477 single base substitution C T intron_variant BRCA-EU 1 236043288 236043288 single base substitution C T intron_variant BRCA-EU 1 236043315 236043315 single base substitution G A intron_variant BRCA-EU 1 236043417 236043417 single base substitution A G intron_variant BRCA-EU 1 236044474 236044474 single base substitution G C intron_variant BRCA-EU 1 236044790 236044790 single base substitution G A intron_variant BRCA-EU 1 236045916 236045916 single base substitution T C intron_variant BRCA-EU 1 236048182 236048182 single base substitution G C upstream_gene_variant BRCA-EU 1 236049317 236049317 single base substitution A C upstream_gene_variant BRCA-EU 1 236049358 236049358 single base substitution G A upstream_gene_variant BRCA-EU 1 236049628 236049628 single base substitution G A upstream_gene_variant BRCA-EU 1 236050743 236050743 deletion of <=200bp T - upstream_gene_variant BRCA-EU 1 236050776 236050776 single base substitution G C upstream_gene_variant BRCA-EU 1 236051851 236051851 single base substitution G C upstream_gene_variant BRCA-FR 1 235839571 235839571 single base substitution C T intron_variant BRCA-FR 1 235854829 235854829 single base substitution A G intron_variant BRCA-FR 1 235860841 235860841 single base substitution G A intron_variant BRCA-FR 1 235862674 235862674 single base substitution G C intron_variant BRCA-FR 1 235862788 235862788 single base substitution T C intron_variant BRCA-FR 1 235863106 235863106 single base substitution G C intron_variant BRCA-FR 1 235868132 235868132 single base substitution C T downstream_gene_variant BRCA-FR 1 235868132 235868132 single base substitution C T intron_variant BRCA-FR 1 235868691 235868691 single base substitution T A downstream_gene_variant BRCA-FR 1 235868691 235868691 single base substitution T A intron_variant BRCA-FR 1 235872500 235872500 single base substitution A G downstream_gene_variant BRCA-FR 1 235872500 235872500 single base substitution A G exon_variant BRCA-FR 1 235872500 235872500 single base substitution A G missense_variant L3345P 10034T>C BRCA-FR 1 235873781 235873781 single base substitution C G downstream_gene_variant BRCA-FR 1 235873781 235873781 single base substitution C G intron_variant BRCA-FR 1 235879081 235879081 single base substitution G C intron_variant BRCA-FR 1 235879081 235879081 single base substitution G C upstream_gene_variant BRCA-FR 1 235879950 235879950 single base substitution C T intron_variant BRCA-FR 1 235879950 235879950 single base substitution C T upstream_gene_variant BRCA-FR 1 235890105 235890105 single base substitution G C intron_variant BRCA-FR 1 235891110 235891110 single base substitution G T intron_variant BRCA-FR 1 235891126 235891126 single base substitution G T intron_variant BRCA-FR 1 235892304 235892304 single base substitution G C intron_variant BRCA-FR 1 235892304 235892304 single base substitution G C upstream_gene_variant BRCA-FR 1 235895057 235895057 single base substitution C T intron_variant BRCA-FR 1 235895057 235895057 single base substitution C T upstream_gene_variant BRCA-FR 1 235899808 235899808 single base substitution G A downstream_gene_variant BRCA-FR 1 235899808 235899808 single base substitution G A exon_variant BRCA-FR 1 235899808 235899808 single base substitution G A intron_variant BRCA-FR 1 235908498 235908498 single base substitution C T downstream_gene_variant BRCA-FR 1 235908498 235908498 single base substitution C T intron_variant BRCA-FR 1 235908498 235908498 single base substitution C T upstream_gene_variant BRCA-FR 1 235914177 235914177 single base substitution G A intron_variant BRCA-FR 1 235917265 235917265 single base substitution C T intron_variant BRCA-FR 1 235917265 235917265 single base substitution C T upstream_gene_variant BRCA-FR 1 235923142 235923142 single base substitution C T intron_variant BRCA-FR 1 235927984 235927984 single base substitution G A intron_variant BRCA-FR 1 235936924 235936924 single base substitution G A intron_variant BRCA-FR 1 235949535 235949535 single base substitution G T downstream_gene_variant BRCA-FR 1 235949535 235949535 single base substitution G T intron_variant BRCA-FR 1 235950818 235950818 single base substitution C T downstream_gene_variant BRCA-FR 1 235950818 235950818 single base substitution C T intron_variant BRCA-FR 1 235955589 235955589 single base substitution G C intron_variant BRCA-FR 1 235955589 235955589 single base substitution G C upstream_gene_variant BRCA-FR 1 235955591 235955591 single base substitution A G intron_variant BRCA-FR 1 235955591 235955591 single base substitution A G upstream_gene_variant BRCA-FR 1 235970518 235970518 single base substitution C A intron_variant BRCA-FR 1 235971988 235971988 single base substitution C T exon_variant BRCA-FR 1 235971988 235971988 single base substitution C T synonymous_variant Q710Q 2130G>A BRCA-FR 1 235977035 235977035 single base substitution A C intron_variant BRCA-FR 1 235977159 235977159 single base substitution G A intron_variant BRCA-FR 1 235977690 235977690 single base substitution G A intron_variant BRCA-FR 1 235982348 235982348 single base substitution C A intron_variant BRCA-FR 1 235990570 235990570 single base substitution G A downstream_gene_variant BRCA-FR 1 235990570 235990570 single base substitution G A intron_variant BRCA-FR 1 235991392 235991392 single base substitution G C downstream_gene_variant BRCA-FR 1 235991392 235991392 single base substitution G C intron_variant BRCA-FR 1 235994520 235994520 single base substitution C G intron_variant BRCA-FR 1 236011205 236011205 single base substitution G C intron_variant BRCA-FR 1 236014178 236014178 single base substitution G C intron_variant BRCA-FR 1 236026602 236026602 single base substitution G C intron_variant BRCA-FR 1 236027716 236027716 single base substitution G A intron_variant BRCA-FR 1 236027925 236027925 single base substitution G C intron_variant BRCA-FR 1 236028793 236028793 single base substitution A G intron_variant BRCA-FR 1 236032088 236032088 single base substitution C T intron_variant BRCA-FR 1 236032088 236032088 single base substitution C T upstream_gene_variant BRCA-FR 1 236032506 236032506 single base substitution C T intron_variant BRCA-FR 1 236032506 236032506 single base substitution C T upstream_gene_variant BRCA-FR 1 236032759 236032759 single base substitution G C intron_variant BRCA-FR 1 236032759 236032759 single base substitution G C upstream_gene_variant BRCA-FR 1 236039171 236039171 single base substitution A C intron_variant BRCA-FR 1 236040595 236040595 single base substitution G C intron_variant BRCA-FR 1 236044474 236044474 single base substitution G C intron_variant BRCA-UK 1 235823248 235823248 single base substitution C G downstream_gene_variant BRCA-UK 1 235824304 235824304 single base substitution T C downstream_gene_variant BRCA-UK 1 235849335 235849335 single base substitution A G intron_variant BRCA-UK 1 235864761 235864761 single base substitution C A intron_variant BRCA-UK 1 235865334 235865334 single base substitution C G intron_variant BRCA-UK 1 235866481 235866481 single base substitution A T intron_variant BRCA-UK 1 235866883 235866883 single base substitution C A intron_variant BRCA-UK 1 235877168 235877168 single base substitution C T intron_variant BRCA-UK 1 235877168 235877168 single base substitution C T upstream_gene_variant BRCA-UK 1 235900726 235900726 single base substitution G T downstream_gene_variant BRCA-UK 1 235900726 235900726 single base substitution G T exon_variant BRCA-UK 1 235900726 235900726 single base substitution G T intron_variant BRCA-UK 1 235911086 235911086 single base substitution A T intron_variant BRCA-UK 1 235911086 235911086 single base substitution A T upstream_gene_variant BRCA-UK 1 235920728 235920728 single base substitution G C downstream_gene_variant BRCA-UK 1 235920728 235920728 single base substitution G C missense_variant C2304W 6912C>G BRCA-UK 1 235922479 235922479 single base substitution C T downstream_gene_variant BRCA-UK 1 235922479 235922479 single base substitution C T exon_variant BRCA-UK 1 235922479 235922479 single base substitution C T missense_variant R2225H 6674G>A BRCA-UK 1 235925870 235925870 single base substitution C G intron_variant BRCA-UK 1 235926105 235926105 single base substitution C G 3_prime_UTR_variant BRCA-UK 1 235926105 235926105 single base substitution C G exon_variant BRCA-UK 1 235926105 235926105 single base substitution C G missense_variant R2056S 6168G>C BRCA-UK 1 235936538 235936538 single base substitution G C intron_variant BRCA-UK 1 235962444 235962444 single base substitution G A intron_variant BRCA-UK 1 235969526 235969526 single base substitution G A exon_variant BRCA-UK 1 235969526 235969526 single base substitution G A synonymous_variant I970I 2910C>T BRCA-UK 1 235969598 235969598 single base substitution G A exon_variant BRCA-UK 1 235969598 235969598 single base substitution G A synonymous_variant L946L 2838C>T BRCA-UK 1 235972068 235972068 single base substitution C T exon_variant BRCA-UK 1 235972068 235972068 single base substitution C T missense_variant E684K 2050G>A BRCA-UK 1 235972232 235972232 single base substitution G T exon_variant BRCA-UK 1 235972232 235972232 single base substitution G T stop_gained S629* 1886C>A BRCA-UK 1 235975794 235975794 single base substitution G T intron_variant BRCA-UK 1 235978493 235978493 single base substitution C G intron_variant BRCA-UK 1 235996516 235996516 single base substitution C G intron_variant BRCA-UK 1 236000632 236000632 single base substitution T A intron_variant BRCA-UK 1 236012551 236012551 single base substitution G C intron_variant BRCA-UK 1 236044148 236044148 single base substitution G A intron_variant BRCA-UK 1 236049965 236049965 single base substitution G C upstream_gene_variant BRCA-UK 1 236050776 236050776 single base substitution G C upstream_gene_variant BRCA-US 1 235856727 235856727 single base substitution C T exon_variant BRCA-US 1 235856727 235856727 single base substitution C T missense_variant A3542T 10624G>A BRCA-US 1 235860498 235860498 single base substitution G T exon_variant BRCA-US 1 235860498 235860498 single base substitution G T synonymous_variant V3483V 10449C>A BRCA-US 1 235872479 235872479 single base substitution T G downstream_gene_variant BRCA-US 1 235872479 235872479 single base substitution T G exon_variant BRCA-US 1 235872479 235872479 single base substitution T G missense_variant Q3352P 10055A>C BRCA-US 1 235872544 235872544 single base substitution C T downstream_gene_variant BRCA-US 1 235872544 235872544 single base substitution C T exon_variant BRCA-US 1 235872544 235872544 single base substitution C T synonymous_variant A3330A 9990G>A BRCA-US 1 235872550 235872550 single base substitution A C downstream_gene_variant BRCA-US 1 235872550 235872550 single base substitution A C exon_variant BRCA-US 1 235872550 235872550 single base substitution A C synonymous_variant P3328P 9984T>G BRCA-US 1 235875443 235875443 single base substitution C G downstream_gene_variant BRCA-US 1 235875443 235875443 single base substitution C G exon_variant BRCA-US 1 235875443 235875443 single base substitution C G missense_variant R3280P 9839G>C BRCA-US 1 235884046 235884046 single base substitution C T exon_variant BRCA-US 1 235884046 235884046 single base substitution C T missense_variant D3159N 9475G>A BRCA-US 1 235891402 235891402 single base substitution T C exon_variant BRCA-US 1 235891402 235891402 single base substitution T C missense_variant N3046D 9136A>G BRCA-US 1 235904748 235904748 single base substitution G C exon_variant BRCA-US 1 235904748 235904748 single base substitution G C missense_variant R2778G 8332C>G BRCA-US 1 235904748 235904748 single base substitution G C upstream_gene_variant BRCA-US 1 235909789 235909789 single base substitution G A synonymous_variant L174L 520C>T BRCA-US 1 235909789 235909789 single base substitution G A synonymous_variant L2607L 7819C>T BRCA-US 1 235909789 235909789 single base substitution G A upstream_gene_variant BRCA-US 1 235909794 235909794 single base substitution G A missense_variant S172L 515C>T BRCA-US 1 235909794 235909794 single base substitution G A missense_variant S2605L 7814C>T BRCA-US 1 235909794 235909794 single base substitution G A upstream_gene_variant BRCA-US 1 235910542 235910542 single base substitution C T intron_variant BRCA-US 1 235910542 235910542 single base substitution C T missense_variant G137S 409G>A BRCA-US 1 235910542 235910542 single base substitution C T upstream_gene_variant BRCA-US 1 235916501 235916501 single base substitution C G missense_variant E2435Q 7303G>C BRCA-US 1 235916501 235916501 single base substitution C G upstream_gene_variant BRCA-US 1 235922289 235922289 single base substitution T A downstream_gene_variant BRCA-US 1 235922289 235922289 single base substitution T A synonymous_variant R2288R 6864A>T BRCA-US 1 235922292 235922292 single base substitution G T downstream_gene_variant BRCA-US 1 235922292 235922292 single base substitution G T missense_variant N2287K 6861C>A BRCA-US 1 235922444 235922444 single base substitution G A downstream_gene_variant BRCA-US 1 235922444 235922444 single base substitution G A stop_gained Q2237* 6709C>T BRCA-US 1 235926116 235926116 single base substitution T C 3_prime_UTR_variant BRCA-US 1 235926116 235926116 single base substitution T C exon_variant BRCA-US 1 235926116 235926116 single base substitution T C missense_variant M2053V 6157A>G BRCA-US 1 235940493 235940493 single base substitution G C 3_prime_UTR_variant BRCA-US 1 235940493 235940493 single base substitution G C exon_variant BRCA-US 1 235940493 235940493 single base substitution G C stop_gained S1777* 5330C>G BRCA-US 1 235945333 235945333 single base substitution A G 3_prime_UTR_variant BRCA-US 1 235945333 235945333 single base substitution A G exon_variant BRCA-US 1 235945333 235945333 single base substitution A G synonymous_variant S1639S 4917T>C BRCA-US 1 235967816 235967816 single base substitution A G exon_variant BRCA-US 1 235967816 235967816 single base substitution A G synonymous_variant A1181A 3543T>C BRCA-US 1 235969126 235969126 single base substitution G C exon_variant BRCA-US 1 235969126 235969126 single base substitution G C missense_variant R1104G 3310C>G BRCA-US 1 235969147 235969147 single base substitution C T exon_variant BRCA-US 1 235969147 235969147 single base substitution C T missense_variant E1097K 3289G>A BRCA-US 1 235969153 235969153 single base substitution C T exon_variant BRCA-US 1 235969153 235969153 single base substitution C T missense_variant E1095K 3283G>A BRCA-US 1 235969744 235969744 insertion of <=200bp - G exon_variant BRCA-US 1 235969744 235969744 insertion of <=200bp - G frameshift_variant I898T? BRCA-US 1 235969747 235969747 insertion of <=200bp - C exon_variant BRCA-US 1 235969747 235969747 insertion of <=200bp - C frameshift_variant T897S? BRCA-US 1 235969927 235969927 single base substitution G A exon_variant BRCA-US 1 235969927 235969927 single base substitution G A missense_variant P837S 2509C>T BRCA-US 1 235972478 235972478 single base substitution C A exon_variant BRCA-US 1 235972478 235972478 single base substitution C A missense_variant C547F 1640G>T BRCA-US 1 235972815 235972815 single base substitution C A exon_variant BRCA-US 1 235972815 235972815 single base substitution C A stop_gained E435* 1303G>T BRCA-US 1 235972931 235972931 single base substitution T C exon_variant BRCA-US 1 235972931 235972931 single base substitution T C missense_variant H396R 1187A>G BRCA-US 1 235973301 235973301 single base substitution C T exon_variant BRCA-US 1 235973301 235973301 single base substitution C T missense_variant V273I 817G>A BRCA-US 1 235993390 235993390 deletion of <=200bp T - exon_variant BRCA-US 1 235993390 235993390 deletion of <=200bp T - intron_variant BTCA-JP 1 235826383 235826383 deletion of <=200bp A - intron_variant BTCA-JP 1 235875559 235875559 single base substitution C T downstream_gene_variant BTCA-JP 1 235875559 235875559 single base substitution C T exon_variant BTCA-JP 1 235875559 235875559 single base substitution C T intron_variant BTCA-JP 1 235878545 235878545 single base substitution A C exon_variant BTCA-JP 1 235878545 235878545 single base substitution A C missense_variant L3247R 9740T>G BTCA-JP 1 235878545 235878545 single base substitution A C upstream_gene_variant BTCA-JP 1 235891542 235891542 single base substitution T C intron_variant BTCA-JP 1 235891542 235891542 single base substitution T C upstream_gene_variant BTCA-JP 1 235907534 235907534 single base substitution A G downstream_gene_variant BTCA-JP 1 235907534 235907534 single base substitution A G intron_variant BTCA-JP 1 235907534 235907534 single base substitution A G upstream_gene_variant BTCA-JP 1 235916449 235916451 deletion of <=200bp AGA - disruptive_inframe_deletion LL2451L BTCA-JP 1 235916449 235916451 deletion of <=200bp AGA - upstream_gene_variant BTCA-JP 1 235937359 235937359 single base substitution T C intron_variant BTCA-JP 1 235938341 235938341 single base substitution G A 3_prime_UTR_variant BTCA-JP 1 235938341 235938341 single base substitution G A exon_variant BTCA-JP 1 235938341 235938341 single base substitution G A stop_gained R1836* 5506C>T BTCA-JP 1 235938389 235938389 deletion of <=200bp A - splice_region_variant BTCA-JP 1 235956781 235956781 single base substitution G T intron_variant BTCA-JP 1 235956781 235956781 single base substitution G T upstream_gene_variant BTCA-JP 1 235971802 235971802 single base substitution G A exon_variant BTCA-JP 1 235971802 235971802 single base substitution G A synonymous_variant D772D 2316C>T BTCA-JP 1 235976438 235976438 single base substitution G A intron_variant BTCA-JP 1 235993743 235993743 deletion of <=200bp A - intron_variant CESC-US 1 235824371 235824371 single base substitution G C 3_prime_UTR_variant CESC-US 1 235824371 235824371 single base substitution G C exon_variant CESC-US 1 235850285 235850285 single base substitution G A exon_variant CESC-US 1 235850285 235850285 single base substitution G A synonymous_variant V3588V 10764C>T CESC-US 1 235944211 235944211 single base substitution C G 3_prime_UTR_variant CESC-US 1 235944211 235944211 single base substitution C G exon_variant CESC-US 1 235944211 235944211 single base substitution C G missense_variant R1723T 5168G>C CESC-US 1 235944340 235944340 single base substitution G C 3_prime_UTR_variant CESC-US 1 235944340 235944340 single base substitution G C exon_variant CESC-US 1 235944340 235944340 single base substitution G C stop_gained S1680* 5039C>G CESC-US 1 235952024 235952024 single base substitution G T 3_prime_UTR_variant CESC-US 1 235952024 235952024 single base substitution G T downstream_gene_variant CESC-US 1 235952024 235952024 single base substitution G T exon_variant CESC-US 1 235952024 235952024 single base substitution G T synonymous_variant P1555P 4665C>A CESC-US 1 235955247 235955247 single base substitution G A exon_variant CESC-US 1 235955247 235955247 single base substitution G A intron_variant CESC-US 1 235955247 235955247 single base substitution G A missense_variant S1432L 4295C>T CESC-US 1 235955247 235955247 single base substitution G A upstream_gene_variant CESC-US 1 235964185 235964185 single base substitution G C exon_variant CESC-US 1 235964185 235964185 single base substitution G C missense_variant L1309V 3925C>G CESC-US 1 235964366 235964366 single base substitution G A exon_variant CESC-US 1 235964366 235964366 single base substitution G A synonymous_variant F1248F 3744C>T CESC-US 1 235969198 235969198 single base substitution C G exon_variant CESC-US 1 235969198 235969198 single base substitution C G missense_variant A1080P 3238G>C CESC-US 1 235969573 235969573 single base substitution C G exon_variant CESC-US 1 235969573 235969573 single base substitution C G missense_variant E955Q 2863G>C CESC-US 1 235973634 235973634 single base substitution G T exon_variant CESC-US 1 235973634 235973634 single base substitution G T missense_variant Q162K 484C>A CLLE-ES 1 235835939 235835939 single base substitution T C intron_variant CLLE-ES 1 235846436 235846436 single base substitution T C intron_variant CLLE-ES 1 235854229 235854229 single base substitution T C intron_variant CLLE-ES 1 235873713 235873713 single base substitution G A downstream_gene_variant CLLE-ES 1 235873713 235873713 single base substitution G A intron_variant CLLE-ES 1 235882866 235882866 single base substitution T G intron_variant CLLE-ES 1 235916696 235916696 single base substitution A G intron_variant CLLE-ES 1 235916696 235916696 single base substitution A G upstream_gene_variant CLLE-ES 1 235934350 235934350 single base substitution T C intron_variant CLLE-ES 1 235938328 235938328 single base substitution G A 3_prime_UTR_variant CLLE-ES 1 235938328 235938328 single base substitution G A exon_variant CLLE-ES 1 235938328 235938328 single base substitution G A missense_variant S1840L 5519C>T CLLE-ES 1 235961879 235961903 deletion of <=200bp AAAAAAAAAAAAAAAAAAAAAAAAA - intron_variant CLLE-ES 1 235975850 235975850 single base substitution A C intron_variant CLLE-ES 1 235990411 235990411 single base substitution C T downstream_gene_variant CLLE-ES 1 235990411 235990411 single base substitution C T intron_variant CLLE-ES 1 236010087 236010087 single base substitution G T intron_variant CLLE-ES 1 236022949 236022949 single base substitution T A intron_variant CLLE-ES 1 236033524 236033524 single base substitution C T intron_variant CLLE-ES 1 236033524 236033524 single base substitution C T upstream_gene_variant CLLE-ES 1 236046118 236046118 single base substitution T C intron_variant COAD-US 1 235827874 235827874 single base substitution C T exon_variant COAD-US 1 235827874 235827874 single base substitution C T missense_variant V3696I 11086G>A COAD-US 1 235856654 235856654 single base substitution T C exon_variant COAD-US 1 235856654 235856654 single base substitution T C missense_variant Y3566C 10697A>G COAD-US 1 235860531 235860531 single base substitution G A exon_variant COAD-US 1 235860531 235860531 single base substitution G A synonymous_variant Y3472Y 10416C>T COAD-US 1 235860557 235860557 single base substitution T C exon_variant COAD-US 1 235860557 235860557 single base substitution T C missense_variant I3464V 10390A>G COAD-US 1 235884060 235884060 single base substitution C T exon_variant COAD-US 1 235884060 235884060 single base substitution C T missense_variant G3154D 9461G>A COAD-US 1 235884120 235884120 single base substitution A C exon_variant COAD-US 1 235884120 235884120 single base substitution A C stop_gained L3134* 9401T>G COAD-US 1 235907315 235907315 single base substitution A C downstream_gene_variant COAD-US 1 235907315 235907315 single base substitution A C exon_variant COAD-US 1 235907315 235907315 single base substitution A C missense_variant I2705M 8115T>G COAD-US 1 235909738 235909738 single base substitution G A downstream_gene_variant COAD-US 1 235909738 235909738 single base substitution G A missense_variant R2624W 7870C>T COAD-US 1 235909738 235909738 single base substitution G A upstream_gene_variant COAD-US 1 235918870 235918870 single base substitution T G downstream_gene_variant COAD-US 1 235918870 235918870 single base substitution T G synonymous_variant L2379L 7137A>C COAD-US 1 235918870 235918870 single base substitution T G upstream_gene_variant COAD-US 1 235922805 235922805 single base substitution C T 3_prime_UTR_variant COAD-US 1 235922805 235922805 single base substitution C T exon_variant COAD-US 1 235922805 235922805 single base substitution C T synonymous_variant T2116T 6348G>A COAD-US 1 235938389 235938389 deletion of <=200bp A - splice_region_variant COAD-US 1 235955345 235955345 single base substitution T C exon_variant COAD-US 1 235955345 235955345 single base substitution T C intron_variant COAD-US 1 235955345 235955345 single base substitution T C synonymous_variant L1399L 4197A>G COAD-US 1 235955345 235955345 single base substitution T C upstream_gene_variant COAD-US 1 235956908 235956908 single base substitution G A exon_variant COAD-US 1 235956908 235956908 single base substitution G A synonymous_variant C1337C 4011C>T COAD-US 1 235956908 235956908 single base substitution G A upstream_gene_variant COAD-US 1 235967852 235967852 single base substitution G A exon_variant COAD-US 1 235967852 235967852 single base substitution G A synonymous_variant L1169L 3507C>T COAD-US 1 235969113 235969113 single base substitution G A exon_variant COAD-US 1 235969113 235969113 single base substitution G A missense_variant A1108V 3323C>T COAD-US 1 235969317 235969317 single base substitution G T exon_variant COAD-US 1 235969317 235969317 single base substitution G T missense_variant S1040Y 3119C>A COAD-US 1 235969866 235969866 single base substitution G T exon_variant COAD-US 1 235969866 235969866 single base substitution G T missense_variant S857Y 2570C>A COAD-US 1 235969998 235969998 single base substitution C T exon_variant COAD-US 1 235969998 235969998 single base substitution C T missense_variant R813Q 2438G>A COAD-US 1 235972351 235972351 single base substitution T G exon_variant COAD-US 1 235972351 235972351 single base substitution T G missense_variant K589N 1767A>C COAD-US 1 235972459 235972459 single base substitution A G exon_variant COAD-US 1 235972459 235972459 single base substitution A G synonymous_variant C553C 1659T>C COAD-US 1 235973040 235973040 single base substitution C T exon_variant COAD-US 1 235973040 235973040 single base substitution C T missense_variant A360T 1078G>A COAD-US 1 235973062 235973062 single base substitution A T exon_variant COAD-US 1 235973062 235973062 single base substitution A T missense_variant N352K 1056T>A COAD-US 1 235973133 235973133 single base substitution G A exon_variant COAD-US 1 235973133 235973133 single base substitution G A stop_gained R329* 985C>T COCA-CN 1 235826190 235826190 single base substitution A C 3_prime_UTR_variant COCA-CN 1 235826190 235826190 single base substitution A C exon_variant COCA-CN 1 235840884 235840884 single base substitution G T exon_variant COCA-CN 1 235840884 235840884 single base substitution G T synonymous_variant L3612L 10836C>A COCA-CN 1 235860500 235860500 single base substitution C T exon_variant COCA-CN 1 235860500 235860500 single base substitution C T missense_variant V3483I 10447G>A COCA-CN 1 235866229 235866229 single base substitution G A exon_variant COCA-CN 1 235866229 235866229 single base substitution G A stop_gained R3398* 10192C>T COCA-CN 1 235872347 235872347 single base substitution T C downstream_gene_variant COCA-CN 1 235872347 235872347 single base substitution T C intron_variant COCA-CN 1 235875408 235875408 single base substitution C A downstream_gene_variant COCA-CN 1 235875408 235875408 single base substitution C A exon_variant COCA-CN 1 235875408 235875408 single base substitution C A stop_gained E3292* 9874G>T COCA-CN 1 235878664 235878664 single base substitution G T splice_region_variant COCA-CN 1 235878664 235878664 single base substitution G T upstream_gene_variant COCA-CN 1 235883949 235883949 single base substitution C A intron_variant COCA-CN 1 235894036 235894036 single base substitution T C intron_variant COCA-CN 1 235894036 235894036 single base substitution T C upstream_gene_variant COCA-CN 1 235894403 235894403 single base substitution C A exon_variant COCA-CN 1 235894403 235894403 single base substitution C A missense_variant R2959M 8876G>T COCA-CN 1 235894403 235894403 single base substitution C A upstream_gene_variant COCA-CN 1 235909728 235909728 single base substitution C T downstream_gene_variant COCA-CN 1 235909728 235909728 single base substitution C T missense_variant S2627N 7880G>A COCA-CN 1 235909728 235909728 single base substitution C T upstream_gene_variant COCA-CN 1 235910572 235910572 single base substitution A G intron_variant COCA-CN 1 235910572 235910572 single base substitution A G missense_variant Y127H 379T>C COCA-CN 1 235910572 235910572 single base substitution A G upstream_gene_variant COCA-CN 1 235916499 235916499 single base substitution C A missense_variant E2435D 7305G>T COCA-CN 1 235916499 235916499 single base substitution C A upstream_gene_variant COCA-CN 1 235918742 235918742 single base substitution G T downstream_gene_variant COCA-CN 1 235918742 235918742 single base substitution G T intron_variant COCA-CN 1 235918742 235918742 single base substitution G T upstream_gene_variant COCA-CN 1 235922805 235922805 single base substitution C T 3_prime_UTR_variant COCA-CN 1 235922805 235922805 single base substitution C T exon_variant COCA-CN 1 235922805 235922805 single base substitution C T synonymous_variant T2116T 6348G>A COCA-CN 1 235933513 235933513 single base substitution A G 3_prime_UTR_variant COCA-CN 1 235933513 235933513 single base substitution A G exon_variant COCA-CN 1 235933513 235933513 single base substitution A G synonymous_variant L1957L 5869T>C COCA-CN 1 235955062 235955062 single base substitution C A exon_variant COCA-CN 1 235955062 235955062 single base substitution C A intron_variant COCA-CN 1 235955062 235955062 single base substitution C A stop_gained G1494* 4480G>T COCA-CN 1 235955062 235955062 single base substitution C A upstream_gene_variant COCA-CN 1 235955437 235955437 single base substitution G T intron_variant COCA-CN 1 235955437 235955437 single base substitution G T upstream_gene_variant COCA-CN 1 235955442 235955442 single base substitution A G intron_variant COCA-CN 1 235955442 235955442 single base substitution A G upstream_gene_variant COCA-CN 1 235963764 235963764 single base substitution C A intron_variant COCA-CN 1 235966392 235966392 single base substitution T G intron_variant COCA-CN 1 235966394 235966394 single base substitution A T intron_variant COCA-CN 1 235967776 235967776 single base substitution G T intron_variant COCA-CN 1 235968032 235968032 single base substitution A G intron_variant COCA-CN 1 235969067 235969067 single base substitution C A exon_variant COCA-CN 1 235969067 235969067 single base substitution C A missense_variant K1123N 3369G>T COCA-CN 1 235970023 235970023 single base substitution C T exon_variant COCA-CN 1 235970023 235970023 single base substitution C T missense_variant E805K 2413G>A COCA-CN 1 235972359 235972359 single base substitution C A exon_variant COCA-CN 1 235972359 235972359 single base substitution C A missense_variant D587Y 1759G>T COCA-CN 1 235972482 235972482 single base substitution G A exon_variant COCA-CN 1 235972482 235972482 single base substitution G A missense_variant R546W 1636C>T COCA-CN 1 235972610 235972610 single base substitution C T exon_variant COCA-CN 1 235972610 235972610 single base substitution C T missense_variant R503Q 1508G>A COCA-CN 1 235993676 235993676 single base substitution G A exon_variant COCA-CN 1 235993676 235993676 single base substitution G A synonymous_variant T14T 42C>T COCA-CN 1 236016452 236016452 single base substitution T G intron_variant EOPC-DE 1 235919351 235919351 single base substitution A G downstream_gene_variant EOPC-DE 1 235919351 235919351 single base substitution A G intron_variant EOPC-DE 1 235919351 235919351 single base substitution A G upstream_gene_variant EOPC-DE 1 235947861 235947861 single base substitution C T downstream_gene_variant EOPC-DE 1 235947861 235947861 single base substitution C T intron_variant ESAD-UK 1 235819348 235819348 single base substitution C A downstream_gene_variant ESAD-UK 1 235820195 235820195 single base substitution T C downstream_gene_variant ESAD-UK 1 235820829 235820829 single base substitution C T downstream_gene_variant ESAD-UK 1 235822690 235822690 single base substitution C A downstream_gene_variant ESAD-UK 1 235822783 235822783 single base substitution T C downstream_gene_variant ESAD-UK 1 235826250 235826250 single base substitution G A exon_variant ESAD-UK 1 235826250 235826250 single base substitution G A missense_variant A3799V 11396C>T ESAD-UK 1 235826480 235826480 single base substitution T A intron_variant ESAD-UK 1 235826821 235826821 single base substitution G A intron_variant ESAD-UK 1 235827376 235827376 single base substitution C G intron_variant ESAD-UK 1 235828019 235828019 single base substitution G T intron_variant ESAD-UK 1 235828635 235828635 single base substitution C T intron_variant ESAD-UK 1 235828999 235828999 single base substitution T G intron_variant ESAD-UK 1 235829079 235829079 single base substitution C G intron_variant ESAD-UK 1 235830955 235830955 single base substitution T A intron_variant ESAD-UK 1 235831065 235831065 single base substitution C T intron_variant ESAD-UK 1 235831504 235831504 insertion of <=200bp - AT intron_variant ESAD-UK 1 235833025 235833025 single base substitution C A intron_variant ESAD-UK 1 235833254 235833254 single base substitution T G intron_variant ESAD-UK 1 235838288 235838288 single base substitution T G intron_variant ESAD-UK 1 235838416 235838416 single base substitution C T intron_variant ESAD-UK 1 235840066 235840066 deletion of <=200bp A - intron_variant ESAD-UK 1 235840733 235840733 single base substitution G A intron_variant ESAD-UK 1 235841016 235841016 single base substitution C T intron_variant ESAD-UK 1 235841318 235841318 single base substitution T A intron_variant ESAD-UK 1 235842303 235842303 single base substitution C A intron_variant ESAD-UK 1 235842399 235842399 single base substitution C T intron_variant ESAD-UK 1 235843344 235843344 single base substitution T G intron_variant ESAD-UK 1 235843959 235843959 single base substitution C T intron_variant ESAD-UK 1 235844833 235844833 single base substitution C A intron_variant ESAD-UK 1 235846476 235846476 single base substitution C A intron_variant ESAD-UK 1 235846983 235846983 deletion of <=200bp G - intron_variant ESAD-UK 1 235847328 235847328 single base substitution C A intron_variant ESAD-UK 1 235849451 235849451 single base substitution G T intron_variant ESAD-UK 1 235849638 235849638 single base substitution G T intron_variant ESAD-UK 1 235850464 235850464 single base substitution T C intron_variant ESAD-UK 1 235856066 235856066 single base substitution A C intron_variant ESAD-UK 1 235856508 235856508 single base substitution T G intron_variant ESAD-UK 1 235857657 235857657 single base substitution A C intron_variant ESAD-UK 1 235861836 235861836 deletion of <=200bp T - intron_variant ESAD-UK 1 235861900 235861900 single base substitution G A intron_variant ESAD-UK 1 235867392 235867392 single base substitution T C intron_variant ESAD-UK 1 235869449 235869449 single base substitution C A downstream_gene_variant ESAD-UK 1 235869449 235869449 single base substitution C A intron_variant ESAD-UK 1 235871011 235871011 single base substitution A G downstream_gene_variant ESAD-UK 1 235871011 235871011 single base substitution A G intron_variant ESAD-UK 1 235871174 235871174 insertion of <=200bp - G downstream_gene_variant ESAD-UK 1 235871174 235871174 insertion of <=200bp - G intron_variant ESAD-UK 1 235872390 235872390 single base substitution C A downstream_gene_variant ESAD-UK 1 235872390 235872390 single base substitution C A splice_donor_variant ESAD-UK 1 235873834 235873834 single base substitution C T downstream_gene_variant ESAD-UK 1 235873834 235873834 single base substitution C T intron_variant ESAD-UK 1 235873876 235873876 single base substitution C T downstream_gene_variant ESAD-UK 1 235873876 235873876 single base substitution C T intron_variant ESAD-UK 1 235875554 235875554 single base substitution C A downstream_gene_variant ESAD-UK 1 235875554 235875554 single base substitution C A exon_variant ESAD-UK 1 235875554 235875554 single base substitution C A intron_variant ESAD-UK 1 235876086 235876086 insertion of <=200bp - C downstream_gene_variant ESAD-UK 1 235876086 235876086 insertion of <=200bp - C intron_variant ESAD-UK 1 235876086 235876086 insertion of <=200bp - C upstream_gene_variant ESAD-UK 1 235876323 235876323 single base substitution A T downstream_gene_variant ESAD-UK 1 235876323 235876323 single base substitution A T intron_variant ESAD-UK 1 235876323 235876323 single base substitution A T upstream_gene_variant ESAD-UK 1 235878307 235878307 single base substitution G A intron_variant ESAD-UK 1 235878307 235878307 single base substitution G A upstream_gene_variant ESAD-UK 1 235880694 235880694 single base substitution C T intron_variant ESAD-UK 1 235880694 235880694 single base substitution C T upstream_gene_variant ESAD-UK 1 235881084 235881084 single base substitution G A intron_variant ESAD-UK 1 235881883 235881883 single base substitution T C intron_variant ESAD-UK 1 235882086 235882086 single base substitution C A intron_variant ESAD-UK 1 235882925 235882925 single base substitution G A intron_variant ESAD-UK 1 235883389 235883389 single base substitution C T intron_variant ESAD-UK 1 235885501 235885501 single base substitution C T intron_variant ESAD-UK 1 235885502 235885502 single base substitution G A intron_variant ESAD-UK 1 235886589 235886589 single base substitution T C intron_variant ESAD-UK 1 235886901 235886901 single base substitution C T intron_variant ESAD-UK 1 235887620 235887620 single base substitution C T intron_variant ESAD-UK 1 235887663 235887663 deletion of <=200bp A - intron_variant ESAD-UK 1 235888161 235888161 single base substitution C T intron_variant ESAD-UK 1 235888362 235888362 single base substitution G T intron_variant ESAD-UK 1 235891336 235891336 single base substitution G A intron_variant ESAD-UK 1 235892103 235892103 single base substitution G C intron_variant ESAD-UK 1 235892103 235892103 single base substitution G C upstream_gene_variant ESAD-UK 1 235892199 235892199 single base substitution G A intron_variant ESAD-UK 1 235892199 235892199 single base substitution G A upstream_gene_variant ESAD-UK 1 235893261 235893261 single base substitution G T intron_variant ESAD-UK 1 235893261 235893261 single base substitution G T upstream_gene_variant ESAD-UK 1 235894114 235894114 single base substitution T C intron_variant ESAD-UK 1 235894114 235894114 single base substitution T C upstream_gene_variant ESAD-UK 1 235894708 235894708 single base substitution C G intron_variant ESAD-UK 1 235894708 235894708 single base substitution C G upstream_gene_variant ESAD-UK 1 235895600 235895600 single base substitution C A intron_variant ESAD-UK 1 235895600 235895600 single base substitution C A upstream_gene_variant ESAD-UK 1 235896043 235896043 single base substitution G T intron_variant ESAD-UK 1 235896043 235896043 single base substitution G T upstream_gene_variant ESAD-UK 1 235899051 235899051 single base substitution T C downstream_gene_variant ESAD-UK 1 235899051 235899051 single base substitution T C exon_variant ESAD-UK 1 235899051 235899051 single base substitution T C intron_variant ESAD-UK 1 235900204 235900204 single base substitution A G downstream_gene_variant ESAD-UK 1 235900204 235900204 single base substitution A G exon_variant ESAD-UK 1 235900204 235900204 single base substitution A G intron_variant ESAD-UK 1 235900344 235900344 deletion of <=200bp A - downstream_gene_variant ESAD-UK 1 235900344 235900344 deletion of <=200bp A - exon_variant ESAD-UK 1 235900344 235900344 deletion of <=200bp A - intron_variant ESAD-UK 1 235900904 235900904 single base substitution A C downstream_gene_variant ESAD-UK 1 235900904 235900904 single base substitution A C exon_variant ESAD-UK 1 235900904 235900904 single base substitution A C intron_variant ESAD-UK 1 235902359 235902359 single base substitution G T intron_variant ESAD-UK 1 235902359 235902359 single base substitution G T upstream_gene_variant ESAD-UK 1 235906487 235906487 single base substitution T C downstream_gene_variant ESAD-UK 1 235906487 235906487 single base substitution T C intron_variant ESAD-UK 1 235907115 235907115 single base substitution C T downstream_gene_variant ESAD-UK 1 235907115 235907115 single base substitution C T intron_variant ESAD-UK 1 235907262 235907262 single base substitution G A downstream_gene_variant ESAD-UK 1 235907262 235907262 single base substitution G A intron_variant ESAD-UK 1 235907347 235907347 single base substitution A G downstream_gene_variant ESAD-UK 1 235907347 235907347 single base substitution A G missense_variant S2695P 8083T>C ESAD-UK 1 235907347 235907347 single base substitution A G upstream_gene_variant ESAD-UK 1 235907844 235907844 single base substitution C T downstream_gene_variant ESAD-UK 1 235907844 235907844 single base substitution C T intron_variant ESAD-UK 1 235907844 235907844 single base substitution C T upstream_gene_variant ESAD-UK 1 235908224 235908224 single base substitution G T downstream_gene_variant ESAD-UK 1 235908224 235908224 single base substitution G T intron_variant ESAD-UK 1 235908224 235908224 single base substitution G T upstream_gene_variant ESAD-UK 1 235908241 235908241 insertion of <=200bp - A downstream_gene_variant ESAD-UK 1 235908241 235908241 insertion of <=200bp - A intron_variant ESAD-UK 1 235908241 235908241 insertion of <=200bp - A upstream_gene_variant ESAD-UK 1 235908517 235908517 deletion of <=200bp T - downstream_gene_variant ESAD-UK 1 235908517 235908517 deletion of <=200bp T - intron_variant ESAD-UK 1 235908517 235908517 deletion of <=200bp T - upstream_gene_variant ESAD-UK 1 235908593 235908593 single base substitution G T downstream_gene_variant ESAD-UK 1 235908593 235908593 single base substitution G T intron_variant ESAD-UK 1 235908593 235908593 single base substitution G T upstream_gene_variant ESAD-UK 1 235911030 235911030 single base substitution G C intron_variant ESAD-UK 1 235911030 235911030 single base substitution G C upstream_gene_variant ESAD-UK 1 235912607 235912607 single base substitution C A intron_variant ESAD-UK 1 235916940 235916940 single base substitution T A intron_variant ESAD-UK 1 235916940 235916940 single base substitution T A upstream_gene_variant ESAD-UK 1 235917365 235917365 single base substitution C T intron_variant ESAD-UK 1 235917365 235917365 single base substitution C T upstream_gene_variant ESAD-UK 1 235917976 235917976 single base substitution G A downstream_gene_variant ESAD-UK 1 235917976 235917976 single base substitution G A intron_variant ESAD-UK 1 235917976 235917976 single base substitution G A upstream_gene_variant ESAD-UK 1 235918889 235918889 single base substitution T C downstream_gene_variant ESAD-UK 1 235918889 235918889 single base substitution T C missense_variant N2373S 7118A>G ESAD-UK 1 235918889 235918889 single base substitution T C upstream_gene_variant ESAD-UK 1 235922858 235922858 single base substitution G A 3_prime_UTR_variant ESAD-UK 1 235922858 235922858 single base substitution G A exon_variant ESAD-UK 1 235922858 235922858 single base substitution G A missense_variant H2099Y 6295C>T ESAD-UK 1 235923706 235923706 single base substitution T G intron_variant ESAD-UK 1 235924411 235924411 single base substitution T A intron_variant ESAD-UK 1 235924824 235924824 single base substitution G T intron_variant ESAD-UK 1 235925166 235925166 single base substitution G T intron_variant ESAD-UK 1 235926164 235926164 insertion of <=200bp - T intron_variant ESAD-UK 1 235926299 235926299 single base substitution G A intron_variant ESAD-UK 1 235926623 235926623 single base substitution C T intron_variant ESAD-UK 1 235930460 235930460 single base substitution A T intron_variant ESAD-UK 1 235930981 235930981 single base substitution T C intron_variant ESAD-UK 1 235931241 235931241 single base substitution T C intron_variant ESAD-UK 1 235931254 235931254 single base substitution G A intron_variant ESAD-UK 1 235932049 235932049 single base substitution T G intron_variant ESAD-UK 1 235932794 235932794 single base substitution C T intron_variant ESAD-UK 1 235933548 235933548 single base substitution G A 3_prime_UTR_variant ESAD-UK 1 235933548 235933548 single base substitution G A exon_variant ESAD-UK 1 235933548 235933548 single base substitution G A missense_variant A1945V 5834C>T ESAD-UK 1 235934744 235934744 single base substitution T C intron_variant ESAD-UK 1 235936589 235936589 single base substitution G T intron_variant ESAD-UK 1 235940324 235940324 single base substitution C T intron_variant ESAD-UK 1 235941580 235941580 single base substitution G T intron_variant ESAD-UK 1 235942117 235942117 single base substitution A C intron_variant ESAD-UK 1 235945141 235945141 deletion of <=200bp A - intron_variant ESAD-UK 1 235945401 235945401 single base substitution A G downstream_gene_variant ESAD-UK 1 235945401 235945401 single base substitution A G intron_variant ESAD-UK 1 235947188 235947188 single base substitution C T downstream_gene_variant ESAD-UK 1 235947188 235947188 single base substitution C T intron_variant ESAD-UK 1 235948276 235948276 single base substitution A T downstream_gene_variant ESAD-UK 1 235948276 235948276 single base substitution A T intron_variant ESAD-UK 1 235951643 235951643 insertion of <=200bp - T downstream_gene_variant ESAD-UK 1 235951643 235951643 insertion of <=200bp - T intron_variant ESAD-UK 1 235953056 235953056 single base substitution T A downstream_gene_variant ESAD-UK 1 235953056 235953056 single base substitution T A intron_variant ESAD-UK 1 235953056 235953056 single base substitution T A upstream_gene_variant ESAD-UK 1 235957129 235957129 single base substitution A T intron_variant ESAD-UK 1 235957129 235957129 single base substitution A T upstream_gene_variant ESAD-UK 1 235961456 235961456 single base substitution C T intron_variant ESAD-UK 1 235964220 235964220 insertion of <=200bp - A exon_variant ESAD-UK 1 235964220 235964220 insertion of <=200bp - A frameshift_variant L1297F? ESAD-UK 1 235964288 235964288 single base substitution C T exon_variant ESAD-UK 1 235964288 235964288 single base substitution C T synonymous_variant L1274L 3822G>A ESAD-UK 1 235964716 235964716 insertion of <=200bp - C intron_variant ESAD-UK 1 235964974 235964974 single base substitution T A intron_variant ESAD-UK 1 235966354 235966354 single base substitution G A exon_variant ESAD-UK 1 235966354 235966354 single base substitution G A missense_variant S1189F 3566C>T ESAD-UK 1 235967152 235967152 single base substitution T C intron_variant ESAD-UK 1 235968578 235968578 single base substitution T A intron_variant ESAD-UK 1 235968970 235968970 single base substitution T A intron_variant ESAD-UK 1 235969366 235969366 single base substitution A G exon_variant ESAD-UK 1 235969366 235969366 single base substitution A G synonymous_variant L1024L 3070T>C ESAD-UK 1 235970459 235970459 single base substitution T C intron_variant ESAD-UK 1 235975987 235975987 single base substitution T C intron_variant ESAD-UK 1 235976360 235976360 single base substitution G C missense_variant A65G 194C>G ESAD-UK 1 235976360 235976360 single base substitution G C splice_region_variant ESAD-UK 1 235978699 235978699 single base substitution T G intron_variant ESAD-UK 1 235979757 235979757 single base substitution T A intron_variant ESAD-UK 1 235979979 235979979 single base substitution G A intron_variant ESAD-UK 1 235983366 235983366 single base substitution A T intron_variant ESAD-UK 1 235991520 235991520 single base substitution A G downstream_gene_variant ESAD-UK 1 235991520 235991520 single base substitution A G intron_variant ESAD-UK 1 235992388 235992388 single base substitution C T downstream_gene_variant ESAD-UK 1 235992388 235992388 single base substitution C T intron_variant ESAD-UK 1 235993244 235993244 single base substitution C T exon_variant ESAD-UK 1 235993244 235993244 single base substitution C T intron_variant ESAD-UK 1 235993787 235993787 single base substitution C G intron_variant ESAD-UK 1 235995403 235995403 single base substitution C T intron_variant ESAD-UK 1 236002084 236002084 single base substitution C A intron_variant ESAD-UK 1 236002891 236002891 single base substitution C T intron_variant ESAD-UK 1 236003865 236003865 single base substitution G A intron_variant ESAD-UK 1 236003906 236003906 single base substitution G A intron_variant ESAD-UK 1 236004359 236004359 single base substitution T G intron_variant ESAD-UK 1 236005956 236005956 single base substitution G A intron_variant ESAD-UK 1 236008123 236008123 single base substitution A C intron_variant ESAD-UK 1 236008459 236008459 single base substitution G A intron_variant ESAD-UK 1 236009272 236009272 single base substitution C T intron_variant ESAD-UK 1 236011082 236011082 single base substitution A T intron_variant ESAD-UK 1 236011439 236011439 single base substitution C T intron_variant ESAD-UK 1 236013036 236013036 single base substitution G T intron_variant ESAD-UK 1 236014104 236014104 single base substitution G C intron_variant ESAD-UK 1 236015507 236015507 single base substitution C T intron_variant ESAD-UK 1 236017951 236017951 single base substitution A G intron_variant ESAD-UK 1 236020049 236020049 single base substitution A G intron_variant ESAD-UK 1 236022144 236022144 single base substitution G T intron_variant ESAD-UK 1 236022725 236022725 single base substitution A C intron_variant ESAD-UK 1 236023294 236023294 single base substitution G A intron_variant ESAD-UK 1 236025086 236025086 single base substitution C T intron_variant ESAD-UK 1 236025780 236025780 single base substitution C A intron_variant ESAD-UK 1 236026230 236026230 single base substitution G C intron_variant ESAD-UK 1 236032780 236032780 single base substitution A T intron_variant ESAD-UK 1 236032780 236032780 single base substitution A T upstream_gene_variant ESAD-UK 1 236033929 236033929 single base substitution T C intron_variant ESAD-UK 1 236033929 236033929 single base substitution T C upstream_gene_variant ESAD-UK 1 236034381 236034381 single base substitution G C intron_variant ESAD-UK 1 236034381 236034381 single base substitution G C upstream_gene_variant ESAD-UK 1 236036964 236036964 single base substitution T C intron_variant ESAD-UK 1 236037438 236037438 single base substitution C A intron_variant ESAD-UK 1 236038415 236038415 single base substitution C T intron_variant ESAD-UK 1 236038964 236038964 single base substitution G C intron_variant ESAD-UK 1 236039663 236039663 insertion of <=200bp - A intron_variant ESAD-UK 1 236043792 236043792 single base substitution C A intron_variant ESAD-UK 1 236045938 236045938 single base substitution A G intron_variant ESCA-CN 1 235824598 235824598 single base substitution A T 3_prime_UTR_variant ESCA-CN 1 235824598 235824598 single base substitution A T exon_variant ESCA-CN 1 235826324 235826324 single base substitution G A exon_variant ESCA-CN 1 235826324 235826324 single base substitution G A synonymous_variant T3774T 11322C>T ESCA-CN 1 235892975 235892975 single base substitution A C intron_variant ESCA-CN 1 235892975 235892975 single base substitution A C upstream_gene_variant ESCA-CN 1 235897013 235897013 deletion of <=200bp C - downstream_gene_variant ESCA-CN 1 235897013 235897013 deletion of <=200bp C - intron_variant ESCA-CN 1 235897191 235897191 single base substitution C T downstream_gene_variant ESCA-CN 1 235897191 235897191 single base substitution C T exon_variant ESCA-CN 1 235897191 235897191 single base substitution C T missense_variant E2851K 8551G>A ESCA-CN 1 235904829 235904829 single base substitution T C downstream_gene_variant ESCA-CN 1 235904829 235904829 single base substitution T C exon_variant ESCA-CN 1 235904829 235904829 single base substitution T C missense_variant I2751V 8251A>G ESCA-CN 1 235904829 235904829 single base substitution T C upstream_gene_variant ESCA-CN 1 235966336 235966336 single base substitution G A exon_variant ESCA-CN 1 235966336 235966336 single base substitution G A missense_variant S1195F 3584C>T ESCA-CN 1 235993566 235993566 single base substitution C A exon_variant ESCA-CN 1 235993566 235993566 single base substitution C A missense_variant G51V 152G>T GBM-US 1 235860518 235860518 single base substitution T C exon_variant GBM-US 1 235860518 235860518 single base substitution T C missense_variant S3477G 10429A>G GBM-US 1 235866229 235866229 single base substitution G A exon_variant GBM-US 1 235866229 235866229 single base substitution G A stop_gained R3398* 10192C>T GBM-US 1 235866238 235866238 single base substitution C T exon_variant GBM-US 1 235866238 235866238 single base substitution C T missense_variant V3395I 10183G>A GBM-US 1 235922440 235922440 single base substitution C T downstream_gene_variant GBM-US 1 235922440 235922440 single base substitution C T missense_variant R2238Q 6713G>A GBM-US 1 235938388 235938388 single base substitution T A splice_acceptor_variant GBM-US 1 235940405 235940405 single base substitution G A 3_prime_UTR_variant GBM-US 1 235940405 235940405 single base substitution G A exon_variant GBM-US 1 235940405 235940405 single base substitution G A synonymous_variant H1806H 5418C>T GBM-US 1 235993676 235993676 single base substitution G A exon_variant GBM-US 1 235993676 235993676 single base substitution G A synonymous_variant T14T 42C>T KIRC-US 1 235884146 235884146 single base substitution A G exon_variant KIRC-US 1 235884146 235884146 single base substitution A G synonymous_variant Y3125Y 9375T>C KIRC-US 1 235894212 235894212 single base substitution A C exon_variant KIRC-US 1 235894212 235894212 single base substitution A C missense_variant F2993L 8979T>G KIRC-US 1 235894212 235894212 single base substitution A C upstream_gene_variant KIRC-US 1 235904825 235904825 single base substitution A C downstream_gene_variant KIRC-US 1 235904825 235904825 single base substitution A C exon_variant KIRC-US 1 235904825 235904825 single base substitution A C missense_variant L2752W 8255T>G KIRC-US 1 235904825 235904825 single base substitution A C upstream_gene_variant KIRC-US 1 235907322 235907322 single base substitution T C downstream_gene_variant KIRC-US 1 235907322 235907322 single base substitution T C exon_variant KIRC-US 1 235907322 235907322 single base substitution T C missense_variant K2703R 8108A>G KIRC-US 1 235918806 235918806 single base substitution A C downstream_gene_variant KIRC-US 1 235918806 235918806 single base substitution A C missense_variant F2401V 7201T>G KIRC-US 1 235918806 235918806 single base substitution A C upstream_gene_variant KIRC-US 1 235918888 235918888 insertion of <=200bp - T downstream_gene_variant KIRC-US 1 235918888 235918888 insertion of <=200bp - T frameshift_variant N2373N? KIRC-US 1 235918888 235918888 insertion of <=200bp - T upstream_gene_variant KIRC-US 1 235944201 235944201 deletion of <=200bp A - 3_prime_UTR_variant KIRC-US 1 235944201 235944201 deletion of <=200bp A - exon_variant KIRC-US 1 235944201 235944201 deletion of <=200bp A - frameshift_variant F1726 KIRC-US 1 235950642 235950642 insertion of <=200bp - T 3_prime_UTR_variant KIRC-US 1 235950642 235950642 insertion of <=200bp - T downstream_gene_variant KIRC-US 1 235950642 235950642 insertion of <=200bp - T exon_variant KIRC-US 1 235950642 235950642 insertion of <=200bp - T frameshift_variant A1574D? KIRC-US 1 235969775 235969775 single base substitution C T exon_variant KIRC-US 1 235969775 235969775 single base substitution C T synonymous_variant K887K 2661G>A KIRC-US 1 235971939 235971939 single base substitution G A exon_variant KIRC-US 1 235971939 235971939 single base substitution G A stop_gained Q727* 2179C>T KIRC-US 1 235971988 235971988 single base substitution C A exon_variant KIRC-US 1 235971988 235971988 single base substitution C A missense_variant Q710H 2130G>T KIRP-US 1 235872510 235872510 single base substitution G A downstream_gene_variant KIRP-US 1 235872510 235872510 single base substitution G A exon_variant KIRP-US 1 235872510 235872510 single base substitution G A missense_variant R3342W 10024C>T KIRP-US 1 235884164 235884164 single base substitution G A exon_variant KIRP-US 1 235884164 235884164 single base substitution G A synonymous_variant L3119L 9357C>T LAML-KR 1 235822435 235822435 single base substitution G T downstream_gene_variant LAML-KR 1 235854277 235854277 single base substitution T C intron_variant LAML-KR 1 235856372 235856372 single base substitution T C intron_variant LAML-KR 1 235896726 235896726 single base substitution C T downstream_gene_variant LAML-KR 1 235896726 235896726 single base substitution C T intron_variant LAML-KR 1 236021084 236021084 single base substitution C T intron_variant LGG-US 1 235964233 235964233 single base substitution A C exon_variant LGG-US 1 235964233 235964233 single base substitution A C missense_variant F1293V 3877T>G LICA-CN 1 235875423 235875423 single base substitution T C downstream_gene_variant LICA-CN 1 235875423 235875423 single base substitution T C exon_variant LICA-CN 1 235875423 235875423 single base substitution T C missense_variant M3287V 9859A>G LICA-CN 1 235883973 235883973 single base substitution A T exon_variant LICA-CN 1 235883973 235883973 single base substitution A T missense_variant L3183Q 9548T>A LICA-CN 1 235904763 235904763 single base substitution G T exon_variant LICA-CN 1 235904763 235904763 single base substitution G T missense_variant H2773N 8317C>A LICA-CN 1 235904763 235904763 single base substitution G T upstream_gene_variant LICA-CN 1 235972725 235972725 single base substitution C T exon_variant LICA-CN 1 235972725 235972725 single base substitution C T missense_variant A465T 1393G>A LICA-FR 1 235852108 235852108 single base substitution C T intron_variant LICA-FR 1 235858930 235858931 deletion of <=200bp TT - intron_variant LICA-FR 1 235863104 235863104 single base substitution T G intron_variant LICA-FR 1 235872446 235872446 single base substitution C T downstream_gene_variant LICA-FR 1 235872446 235872446 single base substitution C T exon_variant LICA-FR 1 235872446 235872446 single base substitution C T missense_variant G3363E 10088G>A LICA-FR 1 235879120 235879120 single base substitution G A intron_variant LICA-FR 1 235879120 235879120 single base substitution G A upstream_gene_variant LICA-FR 1 235893122 235893122 single base substitution T C intron_variant LICA-FR 1 235893122 235893122 single base substitution T C upstream_gene_variant LICA-FR 1 235904811 235904811 single base substitution C A downstream_gene_variant LICA-FR 1 235904811 235904811 single base substitution C A exon_variant LICA-FR 1 235904811 235904811 single base substitution C A missense_variant A2757S 8269G>T LICA-FR 1 235904811 235904811 single base substitution C A upstream_gene_variant LICA-FR 1 235908193 235908195 deletion of <=200bp AAA - downstream_gene_variant LICA-FR 1 235908193 235908195 deletion of <=200bp AAA - intron_variant LICA-FR 1 235908193 235908195 deletion of <=200bp AAA - upstream_gene_variant LICA-FR 1 235915339 235915339 single base substitution T C synonymous_variant G2531G 7593A>G LICA-FR 1 235915339 235915339 single base substitution T C synonymous_variant G44G 132A>G LICA-FR 1 235922363 235922363 single base substitution T C downstream_gene_variant LICA-FR 1 235922363 235922363 single base substitution T C missense_variant S2264G 6790A>G LICA-FR 1 235927641 235927641 single base substitution C A intron_variant LICA-FR 1 235929236 235929236 single base substitution T C intron_variant LICA-FR 1 235961879 235961896 deletion of <=200bp AAAAAAAAAAAAAAAAAA - intron_variant LICA-FR 1 236011251 236011251 single base substitution T C intron_variant LICA-FR 1 236016794 236016794 insertion of <=200bp - A intron_variant LICA-FR 1 236020241 236020244 deletion of <=200bp TTTT - intron_variant LICA-FR 1 236042017 236042017 single base substitution A G intron_variant LIHC-US 1 235904821 235904821 single base substitution C T downstream_gene_variant LIHC-US 1 235904821 235904821 single base substitution C T exon_variant LIHC-US 1 235904821 235904821 single base substitution C T synonymous_variant S2753S 8259G>A LIHC-US 1 235904821 235904821 single base substitution C T upstream_gene_variant LIHC-US 1 235915327 235915327 single base substitution A G synonymous_variant N2535N 7605T>C LIHC-US 1 235915327 235915327 single base substitution A G synonymous_variant N48N 144T>C LIHC-US 1 235922305 235922305 single base substitution T C downstream_gene_variant LIHC-US 1 235922305 235922305 single base substitution T C missense_variant E2283G 6848A>G LIHC-US 1 235937265 235937265 single base substitution T A 3_prime_UTR_variant LIHC-US 1 235937265 235937265 single base substitution T A exon_variant LIHC-US 1 235937265 235937265 single base substitution T A missense_variant E1887D 5661A>T LIHC-US 1 235955200 235955200 single base substitution G C exon_variant LIHC-US 1 235955200 235955200 single base substitution G C intron_variant LIHC-US 1 235955200 235955200 single base substitution G C missense_variant L1448V 4342C>G LIHC-US 1 235955200 235955200 single base substitution G C upstream_gene_variant LIHC-US 1 235964399 235964399 single base substitution T A splice_acceptor_variant LIHC-US 1 235973623 235973623 single base substitution G T exon_variant LIHC-US 1 235973623 235973623 single base substitution G T synonymous_variant T165T 495C>A LINC-JP 1 235824985 235824985 single base substitution A C 3_prime_UTR_variant LINC-JP 1 235824985 235824985 single base substitution A C exon_variant LINC-JP 1 235834251 235834251 single base substitution T C intron_variant LINC-JP 1 235834743 235834743 single base substitution G T intron_variant LINC-JP 1 235840450 235840450 single base substitution G A exon_variant LINC-JP 1 235840450 235840450 single base substitution G A missense_variant P3660L 10979C>T LINC-JP 1 235840689 235840689 single base substitution C T intron_variant LINC-JP 1 235845714 235845714 single base substitution C T intron_variant LINC-JP 1 235850408 235850408 single base substitution T C intron_variant LINC-JP 1 235875443 235875443 single base substitution C A downstream_gene_variant LINC-JP 1 235875443 235875443 single base substitution C A exon_variant LINC-JP 1 235875443 235875443 single base substitution C A missense_variant R3280L 9839G>T LINC-JP 1 235878539 235878539 single base substitution C G exon_variant LINC-JP 1 235878539 235878539 single base substitution C G missense_variant R3249T 9746G>C LINC-JP 1 235878539 235878539 single base substitution C G upstream_gene_variant LINC-JP 1 235881193 235881193 deletion of <=200bp T - intron_variant LINC-JP 1 235892344 235892344 single base substitution A G intron_variant LINC-JP 1 235892344 235892344 single base substitution A G upstream_gene_variant LINC-JP 1 235892866 235892866 single base substitution A G intron_variant LINC-JP 1 235892866 235892866 single base substitution A G upstream_gene_variant LINC-JP 1 235894784 235894784 single base substitution T C intron_variant LINC-JP 1 235894784 235894784 single base substitution T C upstream_gene_variant LINC-JP 1 235897142 235897142 single base substitution T C downstream_gene_variant LINC-JP 1 235897142 235897142 single base substitution T C exon_variant LINC-JP 1 235897142 235897142 single base substitution T C missense_variant N2867S 8600A>G LINC-JP 1 235897645 235897645 single base substitution T C downstream_gene_variant LINC-JP 1 235897645 235897645 single base substitution T C intron_variant LINC-JP 1 235902947 235902947 single base substitution A C intron_variant LINC-JP 1 235902947 235902947 single base substitution A C upstream_gene_variant LINC-JP 1 235903699 235903699 single base substitution C T intron_variant LINC-JP 1 235903699 235903699 single base substitution C T upstream_gene_variant LINC-JP 1 235909889 235909889 single base substitution T C intron_variant LINC-JP 1 235909889 235909889 single base substitution T C upstream_gene_variant LINC-JP 1 235913682 235913682 single base substitution A G intron_variant LINC-JP 1 235921184 235921184 deletion of <=200bp T - downstream_gene_variant LINC-JP 1 235921184 235921184 deletion of <=200bp T - intron_variant LINC-JP 1 235929235 235929235 single base substitution C T intron_variant LINC-JP 1 235938093 235938093 single base substitution T C intron_variant LINC-JP 1 235945225 235945225 single base substitution A G splice_donor_variant LINC-JP 1 235949821 235949821 single base substitution C A downstream_gene_variant LINC-JP 1 235949821 235949821 single base substitution C A intron_variant LINC-JP 1 235949920 235949920 single base substitution T C downstream_gene_variant LINC-JP 1 235949920 235949920 single base substitution T C intron_variant LINC-JP 1 235956864 235956864 deletion of <=200bp C - exon_variant LINC-JP 1 235956864 235956864 deletion of <=200bp C - frameshift_variant R1352 LINC-JP 1 235956864 235956864 deletion of <=200bp C - upstream_gene_variant LINC-JP 1 235964277 235964277 insertion of <=200bp - A exon_variant LINC-JP 1 235964277 235964277 insertion of <=200bp - A frameshift_variant L1278F? LINC-JP 1 235971811 235971811 single base substitution C A exon_variant LINC-JP 1 235971811 235971811 single base substitution C A missense_variant L769F 2307G>T LINC-JP 1 235972330 235972330 single base substitution G C exon_variant LINC-JP 1 235972330 235972330 single base substitution G C synonymous_variant L596L 1788C>G LINC-JP 1 235972428 235972428 single base substitution C T exon_variant LINC-JP 1 235972428 235972428 single base substitution C T missense_variant A564T 1690G>A LINC-JP 1 235973317 235973317 single base substitution T C exon_variant LINC-JP 1 235973317 235973317 single base substitution T C synonymous_variant K267K 801A>G LINC-JP 1 235973922 235973922 insertion of <=200bp - C intron_variant LINC-JP 1 235993467 235993467 single base substitution G T exon_variant LINC-JP 1 235993467 235993467 single base substitution G T intron_variant LINC-JP 1 235998176 235998176 single base substitution C T intron_variant LINC-JP 1 236026761 236026761 deletion of <=200bp A - intron_variant LINC-JP 1 236039598 236039598 single base substitution C T intron_variant LINC-JP 1 236039858 236039858 single base substitution A G intron_variant LINC-JP 1 236047907 236047907 insertion of <=200bp - TT upstream_gene_variant LIRI-JP 1 235823350 235823350 single base substitution C A downstream_gene_variant LIRI-JP 1 235824406 235824406 single base substitution A T 3_prime_UTR_variant LIRI-JP 1 235824406 235824406 single base substitution A T exon_variant LIRI-JP 1 235825272 235825272 single base substitution T C 3_prime_UTR_variant LIRI-JP 1 235825272 235825272 single base substitution T C exon_variant LIRI-JP 1 235826372 235826372 single base substitution T C exon_variant LIRI-JP 1 235826372 235826372 single base substitution T C synonymous_variant T3758T 11274A>G LIRI-JP 1 235828176 235828176 single base substitution A G intron_variant LIRI-JP 1 235829734 235829734 single base substitution T C intron_variant LIRI-JP 1 235835052 235835052 single base substitution G T intron_variant LIRI-JP 1 235835909 235835909 single base substitution T C intron_variant LIRI-JP 1 235836742 235836742 single base substitution T C intron_variant LIRI-JP 1 235837113 235837113 single base substitution T C intron_variant LIRI-JP 1 235841152 235841152 deletion of <=200bp C - intron_variant LIRI-JP 1 235841242 235841242 single base substitution T A intron_variant LIRI-JP 1 235841605 235841605 single base substitution T C intron_variant LIRI-JP 1 235845928 235845928 single base substitution T C intron_variant LIRI-JP 1 235846636 235846636 single base substitution T A intron_variant LIRI-JP 1 235848029 235848029 single base substitution C A intron_variant LIRI-JP 1 235848134 235848134 single base substitution G A intron_variant LIRI-JP 1 235849073 235849073 single base substitution G A intron_variant LIRI-JP 1 235849944 235849944 single base substitution A T intron_variant LIRI-JP 1 235850528 235850528 single base substitution C T intron_variant LIRI-JP 1 235851670 235851670 single base substitution T C intron_variant LIRI-JP 1 235851920 235851920 single base substitution C T intron_variant LIRI-JP 1 235852376 235852376 single base substitution T A intron_variant LIRI-JP 1 235852391 235852391 single base substitution G C intron_variant LIRI-JP 1 235853734 235853734 single base substitution T C intron_variant LIRI-JP 1 235854685 235854685 single base substitution C T intron_variant LIRI-JP 1 235861355 235861355 single base substitution T G intron_variant LIRI-JP 1 235862471 235862471 single base substitution C T intron_variant LIRI-JP 1 235863027 235863027 single base substitution C T intron_variant LIRI-JP 1 235867428 235867428 single base substitution T C downstream_gene_variant LIRI-JP 1 235867428 235867428 single base substitution T C intron_variant LIRI-JP 1 235869551 235869551 single base substitution G A downstream_gene_variant LIRI-JP 1 235869551 235869551 single base substitution G A intron_variant LIRI-JP 1 235869651 235869651 single base substitution C A downstream_gene_variant LIRI-JP 1 235869651 235869651 single base substitution C A intron_variant LIRI-JP 1 235870137 235870137 single base substitution C G downstream_gene_variant LIRI-JP 1 235870137 235870137 single base substitution C G intron_variant LIRI-JP 1 235870196 235870196 single base substitution T C downstream_gene_variant LIRI-JP 1 235870196 235870196 single base substitution T C intron_variant LIRI-JP 1 235871360 235871360 single base substitution G T downstream_gene_variant LIRI-JP 1 235871360 235871360 single base substitution G T intron_variant LIRI-JP 1 235871656 235871656 single base substitution C G downstream_gene_variant LIRI-JP 1 235871656 235871656 single base substitution C G intron_variant LIRI-JP 1 235872378 235872378 single base substitution A C downstream_gene_variant LIRI-JP 1 235872378 235872378 single base substitution A C intron_variant LIRI-JP 1 235878240 235878240 single base substitution T C intron_variant LIRI-JP 1 235878240 235878240 single base substitution T C upstream_gene_variant LIRI-JP 1 235878587 235878587 single base substitution T C exon_variant LIRI-JP 1 235878587 235878587 single base substitution T C missense_variant Y3233C 9698A>G LIRI-JP 1 235878587 235878587 single base substitution T C upstream_gene_variant LIRI-JP 1 235879018 235879018 single base substitution T G intron_variant LIRI-JP 1 235879018 235879018 single base substitution T G upstream_gene_variant LIRI-JP 1 235879291 235879291 single base substitution G T intron_variant LIRI-JP 1 235879291 235879291 single base substitution G T upstream_gene_variant LIRI-JP 1 235879506 235879506 single base substitution T C intron_variant LIRI-JP 1 235879506 235879506 single base substitution T C upstream_gene_variant LIRI-JP 1 235879807 235879807 single base substitution G T intron_variant LIRI-JP 1 235879807 235879807 single base substitution G T upstream_gene_variant LIRI-JP 1 235880243 235880243 single base substitution T C intron_variant LIRI-JP 1 235880243 235880243 single base substitution T C upstream_gene_variant LIRI-JP 1 235881507 235881507 single base substitution G A intron_variant LIRI-JP 1 235884559 235884559 single base substitution C T intron_variant LIRI-JP 1 235887169 235887169 single base substitution A G intron_variant LIRI-JP 1 235887677 235887677 single base substitution T G intron_variant LIRI-JP 1 235888116 235888116 single base substitution C T intron_variant LIRI-JP 1 235889042 235889042 single base substitution T C intron_variant LIRI-JP 1 235890772 235890772 single base substitution C T intron_variant LIRI-JP 1 235891354 235891354 single base substitution A G intron_variant LIRI-JP 1 235892230 235892230 single base substitution C A intron_variant LIRI-JP 1 235892230 235892230 single base substitution C A upstream_gene_variant LIRI-JP 1 235893533 235893533 single base substitution T G intron_variant LIRI-JP 1 235893533 235893533 single base substitution T G upstream_gene_variant LIRI-JP 1 235894606 235894606 single base substitution T C intron_variant LIRI-JP 1 235894606 235894606 single base substitution T C upstream_gene_variant LIRI-JP 1 235894728 235894728 single base substitution C A intron_variant LIRI-JP 1 235894728 235894728 single base substitution C A upstream_gene_variant LIRI-JP 1 235898324 235898324 single base substitution C T downstream_gene_variant LIRI-JP 1 235898324 235898324 single base substitution C T exon_variant LIRI-JP 1 235898324 235898324 single base substitution C T intron_variant LIRI-JP 1 235900274 235900274 single base substitution T C downstream_gene_variant LIRI-JP 1 235900274 235900274 single base substitution T C exon_variant LIRI-JP 1 235900274 235900274 single base substitution T C intron_variant LIRI-JP 1 235901769 235901769 single base substitution A G exon_variant LIRI-JP 1 235901769 235901769 single base substitution A G intron_variant LIRI-JP 1 235901769 235901769 single base substitution A G upstream_gene_variant LIRI-JP 1 235901862 235901862 single base substitution G A exon_variant LIRI-JP 1 235901862 235901862 single base substitution G A intron_variant LIRI-JP 1 235901862 235901862 single base substitution G A upstream_gene_variant LIRI-JP 1 235905472 235905472 single base substitution C A downstream_gene_variant LIRI-JP 1 235905472 235905472 single base substitution C A intron_variant LIRI-JP 1 235905472 235905472 single base substitution C A upstream_gene_variant LIRI-JP 1 235907784 235907784 single base substitution G C downstream_gene_variant LIRI-JP 1 235907784 235907784 single base substitution G C intron_variant LIRI-JP 1 235907784 235907784 single base substitution G C upstream_gene_variant LIRI-JP 1 235907970 235907970 single base substitution C A downstream_gene_variant LIRI-JP 1 235907970 235907970 single base substitution C A intron_variant LIRI-JP 1 235907970 235907970 single base substitution C A upstream_gene_variant LIRI-JP 1 235910823 235910823 single base substitution C T intron_variant LIRI-JP 1 235910823 235910823 single base substitution C T upstream_gene_variant LIRI-JP 1 235911080 235911080 single base substitution C T intron_variant LIRI-JP 1 235911080 235911080 single base substitution C T upstream_gene_variant LIRI-JP 1 235914441 235914441 single base substitution G A intron_variant LIRI-JP 1 235915095 235915101 deletion of <=200bp AACTACT - intron_variant LIRI-JP 1 235916671 235916671 single base substitution A G intron_variant LIRI-JP 1 235916671 235916671 single base substitution A G upstream_gene_variant LIRI-JP 1 235918600 235918600 single base substitution A T downstream_gene_variant LIRI-JP 1 235918600 235918600 single base substitution A T intron_variant LIRI-JP 1 235918600 235918600 single base substitution A T upstream_gene_variant LIRI-JP 1 235918774 235918774 deletion of <=200bp T - downstream_gene_variant LIRI-JP 1 235918774 235918774 deletion of <=200bp T - splice_region_variant LIRI-JP 1 235918774 235918774 deletion of <=200bp T - upstream_gene_variant LIRI-JP 1 235918877 235918877 single base substitution G A downstream_gene_variant LIRI-JP 1 235918877 235918877 single base substitution G A missense_variant S2377F 7130C>T LIRI-JP 1 235918877 235918877 single base substitution G A upstream_gene_variant LIRI-JP 1 235919161 235919161 single base substitution T C downstream_gene_variant LIRI-JP 1 235919161 235919161 single base substitution T C intron_variant LIRI-JP 1 235919161 235919161 single base substitution T C upstream_gene_variant LIRI-JP 1 235921614 235921614 single base substitution T C downstream_gene_variant LIRI-JP 1 235921614 235921614 single base substitution T C intron_variant LIRI-JP 1 235922312 235922312 single base substitution C T downstream_gene_variant LIRI-JP 1 235922312 235922312 single base substitution C T missense_variant G2281S 6841G>A LIRI-JP 1 235923228 235923228 single base substitution T C intron_variant LIRI-JP 1 235924445 235924445 single base substitution T C intron_variant LIRI-JP 1 235925036 235925036 single base substitution C A intron_variant LIRI-JP 1 235925721 235925721 single base substitution G A intron_variant LIRI-JP 1 235926296 235926296 single base substitution C A intron_variant LIRI-JP 1 235928250 235928250 single base substitution T C intron_variant LIRI-JP 1 235928809 235928809 single base substitution T C intron_variant LIRI-JP 1 235928936 235928936 single base substitution T G intron_variant LIRI-JP 1 235931197 235931197 single base substitution A T intron_variant LIRI-JP 1 235932421 235932421 single base substitution T C intron_variant LIRI-JP 1 235933937 235933937 single base substitution T G intron_variant LIRI-JP 1 235935799 235935799 single base substitution T C intron_variant LIRI-JP 1 235936117 235936117 single base substitution C T intron_variant LIRI-JP 1 235937651 235937651 single base substitution G T intron_variant LIRI-JP 1 235939582 235939582 single base substitution G C intron_variant LIRI-JP 1 235940474 235940474 single base substitution G A 3_prime_UTR_variant LIRI-JP 1 235940474 235940474 single base substitution G A exon_variant LIRI-JP 1 235940474 235940474 single base substitution G A synonymous_variant I1783I 5349C>T LIRI-JP 1 235940602 235940602 single base substitution G C 3_prime_UTR_variant LIRI-JP 1 235940602 235940602 single base substitution G C exon_variant LIRI-JP 1 235940602 235940602 single base substitution G C missense_variant L1741V 5221C>G LIRI-JP 1 235941060 235941060 single base substitution T C intron_variant LIRI-JP 1 235941763 235941763 single base substitution C A intron_variant LIRI-JP 1 235942747 235942747 single base substitution C T intron_variant LIRI-JP 1 235944541 235944541 single base substitution T C intron_variant LIRI-JP 1 235946019 235946019 single base substitution C T downstream_gene_variant LIRI-JP 1 235946019 235946019 single base substitution C T intron_variant LIRI-JP 1 235946752 235946752 single base substitution G A downstream_gene_variant LIRI-JP 1 235946752 235946752 single base substitution G A intron_variant LIRI-JP 1 235947160 235947160 single base substitution T C downstream_gene_variant LIRI-JP 1 235947160 235947160 single base substitution T C intron_variant LIRI-JP 1 235952235 235952235 single base substitution T C downstream_gene_variant LIRI-JP 1 235952235 235952235 single base substitution T C intron_variant LIRI-JP 1 235952235 235952235 single base substitution T C upstream_gene_variant LIRI-JP 1 235953739 235953739 single base substitution C A downstream_gene_variant LIRI-JP 1 235953739 235953739 single base substitution C A intron_variant LIRI-JP 1 235953739 235953739 single base substitution C A upstream_gene_variant LIRI-JP 1 235955847 235955847 single base substitution T G intron_variant LIRI-JP 1 235955847 235955847 single base substitution T G upstream_gene_variant LIRI-JP 1 235956172 235956172 single base substitution C T intron_variant LIRI-JP 1 235956172 235956172 single base substitution C T upstream_gene_variant LIRI-JP 1 235956767 235956767 single base substitution T C intron_variant LIRI-JP 1 235956767 235956767 single base substitution T C upstream_gene_variant LIRI-JP 1 235959470 235959470 single base substitution G C intron_variant LIRI-JP 1 235962369 235962369 single base substitution T C intron_variant LIRI-JP 1 235962726 235962726 single base substitution T A intron_variant LIRI-JP 1 235962827 235962827 single base substitution A G intron_variant LIRI-JP 1 235963098 235963098 single base substitution G T intron_variant LIRI-JP 1 235963404 235963404 single base substitution G A intron_variant LIRI-JP 1 235963985 235963985 single base substitution C T intron_variant LIRI-JP 1 235966130 235966130 single base substitution T C intron_variant LIRI-JP 1 235967008 235967008 single base substitution G T intron_variant LIRI-JP 1 235967079 235967079 single base substitution T C intron_variant LIRI-JP 1 235970320 235970320 single base substitution G A intron_variant LIRI-JP 1 235970824 235970824 single base substitution A C intron_variant LIRI-JP 1 235972287 235972287 single base substitution T C exon_variant LIRI-JP 1 235972287 235972287 single base substitution T C missense_variant I611V 1831A>G LIRI-JP 1 235972367 235972367 single base substitution C T exon_variant LIRI-JP 1 235972367 235972367 single base substitution C T missense_variant C584Y 1751G>A LIRI-JP 1 235973781 235973781 single base substitution T A exon_variant LIRI-JP 1 235973781 235973781 single base substitution T A missense_variant S113C 337A>T LIRI-JP 1 235974358 235974358 single base substitution T C intron_variant LIRI-JP 1 235975885 235975885 single base substitution T C intron_variant LIRI-JP 1 235979159 235979159 single base substitution G A intron_variant LIRI-JP 1 235985214 235985214 single base substitution T C intron_variant LIRI-JP 1 235986363 235986363 single base substitution T C intron_variant LIRI-JP 1 235988221 235988221 single base substitution G A downstream_gene_variant LIRI-JP 1 235988221 235988221 single base substitution G A intron_variant LIRI-JP 1 235989467 235989467 single base substitution T G downstream_gene_variant LIRI-JP 1 235989467 235989467 single base substitution T G intron_variant LIRI-JP 1 235991967 235991967 single base substitution A G downstream_gene_variant LIRI-JP 1 235991967 235991967 single base substitution A G intron_variant LIRI-JP 1 235993456 235993456 single base substitution T C exon_variant LIRI-JP 1 235993456 235993456 single base substitution T C intron_variant LIRI-JP 1 235994208 235994208 single base substitution T C intron_variant LIRI-JP 1 235995279 235995279 single base substitution C T intron_variant LIRI-JP 1 235995822 235995857 deletion of <=200bp ATAGGTTAGTGTATATACATGATTACTTGCTTTTAT - intron_variant LIRI-JP 1 235995835 235995835 single base substitution T C intron_variant LIRI-JP 1 235996802 235996802 single base substitution G A intron_variant LIRI-JP 1 235998182 235998182 single base substitution C A intron_variant LIRI-JP 1 235999284 235999284 single base substitution C A intron_variant LIRI-JP 1 236000505 236000505 single base substitution A C intron_variant LIRI-JP 1 236000617 236000617 single base substitution C T intron_variant LIRI-JP 1 236001958 236001958 single base substitution T C intron_variant LIRI-JP 1 236002969 236002969 single base substitution C A intron_variant LIRI-JP 1 236004090 236004090 single base substitution T G intron_variant LIRI-JP 1 236004918 236004918 single base substitution A T intron_variant LIRI-JP 1 236006746 236006746 single base substitution C T intron_variant LIRI-JP 1 236008502 236008502 single base substitution G A intron_variant LIRI-JP 1 236014343 236014343 single base substitution A G intron_variant LIRI-JP 1 236014480 236014480 single base substitution A G intron_variant LIRI-JP 1 236014581 236014581 single base substitution T C intron_variant LIRI-JP 1 236017374 236017374 single base substitution T C intron_variant LIRI-JP 1 236018550 236018550 single base substitution C T intron_variant LIRI-JP 1 236018700 236018700 single base substitution C T intron_variant LIRI-JP 1 236019646 236019646 single base substitution C A intron_variant LIRI-JP 1 236026318 236026318 single base substitution A T intron_variant LIRI-JP 1 236029611 236029611 single base substitution G A intron_variant LIRI-JP 1 236030851 236030851 single base substitution T C intron_variant LIRI-JP 1 236030851 236030851 single base substitution T C upstream_gene_variant LIRI-JP 1 236033700 236033700 single base substitution C G intron_variant LIRI-JP 1 236033700 236033700 single base substitution C G upstream_gene_variant LIRI-JP 1 236035019 236035019 single base substitution T C intron_variant LIRI-JP 1 236035019 236035019 single base substitution T C upstream_gene_variant LIRI-JP 1 236035145 236035145 single base substitution T C intron_variant LIRI-JP 1 236035145 236035145 single base substitution T C upstream_gene_variant LIRI-JP 1 236037717 236037717 single base substitution G A intron_variant LIRI-JP 1 236044053 236044053 single base substitution T C intron_variant LIRI-JP 1 236044694 236044694 single base substitution C T intron_variant LIRI-JP 1 236046023 236046023 insertion of <=200bp - AGCA intron_variant LIRI-JP 1 236046306 236046306 single base substitution C G intron_variant LIRI-JP 1 236048285 236048285 single base substitution T G upstream_gene_variant LIRI-JP 1 236048321 236048321 single base substitution G T upstream_gene_variant LUSC-CN 1 235937104 235937104 single base substitution C A intron_variant LUSC-KR 1 235821994 235821994 single base substitution C T downstream_gene_variant LUSC-KR 1 235831259 235831259 single base substitution C A intron_variant LUSC-KR 1 235836845 235836845 single base substitution C T intron_variant LUSC-KR 1 235837507 235837507 single base substitution G A intron_variant LUSC-KR 1 235841441 235841441 single base substitution T G intron_variant LUSC-KR 1 235841662 235841662 single base substitution G A intron_variant LUSC-KR 1 235849549 235849549 single base substitution C A intron_variant LUSC-KR 1 235851757 235851757 single base substitution G A intron_variant LUSC-KR 1 235852441 235852441 single base substitution T C intron_variant LUSC-KR 1 235854277 235854277 single base substitution T C intron_variant LUSC-KR 1 235856176 235856176 single base substitution C A intron_variant LUSC-KR 1 235857097 235857097 single base substitution T G intron_variant LUSC-KR 1 235872609 235872609 single base substitution C T downstream_gene_variant LUSC-KR 1 235872609 235872609 single base substitution C T splice_acceptor_variant LUSC-KR 1 235886114 235886114 single base substitution C A intron_variant LUSC-KR 1 235887432 235887432 single base substitution C T exon_variant LUSC-KR 1 235887432 235887432 single base substitution C T missense_variant E3071K 9211G>A LUSC-KR 1 235888731 235888731 single base substitution C T intron_variant LUSC-KR 1 235890071 235890071 single base substitution G A intron_variant LUSC-KR 1 235890441 235890441 single base substitution G T intron_variant LUSC-KR 1 235908688 235908688 single base substitution T C downstream_gene_variant LUSC-KR 1 235908688 235908688 single base substitution T C intron_variant LUSC-KR 1 235908688 235908688 single base substitution T C upstream_gene_variant LUSC-KR 1 235913500 235913500 single base substitution A G intron_variant LUSC-KR 1 235919631 235919631 single base substitution C A downstream_gene_variant LUSC-KR 1 235919631 235919631 single base substitution C A intron_variant LUSC-KR 1 235919631 235919631 single base substitution C A upstream_gene_variant LUSC-KR 1 235920957 235920957 single base substitution A G downstream_gene_variant LUSC-KR 1 235920957 235920957 single base substitution A G intron_variant LUSC-KR 1 235925261 235925261 single base substitution C T intron_variant LUSC-KR 1 235930141 235930141 single base substitution T A intron_variant LUSC-KR 1 235933692 235933692 single base substitution G T intron_variant LUSC-KR 1 235940003 235940003 single base substitution A T intron_variant LUSC-KR 1 235940422 235940422 single base substitution T C 3_prime_UTR_variant LUSC-KR 1 235940422 235940422 single base substitution T C exon_variant LUSC-KR 1 235940422 235940422 single base substitution T C missense_variant I1801V 5401A>G LUSC-KR 1 235946900 235946900 single base substitution T A downstream_gene_variant LUSC-KR 1 235946900 235946900 single base substitution T A intron_variant LUSC-KR 1 235952769 235952769 single base substitution G A downstream_gene_variant LUSC-KR 1 235952769 235952769 single base substitution G A intron_variant LUSC-KR 1 235952769 235952769 single base substitution G A upstream_gene_variant LUSC-KR 1 235954788 235954788 single base substitution C T downstream_gene_variant LUSC-KR 1 235954788 235954788 single base substitution C T intron_variant LUSC-KR 1 235954788 235954788 single base substitution C T upstream_gene_variant LUSC-KR 1 235960066 235960066 single base substitution G C intron_variant LUSC-KR 1 235986593 235986593 single base substitution C G intron_variant LUSC-KR 1 235988088 235988088 single base substitution G C downstream_gene_variant LUSC-KR 1 235988088 235988088 single base substitution G C intron_variant LUSC-KR 1 235996815 235996815 single base substitution T A intron_variant LUSC-KR 1 236002771 236002771 single base substitution C A intron_variant LUSC-KR 1 236006689 236006689 single base substitution C A intron_variant LUSC-KR 1 236007103 236007103 single base substitution T C intron_variant LUSC-KR 1 236008140 236008140 single base substitution C T intron_variant LUSC-KR 1 236008322 236008322 single base substitution G T intron_variant LUSC-KR 1 236020555 236020555 single base substitution G C intron_variant LUSC-KR 1 236021084 236021084 single base substitution C T intron_variant LUSC-KR 1 236024467 236024467 single base substitution T A intron_variant LUSC-KR 1 236026775 236026775 single base substitution T A intron_variant LUSC-KR 1 236027508 236027508 single base substitution C G intron_variant LUSC-KR 1 236032708 236032708 single base substitution C A intron_variant LUSC-KR 1 236032708 236032708 single base substitution C A upstream_gene_variant LUSC-KR 1 236032755 236032755 single base substitution G T intron_variant LUSC-KR 1 236032755 236032755 single base substitution G T upstream_gene_variant LUSC-KR 1 236034597 236034597 single base substitution C G intron_variant LUSC-KR 1 236034597 236034597 single base substitution C G upstream_gene_variant LUSC-KR 1 236035131 236035131 single base substitution G T intron_variant LUSC-KR 1 236035131 236035131 single base substitution G T upstream_gene_variant LUSC-KR 1 236037743 236037743 single base substitution G A intron_variant LUSC-KR 1 236037863 236037863 single base substitution C G intron_variant LUSC-KR 1 236038619 236038619 single base substitution A C intron_variant LUSC-KR 1 236041179 236041179 single base substitution A G intron_variant LUSC-KR 1 236047381 236047381 single base substitution A G upstream_gene_variant LUSC-US 1 235827887 235827887 single base substitution C G exon_variant LUSC-US 1 235827887 235827887 single base substitution C G synonymous_variant V3691V 11073G>C LUSC-US 1 235840490 235840490 single base substitution T A splice_acceptor_variant LUSC-US 1 235860456 235860456 single base substitution C A exon_variant LUSC-US 1 235860456 235860456 single base substitution C A missense_variant Q3497H 10491G>T LUSC-US 1 235866082 235866082 single base substitution C G exon_variant LUSC-US 1 235866082 235866082 single base substitution C G missense_variant E3447Q 10339G>C LUSC-US 1 235892930 235892930 single base substitution T C exon_variant LUSC-US 1 235892930 235892930 single base substitution T C synonymous_variant A3024A 9072A>G LUSC-US 1 235892930 235892930 single base substitution T C upstream_gene_variant LUSC-US 1 235896901 235896901 single base substitution C A downstream_gene_variant LUSC-US 1 235896901 235896901 single base substitution C A exon_variant LUSC-US 1 235896901 235896901 single base substitution C A missense_variant E2901D 8703G>T LUSC-US 1 235929511 235929511 single base substitution C A 3_prime_UTR_variant LUSC-US 1 235929511 235929511 single base substitution C A intron_variant LUSC-US 1 235929511 235929511 single base substitution C A missense_variant A1997S 5989G>T LUSC-US 1 235937219 235937219 single base substitution C G 3_prime_UTR_variant LUSC-US 1 235937219 235937219 single base substitution C G exon_variant LUSC-US 1 235937219 235937219 single base substitution C G missense_variant D1903H 5707G>C LUSC-US 1 235944340 235944340 single base substitution G C 3_prime_UTR_variant LUSC-US 1 235944340 235944340 single base substitution G C exon_variant LUSC-US 1 235944340 235944340 single base substitution G C stop_gained S1680* 5039C>G LUSC-US 1 235945292 235945292 single base substitution G T 3_prime_UTR_variant LUSC-US 1 235945292 235945292 single base substitution G T exon_variant LUSC-US 1 235945292 235945292 single base substitution G T stop_gained S1653* 4958C>A LUSC-US 1 235955020 235955020 single base substitution C A exon_variant LUSC-US 1 235955020 235955020 single base substitution C A intron_variant LUSC-US 1 235955020 235955020 single base substitution C A missense_variant D1508Y 4522G>T LUSC-US 1 235955020 235955020 single base substitution C A upstream_gene_variant LUSC-US 1 235967923 235967923 single base substitution G A exon_variant LUSC-US 1 235967923 235967923 single base substitution G A missense_variant L1146F 3436C>T LUSC-US 1 235969140 235969140 single base substitution G T exon_variant LUSC-US 1 235969140 235969140 single base substitution G T stop_gained S1099* 3296C>A LUSC-US 1 235969541 235969541 single base substitution A T exon_variant LUSC-US 1 235969541 235969541 single base substitution A T synonymous_variant S965S 2895T>A LUSC-US 1 235972254 235972254 single base substitution G A exon_variant LUSC-US 1 235972254 235972254 single base substitution G A stop_gained Q622* 1864C>T LUSC-US 1 235972330 235972330 single base substitution G C exon_variant LUSC-US 1 235972330 235972330 single base substitution G C synonymous_variant L596L 1788C>G LUSC-US 1 235972415 235972415 single base substitution C A exon_variant LUSC-US 1 235972415 235972415 single base substitution C A missense_variant S568I 1703G>T LUSC-US 1 235973326 235973326 single base substitution T G exon_variant LUSC-US 1 235973326 235973326 single base substitution T G missense_variant L264F 792A>C MALY-DE 1 235824403 235824403 single base substitution G T 3_prime_UTR_variant MALY-DE 1 235824403 235824403 single base substitution G T exon_variant MALY-DE 1 235836384 235836384 single base substitution T C intron_variant MALY-DE 1 235838771 235838771 single base substitution C T intron_variant MALY-DE 1 235839655 235839655 single base substitution C T intron_variant MALY-DE 1 235846817 235846817 single base substitution T C intron_variant MALY-DE 1 235862996 235862996 single base substitution C T intron_variant MALY-DE 1 235864925 235864925 insertion of <=200bp - TCAA intron_variant MALY-DE 1 235875508 235875508 single base substitution A T downstream_gene_variant MALY-DE 1 235875508 235875508 single base substitution A T exon_variant MALY-DE 1 235875508 235875508 single base substitution A T intron_variant MALY-DE 1 235887443 235887443 single base substitution C A exon_variant MALY-DE 1 235887443 235887443 single base substitution C A missense_variant W3067L 9200G>T MALY-DE 1 235891581 235891581 single base substitution G T intron_variant MALY-DE 1 235891581 235891581 single base substitution G T upstream_gene_variant MALY-DE 1 235909421 235909421 single base substitution T C downstream_gene_variant MALY-DE 1 235909421 235909421 single base substitution T C intron_variant MALY-DE 1 235909421 235909421 single base substitution T C upstream_gene_variant MALY-DE 1 235910979 235910979 single base substitution C T intron_variant MALY-DE 1 235910979 235910979 single base substitution C T upstream_gene_variant MALY-DE 1 235915870 235915870 single base substitution A T intron_variant MALY-DE 1 235915870 235915870 single base substitution A T upstream_gene_variant MALY-DE 1 235924485 235924485 single base substitution A G intron_variant MALY-DE 1 235925084 235925084 single base substitution A C intron_variant MALY-DE 1 235926863 235926863 single base substitution G A intron_variant MALY-DE 1 235936357 235936357 single base substitution C A intron_variant MALY-DE 1 235939404 235939404 single base substitution A G intron_variant MALY-DE 1 235941399 235941400 deletion of <=200bp AT - intron_variant MALY-DE 1 235947473 235947473 single base substitution C T downstream_gene_variant MALY-DE 1 235947473 235947473 single base substitution C T intron_variant MALY-DE 1 235947678 235947678 single base substitution A T downstream_gene_variant MALY-DE 1 235947678 235947678 single base substitution A T intron_variant MALY-DE 1 235959227 235959227 single base substitution G T intron_variant MALY-DE 1 235961879 235961895 deletion of <=200bp AAAAAAAAAAAAAAAAA - intron_variant MALY-DE 1 235966191 235966191 single base substitution C G intron_variant MALY-DE 1 235969212 235969212 single base substitution A G exon_variant MALY-DE 1 235969212 235969212 single base substitution A G missense_variant V1075A 3224T>C MALY-DE 1 235971689 235971689 single base substitution C T intron_variant MALY-DE 1 235972584 235972584 single base substitution G T exon_variant MALY-DE 1 235972584 235972584 single base substitution G T missense_variant H512N 1534C>A MALY-DE 1 235977321 235977321 single base substitution G A intron_variant MALY-DE 1 236032721 236032721 single base substitution G C intron_variant MALY-DE 1 236032721 236032721 single base substitution G C upstream_gene_variant MALY-DE 1 236032772 236032772 insertion of <=200bp - A intron_variant MALY-DE 1 236032772 236032772 insertion of <=200bp - A upstream_gene_variant MALY-DE 1 236034610 236034610 single base substitution G A intron_variant MALY-DE 1 236034610 236034610 single base substitution G A upstream_gene_variant MALY-DE 1 236044926 236044926 single base substitution T G intron_variant MELA-AU 1 235819865 235819865 single base substitution G A downstream_gene_variant MELA-AU 1 235820083 235820083 single base substitution G A downstream_gene_variant MELA-AU 1 235820190 235820190 single base substitution G A downstream_gene_variant MELA-AU 1 235820356 235820356 single base substitution C T downstream_gene_variant MELA-AU 1 235821009 235821009 deletion of <=200bp T - downstream_gene_variant MELA-AU 1 235821071 235821071 single base substitution A T downstream_gene_variant MELA-AU 1 235821124 235821124 single base substitution G A downstream_gene_variant MELA-AU 1 235821220 235821220 single base substitution T G downstream_gene_variant MELA-AU 1 235821578 235821578 single base substitution T C downstream_gene_variant MELA-AU 1 235822063 235822063 single base substitution G A downstream_gene_variant MELA-AU 1 235822508 235822508 single base substitution G A downstream_gene_variant MELA-AU 1 235822680 235822680 single base substitution A G downstream_gene_variant MELA-AU 1 235822850 235822850 single base substitution G A downstream_gene_variant MELA-AU 1 235822852 235822852 single base substitution G A downstream_gene_variant MELA-AU 1 235823081 235823082 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 1 235823373 235823373 single base substitution G A downstream_gene_variant MELA-AU 1 235823430 235823430 single base substitution G A downstream_gene_variant MELA-AU 1 235823465 235823465 single base substitution G A downstream_gene_variant MELA-AU 1 235823690 235823690 single base substitution G A downstream_gene_variant MELA-AU 1 235823764 235823764 single base substitution G A downstream_gene_variant MELA-AU 1 235823841 235823841 single base substitution T C downstream_gene_variant MELA-AU 1 235824104 235824104 single base substitution C T downstream_gene_variant MELA-AU 1 235825955 235825955 single base substitution G A 3_prime_UTR_variant MELA-AU 1 235825955 235825955 single base substitution G A exon_variant MELA-AU 1 235826041 235826041 single base substitution T A 3_prime_UTR_variant MELA-AU 1 235826041 235826041 single base substitution T A exon_variant MELA-AU 1 235826784 235826784 single base substitution G A intron_variant MELA-AU 1 235826914 235826914 single base substitution T A intron_variant MELA-AU 1 235827361 235827361 single base substitution G A splice_region_variant MELA-AU 1 235828337 235828337 single base substitution G A intron_variant MELA-AU 1 235828439 235828439 single base substitution G A intron_variant MELA-AU 1 235828592 235828592 single base substitution G A intron_variant MELA-AU 1 235828838 235828839 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235830477 235830477 single base substitution A C intron_variant MELA-AU 1 235831168 235831168 single base substitution T C intron_variant MELA-AU 1 235831231 235831231 single base substitution G A intron_variant MELA-AU 1 235831686 235831686 single base substitution A G intron_variant MELA-AU 1 235831936 235831936 single base substitution G A intron_variant MELA-AU 1 235832581 235832581 single base substitution G A intron_variant MELA-AU 1 235833416 235833416 single base substitution C T intron_variant MELA-AU 1 235833688 235833688 single base substitution G A intron_variant MELA-AU 1 235834097 235834097 single base substitution G A intron_variant MELA-AU 1 235834360 235834360 single base substitution T G intron_variant MELA-AU 1 235834808 235834808 single base substitution G A intron_variant MELA-AU 1 235834891 235834891 single base substitution A G intron_variant MELA-AU 1 235834945 235834945 single base substitution A G intron_variant MELA-AU 1 235835953 235835954 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235836498 235836498 single base substitution G A intron_variant MELA-AU 1 235836975 235836975 single base substitution C T intron_variant MELA-AU 1 235837471 235837471 single base substitution G A intron_variant MELA-AU 1 235838099 235838099 single base substitution C T intron_variant MELA-AU 1 235838334 235838334 single base substitution C T intron_variant MELA-AU 1 235838380 235838380 single base substitution G A intron_variant MELA-AU 1 235839245 235839245 single base substitution G A intron_variant MELA-AU 1 235839584 235839584 single base substitution G A intron_variant MELA-AU 1 235839818 235839818 single base substitution T G intron_variant MELA-AU 1 235839944 235839944 single base substitution T A intron_variant MELA-AU 1 235840148 235840148 single base substitution G T intron_variant MELA-AU 1 235840153 235840153 single base substitution T C intron_variant MELA-AU 1 235840834 235840834 single base substitution C T exon_variant MELA-AU 1 235840834 235840834 single base substitution C T missense_variant S3629N 10886G>A MELA-AU 1 235841813 235841813 single base substitution G A intron_variant MELA-AU 1 235842577 235842577 single base substitution C G intron_variant MELA-AU 1 235842635 235842635 single base substitution G A intron_variant MELA-AU 1 235843185 235843186 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235843285 235843286 deletion of <=200bp CT - intron_variant MELA-AU 1 235844315 235844315 single base substitution G A intron_variant MELA-AU 1 235844449 235844450 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235844564 235844564 single base substitution G A intron_variant MELA-AU 1 235844639 235844639 single base substitution G A intron_variant MELA-AU 1 235845670 235845670 single base substitution G A intron_variant MELA-AU 1 235845720 235845720 single base substitution G A intron_variant MELA-AU 1 235845942 235845942 single base substitution G A intron_variant MELA-AU 1 235846153 235846153 single base substitution T C intron_variant MELA-AU 1 235846250 235846250 single base substitution G A intron_variant MELA-AU 1 235846266 235846266 deletion of <=200bp A - intron_variant MELA-AU 1 235847087 235847088 multiple base substitution (>=2bp and <=200bp) GT AC intron_variant MELA-AU 1 235847173 235847173 single base substitution G A intron_variant MELA-AU 1 235847530 235847530 single base substitution A G intron_variant MELA-AU 1 235847562 235847562 single base substitution T G intron_variant MELA-AU 1 235847851 235847851 single base substitution G A intron_variant MELA-AU 1 235848834 235848834 single base substitution G A intron_variant MELA-AU 1 235848965 235848965 single base substitution G A intron_variant MELA-AU 1 235849668 235849668 single base substitution A G intron_variant MELA-AU 1 235849782 235849782 single base substitution G A intron_variant MELA-AU 1 235849800 235849800 single base substitution G A intron_variant MELA-AU 1 235850112 235850112 single base substitution T C intron_variant MELA-AU 1 235850847 235850847 single base substitution G A intron_variant MELA-AU 1 235850921 235850921 single base substitution C T intron_variant MELA-AU 1 235851178 235851178 single base substitution C T intron_variant MELA-AU 1 235851327 235851327 single base substitution G A intron_variant MELA-AU 1 235852075 235852075 single base substitution G A intron_variant MELA-AU 1 235852329 235852329 single base substitution C T intron_variant MELA-AU 1 235852509 235852509 single base substitution A G intron_variant MELA-AU 1 235853263 235853263 single base substitution T C intron_variant MELA-AU 1 235853340 235853340 single base substitution G A intron_variant MELA-AU 1 235854077 235854077 single base substitution G A intron_variant MELA-AU 1 235854164 235854164 single base substitution G A intron_variant MELA-AU 1 235854495 235854496 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235854548 235854548 single base substitution G A intron_variant MELA-AU 1 235855451 235855451 single base substitution G T intron_variant MELA-AU 1 235856246 235856246 single base substitution G A intron_variant MELA-AU 1 235856405 235856405 single base substitution G A intron_variant MELA-AU 1 235856543 235856543 single base substitution G A intron_variant MELA-AU 1 235857126 235857126 single base substitution T C intron_variant MELA-AU 1 235857161 235857161 single base substitution G A intron_variant MELA-AU 1 235857445 235857445 single base substitution G A intron_variant MELA-AU 1 235857535 235857535 single base substitution G A intron_variant MELA-AU 1 235857664 235857664 single base substitution G A intron_variant MELA-AU 1 235858131 235858131 single base substitution T A intron_variant MELA-AU 1 235858192 235858192 single base substitution C T intron_variant MELA-AU 1 235858327 235858327 single base substitution C A intron_variant MELA-AU 1 235858439 235858439 single base substitution G A intron_variant MELA-AU 1 235858681 235858681 single base substitution G A intron_variant MELA-AU 1 235859060 235859060 single base substitution G A intron_variant MELA-AU 1 235859067 235859068 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235859096 235859096 single base substitution C T intron_variant MELA-AU 1 235859322 235859322 single base substitution A G intron_variant MELA-AU 1 235859852 235859852 single base substitution C T intron_variant MELA-AU 1 235860210 235860210 single base substitution T C intron_variant MELA-AU 1 235860463 235860463 single base substitution G A exon_variant MELA-AU 1 235860463 235860463 single base substitution G A missense_variant S3495F 10484C>T MELA-AU 1 235860841 235860841 single base substitution G A intron_variant MELA-AU 1 235861157 235861157 single base substitution G A intron_variant MELA-AU 1 235861644 235861644 insertion of <=200bp - C intron_variant MELA-AU 1 235862151 235862151 single base substitution C A intron_variant MELA-AU 1 235862239 235862239 single base substitution T A intron_variant MELA-AU 1 235862507 235862507 single base substitution A G intron_variant MELA-AU 1 235862739 235862739 single base substitution A G intron_variant MELA-AU 1 235863318 235863318 single base substitution G A intron_variant MELA-AU 1 235863492 235863492 single base substitution G A intron_variant MELA-AU 1 235864747 235864747 single base substitution G A intron_variant MELA-AU 1 235864895 235864895 single base substitution T C intron_variant MELA-AU 1 235865294 235865294 single base substitution G A intron_variant MELA-AU 1 235866216 235866216 single base substitution G A exon_variant MELA-AU 1 235866216 235866216 single base substitution G A missense_variant T3402I 10205C>T MELA-AU 1 235868023 235868023 single base substitution G T downstream_gene_variant MELA-AU 1 235868023 235868023 single base substitution G T intron_variant MELA-AU 1 235869339 235869339 single base substitution C A downstream_gene_variant MELA-AU 1 235869339 235869339 single base substitution C A intron_variant MELA-AU 1 235869345 235869346 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 1 235869345 235869346 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235869858 235869858 single base substitution T A downstream_gene_variant MELA-AU 1 235869858 235869858 single base substitution T A intron_variant MELA-AU 1 235870486 235870486 single base substitution G A downstream_gene_variant MELA-AU 1 235870486 235870486 single base substitution G A intron_variant MELA-AU 1 235870708 235870708 single base substitution G T downstream_gene_variant MELA-AU 1 235870708 235870708 single base substitution G T intron_variant MELA-AU 1 235870752 235870752 single base substitution T C downstream_gene_variant MELA-AU 1 235870752 235870752 single base substitution T C intron_variant MELA-AU 1 235871180 235871180 single base substitution G A downstream_gene_variant MELA-AU 1 235871180 235871180 single base substitution G A intron_variant MELA-AU 1 235871246 235871246 single base substitution G A downstream_gene_variant MELA-AU 1 235871246 235871246 single base substitution G A intron_variant MELA-AU 1 235871255 235871255 single base substitution C T downstream_gene_variant MELA-AU 1 235871255 235871255 single base substitution C T intron_variant MELA-AU 1 235871302 235871302 single base substitution G A downstream_gene_variant MELA-AU 1 235871302 235871302 single base substitution G A intron_variant MELA-AU 1 235871999 235871999 single base substitution G A downstream_gene_variant MELA-AU 1 235871999 235871999 single base substitution G A intron_variant MELA-AU 1 235872392 235872392 single base substitution G A downstream_gene_variant MELA-AU 1 235872392 235872392 single base substitution G A missense_variant A3381V 10142C>T MELA-AU 1 235872392 235872392 single base substitution G A splice_region_variant MELA-AU 1 235873633 235873633 single base substitution G A downstream_gene_variant MELA-AU 1 235873633 235873633 single base substitution G A intron_variant MELA-AU 1 235874082 235874082 single base substitution G A downstream_gene_variant MELA-AU 1 235874082 235874082 single base substitution G A intron_variant MELA-AU 1 235875336 235875336 single base substitution A G downstream_gene_variant MELA-AU 1 235875336 235875336 single base substitution A G intron_variant MELA-AU 1 235875704 235875704 single base substitution C T downstream_gene_variant MELA-AU 1 235875704 235875704 single base substitution C T intron_variant MELA-AU 1 235875704 235875704 single base substitution C T upstream_gene_variant MELA-AU 1 235875923 235875923 single base substitution G A downstream_gene_variant MELA-AU 1 235875923 235875923 single base substitution G A intron_variant MELA-AU 1 235875923 235875923 single base substitution G A upstream_gene_variant MELA-AU 1 235876310 235876310 single base substitution G A downstream_gene_variant MELA-AU 1 235876310 235876310 single base substitution G A intron_variant MELA-AU 1 235876310 235876310 single base substitution G A upstream_gene_variant MELA-AU 1 235876319 235876319 single base substitution A G downstream_gene_variant MELA-AU 1 235876319 235876319 single base substitution A G intron_variant MELA-AU 1 235876319 235876319 single base substitution A G upstream_gene_variant MELA-AU 1 235877041 235877041 single base substitution G C intron_variant MELA-AU 1 235877041 235877041 single base substitution G C upstream_gene_variant MELA-AU 1 235878228 235878228 single base substitution G A intron_variant MELA-AU 1 235878228 235878228 single base substitution G A upstream_gene_variant MELA-AU 1 235878260 235878260 single base substitution G A intron_variant MELA-AU 1 235878260 235878260 single base substitution G A upstream_gene_variant MELA-AU 1 235878380 235878380 single base substitution C A intron_variant MELA-AU 1 235878380 235878380 single base substitution C A upstream_gene_variant MELA-AU 1 235879152 235879152 single base substitution G A intron_variant MELA-AU 1 235879152 235879152 single base substitution G A upstream_gene_variant MELA-AU 1 235879500 235879500 single base substitution A G intron_variant MELA-AU 1 235879500 235879500 single base substitution A G upstream_gene_variant MELA-AU 1 235879540 235879540 single base substitution T C intron_variant MELA-AU 1 235879540 235879540 single base substitution T C upstream_gene_variant MELA-AU 1 235879900 235879900 single base substitution G A intron_variant MELA-AU 1 235879900 235879900 single base substitution G A upstream_gene_variant MELA-AU 1 235880136 235880136 single base substitution C T intron_variant MELA-AU 1 235880136 235880136 single base substitution C T upstream_gene_variant MELA-AU 1 235880246 235880246 single base substitution G A intron_variant MELA-AU 1 235880246 235880246 single base substitution G A upstream_gene_variant MELA-AU 1 235880398 235880398 single base substitution G A intron_variant MELA-AU 1 235880398 235880398 single base substitution G A upstream_gene_variant MELA-AU 1 235880633 235880633 single base substitution G A intron_variant MELA-AU 1 235880633 235880633 single base substitution G A upstream_gene_variant MELA-AU 1 235880703 235880703 single base substitution C T intron_variant MELA-AU 1 235880826 235880826 single base substitution G A intron_variant MELA-AU 1 235880856 235880856 single base substitution G A intron_variant MELA-AU 1 235881398 235881398 single base substitution A G intron_variant MELA-AU 1 235882442 235882443 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 235882484 235882484 single base substitution A C intron_variant MELA-AU 1 235882979 235882979 single base substitution G T intron_variant MELA-AU 1 235883611 235883611 single base substitution G A intron_variant MELA-AU 1 235883759 235883759 single base substitution C T intron_variant MELA-AU 1 235884064 235884064 single base substitution C T exon_variant MELA-AU 1 235884064 235884064 single base substitution C T missense_variant A3153T 9457G>A MELA-AU 1 235886000 235886000 single base substitution G A intron_variant MELA-AU 1 235886488 235886488 single base substitution G A intron_variant MELA-AU 1 235886578 235886578 single base substitution G A intron_variant MELA-AU 1 235886807 235886807 single base substitution G A intron_variant MELA-AU 1 235887096 235887096 single base substitution A T intron_variant MELA-AU 1 235887183 235887199 deletion of <=200bp TAACAAAGGCTTCACTT - intron_variant MELA-AU 1 235887248 235887248 single base substitution T C intron_variant MELA-AU 1 235887304 235887304 single base substitution A G intron_variant MELA-AU 1 235887513 235887513 single base substitution T A intron_variant MELA-AU 1 235887664 235887664 single base substitution A G intron_variant MELA-AU 1 235887668 235887668 single base substitution A G intron_variant MELA-AU 1 235887696 235887696 single base substitution T C intron_variant MELA-AU 1 235887852 235887852 single base substitution A C intron_variant MELA-AU 1 235887968 235887968 single base substitution C T intron_variant MELA-AU 1 235888088 235888088 single base substitution A T intron_variant MELA-AU 1 235888395 235888395 single base substitution G A intron_variant MELA-AU 1 235888444 235888444 single base substitution G A intron_variant MELA-AU 1 235888445 235888445 single base substitution G A intron_variant MELA-AU 1 235888918 235888918 single base substitution G T intron_variant MELA-AU 1 235888973 235888973 single base substitution G A intron_variant MELA-AU 1 235888974 235888974 single base substitution G A intron_variant MELA-AU 1 235888985 235888985 single base substitution G A intron_variant MELA-AU 1 235889549 235889549 single base substitution C T intron_variant MELA-AU 1 235889564 235889564 single base substitution T C intron_variant MELA-AU 1 235889910 235889910 single base substitution G A intron_variant MELA-AU 1 235890027 235890027 single base substitution G A intron_variant MELA-AU 1 235891072 235891072 single base substitution G A intron_variant MELA-AU 1 235891377 235891377 single base substitution G A missense_variant S3054L 9161C>T MELA-AU 1 235891377 235891377 single base substitution G A splice_region_variant MELA-AU 1 235891508 235891509 multiple base substitution (>=2bp and <=200bp) GG AC intron_variant MELA-AU 1 235891508 235891509 multiple base substitution (>=2bp and <=200bp) GG AC upstream_gene_variant MELA-AU 1 235891592 235891592 single base substitution G A intron_variant MELA-AU 1 235891592 235891592 single base substitution G A upstream_gene_variant MELA-AU 1 235891789 235891789 single base substitution T C intron_variant MELA-AU 1 235891789 235891789 single base substitution T C upstream_gene_variant MELA-AU 1 235892101 235892101 single base substitution G T intron_variant MELA-AU 1 235892101 235892101 single base substitution G T upstream_gene_variant MELA-AU 1 235892304 235892304 single base substitution G A intron_variant MELA-AU 1 235892304 235892304 single base substitution G A upstream_gene_variant MELA-AU 1 235893623 235893623 single base substitution A G intron_variant MELA-AU 1 235893623 235893623 single base substitution A G upstream_gene_variant MELA-AU 1 235893751 235893751 single base substitution C T intron_variant MELA-AU 1 235893751 235893751 single base substitution C T upstream_gene_variant MELA-AU 1 235894356 235894357 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 1 235894356 235894357 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant LL2974LF MELA-AU 1 235894356 235894357 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 1 235894827 235894827 single base substitution A G intron_variant MELA-AU 1 235894827 235894827 single base substitution A G upstream_gene_variant MELA-AU 1 235894829 235894829 single base substitution A G intron_variant MELA-AU 1 235894829 235894829 single base substitution A G upstream_gene_variant MELA-AU 1 235895269 235895269 single base substitution G A intron_variant MELA-AU 1 235895269 235895269 single base substitution G A upstream_gene_variant MELA-AU 1 235895458 235895458 single base substitution T A intron_variant MELA-AU 1 235895458 235895458 single base substitution T A upstream_gene_variant MELA-AU 1 235895717 235895717 single base substitution C T intron_variant MELA-AU 1 235895717 235895717 single base substitution C T upstream_gene_variant MELA-AU 1 235896740 235896740 single base substitution C T downstream_gene_variant MELA-AU 1 235896740 235896740 single base substitution C T intron_variant MELA-AU 1 235896958 235896958 single base substitution A G downstream_gene_variant MELA-AU 1 235896958 235896958 single base substitution A G exon_variant MELA-AU 1 235896958 235896958 single base substitution A G synonymous_variant D2882D 8646T>C MELA-AU 1 235897089 235897089 single base substitution G A downstream_gene_variant MELA-AU 1 235897089 235897089 single base substitution G A intron_variant MELA-AU 1 235897308 235897308 single base substitution G A downstream_gene_variant MELA-AU 1 235897308 235897308 single base substitution G A intron_variant MELA-AU 1 235897714 235897714 single base substitution A C downstream_gene_variant MELA-AU 1 235897714 235897714 single base substitution A C intron_variant MELA-AU 1 235897914 235897914 single base substitution G A downstream_gene_variant MELA-AU 1 235897914 235897914 single base substitution G A exon_variant MELA-AU 1 235897914 235897914 single base substitution G A missense_variant H2802Y 8404C>T MELA-AU 1 235899676 235899676 single base substitution G A downstream_gene_variant MELA-AU 1 235899676 235899676 single base substitution G A exon_variant MELA-AU 1 235899676 235899676 single base substitution G A intron_variant MELA-AU 1 235899960 235899960 single base substitution T A downstream_gene_variant MELA-AU 1 235899960 235899960 single base substitution T A exon_variant MELA-AU 1 235899960 235899960 single base substitution T A intron_variant MELA-AU 1 235900757 235900757 single base substitution A C downstream_gene_variant MELA-AU 1 235900757 235900757 single base substitution A C exon_variant MELA-AU 1 235900757 235900757 single base substitution A C intron_variant MELA-AU 1 235900823 235900823 single base substitution G A downstream_gene_variant MELA-AU 1 235900823 235900823 single base substitution G A exon_variant MELA-AU 1 235900823 235900823 single base substitution G A intron_variant MELA-AU 1 235901165 235901165 single base substitution C T downstream_gene_variant MELA-AU 1 235901165 235901165 single base substitution C T exon_variant MELA-AU 1 235901165 235901165 single base substitution C T intron_variant MELA-AU 1 235901395 235901395 single base substitution C A exon_variant MELA-AU 1 235901395 235901395 single base substitution C A intron_variant MELA-AU 1 235901395 235901395 single base substitution C A upstream_gene_variant MELA-AU 1 235901880 235901880 single base substitution G A exon_variant MELA-AU 1 235901880 235901880 single base substitution G A intron_variant MELA-AU 1 235901880 235901880 single base substitution G A upstream_gene_variant MELA-AU 1 235901979 235901979 single base substitution G A intron_variant MELA-AU 1 235901979 235901979 single base substitution G A upstream_gene_variant MELA-AU 1 235903029 235903029 insertion of <=200bp - T intron_variant MELA-AU 1 235903029 235903029 insertion of <=200bp - T upstream_gene_variant MELA-AU 1 235903150 235903150 single base substitution G A intron_variant MELA-AU 1 235903150 235903150 single base substitution G A upstream_gene_variant MELA-AU 1 235903369 235903369 single base substitution A G intron_variant MELA-AU 1 235903369 235903369 single base substitution A G upstream_gene_variant MELA-AU 1 235903953 235903953 single base substitution G A intron_variant MELA-AU 1 235903953 235903953 single base substitution G A upstream_gene_variant MELA-AU 1 235904948 235904948 single base substitution G A downstream_gene_variant MELA-AU 1 235904948 235904948 single base substitution G A intron_variant MELA-AU 1 235904948 235904948 single base substitution G A upstream_gene_variant MELA-AU 1 235905177 235905177 single base substitution G A downstream_gene_variant MELA-AU 1 235905177 235905177 single base substitution G A intron_variant MELA-AU 1 235905177 235905177 single base substitution G A upstream_gene_variant MELA-AU 1 235905871 235905872 deletion of <=200bp TA - downstream_gene_variant MELA-AU 1 235905871 235905872 deletion of <=200bp TA - intron_variant MELA-AU 1 235905871 235905872 deletion of <=200bp TA - upstream_gene_variant MELA-AU 1 235906210 235906210 single base substitution G A downstream_gene_variant MELA-AU 1 235906210 235906210 single base substitution G A intron_variant MELA-AU 1 235906210 235906210 single base substitution G A upstream_gene_variant MELA-AU 1 235906456 235906456 single base substitution C T downstream_gene_variant MELA-AU 1 235906456 235906456 single base substitution C T intron_variant MELA-AU 1 235906491 235906491 single base substitution A G downstream_gene_variant MELA-AU 1 235906491 235906491 single base substitution A G intron_variant MELA-AU 1 235907531 235907531 single base substitution G A downstream_gene_variant MELA-AU 1 235907531 235907531 single base substitution G A intron_variant MELA-AU 1 235907531 235907531 single base substitution G A upstream_gene_variant MELA-AU 1 235907689 235907689 single base substitution A T downstream_gene_variant MELA-AU 1 235907689 235907689 single base substitution A T intron_variant MELA-AU 1 235907689 235907689 single base substitution A T upstream_gene_variant MELA-AU 1 235907898 235907898 single base substitution G A downstream_gene_variant MELA-AU 1 235907898 235907898 single base substitution G A intron_variant MELA-AU 1 235907898 235907898 single base substitution G A upstream_gene_variant MELA-AU 1 235908203 235908203 single base substitution A G downstream_gene_variant MELA-AU 1 235908203 235908203 single base substitution A G intron_variant MELA-AU 1 235908203 235908203 single base substitution A G upstream_gene_variant MELA-AU 1 235908839 235908839 single base substitution T A downstream_gene_variant MELA-AU 1 235908839 235908839 single base substitution T A intron_variant MELA-AU 1 235908839 235908839 single base substitution T A upstream_gene_variant MELA-AU 1 235909139 235909139 single base substitution T C downstream_gene_variant MELA-AU 1 235909139 235909139 single base substitution T C intron_variant MELA-AU 1 235909139 235909139 single base substitution T C upstream_gene_variant MELA-AU 1 235909327 235909327 single base substitution G A downstream_gene_variant MELA-AU 1 235909327 235909327 single base substitution G A intron_variant MELA-AU 1 235909327 235909327 single base substitution G A upstream_gene_variant MELA-AU 1 235910390 235910390 single base substitution C T intron_variant MELA-AU 1 235910390 235910390 single base substitution C T upstream_gene_variant MELA-AU 1 235910574 235910574 single base substitution G A intron_variant MELA-AU 1 235910574 235910574 single base substitution G A missense_variant S126F 377C>T MELA-AU 1 235910574 235910574 single base substitution G A upstream_gene_variant MELA-AU 1 235911751 235911751 single base substitution T A intron_variant MELA-AU 1 235911751 235911751 single base substitution T A upstream_gene_variant MELA-AU 1 235912712 235912712 single base substitution G A intron_variant MELA-AU 1 235912807 235912807 single base substitution G A intron_variant MELA-AU 1 235914247 235914247 single base substitution G A intron_variant MELA-AU 1 235915466 235915466 single base substitution G A missense_variant P2489L 7466C>T MELA-AU 1 235915466 235915466 single base substitution G A missense_variant P2L 5C>T MELA-AU 1 235915467 235915467 single base substitution G A missense_variant P2489S 7465C>T MELA-AU 1 235915467 235915467 single base substitution G A missense_variant P2S 4C>T MELA-AU 1 235916127 235916127 single base substitution A C intron_variant MELA-AU 1 235916127 235916127 single base substitution A C upstream_gene_variant MELA-AU 1 235916519 235916519 single base substitution G A missense_variant P2429S 7285C>T MELA-AU 1 235916519 235916519 single base substitution G A upstream_gene_variant MELA-AU 1 235916745 235916745 single base substitution G A intron_variant MELA-AU 1 235916745 235916745 single base substitution G A upstream_gene_variant MELA-AU 1 235917461 235917461 single base substitution T C intron_variant MELA-AU 1 235917461 235917461 single base substitution T C upstream_gene_variant MELA-AU 1 235917666 235917666 single base substitution G A downstream_gene_variant MELA-AU 1 235917666 235917666 single base substitution G A intron_variant MELA-AU 1 235917666 235917666 single base substitution G A upstream_gene_variant MELA-AU 1 235918184 235918184 single base substitution G A downstream_gene_variant MELA-AU 1 235918184 235918184 single base substitution G A intron_variant MELA-AU 1 235918184 235918184 single base substitution G A upstream_gene_variant MELA-AU 1 235918506 235918506 single base substitution G A downstream_gene_variant MELA-AU 1 235918506 235918506 single base substitution G A intron_variant MELA-AU 1 235918506 235918506 single base substitution G A upstream_gene_variant MELA-AU 1 235918633 235918633 single base substitution G A downstream_gene_variant MELA-AU 1 235918633 235918633 single base substitution G A intron_variant MELA-AU 1 235918633 235918633 single base substitution G A upstream_gene_variant MELA-AU 1 235918737 235918737 single base substitution C A downstream_gene_variant MELA-AU 1 235918737 235918737 single base substitution C A intron_variant MELA-AU 1 235918737 235918737 single base substitution C A upstream_gene_variant MELA-AU 1 235919299 235919299 insertion of <=200bp - ATCTAT downstream_gene_variant MELA-AU 1 235919299 235919299 insertion of <=200bp - ATCTAT intron_variant MELA-AU 1 235919299 235919299 insertion of <=200bp - ATCTAT upstream_gene_variant MELA-AU 1 235919351 235919351 single base substitution A G downstream_gene_variant MELA-AU 1 235919351 235919351 single base substitution A G intron_variant MELA-AU 1 235919351 235919351 single base substitution A G upstream_gene_variant MELA-AU 1 235919357 235919357 single base substitution A G downstream_gene_variant MELA-AU 1 235919357 235919357 single base substitution A G intron_variant MELA-AU 1 235919357 235919357 single base substitution A G upstream_gene_variant MELA-AU 1 235919363 235919363 single base substitution G A downstream_gene_variant MELA-AU 1 235919363 235919363 single base substitution G A intron_variant MELA-AU 1 235919363 235919363 single base substitution G A upstream_gene_variant MELA-AU 1 235919665 235919665 single base substitution C T downstream_gene_variant MELA-AU 1 235919665 235919665 single base substitution C T intron_variant MELA-AU 1 235919665 235919665 single base substitution C T upstream_gene_variant MELA-AU 1 235919982 235919982 single base substitution A T downstream_gene_variant MELA-AU 1 235919982 235919982 single base substitution A T intron_variant MELA-AU 1 235919982 235919982 single base substitution A T upstream_gene_variant MELA-AU 1 235920287 235920287 single base substitution G A downstream_gene_variant MELA-AU 1 235920287 235920287 single base substitution G A intron_variant MELA-AU 1 235920287 235920287 single base substitution G A upstream_gene_variant MELA-AU 1 235920337 235920338 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 1 235920337 235920338 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235920337 235920338 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 1 235920527 235920527 single base substitution A G downstream_gene_variant MELA-AU 1 235920527 235920527 single base substitution A G intron_variant MELA-AU 1 235920761 235920761 single base substitution A G downstream_gene_variant MELA-AU 1 235920761 235920761 single base substitution A G splice_region_variant MELA-AU 1 235921382 235921382 single base substitution G A downstream_gene_variant MELA-AU 1 235921382 235921382 single base substitution G A intron_variant MELA-AU 1 235921416 235921416 single base substitution G A downstream_gene_variant MELA-AU 1 235921416 235921416 single base substitution G A intron_variant MELA-AU 1 235921553 235921553 single base substitution C T downstream_gene_variant MELA-AU 1 235921553 235921553 single base substitution C T intron_variant MELA-AU 1 235922109 235922109 single base substitution G A downstream_gene_variant MELA-AU 1 235922109 235922109 single base substitution G A intron_variant MELA-AU 1 235922726 235922727 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 1 235922726 235922727 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 1 235922726 235922727 multiple base substitution (>=2bp and <=200bp) GG AA stop_gained TQ2142T* MELA-AU 1 235922766 235922766 single base substitution G A 3_prime_UTR_variant MELA-AU 1 235922766 235922766 single base substitution G A exon_variant MELA-AU 1 235922766 235922766 single base substitution G A synonymous_variant I2129I 6387C>T MELA-AU 1 235923819 235923819 single base substitution G A intron_variant MELA-AU 1 235924380 235924380 single base substitution C T intron_variant MELA-AU 1 235924817 235924817 single base substitution G C intron_variant MELA-AU 1 235925854 235925854 single base substitution G A intron_variant MELA-AU 1 235926081 235926081 single base substitution G A 3_prime_UTR_variant MELA-AU 1 235926081 235926081 single base substitution G A exon_variant MELA-AU 1 235926081 235926081 single base substitution G A synonymous_variant S2064S 6192C>T MELA-AU 1 235926236 235926236 single base substitution C T intron_variant MELA-AU 1 235926800 235926800 single base substitution G A intron_variant MELA-AU 1 235927419 235927419 single base substitution G A intron_variant MELA-AU 1 235928148 235928148 single base substitution C A intron_variant MELA-AU 1 235929989 235929989 single base substitution G A intron_variant MELA-AU 1 235931710 235931710 single base substitution C T intron_variant MELA-AU 1 235932080 235932080 single base substitution G A intron_variant MELA-AU 1 235932969 235932970 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235933073 235933073 single base substitution C T intron_variant MELA-AU 1 235933122 235933122 single base substitution A C intron_variant MELA-AU 1 235933298 235933298 single base substitution G A intron_variant MELA-AU 1 235933336 235933336 single base substitution G A intron_variant MELA-AU 1 235934901 235934901 single base substitution T A intron_variant MELA-AU 1 235935224 235935224 single base substitution T G intron_variant MELA-AU 1 235935225 235935225 single base substitution T G intron_variant MELA-AU 1 235935571 235935571 single base substitution A G intron_variant MELA-AU 1 235936005 235936005 single base substitution G A intron_variant MELA-AU 1 235936049 235936049 single base substitution C T intron_variant MELA-AU 1 235936178 235936178 single base substitution G A intron_variant MELA-AU 1 235936779 235936779 single base substitution G A intron_variant MELA-AU 1 235936924 235936924 single base substitution G A intron_variant MELA-AU 1 235937119 235937119 single base substitution G A intron_variant MELA-AU 1 235937519 235937519 single base substitution G A intron_variant MELA-AU 1 235937643 235937643 single base substitution G A intron_variant MELA-AU 1 235938219 235938219 single base substitution A C 3_prime_UTR_variant MELA-AU 1 235938219 235938219 single base substitution A C exon_variant MELA-AU 1 235938219 235938219 single base substitution A C missense_variant I1876M 5628T>G MELA-AU 1 235938592 235938592 single base substitution A T intron_variant MELA-AU 1 235938863 235938863 single base substitution G A intron_variant MELA-AU 1 235939078 235939078 single base substitution G A intron_variant MELA-AU 1 235939198 235939198 single base substitution G A intron_variant MELA-AU 1 235939715 235939715 single base substitution G A intron_variant MELA-AU 1 235940260 235940260 single base substitution A G intron_variant MELA-AU 1 235940836 235940837 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235941627 235941627 single base substitution C T intron_variant MELA-AU 1 235942436 235942436 single base substitution G A intron_variant MELA-AU 1 235943478 235943478 single base substitution G A intron_variant MELA-AU 1 235943650 235943650 single base substitution G A intron_variant MELA-AU 1 235943992 235943992 single base substitution G A intron_variant MELA-AU 1 235944059 235944059 single base substitution G A intron_variant MELA-AU 1 235944860 235944860 single base substitution G A intron_variant MELA-AU 1 235945251 235945251 single base substitution G A 3_prime_UTR_variant MELA-AU 1 235945251 235945251 single base substitution G A exon_variant MELA-AU 1 235945251 235945251 single base substitution G A synonymous_variant L1667L 4999C>T MELA-AU 1 235945463 235945463 single base substitution T A downstream_gene_variant MELA-AU 1 235945463 235945463 single base substitution T A intron_variant MELA-AU 1 235945542 235945542 single base substitution C G downstream_gene_variant MELA-AU 1 235945542 235945542 single base substitution C G intron_variant MELA-AU 1 235945625 235945625 single base substitution G A downstream_gene_variant MELA-AU 1 235945625 235945625 single base substitution G A intron_variant MELA-AU 1 235945665 235945665 single base substitution G A downstream_gene_variant MELA-AU 1 235945665 235945665 single base substitution G A intron_variant MELA-AU 1 235945883 235945883 single base substitution G A downstream_gene_variant MELA-AU 1 235945883 235945883 single base substitution G A intron_variant MELA-AU 1 235947521 235947521 insertion of <=200bp - ATCT downstream_gene_variant MELA-AU 1 235947521 235947521 insertion of <=200bp - ATCT intron_variant MELA-AU 1 235948065 235948065 single base substitution G A downstream_gene_variant MELA-AU 1 235948065 235948065 single base substitution G A intron_variant MELA-AU 1 235948825 235948825 single base substitution C T downstream_gene_variant MELA-AU 1 235948825 235948825 single base substitution C T intron_variant MELA-AU 1 235950056 235950056 single base substitution G A downstream_gene_variant MELA-AU 1 235950056 235950056 single base substitution G A intron_variant MELA-AU 1 235950089 235950089 single base substitution G A downstream_gene_variant MELA-AU 1 235950089 235950089 single base substitution G A intron_variant MELA-AU 1 235950221 235950221 single base substitution G A downstream_gene_variant MELA-AU 1 235950221 235950221 single base substitution G A intron_variant MELA-AU 1 235950262 235950262 single base substitution G A downstream_gene_variant MELA-AU 1 235950262 235950262 single base substitution G A intron_variant MELA-AU 1 235950534 235950534 single base substitution G A 3_prime_UTR_variant MELA-AU 1 235950534 235950534 single base substitution G A downstream_gene_variant MELA-AU 1 235950534 235950534 single base substitution G A exon_variant MELA-AU 1 235950534 235950534 single base substitution G A missense_variant H1610Y 4828C>T MELA-AU 1 235951211 235951211 single base substitution T C downstream_gene_variant MELA-AU 1 235951211 235951211 single base substitution T C intron_variant MELA-AU 1 235951384 235951384 single base substitution A G downstream_gene_variant MELA-AU 1 235951384 235951384 single base substitution A G intron_variant MELA-AU 1 235951815 235951815 single base substitution G A downstream_gene_variant MELA-AU 1 235951815 235951815 single base substitution G A intron_variant MELA-AU 1 235952331 235952331 single base substitution G A downstream_gene_variant MELA-AU 1 235952331 235952331 single base substitution G A intron_variant MELA-AU 1 235952331 235952331 single base substitution G A upstream_gene_variant MELA-AU 1 235952579 235952579 single base substitution C T downstream_gene_variant MELA-AU 1 235952579 235952579 single base substitution C T intron_variant MELA-AU 1 235952579 235952579 single base substitution C T upstream_gene_variant MELA-AU 1 235952849 235952849 single base substitution G A downstream_gene_variant MELA-AU 1 235952849 235952849 single base substitution G A intron_variant MELA-AU 1 235952849 235952849 single base substitution G A upstream_gene_variant MELA-AU 1 235953233 235953233 single base substitution G A downstream_gene_variant MELA-AU 1 235953233 235953233 single base substitution G A intron_variant MELA-AU 1 235953233 235953233 single base substitution G A upstream_gene_variant MELA-AU 1 235953996 235953996 single base substitution T C downstream_gene_variant MELA-AU 1 235953996 235953996 single base substitution T C intron_variant MELA-AU 1 235953996 235953996 single base substitution T C upstream_gene_variant MELA-AU 1 235954007 235954007 single base substitution C T downstream_gene_variant MELA-AU 1 235954007 235954007 single base substitution C T intron_variant MELA-AU 1 235954007 235954007 single base substitution C T upstream_gene_variant MELA-AU 1 235954511 235954511 single base substitution G A downstream_gene_variant MELA-AU 1 235954511 235954511 single base substitution G A intron_variant MELA-AU 1 235954511 235954511 single base substitution G A upstream_gene_variant MELA-AU 1 235954543 235954543 single base substitution T A downstream_gene_variant MELA-AU 1 235954543 235954543 single base substitution T A intron_variant MELA-AU 1 235954543 235954543 single base substitution T A upstream_gene_variant MELA-AU 1 235955089 235955089 single base substitution G T exon_variant MELA-AU 1 235955089 235955089 single base substitution G T intron_variant MELA-AU 1 235955089 235955089 single base substitution G T missense_variant H1485N 4453C>A MELA-AU 1 235955089 235955089 single base substitution G T upstream_gene_variant MELA-AU 1 235955170 235955170 single base substitution G A exon_variant MELA-AU 1 235955170 235955170 single base substitution G A intron_variant MELA-AU 1 235955170 235955170 single base substitution G A synonymous_variant L1458L 4372C>T MELA-AU 1 235955170 235955170 single base substitution G A upstream_gene_variant MELA-AU 1 235955416 235955416 single base substitution G A exon_variant MELA-AU 1 235955416 235955416 single base substitution G A intron_variant MELA-AU 1 235955416 235955416 single base substitution G A missense_variant L1376F 4126C>T MELA-AU 1 235955416 235955416 single base substitution G A upstream_gene_variant MELA-AU 1 235955429 235955429 single base substitution G A intron_variant MELA-AU 1 235955429 235955429 single base substitution G A splice_region_variant MELA-AU 1 235955429 235955429 single base substitution G A upstream_gene_variant MELA-AU 1 235955487 235955487 single base substitution G A intron_variant MELA-AU 1 235955487 235955487 single base substitution G A upstream_gene_variant MELA-AU 1 235955622 235955622 single base substitution C T intron_variant MELA-AU 1 235955622 235955622 single base substitution C T upstream_gene_variant MELA-AU 1 235955632 235955632 single base substitution T C intron_variant MELA-AU 1 235955632 235955632 single base substitution T C upstream_gene_variant MELA-AU 1 235955942 235955942 single base substitution T A intron_variant MELA-AU 1 235955942 235955942 single base substitution T A upstream_gene_variant MELA-AU 1 235956097 235956097 single base substitution G A intron_variant MELA-AU 1 235956097 235956097 single base substitution G A upstream_gene_variant MELA-AU 1 235956466 235956466 single base substitution A T intron_variant MELA-AU 1 235956466 235956466 single base substitution A T upstream_gene_variant MELA-AU 1 235956589 235956589 single base substitution G A intron_variant MELA-AU 1 235956589 235956589 single base substitution G A upstream_gene_variant MELA-AU 1 235957256 235957256 single base substitution C T intron_variant MELA-AU 1 235957368 235957368 single base substitution G A intron_variant MELA-AU 1 235957482 235957482 single base substitution G A intron_variant MELA-AU 1 235957596 235957596 single base substitution T C intron_variant MELA-AU 1 235958594 235958594 single base substitution G A intron_variant MELA-AU 1 235958630 235958630 single base substitution G A intron_variant MELA-AU 1 235959933 235959933 single base substitution T C intron_variant MELA-AU 1 235959939 235959939 single base substitution C T intron_variant MELA-AU 1 235960248 235960248 single base substitution G A intron_variant MELA-AU 1 235960566 235960566 single base substitution G A intron_variant MELA-AU 1 235960588 235960588 single base substitution G A intron_variant MELA-AU 1 235961173 235961173 single base substitution T A intron_variant MELA-AU 1 235961181 235961181 single base substitution G A intron_variant MELA-AU 1 235961369 235961369 single base substitution G A intron_variant MELA-AU 1 235961525 235961525 single base substitution G T intron_variant MELA-AU 1 235961723 235961723 single base substitution T G intron_variant MELA-AU 1 235961869 235961869 single base substitution A C intron_variant MELA-AU 1 235961873 235961873 single base substitution T G intron_variant MELA-AU 1 235961909 235961909 single base substitution A G intron_variant MELA-AU 1 235962534 235962534 single base substitution G A intron_variant MELA-AU 1 235963699 235963699 single base substitution A G intron_variant MELA-AU 1 235964002 235964002 single base substitution G A intron_variant MELA-AU 1 235964088 235964088 single base substitution A C intron_variant MELA-AU 1 235964160 235964160 single base substitution G A intron_variant MELA-AU 1 235964481 235964481 single base substitution G A intron_variant MELA-AU 1 235965321 235965321 single base substitution C A intron_variant MELA-AU 1 235965639 235965639 single base substitution G A intron_variant MELA-AU 1 235966816 235966816 single base substitution G A intron_variant MELA-AU 1 235967237 235967237 single base substitution A T intron_variant MELA-AU 1 235967408 235967408 single base substitution T A intron_variant MELA-AU 1 235968050 235968050 single base substitution T C intron_variant MELA-AU 1 235968201 235968201 single base substitution G A intron_variant MELA-AU 1 235968614 235968614 single base substitution C T intron_variant MELA-AU 1 235969149 235969149 single base substitution C T exon_variant MELA-AU 1 235969149 235969149 single base substitution C T missense_variant S1096N 3287G>A MELA-AU 1 235970315 235970315 single base substitution G A intron_variant MELA-AU 1 235970738 235970738 single base substitution G A intron_variant MELA-AU 1 235970756 235970756 single base substitution A C intron_variant MELA-AU 1 235972901 235972901 single base substitution T A exon_variant MELA-AU 1 235972901 235972901 single base substitution T A missense_variant E406V 1217A>T MELA-AU 1 235974139 235974139 single base substitution G A intron_variant MELA-AU 1 235974887 235974887 single base substitution A G intron_variant MELA-AU 1 235975724 235975724 single base substitution T C intron_variant MELA-AU 1 235976010 235976010 single base substitution A C intron_variant MELA-AU 1 235976111 235976111 single base substitution G A intron_variant MELA-AU 1 235976400 235976400 single base substitution G A intron_variant MELA-AU 1 235976677 235976677 single base substitution G A intron_variant MELA-AU 1 235976902 235976902 single base substitution C T intron_variant MELA-AU 1 235977435 235977435 single base substitution G A intron_variant MELA-AU 1 235977682 235977682 single base substitution C T intron_variant MELA-AU 1 235978087 235978088 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235978088 235978088 single base substitution G A intron_variant MELA-AU 1 235978089 235978089 single base substitution G A intron_variant MELA-AU 1 235978348 235978349 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 235978405 235978405 single base substitution C G intron_variant MELA-AU 1 235978998 235978998 single base substitution G A intron_variant MELA-AU 1 235979172 235979172 single base substitution C A intron_variant MELA-AU 1 235979229 235979229 single base substitution G A intron_variant MELA-AU 1 235979742 235979742 single base substitution A G intron_variant MELA-AU 1 235979771 235979771 single base substitution A T intron_variant MELA-AU 1 235980960 235980960 single base substitution A T intron_variant MELA-AU 1 235981387 235981387 single base substitution G A intron_variant MELA-AU 1 235981596 235981596 single base substitution G A intron_variant MELA-AU 1 235981661 235981661 single base substitution G A intron_variant MELA-AU 1 235981676 235981676 single base substitution G A intron_variant MELA-AU 1 235982077 235982077 single base substitution G A intron_variant MELA-AU 1 235982251 235982251 single base substitution G A intron_variant MELA-AU 1 235983131 235983131 single base substitution A G intron_variant MELA-AU 1 235983279 235983279 single base substitution G A intron_variant MELA-AU 1 235983280 235983280 single base substitution G A intron_variant MELA-AU 1 235983329 235983329 single base substitution C A intron_variant MELA-AU 1 235983481 235983481 single base substitution G A intron_variant MELA-AU 1 235983487 235983487 single base substitution G A intron_variant MELA-AU 1 235983771 235983771 single base substitution G A intron_variant MELA-AU 1 235984817 235984817 single base substitution T C intron_variant MELA-AU 1 235984862 235984862 single base substitution T G intron_variant MELA-AU 1 235984944 235984944 single base substitution A G intron_variant MELA-AU 1 235986050 235986050 single base substitution T A intron_variant MELA-AU 1 235987227 235987227 single base substitution C T downstream_gene_variant MELA-AU 1 235987227 235987227 single base substitution C T intron_variant MELA-AU 1 235988104 235988104 single base substitution G A downstream_gene_variant MELA-AU 1 235988104 235988104 single base substitution G A intron_variant MELA-AU 1 235988141 235988141 single base substitution G A downstream_gene_variant MELA-AU 1 235988141 235988141 single base substitution G A intron_variant MELA-AU 1 235989035 235989035 single base substitution T C downstream_gene_variant MELA-AU 1 235989035 235989035 single base substitution T C intron_variant MELA-AU 1 235989600 235989600 single base substitution G A downstream_gene_variant MELA-AU 1 235989600 235989600 single base substitution G A intron_variant MELA-AU 1 235989981 235989981 single base substitution G A downstream_gene_variant MELA-AU 1 235989981 235989981 single base substitution G A intron_variant MELA-AU 1 235990248 235990248 single base substitution A T downstream_gene_variant MELA-AU 1 235990248 235990248 single base substitution A T intron_variant MELA-AU 1 235990747 235990747 deletion of <=200bp A - downstream_gene_variant MELA-AU 1 235990747 235990747 deletion of <=200bp A - intron_variant MELA-AU 1 235991028 235991028 single base substitution G A downstream_gene_variant MELA-AU 1 235991028 235991028 single base substitution G A intron_variant MELA-AU 1 235991032 235991032 single base substitution G A downstream_gene_variant MELA-AU 1 235991032 235991032 single base substitution G A intron_variant MELA-AU 1 235991128 235991128 single base substitution G A downstream_gene_variant MELA-AU 1 235991128 235991128 single base substitution G A intron_variant MELA-AU 1 235991618 235991618 single base substitution G A downstream_gene_variant MELA-AU 1 235991618 235991618 single base substitution G A intron_variant MELA-AU 1 235993084 235993084 single base substitution C T exon_variant MELA-AU 1 235993084 235993084 single base substitution C T intron_variant MELA-AU 1 235993224 235993224 single base substitution G A exon_variant MELA-AU 1 235993224 235993224 single base substitution G A intron_variant MELA-AU 1 235993376 235993376 single base substitution A G exon_variant MELA-AU 1 235993376 235993376 single base substitution A G intron_variant MELA-AU 1 235993567 235993568 deletion of <=200bp CT - exon_variant MELA-AU 1 235993567 235993568 deletion of <=200bp CT - frameshift_variant RG50 MELA-AU 1 235994182 235994182 single base substitution G A intron_variant MELA-AU 1 235994188 235994188 single base substitution C T intron_variant MELA-AU 1 235994479 235994479 single base substitution T G intron_variant MELA-AU 1 235995423 235995423 single base substitution G A intron_variant MELA-AU 1 235995658 235995658 single base substitution G A intron_variant MELA-AU 1 235996065 235996065 single base substitution T A intron_variant MELA-AU 1 235996593 235996593 single base substitution G A intron_variant MELA-AU 1 235997369 235997370 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 1 235997461 235997461 single base substitution G A intron_variant MELA-AU 1 235997545 235997545 single base substitution G A intron_variant MELA-AU 1 235997685 235997685 single base substitution G A intron_variant MELA-AU 1 235998553 235998553 single base substitution G A intron_variant MELA-AU 1 236000008 236000008 single base substitution G A intron_variant MELA-AU 1 236000219 236000219 single base substitution G A intron_variant MELA-AU 1 236000858 236000858 single base substitution G A intron_variant MELA-AU 1 236001049 236001049 single base substitution G A intron_variant MELA-AU 1 236001420 236001420 single base substitution G A intron_variant MELA-AU 1 236002345 236002345 single base substitution G A intron_variant MELA-AU 1 236003122 236003122 single base substitution G A intron_variant MELA-AU 1 236003277 236003277 single base substitution G A intron_variant MELA-AU 1 236003777 236003777 single base substitution T C intron_variant MELA-AU 1 236004221 236004221 single base substitution G A intron_variant MELA-AU 1 236004566 236004566 single base substitution G A intron_variant MELA-AU 1 236004809 236004809 single base substitution G A intron_variant MELA-AU 1 236004954 236004954 single base substitution A G intron_variant MELA-AU 1 236005131 236005131 single base substitution A G intron_variant MELA-AU 1 236005421 236005421 single base substitution G A intron_variant MELA-AU 1 236005461 236005462 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 236005677 236005678 deletion of <=200bp CA - intron_variant MELA-AU 1 236006095 236006095 single base substitution G A intron_variant MELA-AU 1 236006491 236006491 single base substitution G A intron_variant MELA-AU 1 236007060 236007060 single base substitution G A intron_variant MELA-AU 1 236007454 236007454 single base substitution C T intron_variant MELA-AU 1 236008478 236008478 single base substitution G A intron_variant MELA-AU 1 236008519 236008520 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 1 236009411 236009411 single base substitution G A intron_variant MELA-AU 1 236009653 236009653 single base substitution G A intron_variant MELA-AU 1 236009925 236009925 single base substitution G A intron_variant MELA-AU 1 236009941 236009942 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 236010069 236010069 single base substitution G A intron_variant MELA-AU 1 236010136 236010136 single base substitution G A intron_variant MELA-AU 1 236010997 236010997 single base substitution G A intron_variant MELA-AU 1 236011399 236011399 single base substitution G A intron_variant MELA-AU 1 236011400 236011400 single base substitution G A intron_variant MELA-AU 1 236011854 236011854 single base substitution A G intron_variant MELA-AU 1 236012177 236012177 single base substitution A T intron_variant MELA-AU 1 236012348 236012348 single base substitution G A intron_variant MELA-AU 1 236012722 236012722 single base substitution G A intron_variant MELA-AU 1 236013920 236013920 single base substitution A G intron_variant MELA-AU 1 236014145 236014145 single base substitution G A intron_variant MELA-AU 1 236014221 236014221 single base substitution C G intron_variant MELA-AU 1 236014488 236014488 single base substitution G A intron_variant MELA-AU 1 236014684 236014684 single base substitution G A intron_variant MELA-AU 1 236014724 236014724 single base substitution G A intron_variant MELA-AU 1 236015125 236015126 multiple base substitution (>=2bp and <=200bp) GA TT intron_variant MELA-AU 1 236016754 236016754 single base substitution G A intron_variant MELA-AU 1 236016958 236016958 single base substitution A G intron_variant MELA-AU 1 236017675 236017675 single base substitution T G intron_variant MELA-AU 1 236019516 236019516 single base substitution G A intron_variant MELA-AU 1 236020059 236020059 single base substitution C T intron_variant MELA-AU 1 236020093 236020093 single base substitution G A intron_variant MELA-AU 1 236020253 236020253 single base substitution T G intron_variant MELA-AU 1 236021207 236021207 single base substitution G A intron_variant MELA-AU 1 236021365 236021365 single base substitution T A intron_variant MELA-AU 1 236022100 236022100 single base substitution G A intron_variant MELA-AU 1 236022732 236022732 single base substitution G A intron_variant MELA-AU 1 236022799 236022799 single base substitution G A intron_variant MELA-AU 1 236024119 236024119 single base substitution G A intron_variant MELA-AU 1 236024142 236024142 single base substitution C T intron_variant MELA-AU 1 236025815 236025815 single base substitution G A intron_variant MELA-AU 1 236025816 236025817 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 236025859 236025859 single base substitution G A intron_variant MELA-AU 1 236027682 236027682 single base substitution T G intron_variant MELA-AU 1 236027710 236027710 single base substitution T A intron_variant MELA-AU 1 236028106 236028106 single base substitution G A intron_variant MELA-AU 1 236029153 236029153 single base substitution G A intron_variant MELA-AU 1 236030286 236030286 single base substitution C T intron_variant MELA-AU 1 236030286 236030286 single base substitution C T upstream_gene_variant MELA-AU 1 236030338 236030338 single base substitution C T intron_variant MELA-AU 1 236030338 236030338 single base substitution C T upstream_gene_variant MELA-AU 1 236030418 236030418 single base substitution G A intron_variant MELA-AU 1 236030418 236030418 single base substitution G A upstream_gene_variant MELA-AU 1 236031329 236031329 single base substitution G A intron_variant MELA-AU 1 236031329 236031329 single base substitution G A upstream_gene_variant MELA-AU 1 236031782 236031782 single base substitution G A intron_variant MELA-AU 1 236031782 236031782 single base substitution G A upstream_gene_variant MELA-AU 1 236032015 236032018 deletion of <=200bp AGAT - intron_variant MELA-AU 1 236032015 236032018 deletion of <=200bp AGAT - upstream_gene_variant MELA-AU 1 236032748 236032748 single base substitution G A intron_variant MELA-AU 1 236032748 236032748 single base substitution G A upstream_gene_variant MELA-AU 1 236033776 236033776 single base substitution G A intron_variant MELA-AU 1 236033776 236033776 single base substitution G A upstream_gene_variant MELA-AU 1 236034245 236034245 single base substitution G A intron_variant MELA-AU 1 236034245 236034245 single base substitution G A upstream_gene_variant MELA-AU 1 236034669 236034669 single base substitution G A intron_variant MELA-AU 1 236034669 236034669 single base substitution G A upstream_gene_variant MELA-AU 1 236035388 236035388 single base substitution G A intron_variant MELA-AU 1 236035895 236035895 single base substitution G A intron_variant MELA-AU 1 236036313 236036313 single base substitution G A intron_variant MELA-AU 1 236036470 236036470 single base substitution G A intron_variant MELA-AU 1 236036653 236036653 single base substitution A C intron_variant MELA-AU 1 236037009 236037009 single base substitution C T intron_variant MELA-AU 1 236037845 236037845 single base substitution C T intron_variant MELA-AU 1 236037897 236037897 single base substitution T G intron_variant MELA-AU 1 236038306 236038306 single base substitution T A intron_variant MELA-AU 1 236038728 236038728 single base substitution G A intron_variant MELA-AU 1 236038970 236038970 single base substitution A T intron_variant MELA-AU 1 236039758 236039758 single base substitution A G intron_variant MELA-AU 1 236039825 236039825 single base substitution G A intron_variant MELA-AU 1 236041000 236041000 single base substitution C T intron_variant MELA-AU 1 236041130 236041130 single base substitution G A intron_variant MELA-AU 1 236042686 236042686 single base substitution A T intron_variant MELA-AU 1 236042820 236042820 single base substitution G A intron_variant MELA-AU 1 236043367 236043367 single base substitution G A intron_variant MELA-AU 1 236044604 236044604 single base substitution G A intron_variant MELA-AU 1 236044639 236044639 single base substitution A G intron_variant MELA-AU 1 236045471 236045471 single base substitution G A intron_variant MELA-AU 1 236045882 236045882 single base substitution C T intron_variant MELA-AU 1 236046279 236046279 single base substitution T C intron_variant MELA-AU 1 236048048 236048048 single base substitution T C upstream_gene_variant MELA-AU 1 236048318 236048318 single base substitution C T upstream_gene_variant MELA-AU 1 236048566 236048566 single base substitution C T upstream_gene_variant MELA-AU 1 236049254 236049254 single base substitution C T upstream_gene_variant MELA-AU 1 236050029 236050029 single base substitution C T upstream_gene_variant MELA-AU 1 236051230 236051230 single base substitution G A upstream_gene_variant MELA-AU 1 236051925 236051925 single base substitution C T upstream_gene_variant ORCA-IN 1 235826154 235826154 single base substitution T C 3_prime_UTR_variant ORCA-IN 1 235826154 235826154 single base substitution T C exon_variant ORCA-IN 1 235829522 235829531 deletion of <=200bp ACATACACAC - intron_variant ORCA-IN 1 235944223 235944223 single base substitution C A 3_prime_UTR_variant ORCA-IN 1 235944223 235944223 single base substitution C A exon_variant ORCA-IN 1 235944223 235944223 single base substitution C A missense_variant C1719F 5156G>T ORCA-IN 1 235950531 235950531 single base substitution C A 3_prime_UTR_variant ORCA-IN 1 235950531 235950531 single base substitution C A downstream_gene_variant ORCA-IN 1 235950531 235950531 single base substitution C A exon_variant ORCA-IN 1 235950531 235950531 single base substitution C A missense_variant G1611W 4831G>T ORCA-IN 1 235952521 235952521 single base substitution A T downstream_gene_variant ORCA-IN 1 235952521 235952521 single base substitution A T intron_variant ORCA-IN 1 235952521 235952521 single base substitution A T upstream_gene_variant ORCA-IN 1 235954766 235954766 single base substitution T A downstream_gene_variant ORCA-IN 1 235954766 235954766 single base substitution T A intron_variant ORCA-IN 1 235954766 235954766 single base substitution T A upstream_gene_variant ORCA-IN 1 235960593 235960593 single base substitution G C intron_variant ORCA-IN 1 235973697 235973697 single base substitution G A exon_variant ORCA-IN 1 235973697 235973697 single base substitution G A stop_gained R141* 421C>T ORCA-IN 1 236014708 236014708 single base substitution G A intron_variant ORCA-IN 1 236024580 236024580 single base substitution G C intron_variant ORCA-IN 1 236024798 236024798 single base substitution G C intron_variant ORCA-IN 1 236032433 236032433 single base substitution A T intron_variant ORCA-IN 1 236032433 236032433 single base substitution A T upstream_gene_variant ORCA-IN 1 236041842 236041842 single base substitution G C intron_variant ORCA-IN 1 236050727 236050727 single base substitution G C upstream_gene_variant OV-AU 1 235822043 235822043 single base substitution T A downstream_gene_variant OV-AU 1 235827160 235827160 single base substitution G T intron_variant OV-AU 1 235827373 235827373 single base substitution C G intron_variant OV-AU 1 235828933 235828933 single base substitution T C intron_variant OV-AU 1 235833424 235833424 single base substitution G C intron_variant OV-AU 1 235845657 235845657 single base substitution C A intron_variant OV-AU 1 235848886 235848886 single base substitution C T intron_variant OV-AU 1 235852695 235852695 single base substitution C A intron_variant OV-AU 1 235861097 235861097 single base substitution T G intron_variant OV-AU 1 235868410 235868410 single base substitution G C downstream_gene_variant OV-AU 1 235868410 235868410 single base substitution G C intron_variant OV-AU 1 235870096 235870096 single base substitution T A downstream_gene_variant OV-AU 1 235870096 235870096 single base substitution T A intron_variant OV-AU 1 235877759 235877759 single base substitution G C intron_variant OV-AU 1 235877759 235877759 single base substitution G C upstream_gene_variant OV-AU 1 235880146 235880146 single base substitution C G intron_variant OV-AU 1 235880146 235880146 single base substitution C G upstream_gene_variant OV-AU 1 235882763 235882763 single base substitution A T intron_variant OV-AU 1 235884275 235884275 single base substitution C T intron_variant OV-AU 1 235888816 235888816 single base substitution A C intron_variant OV-AU 1 235898102 235898102 single base substitution T C downstream_gene_variant OV-AU 1 235898102 235898102 single base substitution T C exon_variant OV-AU 1 235898102 235898102 single base substitution T C intron_variant OV-AU 1 235906195 235906195 single base substitution C T downstream_gene_variant OV-AU 1 235906195 235906195 single base substitution C T intron_variant OV-AU 1 235906195 235906195 single base substitution C T upstream_gene_variant OV-AU 1 235907844 235907844 single base substitution C T downstream_gene_variant OV-AU 1 235907844 235907844 single base substitution C T intron_variant OV-AU 1 235907844 235907844 single base substitution C T upstream_gene_variant OV-AU 1 235914601 235914601 single base substitution G T synonymous_variant T2563T 7689C>A OV-AU 1 235914601 235914601 single base substitution G T synonymous_variant T76T 228C>A OV-AU 1 235915513 235915513 single base substitution A G intron_variant OV-AU 1 235915513 235915513 single base substitution A G upstream_gene_variant OV-AU 1 235916567 235916567 single base substitution G A synonymous_variant L2413L 7237C>T OV-AU 1 235916567 235916567 single base substitution G A upstream_gene_variant OV-AU 1 235930604 235930604 single base substitution T A intron_variant OV-AU 1 235930697 235930697 single base substitution C G intron_variant OV-AU 1 235932428 235932428 single base substitution A G intron_variant OV-AU 1 235933582 235933582 single base substitution T C 3_prime_UTR_variant OV-AU 1 235933582 235933582 single base substitution T C exon_variant OV-AU 1 235933582 235933582 single base substitution T C missense_variant T1934A 5800A>G OV-AU 1 235933936 235933936 single base substitution T C intron_variant OV-AU 1 235933987 235933987 single base substitution C A intron_variant OV-AU 1 235948656 235948656 single base substitution A T downstream_gene_variant OV-AU 1 235948656 235948656 single base substitution A T intron_variant OV-AU 1 235951932 235951932 single base substitution C A downstream_gene_variant OV-AU 1 235951932 235951932 single base substitution C A intron_variant OV-AU 1 235956964 235956964 single base substitution T C intron_variant OV-AU 1 235956964 235956964 single base substitution T C upstream_gene_variant OV-AU 1 235958645 235958645 single base substitution T C intron_variant OV-AU 1 235959629 235959629 single base substitution C A intron_variant OV-AU 1 235966093 235966093 single base substitution C T intron_variant OV-AU 1 235967698 235967698 single base substitution C T intron_variant OV-AU 1 235968601 235968601 single base substitution A G intron_variant OV-AU 1 235969600 235969600 single base substitution G T exon_variant OV-AU 1 235969600 235969600 single base substitution G T missense_variant L946I 2836C>A OV-AU 1 235970186 235970186 single base substitution C G intron_variant OV-AU 1 235979290 235979290 single base substitution C T intron_variant OV-AU 1 235980641 235980641 single base substitution A G intron_variant OV-AU 1 235986789 235986789 single base substitution C G intron_variant OV-AU 1 235987684 235987684 single base substitution C T downstream_gene_variant OV-AU 1 235987684 235987684 single base substitution C T intron_variant OV-AU 1 235990268 235990268 single base substitution G T downstream_gene_variant OV-AU 1 235990268 235990268 single base substitution G T intron_variant OV-AU 1 235991302 235991302 single base substitution C A downstream_gene_variant OV-AU 1 235991302 235991302 single base substitution C A intron_variant OV-AU 1 235996486 235996486 single base substitution C A intron_variant OV-AU 1 235999437 235999437 single base substitution A G intron_variant OV-AU 1 236005467 236005467 single base substitution G A intron_variant OV-AU 1 236005574 236005574 single base substitution C A intron_variant OV-AU 1 236008396 236008396 single base substitution C T intron_variant OV-AU 1 236012949 236012949 single base substitution G C intron_variant OV-AU 1 236020105 236020105 single base substitution G T intron_variant OV-AU 1 236021254 236021254 single base substitution A T intron_variant OV-AU 1 236023093 236023093 single base substitution G C intron_variant OV-AU 1 236034725 236034725 single base substitution C T intron_variant OV-AU 1 236034725 236034725 single base substitution C T upstream_gene_variant OV-AU 1 236038332 236038332 single base substitution A G intron_variant OV-AU 1 236043227 236043227 single base substitution G A intron_variant OV-AU 1 236048503 236048503 single base substitution T C upstream_gene_variant OV-AU 1 236048703 236048703 single base substitution C T upstream_gene_variant OV-AU 1 236048833 236048833 single base substitution A T upstream_gene_variant OV-US 1 235897870 235897870 single base substitution C T downstream_gene_variant OV-US 1 235897870 235897870 single base substitution C T exon_variant OV-US 1 235897870 235897870 single base substitution C T synonymous_variant L2816L 8448G>A OV-US 1 235966296 235966296 single base substitution C A exon_variant OV-US 1 235966296 235966296 single base substitution C A missense_variant Q1208H 3624G>T OV-US 1 235969927 235969927 single base substitution G A exon_variant OV-US 1 235969927 235969927 single base substitution G A missense_variant P837S 2509C>T PACA-AU 1 235820746 235820746 single base substitution C T downstream_gene_variant PACA-AU 1 235823150 235823150 single base substitution C A downstream_gene_variant PACA-AU 1 235824714 235824714 single base substitution G A 3_prime_UTR_variant PACA-AU 1 235824714 235824714 single base substitution G A exon_variant PACA-AU 1 235825114 235825114 single base substitution T C 3_prime_UTR_variant PACA-AU 1 235825114 235825114 single base substitution T C exon_variant PACA-AU 1 235825763 235825763 single base substitution A C 3_prime_UTR_variant PACA-AU 1 235825763 235825763 single base substitution A C exon_variant PACA-AU 1 235825878 235825878 single base substitution C T 3_prime_UTR_variant PACA-AU 1 235825878 235825878 single base substitution C T exon_variant PACA-AU 1 235840669 235840669 single base substitution C T intron_variant PACA-AU 1 235842589 235842595 deletion of <=200bp TGGGATA - intron_variant PACA-AU 1 235846801 235846801 single base substitution C T intron_variant PACA-AU 1 235853658 235853658 single base substitution T C intron_variant PACA-AU 1 235854500 235854500 single base substitution G C intron_variant PACA-AU 1 235860648 235860648 single base substitution A C intron_variant PACA-AU 1 235862996 235862996 single base substitution C T intron_variant PACA-AU 1 235865389 235865389 insertion of <=200bp - C intron_variant PACA-AU 1 235865789 235865789 single base substitution T A intron_variant PACA-AU 1 235868691 235868691 single base substitution T A downstream_gene_variant PACA-AU 1 235868691 235868691 single base substitution T A intron_variant PACA-AU 1 235869551 235869551 single base substitution G A downstream_gene_variant PACA-AU 1 235869551 235869551 single base substitution G A intron_variant PACA-AU 1 235872728 235872728 single base substitution T C downstream_gene_variant PACA-AU 1 235872728 235872728 single base substitution T C intron_variant PACA-AU 1 235876436 235876436 single base substitution T C exon_variant PACA-AU 1 235876436 235876436 single base substitution T C intron_variant PACA-AU 1 235876436 235876436 single base substitution T C upstream_gene_variant PACA-AU 1 235876648 235876648 single base substitution T A intron_variant PACA-AU 1 235876648 235876648 single base substitution T A upstream_gene_variant PACA-AU 1 235888721 235888721 single base substitution G A intron_variant PACA-AU 1 235891449 235891482 deletion of <=200bp ATATAAGGGTTTTAAAATGTATGTGCACACTACC - intron_variant PACA-AU 1 235891449 235891482 deletion of <=200bp ATATAAGGGTTTTAAAATGTATGTGCACACTACC - upstream_gene_variant PACA-AU 1 235893042 235893042 single base substitution T C intron_variant PACA-AU 1 235893042 235893042 single base substitution T C upstream_gene_variant PACA-AU 1 235893214 235893215 deletion of <=200bp AA - intron_variant PACA-AU 1 235893214 235893215 deletion of <=200bp AA - upstream_gene_variant PACA-AU 1 235894091 235894091 single base substitution T C intron_variant PACA-AU 1 235894091 235894091 single base substitution T C upstream_gene_variant PACA-AU 1 235894735 235894735 single base substitution A T intron_variant PACA-AU 1 235894735 235894735 single base substitution A T upstream_gene_variant PACA-AU 1 235897710 235897710 deletion of <=200bp A - downstream_gene_variant PACA-AU 1 235897710 235897710 deletion of <=200bp A - intron_variant PACA-AU 1 235900322 235900322 insertion of <=200bp - A downstream_gene_variant PACA-AU 1 235900322 235900322 insertion of <=200bp - A exon_variant PACA-AU 1 235900322 235900322 insertion of <=200bp - A intron_variant PACA-AU 1 235900739 235900739 single base substitution C A downstream_gene_variant PACA-AU 1 235900739 235900739 single base substitution C A exon_variant PACA-AU 1 235900739 235900739 single base substitution C A intron_variant PACA-AU 1 235903616 235903616 single base substitution G C intron_variant PACA-AU 1 235903616 235903616 single base substitution G C upstream_gene_variant PACA-AU 1 235905944 235905944 insertion of <=200bp - A downstream_gene_variant PACA-AU 1 235905944 235905944 insertion of <=200bp - A intron_variant PACA-AU 1 235905944 235905944 insertion of <=200bp - A upstream_gene_variant PACA-AU 1 235909137 235909137 single base substitution A C downstream_gene_variant PACA-AU 1 235909137 235909137 single base substitution A C intron_variant PACA-AU 1 235909137 235909137 single base substitution A C upstream_gene_variant PACA-AU 1 235914600 235914600 single base substitution C T missense_variant A2564T 7690G>A PACA-AU 1 235914600 235914600 single base substitution C T missense_variant A77T 229G>A PACA-AU 1 235918185 235918185 single base substitution G C downstream_gene_variant PACA-AU 1 235918185 235918185 single base substitution G C intron_variant PACA-AU 1 235918185 235918185 single base substitution G C upstream_gene_variant PACA-AU 1 235920771 235920771 single base substitution C A downstream_gene_variant PACA-AU 1 235920771 235920771 single base substitution C A intron_variant PACA-AU 1 235920772 235920772 single base substitution C A downstream_gene_variant PACA-AU 1 235920772 235920772 single base substitution C A intron_variant PACA-AU 1 235921892 235921892 single base substitution C T downstream_gene_variant PACA-AU 1 235921892 235921892 single base substitution C T intron_variant PACA-AU 1 235925339 235925339 single base substitution G A intron_variant PACA-AU 1 235929544 235929544 single base substitution G A 3_prime_UTR_variant PACA-AU 1 235929544 235929544 single base substitution G A exon_variant PACA-AU 1 235929544 235929544 single base substitution G A stop_gained R1986* 5956C>T PACA-AU 1 235930863 235930863 single base substitution C A intron_variant PACA-AU 1 235938344 235938344 single base substitution G C 3_prime_UTR_variant PACA-AU 1 235938344 235938344 single base substitution G C exon_variant PACA-AU 1 235938344 235938344 single base substitution G C missense_variant L1835V 5503C>G PACA-AU 1 235941544 235941544 single base substitution C T intron_variant PACA-AU 1 235950663 235950664 multiple base substitution (>=2bp and <=200bp) CC AT 3_prime_UTR_variant PACA-AU 1 235950663 235950664 multiple base substitution (>=2bp and <=200bp) CC AT downstream_gene_variant PACA-AU 1 235950663 235950664 multiple base substitution (>=2bp and <=200bp) CC AT exon_variant PACA-AU 1 235950663 235950664 multiple base substitution (>=2bp and <=200bp) CC AT missense_variant MD1566IY PACA-AU 1 235952567 235952567 single base substitution A T downstream_gene_variant PACA-AU 1 235952567 235952567 single base substitution A T intron_variant PACA-AU 1 235952567 235952567 single base substitution A T upstream_gene_variant PACA-AU 1 235954342 235954342 single base substitution G A downstream_gene_variant PACA-AU 1 235954342 235954342 single base substitution G A intron_variant PACA-AU 1 235954342 235954342 single base substitution G A upstream_gene_variant PACA-AU 1 235956907 235956907 single base substitution G T exon_variant PACA-AU 1 235956907 235956907 single base substitution G T missense_variant Q1338K 4012C>A PACA-AU 1 235956907 235956907 single base substitution G T upstream_gene_variant PACA-AU 1 235958572 235958572 single base substitution G T intron_variant PACA-AU 1 235967703 235967703 single base substitution C T intron_variant PACA-AU 1 235968627 235968627 single base substitution C A intron_variant PACA-AU 1 235968853 235968853 single base substitution A G intron_variant PACA-AU 1 235968982 235968982 single base substitution G A intron_variant PACA-AU 1 235970693 235970694 deletion of <=200bp TT - intron_variant PACA-AU 1 235971053 235971053 single base substitution T C intron_variant PACA-AU 1 235973433 235973433 single base substitution G A exon_variant PACA-AU 1 235973433 235973433 single base substitution G A missense_variant P229S 685C>T PACA-AU 1 235977361 235977361 single base substitution A C intron_variant PACA-AU 1 235982455 235982455 single base substitution C T intron_variant PACA-AU 1 235983238 235983238 single base substitution G A intron_variant PACA-AU 1 235989242 235989242 single base substitution C T downstream_gene_variant PACA-AU 1 235989242 235989242 single base substitution C T intron_variant PACA-AU 1 236001659 236001659 insertion of <=200bp - GT intron_variant PACA-AU 1 236016709 236016709 single base substitution G T intron_variant PACA-AU 1 236016730 236016730 deletion of <=200bp T - intron_variant PACA-AU 1 236016760 236016760 single base substitution T G intron_variant PACA-AU 1 236020535 236020535 single base substitution C T intron_variant PACA-AU 1 236021403 236021403 single base substitution A C intron_variant PACA-AU 1 236035130 236035130 single base substitution C T intron_variant PACA-AU 1 236035130 236035130 single base substitution C T upstream_gene_variant PACA-AU 1 236038920 236038920 single base substitution C T intron_variant PACA-AU 1 236039129 236039129 single base substitution G A intron_variant PACA-AU 1 236044959 236044959 insertion of <=200bp - AT intron_variant PACA-AU 1 236050583 236050583 single base substitution G A upstream_gene_variant PACA-AU 1 236050593 236050593 single base substitution G C upstream_gene_variant PACA-AU 1 236050633 236050633 single base substitution G A upstream_gene_variant PACA-AU 1 236051005 236051005 single base substitution G T upstream_gene_variant PACA-AU 1 236051563 236051564 deletion of <=200bp AG - upstream_gene_variant PACA-CA 1 235821056 235821056 single base substitution A T downstream_gene_variant PACA-CA 1 235824583 235824583 single base substitution T A 3_prime_UTR_variant PACA-CA 1 235824583 235824583 single base substitution T A exon_variant PACA-CA 1 235827246 235827246 single base substitution A T intron_variant PACA-CA 1 235829907 235829907 single base substitution T C intron_variant PACA-CA 1 235829909 235829909 single base substitution C T intron_variant PACA-CA 1 235833643 235833643 single base substitution G A intron_variant PACA-CA 1 235843099 235843099 single base substitution C G intron_variant PACA-CA 1 235843114 235843114 single base substitution C G intron_variant PACA-CA 1 235848847 235848847 single base substitution A G intron_variant PACA-CA 1 235850186 235850186 single base substitution T C intron_variant PACA-CA 1 235851743 235851743 single base substitution G C intron_variant PACA-CA 1 235853603 235853603 single base substitution A G intron_variant PACA-CA 1 235854772 235854772 single base substitution G A intron_variant PACA-CA 1 235856115 235856115 single base substitution G C intron_variant PACA-CA 1 235857454 235857454 single base substitution C T intron_variant PACA-CA 1 235858349 235858349 single base substitution T C intron_variant PACA-CA 1 235866900 235866909 deletion of <=200bp TTTTCGTATA - intron_variant PACA-CA 1 235875537 235875537 single base substitution C A downstream_gene_variant PACA-CA 1 235875537 235875537 single base substitution C A exon_variant PACA-CA 1 235875537 235875537 single base substitution C A intron_variant PACA-CA 1 235876600 235876600 single base substitution G C intron_variant PACA-CA 1 235876600 235876600 single base substitution G C upstream_gene_variant PACA-CA 1 235878074 235878074 single base substitution T C intron_variant PACA-CA 1 235878074 235878074 single base substitution T C upstream_gene_variant PACA-CA 1 235878708 235878708 single base substitution C T intron_variant PACA-CA 1 235878708 235878708 single base substitution C T upstream_gene_variant PACA-CA 1 235882041 235882041 single base substitution T C intron_variant PACA-CA 1 235882330 235882330 deletion of <=200bp T - intron_variant PACA-CA 1 235884516 235884516 single base substitution G A intron_variant PACA-CA 1 235892125 235892125 single base substitution G A intron_variant PACA-CA 1 235892125 235892125 single base substitution G A upstream_gene_variant PACA-CA 1 235892126 235892126 single base substitution C G intron_variant PACA-CA 1 235892126 235892126 single base substitution C G upstream_gene_variant PACA-CA 1 235900838 235900838 single base substitution T C downstream_gene_variant PACA-CA 1 235900838 235900838 single base substitution T C exon_variant PACA-CA 1 235900838 235900838 single base substitution T C intron_variant PACA-CA 1 235906334 235906334 insertion of <=200bp - A downstream_gene_variant PACA-CA 1 235906334 235906334 insertion of <=200bp - A intron_variant PACA-CA 1 235908240 235908240 insertion of <=200bp - A downstream_gene_variant PACA-CA 1 235908240 235908240 insertion of <=200bp - A intron_variant PACA-CA 1 235908240 235908240 insertion of <=200bp - A upstream_gene_variant PACA-CA 1 235908302 235908302 single base substitution T C downstream_gene_variant PACA-CA 1 235908302 235908302 single base substitution T C intron_variant PACA-CA 1 235908302 235908302 single base substitution T C upstream_gene_variant PACA-CA 1 235910101 235910101 deletion of <=200bp A - intron_variant PACA-CA 1 235910101 235910101 deletion of <=200bp A - upstream_gene_variant PACA-CA 1 235912734 235912734 insertion of <=200bp - AG intron_variant PACA-CA 1 235912979 235912979 single base substitution G T intron_variant PACA-CA 1 235913079 235913079 single base substitution C A intron_variant PACA-CA 1 235917846 235917846 single base substitution C A downstream_gene_variant PACA-CA 1 235917846 235917846 single base substitution C A intron_variant PACA-CA 1 235917846 235917846 single base substitution C A upstream_gene_variant PACA-CA 1 235918290 235918290 single base substitution C T downstream_gene_variant PACA-CA 1 235918290 235918290 single base substitution C T intron_variant PACA-CA 1 235918290 235918290 single base substitution C T upstream_gene_variant PACA-CA 1 235919674 235919674 single base substitution T C downstream_gene_variant PACA-CA 1 235919674 235919674 single base substitution T C intron_variant PACA-CA 1 235919674 235919674 single base substitution T C upstream_gene_variant PACA-CA 1 235920491 235920491 single base substitution G T downstream_gene_variant PACA-CA 1 235920491 235920491 single base substitution G T intron_variant PACA-CA 1 235920979 235920979 single base substitution T C downstream_gene_variant PACA-CA 1 235920979 235920979 single base substitution T C intron_variant PACA-CA 1 235924404 235924404 single base substitution T A intron_variant PACA-CA 1 235925535 235925535 single base substitution G C intron_variant PACA-CA 1 235926927 235926927 single base substitution C T intron_variant PACA-CA 1 235933398 235933398 single base substitution T C intron_variant PACA-CA 1 235933646 235933646 single base substitution G A intron_variant PACA-CA 1 235936871 235936871 single base substitution C A intron_variant PACA-CA 1 235946953 235946953 single base substitution T C downstream_gene_variant PACA-CA 1 235946953 235946953 single base substitution T C intron_variant PACA-CA 1 235948604 235948604 single base substitution A T downstream_gene_variant PACA-CA 1 235948604 235948604 single base substitution A T intron_variant PACA-CA 1 235948985 235948985 single base substitution C G downstream_gene_variant PACA-CA 1 235948985 235948985 single base substitution C G intron_variant PACA-CA 1 235954347 235954347 single base substitution G A downstream_gene_variant PACA-CA 1 235954347 235954347 single base substitution G A intron_variant PACA-CA 1 235954347 235954347 single base substitution G A upstream_gene_variant PACA-CA 1 235958408 235958408 single base substitution G A intron_variant PACA-CA 1 235958636 235958636 single base substitution G A intron_variant PACA-CA 1 235960516 235960557 deletion of <=200bp GTCCATCAACTGATGAATGGATAAATCAAATGCAGTATATCC - intron_variant PACA-CA 1 235963698 235963698 single base substitution A C intron_variant PACA-CA 1 235964433 235964433 single base substitution C G intron_variant PACA-CA 1 235964716 235964716 deletion of <=200bp C - intron_variant PACA-CA 1 235968980 235968980 single base substitution A G intron_variant PACA-CA 1 235971139 235971139 single base substitution A G intron_variant PACA-CA 1 235976960 235976960 single base substitution A G intron_variant PACA-CA 1 235976999 235976999 single base substitution A G intron_variant PACA-CA 1 235978266 235978266 single base substitution A G intron_variant PACA-CA 1 235985246 235985246 single base substitution G T intron_variant PACA-CA 1 235988828 235988828 single base substitution A G downstream_gene_variant PACA-CA 1 235988828 235988828 single base substitution A G intron_variant PACA-CA 1 235992322 235992322 single base substitution G A downstream_gene_variant PACA-CA 1 235992322 235992322 single base substitution G A exon_variant PACA-CA 1 235992322 235992322 single base substitution G A intron_variant PACA-CA 1 235994182 235994182 single base substitution G T intron_variant PACA-CA 1 235996187 235996187 single base substitution T C intron_variant PACA-CA 1 235996538 235996538 single base substitution A G intron_variant PACA-CA 1 236001754 236001754 single base substitution A G intron_variant PACA-CA 1 236003180 236003180 single base substitution A G intron_variant PACA-CA 1 236005934 236005934 single base substitution T G intron_variant PACA-CA 1 236007067 236007067 single base substitution C A intron_variant PACA-CA 1 236007406 236007406 single base substitution A T intron_variant PACA-CA 1 236007692 236007692 single base substitution A G intron_variant PACA-CA 1 236008079 236008079 single base substitution G A intron_variant PACA-CA 1 236011189 236011189 single base substitution A G intron_variant PACA-CA 1 236014714 236014714 deletion of <=200bp G - intron_variant PACA-CA 1 236015887 236015887 single base substitution A G intron_variant PACA-CA 1 236019927 236019950 deletion of <=200bp GTTTTTTAAAAAATAAGGTGAAGA - intron_variant PACA-CA 1 236020603 236020603 single base substitution T A intron_variant PACA-CA 1 236031362 236031362 single base substitution C A intron_variant PACA-CA 1 236031362 236031362 single base substitution C A upstream_gene_variant PACA-CA 1 236032629 236032629 single base substitution G A intron_variant PACA-CA 1 236032629 236032629 single base substitution G A upstream_gene_variant PACA-CA 1 236035545 236035545 single base substitution A T intron_variant PACA-CA 1 236037193 236037193 single base substitution G A intron_variant PACA-CA 1 236037401 236037401 single base substitution G A intron_variant PACA-CA 1 236037440 236037440 single base substitution G C intron_variant PACA-CA 1 236038511 236038511 single base substitution C G intron_variant PACA-CA 1 236039938 236039938 single base substitution A T intron_variant PACA-CA 1 236042216 236042216 single base substitution A C intron_variant PACA-CA 1 236044821 236044821 single base substitution C G intron_variant PACA-CA 1 236050279 236050279 single base substitution C T upstream_gene_variant PACA-CA 1 236050369 236050369 single base substitution G A upstream_gene_variant PAEN-AU 1 235890051 235890051 single base substitution T C intron_variant PAEN-AU 1 235918737 235918737 single base substitution C A downstream_gene_variant PAEN-AU 1 235918737 235918737 single base substitution C A intron_variant PAEN-AU 1 235918737 235918737 single base substitution C A upstream_gene_variant PAEN-AU 1 235958199 235958199 single base substitution T C intron_variant PAEN-AU 1 235975516 235975516 single base substitution C T intron_variant PAEN-AU 1 236032492 236032492 single base substitution G A intron_variant PAEN-AU 1 236032492 236032492 single base substitution G A upstream_gene_variant PAEN-IT 1 235852992 235852992 single base substitution G A intron_variant PAEN-IT 1 235961833 235961833 single base substitution G A intron_variant PAEN-IT 1 236005556 236005556 single base substitution G A intron_variant PAEN-IT 1 236006417 236006417 single base substitution A C intron_variant PAEN-IT 1 236036365 236036365 single base substitution G A intron_variant PBCA-DE 1 235828210 235828210 single base substitution C A intron_variant PBCA-DE 1 235842224 235842225 deletion of <=200bp TC - intron_variant PBCA-DE 1 235843285 235843286 deletion of <=200bp CT - intron_variant PBCA-DE 1 235857477 235857477 insertion of <=200bp - T intron_variant PBCA-DE 1 235870758 235870758 insertion of <=200bp - T downstream_gene_variant PBCA-DE 1 235870758 235870758 insertion of <=200bp - T intron_variant PBCA-DE 1 235870762 235870762 insertion of <=200bp - T downstream_gene_variant PBCA-DE 1 235870762 235870762 insertion of <=200bp - T intron_variant PBCA-DE 1 235883304 235883304 deletion of <=200bp T - intron_variant PBCA-DE 1 235903183 235903183 single base substitution G A intron_variant PBCA-DE 1 235903183 235903183 single base substitution G A upstream_gene_variant PBCA-DE 1 235915720 235915720 single base substitution T C intron_variant PBCA-DE 1 235915720 235915720 single base substitution T C upstream_gene_variant PBCA-DE 1 235919357 235919357 single base substitution A G downstream_gene_variant PBCA-DE 1 235919357 235919357 single base substitution A G intron_variant PBCA-DE 1 235919357 235919357 single base substitution A G upstream_gene_variant PBCA-DE 1 235919363 235919363 single base substitution G A downstream_gene_variant PBCA-DE 1 235919363 235919363 single base substitution G A intron_variant PBCA-DE 1 235919363 235919363 single base substitution G A upstream_gene_variant PBCA-DE 1 235922371 235922371 single base substitution C T downstream_gene_variant PBCA-DE 1 235922371 235922371 single base substitution C T missense_variant R2261H 6782G>A PBCA-DE 1 235925076 235925076 insertion of <=200bp - A intron_variant PBCA-DE 1 235929764 235929764 single base substitution T C intron_variant PBCA-DE 1 235941399 235941400 deletion of <=200bp AT - intron_variant PBCA-DE 1 235956588 235956588 single base substitution C T intron_variant PBCA-DE 1 235956588 235956588 single base substitution C T upstream_gene_variant PBCA-DE 1 235964686 235964686 insertion of <=200bp - A intron_variant PBCA-DE 1 235993964 235993964 single base substitution G T intron_variant PBCA-DE 1 235998219 235998219 single base substitution A G intron_variant PBCA-DE 1 236002549 236002550 deletion of <=200bp AT - intron_variant PBCA-DE 1 236003860 236003860 single base substitution C T intron_variant PBCA-DE 1 236007985 236007985 single base substitution C G intron_variant PBCA-DE 1 236012676 236012676 single base substitution A G intron_variant PBCA-DE 1 236018207 236018207 single base substitution T C intron_variant PBCA-DE 1 236027067 236027067 single base substitution C T intron_variant PBCA-DE 1 236030045 236030045 single base substitution A T intron_variant PBCA-DE 1 236031001 236031001 single base substitution G A intron_variant PBCA-DE 1 236031001 236031001 single base substitution G A upstream_gene_variant PBCA-DE 1 236039663 236039663 insertion of <=200bp - A intron_variant PBCA-DE 1 236050247 236050247 single base substitution C A upstream_gene_variant PRAD-CA 1 235829907 235829907 single base substitution T C intron_variant PRAD-CA 1 235850724 235850724 single base substitution C T intron_variant PRAD-CA 1 235852326 235852326 single base substitution T C intron_variant PRAD-CA 1 235887221 235887221 single base substitution G A intron_variant PRAD-CA 1 235897565 235897565 single base substitution G A downstream_gene_variant PRAD-CA 1 235897565 235897565 single base substitution G A intron_variant PRAD-CA 1 235908204 235908204 single base substitution G A downstream_gene_variant PRAD-CA 1 235908204 235908204 single base substitution G A intron_variant PRAD-CA 1 235908204 235908204 single base substitution G A upstream_gene_variant PRAD-CA 1 235908205 235908205 single base substitution A G downstream_gene_variant PRAD-CA 1 235908205 235908205 single base substitution A G intron_variant PRAD-CA 1 235908205 235908205 single base substitution A G upstream_gene_variant PRAD-CA 1 235908206 235908206 single base substitution A G downstream_gene_variant PRAD-CA 1 235908206 235908206 single base substitution A G intron_variant PRAD-CA 1 235908206 235908206 single base substitution A G upstream_gene_variant PRAD-CA 1 235917245 235917245 single base substitution C T intron_variant PRAD-CA 1 235917245 235917245 single base substitution C T upstream_gene_variant PRAD-CA 1 235919357 235919357 single base substitution A G downstream_gene_variant PRAD-CA 1 235919357 235919357 single base substitution A G intron_variant PRAD-CA 1 235919357 235919357 single base substitution A G upstream_gene_variant PRAD-CA 1 235977947 235977947 single base substitution C T intron_variant PRAD-CA 1 236032409 236032409 single base substitution G T intron_variant PRAD-CA 1 236032409 236032409 single base substitution G T upstream_gene_variant PRAD-CA 1 236034509 236034509 single base substitution C A intron_variant PRAD-CA 1 236034509 236034509 single base substitution C A upstream_gene_variant PRAD-CA 1 236035167 236035167 single base substitution G A intron_variant PRAD-CA 1 236035167 236035167 single base substitution G A upstream_gene_variant PRAD-CA 1 236051634 236051634 single base substitution C T upstream_gene_variant PRAD-UK 1 235821230 235821230 single base substitution A G downstream_gene_variant PRAD-UK 1 235833987 235833987 single base substitution G A intron_variant PRAD-UK 1 235839158 235839158 single base substitution C A intron_variant PRAD-UK 1 235868691 235868691 single base substitution T A downstream_gene_variant PRAD-UK 1 235868691 235868691 single base substitution T A intron_variant PRAD-UK 1 235889211 235889211 single base substitution T C intron_variant PRAD-UK 1 235891143 235891143 single base substitution T C intron_variant PRAD-UK 1 235906757 235906757 single base substitution T A downstream_gene_variant PRAD-UK 1 235906757 235906757 single base substitution T A intron_variant PRAD-UK 1 235922805 235922805 single base substitution C T 3_prime_UTR_variant PRAD-UK 1 235922805 235922805 single base substitution C T exon_variant PRAD-UK 1 235922805 235922805 single base substitution C T synonymous_variant T2116T 6348G>A PRAD-UK 1 235924403 235924403 single base substitution A T intron_variant PRAD-UK 1 235929663 235929663 single base substitution A G intron_variant PRAD-UK 1 235932503 235932503 single base substitution T A intron_variant PRAD-UK 1 235941147 235941147 deletion of <=200bp A - intron_variant PRAD-UK 1 235981937 235981937 single base substitution T A intron_variant PRAD-UK 1 235985971 235985971 single base substitution G C intron_variant PRAD-UK 1 235989011 235989011 single base substitution G A downstream_gene_variant PRAD-UK 1 235989011 235989011 single base substitution G A intron_variant PRAD-UK 1 236010053 236010057 deletion of <=200bp AACTA - intron_variant PRAD-UK 1 236013468 236013468 insertion of <=200bp - A intron_variant PRAD-UK 1 236016012 236016012 single base substitution T C intron_variant PRAD-UK 1 236038329 236038329 single base substitution C G intron_variant PRAD-UK 1 236042213 236042213 single base substitution G A intron_variant PRAD-US 1 235840808 235840808 single base substitution C T exon_variant PRAD-US 1 235840808 235840808 single base substitution C T missense_variant G3638R 10912G>A PRAD-US 1 235950607 235950607 single base substitution A G 3_prime_UTR_variant PRAD-US 1 235950607 235950607 single base substitution A G downstream_gene_variant PRAD-US 1 235950607 235950607 single base substitution A G exon_variant PRAD-US 1 235950607 235950607 single base substitution A G synonymous_variant N1585N 4755T>C READ-US 1 235850291 235850291 single base substitution G A exon_variant READ-US 1 235850291 235850291 single base substitution G A synonymous_variant C3586C 10758C>T READ-US 1 235884002 235884002 single base substitution G A exon_variant READ-US 1 235884002 235884002 single base substitution G A synonymous_variant Y3173Y 9519C>T READ-US 1 235884202 235884202 single base substitution G A exon_variant READ-US 1 235884202 235884202 single base substitution G A missense_variant R3107C 9319C>T READ-US 1 235907320 235907320 single base substitution C A downstream_gene_variant READ-US 1 235907320 235907320 single base substitution C A exon_variant READ-US 1 235907320 235907320 single base substitution C A stop_gained E2704* 8110G>T READ-US 1 235929404 235929404 single base substitution C T 3_prime_UTR_variant READ-US 1 235929404 235929404 single base substitution C T intron_variant READ-US 1 235929404 235929404 single base substitution C T synonymous_variant T2032T 6096G>A READ-US 1 235940455 235940455 single base substitution G T 3_prime_UTR_variant READ-US 1 235940455 235940455 single base substitution G T exon_variant READ-US 1 235940455 235940455 single base substitution G T missense_variant L1790I 5368C>A READ-US 1 235944209 235944209 single base substitution C A 3_prime_UTR_variant READ-US 1 235944209 235944209 single base substitution C A exon_variant READ-US 1 235944209 235944209 single base substitution C A stop_gained E1724* 5170G>T READ-US 1 235955338 235955338 single base substitution C T exon_variant READ-US 1 235955338 235955338 single base substitution C T intron_variant READ-US 1 235955338 235955338 single base substitution C T missense_variant A1402T 4204G>A READ-US 1 235955338 235955338 single base substitution C T upstream_gene_variant READ-US 1 235969720 235969720 single base substitution A C exon_variant READ-US 1 235969720 235969720 single base substitution A C missense_variant F906V 2716T>G READ-US 1 235969959 235969959 single base substitution C T exon_variant READ-US 1 235969959 235969959 single base substitution C T missense_variant S826N 2477G>A READ-US 1 235969998 235969998 single base substitution C T exon_variant READ-US 1 235969998 235969998 single base substitution C T missense_variant R813Q 2438G>A READ-US 1 235972282 235972282 single base substitution C A exon_variant READ-US 1 235972282 235972282 single base substitution C A missense_variant L612F 1836G>T READ-US 1 235973320 235973320 single base substitution T G exon_variant READ-US 1 235973320 235973320 single base substitution T G missense_variant E266D 798A>C RECA-EU 1 235819640 235819640 single base substitution C A downstream_gene_variant RECA-EU 1 235821947 235821947 single base substitution C A downstream_gene_variant RECA-EU 1 235823639 235823639 single base substitution C A downstream_gene_variant RECA-EU 1 235823961 235823961 single base substitution G A downstream_gene_variant RECA-EU 1 235830539 235830539 single base substitution C T intron_variant RECA-EU 1 235837781 235837781 single base substitution G T intron_variant RECA-EU 1 235844144 235844144 single base substitution C A intron_variant RECA-EU 1 235851651 235851651 single base substitution A G intron_variant RECA-EU 1 235860332 235860332 single base substitution A C intron_variant RECA-EU 1 235868261 235868261 single base substitution T A downstream_gene_variant RECA-EU 1 235868261 235868261 single base substitution T A intron_variant RECA-EU 1 235870942 235870942 single base substitution A T downstream_gene_variant RECA-EU 1 235870942 235870942 single base substitution A T intron_variant RECA-EU 1 235892374 235892374 single base substitution T C intron_variant RECA-EU 1 235892374 235892374 single base substitution T C upstream_gene_variant RECA-EU 1 235898546 235898546 single base substitution C G downstream_gene_variant RECA-EU 1 235898546 235898546 single base substitution C G exon_variant RECA-EU 1 235898546 235898546 single base substitution C G intron_variant RECA-EU 1 235904376 235904376 single base substitution C T intron_variant RECA-EU 1 235904376 235904376 single base substitution C T upstream_gene_variant RECA-EU 1 235906523 235906523 single base substitution T A downstream_gene_variant RECA-EU 1 235906523 235906523 single base substitution T A intron_variant RECA-EU 1 235913879 235913879 single base substitution T C intron_variant RECA-EU 1 235916761 235916761 single base substitution G A intron_variant RECA-EU 1 235916761 235916761 single base substitution G A upstream_gene_variant RECA-EU 1 235917941 235917941 single base substitution A T downstream_gene_variant RECA-EU 1 235917941 235917941 single base substitution A T intron_variant RECA-EU 1 235917941 235917941 single base substitution A T upstream_gene_variant RECA-EU 1 235919357 235919357 single base substitution A G downstream_gene_variant RECA-EU 1 235919357 235919357 single base substitution A G intron_variant RECA-EU 1 235919357 235919357 single base substitution A G upstream_gene_variant RECA-EU 1 235921223 235921223 single base substitution T G downstream_gene_variant RECA-EU 1 235921223 235921223 single base substitution T G intron_variant RECA-EU 1 235924329 235924329 single base substitution G A intron_variant RECA-EU 1 235926834 235926834 single base substitution T A intron_variant RECA-EU 1 235955478 235955478 single base substitution A G intron_variant RECA-EU 1 235955478 235955478 single base substitution A G upstream_gene_variant RECA-EU 1 235973516 235973516 single base substitution G T exon_variant RECA-EU 1 235973516 235973516 single base substitution G T missense_variant P201H 602C>A RECA-EU 1 236018158 236018158 single base substitution T A intron_variant RECA-EU 1 236024310 236024310 single base substitution C T intron_variant RECA-EU 1 236039560 236039560 single base substitution A T intron_variant RECA-EU 1 236039985 236039985 single base substitution T A intron_variant RECA-EU 1 236048631 236048631 single base substitution A G upstream_gene_variant RECA-EU 1 236049004 236049004 single base substitution A T upstream_gene_variant SKCA-BR 1 235820263 235820263 insertion of <=200bp - GAAAC downstream_gene_variant SKCA-BR 1 235820731 235820731 single base substitution G A downstream_gene_variant SKCA-BR 1 235821953 235821953 single base substitution T A downstream_gene_variant SKCA-BR 1 235822422 235822422 insertion of <=200bp - GT downstream_gene_variant SKCA-BR 1 235825452 235825452 single base substitution T C 3_prime_UTR_variant SKCA-BR 1 235825452 235825452 single base substitution T C exon_variant SKCA-BR 1 235827340 235827340 single base substitution C T exon_variant SKCA-BR 1 235827340 235827340 single base substitution C T stop_gained W3737* 11211G>A SKCA-BR 1 235834639 235834639 single base substitution G A intron_variant SKCA-BR 1 235835911 235835911 single base substitution T C intron_variant SKCA-BR 1 235836673 235836673 single base substitution A C intron_variant SKCA-BR 1 235836962 235836962 single base substitution C T intron_variant SKCA-BR 1 235837189 235837189 single base substitution G A intron_variant SKCA-BR 1 235850547 235850547 single base substitution T C intron_variant SKCA-BR 1 235852323 235852323 single base substitution T C intron_variant SKCA-BR 1 235852326 235852326 insertion of <=200bp - TAATAATAACAAC intron_variant SKCA-BR 1 235852326 235852326 single base substitution T C intron_variant SKCA-BR 1 235855879 235855879 single base substitution T C intron_variant SKCA-BR 1 235857311 235857311 insertion of <=200bp - CT intron_variant SKCA-BR 1 235858582 235858582 single base substitution G A intron_variant SKCA-BR 1 235859819 235859819 single base substitution G A intron_variant SKCA-BR 1 235863373 235863373 single base substitution A G intron_variant SKCA-BR 1 235865904 235865904 single base substitution T A intron_variant SKCA-BR 1 235866437 235866437 single base substitution A G intron_variant SKCA-BR 1 235866463 235866463 insertion of <=200bp - CA intron_variant SKCA-BR 1 235869420 235869420 single base substitution G A downstream_gene_variant SKCA-BR 1 235869420 235869420 single base substitution G A intron_variant SKCA-BR 1 235879181 235879181 single base substitution G A intron_variant SKCA-BR 1 235879181 235879181 single base substitution G A upstream_gene_variant SKCA-BR 1 235879702 235879702 single base substitution G A intron_variant SKCA-BR 1 235879702 235879702 single base substitution G A upstream_gene_variant SKCA-BR 1 235884660 235884660 single base substitution A G intron_variant SKCA-BR 1 235885313 235885313 single base substitution G A intron_variant SKCA-BR 1 235886582 235886582 single base substitution T A intron_variant SKCA-BR 1 235890518 235890518 single base substitution G T intron_variant SKCA-BR 1 235890615 235890615 single base substitution G A intron_variant SKCA-BR 1 235895869 235895869 single base substitution A C intron_variant SKCA-BR 1 235895869 235895869 single base substitution A C upstream_gene_variant SKCA-BR 1 235897676 235897676 single base substitution A T downstream_gene_variant SKCA-BR 1 235897676 235897676 single base substitution A T intron_variant SKCA-BR 1 235900854 235900854 single base substitution G A downstream_gene_variant SKCA-BR 1 235900854 235900854 single base substitution G A exon_variant SKCA-BR 1 235900854 235900854 single base substitution G A intron_variant SKCA-BR 1 235902108 235902108 single base substitution T G intron_variant SKCA-BR 1 235902108 235902108 single base substitution T G upstream_gene_variant SKCA-BR 1 235904572 235904572 single base substitution C T intron_variant SKCA-BR 1 235904572 235904572 single base substitution C T upstream_gene_variant SKCA-BR 1 235905621 235905621 single base substitution G T downstream_gene_variant SKCA-BR 1 235905621 235905621 single base substitution G T intron_variant SKCA-BR 1 235905621 235905621 single base substitution G T upstream_gene_variant SKCA-BR 1 235905622 235905622 single base substitution G A downstream_gene_variant SKCA-BR 1 235905622 235905622 single base substitution G A intron_variant SKCA-BR 1 235905622 235905622 single base substitution G A upstream_gene_variant SKCA-BR 1 235908204 235908205 deletion of <=200bp GA - downstream_gene_variant SKCA-BR 1 235908204 235908205 deletion of <=200bp GA - intron_variant SKCA-BR 1 235908204 235908205 deletion of <=200bp GA - upstream_gene_variant SKCA-BR 1 235909403 235909403 single base substitution A T downstream_gene_variant SKCA-BR 1 235909403 235909403 single base substitution A T intron_variant SKCA-BR 1 235909403 235909403 single base substitution A T upstream_gene_variant SKCA-BR 1 235914653 235914653 single base substitution A C missense_variant V2546G 7637T>G SKCA-BR 1 235914653 235914653 single base substitution A C missense_variant V59G 176T>G SKCA-BR 1 235917529 235917529 single base substitution C T downstream_gene_variant SKCA-BR 1 235917529 235917529 single base substitution C T intron_variant SKCA-BR 1 235917529 235917529 single base substitution C T upstream_gene_variant SKCA-BR 1 235919298 235919304 deletion of <=200bp AATCTAT - downstream_gene_variant SKCA-BR 1 235919298 235919304 deletion of <=200bp AATCTAT - intron_variant SKCA-BR 1 235919298 235919304 deletion of <=200bp AATCTAT - upstream_gene_variant SKCA-BR 1 235921525 235921525 single base substitution T A downstream_gene_variant SKCA-BR 1 235921525 235921525 single base substitution T A intron_variant SKCA-BR 1 235921746 235921746 single base substitution C T downstream_gene_variant SKCA-BR 1 235921746 235921746 single base substitution C T intron_variant SKCA-BR 1 235921989 235921989 single base substitution C A downstream_gene_variant SKCA-BR 1 235921989 235921989 single base substitution C A intron_variant SKCA-BR 1 235924328 235924328 single base substitution T G intron_variant SKCA-BR 1 235924403 235924403 single base substitution A T intron_variant SKCA-BR 1 235927482 235927482 single base substitution G A intron_variant SKCA-BR 1 235929528 235929528 single base substitution G A 3_prime_UTR_variant SKCA-BR 1 235929528 235929528 single base substitution G A intron_variant SKCA-BR 1 235929528 235929528 single base substitution G A missense_variant S1991L 5972C>T SKCA-BR 1 235932786 235932786 single base substitution A C intron_variant SKCA-BR 1 235933348 235933348 insertion of <=200bp - GA intron_variant SKCA-BR 1 235934765 235934765 single base substitution T C intron_variant SKCA-BR 1 235935216 235935217 deletion of <=200bp TG - intron_variant SKCA-BR 1 235935217 235935217 single base substitution G T intron_variant SKCA-BR 1 235935217 235935218 deletion of <=200bp GT - intron_variant SKCA-BR 1 235937267 235937267 single base substitution C A 3_prime_UTR_variant SKCA-BR 1 235937267 235937267 single base substitution C A exon_variant SKCA-BR 1 235937267 235937267 single base substitution C A stop_gained E1887* 5659G>T SKCA-BR 1 235941398 235941398 insertion of <=200bp - AATATAT intron_variant SKCA-BR 1 235941398 235941398 insertion of <=200bp - AAT intron_variant SKCA-BR 1 235944785 235944785 single base substitution A C intron_variant SKCA-BR 1 235945460 235945460 single base substitution A T downstream_gene_variant SKCA-BR 1 235945460 235945460 single base substitution A T intron_variant SKCA-BR 1 235945644 235945644 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 1 235945644 235945644 insertion of <=200bp - AT intron_variant SKCA-BR 1 235946793 235946793 single base substitution C G downstream_gene_variant SKCA-BR 1 235946793 235946793 single base substitution C G intron_variant SKCA-BR 1 235947941 235947941 single base substitution T C downstream_gene_variant SKCA-BR 1 235947941 235947941 single base substitution T C intron_variant SKCA-BR 1 235951321 235951321 single base substitution G A downstream_gene_variant SKCA-BR 1 235951321 235951321 single base substitution G A intron_variant SKCA-BR 1 235954741 235954741 single base substitution G A downstream_gene_variant SKCA-BR 1 235954741 235954741 single base substitution G A intron_variant SKCA-BR 1 235954741 235954741 single base substitution G A upstream_gene_variant SKCA-BR 1 235956287 235956287 single base substitution A G intron_variant SKCA-BR 1 235956287 235956287 single base substitution A G upstream_gene_variant SKCA-BR 1 235957330 235957330 single base substitution A C intron_variant SKCA-BR 1 235962870 235962870 single base substitution A G intron_variant SKCA-BR 1 235964559 235964559 single base substitution G A intron_variant SKCA-BR 1 235964685 235964685 insertion of <=200bp - TA intron_variant SKCA-BR 1 235967215 235967227 deletion of <=200bp CAACTAAAGGTAA - intron_variant SKCA-BR 1 235969927 235969927 single base substitution G A exon_variant SKCA-BR 1 235969927 235969927 single base substitution G A missense_variant P837S 2509C>T SKCA-BR 1 235972850 235972850 single base substitution G A exon_variant SKCA-BR 1 235972850 235972850 single base substitution G A missense_variant P423L 1268C>T SKCA-BR 1 235973564 235973564 single base substitution G T exon_variant SKCA-BR 1 235973564 235973564 single base substitution G T missense_variant P185H 554C>A SKCA-BR 1 235973579 235973579 single base substitution T C exon_variant SKCA-BR 1 235973579 235973579 single base substitution T C missense_variant N180S 539A>G SKCA-BR 1 235975794 235975794 single base substitution G A intron_variant SKCA-BR 1 235978665 235978665 single base substitution G A intron_variant SKCA-BR 1 235979037 235979037 single base substitution A G intron_variant SKCA-BR 1 235979763 235979764 deletion of <=200bp AT - intron_variant SKCA-BR 1 235981937 235981937 insertion of <=200bp - TA intron_variant SKCA-BR 1 235993759 235993759 single base substitution G A intron_variant SKCA-BR 1 235993985 235993985 single base substitution G A intron_variant SKCA-BR 1 235996926 235996928 deletion of <=200bp CAT - 5_prime_UTR_variant SKCA-BR 1 235996926 235996928 deletion of <=200bp CAT - exon_variant SKCA-BR 1 235997724 235997724 single base substitution G A intron_variant SKCA-BR 1 236001935 236001935 single base substitution C T intron_variant SKCA-BR 1 236002365 236002365 single base substitution A C intron_variant SKCA-BR 1 236006425 236006425 single base substitution G A intron_variant SKCA-BR 1 236008230 236008230 single base substitution A G intron_variant SKCA-BR 1 236009973 236009973 single base substitution G A intron_variant SKCA-BR 1 236012233 236012233 single base substitution C A intron_variant SKCA-BR 1 236013117 236013117 single base substitution A T intron_variant SKCA-BR 1 236014798 236014798 single base substitution A C intron_variant SKCA-BR 1 236023158 236023158 single base substitution G A intron_variant SKCA-BR 1 236023461 236023461 single base substitution C T intron_variant SKCA-BR 1 236024622 236024622 single base substitution A T intron_variant SKCA-BR 1 236026148 236026148 insertion of <=200bp - CACACACAT intron_variant SKCA-BR 1 236035178 236035178 single base substitution A T intron_variant SKCA-BR 1 236035178 236035178 single base substitution A T upstream_gene_variant SKCA-BR 1 236038791 236038791 single base substitution T G intron_variant SKCA-BR 1 236038806 236038806 single base substitution A T intron_variant SKCA-BR 1 236039550 236039550 single base substitution T A intron_variant SKCA-BR 1 236039785 236039785 single base substitution C T intron_variant SKCA-BR 1 236041155 236041155 insertion of <=200bp - CAA intron_variant SKCA-BR 1 236043040 236043041 deletion of <=200bp CT - intron_variant SKCM-US 1 235827771 235827771 single base substitution A C exon_variant SKCM-US 1 235827771 235827771 single base substitution A C missense_variant I3730S 11189T>G SKCM-US 1 235840451 235840451 single base substitution G A exon_variant SKCM-US 1 235840451 235840451 single base substitution G A missense_variant P3660S 10978C>T SKCM-US 1 235860390 235860390 single base substitution C T exon_variant SKCM-US 1 235860390 235860390 single base substitution C T synonymous_variant K3519K 10557G>A SKCM-US 1 235860522 235860522 single base substitution G A exon_variant SKCM-US 1 235860522 235860522 single base substitution G A synonymous_variant S3475S 10425C>T SKCM-US 1 235866078 235866078 single base substitution G A exon_variant SKCM-US 1 235866078 235866078 single base substitution G A missense_variant T3448I 10343C>T SKCM-US 1 235866213 235866213 single base substitution A G exon_variant SKCM-US 1 235866213 235866213 single base substitution A G missense_variant M3403T 10208T>C SKCM-US 1 235884159 235884159 single base substitution T A exon_variant SKCM-US 1 235884159 235884159 single base substitution T A missense_variant N3121I 9362A>T SKCM-US 1 235887328 235887328 single base substitution C T splice_region_variant SKCM-US 1 235891379 235891379 single base substitution A G exon_variant SKCM-US 1 235891379 235891379 single base substitution A G synonymous_variant S3053S 9159T>C SKCM-US 1 235904728 235904728 single base substitution G A exon_variant SKCM-US 1 235904728 235904728 single base substitution G A synonymous_variant S2784S 8352C>T SKCM-US 1 235904728 235904728 single base substitution G A upstream_gene_variant SKCM-US 1 235907411 235907411 single base substitution T G downstream_gene_variant SKCM-US 1 235907411 235907411 single base substitution T G synonymous_variant V2673V 8019A>C SKCM-US 1 235907411 235907411 single base substitution T G upstream_gene_variant SKCM-US 1 235915467 235915467 single base substitution G A missense_variant P2489S 7465C>T SKCM-US 1 235915467 235915467 single base substitution G A missense_variant P2S 4C>T SKCM-US 1 235922487 235922487 single base substitution G A downstream_gene_variant SKCM-US 1 235922487 235922487 single base substitution G A exon_variant SKCM-US 1 235922487 235922487 single base substitution G A synonymous_variant S2222S 6666C>T SKCM-US 1 235922514 235922514 single base substitution T G downstream_gene_variant SKCM-US 1 235922514 235922514 single base substitution T G exon_variant SKCM-US 1 235922514 235922514 single base substitution T G synonymous_variant S2213S 6639A>C SKCM-US 1 235922707 235922707 single base substitution G C 3_prime_UTR_variant SKCM-US 1 235922707 235922707 single base substitution G C exon_variant SKCM-US 1 235922707 235922707 single base substitution G C missense_variant S2149C 6446C>G SKCM-US 1 235929509 235929509 single base substitution T C 3_prime_UTR_variant SKCM-US 1 235929509 235929509 single base substitution T C intron_variant SKCM-US 1 235929509 235929509 single base substitution T C synonymous_variant A1997A 5991A>G SKCM-US 1 235950601 235950601 single base substitution G A 3_prime_UTR_variant SKCM-US 1 235950601 235950601 single base substitution G A downstream_gene_variant SKCM-US 1 235950601 235950601 single base substitution G A exon_variant SKCM-US 1 235950601 235950601 single base substitution G A synonymous_variant F1587F 4761C>T SKCM-US 1 235950643 235950643 single base substitution T C 3_prime_UTR_variant SKCM-US 1 235950643 235950643 single base substitution T C downstream_gene_variant SKCM-US 1 235950643 235950643 single base substitution T C exon_variant SKCM-US 1 235950643 235950643 single base substitution T C synonymous_variant K1573K 4719A>G SKCM-US 1 235955205 235955205 single base substitution C T exon_variant SKCM-US 1 235955205 235955205 single base substitution C T intron_variant SKCM-US 1 235955205 235955205 single base substitution C T missense_variant R1446Q 4337G>A SKCM-US 1 235955205 235955205 single base substitution C T upstream_gene_variant SKCM-US 1 235955367 235955367 single base substitution G T exon_variant SKCM-US 1 235955367 235955367 single base substitution G T intron_variant SKCM-US 1 235955367 235955367 single base substitution G T stop_gained S1392* 4175C>A SKCM-US 1 235955367 235955367 single base substitution G T upstream_gene_variant SKCM-US 1 235956850 235956850 single base substitution C T exon_variant SKCM-US 1 235956850 235956850 single base substitution C T missense_variant E1357K 4069G>A SKCM-US 1 235956850 235956850 single base substitution C T upstream_gene_variant SKCM-US 1 235967804 235967804 single base substitution C T splice_region_variant SKCM-US 1 235969062 235969062 single base substitution T C exon_variant SKCM-US 1 235969062 235969062 single base substitution T C missense_variant E1125G 3374A>G SKCM-US 1 235969138 235969138 single base substitution G A exon_variant SKCM-US 1 235969138 235969138 single base substitution G A missense_variant L1100F 3298C>T SKCM-US 1 235969220 235969220 single base substitution G A exon_variant SKCM-US 1 235969220 235969220 single base substitution G A synonymous_variant S1072S 3216C>T SKCM-US 1 235969221 235969221 single base substitution G A exon_variant SKCM-US 1 235969221 235969221 single base substitution G A missense_variant S1072F 3215C>T SKCM-US 1 235969576 235969576 single base substitution G A exon_variant SKCM-US 1 235969576 235969576 single base substitution G A missense_variant P954S 2860C>T SKCM-US 1 235969602 235969602 single base substitution G A exon_variant SKCM-US 1 235969602 235969602 single base substitution G A missense_variant S945F 2834C>T SKCM-US 1 235972340 235972340 single base substitution A G exon_variant SKCM-US 1 235972340 235972340 single base substitution A G missense_variant I593T 1778T>C SKCM-US 1 235972583 235972583 single base substitution T C exon_variant SKCM-US 1 235972583 235972583 single base substitution T C missense_variant H512R 1535A>G SKCM-US 1 235972605 235972605 single base substitution C T exon_variant SKCM-US 1 235972605 235972605 single base substitution C T missense_variant E505K 1513G>A SKCM-US 1 235973240 235973240 single base substitution A G exon_variant SKCM-US 1 235973240 235973240 single base substitution A G missense_variant L293P 878T>C SKCM-US 1 235973317 235973317 single base substitution T C exon_variant SKCM-US 1 235973317 235973317 single base substitution T C synonymous_variant K267K 801A>G SKCM-US 1 235973358 235973358 single base substitution G A exon_variant SKCM-US 1 235973358 235973358 single base substitution G A missense_variant P254S 760C>T SKCM-US 1 235973516 235973516 single base substitution G A exon_variant SKCM-US 1 235973516 235973516 single base substitution G A missense_variant P201L 602C>T SKCM-US 1 235973692 235973692 single base substitution T G exon_variant SKCM-US 1 235973692 235973692 single base substitution T G missense_variant K142N 426A>C SKCM-US 1 235973733 235973733 single base substitution G A exon_variant SKCM-US 1 235973733 235973733 single base substitution G A synonymous_variant L129L 385C>T SKCM-US 1 235973803 235973803 single base substitution G A exon_variant SKCM-US 1 235973803 235973803 single base substitution G A synonymous_variant I105I 315C>T STAD-US 1 235827885 235827885 single base substitution T C exon_variant STAD-US 1 235827885 235827885 single base substitution T C missense_variant N3692S 11075A>G STAD-US 1 235840481 235840481 single base substitution A C exon_variant STAD-US 1 235840481 235840481 single base substitution A C missense_variant Y3650D 10948T>G STAD-US 1 235866168 235866168 single base substitution G A exon_variant STAD-US 1 235866168 235866168 single base substitution G A missense_variant A3418V 10253C>T STAD-US 1 235866229 235866229 single base substitution G A exon_variant STAD-US 1 235866229 235866229 single base substitution G A stop_gained R3398* 10192C>T STAD-US 1 235884029 235884029 single base substitution A G exon_variant STAD-US 1 235884029 235884029 single base substitution A G synonymous_variant P3164P 9492T>C STAD-US 1 235884124 235884124 single base substitution T A exon_variant STAD-US 1 235884124 235884124 single base substitution T A missense_variant N3133Y 9397A>T STAD-US 1 235884191 235884191 single base substitution T C exon_variant STAD-US 1 235884191 235884191 single base substitution T C synonymous_variant V3110V 9330A>G STAD-US 1 235887376 235887376 single base substitution G T exon_variant STAD-US 1 235887376 235887376 single base substitution G T synonymous_variant I3089I 9267C>A STAD-US 1 235887386 235887386 single base substitution G T exon_variant STAD-US 1 235887386 235887386 single base substitution G T missense_variant A3086D 9257C>A STAD-US 1 235894451 235894451 single base substitution T C exon_variant STAD-US 1 235894451 235894451 single base substitution T C missense_variant Y2943C 8828A>G STAD-US 1 235894451 235894451 single base substitution T C upstream_gene_variant STAD-US 1 235896835 235896835 single base substitution C T downstream_gene_variant STAD-US 1 235896835 235896835 single base substitution C T exon_variant STAD-US 1 235896835 235896835 single base substitution C T stop_gained W2923* 8769G>A STAD-US 1 235897198 235897198 single base substitution C A downstream_gene_variant STAD-US 1 235897198 235897198 single base substitution C A exon_variant STAD-US 1 235897198 235897198 single base substitution C A missense_variant K2848N 8544G>T STAD-US 1 235904748 235904748 single base substitution G A exon_variant STAD-US 1 235904748 235904748 single base substitution G A stop_gained R2778* 8332C>T STAD-US 1 235904748 235904748 single base substitution G A upstream_gene_variant STAD-US 1 235914579 235914579 single base substitution G A missense_variant L2571F 7711C>T STAD-US 1 235914579 235914579 single base substitution G A missense_variant L84F 250C>T STAD-US 1 235916455 235916455 single base substitution A C missense_variant L2450R 7349T>G STAD-US 1 235916455 235916455 single base substitution A C upstream_gene_variant STAD-US 1 235916502 235916502 single base substitution T C missense_variant I2434M 7302A>G STAD-US 1 235916502 235916502 single base substitution T C upstream_gene_variant STAD-US 1 235918837 235918837 single base substitution T G downstream_gene_variant STAD-US 1 235918837 235918837 single base substitution T G missense_variant Q2390H 7170A>C STAD-US 1 235918837 235918837 single base substitution T G upstream_gene_variant STAD-US 1 235918947 235918947 single base substitution G C downstream_gene_variant STAD-US 1 235918947 235918947 single base substitution G C missense_variant L2354V 7060C>G STAD-US 1 235918947 235918947 single base substitution G C upstream_gene_variant STAD-US 1 235920596 235920596 single base substitution T C downstream_gene_variant STAD-US 1 235920596 235920596 single base substitution T C synonymous_variant Q2348Q 7044A>G STAD-US 1 235920623 235920623 single base substitution G A downstream_gene_variant STAD-US 1 235920623 235920623 single base substitution G A synonymous_variant L2339L 7017C>T STAD-US 1 235922628 235922631 deletion of <=200bp ACAA - 3_prime_UTR_variant STAD-US 1 235922628 235922631 deletion of <=200bp ACAA - exon_variant STAD-US 1 235922628 235922631 deletion of <=200bp ACAA - frameshift_variant VC2174 STAD-US 1 235922666 235922666 single base substitution C T 3_prime_UTR_variant STAD-US 1 235922666 235922666 single base substitution C T exon_variant STAD-US 1 235922666 235922666 single base substitution C T missense_variant A2163T 6487G>A STAD-US 1 235922861 235922861 single base substitution C T 3_prime_UTR_variant STAD-US 1 235922861 235922861 single base substitution C T exon_variant STAD-US 1 235922861 235922861 single base substitution C T missense_variant A2098T 6292G>A STAD-US 1 235922883 235922883 single base substitution A G 3_prime_UTR_variant STAD-US 1 235922883 235922883 single base substitution A G exon_variant STAD-US 1 235922883 235922883 single base substitution A G synonymous_variant N2090N 6270T>C STAD-US 1 235929422 235929422 single base substitution G A 3_prime_UTR_variant STAD-US 1 235929422 235929422 single base substitution G A intron_variant STAD-US 1 235929422 235929422 single base substitution G A synonymous_variant Y2026Y 6078C>T STAD-US 1 235944236 235944236 single base substitution C A 3_prime_UTR_variant STAD-US 1 235944236 235944236 single base substitution C A exon_variant STAD-US 1 235944236 235944236 single base substitution C A stop_gained E1715* 5143G>T STAD-US 1 235964220 235964220 insertion of <=200bp - A exon_variant STAD-US 1 235964220 235964220 insertion of <=200bp - A frameshift_variant L1297F? STAD-US 1 235966262 235966264 deletion of <=200bp CTT - disruptive_inframe_deletion EG1219G STAD-US 1 235966262 235966264 deletion of <=200bp CTT - exon_variant STAD-US 1 235967817 235967817 single base substitution G A exon_variant STAD-US 1 235967817 235967817 single base substitution G A missense_variant A1181V 3542C>T STAD-US 1 235969041 235969041 single base substitution A G splice_donor_variant STAD-US 1 235969335 235969335 single base substitution A G exon_variant STAD-US 1 235969335 235969335 single base substitution A G missense_variant M1034T 3101T>C STAD-US 1 235969716 235969716 deletion of <=200bp A - exon_variant STAD-US 1 235969716 235969716 deletion of <=200bp A - frameshift_variant L907 STAD-US 1 235971775 235971775 single base substitution C T exon_variant STAD-US 1 235971775 235971775 single base substitution C T synonymous_variant L781L 2343G>A STAD-US 1 235971943 235971943 single base substitution A G exon_variant STAD-US 1 235971943 235971943 single base substitution A G synonymous_variant V725V 2175T>C STAD-US 1 235972028 235972028 single base substitution T G exon_variant STAD-US 1 235972028 235972028 single base substitution T G missense_variant Q697P 2090A>C STAD-US 1 235972663 235972663 insertion of <=200bp - T exon_variant STAD-US 1 235972663 235972663 insertion of <=200bp - T frameshift_variant K485K? STAD-US 1 235972915 235972915 single base substitution T C exon_variant STAD-US 1 235972915 235972915 single base substitution T C synonymous_variant L401L 1203A>G STAD-US 1 235973006 235973006 single base substitution G T exon_variant STAD-US 1 235973006 235973006 single base substitution G T missense_variant P371H 1112C>A STAD-US 1 235973152 235973152 single base substitution C A exon_variant STAD-US 1 235973152 235973152 single base substitution C A missense_variant L322F 966G>T STAD-US 1 235973208 235973208 single base substitution C T exon_variant STAD-US 1 235973208 235973208 single base substitution C T missense_variant D304N 910G>A STAD-US 1 235973499 235973499 single base substitution G A exon_variant STAD-US 1 235973499 235973499 single base substitution G A missense_variant R207C 619C>T STAD-US 1 235973738 235973741 deletion of <=200bp CTTC - exon_variant STAD-US 1 235973738 235973741 deletion of <=200bp CTTC - frameshift_variant GS126 STAD-US 1 235976313 235976313 single base substitution G C exon_variant STAD-US 1 235976313 235976313 single base substitution G C missense_variant P81A 241C>G STAD-US 1 235976350 235976350 single base substitution A G exon_variant STAD-US 1 235976350 235976350 single base substitution A G synonymous_variant C68C 204T>C STAD-US 1 235993555 235993555 single base substitution G C exon_variant STAD-US 1 235993555 235993555 single base substitution G C missense_variant L55V 163C>G STAD-US 1 235993568 235993568 single base substitution T G exon_variant STAD-US 1 235993568 235993568 single base substitution T G synonymous_variant R50R 150A>C THCA-US 1 235920719 235920719 single base substitution T C downstream_gene_variant THCA-US 1 235920719 235920719 single base substitution T C synonymous_variant L2307L 6921A>G THCA-US 1 235952076 235952076 single base substitution T C 3_prime_UTR_variant THCA-US 1 235952076 235952076 single base substitution T C downstream_gene_variant THCA-US 1 235952076 235952076 single base substitution T C exon_variant THCA-US 1 235952076 235952076 single base substitution T C missense_variant H1538R 4613A>G UCEC-US 1 235826246 235826246 single base substitution G A exon_variant UCEC-US 1 235826246 235826246 single base substitution G A synonymous_variant A3800A 11400C>T UCEC-US 1 235827794 235827794 single base substitution G A exon_variant UCEC-US 1 235827794 235827794 single base substitution G A synonymous_variant I3722I 11166C>T UCEC-US 1 235827867 235827867 single base substitution T C exon_variant UCEC-US 1 235827867 235827867 single base substitution T C missense_variant H3698R 11093A>G UCEC-US 1 235840412 235840412 single base substitution T C exon_variant UCEC-US 1 235840412 235840412 single base substitution T C missense_variant I3673V 11017A>G UCEC-US 1 235840918 235840918 single base substitution G A missense_variant P3601L 10802C>T UCEC-US 1 235840918 235840918 single base substitution G A splice_region_variant UCEC-US 1 235856784 235856784 single base substitution C T missense_variant V3523M 10567G>A UCEC-US 1 235856784 235856784 single base substitution C T splice_region_variant UCEC-US 1 235872587 235872587 single base substitution T C downstream_gene_variant UCEC-US 1 235872587 235872587 single base substitution T C exon_variant UCEC-US 1 235872587 235872587 single base substitution T C missense_variant Q3316R 9947A>G UCEC-US 1 235875362 235875362 single base substitution C T downstream_gene_variant UCEC-US 1 235875362 235875362 single base substitution C T exon_variant UCEC-US 1 235875362 235875362 single base substitution C T missense_variant R3307H 9920G>A UCEC-US 1 235875429 235875429 single base substitution C A downstream_gene_variant UCEC-US 1 235875429 235875429 single base substitution C A exon_variant UCEC-US 1 235875429 235875429 single base substitution C A stop_gained E3285* 9853G>T UCEC-US 1 235878638 235878638 single base substitution C T exon_variant UCEC-US 1 235878638 235878638 single base substitution C T missense_variant R3216H 9647G>A UCEC-US 1 235878638 235878638 single base substitution C T upstream_gene_variant UCEC-US 1 235878639 235878639 single base substitution G A exon_variant UCEC-US 1 235878639 235878639 single base substitution G A missense_variant R3216C 9646C>T UCEC-US 1 235878639 235878639 single base substitution G A upstream_gene_variant UCEC-US 1 235880032 235880032 single base substitution G A exon_variant UCEC-US 1 235880032 235880032 single base substitution G A missense_variant R3203C 9607C>T UCEC-US 1 235880032 235880032 single base substitution G A upstream_gene_variant UCEC-US 1 235884030 235884030 single base substitution G T exon_variant UCEC-US 1 235884030 235884030 single base substitution G T missense_variant P3164H 9491C>A UCEC-US 1 235884202 235884202 single base substitution G A exon_variant UCEC-US 1 235884202 235884202 single base substitution G A missense_variant R3107C 9319C>T UCEC-US 1 235891377 235891377 single base substitution G A missense_variant S3054L 9161C>T UCEC-US 1 235891377 235891377 single base substitution G A splice_region_variant UCEC-US 1 235892950 235892950 single base substitution G A exon_variant UCEC-US 1 235892950 235892950 single base substitution G A stop_gained R3018* 9052C>T UCEC-US 1 235892950 235892950 single base substitution G A upstream_gene_variant UCEC-US 1 235894359 235894359 single base substitution G T exon_variant UCEC-US 1 235894359 235894359 single base substitution G T missense_variant L2974I 8920C>A UCEC-US 1 235894359 235894359 single base substitution G T upstream_gene_variant UCEC-US 1 235894438 235894438 single base substitution C T exon_variant UCEC-US 1 235894438 235894438 single base substitution C T stop_gained W2947* 8841G>A UCEC-US 1 235894438 235894438 single base substitution C T upstream_gene_variant UCEC-US 1 235904858 235904858 single base substitution C T downstream_gene_variant UCEC-US 1 235904858 235904858 single base substitution C T exon_variant UCEC-US 1 235904858 235904858 single base substitution C T missense_variant R2741Q 8222G>A UCEC-US 1 235904858 235904858 single base substitution C T upstream_gene_variant UCEC-US 1 235907331 235907331 single base substitution G T downstream_gene_variant UCEC-US 1 235907331 235907331 single base substitution G T exon_variant UCEC-US 1 235907331 235907331 single base substitution G T missense_variant P2700Q 8099C>A UCEC-US 1 235907458 235907458 single base substitution C A downstream_gene_variant UCEC-US 1 235907458 235907458 single base substitution C A splice_acceptor_variant UCEC-US 1 235907458 235907458 single base substitution C A upstream_gene_variant UCEC-US 1 235909822 235909822 single base substitution G A stop_gained R163* 487C>T UCEC-US 1 235909822 235909822 single base substitution G A stop_gained R2596* 7786C>T UCEC-US 1 235909822 235909822 single base substitution G A upstream_gene_variant UCEC-US 1 235916455 235916455 single base substitution A C missense_variant L2450R 7349T>G UCEC-US 1 235916455 235916455 single base substitution A C upstream_gene_variant UCEC-US 1 235916465 235916465 single base substitution C T missense_variant A2447T 7339G>A UCEC-US 1 235916465 235916465 single base substitution C T upstream_gene_variant UCEC-US 1 235916528 235916528 single base substitution A G missense_variant S2426P 7276T>C UCEC-US 1 235916528 235916528 single base substitution A G upstream_gene_variant UCEC-US 1 235918789 235918789 single base substitution G A downstream_gene_variant UCEC-US 1 235918789 235918789 single base substitution G A synonymous_variant G2406G 7218C>T UCEC-US 1 235918789 235918789 single base substitution G A upstream_gene_variant UCEC-US 1 235918821 235918821 single base substitution A C downstream_gene_variant UCEC-US 1 235918821 235918821 single base substitution A C missense_variant F2396V 7186T>G UCEC-US 1 235918821 235918821 single base substitution A C upstream_gene_variant UCEC-US 1 235918881 235918881 single base substitution A G downstream_gene_variant UCEC-US 1 235918881 235918881 single base substitution A G missense_variant F2376L 7126T>C UCEC-US 1 235918881 235918881 single base substitution A G upstream_gene_variant UCEC-US 1 235918905 235918905 single base substitution C A downstream_gene_variant UCEC-US 1 235918905 235918905 single base substitution C A missense_variant D2368Y 7102G>T UCEC-US 1 235918905 235918905 single base substitution C A upstream_gene_variant UCEC-US 1 235918923 235918923 single base substitution C T downstream_gene_variant UCEC-US 1 235918923 235918923 single base substitution C T missense_variant A2362T 7084G>A UCEC-US 1 235918923 235918923 single base substitution C T upstream_gene_variant UCEC-US 1 235920622 235920622 single base substitution C T downstream_gene_variant UCEC-US 1 235920622 235920622 single base substitution C T missense_variant V2340I 7018G>A UCEC-US 1 235920694 235920694 single base substitution G T downstream_gene_variant UCEC-US 1 235920694 235920694 single base substitution G T missense_variant L2316I 6946C>A UCEC-US 1 235922751 235922751 single base substitution A G 3_prime_UTR_variant UCEC-US 1 235922751 235922751 single base substitution A G exon_variant UCEC-US 1 235922751 235922751 single base substitution A G synonymous_variant N2134N 6402T>C UCEC-US 1 235922765 235922765 single base substitution C T 3_prime_UTR_variant UCEC-US 1 235922765 235922765 single base substitution C T exon_variant UCEC-US 1 235922765 235922765 single base substitution C T missense_variant D2130N 6388G>A UCEC-US 1 235922848 235922848 single base substitution C T 3_prime_UTR_variant UCEC-US 1 235922848 235922848 single base substitution C T exon_variant UCEC-US 1 235922848 235922848 single base substitution C T missense_variant R2102H 6305G>A UCEC-US 1 235926125 235926125 single base substitution G A 3_prime_UTR_variant UCEC-US 1 235926125 235926125 single base substitution G A exon_variant UCEC-US 1 235926125 235926125 single base substitution G A missense_variant R2050W 6148C>T UCEC-US 1 235929422 235929422 single base substitution G A 3_prime_UTR_variant UCEC-US 1 235929422 235929422 single base substitution G A intron_variant UCEC-US 1 235929422 235929422 single base substitution G A synonymous_variant Y2026Y 6078C>T UCEC-US 1 235940529 235940529 single base substitution T C 3_prime_UTR_variant UCEC-US 1 235940529 235940529 single base substitution T C exon_variant UCEC-US 1 235940529 235940529 single base substitution T C missense_variant Q1765R 5294A>G UCEC-US 1 235944236 235944236 single base substitution C A 3_prime_UTR_variant UCEC-US 1 235944236 235944236 single base substitution C A exon_variant UCEC-US 1 235944236 235944236 single base substitution C A stop_gained E1715* 5143G>T UCEC-US 1 235945322 235945322 single base substitution T G 3_prime_UTR_variant UCEC-US 1 235945322 235945322 single base substitution T G exon_variant UCEC-US 1 235945322 235945322 single base substitution T G missense_variant K1643T 4928A>C UCEC-US 1 235952058 235952058 single base substitution G A 3_prime_UTR_variant UCEC-US 1 235952058 235952058 single base substitution G A downstream_gene_variant UCEC-US 1 235952058 235952058 single base substitution G A exon_variant UCEC-US 1 235952058 235952058 single base substitution G A missense_variant S1544F 4631C>T UCEC-US 1 235955081 235955081 single base substitution A G exon_variant UCEC-US 1 235955081 235955081 single base substitution A G intron_variant UCEC-US 1 235955081 235955081 single base substitution A G synonymous_variant A1487A 4461T>C UCEC-US 1 235955081 235955081 single base substitution A G upstream_gene_variant UCEC-US 1 235955093 235955093 single base substitution A G exon_variant UCEC-US 1 235955093 235955093 single base substitution A G intron_variant UCEC-US 1 235955093 235955093 single base substitution A G synonymous_variant C1483C 4449T>C UCEC-US 1 235955093 235955093 single base substitution A G upstream_gene_variant UCEC-US 1 235955161 235955161 single base substitution G T exon_variant UCEC-US 1 235955161 235955161 single base substitution G T intron_variant UCEC-US 1 235955161 235955161 single base substitution G T missense_variant L1461M 4381C>A UCEC-US 1 235955161 235955161 single base substitution G T upstream_gene_variant UCEC-US 1 235955237 235955237 single base substitution C A exon_variant UCEC-US 1 235955237 235955237 single base substitution C A intron_variant UCEC-US 1 235955237 235955237 single base substitution C A missense_variant K1435N 4305G>T UCEC-US 1 235955237 235955237 single base substitution C A upstream_gene_variant UCEC-US 1 235956838 235956838 single base substitution G T exon_variant UCEC-US 1 235956838 235956838 single base substitution G T missense_variant L1361I 4081C>A UCEC-US 1 235956838 235956838 single base substitution G T upstream_gene_variant UCEC-US 1 235956908 235956908 single base substitution G A exon_variant UCEC-US 1 235956908 235956908 single base substitution G A synonymous_variant C1337C 4011C>T UCEC-US 1 235956908 235956908 single base substitution G A upstream_gene_variant UCEC-US 1 235963685 235963685 single base substitution C A missense_variant G1314V 3941G>T UCEC-US 1 235963685 235963685 single base substitution C A splice_region_variant UCEC-US 1 235966234 235966234 single base substitution G T exon_variant UCEC-US 1 235966234 235966234 single base substitution G T missense_variant P1229H 3686C>A UCEC-US 1 235966256 235966256 single base substitution C T exon_variant UCEC-US 1 235966256 235966256 single base substitution C T missense_variant E1222K 3664G>A UCEC-US 1 235969067 235969067 single base substitution C T exon_variant UCEC-US 1 235969067 235969067 single base substitution C T synonymous_variant K1123K 3369G>A UCEC-US 1 235969240 235969240 single base substitution C T exon_variant UCEC-US 1 235969240 235969240 single base substitution C T missense_variant E1066K 3196G>A UCEC-US 1 235969265 235969265 single base substitution C A exon_variant UCEC-US 1 235969265 235969265 single base substitution C A missense_variant K1057N 3171G>T UCEC-US 1 235969296 235969296 single base substitution G T exon_variant UCEC-US 1 235969296 235969296 single base substitution G T missense_variant P1047H 3140C>A UCEC-US 1 235969320 235969320 single base substitution A G exon_variant UCEC-US 1 235969320 235969320 single base substitution A G missense_variant L1039S 3116T>C UCEC-US 1 235969359 235969359 single base substitution C A exon_variant UCEC-US 1 235969359 235969359 single base substitution C A missense_variant R1026I 3077G>T UCEC-US 1 235969378 235969378 single base substitution C A exon_variant UCEC-US 1 235969378 235969378 single base substitution C A stop_gained E1020* 3058G>T UCEC-US 1 235969493 235969493 single base substitution A C exon_variant UCEC-US 1 235969493 235969493 single base substitution A C missense_variant F981L 2943T>G UCEC-US 1 235969712 235969712 single base substitution G A exon_variant UCEC-US 1 235969712 235969712 single base substitution G A synonymous_variant C908C 2724C>T UCEC-US 1 235969732 235969732 single base substitution G T exon_variant UCEC-US 1 235969732 235969732 single base substitution G T missense_variant L902I 2704C>A UCEC-US 1 235969939 235969939 single base substitution C A exon_variant UCEC-US 1 235969939 235969939 single base substitution C A missense_variant D833Y 2497G>T UCEC-US 1 235969998 235969998 single base substitution C A exon_variant UCEC-US 1 235969998 235969998 single base substitution C A missense_variant R813L 2438G>T UCEC-US 1 235969998 235969998 single base substitution C T exon_variant UCEC-US 1 235969998 235969998 single base substitution C T missense_variant R813Q 2438G>A UCEC-US 1 235971814 235971814 single base substitution G A exon_variant UCEC-US 1 235971814 235971814 single base substitution G A synonymous_variant C768C 2304C>T UCEC-US 1 235972036 235972036 single base substitution C A exon_variant UCEC-US 1 235972036 235972036 single base substitution C A missense_variant K694N 2082G>T UCEC-US 1 235972195 235972195 single base substitution A G exon_variant UCEC-US 1 235972195 235972195 single base substitution A G synonymous_variant T641T 1923T>C UCEC-US 1 235972332 235972332 single base substitution G A exon_variant UCEC-US 1 235972332 235972332 single base substitution G A missense_variant L596F 1786C>T UCEC-US 1 235972457 235972457 single base substitution G A exon_variant UCEC-US 1 235972457 235972457 single base substitution G A missense_variant A554V 1661C>T UCEC-US 1 235972728 235972728 single base substitution C T exon_variant UCEC-US 1 235972728 235972728 single base substitution C T missense_variant E464K 1390G>A UCEC-US 1 235972773 235972773 single base substitution C T exon_variant UCEC-US 1 235972773 235972773 single base substitution C T missense_variant V449I 1345G>A UCEC-US 1 235972796 235972796 single base substitution C A exon_variant UCEC-US 1 235972796 235972796 single base substitution C A missense_variant G441V 1322G>T UCEC-US 1 235972815 235972815 single base substitution C A exon_variant UCEC-US 1 235972815 235972815 single base substitution C A stop_gained E435* 1303G>T UCEC-US 1 235972935 235972935 single base substitution G A exon_variant UCEC-US 1 235972935 235972935 single base substitution G A missense_variant R395C 1183C>T UCEC-US 1 235973226 235973226 single base substitution C T exon_variant UCEC-US 1 235973226 235973226 single base substitution C T missense_variant D298N 892G>A UCEC-US 1 235973331 235973331 single base substitution A G exon_variant UCEC-US 1 235973331 235973331 single base substitution A G missense_variant S263P 787T>C UCEC-US 1 235973498 235973498 single base substitution C T exon_variant UCEC-US 1 235973498 235973498 single base substitution C T missense_variant R207H 620G>A UCEC-US 1 235973536 235973536 single base substitution C T exon_variant UCEC-US 1 235973536 235973536 single base substitution C T synonymous_variant S194S 582G>A UCEC-US 1 235973575 235973575 single base substitution C A exon_variant UCEC-US 1 235973575 235973575 single base substitution C A missense_variant K181N 543G>T UCEC-US 1 235993653 235993653 single base substitution G A exon_variant UCEC-US 1 235993653 235993653 single base substitution G A missense_variant A22V 65C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-AX-A05Z-01 COSM905917 c.3058G>T p.E1020* Substitution - Nonsense 1:235806078-235806078 - T5 COSM3746868 c.1683A>G p.L561L Substitution - coding silent 1:235809135-235809135 - TCGA-BT-A42C-01 COSM4390543 c.9471C>T p.F3157F Substitution - coding silent 1:235720750-235720750 - MM1S COSM1235519 c.2898G>A p.M966I Substitution - Missense 1:235806238-235806238 - PD4847a COSM5778154 c.3737A>G p.E1246G Substitution - Missense 1:235801073-235801073 - T578 COSM4699646 c.1873G>T p.G625* Substitution - Nonsense 1:235808945-235808945 - Pat_41_B COSM5845913 c.6679C>T p.P2227S Substitution - Missense 1:235759174-235759174 - TCGA-D1-A103-01 COSM905878 c.7973-1G>T p.? Unknown 1:235744158-235744158 - TCGA-DK-A2I4-01 COSM288607 c.7017C>T p.L2339L Substitution - coding silent 1:235757323-235757323 - PDA_079 COSM5002399 c.944G>T p.W315L Substitution - Missense 1:235809874-235809874 - TCGA-A5-A0GA-01 COSM905875 c.8769G>A p.W2923* Substitution - Nonsense 1:235733535-235733535 - T3099 COSM1296024 c.5957G>A p.R1986Q Substitution - Missense 1:235766243-235766243 - HCC108T COSM1601941 c.4055delG p.R1352fs*7 Deletion - Frameshift 1:235793564-235793564 - TCGA-D3-A51J-06 COSM3485574 c.315C>T p.I105I Substitution - coding silent 1:235810503-235810503 - HN_63081 COSM124255 c.2380T>C p.F794L Substitution - Missense 1:235806756-235806756 - ESO-152 COSM1257020 c.4170C>T p.S1390S Substitution - coding silent 1:235792072-235792072 - TCGA-EJ-7125-01 COSM533616 c.10965G>T p.A3655A Substitution - coding silent 1:235677164-235677164 - Au2 COSM5599871 c.1720C>T p.L574L Substitution - coding silent 1:235809098-235809098 - CSCC-31-T COSM4462934 c.1268C>T p.P423L Substitution - Missense 1:235809550-235809550 - HN_62671 COSM124257 c.44A>T p.D15V Substitution - Missense 1:235830374-235830374 - DLBCL824 COSM1581210 c.6214G>A p.V2072I Substitution - Missense 1:235762759-235762759 - 1731645 COSM327846 c.4370A>C p.H1457P Substitution - Missense 1:235791872-235791872 - TCGA-EI-6917-01 COSM905869 c.9319C>T p.R3107C Substitution - Missense 1:235720902-235720902 - HN_62421 COSM124254 c.6799G>C p.D2267H Substitution - Missense 1:235759054-235759054 - PT49 COSM5934330 c.7159C>T p.R2387* Substitution - Nonsense 1:235755548-235755548 - B15-Tumor COSM1748238 c.4866G>T p.K1622N Substitution - Missense 1:235782084-235782084 - CSCC-31-T COSM4562320 c.921G>A p.E307E Substitution - coding silent 1:235809897-235809897 - 1_PRE-TREATMENT COSM1719418 c.7448G>A p.G2483E Substitution - Missense 1:235753056-235753056 - S00833 COSM312677 c.3697G>A p.E1233K Substitution - Missense 1:235802923-235802923 - TCGA-AA-A010-01 COSM282595 c.10379C>A p.P3460H Substitution - Missense 1:235697268-235697268 - HCC011T COSM5820007 c.9548T>A p.L3183Q Substitution - Missense 1:235720673-235720673 - S02277 COSM5682964 c.8264C>T p.A2755V Substitution - Missense 1:235741516-235741516 - TCGA-B5-A0JY-01 COSM905909 c.3664G>A p.E1222K Substitution - Missense 1:235802956-235802956 - TCGA-AA-3715-01 COSM269534 c.5290G>T p.G1764C Substitution - Missense 1:235777233-235777233 - YUPAER COSM5380154 c.8830C>T p.P2944S Substitution - Missense 1:235731149-235731149 - GC8_T COSM146828 c.368A>G p.H123R Substitution - Missense 1:235810450-235810450 - TCGA-IR-A3LH-01 COSM4833038 c.3744C>T p.F1248F Substitution - coding silent 1:235801066-235801066 - TCGA-GC-A3RB-01 COSM1296025 c.4678C>G p.L1560V Substitution - Missense 1:235788711-235788711 - TCGA-BS-A0UF-01 COSM905913 c.3171G>T p.K1057N Substitution - Missense 1:235805965-235805965 - LS411 COSM2000158 c.11322C>T p.T3774T Substitution - coding silent 1:235663024-235663024 - AOCS-093-1-9 COSM3943706 c.7689C>A p.T2563T Substitution - coding silent 1:235751301-235751301 - TCGA-F5-6814-01 COSM3418925 c.1836G>T p.L612F Substitution - Missense 1:235808982-235808982 - TCGA-AP-A051-01 COSM905927 c.1786C>T p.L596F Substitution - Missense 1:235809032-235809032 - TCGA-BR-8680-01 COSM4029744 c.8544G>T p.K2848N Substitution - Missense 1:235733898-235733898 - 2492702 COSM5716228 c.6132C>T p.I2044I Substitution - coding silent 1:235762841-235762841 - TCGA-EE-A181-06 COSM3485573 c.426A>C p.K142N Substitution - Missense 1:235810392-235810392 - RK069_C01 COSM1626908 c.7130C>T p.S2377F Substitution - Missense 1:235755577-235755577 - SNU-283 COSM2000308 c.3740G>A p.G1247D Substitution - Missense 1:235801070-235801070 - TCGA-AP-A051-01 COSM905883 c.7339G>A p.A2447T Substitution - Missense 1:235753165-235753165 - TCGA-HU-A4H4-01 COSM4029766 c.204T>C p.C68C Substitution - coding silent 1:235813050-235813050 - TCGA-22-5489-01 COSM678965 c.1864C>T p.Q622* Substitution - Nonsense 1:235808954-235808954 - TCGA-AO-A0JE-01 COSM425641 c.817G>A p.V273I Substitution - Missense 1:235810001-235810001 - 8031121 COSM3385910 c.4012C>A p.Q1338K Substitution - Missense 1:235793607-235793607 - HCC2998 COSM1668586 c.1407G>T p.L469F Substitution - Missense 1:235809411-235809411 - TCGA-AP-A0LM-01 COSM905926 c.1923T>C p.T641T Substitution - coding silent 1:235808895-235808895 - EGC20 COSM5053247 c.911A>G p.D304G Substitution - Missense 1:235809907-235809907 - SJHGG034_D COSM905876 c.8222G>A p.R2741Q Substitution - Missense 1:235741558-235741558 - pfg020T COSM1639754 c.11155A>G p.I3719V Substitution - Missense 1:235664505-235664505 - TCGA-BR-4361-01 COSM4029761 c.1112C>A p.P371H Substitution - Missense 1:235809706-235809706 - 2492703 COSM5716228 c.6132C>T p.I2044I Substitution - coding silent 1:235762841-235762841 - 473 COSM4438078 c.9567C>G p.L3189L Substitution - coding silent 1:235716772-235716772 - TCGA-AX-A0J0-01 COSM905920 c.2704C>A p.L902I Substitution - Missense 1:235806432-235806432 - TCGA-AG-3890-01 COSM288607 c.7017C>T p.L2339L Substitution - coding silent 1:235757323-235757323 - TCGA-66-2742-01 COSM678979 c.10491G>T p.Q3497H Substitution - Missense 1:235697156-235697156 - YULONE COSM5380153 c.10464C>T p.P3488P Substitution - coding silent 1:235697183-235697183 - HCC2998 COSM1668580 c.11300A>G p.Y3767C Substitution - Missense 1:235663046-235663046 - 88 COSM5014198 c.10878A>T p.K3626N Substitution - Missense 1:235677542-235677542 - Pat_66_A COSM5845918 c.1364T>C p.L455P Substitution - Missense 1:235809454-235809454 - 587376 COSM1214131 c.4055G>T p.R1352I Substitution - Missense 1:235793564-235793564 - AOCS-093-8-4 COSM3943706 c.7689C>A p.T2563T Substitution - coding silent 1:235751301-235751301 - LUAD-RT-S01818 COSM383773 c.8321A>G p.Q2774R Substitution - Missense 1:235741459-235741459 - HCC147T COSM3705647 c.5023+2T>C p.? Unknown 1:235781925-235781925 - TCGA-BR-7717-01 COSM4029767 c.163C>G p.L55V Substitution - Missense 1:235830255-235830255 - TCGA-CZ-5469-01 COSM464185 c.4343T>C p.L1448P Substitution - Missense 1:235791899-235791899 - ESO-0123 COSM1257016 c.2131A>T p.I711F Substitution - Missense 1:235808687-235808687 - T2269 COSM4699645 c.2259C>T p.S753S Substitution - coding silent 1:235808559-235808559 - EGC15 COSM5053245 c.6201C>T p.S2067S Substitution - coding silent 1:235762772-235762772 - TCGA-D1-A16Y-01 COSM905896 c.6078C>T p.Y2026Y Substitution - coding silent 1:235766122-235766122 - TCGA-F5-6814-01 COSM3418926 c.798A>C p.E266D Substitution - Missense 1:235810020-235810020 - TCGA-BS-A0UF-01 COSM905867 c.9607C>T p.R3203C Substitution - Missense 1:235716732-235716732 - SH-0622 COSM1340319 c.575delT p.L192fs*1 Deletion - Frameshift 1:235810243-235810243 - S02234 COSM5675903 c.1551A>T p.S517S Substitution - coding silent 1:235809267-235809267 - TCGA-AP-A051-01 COSM905897 c.5294A>G p.Q1765R Substitution - Missense 1:235777229-235777229 - TCGA-CG-5726-01 COSM4029742 c.9257C>A p.A3086D Substitution - Missense 1:235724086-235724086 - C0074T COSM4136033 c.602C>A p.P201H Substitution - Missense 1:235810216-235810216 - TCGA-CZ-4863-01 COSM464188 c.327A>G p.E109E Substitution - coding silent 1:235810491-235810491 - Pat_41_B COSM5845915 c.6121+1G>A p.? Unknown 1:235766078-235766078 - LUAD-TLLGS COSM347602 c.10962G>T p.L3654L Substitution - coding silent 1:235677167-235677167 - LC_S15 COSM1185794 c.10389G>T p.W3463C Substitution - Missense 1:235697258-235697258 - TCGA-AA-3947-01 COSM272250 c.914_915insA p.N305fs*36 Insertion - Frameshift 1:235809903-235809904 - ESCC_160 COSM3485569 c.1513G>A p.E505K Substitution - Missense 1:235809305-235809305 - CSCC-16-T COSM1340319 c.575delT p.L192fs*1 Deletion - Frameshift 1:235810243-235810243 - LUAD-NYU1021 COSM367987 c.6921A>G p.L2307L Substitution - coding silent 1:235757419-235757419 - B89-12 COSM1748239 c.3974G>A p.S1325N Substitution - Missense 1:235800352-235800352 - 74 COSM327846 c.4370A>C p.H1457P Substitution - Missense 1:235791872-235791872 - TCGA-AN-A046-01 COSM2000224 c.7814C>T p.S2605L Substitution - Missense 1:235746494-235746494 - CSCC-62-T COSM4510249 c.8317C>T p.H2773Y Substitution - Missense 1:235741463-235741463 - 2492703 COSM5599870 c.7269G>A p.Q2423Q Substitution - coding silent 1:235753235-235753235 - PD22361a COSM5790668 c.9465A>T p.R3155R Substitution - coding silent 1:235720756-235720756 - TCGA-GN-A266-06 COSM3485569 c.1513G>A p.E505K Substitution - Missense 1:235809305-235809305 - TCGA-EI-6882-01 COSM3418917 c.9519C>T p.Y3173Y Substitution - coding silent 1:235720702-235720702 - TCGA-EE-A2GO-06 COSM3485552 c.9315G>A p.K3105K Substitution - coding silent 1:235724028-235724028 - KM12 COSM1668582 c.10030G>A p.A3344T Substitution - Missense 1:235709204-235709204 - S02375 COSM5696351 c.5297T>G p.M1766R Substitution - Missense 1:235777226-235777226 - 1N45-VS-1T45 COSM4975736 c.516A>C p.S172S Substitution - coding silent 1:235810302-235810302 - CSCC-11-T COSM4493949 c.4243C>T p.P1415S Substitution - Missense 1:235791999-235791999 - CHC205T COSM3746866 c.5373G>A p.K1791K Substitution - coding silent 1:235777150-235777150 - BD124T COSM5491310 c.11268-5delT p.? Unknown 1:235663083-235663083 - Gp2D COSM2000338 c.1918T>C p.C640R Substitution - Missense 1:235808900-235808900 - TCGA-AX-A05Z-01 COSM905904 c.4305G>T p.K1435N Substitution - Missense 1:235791937-235791937 - TCGA-AD-6895-01 COSM1340300 c.9461G>A p.G3154D Substitution - Missense 1:235720760-235720760 - PD5935a COSM5771996 c.7973-1G>A p.? Unknown 1:235744158-235744158 - TCGA-A6-5661-01 COSM1340295 c.10390A>G p.I3464V Substitution - Missense 1:235697257-235697257 - TCGA-F5-6814-01 COSM3418920 c.5368C>A p.L1790I Substitution - Missense 1:235777155-235777155 - 22T COSM3710646 c.421C>T p.R141* Substitution - Nonsense 1:235810397-235810397 - TCGA-DD-A1EF-01 COSM4915675 c.8259G>A p.S2753S Substitution - coding silent 1:235741521-235741521 - CSCC-41-T COSM4495957 c.4647C>T p.I1549I Substitution - coding silent 1:235788742-235788742 - Pat_41_B COSM5845912 c.8230C>T p.L2744F Substitution - Missense 1:235741550-235741550 - TCGA-IR-A3LH-01 COSM4832842 c.3925C>G p.L1309V Substitution - Missense 1:235800885-235800885 - TCGA-66-2778-01 COSM678977 c.10339G>C p.E3447Q Substitution - Missense 1:235702782-235702782 - TCGA-HU-A4G8-01 COSM4029754 c.3542C>T p.A1181V Substitution - Missense 1:235804517-235804517 - LAU165 COSM234941 c.10800G>C p.T3600T Substitution - coding silent 1:235686949-235686949 - PA182 COSM1162577 c.1075G>A p.A359T Substitution - Missense 1:235809743-235809743 - CHC1700T COSM4800449 c.7593A>G p.G2531G Substitution - coding silent 1:235752039-235752039 - 18195 COSM1296030 c.331A>T p.N111Y Substitution - Missense 1:235810487-235810487 - HCC5T COSM3705648 c.2307G>T p.L769F Substitution - Missense 1:235808511-235808511 - TCGA-37-3783-01 COSM678972 c.5707G>C p.D1903H Substitution - Missense 1:235773919-235773919 - Gp2D COSM4627065 c.7512C>A p.F2504L Substitution - Missense 1:235752120-235752120 - TCGA-AR-A256-01 COSM1473633 c.10449C>A p.V3483V Substitution - coding silent 1:235697198-235697198 - AOCS-064-3-3 COSM3943707 c.7237C>T p.L2413L Substitution - coding silent 1:235753267-235753267 - TCGA-AA-A00N-01 COSM275953 c.2103T>C p.F701F Substitution - coding silent 1:235808715-235808715 - TCGA-BR-7958-01 COSM905882 c.7349T>G p.L2450R Substitution - Missense 1:235753155-235753155 - TCGA-B7-5818-01 COSM4029743 c.8828A>G p.Y2943C Substitution - Missense 1:235731151-235731151 - 2492710 COSM5716985 c.2730T>G p.S910R Substitution - Missense 1:235806406-235806406 - HCC141 COSM1601942 c.801A>G p.K267K Substitution - coding silent 1:235810017-235810017 - PD11399a COSM5795668 c.272A>G p.E91G Substitution - Missense 1:235812982-235812982 - LUAD-RT-S01813 COSM383006 c.139G>C p.V47L Substitution - Missense 1:235830279-235830279 - TCGA-EB-A299-01 COSM3485557 c.6639A>C p.S2213S Substitution - coding silent 1:235759214-235759214 - MN-54 COSM1578615 c.8825A>G p.Y2942C Substitution - Missense 1:235731154-235731154 - CSCC-56-T COSM4539898 c.2750G>A p.R917K Substitution - Missense 1:235806386-235806386 - HCC1395 COSM50242 c.5923-26_5923del27 p.? Unknown 1:235766277-235766303 - HT115 COSM2000212 c.8498C>A p.A2833E Substitution - Missense 1:235734520-235734520 - LUAD-NYU1096 COSM369128 c.3104A>C p.K1035T Substitution - Missense 1:235806032-235806032 - BK0027 COSM4186591 c.3880G>C p.E1294Q Substitution - Missense 1:235800930-235800930 - PD13771a COSM5780432 c.2774A>T p.D925V Substitution - Missense 1:235806362-235806362 - TCGA-HU-A4H8-01 COSM4029751 c.6487G>A p.A2163T Substitution - Missense 1:235759366-235759366 - TCGA-BS-A0U5-01 COSM905907 c.3941G>T p.G1314V Substitution - Missense 1:235800385-235800385 - RK095_C01 COSM3700659 c.5349C>T p.I1783I Substitution - coding silent 1:235777174-235777174 - TCGA-B5-A11E-01 COSM905911 c.3369G>A p.K1123K Substitution - coding silent 1:235805767-235805767 - TCGA-AO-A03M-01 COSM3804434 c.7303G>C p.E2435Q Substitution - Missense 1:235753201-235753201 - Br27P COSM40287 c.4061G>A p.C1354Y Substitution - Missense 1:235793558-235793558 - TCGA-AP-A0LQ-01 COSM905910 c.3470C>A p.A1157E Substitution - Missense 1:235804589-235804589 - TCGA-BR-8485-01 COSM4029745 c.8332C>T p.R2778* Substitution - Nonsense 1:235741448-235741448 - TCGA-DD-A73B-01 COSM4921160 c.7605T>C p.N2535N Substitution - coding silent 1:235752027-235752027 - TCGA-AZ-4315-01 COSM1340311 c.3119C>A p.S1040Y Substitution - Missense 1:235806017-235806017 - TCGA-BR-8589-01 COSM4029739 c.9397A>T p.N3133Y Substitution - Missense 1:235720824-235720824 - TCGA-FD-A3B5-01 COSM1296021 c.8001G>C p.L2667F Substitution - Missense 1:235744129-235744129 - Br27P COSM40286 c.10772C>T p.A3591V Substitution - Missense 1:235686977-235686977 - OSCC-GB_00980111 COSM4882150 c.4831G>T p.G1611W Substitution - Missense 1:235787231-235787231 - PD9756a COSM5794712 c.10271G>C p.G3424A Substitution - Missense 1:235702850-235702850 - PD4203a COSM162304 c.2050G>A p.E684K Substitution - Missense 1:235808768-235808768 - TCGA-33-4547-01 COSM678970 c.4958C>A p.S1653* Substitution - Nonsense 1:235781992-235781992 - sysucc-311T COSM5478209 c.7305G>T p.E2435D Substitution - Missense 1:235753199-235753199 - S02360 COSM5695884 c.4204G>T p.A1402S Substitution - Missense 1:235792038-235792038 - sysucc-1163T COSM1340304 c.6348G>A p.T2116T Substitution - coding silent 1:235759505-235759505 - PT34 COSM5910193 c.3955C>T p.L1319F Substitution - Missense 1:235800371-235800371 - TCGA-BP-4782-01 COSM464182 c.8108A>G p.K2703R Substitution - Missense 1:235744022-235744022 - TCGA-DK-A2I1-01 COSM1296023 c.6643G>A p.D2215N Substitution - Missense 1:235759210-235759210 - SJHGG028_D COSM4969559 c.10025G>A p.R3342Q Substitution - Missense 1:235709209-235709209 - TCGA-DR-A0ZM-01 COSM459535 c.4295C>T p.S1432L Substitution - Missense 1:235791947-235791947 - 8066738 COSM3771659 c.685C>T p.P229S Substitution - Missense 1:235810133-235810133 - PD6763a COSM1638080 c.10154G>A p.G3385E Substitution - Missense 1:235702967-235702967 - YUBER COSM1689993 c.6091C>T p.P2031S Substitution - Missense 1:235766109-235766109 - TCGA-GU-A42R-01 COSM3789679 c.586C>A p.P196T Substitution - Missense 1:235810232-235810232 - BN23T COSM3705645 c.10979C>T p.P3660L Substitution - Missense 1:235677150-235677150 - TCGA-F1-A448-01 COSM4029755 c.3393+2T>C p.? Unknown 1:235805741-235805741 - TCGA-AX-A05Z-01 COSM905935 c.787T>C p.S263P Substitution - Missense 1:235810031-235810031 - TCGA-BR-8589-01 COSM4029768 c.150A>C p.R50R Substitution - coding silent 1:235830268-235830268 - ESCC_40 COSM5629285 c.5789G>T p.G1930V Substitution - Missense 1:235770293-235770293 - TCGA-CJ-5672-01 COSM464186 c.2661G>A p.K887K Substitution - coding silent 1:235806475-235806475 - CLL119 COSM1290145 c.302C>T p.S101L Substitution - Missense 1:235810516-235810516 - TCGA-RC-A7S9-01 COSM4940286 c.4342C>G p.L1448V Substitution - Missense 1:235791900-235791900 - TCGA-FU-A23K-01 COSM459534 c.3238G>C p.A1080P Substitution - Missense 1:235805898-235805898 - ESO-887 COSM1257022 c.9412G>T p.G3138W Substitution - Missense 1:235720809-235720809 - 2492701 COSM5599871 c.1720C>T p.L574L Substitution - coding silent 1:235809098-235809098 - TCGA-CA-6717-01 COSM1340315 c.1767A>C p.K589N Substitution - Missense 1:235809051-235809051 - HCC2998 COSM1668580 c.11300A>G p.Y3767C Substitution - Missense 1:235663046-235663046 - TCGA-B5-A0JY-01 COSM905871 c.9052C>T p.R3018* Substitution - Nonsense 1:235729650-235729650 - 3T COSM3733936 c.9670C>T p.P3224S Substitution - Missense 1:235715315-235715315 - TCGA-F5-6814-01 COSM3418922 c.4204G>A p.A1402T Substitution - Missense 1:235792038-235792038 - T3064 COSM4699648 c.439C>T p.R147C Substitution - Missense 1:235810379-235810379 - TCGA-23-1123-01 COSM75326 c.3624G>T p.Q1208H Substitution - Missense 1:235802996-235802996 - HCC120 COSM3705646 c.9839G>T p.R3280L Substitution - Missense 1:235712143-235712143 - pfg052T COSM4764851 c.1201T>G p.L401V Substitution - Missense 1:235809617-235809617 - M013 COSM1738437 c.340T>A p.S114T Substitution - Missense 1:235810478-235810478 - 15 COSM2000366 c.433C>T p.R145* Substitution - Nonsense 1:235810385-235810385 - TCGA-AO-A128-01 COSM3804429 c.9990G>A p.A3330A Substitution - coding silent 1:235709244-235709244 - TCGA-AN-A046-01 COSM905932 c.1303G>T p.E435* Substitution - Nonsense 1:235809515-235809515 - ESO-717 COSM1242487 c.6690A>G p.L2230L Substitution - coding silent 1:235759163-235759163 - TCGA-A6-5661-01 COSM253020 c.5461-3delT p.? Unknown 1:235775089-235775089 - TCGA-ER-A19O-06 COSM3485570 c.878T>C p.L293P Substitution - Missense 1:235809940-235809940 - TCGA-BR-8680-01 COSM4029760 c.1203A>G p.L401L Substitution - coding silent 1:235809615-235809615 - CSCC-62-T COSM4505074 c.6838C>A p.L2280I Substitution - Missense 1:235759015-235759015 - TCGA-D1-A174-01 COSM905938 c.543G>T p.K181N Substitution - Missense 1:235810275-235810275 - PD4116a COSM219497 c.6168G>C p.R2056S Substitution - Missense 1:235762805-235762805 - HCC152T COSM3705649 c.1690G>A p.A564T Substitution - Missense 1:235809128-235809128 - ESO-120 COSM1257018 c.2826A>G p.P942P Substitution - coding silent 1:235806310-235806310 - HCC138T COSM5819037 c.8317C>A p.H2773N Substitution - Missense 1:235741463-235741463 - TCGA-HG-A2PA-01 COSM4823629 c.484C>A p.Q162K Substitution - Missense 1:235810334-235810334 - TCGA-BS-A0UV-01 COSM905923 c.2438G>T p.R813L Substitution - Missense 1:235806698-235806698 - TCGA-D1-A17H-01 COSM905858 c.11093A>G p.H3698R Substitution - Missense 1:235664567-235664567 - TCGA-FW-A3R5-06 COSM3864851 c.3215C>T p.S1072F Substitution - Missense 1:235805921-235805921 - TCGA-AO-A128-01 COSM5832524 c.2688_2689insG p.T897fs*15 Insertion - Frameshift 1:235806447-235806448 - 19 COSM5745830 c.10214A>G p.K3405R Substitution - Missense 1:235702907-235702907 - TCGA-CG-4442-01 COSM4029736 c.10948T>G p.Y3650D Substitution - Missense 1:235677181-235677181 - LC_S15 COSM1185795 c.7610A>G p.K2537R Substitution - Missense 1:235752022-235752022 - TCGA-AP-A051-01 COSM905866 c.9646C>T p.R3216C Substitution - Missense 1:235715339-235715339 - TCGA-B5-A11E-01 COSM905860 c.10802C>T p.P3601L Substitution - Missense 1:235677618-235677618 - J33_T COSM3977217 c.9926-1G>A p.? Unknown 1:235709309-235709309 - PD24225a COSM5784757 c.7125A>G p.G2375G Substitution - coding silent 1:235755582-235755582 - TCGA-AM-5821-01 COSM3751013 c.7137A>C p.L2379L Substitution - coding silent 1:235755570-235755570 - TCGA-A6-6141-01 COSM261876 c.985C>T p.R329* Substitution - Nonsense 1:235809833-235809833 - TCGA-AC-A23H-01 COSM3804432 c.9475G>A p.D3159N Substitution - Missense 1:235720746-235720746 - TCGA-CD-8529-01 COSM4029765 c.241C>G p.P81A Substitution - Missense 1:235813013-235813013 - TCGA-BR-8680-01 COSM905898 c.5143G>T p.E1715* Substitution - Nonsense 1:235780936-235780936 - PT08_1 COSM5892611 c.5878G>A p.A1960T Substitution - Missense 1:235770204-235770204 - 3P3 COSM3733936 c.9670C>T p.P3224S Substitution - Missense 1:235715315-235715315 - HN_62860 COSM124256 c.577A>C p.T193P Substitution - Missense 1:235810241-235810241 - 2293776 COSM4607435 c.3688G>T p.E1230* Substitution - Nonsense 1:235802932-235802932 - TCGA-AP-A056-01 COSM905898 c.5143G>T p.E1715* Substitution - Nonsense 1:235780936-235780936 - TCGA-B5-A0JZ-01 COSM905881 c.7462A>G p.I2488V Substitution - Missense 1:235752170-235752170 - TCGA-14-1455 COSM2155520 c.7832_7833delGT p.R2611fs*5 Deletion - Frameshift 1:235746475-235746476 - TCGA-DK-A3IN-01 COSM3789674 c.8857G>A p.E2953K Substitution - Missense 1:235731122-235731122 - TCGA-AP-A0LM-01 COSM905931 c.1322G>T p.G441V Substitution - Missense 1:235809496-235809496 - Pat_59_B COSM5845914 c.6368G>A p.G2123E Substitution - Missense 1:235759485-235759485 - SS6003312 COSM3716889 c.5834C>T p.A1945V Substitution - Missense 1:235770248-235770248 - TCGA-EE-A2MS-06 COSM3485571 c.760C>T p.P254S Substitution - Missense 1:235810058-235810058 - TCGA-Q1-A73O-01 COSM4836355 c.10764C>T p.V3588V Substitution - coding silent 1:235686985-235686985 - TCGA-BG-A0VW-01 COSM905906 c.4011C>T p.C1337C Substitution - coding silent 1:235793608-235793608 - TCGA-06-0122 COSM2149205 c.3242_3244delCTG p.T1081_E1082>K Complex - deletion inframe 1:235805892-235805894 - TCGA-BR-6706-01 COSM4029748 c.7170A>C p.Q2390H Substitution - Missense 1:235755537-235755537 - AOCS-001-1-7 COSM3943709 c.2836C>A p.L946I Substitution - Missense 1:235806300-235806300 - TCGA-AO-A03N-01 COSM75327 c.2509C>T p.P837S Substitution - Missense 1:235806627-235806627 - TCGA-A5-A0GP-01 COSM905891 c.6946C>A p.L2316I Substitution - Missense 1:235757394-235757394 - TCGA-DU-7299-01 COSM3966371 c.3877T>G p.F1293V Substitution - Missense 1:235800933-235800933 - 01-P8014 COSM4577037 c.3153A>G p.E1051E Substitution - coding silent 1:235805983-235805983 - TCGA-DD-A4NQ-01 COSM4941072 c.495C>A p.T165T Substitution - coding silent 1:235810323-235810323 - OSCC-GB_00430111 COSM3711275 c.5156G>T p.C1719F Substitution - Missense 1:235780923-235780923 - Pat_41_B COSM5845910 c.10268C>T p.P3423L Substitution - Missense 1:235702853-235702853 - LUAD-F00057 COSM339393 c.10649G>A p.S3550N Substitution - Missense 1:235693402-235693402 - WA19 COSM240563 c.1459_1468del10 p.K487fs*77 Deletion - Frameshift 1:235809350-235809359 - TCGA-CG-5721-01 COSM4029735 c.11075A>G p.N3692S Substitution - Missense 1:235664585-235664585 - TCGA-BP-5191-01 COSM464183 c.7201T>G p.F2401V Substitution - Missense 1:235755506-235755506 - YUPROST COSM1685417 c.10119A>G p.Q3373Q Substitution - coding silent 1:235709115-235709115 - CSCC-7-T COSM4548920 c.4603G>A p.G1535R Substitution - Missense 1:235788786-235788786 - ESO-0292 COSM1241392 c.1659_1660delTG p.A554fs*25 Deletion - Frameshift 1:235809158-235809159 - TCGA-EE-A2MJ-06 COSM3485547 c.10978C>T p.P3660S Substitution - Missense 1:235677151-235677151 - TCGA-06-5418 COSM2149205 c.3242_3244delCTG p.T1081_E1082>K Complex - deletion inframe 1:235805892-235805894 - T3535 COSM905894 c.6305G>A p.R2102H Substitution - Missense 1:235759548-235759548 - 2492700 COSM5599871 c.1720C>T p.L574L Substitution - coding silent 1:235809098-235809098 - TCGA-AX-A05Z-01 COSM905932 c.1303G>T p.E435* Substitution - Nonsense 1:235809515-235809515 - TCGA-B5-A11E-01 COSM905919 c.2724C>T p.C908C Substitution - coding silent 1:235806412-235806412 - TCGA-A2-A0CR-01 COSM3804436 c.6709C>T p.Q2237* Substitution - Nonsense 1:235759144-235759144 - CSCC-27-T COSM4483466 c.2703C>T p.F901F Substitution - coding silent 1:235806433-235806433 - 2492702 COSM5599870 c.7269G>A p.Q2423Q Substitution - coding silent 1:235753235-235753235 - H2171 COSM312676 c.440G>T p.R147L Substitution - Missense 1:235810378-235810378 - WA32 COSM240562 c.8560G>C p.E2854Q Substitution - Missense 1:235733882-235733882 - TCGA-MH-A55Z-01 COSM3984859 c.9357C>T p.L3119L Substitution - coding silent 1:235720864-235720864 - PD6047a COSM5796538 c.642T>G p.T214T Substitution - coding silent 1:235810176-235810176 - TCGA-D3-A5GR-06 COSM3485564 c.3555G>A p.K1185K Substitution - coding silent 1:235804504-235804504 - TCGA-AX-A0J0-01 COSM905924 c.2304C>T p.C768C Substitution - coding silent 1:235808514-235808514 - TCGA-AA-3663-01 COSM1340317 c.1078G>A p.A360T Substitution - Missense 1:235809740-235809740 - SNU-C2B COSM2000232 c.7636G>A p.V2546I Substitution - Missense 1:235751354-235751354 - PD4137a COSM162305 c.1886C>A p.S629* Substitution - Nonsense 1:235808932-235808932 - TCGA-FT-A3EE-01 COSM3789673 c.9334C>G p.H3112D Substitution - Missense 1:235720887-235720887 - CSCC-11-T COSM4483471 c.2704C>T p.L902F Substitution - Missense 1:235806432-235806432 - Pat_41_B COSM3984858 c.10024C>T p.R3342W Substitution - Missense 1:235709210-235709210 - PCA17-1 COSM210418 c.2413G>A p.E805K Substitution - Missense 1:235806723-235806723 - 2521259 COSM5889541 c.8732G>A p.G2911E Substitution - Missense 1:235733572-235733572 - SJHGG118_A COSM4972028 c.4614T>G p.H1538Q Substitution - Missense 1:235788775-235788775 - ESCC_BICR_052T COSM5434637 c.8251A>G p.I2751V Substitution - Missense 1:235741529-235741529 - LUAD_E01419 COSM354855 c.10133T>G p.F3378C Substitution - Missense 1:235709101-235709101 - B80 COSM1748240 c.2979A>C p.L993F Substitution - Missense 1:235806157-235806157 - CSCC-31-T COSM4566995 c.5320_5321CC>TT p.P1774F Substitution - Missense 1:235777202-235777203 - 3N01-VS-3T01 COSM4978243 c.3509G>A p.G1170E Substitution - Missense 1:235804550-235804550 - LUAD-NYU739 COSM376232 c.10896A>C p.I3632I Substitution - coding silent 1:235677524-235677524 - TCGA-GV-A3QI-01 COSM1296027 c.3882G>A p.E1294E Substitution - coding silent 1:235800928-235800928 - Pat_59_A COSM5845916 c.5380C>A p.Q1794K Substitution - Missense 1:235777143-235777143 - AOCS-135-3-1 COSM3943708 c.5800A>G p.T1934A Substitution - Missense 1:235770282-235770282 - BCM617T COSM4955981 c.6790A>G p.S2264G Substitution - Missense 1:235759063-235759063 - ICC010T COSM5813939 c.1393G>A p.A465T Substitution - Missense 1:235809425-235809425 - TCGA-D5-6928-01 COSM1340318 c.1056T>A p.N352K Substitution - Missense 1:235809762-235809762 - TCGA-AX-A05Z-01 COSM905915 c.3116T>C p.L1039S Substitution - Missense 1:235806020-235806020 - HN_62984 COSM124253 c.9053G>A p.R3018Q Substitution - Missense 1:235729649-235729649 - T578 COSM4699642 c.5419G>A p.E1807K Substitution - Missense 1:235777104-235777104 - HCC1937 COSM50334 c.5512A>G p.I1838V Substitution - Missense 1:235775035-235775035 - TCGA-ER-A3PL-06 COSM3485548 c.10557G>A p.K3519K Substitution - coding silent 1:235697090-235697090 - TCGA-BK-A0C9-01 COSM905873 c.8897A>G p.Y2966C Substitution - Missense 1:235731082-235731082 - RK047_C01 COSM1626909 c.6841G>A p.G2281S Substitution - Missense 1:235759012-235759012 - TCGA-AP-A059-01 COSM905887 c.7126T>C p.F2376L Substitution - Missense 1:235755581-235755581 - PD6754a COSM1637821 c.6713G>A p.R2238Q Substitution - Missense 1:235759140-235759140 - TCGA-D1-A16S-01 COSM905922 c.2447C>T p.S816F Substitution - Missense 1:235806689-235806689 - ESO-913 COSM1257023 c.10425C>T p.S3475S Substitution - coding silent 1:235697222-235697222 - PDA_104 COSM5003721 c.7056_7057insT p.K2353fs*1 Insertion - Frameshift 1:235757283-235757284 - TCGA-EE-A29B-06 COSM3485565 c.3374A>G p.E1125G Substitution - Missense 1:235805762-235805762 - TCGA-F5-6814-01 COSM3418923 c.2716T>G p.F906V Substitution - Missense 1:235806420-235806420 - TCGA-D1-A16Y-01 COSM905864 c.9853G>T p.E3285* Substitution - Nonsense 1:235712129-235712129 - TCGA-A2-A25E-01 COSM1473634 c.9136A>G p.N3046D Substitution - Missense 1:235728102-235728102 - TCGA-BT-A3PJ-01 COSM3789678 c.1481C>T p.S494L Substitution - Missense 1:235809337-235809337 - TCGA-B5-A0JY-01 COSM905892 c.6402T>C p.N2134N Substitution - coding silent 1:235759451-235759451 - TCGA-FS-A1ZM-06 COSM3485572 c.602C>T p.P201L Substitution - Missense 1:235810216-235810216 - TCGA-AA-3510-01 COSM3689447 c.2570C>A p.S857Y Substitution - Missense 1:235806566-235806566 - HCT8 COSM4633634 c.4277T>C p.L1426S Substitution - Missense 1:235791965-235791965 - LUAD-CHTN-Z4716A COSM361449 c.8949T>C p.D2983D Substitution - coding silent 1:235730942-235730942 - YUWAND COSM1689995 c.4598A>G p.E1533G Substitution - Missense 1:235788791-235788791 - 2492702 COSM5599871 c.1720C>T p.L574L Substitution - coding silent 1:235809098-235809098 - SJDOSTEOS005 COSM3771658 c.5956C>T p.R1986* Substitution - Nonsense 1:235766244-235766244 - TCGA-13-0903-01 COSM75327 c.2509C>T p.P837S Substitution - Missense 1:235806627-235806627 - TCGA-EE-A182-06 COSM3485567 c.1778T>C p.I593T Substitution - Missense 1:235809040-235809040 - TCGA-EE-A2GC-06 COSM3485553 c.9159T>C p.S3053S Substitution - coding silent 1:235728079-235728079 - SW1222 COSM4654702 c.8069T>C p.I2690T Substitution - Missense 1:235744061-235744061 - HCT116 COSM2000343 c.1671C>T p.C557C Substitution - coding silent 1:235809147-235809147 - TCGA-23-2072-01 COSM71520 c.10838A>G p.Y3613C Substitution - Missense 1:235677582-235677582 - 0127_CRUK_PC_0127_T1_DNA COSM1340304 c.6348G>A p.T2116T Substitution - coding silent 1:235759505-235759505 - 20 COSM5732176 c.6676C>T p.R2226* Substitution - Nonsense 1:235759177-235759177 - TCGA-DJ-A2PP-01 COSM367987 c.6921A>G p.L2307L Substitution - coding silent 1:235757419-235757419 - LUAD-D01382 COSM337073 c.2956G>A p.G986S Substitution - Missense 1:235806180-235806180 - P149 COSM253020 c.5461-3delT p.? Unknown 1:235775089-235775089 - T70 COSM1177965 c.9942G>A p.V3314V Substitution - coding silent 1:235709292-235709292 - CHC205T COSM3746868 c.1683A>G p.L561L Substitution - coding silent 1:235809135-235809135 - TC32 COSM4577036 c.10235G>A p.R3412H Substitution - Missense 1:235702886-235702886 - TCGA-EE-A29S-06 COSM3485556 c.6666C>T p.S2222S Substitution - coding silent 1:235759187-235759187 - TCGA-AX-A0J1-01 COSM905894 c.6305G>A p.R2102H Substitution - Missense 1:235759548-235759548 - CHC1700T COSM4800449 c.7593A>G p.G2531G Substitution - coding silent 1:235752039-235752039 - CSCC-27-T COSM4510037 c.8258C>T p.S2753L Substitution - Missense 1:235741522-235741522 - PT33 COSM5907949 c.11378C>T p.S3793F Substitution - Missense 1:235662968-235662968 - sysucc-311T COSM5478210 c.1759G>T p.D587Y Substitution - Missense 1:235809059-235809059 - TCGA-D1-A17Q-01 COSM905870 c.9161C>T p.S3054L Substitution - Missense 1:235728077-235728077 - TCGA-D3-A51G-06 COSM1601942 c.801A>G p.K267K Substitution - coding silent 1:235810017-235810017 - TCGA-AM-5821-01 COSM3689446 c.3507C>T p.L1169L Substitution - coding silent 1:235804552-235804552 - TCGA-AG-A002-01 COSM261876 c.985C>T p.R329* Substitution - Nonsense 1:235809833-235809833 - SA231 COSM212708 c.10341G>C p.E3447D Substitution - Missense 1:235702780-235702780 - TCGA-EJ-5531-01 COSM1127103 c.10411G>A p.E3471K Substitution - Missense 1:235697236-235697236 - T2269 COSM3710646 c.421C>T p.R141* Substitution - Nonsense 1:235810397-235810397 - TCGA-CD-A4MI-01 COSM4029737 c.10253C>T p.A3418V Substitution - Missense 1:235702868-235702868 - TCGA-12-3649-01 COSM3400475 c.10192C>T p.R3398* Substitution - Nonsense 1:235702929-235702929 - DLD1 COSM4622595 c.7631T>A p.M2544K Substitution - Missense 1:235751359-235751359 - TCGA-A5-A0G9-01 COSM905914 c.3140C>A p.P1047H Substitution - Missense 1:235805996-235805996 - S00838 COSM5661357 c.11002G>A p.E3668K Substitution - Missense 1:235677127-235677127 - TCGA-AP-A051-01 COSM905925 c.2082G>T p.K694N Substitution - Missense 1:235808736-235808736 - I2L-P19Ta-Tumor-Organoid COSM5353010 c.5784+1G>A p.? Unknown 1:235773841-235773841 - TCGA-BS-A0UF-01 COSM905888 c.7102G>T p.D2368Y Substitution - Missense 1:235755605-235755605 - T3724 COSM905914 c.3140C>A p.P1047H Substitution - Missense 1:235805996-235805996 - 2318492 COSM4777099 c.6946C>G p.L2316V Substitution - Missense 1:235757394-235757394 - BICR_22 COSM2000169 c.10845C>G p.H3615Q Substitution - Missense 1:235677575-235677575 - 61 COSM5735905 c.10517G>A p.G3506D Substitution - Missense 1:235697130-235697130 - TCGA-EE-A2GR-06 COSM3485546 c.11189T>G p.I3730S Substitution - Missense 1:235664471-235664471 - T3091 COSM4699640 c.6872G>A p.S2291N Substitution - Missense 1:235758981-235758981 - S01578 COSM312678 c.4939A>G p.M1647V Substitution - Missense 1:235782011-235782011 - TCGA-AX-A05Z-01 COSM905882 c.7349T>G p.L2450R Substitution - Missense 1:235753155-235753155 - TCGA-ER-A19F-06 COSM1257023 c.10425C>T p.S3475S Substitution - coding silent 1:235697222-235697222 - 479 COSM4439028 c.2830A>G p.I944V Substitution - Missense 1:235806306-235806306 - BRC41 COSM5025543 c.1573A>T p.K525* Substitution - Nonsense 1:235809245-235809245 - SC_9081 COSM5571994 c.2725G>A p.V909I Substitution - Missense 1:235806411-235806411 - TCGA-18-3414-01 COSM678980 c.10941-2A>T p.? Unknown 1:235677190-235677190 - TCGA-AZ-6598-01 COSM1340291 c.11086G>A p.V3696I Substitution - Missense 1:235664574-235664574 - STC252 COSM5053244 c.7837G>A p.V2613M Substitution - Missense 1:235746471-235746471 - PT08_2 COSM5892611 c.5878G>A p.A1960T Substitution - Missense 1:235770204-235770204 - T2269 COSM4699639 c.8589A>C p.K2863N Substitution - Missense 1:235733853-235733853 - TCGA-AA-A010-01 COSM282596 c.5177T>G p.F1726C Substitution - Missense 1:235780902-235780902 - TCGA-BH-A0B6-01 COSM2000223 c.7819C>T p.L2607L Substitution - coding silent 1:235746489-235746489 - TCGA-D1-A17Q-01 COSM905869 c.9319C>T p.R3107C Substitution - Missense 1:235720902-235720902 - TCGA-K4-A3WU-01 COSM3789677 c.1994C>T p.S665L Substitution - Missense 1:235808824-235808824 - TCGA-FS-A1Z3-06 COSM3485563 c.4175C>A p.S1392* Substitution - Nonsense 1:235792067-235792067 - ESO-120 COSM1257017 c.7128T>C p.F2376F Substitution - coding silent 1:235755579-235755579 - AOCS-064-1-6 COSM3943707 c.7237C>T p.L2413L Substitution - coding silent 1:235753267-235753267 - TCGA-25-1313-01 COSM71521 c.1781C>A p.P594H Substitution - Missense 1:235809037-235809037 - 2492700 COSM5599870 c.7269G>A p.Q2423Q Substitution - coding silent 1:235753235-235753235 - TCGA-D8-A1XK-01 COSM3804433 c.8332C>G p.R2778G Substitution - Missense 1:235741448-235741448 - HCC147 COSM3705647 c.5023+2T>C p.? Unknown 1:235781925-235781925 - HCC49T COSM1601940 c.8600A>G p.N2867S Substitution - Missense 1:235733842-235733842 - PD8621a COSM5789293 c.9355C>T p.L3119F Substitution - Missense 1:235720866-235720866 - Gp5D COSM2000338 c.1918T>C p.C640R Substitution - Missense 1:235808900-235808900 - 308_T COSM3977220 c.3940G>A p.G1314R Substitution - Missense 1:235800386-235800386 - LUAD-D01603 COSM337652 c.6296A>G p.H2099R Substitution - Missense 1:235759557-235759557 - HCC97T COSM678964 c.1788C>G p.L596L Substitution - coding silent 1:235809030-235809030 - 587378 COSM1214130 c.10211T>C p.I3404T Substitution - Missense 1:235702910-235702910 - ZZUFHECRKL-G045T COSM2000158 c.11322C>T p.T3774T Substitution - coding silent 1:235663024-235663024 - TCGA-F5-6814-01 COSM3418918 c.8110G>T p.E2704* Substitution - Nonsense 1:235744020-235744020 - TCGA-E5-A2PC-01 COSM1296030 c.331A>T p.N111Y Substitution - Missense 1:235810487-235810487 - HCC2998 COSM1668586 c.1407G>T p.L469F Substitution - Missense 1:235809411-235809411 - 2290930 COSM4439843 c.377G>A p.G126E Substitution - Missense 1:235810441-235810441 - TCGA-EB-A5UM-01 COSM3485558 c.6446C>G p.S2149C Substitution - Missense 1:235759407-235759407 - RK135_C01 COSM3741111 c.11274A>G p.T3758T Substitution - coding silent 1:235663072-235663072 - TCGA-CH-5739-01 COSM1470246 c.4755T>C p.N1585N Substitution - coding silent 1:235787307-235787307 - HCC152 COSM3705649 c.1690G>A p.A564T Substitution - Missense 1:235809128-235809128 - TCGA-HU-A4GN-01 COSM4029747 c.7302A>G p.I2434M Substitution - Missense 1:235753202-235753202 - TCGA-46-6025-01 COSM678963 c.1703G>T p.S568I Substitution - Missense 1:235809115-235809115 - HCC080T COSM5810525 c.9859A>G p.M3287V Substitution - Missense 1:235712123-235712123 - TCGA-BR-6452-01 COSM4029752 c.6292G>A p.A2098T Substitution - Missense 1:235759561-235759561 - DLBCL799 COSM1581212 c.452A>G p.H151R Substitution - Missense 1:235810366-235810366 - YUAKER COSM1689996 c.4427C>T p.S1476F Substitution - Missense 1:235791815-235791815 - ESO-0292 COSM1241390 c.2102T>C p.F701S Substitution - Missense 1:235808716-235808716 - 587374 COSM1214133 c.43G>A p.D15N Substitution - Missense 1:235830375-235830375 - TCGA-BH-A18G-01 COSM3804427 c.10624G>A p.A3542T Substitution - Missense 1:235693427-235693427 - 1_RESISTANT COSM1719419 c.1586C>T p.S529F Substitution - Missense 1:235809232-235809232 - BB14T COSM50335 c.9485A>G p.Q3162R Substitution - Missense 1:235720736-235720736 - DLD1 COSM2000278 c.5113G>T p.V1705F Substitution - Missense 1:235780966-235780966 - RMS2051 COSM5880686 c.1356G>A p.M452I Substitution - Missense 1:235809462-235809462 - SA214 COSM213984 c.4398G>A p.W1466* Substitution - Nonsense 1:235791844-235791844 - OV207 COSM253020 c.5461-3delT p.? Unknown 1:235775089-235775089 - T2939 COSM4699647 c.440G>A p.R147H Substitution - Missense 1:235810378-235810378 - TCGA-D8-A27G-01 COSM3804441 c.3289G>A p.E1097K Substitution - Missense 1:235805847-235805847 - TCGA-66-2785-01 COSM678973 c.5989G>T p.A1997S Substitution - Missense 1:235766211-235766211 - TCGA-BS-A0UV-01 COSM905912 c.3196G>A p.E1066K Substitution - Missense 1:235805940-235805940 - TCGA-B0-4813-01 COSM3360747 c.2130G>T p.Q710H Substitution - Missense 1:235808688-235808688 - TCGA-AX-A1C8-01 COSM905939 c.346A>G p.R116G Substitution - Missense 1:235810472-235810472 - TCGA-A8-A09Z-01 COSM3804438 c.4917T>C p.S1639S Substitution - coding silent 1:235782033-235782033 - ESCC_BICR_042T COSM5443628 c.8551G>A p.E2851K Substitution - Missense 1:235733891-235733891 - sysucc-1397T COSM5473371 c.3369G>T p.K1123N Substitution - Missense 1:235805767-235805767 - 136 COSM145604 c.5519C>T p.S1840L Substitution - Missense 1:235775028-235775028 - TCGA-DI-A0WH-01 COSM905879 c.7831C>T p.R2611C Substitution - Missense 1:235746477-235746477 - Gp2D COSM4627064 c.10527G>A p.R3509R Substitution - coding silent 1:235697120-235697120 - TCGA-B5-A11E-01 COSM905936 c.620G>A p.R207H Substitution - Missense 1:235810198-235810198 - TCGA-RA-A741-01 COSM4818888 c.4665C>A p.P1555P Substitution - coding silent 1:235788724-235788724 - LP6007508-DNA_A01 COSM5951580 c.7118A>G p.N2373S Substitution - Missense 1:235755589-235755589 - LUAD-S01315 COSM345007 c.10849G>A p.E3617K Substitution - Missense 1:235677571-235677571 - Pat_45_B COSM5845919 c.136C>T p.L46F Substitution - Missense 1:235830282-235830282 - TCGA-AY-6197-01 COSM1340293 c.10697A>G p.Y3566C Substitution - Missense 1:235693354-235693354 - BD57T COSM253020 c.5461-3delT p.? Unknown 1:235775089-235775089 - 313 COSM1741942 c.5330C>G p.S1777* Substitution - Nonsense 1:235777193-235777193 - BD72T COSM5511663 c.2316C>T p.D772D Substitution - coding silent 1:235808502-235808502 - BD183T COSM5508001 c.9740T>G p.L3247R Substitution - Missense 1:235715245-235715245 - CSCC-2-T COSM4510871 c.8504C>A p.T2835K Substitution - Missense 1:235734514-235734514 - TCGA-D7-6521-01 COSM4029764 c.619C>T p.R207C Substitution - Missense 1:235810199-235810199 - TCGA-EE-A3JB-06 COSM4898713 c.4069G>A p.E1357K Substitution - Missense 1:235793550-235793550 - TCGA-60-2698-01 COSM678971 c.5039C>G p.S1680* Substitution - Nonsense 1:235781040-235781040 - TCGA-HU-A4GN-01 COSM4029750 c.7044A>G p.Q2348Q Substitution - coding silent 1:235757296-235757296 - TCGA-RP-A693-06 COSM4895135 c.3298C>T p.L1100F Substitution - Missense 1:235805838-235805838 - 1_PRE-TREATMENT COSM1719419 c.1586C>T p.S529F Substitution - Missense 1:235809232-235809232 - 1115202 COSM5567324 c.3845G>T p.S1282I Substitution - Missense 1:235800965-235800965 - TCGA-EI-6917-01 COSM3418919 c.6096G>A p.T2032T Substitution - coding silent 1:235766104-235766104 - LUAD-F00134 COSM339968 c.5837A>G p.D1946G Substitution - Missense 1:235770245-235770245 - TCGA-BS-A0UV-01 COSM905893 c.6388G>A p.D2130N Substitution - Missense 1:235759465-235759465 - RK216_C01 COSM3741113 c.337A>T p.S113C Substitution - Missense 1:235810481-235810481 - 43T COSM3711275 c.5156G>T p.C1719F Substitution - Missense 1:235780923-235780923 - 1N62-VS-1T62 COSM4977829 c.11143G>C p.E3715Q Substitution - Missense 1:235664517-235664517 - CHC892T COSM4797790 c.10088G>A p.G3363E Substitution - Missense 1:235709146-235709146 - LP6005334-DNA_E03 COSM4412957 c.3070T>C p.L1024L Substitution - coding silent 1:235806066-235806066 - TCGA-B0-4815-01 COSM464181 c.8268C>T p.H2756H Substitution - coding silent 1:235741512-235741512 - TCGA-DK-A3IU-01 COSM3789676 c.2613C>T p.L871L Substitution - coding silent 1:235806523-235806523 - CSCC-6-T COSM4390543 c.9471C>T p.F3157F Substitution - coding silent 1:235720750-235720750 - TCGA-AZ-6598-01 COSM1340316 c.1659T>C p.C553C Substitution - coding silent 1:235809159-235809159 - TCGA-BR-8363-01 COSM4029740 c.9330A>G p.V3110V Substitution - coding silent 1:235720891-235720891 - TCGA-D1-A103-01 COSM905861 c.10567G>A p.V3523M Substitution - Missense 1:235693484-235693484 - LS411 COSM2000364 c.525A>G p.K175K Substitution - coding silent 1:235810293-235810293 - TCGA-F5-6814-01 COSM210417 c.2438G>A p.R813Q Substitution - Missense 1:235806698-235806698 - TCGA-D1-A176-01 COSM905885 c.7218C>T p.G2406G Substitution - coding silent 1:235755489-235755489 - TCGA-BT-A3PH-01 COSM1296024 c.5957G>A p.R1986Q Substitution - Missense 1:235766243-235766243 - SS6003311 COSM3716889 c.5834C>T p.A1945V Substitution - Missense 1:235770248-235770248 - TCGA-BC-A10W-01 COSM4937336 c.6848A>G p.E2283G Substitution - Missense 1:235759005-235759005 - TCGA-D1-A16Y-01 COSM905934 c.892G>A p.D298N Substitution - Missense 1:235809926-235809926 - C467 COSM4441877 c.3596A>T p.D1199V Substitution - Missense 1:235803024-235803024 - TCGA-A8-A07R-01 COSM3804431 c.9839G>C p.R3280P Substitution - Missense 1:235712143-235712143 - TCGA-FD-A3B5-01 COSM1296022 c.7973-1G>C p.? Unknown 1:235744158-235744158 - TCGA-CG-5721-01 COSM905875 c.8769G>A p.W2923* Substitution - Nonsense 1:235733535-235733535 - 447 COSM1340308 c.4062T>C p.C1354C Substitution - coding silent 1:235793557-235793557 - T3090 COSM4699641 c.5662G>T p.D1888Y Substitution - Missense 1:235773964-235773964 - TCGA-AD-6899-01 COSM533613 c.10416C>T p.Y3472Y Substitution - coding silent 1:235697231-235697231 - CSCC-7-T COSM4455039 c.6472A>C p.K2158Q Substitution - Missense 1:235759381-235759381 - TCGA-BR-8487-01 COSM4029756 c.3101T>C p.M1034T Substitution - Missense 1:235806035-235806035 - SNU-175 COSM2000303 c.3902G>A p.R1301K Substitution - Missense 1:235800908-235800908 - TCGA-AM-5820-01 COSM905906 c.4011C>T p.C1337C Substitution - coding silent 1:235793608-235793608 - LS180 COSM2000155 c.11399C>T p.A3800V Substitution - Missense 1:235662947-235662947 - TCGA-AP-A051-01 COSM905874 c.8841G>A p.W2947* Substitution - Nonsense 1:235731138-235731138 - 43 COSM1340308 c.4062T>C p.C1354C Substitution - coding silent 1:235793557-235793557 - S02397 COSM5698989 c.2134G>A p.A712T Substitution - Missense 1:235808684-235808684 - TCGA-HU-A4GT-01 COSM4029758 c.2175T>C p.V725V Substitution - coding silent 1:235808643-235808643 - 8015299 COSM3771658 c.5956C>T p.R1986* Substitution - Nonsense 1:235766244-235766244 - TCGA-G3-A3CH-01 COSM4918009 c.5661A>T p.E1887D Substitution - Missense 1:235773965-235773965 - BN23 COSM3705645 c.10979C>T p.P3660L Substitution - Missense 1:235677150-235677150 - 1N30-VS-1T30 COSM4973979 c.7327C>T p.L2443F Substitution - Missense 1:235753177-235753177 - TCGA-GV-A3JV-01 COSM905894 c.6305G>A p.R2102H Substitution - Missense 1:235759548-235759548 - TCGA-BS-A0UV-01 COSM905863 c.9920G>A p.R3307H Substitution - Missense 1:235712062-235712062 - S02289 COSM5685854 c.4569G>C p.E1523D Substitution - Missense 1:235788820-235788820 - PTC-14C COSM4143541 c.3475C>A p.P1159T Substitution - Missense 1:235804584-235804584 - S02245 COSM5702000 c.6597_6598GG>TT p.V2200F Substitution - Missense 1:235759255-235759256 - TCGA-BT-A20O-01 COSM414563 c.2089C>T p.Q697* Substitution - Nonsense 1:235808729-235808729 - TCGA-AP-A054-01 COSM905862 c.9947A>G p.Q3316R Substitution - Missense 1:235709287-235709287 - KM12 COSM1668582 c.10030G>A p.A3344T Substitution - Missense 1:235709204-235709204 - KM12 COSM2000192 c.10011delT p.F3337fs*9 Deletion - Frameshift 1:235709223-235709223 - HCC107 COSM1601939 c.9746G>C p.R3249T Substitution - Missense 1:235715239-235715239 - HCC107T COSM1601939 c.9746G>C p.R3249T Substitution - Missense 1:235715239-235715239 - Pat_41_B COSM5845917 c.2506G>A p.V836I Substitution - Missense 1:235806630-235806630 - ESO-2143 COSM1257021 c.7170A>G p.Q2390Q Substitution - coding silent 1:235755537-235755537 - TCGA-12-0619-01 COSM2153669 c.10429A>G p.S3477G Substitution - Missense 1:235697218-235697218 - TCGA-B5-A11E-01 COSM905857 c.11166C>T p.I3722I Substitution - coding silent 1:235664494-235664494 - TCGA-IR-A3LI-01 COSM4846390 c.5168G>C p.R1723T Substitution - Missense 1:235780911-235780911 - 19 COSM5745829 c.10216delA p.T3406fs*15 Deletion - Frameshift 1:235702905-235702905 - PT20_2 COSM5900656 c.6266C>T p.S2089F Substitution - Missense 1:235759587-235759587 - ESO-130 COSM1257019 c.6089A>G p.N2030S Substitution - Missense 1:235766111-235766111 - HCT15 COSM2000278 c.5113G>T p.V1705F Substitution - Missense 1:235780966-235780966 - UM-SCC-17B COSM4598337 c.3065A>G p.Q1022R Substitution - Missense 1:235806071-235806071 - ESCC_BICR_023T COSM5436328 c.3584C>T p.S1195F Substitution - Missense 1:235803036-235803036 - AOCS-135-8-X COSM3943708 c.5800A>G p.T1934A Substitution - Missense 1:235770282-235770282 - BK0052 COSM4188062 c.7270A>T p.K2424* Substitution - Nonsense 1:235753234-235753234 - LUAD-NYU259 COSM371648 c.149G>T p.R50L Substitution - Missense 1:235830269-235830269 - TCGA-D1-A0ZS-01 COSM905901 c.4461T>C p.A1487A Substitution - coding silent 1:235791781-235791781 - TCGA-EE-A2MD-06 COSM3485555 c.7465C>T p.P2489S Substitution - Missense 1:235752167-235752167 - TCGA-EJ-5498-01 COSM1127104 c.10912G>A p.G3638R Substitution - Missense 1:235677508-235677508 - COLO320-DM COSM261876 c.985C>T p.R329* Substitution - Nonsense 1:235809833-235809833 - HCC1395 COSM50243 c.5923-4_5923delTCAGG p.? Unknown 1:235766277-235766281 - T3724 COSM4699638 c.9314A>T p.K3105M Substitution - Missense 1:235724029-235724029 - Pat_45_B COSM5612050 c.1967G>A p.G656E Substitution - Missense 1:235808851-235808851 - QC2-35-T2 COSM5655064 c.5415G>T p.L1805L Substitution - coding silent 1:235777108-235777108 - TCGA-B5-A0JY-01 COSM905880 c.7786C>T p.R2596* Substitution - Nonsense 1:235746522-235746522 - TCGA-D1-A167-01 COSM905856 c.11400C>T p.A3800A Substitution - coding silent 1:235662946-235662946 - TCGA-BS-A0UF-01 COSM210417 c.2438G>A p.R813Q Substitution - Missense 1:235806698-235806698 - ESO-0292 COSM1241391 c.4548C>T p.S1516S Substitution - coding silent 1:235788841-235788841 - TCGA-CJ-4873-01 COSM3359492 c.8255T>G p.L2752W Substitution - Missense 1:235741525-235741525 - DN1122F COSM5782744 c.10034T>C p.L3345P Substitution - Missense 1:235709200-235709200 - LUAD-S01354 COSM385816 c.7929A>T p.L2643L Substitution - coding silent 1:235746379-235746379 - TCGA-AG-3892-01 COSM288673 c.4522G>T p.D1508Y Substitution - Missense 1:235791720-235791720 - PD4116a COSM219497 c.6168G>C p.R2056S Substitution - Missense 1:235762805-235762805 - TCGA-BS-A0UV-01 COSM905876 c.8222G>A p.R2741Q Substitution - Missense 1:235741558-235741558 - 2492701 COSM5599870 c.7269G>A p.Q2423Q Substitution - coding silent 1:235753235-235753235 - TCGA-A5-A0G9-01 COSM905933 c.1183C>T p.R395C Substitution - Missense 1:235809635-235809635 - TCGA-A2-A04T-01 COSM3804428 c.10055A>C p.Q3352P Substitution - Missense 1:235709179-235709179 - TCGA-22-5482-01 COSM678975 c.8703G>T p.E2901D Substitution - Missense 1:235733601-235733601 - TCGA-AP-A059-01 COSM905940 c.65C>T p.A22V Substitution - Missense 1:235830353-235830353 - DLBCL685 COSM1581211 c.5598C>G p.I1866M Substitution - Missense 1:235774949-235774949 - TCGA-D3-A3C8-06 COSM3485562 c.4337G>A p.R1446Q Substitution - Missense 1:235791905-235791905 - 2492709 COSM5716985 c.2730T>G p.S910R Substitution - Missense 1:235806406-235806406 - PT37 COSM5917269 c.8948-8C>T p.? Unknown 1:235730951-235730951 - NCI-H716 COSM2000175 c.10467C>T p.H3489H Substitution - coding silent 1:235697180-235697180 - sysucc-880T COSM3400475 c.10192C>T p.R3398* Substitution - Nonsense 1:235702929-235702929 - B15 COSM1748238 c.4866G>T p.K1622N Substitution - Missense 1:235782084-235782084 - TCGA-12-0619 COSM2153669 c.10429A>G p.S3477G Substitution - Missense 1:235697218-235697218 - B80-Tumor COSM1748240 c.2979A>C p.L993F Substitution - Missense 1:235806157-235806157 - TCGA-G2-A2EK-01 COSM1296026 c.4622C>T p.S1541L Substitution - Missense 1:235788767-235788767 - TCGA-18-3409-01 COSM678969 c.3436C>T p.L1146F Substitution - Missense 1:235804623-235804623 - TCGA-AP-A0LT-01 COSM905895 c.6148C>T p.R2050W Substitution - Missense 1:235762825-235762825 - HT115 COSM2000296 c.3951A>C p.K1317N Substitution - Missense 1:235800375-235800375 - TCGA-32-1982-01 COSM3400478 c.42C>T p.T14T Substitution - coding silent 1:235830376-235830376 - TCGA-FU-A23K-01 COSM459533 c.2863G>C p.E955Q Substitution - Missense 1:235806273-235806273 - TCGA-66-2785-01 COSM678981 c.11073G>C p.V3691V Substitution - coding silent 1:235664587-235664587 - TCGA-06-0214-01 COSM3400477 c.5418C>T p.H1806H Substitution - coding silent 1:235777105-235777105 - TCGA-D1-A103-01 COSM905918 c.2943T>G p.F981L Substitution - Missense 1:235806193-235806193 - TCGA-GM-A2DB-01 COSM1741942 c.5330C>G p.S1777* Substitution - Nonsense 1:235777193-235777193 - 2492708 COSM5716985 c.2730T>G p.S910R Substitution - Missense 1:235806406-235806406 - TCGA-BG-A18B-01 COSM905890 c.7018G>A p.V2340I Substitution - Missense 1:235757322-235757322 - TCGA-AP-A051-01 COSM905868 c.9491C>A p.P3164H Substitution - Missense 1:235720730-235720730 - RK135_C01 COSM3741112 c.9698A>G p.Y3233C Substitution - Missense 1:235715287-235715287 - PT37 COSM5917268 c.5305C>T p.Q1769* Substitution - Nonsense 1:235777218-235777218 - CSB1 COSM5025542 c.10455C>T p.F3485F Substitution - coding silent 1:235697192-235697192 - KM12 COSM1668585 c.4640T>C p.L1547S Substitution - Missense 1:235788749-235788749 - K-562 COSM1668581 c.10537C>A p.L3513I Substitution - Missense 1:235697110-235697110 - BCM617T COSM4955981 c.6790A>G p.S2264G Substitution - Missense 1:235759063-235759063 - HCT-116 COSM1668583 c.9682G>A p.V3228M Substitution - Missense 1:235715303-235715303 - TCGA-J8-A4HW-01 COSM3369618 c.4613A>G p.H1538R Substitution - Missense 1:235788776-235788776 - 587278 COSM1214129 c.10759G>A p.G3587S Substitution - Missense 1:235686990-235686990 - TCGA-CZ-4865-01 COSM3360746 c.9375T>C p.Y3125Y Substitution - coding silent 1:235720846-235720846 - TCGA-HU-A4H5-01 COSM3400475 c.10192C>T p.R3398* Substitution - Nonsense 1:235702929-235702929 - LUAD-NYU847 COSM376532 c.10270G>T p.G3424* Substitution - Nonsense 1:235702851-235702851 - CSCC-55-T COSM4500773 c.5737C>T p.L1913L Substitution - coding silent 1:235773889-235773889 - COLO320-DM COSM4621409 c.9520G>A p.V3174I Substitution - Missense 1:235720701-235720701 - TCGA-85-6560-01 COSM678976 c.9072A>G p.A3024A Substitution - coding silent 1:235729630-235729630 - S00833 COSM312677 c.3697G>A p.E1233K Substitution - Missense 1:235802923-235802923 - TCGA-EE-A2MJ-06 COSM3485551 c.9362A>T p.N3121I Substitution - Missense 1:235720859-235720859 - TCGA-DC-5337-01 COSM1560179 c.10758C>T p.C3586C Substitution - coding silent 1:235686991-235686991 - HCT116 COSM1668583 c.9682G>A p.V3228M Substitution - Missense 1:235715303-235715303 - TCGA-A6-5661-01 COSM1340304 c.6348G>A p.T2116T Substitution - coding silent 1:235759505-235759505 - J46_T COSM3977219 c.5401A>G p.I1801V Substitution - Missense 1:235777122-235777122 - 8014573 COSM3385909 c.5503C>G p.L1835V Substitution - Missense 1:235775044-235775044 - TCGA-BR-8680-01 COSM4029741 c.9267C>A p.I3089I Substitution - coding silent 1:235724076-235724076 - LP6005409-DNA_F02 COSM4408854 c.10143+1G>T p.? Unknown 1:235709090-235709090 - tumor_4111326 COSM5950030 c.9200G>T p.W3067L Substitution - Missense 1:235724143-235724143 - CSCC-44-T COSM4458378 c.10834C>T p.L3612F Substitution - Missense 1:235677586-235677586 - CHC205T COSM3746869 c.1251A>G p.Q417Q Substitution - coding silent 1:235809567-235809567 - 136-02-3TD COSM145604 c.5519C>T p.S1840L Substitution - Missense 1:235775028-235775028 - TCGA-AP-A051-01 COSM905900 c.4631C>T p.S1544F Substitution - Missense 1:235788758-235788758 - TCGA-AZ-4315-01 COSM1340303 c.8115T>G p.I2705M Substitution - Missense 1:235744015-235744015 - PT13 COSM5895496 c.9713C>T p.S3238F Substitution - Missense 1:235715272-235715272 - TCGA-EE-A3J7-06 COSM2000322 c.2860C>T p.P954S Substitution - Missense 1:235806276-235806276 - TCGA-EE-A2MJ-06 COSM3485561 c.4719A>G p.K1573K Substitution - coding silent 1:235787343-235787343 - PD11326a COSM5789703 c.9824C>T p.T3275I Substitution - Missense 1:235712158-235712158 - ESCC_123 COSM5640835 c.10628A>G p.D3543G Substitution - Missense 1:235693423-235693423 - HT115 COSM2000358 c.979C>T p.L327F Substitution - Missense 1:235809839-235809839 - PT15_1 COSM5897298 c.2875C>T p.Q959* Substitution - Nonsense 1:235806261-235806261 - HT115 COSM2000362 c.836C>T p.S279F Substitution - Missense 1:235809982-235809982 - TCGA-D1-A163-01 COSM905908 c.3686C>A p.P1229H Substitution - Missense 1:235802934-235802934 - ESO-916 COSM1257024 c.291C>A p.N97K Substitution - Missense 1:235810527-235810527 - CSCC-27-T COSM4465524 c.1388C>T p.P463L Substitution - Missense 1:235809430-235809430 - 046T COSM1731523 c.2012_2014delCTT p.S671delS Deletion - In frame 1:235808804-235808806 - TCGA-D3-A2JO-06 COSM3485554 c.8019A>C p.V2673V Substitution - coding silent 1:235744111-235744111 - TCGA-BH-A18G-01 COSM3804443 c.1187A>G p.H396R Substitution - Missense 1:235809631-235809631 - HCT15 COSM2000379 c.15T>C p.S5S Substitution - coding silent 1:235830403-235830403 - HCC5 COSM3705648 c.2307G>T p.L769F Substitution - Missense 1:235808511-235808511 - I2L-P23-Tumor-Biopsy COSM5353177 c.2166C>A p.G722G Substitution - coding silent 1:235808652-235808652 - TCGA-AP-A054-01 COSM905859 c.11017A>G p.I3673V Substitution - Missense 1:235677112-235677112 - COLO678 COSM2000226 c.7765C>T p.R2589W Substitution - Missense 1:235751225-235751225 - MD-289 COSM302600 c.10843C>G p.H3615D Substitution - Missense 1:235677577-235677577 - BHY COSM4592124 c.8368A>C p.K2790Q Substitution - Missense 1:235734650-235734650 - T3091 COSM4699637 c.9773delT p.L3258fs*1 Deletion - Frameshift 1:235715212-235715212 - S02248 COSM5679334 c.8077G>T p.E2693* Substitution - Nonsense 1:235744053-235744053 - HCC2998 COSM905932 c.1303G>T p.E435* Substitution - Nonsense 1:235809515-235809515 - HCC49 COSM1601940 c.8600A>G p.N2867S Substitution - Missense 1:235733842-235733842 - TCGA-AA-A02W-01 COSM287583 c.11299T>C p.Y3767H Substitution - Missense 1:235663047-235663047 - PD23558a COSM5777588 c.4356C>G p.H1452Q Substitution - Missense 1:235791886-235791886 - HCC141T COSM1601942 c.801A>G p.K267K Substitution - coding silent 1:235810017-235810017 - CSCC-10-T COSM4514448 c.9755C>T p.P3252L Substitution - Missense 1:235715230-235715230 - TCGA-AP-A0LM-01 COSM905937 c.582G>A p.S194S Substitution - coding silent 1:235810236-235810236 - CSCC-55-T COSM4560685 c.8535G>A p.E2845E Substitution - coding silent 1:235734483-235734483 - CSCC-29-T COSM4555448 c.6559G>T p.V2187F Substitution - Missense 1:235759294-235759294 - TCGA-37-4135-01 COSM678966 c.2895T>A p.S965S Substitution - coding silent 1:235806241-235806241 - TCGA-AC-A23H-01 COSM3804440 c.3310C>G p.R1104G Substitution - Missense 1:235805826-235805826 - TCGA-AO-A128-01 COSM5832523 c.2691_2692insC p.I898fs*14 Insertion - Frameshift 1:235806444-235806445 - TCGA-AX-A0J0-01 COSM905929 c.1390G>A p.E464K Substitution - Missense 1:235809428-235809428 - TCGA-AX-A0J1-01 COSM905865 c.9647G>A p.R3216H Substitution - Missense 1:235715338-235715338 - YUPROST COSM1685392 c.10117C>G p.Q3373E Substitution - Missense 1:235709117-235709117 - ICGC_MB70 COSM3670151 c.6782G>A p.R2261H Substitution - Missense 1:235759071-235759071 - TCGA-BR-8591-01 COSM905896 c.6078C>T p.Y2026Y Substitution - coding silent 1:235766122-235766122 - Pat_11_A COSM5845911 c.10003C>T p.R3335C Substitution - Missense 1:235709231-235709231 - CSCC-7-T COSM4496824 c.4839C>T p.I1613I Substitution - coding silent 1:235787223-235787223 - 517 COSM5612050 c.1967G>A p.G656E Substitution - Missense 1:235808851-235808851 - P147 COSM1737232 c.4249A>T p.I1417F Substitution - Missense 1:235791993-235791993 - PD4116a COSM219497 c.6168G>C p.R2056S Substitution - Missense 1:235762805-235762805 - LPJ041 COSM1316019 c.6454A>T p.S2152C Substitution - Missense 1:235759399-235759399 - TCGA-AO-A128-01 COSM3804439 c.3543T>C p.A1181A Substitution - coding silent 1:235804516-235804516 - CSCC-31-T COSM4507708 c.7541C>T p.S2514F Substitution - Missense 1:235752091-235752091 - LP6008051-DNA_A02 COSM5951325 c.8083T>C p.S2695P Substitution - Missense 1:235744047-235744047 - ESCC_152 COSM5645324 c.6347C>T p.T2116M Substitution - Missense 1:235759506-235759506 - T3064 COSM1214128 c.10964C>T p.A3655V Substitution - Missense 1:235677165-235677165 - PD23574a COSM5793729 c.2254C>G p.L752V Substitution - Missense 1:235808564-235808564 - HCC97 COSM678964 c.1788C>G p.L596L Substitution - coding silent 1:235809030-235809030 - CCK81 COSM2000277 c.5131T>C p.Y1711H Substitution - Missense 1:235780948-235780948 - TCGA-B5-A0JY-01 COSM905921 c.2497G>T p.D833Y Substitution - Missense 1:235806639-235806639 - HCC2998 COSM905932 c.1303G>T p.E435* Substitution - Nonsense 1:235809515-235809515 - NB-1100 COSM1286038 c.7637T>G p.V2546G Substitution - Missense 1:235751353-235751353 - 9583_PT COSM5156103 c.110C>T p.T37M Substitution - Missense 1:235830308-235830308 - YUMOBER COSM5380157 c.1945C>T p.Q649* Substitution - Nonsense 1:235808873-235808873 - TCGA-HF-7132-01 COSM4029738 c.9492T>C p.P3164P Substitution - coding silent 1:235720729-235720729 - LUAD-RT-S01818 COSM383772 c.8967C>G p.L2989L Substitution - coding silent 1:235730924-235730924 - TCGA-BF-A1PZ-01 COSM4399360 c.3216C>T p.S1072S Substitution - coding silent 1:235805920-235805920 - RK148_C01 COSM1626910 c.5221C>G p.L1741V Substitution - Missense 1:235777302-235777302 - EGC3 COSM5053246 c.4946G>A p.G1649D Substitution - Missense 1:235782004-235782004 - T3658 COSM2000327 c.2720delT p.L907fs*3 Deletion - Frameshift 1:235806416-235806416 - LUAD-YINHD COSM350000 c.4644_4645GA>TT p.M1548>? Complex 1:235788744-235788745 - TCGA-66-2795-01 COSM678968 c.3296C>A p.S1099* Substitution - Nonsense 1:235805840-235805840 - S00936 COSM312678 c.4939A>G p.M1647V Substitution - Missense 1:235782011-235782011 - ESO-081 COSM1243386 c.9701G>A p.G3234D Substitution - Missense 1:235715284-235715284 - Au1 COSM5597042 c.4333C>T p.H1445Y Substitution - Missense 1:235791909-235791909 - TCGA-BS-A0UF-01 COSM905884 c.7276T>C p.S2426P Substitution - Missense 1:235753228-235753228 - TCGA-BR-4280-01 COSM4029746 c.7711C>T p.L2571F Substitution - Missense 1:235751279-235751279 - TCGA-33-4583-01 COSM678961 c.792A>C p.L264F Substitution - Missense 1:235810026-235810026 - TCGA-AP-A051-01 COSM905903 c.4381C>A p.L1461M Substitution - Missense 1:235791861-235791861 - 49M COSM5591747 c.3145C>T p.P1049S Substitution - Missense 1:235805991-235805991 - Capan-1 COSM328091 c.6482A>C p.E2161A Substitution - Missense 1:235759371-235759371 - ESO-157 COSM1257015 c.408_409insA p.V137fs*12 Insertion - Frameshift 1:235810409-235810410 - ESCC_154 COSM2000226 c.7765C>T p.R2589W Substitution - Missense 1:235751225-235751225 - J90_T COSM3977218 c.9211G>T p.E3071* Substitution - Nonsense 1:235724132-235724132 - T3225 COSM4699643 c.4329T>C p.F1443F Substitution - coding silent 1:235791913-235791913 - 2492730 COSM5729399 c.8188A>G p.T2730A Substitution - Missense 1:235741592-235741592 - OSCC-GB_00220111 COSM3710646 c.421C>T p.R141* Substitution - Nonsense 1:235810397-235810397 - CHC155T COSM2000217 c.8269G>T p.A2757S Substitution - Missense 1:235741511-235741511 - NCI-H460 COSM1668584 c.7120C>T p.R2374C Substitution - Missense 1:235755587-235755587 - TCGA-G3-A5SJ-01 COSM4914838 c.3713-2A>T p.? Unknown 1:235801099-235801099 - TCGA-D3-A51J-06 COSM3485560 c.4761C>T p.F1587F Substitution - coding silent 1:235787301-235787301 - TCGA-AX-A05Z-01 COSM905902 c.4449T>C p.C1483C Substitution - coding silent 1:235791793-235791793 - HCC120T COSM3705646 c.9839G>T p.R3280L Substitution - Missense 1:235712143-235712143 - TCGA-AC-A2FO-01 COSM3804435 c.6861C>A p.N2287K Substitution - Missense 1:235758992-235758992 - T2269 COSM4699644 c.4145T>C p.I1382T Substitution - Missense 1:235792097-235792097 - TCGA-13-1411-01 COSM81403 c.8448G>A p.L2816L Substitution - coding silent 1:235734570-235734570 - AOCS-093-3-6 COSM3943706 c.7689C>A p.T2563T Substitution - coding silent 1:235751301-235751301 - TCGA-ER-A19P-06 COSM3485559 c.5991A>G p.A1997A Substitution - coding silent 1:235766209-235766209 - Gp2D COSM4627063 c.11150T>C p.V3717A Substitution - Missense 1:235664510-235664510 - LUAD-U6SJ7 COSM405225 c.616delG p.D206fs*3 Deletion - Frameshift 1:235810202-235810202 - YUROC COSM5380155 c.8695G>A p.G2899R Substitution - Missense 1:235733609-235733609 - ATL074 COSM5705320 c.6547G>T p.A2183S Substitution - Missense 1:235759306-235759306 - CHC205T COSM3746867 c.4956A>G p.L1652L Substitution - coding silent 1:235781994-235781994 - TCGA-CU-A3KJ-01 COSM1296029 c.467G>C p.R156T Substitution - Missense 1:235810351-235810351 - CSCC-44-T COSM4457742 c.10586C>T p.T3529M Substitution - Missense 1:235693465-235693465 - B89-12-Tumor COSM1748239 c.3974G>A p.S1325N Substitution - Missense 1:235800352-235800352 - I2L-P23-Tumor-Organoid COSM5353177 c.2166C>A p.G722G Substitution - coding silent 1:235808652-235808652 - TCGA-26-5132-01 COSM1637821 c.6713G>A p.R2238Q Substitution - Missense 1:235759140-235759140 - 587256 COSM1214132 c.1697T>C p.L566S Substitution - Missense 1:235809121-235809121 - 258 COSM3722440 c.9544G>T p.D3182Y Substitution - Missense 1:235720677-235720677 - TCGA-HU-A4GF-01 COSM4029749 c.7060C>G p.L2354V Substitution - Missense 1:235755647-235755647 - Au2 COSM5599870 c.7269G>A p.Q2423Q Substitution - coding silent 1:235753235-235753235 - TCGA-HE-A5NL-01 COSM3984858 c.10024C>T p.R3342W Substitution - Missense 1:235709210-235709210 - 6 COSM1237119 c.746A>G p.N249S Substitution - Missense 1:235810072-235810072 - TCGA-DK-A1AG-01 COSM1296028 c.3709G>A p.D1237N Substitution - Missense 1:235802911-235802911 - DLD1 COSM4611595 c.7633delG p.A2545fs*16 Deletion - Frameshift 1:235751357-235751357 - ME043T COSM228298 c.1897A>T p.K633* Substitution - Nonsense 1:235808921-235808921 - STC252 COSM5053243 c.9342A>G p.I3114M Substitution - Missense 1:235720879-235720879 - 2492700 COSM5716228 c.6132C>T p.I2044I Substitution - coding silent 1:235762841-235762841 - 8069332 COSM4406724 c.7690G>A p.A2564T Substitution - Missense 1:235751300-235751300 - PD4003a COSM162303 c.6912C>G p.C2304W Substitution - Missense 1:235757428-235757428 - CSCC-44-T COSM2000177 c.10372C>T p.P3458S Substitution - Missense 1:235702749-235702749 - TCGA-CZ-5452-01 COSM464187 c.2179C>T p.Q727* Substitution - Nonsense 1:235808639-235808639 - LUAD-RT-S01818 COSM383771 c.9038C>G p.S3013C Substitution - Missense 1:235730853-235730853 - TCGA-BR-8487-01 COSM4029757 c.2343G>A p.L781L Substitution - coding silent 1:235808475-235808475 - PD4108a COSM162306 c.2910C>T p.I970I Substitution - coding silent 1:235806226-235806226 - TCGA-B0-5088-01 COSM464180 c.8979T>G p.F2993L Substitution - Missense 1:235730912-235730912 - C086 COSM5380154 c.8830C>T p.P2944S Substitution - Missense 1:235731149-235731149 - QGP1 COSM2000369 c.281C>T p.T94I Substitution - Missense 1:235812973-235812973 - TCGA-OL-A66I-01 COSM3804442 c.1640G>T p.C547F Substitution - Missense 1:235809178-235809178 - LUAD-QJN9L COSM342693 c.2125A>G p.I709V Substitution - Missense 1:235808693-235808693 - TCGA-AA-A00N-01 COSM275952 c.3024G>T p.E1008D Substitution - Missense 1:235806112-235806112 - sysucc-863T COSM3400478 c.42C>T p.T14T Substitution - coding silent 1:235830376-235830376 - TCGA-AP-A051-01 COSM905916 c.3077G>T p.R1026I Substitution - Missense 1:235806059-235806059 - TCGA-BH-A18G-01 COSM3804437 c.6157A>G p.M2053V Substitution - Missense 1:235762816-235762816 - TCGA-06-0155-01 COSM3747833 c.5461-2A>T p.? Unknown 1:235775088-235775088 - C547 COSM2000162 c.11167G>A p.A3723T Substitution - Missense 1:235664493-235664493 - TCGA-B0-4814-01 COSM3360747 c.2130G>T p.Q710H Substitution - Missense 1:235808688-235808688 - 523LT COSM4386642 c.4963C>A p.Q1655K Substitution - Missense 1:235781987-235781987 - TCGA-FS-A1ZQ-06 COSM3485566 c.2834C>T p.S945F Substitution - Missense 1:235806302-235806302 - TCGA-EE-A2A2-06 COSM3485568 c.1535A>G p.H512R Substitution - Missense 1:235809283-235809283 - 2292383 COSM1286038 c.7637T>G p.V2546G Substitution - Missense 1:235751353-235751353 - YULONE COSM5380152 c.10465C>T p.H3489Y Substitution - Missense 1:235697182-235697182 - ME032T COSM227209 c.2965G>A p.V989I Substitution - Missense 1:235806171-235806171 - TCGA-EI-6917-01 COSM3418924 c.2477G>A p.S826N Substitution - Missense 1:235806659-235806659 - TCGA-EE-A3J7-06 COSM3864852 c.385C>T p.L129L Substitution - coding silent 1:235810433-235810433 - TCGA-BS-A0UF-01 COSM905930 c.1345G>A p.V449I Substitution - Missense 1:235809473-235809473 - TCGA-AM-5821-01 COSM3751012 c.7870C>T p.R2624W Substitution - Missense 1:235746438-235746438 - YULAN COSM1689994 c.4663C>T p.P1555S Substitution - Missense 1:235788726-235788726 - CSCC-41-T COSM4464694 c.1348C>T p.L450F Substitution - Missense 1:235809470-235809470 - CHC155T COSM2000217 c.8269G>T p.A2757S Substitution - Missense 1:235741511-235741511 - PD4002a COSM162302 c.6674G>A p.R2225H Substitution - Missense 1:235759179-235759179 - TCGA-A7-A0DA-01 COSM425638 c.6864A>T p.R2288R Substitution - coding silent 1:235758989-235758989 - LUAD-YINHD COSM350001 c.146G>A p.G49D Substitution - Missense 1:235830272-235830272 - ACINAR28 COSM253020 c.5461-3delT p.? Unknown 1:235775089-235775089 - TCGA-AP-A051-01 COSM905872 c.8920C>A p.L2974I Substitution - Missense 1:235731059-235731059 - 2492703 COSM5599871 c.1720C>T p.L574L Substitution - coding silent 1:235809098-235809098 - TCGA-41-2572-01 COSM3747833 c.5461-2A>T p.? Unknown 1:235775088-235775088 - TCGA-AX-A0J0-01 COSM905878 c.7973-1G>T p.? Unknown 1:235744158-235744158 - TCGA-AD-6964-01 COSM1340309 c.3323C>T p.A1108V Substitution - Missense 1:235805813-235805813 - TCGA-06-0168-01 COSM2150251 c.2712G>A p.V904V Substitution - coding silent 1:235806424-235806424 - TCGA-GC-A3YS-01 COSM3789675 c.2706C>G p.L902L Substitution - coding silent 1:235806430-235806430 - TCGA-AX-A0J1-01 COSM905928 c.1661C>T p.A554V Substitution - Missense 1:235809157-235809157 - TCGA-B5-A11E-01 COSM905889 c.7084G>A p.A2362T Substitution - Missense 1:235755623-235755623 - DLBCL1058 COSM1581209 c.8027G>T p.S2676I Substitution - Missense 1:235744103-235744103 - TCGA-EB-A553-01 COSM3485549 c.10343C>T p.T3448I Substitution - Missense 1:235702778-235702778 - HCT116 COSM4632035 c.10324C>T p.Q3442* Substitution - Nonsense 1:235702797-235702797 - PTC-28C COSM4143542 c.95A>G p.E32G Substitution - Missense 1:235830323-235830323 - TCGA-B5-A11E-01 COSM905899 c.4928A>C p.K1643T Substitution - Missense 1:235782022-235782022 - TCGA-25-1319-01 COSM71522 c.82G>A p.E28K Substitution - Missense 1:235830336-235830336 - CSCC-7-T COSM4559689 c.8152G>A p.G2718S Substitution - Missense 1:235741628-235741628 - TCGA-AA-A010-01 COSM282597 c.1526T>G p.F509C Substitution - Missense 1:235809292-235809292 - TCGA-06-0168 COSM2150251 c.2712G>A p.V904V Substitution - coding silent 1:235806424-235806424 - BZ38 COSM5759273 c.2529C>G p.D843E Substitution - Missense 1:235806607-235806607 - TCGA-A6-6654-01 COSM253020 c.5461-3delT p.? Unknown 1:235775089-235775089 - TCGA-F5-6814-01 COSM3418921 c.5170G>T p.E1724* Substitution - Nonsense 1:235780909-235780909 - TCGA-BR-7851-01 COSM4029763 c.910G>A p.D304N Substitution - Missense 1:235809908-235809908 - 2492701 COSM5716228 c.6132C>T p.I2044I Substitution - coding silent 1:235762841-235762841 - TCGA-22-5489-01 COSM678964 c.1788C>G p.L596L Substitution - coding silent 1:235809030-235809030 - LUAD-NYU284 COSM372590 c.10480G>T p.G3494C Substitution - Missense 1:235697167-235697167 - ccRCC-15 COSM1662657 c.10373C>T p.P3458L Substitution - Missense 1:235702748-235702748 - TCGA-K4-A3WU-01 COSM3789672 c.11358G>A p.L3786L Substitution - coding silent 1:235662988-235662988 - CHC892T COSM4797790 c.10088G>A p.G3363E Substitution - Missense 1:235709146-235709146 - KM12 COSM1668585 c.4640T>C p.L1547S Substitution - Missense 1:235788749-235788749 - TCGA-14-4157-01 COSM3400476 c.10183G>A p.V3395I Substitution - Missense 1:235702938-235702938 - TCGA-HU-A4GP-01 COSM4029762 c.966G>T p.L322F Substitution - Missense 1:235809852-235809852 - 1_RESISTANT COSM1719418 c.7448G>A p.G2483E Substitution - Missense 1:235753056-235753056 - PD11344a COSM5782744 c.10034T>C p.L3345P Substitution - Missense 1:235709200-235709200 - TCGA-AX-A05Z-01 COSM210417 c.2438G>A p.R813Q Substitution - Missense 1:235806698-235806698 - TCGA-AP-A056-01 COSM905877 c.8099C>A p.P2700Q Substitution - Missense 1:235744031-235744031 - YUNEKI COSM5380156 c.4508C>T p.S1503L Substitution - Missense 1:235791734-235791734 - TCGA-CG-5721-01 COSM4029753 c.6270T>C p.N2090N Substitution - coding silent 1:235759583-235759583 - TCGA-B5-A0JY-01 COSM905886 c.7186T>G p.F2396V Substitution - Missense 1:235755521-235755521 - CSCC-27-T COSM4499800 c.5503C>T p.L1835L Substitution - coding silent 1:235775044-235775044 - 587228 COSM1214128 c.10964C>T p.A3655V Substitution - Missense 1:235677165-235677165 - TCGA-61-1740-01 COSM1320363 c.5927A>G p.Y1976C Substitution - Missense 1:235766273-235766273 - TCGA-66-2785-01 COSM288673 c.4522G>T p.D1508Y Substitution - Missense 1:235791720-235791720 - ESCC_BICR_058T COSM5430524 c.152G>T p.G51V Substitution - Missense 1:235830266-235830266 - TCGA-BR-8680-01 COSM4029759 c.2090A>C p.Q697P Substitution - Missense 1:235808728-235808728 - DLBCL1021 COSM1582038 c.7355_7356delTC p.L2452fs*8 Deletion - Frameshift 1:235753148-235753149 - TCGA-AD-6888-01 COSM1340301 c.9401T>G p.L3134* Substitution - Nonsense 1:235720820-235720820 - TCGA-FS-A1ZK-06 COSM2000214 c.8352C>T p.S2784S Substitution - coding silent 1:235741428-235741428 - S00501 COSM5658084 c.5461-4_5461-3delTT p.? Unknown 1:235775089-235775090 - TCGA-BR-6452-01 COSM288607 c.7017C>T p.L2339L Substitution - coding silent 1:235757323-235757323 - 406 COSM4430153 c.1013A>G p.D338G Substitution - Missense 1:235809805-235809805 - TCGA-CA-6717-01 COSM1340307 c.4197A>G p.L1399L Substitution - coding silent 1:235792045-235792045 - TCGA-A2-A0CT-01 COSM425640 c.3283G>A p.E1095K Substitution - Missense 1:235805853-235805853 - LUAD-F00365 COSM340558 c.1511G>T p.C504F Substitution - Missense 1:235809307-235809307 - T276 COSM4699649 c.47T>C p.V16A Substitution - Missense 1:235830371-235830371 - TCGA-EE-A29M-06 COSM3485550 c.10208T>C p.M3403T Substitution - Missense 1:235702913-235702913 - TCGA-C5-A1MH-01 COSM678971 c.5039C>G p.S1680* Substitution - Nonsense 1:235781040-235781040 - DLBCL1021 COSM1582025 c.7348_7350delCTT p.L2452delL Deletion - In frame 1:235753154-235753156 - TCGA-CA-6717-01 COSM210417 c.2438G>A p.R813Q Substitution - Missense 1:235806698-235806698 - CSCC-38-T COSM4457404 c.10449C>T p.V3483V Substitution - coding silent 1:235697198-235697198 - TCGA-GM-A3NW-01 COSM3804430 c.9984T>G p.P3328P Substitution - coding silent 1:235709250-235709250 - TCGA-B5-A11E-01 COSM905905 c.4081C>A p.L1361I Substitution - Missense 1:235793538-235793538 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.532407;Hs.532411 1q42.1-q42.2 606897

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.F1293V c.3877T>G 1 235964233 LGG A C Missense p.F2401V c.7201T>G 1 235918806 RCCC A C Missense p.F2993L c.8979T>G 1 235894212 RCCC A C Missense p.I3730S c.11189T>G 1 235827771 CM A C Missense p.L2752W c.8255T>G 1 235904825 RCCC A - Frameshift p.F1726Lfs*2 c.5178delT 1 235944201 RCCC A G IntronicSNV . c.8358+3203T>C 1 235901519 CM A G Missense p.F794L c.2380T>C 1 235970056 HNSC A G Missense p.I593T c.1778T>C 1 235972340 CM A G Missense p.L187P c.560T>C 1 235973558 LUAD A G Missense p.L2496P c.7487T>C 1 235915445 HNSC A G Missense p.L293P c.878T>C 1 235973240 CM A G Missense p.M3403T c.10208T>C 1 235866213 CM A G Missense p.Y3767H c.11299T>C 1 235826347 COREAD A G Synonymous p.A1487A c.4461T>C 1 235955081 UCEC A G Synonymous p.A905A c.2715T>C 1 235969721 CM A G Synonymous p.F2376F c.7128T>C 1 235918879 ESCA A G Synonymous p.S3053S c.9159T>C 1 235891379 CM A G Synonymous p.Y3125Y c.9375T>C 1 235884146 RCCC A T IntronicSNV . c.9785-11T>A 1 235875508 DLBCL A T Synonymous p.S965S c.2895T>A 1 235969541 LUSC C A IntronicSNV . c.3555+32G>T 1 235967772 NSCLC C A Missense p.A2290S c.6868G>T 1 235922285 LUAD C A Missense p.A360S c.1078G>T 1 235973040 LUAD C A Missense p.E2901D c.8703G>T 1 235896901 LUSC C A Missense p.G1314V c.3941G>T 1 235963685 UCEC C A Missense p.G3138W c.9412G>T 1 235884109 ESCA C A Missense p.G877V c.2630G>T 1 235969806 LUAD C A Missense p.K181N c.543G>T 1 235973575 UCEC C A Missense p.M1630I c.4890G>T 1 235945360 LUAD C A Missense p.Q1208H c.3624G>T 1 235966296 OV C A Missense p.Q3497H c.10491G>T 1 235860456 LUSC C A Missense p.Q710H c.2130G>T 1 235971988 RCCC C A Missense p.R2961L c.8882G>T 1 235894397 LUAD C A Missense p.S568I c.1703G>T 1 235972415 LUSC C A Missense p.V3228L c.9682G>T 1 235878603 LUAD C A Missense p.W3689L c.11066G>T 1 235827894 LUAD C A Nonsense p.E3285* c.9853G>T 1 235875429 UCEC C A Synonymous p.A3655A c.10965G>T 1 235840464 STAD C A Synonymous p.L1968L c.5904G>T 1 235933478 LUAD C - Frameshift p.G2193Efs*38 c.6578delG 1 235922575 LUAD C G Missense p.A102P c.304G>C 1 235973814 CM C G Missense p.A636P c.1906G>C 1 235972212 LUAD C G Missense p.D1903H c.5707G>C 1 235937219 LUSC C G Missense p.D2267H c.6799G>C 1 235922354 HNSC C G Missense p.E3447D c.10341G>C 1 235866080 BRCA C G Missense p.E3447Q c.10339G>C 1 235866082 LUSC C G Missense p.K2677N c.8031G>C 1 235907399 BRCA C G Missense p.L2667F c.8001G>C 1 235907429 BLCA C G Missense p.R156T c.467G>C 1 235973651 BLCA C G Missense p.R2741P c.8222G>C 1 235904858 LUAD C G Missense p.R377T c.1130G>C 1 235972988 HNSC C G SpliceAcceptorSNV . c.7973-1G>C 1 235907458 BLCA C G Synonymous p.L3131L c.9393G>C 1 235884128 COREAD C T IntronicSNV . c.9316-134G>A 1 235884339 NSCLC C T Missense p.A3591V c.10772C>T 1 235850277 GBM C T Missense p.C808Y c.2423G>A 1 235970013 LUAD C T Missense p.D1237N c.3709G>A 1 235966211 BLCA C T Missense p.D2215N c.6643G>A 1 235922510 BLCA C T Missense p.D298N c.892G>A 1 235973226 UCEC C T Missense p.E1095K c.3283G>A 1 235969153 BRCA C T Missense p.E1233K c.3697G>A 1 235966223 SCLC C T Missense p.E1357K c.4069G>A 1 235956850 CM C T Missense p.E28K c.82G>A 1 235993636 OV C T Missense p.E2953K c.8857G>A 1 235894422 BLCA C T Missense p.E3176K c.9526G>A 1 235883995 BRCA C T Missense p.E684K c.2050G>A 1 235972068 BRCA C T Missense p.E955K c.2863G>A 1 235969573 HNSC C T Missense p.G2281S c.6841G>A 1 235922312 HC C T Missense p.G3638R c.10912G>A 1 235840808 PRAD C T Missense p.G986S c.2956G>A 1 235969480 LUAD C T Missense p.M1I c.3G>A 1 235993715 LUAD C T Missense p.R1446Q c.4337G>A 1 235955205 CM C T Missense p.R1986Q c.5957G>A 1 235929543 BLCA C T Missense p.R2102H c.6305G>A 1 235922848 BLCA C T Missense p.R2225H c.6674G>A 1 235922479 BRCA C T Missense p.R2238Q c.6713G>A 1 235922440 GBM C T Missense p.R2261H c.6782G>A 1 235922371 MB C T Missense p.R2611H c.7832G>A 1 235909776 LUAD C T Missense p.R3018Q c.9053G>A 1 235892949 HNSC C T Missense p.R3078H c.9233G>A 1 235887410 COREAD C T Missense p.V2340I c.7018G>A 1 235920622 UCEC C T Missense p.V273I c.817G>A 1 235973301 BRCA C T Missense p.V3395I c.10183G>A 1 235866238 GBM C T Missense p.V3473M c.10417G>A 1 235860530 HNSC C T Missense p.V836I c.2506G>A 1 235969930 CM C T Nonsense p.W1466* c.4398G>A 1 235955144 BRCA C T Synonymous p.E1294E c.3882G>A 1 235964228 BLCA C T Synonymous p.K3105K c.9315G>A 1 235887328 CM C T Synonymous p.K887K c.2661G>A 1 235969775 RCCC C T Synonymous p.L2816L c.8448G>A 1 235897870 OV C T Synonymous p.V904V c.2712G>A 1 235969724 GBM CT TA Missense p.E2617V c.7850_7851delinsTA 1 235909757 CM G A IntronicSNV . c.8358+2458C>T 1 235902264 CM G A IntronicSNV . c.9926-1105C>T 1 235873713 CLL G A Missense p.A3572V c.10715C>T 1 235850334 HNSC G A Missense p.C1354Y c.4061G>A 1 235956858 GBM G A Missense p.H2756Y c.8266C>T 1 235904814 HNSC G A Missense p.L2571F c.7711C>T 1 235914579 STAD G A Missense p.P1254L c.3761C>T 1 235964349 CM G A Missense p.P201L c.602C>T 1 235973516 CM G A Missense p.P2489S c.7465C>T 1 235915467 CM G A Missense p.P254S c.760C>T 1 235973358 CM G A Missense p.P3327S c.9979C>T 1 235872555 CM G A Missense p.P3660S c.10978C>T 1 235840451 CM G A Missense p.P837S c.2509C>T 1 235969927 BRCA G A Missense p.P837S c.2509C>T 1 235969927 OV G A Missense p.P87L c.260C>T 1 235976294 LUAD G A Missense p.P954S c.2860C>T 1 235969576 CM G A Missense p.R2050W c.6148C>T 1 235926125 UCEC G A Missense p.R207C c.619C>T 1 235973499 HNSC G A Missense p.R2225C c.6673C>T 1 235922480 HNSC G A Missense p.R2261C c.6781C>T 1 235922372 RCCC G A Missense p.R395C c.1183C>T 1 235972935 UCEC G A Missense p.S101L c.302C>T 1 235973816 CLL G A Missense p.S1541L c.4622C>T 1 235952067 BLCA G A Missense p.S2377F c.7130C>T 1 235918877 HC G A Missense p.S2679L c.8036C>T 1 235907394 LUAD G A Missense p.S494L c.1481C>T 1 235972637 BLCA G A Missense p.S945F c.2834C>T 1 235969602 CM G A Missense p.T210I c.629C>T 1 235973489 LUAD G A Nonsense p.Q2534* c.7600C>T 1 235915332 HNSC G A Nonsense p.Q622* c.1864C>T 1 235972254 LUSC G A Nonsense p.Q697* c.2089C>T 1 235972029 BLCA G A Nonsense p.Q727* c.2179C>T 1 235971939 RCCC G A Nonsense p.R3398* c.10192C>T 1 235866229 GBM G A Synonymous p.C1337C c.4011C>T 1 235956908 UCEC G A Synonymous p.F3485F c.10455C>T 1 235860492 BRCA G A Synonymous p.G2406G c.7218C>T 1 235918789 UCEC G A Synonymous p.H1806H c.5418C>T 1 235940405 GBM G A Synonymous p.H2756H c.8268C>T 1 235904812 HNSC G A Synonymous p.I970I c.2910C>T 1 235969526 BRCA G A Synonymous p.L129L c.385C>T 1 235973733 CM G A Synonymous p.L1588L c.4764C>T 1 235950598 LUAD G A Synonymous p.L2339L c.7017C>T 1 235920623 BLCA G A Synonymous p.L2339L c.7017C>T 1 235920623 COREAD G A Synonymous p.L871L c.2613C>T 1 235969823 BLCA G A Synonymous p.S1072S c.3216C>T 1 235969220 CM G A Synonymous p.S1390S c.4170C>T 1 235955372 ESCA G A Synonymous p.S1782S c.5346C>T 1 235940477 HNSC G A Synonymous p.S2153S c.6459C>T 1 235922694 COREAD G A Synonymous p.S2222S c.6666C>T 1 235922487 CM G A Synonymous p.S2784S c.8352C>T 1 235904728 CM G A Synonymous p.S3475S c.10425C>T 1 235860522 CM G A Synonymous p.S3475S c.10425C>T 1 235860522 ESCA G A Synonymous p.T14T c.42C>T 1 235993676 GBM G A Synonymous p.Y2026Y c.6078C>T 1 235929422 UCEC G A Synonymous p.Y3472Y c.10416C>T 1 235860531 LUAD G C Missense p.C2304W c.6912C>G 1 235920728 BRCA G C Missense p.I1908M c.5724C>G 1 235937202 HNSC G C Missense p.L1560V c.4678C>G 1 235952011 BLCA G C Missense p.Q438E c.1312C>G 1 235972806 CM G C Missense p.S683C c.2048C>G 1 235972070 LUAD G C Missense p.S965C c.2894C>G 1 235969542 LUAD G C Synonymous p.L596L c.1788C>G 1 235972330 LUSC GG AA Missense p.H3419Y c.10254_10255delinsTT 1 235866166 CM GG AA Missense p.T3402I c.10205_10206delinsTT 1 235866215 CM G T Missense p.A3086D c.9257C>A 1 235887386 STAD G T Missense p.H2756N c.8266C>A 1 235904814 LUAD G T Missense p.L187M c.559C>A 1 235973559 COREAD G T Missense p.L2316I c.6946C>A 1 235920694 UCEC G T Missense p.N97K c.291C>A 1 235973827 ESCA G T Missense p.P1047H c.3140C>A 1 235969296 UCEC G T Missense p.P1229H c.3686C>A 1 235966234 UCEC G T Missense p.P594H c.1781C>A 1 235972337 OV G T Missense p.Q1022K c.3064C>A 1 235969372 LUAD G T Missense p.S1544Y c.4631C>A 1 235952058 HNSC G T Missense p.T3593K c.10778C>A 1 235850271 LUAD G T Nonsense p.S1099* c.3296C>A 1 235969140 LUSC G T Nonsense p.S1392* c.4175C>A 1 235955367 CM G T Nonsense p.S1653* c.4958C>A 1 235945292 LUSC G T Nonsense p.S629* c.1886C>A 1 235972232 BRCA G T Synonymous p.P1085P c.3255C>A 1 235969181 CM G T Synonymous p.P1085P c.3255C>A 1 235969181 LUAD G T Synonymous p.R329R c.985C>A 1 235973133 LUAD G T Synonymous p.V3483V c.10449C>A 1 235860498 BRCA T A Missense p.D15V c.44A>T 1 235993674 HNSC T A Missense p.I711F c.2131A>T 1 235971987 ESCA T A Missense p.N111Y c.331A>T 1 235973787 BLCA T A Missense p.N3121I c.9362A>T 1 235884159 CM T A Nonsense p.K2372* c.7114A>T 1 235918893 LUAD T A Nonsense p.K525* c.1573A>T 1 235972545 BRCA T A Nonsense p.K633* c.1897A>T 1 235972221 CM T A SpliceAcceptorSNV . c.10941-2A>T 1 235840490 LUSC T A SpliceAcceptorSNV . c.5461-2A>T 1 235938388 GBM T A Synonymous p.I3642I c.10926A>T 1 235840794 LUAD T A Synonymous p.R2288R c.6864A>T 1 235922289 BRCA T C 3-UTRSNV . c.11403+29A>G 1 235826214 MM T C Missense p.E1125G c.3374A>G 1 235969062 CM T C Missense p.H3698R c.11093A>G 1 235827867 UCEC T C Missense p.H512R c.1535A>G 1 235972583 CM T C Missense p.I2505M c.7515A>G 1 235915417 LUAD T C Missense p.I3673V c.11017A>G 1 235840412 UCEC T C Missense p.I3719V c.11155A>G 1 235827805 STAD T C Missense p.K2703R c.8108A>G 1 235907322 RCCC T C Missense p.K884R c.2651A>G 1 235969785 LUAD T C Missense p.M1647V c.4939A>G 1 235945311 SCLC T C Missense p.N3046D c.9136A>G 1 235891402 BRCA T C Missense p.N3712D c.11134A>G 1 235827826 HNSC T C Missense p.Q3316R c.9947A>G 1 235872587 UCEC T C Missense p.R144G c.430A>G 1 235973688 LUAD T C Missense p.S3477G c.10429A>G 1 235860518 GBM T C Missense p.T1092A c.3274A>G 1 235969162 LUAD T C Missense p.Y1701C c.5102A>G 1 235944277 LUAD T C Missense p.Y2943C c.8828A>G 1 235894451 STAD T C Missense p.Y3613C c.10838A>G 1 235840882 OV T C Synonymous p.A1997A c.5991A>G 1 235929509 CM T C Synonymous p.A3024A c.9072A>G 1 235892930 LUSC T C Synonymous p.K1573K c.4719A>G 1 235950643 CM T C Synonymous p.L2307L c.6921A>G 1 235920719 THCA T C Synonymous p.L2379L c.7137A>G 1 235918870 STAD T C Synonymous p.Q2390Q c.7170A>G 1 235918837 ESCA T C Synonymous p.S1840S c.5520A>G 1 235938327 STAD - T Frameshift p.A1574Sfs*8 c.4719dupA 1 235950643 RCCC - T Frameshift p.N2373Kfs*36 c.7118dupA 1 235918889 RCCC - T Frameshift p.V137Sfs*12 c.408dupA 1 235973710 ESCA T G Missense p.K142N c.426A>C 1 235973692 CM T G Missense p.L1241F c.3723A>C 1 235964387 MM T G Missense p.L264F c.792A>C 1 235973326 LUSC T G Missense p.T193P c.577A>C 1 235973541 HNSC T G Synonymous p.S2213S c.6639A>C 1 235922514 CM T G Synonymous p.V2673V c.8019A>C 1 235907411 CM TGTTAT - MultiAAMissense p.H578_I580delinsL c.1733_1738delATAACA 1 235972380 HNSC T - IntronicDeletion . c.192+136delA 1 235993390 RCCC T - IntronicDeletion . c.192+136delA 1 235993390 STAD TTCCCCTTGAGTG - Frameshift p.T1262*fs*1 c.3783_3795delCACTCAAGGGGAA 1 235964315 HNSC TT - IntronicDeletion . c.192+135_192+136delAA 1 235993390 STAD TTTCGAGGACC - SpliceAcceptorDeletion . c.7781-1_7790delGGTCCTCGAAA 1 235909818 BRCA