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 19 8587291 8587291 + Missense_Mutation SNP C C T TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr19:8587291C>T c.3190G>A c.(3190-3192)Gtg>Atg p.V1064M ACC 19 8595175 8595175 + Missense_Mutation SNP C C A TCGA-OR-A5LC-01A-11D-A29I-10 TCGA-OR-A5LC-10A-01D-A29L-10 g.chr19:8595175C>A c.2233G>T c.(2233-2235)Ggg>Tgg p.G745W ACC 19 8604874 8604874 + Missense_Mutation SNP C C T TCGA-OR-A5J4-01A-11D-A29I-10 TCGA-OR-A5J4-10A-01D-A29L-10 g.chr19:8604874C>T c.1649G>A c.(1648-1650)gGa>gAa p.G550E BLCA 19 8587285 8587285 + Missense_Mutation SNP C C T TCGA-UY-A9PH-01A-11D-A38G-08 TCGA-UY-A9PH-10A-01D-A38J-08 g.chr19:8587285C>T c.3196G>A c.(3196-3198)Gag>Aag p.E1066K BLCA 19 8587680 8587680 + Missense_Mutation SNP C C G TCGA-C4-A0F6-01A-11D-A10S-08 TCGA-C4-A0F6-10A-01D-A10S-08 g.chr19:8587680C>G c.2888G>C c.(2887-2889)aGa>aCa p.R963T BLCA 19 8591788 8591788 + Missense_Mutation SNP C C G TCGA-K4-A3WU-01B-11D-A23M-08 TCGA-K4-A3WU-10A-01D-A23K-08 g.chr19:8591788C>G c.2506G>C c.(2506-2508)Gag>Cag p.E836Q BLCA 19 8606846 8606846 + Missense_Mutation SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr19:8606846C>G c.1554G>C c.(1552-1554)gaG>gaC p.E518D BLCA 19 8609262 8609262 + Missense_Mutation SNP C C G TCGA-4Z-AA87-01A-11D-A391-08 TCGA-4Z-AA87-10A-01D-A394-08 g.chr19:8609262C>G c.1443G>C c.(1441-1443)caG>caC p.Q481H BLCA 19 8609274 8609274 + Missense_Mutation SNP C C G TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr19:8609274C>G c.1431G>C c.(1429-1431)caG>caC p.Q477H BLCA 19 8609325 8609325 + Silent SNP G G A TCGA-FJ-A3ZE-01A-11D-A23M-08 TCGA-FJ-A3ZE-10A-01D-A23K-08 g.chr19:8609325G>A c.1380C>T c.(1378-1380)gtC>gtT p.V460V BLCA 19 8615059 8615059 + Silent SNP G G A TCGA-XF-AAMQ-01A-11D-A42E-08 TCGA-XF-AAMQ-10A-01D-A42H-08 g.chr19:8615059G>A c.1086C>T c.(1084-1086)ttC>ttT p.F362F BLCA 19 8615474 8615474 + Silent SNP C C T TCGA-G2-A3IE-01A-11D-A20D-08 TCGA-G2-A3IE-10A-01D-A20D-08 g.chr19:8615474C>T c.876G>A c.(874-876)ggG>ggA p.G292G BLCA 19 8615562 8615562 + Missense_Mutation SNP A A T TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr19:8615562A>T c.788T>A c.(787-789)aTt>aAt p.I263N BLCA 19 8615579 8615579 + Splice_Site SNP C C G TCGA-FD-A6TF-01A-52D-A32B-08 TCGA-FD-A6TF-10A-21D-A329-08 g.chr19:8615579C>G c.e9-1 BLCA 19 8616632 8616632 + Missense_Mutation SNP C C T TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr19:8616632C>T c.763G>A c.(763-765)Gag>Aag p.E255K BLCA 19 8616983 8616983 + Missense_Mutation SNP G G T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr19:8616983G>T c.570C>A c.(568-570)ttC>ttA p.F190L BLCA 19 8617036 8617036 + Missense_Mutation SNP C C G TCGA-DK-A3IQ-01A-31D-A20D-08 TCGA-DK-A3IQ-10A-01D-A20D-08 g.chr19:8617036C>G c.517G>C c.(517-519)Gag>Cag p.E173Q BLCA 19 8617036 8617036 + Missense_Mutation SNP C C G TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr19:8617036C>G c.517G>C c.(517-519)Gag>Cag p.E173Q BLCA 19 8618073 8618073 + Missense_Mutation SNP C C T TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr19:8618073C>T c.454G>A c.(454-456)Gag>Aag p.E152K BLCA 19 8618223 8618246 + Splice_Site DEL CCTCGTCTCACCTGGACCTTCTCG CCTCGTCTCACCTGGACCTTCTCG - TCGA-DK-AA75-01A-11D-A391-08 TCGA-DK-AA75-10A-01D-A394-08 g.chr19:8618223_8618246delCCTCGTCTCACCTGGACCTTCTCG c.402_415delCGAGAAGGTCCAGGTGAGACGAGG c.(400-417)ggcgagaaggtccaggtg>ggtg p.EKVQV135del BLCA 19 8619436 8619436 + Missense_Mutation SNP G G A TCGA-4Z-AA7W-01A-11D-A391-08 TCGA-4Z-AA7W-10A-01D-A394-08 g.chr19:8619436G>A c.251C>T c.(250-252)cCg>cTg p.P84L BLCA 19 8619448 8619448 + Missense_Mutation SNP T T C TCGA-ZF-A9R5-01A-12D-A42E-08 TCGA-ZF-A9R5-10A-01D-A42H-08 g.chr19:8619448T>C c.239A>G c.(238-240)tAt>tGt p.Y80C BLCA 19 8619567 8619567 + Missense_Mutation SNP C C T TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr19:8619567C>T c.202G>A c.(202-204)Gac>Aac p.D68N BLCA 19 8620604 8620604 + Missense_Mutation SNP T T G TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr19:8620604T>G c.80A>C c.(79-81)cAg>cCg p.Q27P BLCA 19 8620611 8620611 + Missense_Mutation SNP G G A TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr19:8620611G>A c.73C>T c.(73-75)Ctt>Ttt p.L25F BRCA 19 8587599 8587599 + Missense_Mutation SNP C C G TCGA-E9-A1R4-01A-21D-A14G-09 TCGA-E9-A1R4-10A-01D-A14G-09 g.chr19:8587599C>G c.2969G>C c.(2968-2970)gGa>gCa p.G990A BRCA 19 8587613 8587613 + Silent SNP C C A TCGA-BH-A5IZ-01A-11D-A27P-09 TCGA-BH-A5IZ-11A-13D-A27P-09 g.chr19:8587613C>A c.2955G>T c.(2953-2955)ccG>ccT p.P985P BRCA 19 8592341 8592341 + Silent SNP C C T TCGA-BH-A0E6-01A-11W-A050-09 TCGA-BH-A0E6-10A-01W-A055-09 g.chr19:8592341C>T c.2355G>A c.(2353-2355)acG>acA p.T785T BRCA 19 8601262 8601262 + Silent SNP G G A TCGA-AR-A1AR-01A-31D-A135-09 TCGA-AR-A1AR-10A-01D-A135-09 g.chr19:8601262G>A c.1917C>T c.(1915-1917)ccC>ccT p.P639P BRCA 19 8615476 8615476 + Missense_Mutation SNP C C T TCGA-A8-A07E-01A-11W-A050-09 TCGA-A8-A07E-10A-01W-A055-09 g.chr19:8615476C>T c.874G>A c.(874-876)Ggg>Agg p.G292R BRCA 19 8615498 8615498 + Silent SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr19:8615498C>T c.852G>A c.(850-852)ggG>ggA p.G284G BRCA 19 8620576 8620576 + Missense_Mutation SNP G G T TCGA-AO-A129-01A-21D-A10M-09 TCGA-AO-A129-10A-01D-A10M-09 g.chr19:8620576G>T c.108C>A c.(106-108)aaC>aaA p.N36K CESC 19 8587697 8587697 + Silent SNP C C A TCGA-C5-A2LX-01A-11D-A18J-09 TCGA-C5-A2LX-10A-01D-A18J-09 g.chr19:8587697C>A c.2871G>T c.(2869-2871)ggG>ggT p.G957G CESC 19 8595361 8595361 + Missense_Mutation SNP C C T TCGA-EK-A3GJ-01A-21D-A20U-09 TCGA-EK-A3GJ-11A-11D-A20U-09 g.chr19:8595361C>T c.2140G>A c.(2140-2142)Gag>Aag p.E714K CESC 19 8616752 8616752 + Nonsense_Mutation SNP C C A TCGA-IR-A3LH-01A-21D-A20U-09 TCGA-IR-A3LH-10A-01D-A20U-09 g.chr19:8616752C>A c.643G>T c.(643-645)Gaa>Taa p.E215* CESC 19 8620554 8620554 + Missense_Mutation SNP C C T TCGA-C5-A1MH-01A-11D-A14W-08 TCGA-C5-A1MH-10A-01D-A14W-08 g.chr19:8620554C>T c.130G>A c.(130-132)Gac>Aac p.D44N COAD 19 8587343 8587343 + Silent SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr19:8587343G>A c.3138C>T c.(3136-3138)tgC>tgT p.C1046C COAD 19 8587669 8587669 + Frame_Shift_Del DEL G G - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr19:8587669delG c.2899delC c.(2899-2901)ctgfs p.L967fs COAD 19 8591709 8591709 + Missense_Mutation SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr19:8591709G>A c.2585C>T c.(2584-2586)gCg>gTg p.A862V COAD 19 8591767 8591767 + Missense_Mutation SNP G G T TCGA-DM-A282-01A-12D-A16V-10 TCGA-DM-A282-10A-01D-A16V-10 g.chr19:8591767G>T c.2527C>A c.(2527-2529)Ctg>Atg p.L843M COAD 19 8592319 8592319 + Missense_Mutation SNP C C A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr19:8592319C>A c.2377G>T c.(2377-2379)Ggg>Tgg p.G793W COAD 19 8595116 8595116 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr19:8595116G>A c.2292C>T c.(2290-2292)ttC>ttT p.F764F COAD 19 8595157 8595157 + Missense_Mutation SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr19:8595157C>T c.2251G>A c.(2251-2253)Gag>Aag p.E751K COAD 19 8595422 8595422 + Silent SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr19:8595422G>A c.2079C>T c.(2077-2079)ttC>ttT p.F693F COAD 19 8601412 8601412 + Silent SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr19:8601412G>A c.1869C>T c.(1867-1869)taC>taT p.Y623Y COAD 19 8601852 8601852 + Nonsense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr19:8601852G>A c.1780C>T c.(1780-1782)Cga>Tga p.R594* COAD 19 8609251 8609251 + Missense_Mutation SNP G G A TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr19:8609251G>A c.1454C>T c.(1453-1455)gCg>gTg p.A485V COAD 19 8609319 8609319 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr19:8609319G>A c.1386C>T c.(1384-1386)gaC>gaT p.D462D COAD 19 8612995 8612995 + Silent SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr19:8612995G>A c.1194C>T c.(1192-1194)ttC>ttT p.F398F COAD 19 8612995 8612995 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr19:8612995G>A c.1194C>T c.(1192-1194)ttC>ttT p.F398F COAD 19 8613157 8613157 + Silent SNP G G A TCGA-CM-6675-01A-11D-1835-10 TCGA-CM-6675-10A-01D-1835-10 g.chr19:8613157G>A c.1146C>T c.(1144-1146)atC>atT p.I382I COAD 19 8615468 8615468 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr19:8615468G>A c.882C>T c.(880-882)taC>taT p.Y294Y COAD 19 8615496 8615496 + Missense_Mutation SNP T T C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr19:8615496T>C c.854A>G c.(853-855)aAc>aGc p.N285S COAD 19 8616651 8616651 + Silent SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr19:8616651G>A c.744C>T c.(742-744)gaC>gaT p.D248D COAD 19 8616669 8616669 + Silent SNP G G A TCGA-CA-5255-01A-11D-1835-10 TCGA-CA-5255-10A-01D-1835-10 g.chr19:8616669G>A c.726C>T c.(724-726)taC>taT p.Y242Y COAD 19 8616671 8616671 + Missense_Mutation SNP A A G TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr19:8616671A>G c.724T>C c.(724-726)Tac>Cac p.Y242H COAD 19 8616671 8616671 + Missense_Mutation SNP A A T TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr19:8616671A>T c.724T>A c.(724-726)Tac>Aac p.Y242N COAD 19 8617025 8617025 + Silent SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr19:8617025G>A c.528C>T c.(526-528)ttC>ttT p.F176F COAD 19 8619398 8619398 + Missense_Mutation SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr19:8619398T>C c.289A>G c.(289-291)Atg>Gtg p.M97V COAD 19 8619403 8619403 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr19:8619403C>T c.284G>A c.(283-285)cGg>cAg p.R95Q COAD 19 8619421 8619421 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr19:8619421A>G c.266T>C c.(265-267)cTc>cCc p.L89P COAD 19 8619436 8619436 + Frame_Shift_Del DEL G G - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr19:8619436delG c.251delC c.(250-252)ccgfs p.P84fs COAD 19 8619538 8619538 + Splice_Site SNP C C T TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr19:8619538C>T c.231G>A c.(229-231)gcG>gcA p.A77A COAD 19 8619556 8619556 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr19:8619556G>A c.213C>T c.(211-213)atC>atT p.I71I COAD 19 8619618 8619618 + Missense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr19:8619618C>T c.151G>A c.(151-153)Ggc>Agc p.G51S COAD 19 8620542 8620542 + Splice_Site SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr19:8620542C>T c.e2+1 COAD 19 8620640 8620640 + Missense_Mutation SNP T T C TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr19:8620640T>C c.44A>G c.(43-45)aAg>aGg p.K15R COAD 19 8620640 8620640 + Missense_Mutation SNP T T C TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr19:8620640T>C c.44A>G c.(43-45)aAg>aGg p.K15R COADREAD 19 8587343 8587343 + Silent SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr19:8587343G>A c.3138C>T c.(3136-3138)tgC>tgT p.C1046C COADREAD 19 8587669 8587669 + Frame_Shift_Del DEL G G - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr19:8587669delG c.2899delC c.(2899-2901)ctgfs p.L967fs COADREAD 19 8591709 8591709 + Missense_Mutation SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr19:8591709G>A c.2585C>T c.(2584-2586)gCg>gTg p.A862V COADREAD 19 8591767 8591767 + Missense_Mutation SNP G G T TCGA-DM-A282-01A-12D-A16V-10 TCGA-DM-A282-10A-01D-A16V-10 g.chr19:8591767G>T c.2527C>A c.(2527-2529)Ctg>Atg p.L843M COADREAD 19 8592319 8592319 + Missense_Mutation SNP C C A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr19:8592319C>A c.2377G>T c.(2377-2379)Ggg>Tgg p.G793W COADREAD 19 8595116 8595116 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr19:8595116G>A c.2292C>T c.(2290-2292)ttC>ttT p.F764F COADREAD 19 8595157 8595157 + Missense_Mutation SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr19:8595157C>T c.2251G>A c.(2251-2253)Gag>Aag p.E751K COADREAD 19 8595422 8595422 + Silent SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr19:8595422G>A c.2079C>T c.(2077-2079)ttC>ttT p.F693F COADREAD 19 8601412 8601412 + Silent SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr19:8601412G>A c.1869C>T c.(1867-1869)taC>taT p.Y623Y COADREAD 19 8601852 8601852 + Nonsense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr19:8601852G>A c.1780C>T c.(1780-1782)Cga>Tga p.R594* COADREAD 19 8609251 8609251 + Missense_Mutation SNP G G A TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr19:8609251G>A c.1454C>T c.(1453-1455)gCg>gTg p.A485V COADREAD 19 8609319 8609319 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr19:8609319G>A c.1386C>T c.(1384-1386)gaC>gaT p.D462D COADREAD 19 8612995 8612995 + Silent SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr19:8612995G>A c.1194C>T c.(1192-1194)ttC>ttT p.F398F COADREAD 19 8612995 8612995 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr19:8612995G>A c.1194C>T c.(1192-1194)ttC>ttT p.F398F COADREAD 19 8613157 8613157 + Silent SNP G G A TCGA-CM-6675-01A-11D-1835-10 TCGA-CM-6675-10A-01D-1835-10 g.chr19:8613157G>A c.1146C>T c.(1144-1146)atC>atT p.I382I COADREAD 19 8615468 8615468 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr19:8615468G>A c.882C>T c.(880-882)taC>taT p.Y294Y COADREAD 19 8615496 8615496 + Missense_Mutation SNP T T C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr19:8615496T>C c.854A>G c.(853-855)aAc>aGc p.N285S COADREAD 19 8616651 8616651 + Silent SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr19:8616651G>A c.744C>T c.(742-744)gaC>gaT p.D248D COADREAD 19 8616669 8616669 + Silent SNP G G A TCGA-CA-5255-01A-11D-1835-10 TCGA-CA-5255-10A-01D-1835-10 g.chr19:8616669G>A c.726C>T c.(724-726)taC>taT p.Y242Y COADREAD 19 8616671 8616671 + Missense_Mutation SNP A A G TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr19:8616671A>G c.724T>C c.(724-726)Tac>Cac p.Y242H COADREAD 19 8616671 8616671 + Missense_Mutation SNP A A T TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr19:8616671A>T c.724T>A c.(724-726)Tac>Aac p.Y242N COADREAD 19 8617025 8617025 + Silent SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr19:8617025G>A c.528C>T c.(526-528)ttC>ttT p.F176F COADREAD 19 8619398 8619398 + Missense_Mutation SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr19:8619398T>C c.289A>G c.(289-291)Atg>Gtg p.M97V COADREAD 19 8619403 8619403 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr19:8619403C>T c.284G>A c.(283-285)cGg>cAg p.R95Q COADREAD 19 8619421 8619421 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr19:8619421A>G c.266T>C c.(265-267)cTc>cCc p.L89P COADREAD 19 8619436 8619436 + Frame_Shift_Del DEL G G - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr19:8619436delG c.251delC c.(250-252)ccgfs p.P84fs COADREAD 19 8619538 8619538 + Splice_Site SNP C C T TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr19:8619538C>T c.231G>A c.(229-231)gcG>gcA p.A77A COADREAD 19 8619556 8619556 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr19:8619556G>A c.213C>T c.(211-213)atC>atT p.I71I COADREAD 19 8619618 8619618 + Missense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr19:8619618C>T c.151G>A c.(151-153)Ggc>Agc p.G51S COADREAD 19 8620542 8620542 + Splice_Site SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr19:8620542C>T c.e2+1 COADREAD 19 8620640 8620640 + Missense_Mutation SNP T T C TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr19:8620640T>C c.44A>G c.(43-45)aAg>aGg p.K15R COADREAD 19 8620640 8620640 + Missense_Mutation SNP T T C TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr19:8620640T>C c.44A>G c.(43-45)aAg>aGg p.K15R DLBC 19 8601222 8601222 + Missense_Mutation SNP C C T TCGA-FF-8042-01A-11D-2210-10 TCGA-FF-8042-10A-01D-2210-10 g.chr19:8601222C>T c.1957G>A c.(1957-1959)Gtc>Atc p.V653I DLBC 19 8616999 8616999 + Missense_Mutation SNP C C T TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr19:8616999C>T c.554G>A c.(553-555)gGc>gAc p.G185D DLBC 19 8620636 8620636 + Silent SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr19:8620636C>T c.48G>A c.(46-48)caG>caA p.Q16Q ESCA 19 8587367 8587367 + Missense_Mutation SNP C C G TCGA-IG-A625-01A-11D-A31U-09 TCGA-IG-A625-10A-01D-A31U-09 g.chr19:8587367C>G c.3114G>C c.(3112-3114)caG>caC p.Q1038H ESCA 19 8587572 8587572 + Missense_Mutation SNP G G A TCGA-2H-A9GL-01A-12D-A37C-09 TCGA-2H-A9GL-11A-11D-A37F-09 g.chr19:8587572G>A c.2996C>T c.(2995-2997)cCg>cTg p.P999L ESCA 19 8587613 8587613 + Silent SNP C C G TCGA-LN-A7HY-01A-12D-A351-09 TCGA-LN-A7HY-10A-01D-A351-09 g.chr19:8587613C>G c.2955G>C c.(2953-2955)ccG>ccC p.P985P ESCA 19 8592306 8592306 + Missense_Mutation SNP A A G TCGA-L5-A4OQ-01A-11D-A27G-09 TCGA-L5-A4OQ-11A-12D-A27G-09 g.chr19:8592306A>G c.2390T>C c.(2389-2391)gTg>gCg p.V797A ESCA 19 8595219 8595219 + Missense_Mutation SNP C C T TCGA-V5-A7RB-01A-11D-A351-09 TCGA-V5-A7RB-10A-01D-A351-09 g.chr19:8595219C>T c.2189G>A c.(2188-2190)cGg>cAg p.R730Q GBM 19 8616651 8616651 + Silent SNP G G A TCGA-76-6661-01B-11D-1845-08 TCGA-76-6661-10A-01D-1845-08 g.chr19:8616651G>A c.744C>T c.(742-744)gaC>gaT p.D248D GBMLGG 19 8587611 8587611 + Missense_Mutation SNP G G A TCGA-TQ-A7RQ-01A-11D-A33T-08 TCGA-TQ-A7RQ-10A-01D-A33W-08 g.chr19:8587611G>A c.2957C>T c.(2956-2958)tCc>tTc p.S986F GBMLGG 19 8601203 8601203 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:8601203G>A c.1976C>T c.(1975-1977)gCg>gTg p.A659V GBMLGG 19 8601249 8601249 + Missense_Mutation SNP G G A TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr19:8601249G>A c.1930C>T c.(1930-1932)Cgg>Tgg p.R644W GBMLGG 19 8606809 8606809 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:8606809G>T c.1591C>A c.(1591-1593)Ctg>Atg p.L531M GBMLGG 19 8609329 8609329 + Missense_Mutation SNP C C G TCGA-E1-A7YW-01A-11D-A34J-08 TCGA-E1-A7YW-10A-01D-A34M-08 g.chr19:8609329C>G c.1376G>C c.(1375-1377)aGc>aCc p.S459T GBMLGG 19 8616651 8616651 + Silent SNP G G A TCGA-76-6661-01B-11D-1845-08 TCGA-76-6661-10A-01D-1845-08 g.chr19:8616651G>A c.744C>T c.(742-744)gaC>gaT p.D248D GBMLGG 19 8617006 8617006 + Missense_Mutation SNP C C G TCGA-P5-A5EV-01A-11D-A27K-08 TCGA-P5-A5EV-10A-01D-A27N-08 g.chr19:8617006C>G c.547G>C c.(547-549)Gat>Cat p.D183H GBMLGG 19 8619587 8619587 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:8619587T>C c.182A>G c.(181-183)aAg>aGg p.K61R GBMLGG 19 8620581 8620581 + Missense_Mutation SNP C C T TCGA-HT-7855-01A-11D-2395-08 TCGA-HT-7855-10A-01D-2396-08 g.chr19:8620581C>T c.103G>A c.(103-105)Gcc>Acc p.A35T HNSC 19 8587264 8587264 + Missense_Mutation SNP C C T TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr19:8587264C>T c.3217G>A c.(3217-3219)Gaa>Aaa p.E1073K HNSC 19 8587564 8587564 + Missense_Mutation SNP C C T TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr19:8587564C>T c.3004G>A c.(3004-3006)Gag>Aag p.E1002K HNSC 19 8587614 8587614 + Missense_Mutation SNP G G A TCGA-CN-5356-01A-01D-1434-08 TCGA-CN-5356-10A-01D-1434-08 g.chr19:8587614G>A c.2954C>T c.(2953-2955)cCg>cTg p.P985L HNSC 19 8592316 8592316 + Silent SNP G G T TCGA-CQ-7064-01A-11D-2394-08 TCGA-CQ-7064-10A-01D-2394-08 g.chr19:8592316G>T c.2380C>A c.(2380-2382)Cga>Aga p.R794R HNSC 19 8601169 8601169 + Silent SNP C C T TCGA-QK-A64Z-01A-11D-A30E-08 TCGA-QK-A64Z-10A-01D-A30H-08 g.chr19:8601169C>T c.2010G>A c.(2008-2010)ggG>ggA p.G670G HNSC 19 8601428 8601428 + Missense_Mutation SNP C C G TCGA-BA-4077-01B-01D-1434-08 TCGA-BA-4077-10A-01D-1434-08 g.chr19:8601428C>G c.1853G>C c.(1852-1854)aGa>aCa p.R618T HNSC 19 8606807 8606807 + Silent SNP C C G TCGA-CV-5442-01A-01D-1512-08 TCGA-CV-5442-11A-01D-1512-08 g.chr19:8606807C>G c.1593G>C c.(1591-1593)ctG>ctC p.L531L HNSC 19 8615225 8615225 + Missense_Mutation SNP G G A TCGA-C9-A480-01A-12D-A24D-08 TCGA-C9-A480-10A-01D-A24F-08 g.chr19:8615225G>A c.920C>T c.(919-921)gCc>gTc p.A307V HNSC 19 8616943 8616943 + Missense_Mutation SNP C C G TCGA-CN-6992-01A-11D-1912-08 TCGA-CN-6992-10A-01D-1912-08 g.chr19:8616943C>G c.610G>C c.(610-612)Gag>Cag p.E204Q HNSC 19 8618065 8618065 + Silent SNP G G A TCGA-CV-7407-01A-11D-2078-08 TCGA-CV-7407-10A-01D-2078-08 g.chr19:8618065G>A c.462C>T c.(460-462)ttC>ttT p.F154F HNSC 19 8618294 8618294 + Silent SNP C C G TCGA-CR-7368-01A-11D-2129-08 TCGA-CR-7368-10A-01D-2129-08 g.chr19:8618294C>G c.354G>C c.(352-354)gtG>gtC p.V118V HNSC 19 8619427 8619427 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr19:8619427T>C c.260A>G c.(259-261)tAc>tGc p.Y87C HNSC 19 8619446 8619446 + Missense_Mutation SNP C C T TCGA-CV-7406-01A-11D-2078-08 TCGA-CV-7406-10A-01D-2078-08 g.chr19:8619446C>T c.241G>A c.(241-243)Gag>Aag p.E81K KICH 19 8592315 8592315 + Missense_Mutation SNP C C T TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr19:8592315C>T c.2381G>A c.(2380-2382)cGa>cAa p.R794Q KICH 19 8615207 8615207 + Missense_Mutation SNP T T A TCGA-KM-8443-01A-11D-2310-10 TCGA-KM-8443-10A-01D-2311-10 g.chr19:8615207T>A c.938A>T c.(937-939)gAc>gTc p.D313V KIPAN 19 8592225 8592225 + Missense_Mutation SNP A A T TCGA-B0-5119-01A-02D-1421-08 TCGA-B0-5119-11A-01D-1421-08 g.chr19:8592225A>T c.2471T>A c.(2470-2472)cTc>cAc p.L824H KIPAN 19 8592315 8592315 + Missense_Mutation SNP C C T TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr19:8592315C>T c.2381G>A c.(2380-2382)cGa>cAa p.R794Q KIPAN 19 8595162 8595162 + Missense_Mutation SNP C C T TCGA-CZ-5457-01A-01D-1501-10 TCGA-CZ-5457-11A-01D-1501-10 g.chr19:8595162C>T c.2246G>A c.(2245-2247)cGg>cAg p.R749Q KIPAN 19 8604865 8604865 + Missense_Mutation SNP T T G TCGA-BQ-5889-01A-11D-1589-08 TCGA-BQ-5889-11A-01D-1589-08 g.chr19:8604865T>G c.1658A>C c.(1657-1659)aAg>aCg p.K553T KIPAN 19 8606866 8606866 + Missense_Mutation SNP C C T TCGA-BP-4992-01A-01D-1462-08 TCGA-BP-4992-11A-01D-1462-08 g.chr19:8606866C>T c.1534G>A c.(1534-1536)Gac>Aac p.D512N KIPAN 19 8609279 8609279 + Missense_Mutation SNP C C A TCGA-EV-5902-01A-11D-1589-08 TCGA-EV-5902-10A-01D-1589-08 g.chr19:8609279C>A c.1426G>T c.(1426-1428)Gac>Tac p.D476Y KIPAN 19 8612963 8612963 + Missense_Mutation SNP T T A TCGA-BP-4352-01A-01D-1366-10 TCGA-BP-4352-11A-01D-1366-10 g.chr19:8612963T>A c.1226A>T c.(1225-1227)aAg>aTg p.K409M KIPAN 19 8615148 8615148 + Missense_Mutation SNP G G C TCGA-5P-A9JY-01A-11D-A42J-10 TCGA-5P-A9JY-10A-01D-A42M-10 g.chr19:8615148G>C c.997C>G c.(997-999)Cgc>Ggc p.R333G KIPAN 19 8615207 8615207 + Missense_Mutation SNP T T A TCGA-KM-8443-01A-11D-2310-10 TCGA-KM-8443-10A-01D-2311-10 g.chr19:8615207T>A c.938A>T c.(937-939)gAc>gTc p.D313V KIPAN 19 8616967 8616967 + Missense_Mutation SNP G G T TCGA-DZ-6132-01A-11D-1961-08 TCGA-DZ-6132-11A-01D-1961-08 g.chr19:8616967G>T c.586C>A c.(586-588)Cgc>Agc p.R196S KIPAN 19 8642191 8642191 + Splice_Site SNP C C G TCGA-A4-A48D-01A-11D-A25F-10 TCGA-A4-A48D-10A-01D-A25F-10 g.chr19:8642191C>G c.3G>C c.(1-3)atG>atC p.M1I KIRC 19 8592225 8592225 + Missense_Mutation SNP A A T TCGA-B0-5119-01A-02D-1421-08 TCGA-B0-5119-11A-01D-1421-08 g.chr19:8592225A>T c.2471T>A c.(2470-2472)cTc>cAc p.L824H KIRC 19 8595162 8595162 + Missense_Mutation SNP C C T TCGA-CZ-5457-01A-01D-1501-10 TCGA-CZ-5457-11A-01D-1501-10 g.chr19:8595162C>T c.2246G>A c.(2245-2247)cGg>cAg p.R749Q KIRC 19 8606866 8606866 + Missense_Mutation SNP C C T TCGA-BP-4992-01A-01D-1462-08 TCGA-BP-4992-11A-01D-1462-08 g.chr19:8606866C>T c.1534G>A c.(1534-1536)Gac>Aac p.D512N KIRC 19 8612963 8612963 + Missense_Mutation SNP T T A TCGA-BP-4352-01A-01D-1366-10 TCGA-BP-4352-11A-01D-1366-10 g.chr19:8612963T>A c.1226A>T c.(1225-1227)aAg>aTg p.K409M KIRP 19 8604865 8604865 + Missense_Mutation SNP T T G TCGA-BQ-5889-01A-11D-1589-08 TCGA-BQ-5889-11A-01D-1589-08 g.chr19:8604865T>G c.1658A>C c.(1657-1659)aAg>aCg p.K553T KIRP 19 8609279 8609279 + Missense_Mutation SNP C C A TCGA-EV-5902-01A-11D-1589-08 TCGA-EV-5902-10A-01D-1589-08 g.chr19:8609279C>A c.1426G>T c.(1426-1428)Gac>Tac p.D476Y KIRP 19 8615148 8615148 + Missense_Mutation SNP G G C TCGA-5P-A9JY-01A-11D-A42J-10 TCGA-5P-A9JY-10A-01D-A42M-10 g.chr19:8615148G>C c.997C>G c.(997-999)Cgc>Ggc p.R333G KIRP 19 8616967 8616967 + Missense_Mutation SNP G G T TCGA-DZ-6132-01A-11D-1961-08 TCGA-DZ-6132-11A-01D-1961-08 g.chr19:8616967G>T c.586C>A c.(586-588)Cgc>Agc p.R196S KIRP 19 8642191 8642191 + Splice_Site SNP C C G TCGA-A4-A48D-01A-11D-A25F-10 TCGA-A4-A48D-10A-01D-A25F-10 g.chr19:8642191C>G c.3G>C c.(1-3)atG>atC p.M1I LAML 19 8606789 8606789 + Splice_Site SNP C C T TCGA-AB-3002-03A-01D-0739-09 TCGA-AB-3002-11A-01D-0739-09 g.chr19:8606789C>T c.e15+1 LGG 19 8587611 8587611 + Missense_Mutation SNP G G A TCGA-TQ-A7RQ-01A-11D-A33T-08 TCGA-TQ-A7RQ-10A-01D-A33W-08 g.chr19:8587611G>A c.2957C>T c.(2956-2958)tCc>tTc p.S986F LGG 19 8601203 8601203 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:8601203G>A c.1976C>T c.(1975-1977)gCg>gTg p.A659V LGG 19 8601249 8601249 + Missense_Mutation SNP G G A TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr19:8601249G>A c.1930C>T c.(1930-1932)Cgg>Tgg p.R644W LGG 19 8606809 8606809 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:8606809G>T c.1591C>A c.(1591-1593)Ctg>Atg p.L531M LGG 19 8609329 8609329 + Missense_Mutation SNP C C G TCGA-E1-A7YW-01A-11D-A34J-08 TCGA-E1-A7YW-10A-01D-A34M-08 g.chr19:8609329C>G c.1376G>C c.(1375-1377)aGc>aCc p.S459T LGG 19 8617006 8617006 + Missense_Mutation SNP C C G TCGA-P5-A5EV-01A-11D-A27K-08 TCGA-P5-A5EV-10A-01D-A27N-08 g.chr19:8617006C>G c.547G>C c.(547-549)Gat>Cat p.D183H LGG 19 8619587 8619587 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:8619587T>C c.182A>G c.(181-183)aAg>aGg p.K61R LGG 19 8620581 8620581 + Missense_Mutation SNP C C T TCGA-HT-7855-01A-11D-2395-08 TCGA-HT-7855-10A-01D-2396-08 g.chr19:8620581C>T c.103G>A c.(103-105)Gcc>Acc p.A35T LIHC 19 8587279 8587279 + Missense_Mutation SNP T T C TCGA-DD-AACY-01A-11D-A40R-10 TCGA-DD-AACY-10A-01D-A40U-10 g.chr19:8587279T>C c.3202A>G c.(3202-3204)Att>Gtt p.I1068V LIHC 19 8619381 8619395 + In_Frame_Del DEL CTCACAGTCGATAAG CTCACAGTCGATAAG - TCGA-CC-A7II-01A-11D-A33K-10 TCGA-CC-A7II-10A-01D-A33K-10 g.chr19:8619381_8619395delCTCACAGTCGATAAG c.292_306delCTTATCGACTGTGAG c.(292-306)cttatcgactgtgagdel p.LIDCE98del LUAD 19 8587292 8587292 + Silent SNP G G A TCGA-17-Z037-01A-01W-0746-08 TCGA-17-Z037-11A-01W-0746-08 g.chr19:8587292G>A c.3189C>T c.(3187-3189)aaC>aaT p.N1063N LUAD 19 8590439 8590439 + Silent SNP C C A TCGA-55-8301-01A-11D-2284-08 TCGA-55-8301-10A-01D-2284-08 g.chr19:8590439C>A c.2778G>T c.(2776-2778)acG>acT p.T926T LUAD 19 8590441 8590441 + Missense_Mutation SNP T T A TCGA-17-Z014-01A-01W-0746-08 TCGA-17-Z014-11A-01W-0746-08 g.chr19:8590441T>A c.2776A>T c.(2776-2778)Acg>Tcg p.T926S LUAD 19 8591385 8591385 + Missense_Mutation SNP C C T TCGA-55-1592-01A-01D-0969-08 TCGA-55-1592-11A-01D-0969-08 g.chr19:8591385C>T c.2722G>A c.(2722-2724)Ggt>Agt p.G908S LUAD 19 8592263 8592263 + Silent SNP C C T TCGA-05-5425-01A-02D-1625-08 TCGA-05-5425-10A-01D-1625-08 g.chr19:8592263C>T c.2433G>A c.(2431-2433)aaG>aaA p.K811K LUAD 19 8595209 8595209 + Missense_Mutation SNP G G T TCGA-55-A493-01A-11D-A24D-08 TCGA-55-A493-10A-01D-A24F-08 g.chr19:8595209G>T c.2199C>A c.(2197-2199)aaC>aaA p.N733K LUAD 19 8595209 8595209 + Missense_Mutation SNP G G T TCGA-95-7944-01A-11D-2184-08 TCGA-95-7944-10A-01D-2184-08 g.chr19:8595209G>T c.2199C>A c.(2197-2199)aaC>aaA p.N733K LUAD 19 8595413 8595413 + Silent SNP A A G TCGA-17-Z027-01A-01W-0746-08 TCGA-17-Z027-11A-01W-0746-08 g.chr19:8595413A>G c.2088T>C c.(2086-2088)ttT>ttC p.F696F LUAD 19 8601171 8601171 + Missense_Mutation SNP C C T TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr19:8601171C>T c.2008G>A c.(2008-2010)Ggg>Agg p.G670R LUAD 19 8601175 8601175 + Missense_Mutation SNP C C G TCGA-97-A4M5-01A-11D-A24P-08 TCGA-97-A4M5-10A-01D-A24P-08 g.chr19:8601175C>G c.2004G>C c.(2002-2004)caG>caC p.Q668H LUAD 19 8601438 8601438 + Silent SNP T T G TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chr19:8601438T>G c.1843A>C c.(1843-1845)Agg>Cgg p.R615R LUAD 19 8601852 8601852 + Silent SNP G G T TCGA-17-Z049-01A-01W-0746-08 TCGA-17-Z049-11A-01W-0747-08 g.chr19:8601852G>T c.1780C>A c.(1780-1782)Cga>Aga p.R594R LUAD 19 8615069 8615069 + Missense_Mutation SNP G G T TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr19:8615069G>T c.1076C>A c.(1075-1077)gCc>gAc p.A359D LUAD 19 8615202 8615202 + Missense_Mutation SNP C C T TCGA-69-8254-01A-11D-2284-08 TCGA-69-8254-10A-01D-2284-08 g.chr19:8615202C>T c.943G>A c.(943-945)Ggg>Agg p.G315R LUAD 19 8615449 8615449 + Missense_Mutation SNP C C A TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr19:8615449C>A c.901G>T c.(901-903)Gac>Tac p.D301Y LUAD 19 8619559 8619559 + Missense_Mutation SNP C C G TCGA-50-5049-01A-01D-1625-08 TCGA-50-5049-10A-01D-1625-08 g.chr19:8619559C>G c.210G>C c.(208-210)gaG>gaC p.E70D LUAD 19 8619594 8619594 + Missense_Mutation SNP G G T TCGA-55-8094-01A-11D-2238-08 TCGA-55-8094-10A-01D-2238-08 g.chr19:8619594G>T c.175C>A c.(175-177)Ccc>Acc p.P59T LUSC 19 8586456 8586456 + Missense_Mutation SNP C C T TCGA-33-4586-01A-01D-1441-08 TCGA-33-4586-11A-01D-1441-08 g.chr19:8586456C>T c.3253G>A c.(3253-3255)Ggc>Agc p.G1085S LUSC 19 8595157 8595157 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr19:8595157C>T c.2251G>A c.(2251-2253)Gag>Aag p.E751K LUSC 19 8595448 8595448 + Missense_Mutation SNP G G T TCGA-66-2763-01A-01D-1522-08 TCGA-66-2763-11A-01D-1522-08 g.chr19:8595448G>T c.2053C>A c.(2053-2055)Ctg>Atg p.L685M LUSC 19 8601411 8601411 + Missense_Mutation SNP G G T TCGA-39-5028-01A-01D-1441-08 TCGA-39-5028-11A-01D-1441-08 g.chr19:8601411G>T c.1870C>A c.(1870-1872)Cgc>Agc p.R624S LUSC 19 8601932 8601932 + Missense_Mutation SNP G G T TCGA-22-4601-01A-01D-1441-08 TCGA-22-4601-11A-01D-1441-08 g.chr19:8601932G>T c.1700C>A c.(1699-1701)gCc>gAc p.A567D LUSC 19 8609217 8609217 + Nonsense_Mutation SNP C C T TCGA-46-3767-01A-01D-0983-08 TCGA-46-3767-10A-01D-0983-08 g.chr19:8609217C>T c.1488G>A c.(1486-1488)tgG>tgA p.W496* OV 19 8587323 8587323 + Missense_Mutation SNP A A G TCGA-24-1426-01A-01W-0549-09 TCGA-24-1426-10A-01W-0549-09 g.chr19:8587323A>G c.3158T>C c.(3157-3159)gTg>gCg p.V1053A OV 19 8616669 8616669 + Silent SNP G G A TCGA-24-1604-01A-01W-0552-10 TCGA-24-1604-10A-01W-0552-10 g.chr19:8616669G>A c.726C>T c.(724-726)taC>taT p.Y242Y OV 19 8620639 8620639 + Missense_Mutation SNP C C G TCGA-23-1123-01A-01W-0488-09 TCGA-23-1123-10A-01W-0488-09 g.chr19:8620639C>G c.45G>C c.(43-45)aaG>aaC p.K15N PAAD 19 8595095 8595095 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:8595095G>A c.2313C>T c.(2311-2313)taC>taT p.Y771Y PAAD 19 8595429 8595429 + Missense_Mutation SNP C C T TCGA-2L-AAQA-01A-21D-A38G-08 TCGA-2L-AAQA-11A-11D-A38J-08 g.chr19:8595429C>T c.2072G>A c.(2071-2073)cGa>cAa p.R691Q PAAD 19 8612995 8612995 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:8612995G>A c.1194C>T c.(1192-1194)ttC>ttT p.F398F PAAD 19 8619390 8619390 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:8619390G>A c.297C>T c.(295-297)atC>atT p.I99I PRAD 19 8604860 8604860 + Missense_Mutation SNP G G A TCGA-EJ-5532-01A-01D-1576-08 TCGA-EJ-5532-10A-01D-1577-08 g.chr19:8604860G>A c.1663C>T c.(1663-1665)Cgc>Tgc p.R555C PRAD 19 8612935 8612935 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:8612935G>A c.1254C>T c.(1252-1254)acC>acT p.T418T PRAD 19 8612974 8612974 + Silent SNP G G A TCGA-J9-A52C-01A-11D-A26M-08 TCGA-J9-A52C-10A-01D-A26K-08 g.chr19:8612974G>A c.1215C>T c.(1213-1215)ttC>ttT p.F405F PRAD 19 8613157 8613157 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:8613157G>A c.1146C>T c.(1144-1146)atC>atT p.I382I SARC 19 8586453 8586453 + Nonsense_Mutation SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr19:8586453G>A c.3256C>T c.(3256-3258)Cag>Tag p.Q1086* SARC 19 8587306 8587306 + Missense_Mutation SNP C C G TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr19:8587306C>G c.3175G>C c.(3175-3177)Gag>Cag p.E1059Q SARC 19 8601180 8601180 + Missense_Mutation SNP A A T TCGA-DX-A1L0-01A-11D-A24N-09 TCGA-DX-A1L0-10A-01D-A24N-09 g.chr19:8601180A>T c.1999T>A c.(1999-2001)Tac>Aac p.Y667N SARC 19 8601415 8601415 + Silent SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr19:8601415G>A c.1866C>T c.(1864-1866)gcC>gcT p.A622A SKCM 19 8587285 8587285 + Missense_Mutation SNP C C T TCGA-GN-A268-06A-11D-A196-08 TCGA-GN-A268-10A-01D-A198-08 g.chr19:8587285C>T c.3196G>A c.(3196-3198)Gag>Aag p.E1066K SKCM 19 8587370 8587370 + Silent SNP G G A TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chr19:8587370G>A c.3111C>T c.(3109-3111)ccC>ccT p.P1037P SKCM 19 8587371 8587371 + Missense_Mutation SNP G G A TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chr19:8587371G>A c.3110C>T c.(3109-3111)cCc>cTc p.P1037L SKCM 19 8587587 8587587 + Missense_Mutation SNP C C T TCGA-D3-A1Q7-06A-11D-A19A-08 TCGA-D3-A1Q7-10A-01D-A19A-08 g.chr19:8587587C>T c.2981G>A c.(2980-2982)cGa>cAa p.R994Q SKCM 19 8590392 8590392 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:8590392G>A c.2825C>T c.(2824-2826)cCt>cTt p.P942L SKCM 19 8590433 8590433 + Silent SNP C C T TCGA-D9-A1JX-06A-11D-A19A-08 TCGA-D9-A1JX-10A-01D-A19A-08 g.chr19:8590433C>T c.2784G>A c.(2782-2784)aaG>aaA p.K928K SKCM 19 8590433 8590433 + Silent SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr19:8590433C>T c.2784G>A c.(2782-2784)aaG>aaA p.K928K SKCM 19 8591700 8591700 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:8591700C>T c.2594G>A c.(2593-2595)aGg>aAg p.R865K SKCM 19 8592300 8592300 + Missense_Mutation SNP T T G TCGA-D3-A3MU-06A-11D-A21A-08 TCGA-D3-A3MU-10A-01D-A21A-08 g.chr19:8592300T>G c.2396A>C c.(2395-2397)aAg>aCg p.K799T SKCM 19 8595250 8595250 + Splice_Site SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr19:8595250C>T c.e21-1 SKCM 19 8595349 8595349 + Missense_Mutation SNP C C T TCGA-D3-A1Q5-06A-11D-A196-08 TCGA-D3-A1Q5-10A-01D-A198-08 g.chr19:8595349C>T c.2152G>A c.(2152-2154)Gag>Aag p.E718K SKCM 19 8595349 8595349 + Missense_Mutation SNP C C T TCGA-ER-A42K-06A-11D-A24R-08 TCGA-ER-A42K-10A-01D-A24R-08 g.chr19:8595349C>T c.2152G>A c.(2152-2154)Gag>Aag p.E718K SKCM 19 8595445 8595445 + Missense_Mutation SNP C C T TCGA-EE-A3AB-06A-11D-A196-08 TCGA-EE-A3AB-10A-01D-A198-08 g.chr19:8595445C>T c.2056G>A c.(2056-2058)Gag>Aag p.E686K SKCM 19 8595446 8595446 + Silent SNP C C T TCGA-EE-A3AB-06A-11D-A196-08 TCGA-EE-A3AB-10A-01D-A198-08 g.chr19:8595446C>T c.2055G>A c.(2053-2055)ctG>ctA p.L685L SKCM 19 8601135 8601135 + Splice_Site SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:8601135C>T c.e19+1 SKCM 19 8601239 8601239 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:8601239C>T c.1940G>A c.(1939-1941)gGg>gAg p.G647E SKCM 19 8604837 8604837 + Silent SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr19:8604837C>T c.1686G>A c.(1684-1686)aaG>aaA p.K562K SKCM 19 8604855 8604855 + Silent SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr19:8604855G>A c.1668C>T c.(1666-1668)ccC>ccT p.P556P SKCM 19 8604862 8604862 + Missense_Mutation SNP C C T TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr19:8604862C>T c.1661G>A c.(1660-1662)gGg>gAg p.G554E SKCM 19 8604875 8604875 + Missense_Mutation SNP C C T TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chr19:8604875C>T c.1648G>A c.(1648-1650)Gga>Aga p.G550R SKCM 19 8606848 8606848 + Missense_Mutation SNP C C T TCGA-EE-A2GE-06A-11D-A196-08 TCGA-EE-A2GE-10A-01D-A198-08 g.chr19:8606848C>T c.1552G>A c.(1552-1554)Gag>Aag p.E518K SKCM 19 8606866 8606866 + Missense_Mutation SNP C C T TCGA-D3-A3MV-06A-11D-A21A-08 TCGA-D3-A3MV-10A-01D-A21A-08 g.chr19:8606866C>T c.1534G>A c.(1534-1536)Gac>Aac p.D512N SKCM 19 8609209 8609209 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr19:8609209C>T c.1496G>A c.(1495-1497)gGc>gAc p.G499D SKCM 19 8609249 8609249 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:8609249C>T c.1456G>A c.(1456-1458)Gct>Act p.A486T SKCM 19 8609284 8609284 + Missense_Mutation SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr19:8609284C>T c.1421G>A c.(1420-1422)gGa>gAa p.G474E SKCM 19 8609287 8609287 + Missense_Mutation SNP C C T TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr19:8609287C>T c.1418G>A c.(1417-1419)gGg>gAg p.G473E SKCM 19 8610545 8610545 + Missense_Mutation SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr19:8610545C>T c.1345G>A c.(1345-1347)Gaa>Aaa p.E449K SKCM 19 8610561 8610561 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:8610561G>A c.1329C>T c.(1327-1329)gtC>gtT p.V443V SKCM 19 8610586 8610586 + Missense_Mutation SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr19:8610586G>A c.1304C>T c.(1303-1305)cCa>cTa p.P435L SKCM 19 8610586 8610586 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr19:8610586G>A c.1304C>T c.(1303-1305)cCa>cTa p.P435L SKCM 19 8610589 8610589 + Missense_Mutation SNP G G A TCGA-RP-A694-06A-11D-A30X-08 TCGA-RP-A694-10A-01D-A30X-08 g.chr19:8610589G>A c.1301C>T c.(1300-1302)aCt>aTt p.T434I SKCM 19 8610597 8610597 + Silent SNP G G A TCGA-DA-A1IA-06A-11D-A196-08 TCGA-DA-A1IA-10A-01D-A198-08 g.chr19:8610597G>A c.1293C>T c.(1291-1293)atC>atT p.I431I SKCM 19 8615459 8615459 + Silent SNP C C T TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr19:8615459C>T c.891G>A c.(889-891)gtG>gtA p.V297V SKCM 19 8615533 8615533 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr19:8615533C>T c.817G>A c.(817-819)Gtc>Atc p.V273I SKCM 19 8615558 8615558 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:8615558C>T c.792G>A c.(790-792)ggG>ggA p.G264G SKCM 19 8616642 8616642 + Silent SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr19:8616642G>A c.753C>T c.(751-753)agC>agT p.S251S SKCM 19 8616665 8616665 + Missense_Mutation SNP C C T TCGA-EE-A2A0-06A-11D-A196-08 TCGA-EE-A2A0-10A-01D-A198-08 g.chr19:8616665C>T c.730G>A c.(730-732)Gtg>Atg p.V244M SKCM 19 8616666 8616666 + Silent SNP C C T TCGA-EE-A2A0-06A-11D-A196-08 TCGA-EE-A2A0-10A-01D-A198-08 g.chr19:8616666C>T c.729G>A c.(727-729)caG>caA p.Q243Q SKCM 19 8618077 8618077 + Silent SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr19:8618077C>T c.450G>A c.(448-450)ctG>ctA p.L150L SKCM 19 8618261 8618261 + Silent SNP C C T TCGA-DA-A1I1-06A-12D-A196-08 TCGA-DA-A1I1-10A-01D-A198-08 g.chr19:8618261C>T c.387G>A c.(385-387)aaG>aaA p.K129K SKCM 19 8618320 8618320 + Splice_Site SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr19:8618320C>T c.328G>A c.(328-330)Gga>Aga p.G110R SKCM 19 8619417 8619417 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:8619417C>T c.270G>A c.(268-270)acG>acA p.T90T SKCM 19 8620543 8620543 + Splice_Site SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr19:8620543G>A c.141C>T c.(139-141)ttC>ttT p.F47F SKCM 19 8620596 8620596 + Missense_Mutation SNP C C T TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr19:8620596C>T c.88G>A c.(88-90)Gaa>Aaa p.E30K SKCM 19 8620608 8620608 + Missense_Mutation SNP G G A TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr19:8620608G>A c.76C>T c.(76-78)Ccc>Tcc p.P26S SKCM 19 8620618 8620618 + Missense_Mutation SNP C C T TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr19:8620618C>T c.66G>A c.(64-66)atG>atA p.M22I

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 19 8591788 8591788 single base substitution C T 3_prime_UTR_variant BLCA-CN 19 8591788 8591788 single base substitution C T downstream_gene_variant BLCA-CN 19 8591788 8591788 single base substitution C T exon_variant BLCA-CN 19 8591788 8591788 single base substitution C T missense_variant E836K 2506G>A BLCA-CN 19 8591788 8591788 single base substitution C T upstream_gene_variant BLCA-CN 19 8595112 8595112 single base substitution C T exon_variant BLCA-CN 19 8595112 8595112 single base substitution C T missense_variant D766N 2296G>A BLCA-CN 19 8595112 8595112 single base substitution C T upstream_gene_variant BLCA-CN 19 8617018 8617018 single base substitution C T downstream_gene_variant BLCA-CN 19 8617018 8617018 single base substitution C T exon_variant BLCA-CN 19 8617018 8617018 single base substitution C T missense_variant G179S 535G>A BLCA-CN 19 8617018 8617018 single base substitution C T upstream_gene_variant BLCA-US 19 8587680 8587680 single base substitution C G downstream_gene_variant BLCA-US 19 8587680 8587680 single base substitution C G missense_variant R963T 2888G>C BLCA-US 19 8591788 8591788 single base substitution C G 3_prime_UTR_variant BLCA-US 19 8591788 8591788 single base substitution C G downstream_gene_variant BLCA-US 19 8591788 8591788 single base substitution C G exon_variant BLCA-US 19 8591788 8591788 single base substitution C G missense_variant E836Q 2506G>C BLCA-US 19 8591788 8591788 single base substitution C G upstream_gene_variant BLCA-US 19 8609325 8609325 single base substitution G A downstream_gene_variant BLCA-US 19 8609325 8609325 single base substitution G A exon_variant BLCA-US 19 8609325 8609325 single base substitution G A synonymous_variant V460V 1380C>T BLCA-US 19 8609325 8609325 single base substitution G A upstream_gene_variant BLCA-US 19 8615474 8615474 single base substitution C T downstream_gene_variant BLCA-US 19 8615474 8615474 single base substitution C T exon_variant BLCA-US 19 8615474 8615474 single base substitution C T synonymous_variant G292G 876G>A BLCA-US 19 8615474 8615474 single base substitution C T upstream_gene_variant BLCA-US 19 8617036 8617036 single base substitution C G downstream_gene_variant BLCA-US 19 8617036 8617036 single base substitution C G exon_variant BLCA-US 19 8617036 8617036 single base substitution C G missense_variant E173Q 517G>C BLCA-US 19 8617036 8617036 single base substitution C G upstream_gene_variant BRCA-EU 19 8582848 8582848 deletion of <=200bp C - downstream_gene_variant BRCA-EU 19 8584078 8584078 single base substitution G A downstream_gene_variant BRCA-EU 19 8585590 8585590 single base substitution C T downstream_gene_variant BRCA-EU 19 8585760 8585760 single base substitution C T 3_prime_UTR_variant BRCA-EU 19 8585760 8585760 single base substitution C T downstream_gene_variant BRCA-EU 19 8585801 8585801 single base substitution G A 3_prime_UTR_variant BRCA-EU 19 8585801 8585801 single base substitution G A downstream_gene_variant BRCA-EU 19 8586010 8586010 single base substitution G A 3_prime_UTR_variant BRCA-EU 19 8586010 8586010 single base substitution G A downstream_gene_variant BRCA-EU 19 8586063 8586063 single base substitution C A 3_prime_UTR_variant BRCA-EU 19 8586063 8586063 single base substitution C A downstream_gene_variant BRCA-EU 19 8587912 8587912 single base substitution T A downstream_gene_variant BRCA-EU 19 8587912 8587912 single base substitution T A intron_variant BRCA-EU 19 8588208 8588208 single base substitution C T downstream_gene_variant BRCA-EU 19 8588208 8588208 single base substitution C T intron_variant BRCA-EU 19 8588257 8588257 single base substitution C G downstream_gene_variant BRCA-EU 19 8588257 8588257 single base substitution C G intron_variant BRCA-EU 19 8591386 8591386 single base substitution G T 3_prime_UTR_variant BRCA-EU 19 8591386 8591386 single base substitution G T downstream_gene_variant BRCA-EU 19 8591386 8591386 single base substitution G T exon_variant BRCA-EU 19 8591386 8591386 single base substitution G T synonymous_variant G907G 2721C>A BRCA-EU 19 8593300 8593300 single base substitution T G downstream_gene_variant BRCA-EU 19 8593300 8593300 single base substitution T G intron_variant BRCA-EU 19 8593300 8593300 single base substitution T G upstream_gene_variant BRCA-EU 19 8593582 8593582 single base substitution G C downstream_gene_variant BRCA-EU 19 8593582 8593582 single base substitution G C intron_variant BRCA-EU 19 8593582 8593582 single base substitution G C upstream_gene_variant BRCA-EU 19 8594780 8594780 single base substitution G A downstream_gene_variant BRCA-EU 19 8594780 8594780 single base substitution G A exon_variant BRCA-EU 19 8594780 8594780 single base substitution G A intron_variant BRCA-EU 19 8594780 8594780 single base substitution G A upstream_gene_variant BRCA-EU 19 8595001 8595001 single base substitution G A downstream_gene_variant BRCA-EU 19 8595001 8595001 single base substitution G A exon_variant BRCA-EU 19 8595001 8595001 single base substitution G A intron_variant BRCA-EU 19 8595001 8595001 single base substitution G A upstream_gene_variant BRCA-EU 19 8595802 8595802 single base substitution C A intron_variant BRCA-EU 19 8595802 8595802 single base substitution C A upstream_gene_variant BRCA-EU 19 8596022 8596022 single base substitution G A intron_variant BRCA-EU 19 8596022 8596022 single base substitution G A upstream_gene_variant BRCA-EU 19 8596620 8596620 single base substitution C T intron_variant BRCA-EU 19 8596620 8596620 single base substitution C T upstream_gene_variant BRCA-EU 19 8597083 8597083 single base substitution T C intron_variant BRCA-EU 19 8597083 8597083 single base substitution T C upstream_gene_variant BRCA-EU 19 8599479 8599479 single base substitution C T intron_variant BRCA-EU 19 8599479 8599479 single base substitution C T upstream_gene_variant BRCA-EU 19 8600062 8600062 single base substitution C G intron_variant BRCA-EU 19 8600062 8600062 single base substitution C G upstream_gene_variant BRCA-EU 19 8600586 8600586 single base substitution C G downstream_gene_variant BRCA-EU 19 8600586 8600586 single base substitution C G intron_variant BRCA-EU 19 8601203 8601203 single base substitution G A downstream_gene_variant BRCA-EU 19 8601203 8601203 single base substitution G A exon_variant BRCA-EU 19 8601203 8601203 single base substitution G A missense_variant A659V 1976C>T BRCA-EU 19 8601865 8601865 single base substitution C T downstream_gene_variant BRCA-EU 19 8601865 8601865 single base substitution C T exon_variant BRCA-EU 19 8601865 8601865 single base substitution C T synonymous_variant E589E 1767G>A BRCA-EU 19 8603962 8603962 single base substitution G C downstream_gene_variant BRCA-EU 19 8603962 8603962 single base substitution G C intron_variant BRCA-EU 19 8604902 8604902 single base substitution G A downstream_gene_variant BRCA-EU 19 8604902 8604902 single base substitution G A exon_variant BRCA-EU 19 8604902 8604902 single base substitution G A missense_variant R541W 1621C>T BRCA-EU 19 8605095 8605095 single base substitution G A downstream_gene_variant BRCA-EU 19 8605095 8605095 single base substitution G A intron_variant BRCA-EU 19 8605095 8605095 single base substitution G A upstream_gene_variant BRCA-EU 19 8605572 8605572 single base substitution C T downstream_gene_variant BRCA-EU 19 8605572 8605572 single base substitution C T intron_variant BRCA-EU 19 8605572 8605572 single base substitution C T upstream_gene_variant BRCA-EU 19 8605877 8605877 deletion of <=200bp T - downstream_gene_variant BRCA-EU 19 8605877 8605877 deletion of <=200bp T - intron_variant BRCA-EU 19 8605877 8605877 deletion of <=200bp T - upstream_gene_variant BRCA-EU 19 8606818 8606818 single base substitution G A downstream_gene_variant BRCA-EU 19 8606818 8606818 single base substitution G A exon_variant BRCA-EU 19 8606818 8606818 single base substitution G A missense_variant L528F 1582C>T BRCA-EU 19 8606818 8606818 single base substitution G A upstream_gene_variant BRCA-EU 19 8609641 8609641 single base substitution T C downstream_gene_variant BRCA-EU 19 8609641 8609641 single base substitution T C intron_variant BRCA-EU 19 8609641 8609641 single base substitution T C upstream_gene_variant BRCA-EU 19 8610422 8610422 single base substitution G T downstream_gene_variant BRCA-EU 19 8610422 8610422 single base substitution G T exon_variant BRCA-EU 19 8610422 8610422 single base substitution G T intron_variant BRCA-EU 19 8610422 8610422 single base substitution G T upstream_gene_variant BRCA-EU 19 8610595 8610595 single base substitution C T downstream_gene_variant BRCA-EU 19 8610595 8610595 single base substitution C T exon_variant BRCA-EU 19 8610595 8610595 single base substitution C T missense_variant R432H 1295G>A BRCA-EU 19 8610595 8610595 single base substitution C T upstream_gene_variant BRCA-EU 19 8610998 8610998 single base substitution G C downstream_gene_variant BRCA-EU 19 8610998 8610998 single base substitution G C intron_variant BRCA-EU 19 8610998 8610998 single base substitution G C upstream_gene_variant BRCA-EU 19 8611042 8611042 single base substitution G A downstream_gene_variant BRCA-EU 19 8611042 8611042 single base substitution G A intron_variant BRCA-EU 19 8611042 8611042 single base substitution G A upstream_gene_variant BRCA-EU 19 8611723 8611723 single base substitution T G downstream_gene_variant BRCA-EU 19 8611723 8611723 single base substitution T G intron_variant BRCA-EU 19 8611723 8611723 single base substitution T G upstream_gene_variant BRCA-EU 19 8613339 8613339 single base substitution C T downstream_gene_variant BRCA-EU 19 8613339 8613339 single base substitution C T intron_variant BRCA-EU 19 8613339 8613339 single base substitution C T upstream_gene_variant BRCA-EU 19 8613699 8613699 single base substitution C T downstream_gene_variant BRCA-EU 19 8613699 8613699 single base substitution C T intron_variant BRCA-EU 19 8613699 8613699 single base substitution C T upstream_gene_variant BRCA-EU 19 8613907 8613907 single base substitution T A downstream_gene_variant BRCA-EU 19 8613907 8613907 single base substitution T A intron_variant BRCA-EU 19 8613907 8613907 single base substitution T A upstream_gene_variant BRCA-EU 19 8614188 8614188 single base substitution G A downstream_gene_variant BRCA-EU 19 8614188 8614188 single base substitution G A intron_variant BRCA-EU 19 8614188 8614188 single base substitution G A upstream_gene_variant BRCA-EU 19 8614356 8614356 single base substitution G A downstream_gene_variant BRCA-EU 19 8614356 8614356 single base substitution G A intron_variant BRCA-EU 19 8614356 8614356 single base substitution G A upstream_gene_variant BRCA-EU 19 8615966 8615966 single base substitution C T downstream_gene_variant BRCA-EU 19 8615966 8615966 single base substitution C T intron_variant BRCA-EU 19 8615966 8615966 single base substitution C T upstream_gene_variant BRCA-EU 19 8617394 8617394 single base substitution G A downstream_gene_variant BRCA-EU 19 8617394 8617394 single base substitution G A intron_variant BRCA-EU 19 8617394 8617394 single base substitution G A upstream_gene_variant BRCA-EU 19 8617577 8617577 deletion of <=200bp T - downstream_gene_variant BRCA-EU 19 8617577 8617577 deletion of <=200bp T - intron_variant BRCA-EU 19 8617577 8617577 deletion of <=200bp T - upstream_gene_variant BRCA-EU 19 8617830 8617830 single base substitution C T downstream_gene_variant BRCA-EU 19 8617830 8617830 single base substitution C T intron_variant BRCA-EU 19 8617830 8617830 single base substitution C T upstream_gene_variant BRCA-EU 19 8618661 8618661 single base substitution C T downstream_gene_variant BRCA-EU 19 8618661 8618661 single base substitution C T intron_variant BRCA-EU 19 8618661 8618661 single base substitution C T upstream_gene_variant BRCA-EU 19 8620034 8620034 single base substitution C G downstream_gene_variant BRCA-EU 19 8620034 8620034 single base substitution C G intron_variant BRCA-EU 19 8620034 8620034 single base substitution C G upstream_gene_variant BRCA-EU 19 8620566 8620566 single base substitution G A exon_variant BRCA-EU 19 8620566 8620566 single base substitution G A missense_variant R40C 118C>T BRCA-EU 19 8620566 8620566 single base substitution G A upstream_gene_variant BRCA-EU 19 8620863 8620863 single base substitution C G intron_variant BRCA-EU 19 8620863 8620863 single base substitution C G upstream_gene_variant BRCA-EU 19 8623240 8623240 single base substitution G T intron_variant BRCA-EU 19 8623240 8623240 single base substitution G T upstream_gene_variant BRCA-EU 19 8625241 8625241 single base substitution C T intron_variant BRCA-EU 19 8625241 8625241 single base substitution C T upstream_gene_variant BRCA-EU 19 8625713 8625713 single base substitution C G intron_variant BRCA-EU 19 8626455 8626455 single base substitution C T intron_variant BRCA-EU 19 8630127 8630127 single base substitution C T intron_variant BRCA-EU 19 8630418 8630418 single base substitution C T intron_variant BRCA-EU 19 8631164 8631164 single base substitution G T intron_variant BRCA-EU 19 8631405 8631405 single base substitution T A intron_variant BRCA-EU 19 8633438 8633438 single base substitution T C intron_variant BRCA-EU 19 8633625 8633625 single base substitution T C intron_variant BRCA-EU 19 8636733 8636733 single base substitution G A downstream_gene_variant BRCA-EU 19 8636733 8636733 single base substitution G A intron_variant BRCA-EU 19 8637163 8637163 insertion of <=200bp - C downstream_gene_variant BRCA-EU 19 8637163 8637163 insertion of <=200bp - C intron_variant BRCA-EU 19 8637174 8637174 single base substitution C T downstream_gene_variant BRCA-EU 19 8637174 8637174 single base substitution C T intron_variant BRCA-EU 19 8637236 8637236 single base substitution C T downstream_gene_variant BRCA-EU 19 8637236 8637236 single base substitution C T intron_variant BRCA-EU 19 8639250 8639250 single base substitution T A downstream_gene_variant BRCA-EU 19 8639250 8639250 single base substitution T A intron_variant BRCA-EU 19 8640068 8640068 single base substitution C T downstream_gene_variant BRCA-EU 19 8640068 8640068 single base substitution C T intron_variant BRCA-EU 19 8641079 8641079 single base substitution C T downstream_gene_variant BRCA-EU 19 8641079 8641079 single base substitution C T intron_variant BRCA-EU 19 8641256 8641256 single base substitution C G downstream_gene_variant BRCA-EU 19 8641256 8641256 single base substitution C G intron_variant BRCA-EU 19 8641374 8641374 single base substitution G A exon_variant BRCA-EU 19 8641374 8641374 single base substitution G A intron_variant BRCA-EU 19 8641507 8641507 single base substitution G A exon_variant BRCA-EU 19 8641507 8641507 single base substitution G A intron_variant BRCA-EU 19 8641638 8641638 single base substitution A G exon_variant BRCA-EU 19 8641638 8641638 single base substitution A G intron_variant BRCA-EU 19 8643322 8643322 single base substitution C G upstream_gene_variant BRCA-EU 19 8643858 8643858 single base substitution C G upstream_gene_variant BRCA-EU 19 8644613 8644613 single base substitution C T upstream_gene_variant BRCA-EU 19 8644885 8644885 single base substitution G A upstream_gene_variant BRCA-EU 19 8645430 8645430 single base substitution C G upstream_gene_variant BRCA-FR 19 8585760 8585760 single base substitution C T 3_prime_UTR_variant BRCA-FR 19 8585760 8585760 single base substitution C T downstream_gene_variant BRCA-FR 19 8586010 8586010 single base substitution G A 3_prime_UTR_variant BRCA-FR 19 8586010 8586010 single base substitution G A downstream_gene_variant BRCA-FR 19 8588257 8588257 single base substitution C G downstream_gene_variant BRCA-FR 19 8588257 8588257 single base substitution C G intron_variant BRCA-FR 19 8606529 8606529 single base substitution T C downstream_gene_variant BRCA-FR 19 8606529 8606529 single base substitution T C intron_variant BRCA-FR 19 8606529 8606529 single base substitution T C upstream_gene_variant BRCA-FR 19 8617830 8617830 single base substitution C T downstream_gene_variant BRCA-FR 19 8617830 8617830 single base substitution C T intron_variant BRCA-FR 19 8617830 8617830 single base substitution C T upstream_gene_variant BRCA-FR 19 8633625 8633625 single base substitution T C intron_variant BRCA-FR 19 8640068 8640068 single base substitution C T downstream_gene_variant BRCA-FR 19 8640068 8640068 single base substitution C T intron_variant BRCA-FR 19 8641507 8641507 single base substitution G A exon_variant BRCA-FR 19 8641507 8641507 single base substitution G A intron_variant BRCA-FR 19 8643858 8643858 single base substitution C G upstream_gene_variant BRCA-FR 19 8644613 8644613 single base substitution C T upstream_gene_variant BRCA-FR 19 8645430 8645430 single base substitution C G upstream_gene_variant BRCA-UK 19 8618310 8618310 single base substitution C T 3_prime_UTR_variant BRCA-UK 19 8618310 8618310 single base substitution C T downstream_gene_variant BRCA-UK 19 8618310 8618310 single base substitution C T exon_variant BRCA-UK 19 8618310 8618310 single base substitution C T missense_variant G109E 326G>A BRCA-UK 19 8618310 8618310 single base substitution C T missense_variant G113E 338G>A BRCA-UK 19 8618310 8618310 single base substitution C T upstream_gene_variant BRCA-UK 19 8630127 8630127 single base substitution C T intron_variant BRCA-US 19 8587599 8587599 single base substitution C G downstream_gene_variant BRCA-US 19 8587599 8587599 single base substitution C G missense_variant G990A 2969G>C BRCA-US 19 8592341 8592341 single base substitution C T downstream_gene_variant BRCA-US 19 8592341 8592341 single base substitution C T exon_variant BRCA-US 19 8592341 8592341 single base substitution C T synonymous_variant T785T 2355G>A BRCA-US 19 8592341 8592341 single base substitution C T upstream_gene_variant BRCA-US 19 8601262 8601262 single base substitution G A downstream_gene_variant BRCA-US 19 8601262 8601262 single base substitution G A exon_variant BRCA-US 19 8601262 8601262 single base substitution G A synonymous_variant P639P 1917C>T BRCA-US 19 8615476 8615476 single base substitution C T downstream_gene_variant BRCA-US 19 8615476 8615476 single base substitution C T exon_variant BRCA-US 19 8615476 8615476 single base substitution C T missense_variant G292R 874G>A BRCA-US 19 8615476 8615476 single base substitution C T upstream_gene_variant BRCA-US 19 8615498 8615498 single base substitution C T downstream_gene_variant BRCA-US 19 8615498 8615498 single base substitution C T exon_variant BRCA-US 19 8615498 8615498 single base substitution C T synonymous_variant G284G 852G>A BRCA-US 19 8615498 8615498 single base substitution C T upstream_gene_variant BRCA-US 19 8620576 8620576 single base substitution G T exon_variant BRCA-US 19 8620576 8620576 single base substitution G T missense_variant N36K 108C>A BRCA-US 19 8620576 8620576 single base substitution G T upstream_gene_variant BTCA-JP 19 8587197 8587197 single base substitution C T downstream_gene_variant BTCA-JP 19 8587197 8587197 single base substitution C T intron_variant BTCA-JP 19 8591534 8591534 single base substitution C T downstream_gene_variant BTCA-JP 19 8591534 8591534 single base substitution C T exon_variant BTCA-JP 19 8591534 8591534 single base substitution C T intron_variant BTCA-JP 19 8591534 8591534 single base substitution C T upstream_gene_variant BTCA-JP 19 8595095 8595095 single base substitution G A exon_variant BTCA-JP 19 8595095 8595095 single base substitution G A synonymous_variant Y771Y 2313C>T BTCA-JP 19 8595095 8595095 single base substitution G A upstream_gene_variant BTCA-JP 19 8601821 8601821 insertion of <=200bp - G downstream_gene_variant BTCA-JP 19 8601821 8601821 insertion of <=200bp - G intron_variant BTCA-JP 19 8615118 8615118 single base substitution C T downstream_gene_variant BTCA-JP 19 8615118 8615118 single base substitution C T exon_variant BTCA-JP 19 8615118 8615118 single base substitution C T missense_variant V343M 1027G>A BTCA-JP 19 8615118 8615118 single base substitution C T upstream_gene_variant BTCA-JP 19 8616655 8616655 single base substitution G A downstream_gene_variant BTCA-JP 19 8616655 8616655 single base substitution G A exon_variant BTCA-JP 19 8616655 8616655 single base substitution G A missense_variant T247M 740C>T BTCA-JP 19 8616655 8616655 single base substitution G A upstream_gene_variant BTCA-JP 19 8618346 8618346 single base substitution G T downstream_gene_variant BTCA-JP 19 8618346 8618346 single base substitution G T intron_variant BTCA-JP 19 8618346 8618346 single base substitution G T upstream_gene_variant BTCA-JP 19 8645692 8645692 deletion of <=200bp C - upstream_gene_variant CESC-US 19 8587697 8587697 single base substitution C A downstream_gene_variant CESC-US 19 8587697 8587697 single base substitution C A exon_variant CESC-US 19 8587697 8587697 single base substitution C A synonymous_variant G957G 2871G>T CESC-US 19 8595361 8595361 single base substitution C T exon_variant CESC-US 19 8595361 8595361 single base substitution C T missense_variant E714K 2140G>A CESC-US 19 8595361 8595361 single base substitution C T upstream_gene_variant CESC-US 19 8616752 8616752 single base substitution C A downstream_gene_variant CESC-US 19 8616752 8616752 single base substitution C A exon_variant CESC-US 19 8616752 8616752 single base substitution C A stop_gained E215* 643G>T CESC-US 19 8616752 8616752 single base substitution C A upstream_gene_variant CESC-US 19 8620554 8620554 single base substitution C T exon_variant CESC-US 19 8620554 8620554 single base substitution C T missense_variant D44N 130G>A CESC-US 19 8620554 8620554 single base substitution C T upstream_gene_variant CESC-US 19 8645823 8645823 single base substitution C T upstream_gene_variant CLLE-ES 19 8584424 8584424 single base substitution T G downstream_gene_variant CLLE-ES 19 8617959 8617959 single base substitution G A downstream_gene_variant CLLE-ES 19 8617959 8617959 single base substitution G A intron_variant CLLE-ES 19 8617959 8617959 single base substitution G A upstream_gene_variant CLLE-ES 19 8618577 8618577 single base substitution T A downstream_gene_variant CLLE-ES 19 8618577 8618577 single base substitution T A intron_variant CLLE-ES 19 8618577 8618577 single base substitution T A upstream_gene_variant CLLE-ES 19 8636246 8636246 single base substitution C T intron_variant COAD-US 19 8587343 8587343 single base substitution G A downstream_gene_variant COAD-US 19 8587343 8587343 single base substitution G A synonymous_variant C1046C 3138C>T COAD-US 19 8587669 8587669 deletion of <=200bp G - downstream_gene_variant COAD-US 19 8587669 8587669 deletion of <=200bp G - frameshift_variant L967 COAD-US 19 8591767 8591767 single base substitution G T 3_prime_UTR_variant COAD-US 19 8591767 8591767 single base substitution G T downstream_gene_variant COAD-US 19 8591767 8591767 single base substitution G T exon_variant COAD-US 19 8591767 8591767 single base substitution G T missense_variant L843M 2527C>A COAD-US 19 8591767 8591767 single base substitution G T upstream_gene_variant COAD-US 19 8595116 8595116 single base substitution G A exon_variant COAD-US 19 8595116 8595116 single base substitution G A synonymous_variant F764F 2292C>T COAD-US 19 8595116 8595116 single base substitution G A upstream_gene_variant COAD-US 19 8595157 8595157 single base substitution C T exon_variant COAD-US 19 8595157 8595157 single base substitution C T missense_variant E751K 2251G>A COAD-US 19 8595157 8595157 single base substitution C T upstream_gene_variant COAD-US 19 8595163 8595163 single base substitution G A exon_variant COAD-US 19 8595163 8595163 single base substitution G A missense_variant R749W 2245C>T COAD-US 19 8595163 8595163 single base substitution G A upstream_gene_variant COAD-US 19 8595422 8595422 single base substitution G A exon_variant COAD-US 19 8595422 8595422 single base substitution G A synonymous_variant F693F 2079C>T COAD-US 19 8595422 8595422 single base substitution G A upstream_gene_variant COAD-US 19 8601412 8601412 single base substitution G A downstream_gene_variant COAD-US 19 8601412 8601412 single base substitution G A exon_variant COAD-US 19 8601412 8601412 single base substitution G A synonymous_variant Y623Y 1869C>T COAD-US 19 8601427 8601427 single base substitution T G downstream_gene_variant COAD-US 19 8601427 8601427 single base substitution T G exon_variant COAD-US 19 8601427 8601427 single base substitution T G missense_variant R618S 1854A>C COAD-US 19 8609251 8609251 single base substitution G A downstream_gene_variant COAD-US 19 8609251 8609251 single base substitution G A exon_variant COAD-US 19 8609251 8609251 single base substitution G A missense_variant A485V 1454C>T COAD-US 19 8609251 8609251 single base substitution G A upstream_gene_variant COAD-US 19 8612995 8612995 single base substitution G A downstream_gene_variant COAD-US 19 8612995 8612995 single base substitution G A exon_variant COAD-US 19 8612995 8612995 single base substitution G A synonymous_variant F398F 1194C>T COAD-US 19 8612995 8612995 single base substitution G A upstream_gene_variant COAD-US 19 8613001 8613001 insertion of <=200bp - T downstream_gene_variant COAD-US 19 8613001 8613001 insertion of <=200bp - T exon_variant COAD-US 19 8613001 8613001 insertion of <=200bp - T frameshift_variant N396N? COAD-US 19 8613001 8613001 insertion of <=200bp - T upstream_gene_variant COAD-US 19 8613157 8613157 single base substitution G A downstream_gene_variant COAD-US 19 8613157 8613157 single base substitution G A exon_variant COAD-US 19 8613157 8613157 single base substitution G A synonymous_variant I382I 1146C>T COAD-US 19 8613157 8613157 single base substitution G A upstream_gene_variant COAD-US 19 8615049 8615049 single base substitution C T downstream_gene_variant COAD-US 19 8615049 8615049 single base substitution C T exon_variant COAD-US 19 8615049 8615049 single base substitution C T missense_variant V366M 1096G>A COAD-US 19 8615049 8615049 single base substitution C T upstream_gene_variant COAD-US 19 8617025 8617025 single base substitution G A downstream_gene_variant COAD-US 19 8617025 8617025 single base substitution G A exon_variant COAD-US 19 8617025 8617025 single base substitution G A synonymous_variant F176F 528C>T COAD-US 19 8617025 8617025 single base substitution G A upstream_gene_variant COAD-US 19 8619398 8619398 single base substitution T C 3_prime_UTR_variant COAD-US 19 8619398 8619398 single base substitution T C downstream_gene_variant COAD-US 19 8619398 8619398 single base substitution T C exon_variant COAD-US 19 8619398 8619398 single base substitution T C missense_variant M93V 277A>G COAD-US 19 8619398 8619398 single base substitution T C missense_variant M97V 289A>G COAD-US 19 8619398 8619398 single base substitution T C upstream_gene_variant COAD-US 19 8619403 8619403 single base substitution C T 3_prime_UTR_variant COAD-US 19 8619403 8619403 single base substitution C T downstream_gene_variant COAD-US 19 8619403 8619403 single base substitution C T exon_variant COAD-US 19 8619403 8619403 single base substitution C T missense_variant R91Q 272G>A COAD-US 19 8619403 8619403 single base substitution C T missense_variant R95Q 284G>A COAD-US 19 8619403 8619403 single base substitution C T upstream_gene_variant COAD-US 19 8619421 8619421 single base substitution A G 3_prime_UTR_variant COAD-US 19 8619421 8619421 single base substitution A G downstream_gene_variant COAD-US 19 8619421 8619421 single base substitution A G exon_variant COAD-US 19 8619421 8619421 single base substitution A G missense_variant L85P 254T>C COAD-US 19 8619421 8619421 single base substitution A G missense_variant L89P 266T>C COAD-US 19 8619421 8619421 single base substitution A G upstream_gene_variant COAD-US 19 8619436 8619436 deletion of <=200bp G - 3_prime_UTR_variant COAD-US 19 8619436 8619436 deletion of <=200bp G - downstream_gene_variant COAD-US 19 8619436 8619436 deletion of <=200bp G - exon_variant COAD-US 19 8619436 8619436 deletion of <=200bp G - frameshift_variant P80 COAD-US 19 8619436 8619436 deletion of <=200bp G - frameshift_variant P84 COAD-US 19 8619436 8619436 deletion of <=200bp G - upstream_gene_variant COAD-US 19 8619556 8619556 single base substitution G A 3_prime_UTR_variant COAD-US 19 8619556 8619556 single base substitution G A downstream_gene_variant COAD-US 19 8619556 8619556 single base substitution G A exon_variant COAD-US 19 8619556 8619556 single base substitution G A synonymous_variant I67I 201C>T COAD-US 19 8619556 8619556 single base substitution G A synonymous_variant I71I 213C>T COAD-US 19 8619556 8619556 single base substitution G A upstream_gene_variant COAD-US 19 8619618 8619618 single base substitution C T downstream_gene_variant COAD-US 19 8619618 8619618 single base substitution C T exon_variant COAD-US 19 8619618 8619618 single base substitution C T intron_variant COAD-US 19 8619618 8619618 single base substitution C T missense_variant G51S 151G>A COAD-US 19 8619618 8619618 single base substitution C T upstream_gene_variant COAD-US 19 8620542 8620542 single base substitution C T exon_variant COAD-US 19 8620542 8620542 single base substitution C T missense_variant V48I 142G>A COAD-US 19 8620542 8620542 single base substitution C T splice_donor_variant COAD-US 19 8620542 8620542 single base substitution C T upstream_gene_variant COAD-US 19 8620596 8620596 single base substitution C T exon_variant COAD-US 19 8620596 8620596 single base substitution C T missense_variant E30K 88G>A COAD-US 19 8620596 8620596 single base substitution C T upstream_gene_variant COCA-CN 19 8591886 8591886 single base substitution G T downstream_gene_variant COCA-CN 19 8591886 8591886 single base substitution G T intron_variant COCA-CN 19 8591886 8591886 single base substitution G T upstream_gene_variant COCA-CN 19 8601257 8601257 single base substitution G A downstream_gene_variant COCA-CN 19 8601257 8601257 single base substitution G A exon_variant COCA-CN 19 8601257 8601257 single base substitution G A missense_variant T641M 1922C>T COCA-CN 19 8601868 8601868 single base substitution G A downstream_gene_variant COCA-CN 19 8601868 8601868 single base substitution G A exon_variant COCA-CN 19 8601868 8601868 single base substitution G A synonymous_variant N588N 1764C>T COCA-CN 19 8606756 8606756 single base substitution G A 3_prime_UTR_variant COCA-CN 19 8606756 8606756 single base substitution G A downstream_gene_variant COCA-CN 19 8606756 8606756 single base substitution G A intron_variant COCA-CN 19 8606756 8606756 single base substitution G A upstream_gene_variant COCA-CN 19 8606835 8606835 single base substitution T C downstream_gene_variant COCA-CN 19 8606835 8606835 single base substitution T C exon_variant COCA-CN 19 8606835 8606835 single base substitution T C missense_variant D522G 1565A>G COCA-CN 19 8606835 8606835 single base substitution T C upstream_gene_variant COCA-CN 19 8608577 8608577 single base substitution G C downstream_gene_variant COCA-CN 19 8608577 8608577 single base substitution G C intron_variant COCA-CN 19 8608577 8608577 single base substitution G C upstream_gene_variant COCA-CN 19 8609222 8609222 single base substitution T C downstream_gene_variant COCA-CN 19 8609222 8609222 single base substitution T C exon_variant COCA-CN 19 8609222 8609222 single base substitution T C missense_variant S495G 1483A>G COCA-CN 19 8609222 8609222 single base substitution T C upstream_gene_variant COCA-CN 19 8609370 8609370 single base substitution G A downstream_gene_variant COCA-CN 19 8609370 8609370 single base substitution G A intron_variant COCA-CN 19 8609370 8609370 single base substitution G A upstream_gene_variant COCA-CN 19 8612875 8612875 single base substitution A C downstream_gene_variant COCA-CN 19 8612875 8612875 single base substitution A C exon_variant COCA-CN 19 8612875 8612875 single base substitution A C intron_variant COCA-CN 19 8612875 8612875 single base substitution A C upstream_gene_variant COCA-CN 19 8612914 8612914 single base substitution G A downstream_gene_variant COCA-CN 19 8612914 8612914 single base substitution G A exon_variant COCA-CN 19 8612914 8612914 single base substitution G A intron_variant COCA-CN 19 8612914 8612914 single base substitution G A splice_region_variant COCA-CN 19 8612914 8612914 single base substitution G A upstream_gene_variant COCA-CN 19 8615395 8615395 single base substitution G C downstream_gene_variant COCA-CN 19 8615395 8615395 single base substitution G C intron_variant COCA-CN 19 8615395 8615395 single base substitution G C upstream_gene_variant COCA-CN 19 8616964 8616964 single base substitution C T downstream_gene_variant COCA-CN 19 8616964 8616964 single base substitution C T exon_variant COCA-CN 19 8616964 8616964 single base substitution C T missense_variant V197M 589G>A COCA-CN 19 8616964 8616964 single base substitution C T upstream_gene_variant COCA-CN 19 8619532 8619532 single base substitution C T downstream_gene_variant COCA-CN 19 8619532 8619532 single base substitution C T exon_variant COCA-CN 19 8619532 8619532 single base substitution C T splice_region_variant COCA-CN 19 8619532 8619532 single base substitution C T upstream_gene_variant EOPC-DE 19 8605367 8605367 single base substitution G A downstream_gene_variant EOPC-DE 19 8605367 8605367 single base substitution G A intron_variant EOPC-DE 19 8605367 8605367 single base substitution G A upstream_gene_variant EOPC-DE 19 8620823 8620823 single base substitution A G intron_variant EOPC-DE 19 8620823 8620823 single base substitution A G upstream_gene_variant EOPC-DE 19 8636444 8636444 single base substitution G A downstream_gene_variant EOPC-DE 19 8636444 8636444 single base substitution G A intron_variant EOPC-DE 19 8643135 8643135 single base substitution G C upstream_gene_variant ESAD-UK 19 8580823 8580823 single base substitution A T downstream_gene_variant ESAD-UK 19 8583723 8583723 single base substitution C T downstream_gene_variant ESAD-UK 19 8586061 8586061 deletion of <=200bp C - 3_prime_UTR_variant ESAD-UK 19 8586061 8586061 deletion of <=200bp C - downstream_gene_variant ESAD-UK 19 8587426 8587426 single base substitution G T downstream_gene_variant ESAD-UK 19 8587426 8587426 single base substitution G T missense_variant Q1019K 3055C>A ESAD-UK 19 8589162 8589162 single base substitution T C downstream_gene_variant ESAD-UK 19 8589162 8589162 single base substitution T C intron_variant ESAD-UK 19 8590504 8590504 single base substitution C T downstream_gene_variant ESAD-UK 19 8590504 8590504 single base substitution C T intron_variant ESAD-UK 19 8594051 8594051 single base substitution T C downstream_gene_variant ESAD-UK 19 8594051 8594051 single base substitution T C intron_variant ESAD-UK 19 8594051 8594051 single base substitution T C upstream_gene_variant ESAD-UK 19 8595090 8595090 single base substitution C T exon_variant ESAD-UK 19 8595090 8595090 single base substitution C T missense_variant R773H 2318G>A ESAD-UK 19 8595090 8595090 single base substitution C T upstream_gene_variant ESAD-UK 19 8595617 8595617 single base substitution G A intron_variant ESAD-UK 19 8595617 8595617 single base substitution G A upstream_gene_variant ESAD-UK 19 8596485 8596485 single base substitution C A intron_variant ESAD-UK 19 8596485 8596485 single base substitution C A upstream_gene_variant ESAD-UK 19 8598078 8598078 insertion of <=200bp - T intron_variant ESAD-UK 19 8598078 8598078 insertion of <=200bp - T upstream_gene_variant ESAD-UK 19 8600757 8600757 single base substitution C T downstream_gene_variant ESAD-UK 19 8600757 8600757 single base substitution C T intron_variant ESAD-UK 19 8603581 8603581 single base substitution C T downstream_gene_variant ESAD-UK 19 8603581 8603581 single base substitution C T intron_variant ESAD-UK 19 8603683 8603683 single base substitution C G downstream_gene_variant ESAD-UK 19 8603683 8603683 single base substitution C G intron_variant ESAD-UK 19 8604189 8604189 single base substitution T C downstream_gene_variant ESAD-UK 19 8604189 8604189 single base substitution T C intron_variant ESAD-UK 19 8605222 8605222 single base substitution A T 3_prime_UTR_variant ESAD-UK 19 8605222 8605222 single base substitution A T downstream_gene_variant ESAD-UK 19 8605222 8605222 single base substitution A T intron_variant ESAD-UK 19 8605222 8605222 single base substitution A T upstream_gene_variant ESAD-UK 19 8605467 8605467 single base substitution G A downstream_gene_variant ESAD-UK 19 8605467 8605467 single base substitution G A intron_variant ESAD-UK 19 8605467 8605467 single base substitution G A upstream_gene_variant ESAD-UK 19 8605636 8605636 single base substitution G A downstream_gene_variant ESAD-UK 19 8605636 8605636 single base substitution G A intron_variant ESAD-UK 19 8605636 8605636 single base substitution G A upstream_gene_variant ESAD-UK 19 8606546 8606546 single base substitution C T downstream_gene_variant ESAD-UK 19 8606546 8606546 single base substitution C T intron_variant ESAD-UK 19 8606546 8606546 single base substitution C T upstream_gene_variant ESAD-UK 19 8606863 8606863 single base substitution C T downstream_gene_variant ESAD-UK 19 8606863 8606863 single base substitution C T exon_variant ESAD-UK 19 8606863 8606863 single base substitution C T missense_variant V513I 1537G>A ESAD-UK 19 8606863 8606863 single base substitution C T upstream_gene_variant ESAD-UK 19 8609190 8609190 single base substitution G A downstream_gene_variant ESAD-UK 19 8609190 8609190 single base substitution G A exon_variant ESAD-UK 19 8609190 8609190 single base substitution G A synonymous_variant Y505Y 1515C>T ESAD-UK 19 8609190 8609190 single base substitution G A upstream_gene_variant ESAD-UK 19 8609289 8609289 single base substitution G A downstream_gene_variant ESAD-UK 19 8609289 8609289 single base substitution G A exon_variant ESAD-UK 19 8609289 8609289 single base substitution G A synonymous_variant G472G 1416C>T ESAD-UK 19 8609289 8609289 single base substitution G A upstream_gene_variant ESAD-UK 19 8609981 8609981 single base substitution A T downstream_gene_variant ESAD-UK 19 8609981 8609981 single base substitution A T intron_variant ESAD-UK 19 8609981 8609981 single base substitution A T upstream_gene_variant ESAD-UK 19 8611074 8611074 single base substitution G A downstream_gene_variant ESAD-UK 19 8611074 8611074 single base substitution G A intron_variant ESAD-UK 19 8611074 8611074 single base substitution G A upstream_gene_variant ESAD-UK 19 8611550 8611550 single base substitution G C downstream_gene_variant ESAD-UK 19 8611550 8611550 single base substitution G C intron_variant ESAD-UK 19 8611550 8611550 single base substitution G C upstream_gene_variant ESAD-UK 19 8612034 8612036 deletion of <=200bp TAT - downstream_gene_variant ESAD-UK 19 8612034 8612036 deletion of <=200bp TAT - intron_variant ESAD-UK 19 8612034 8612036 deletion of <=200bp TAT - upstream_gene_variant ESAD-UK 19 8613205 8613205 single base substitution C T downstream_gene_variant ESAD-UK 19 8613205 8613205 single base substitution C T intron_variant ESAD-UK 19 8613205 8613205 single base substitution C T splice_region_variant ESAD-UK 19 8613205 8613205 single base substitution C T upstream_gene_variant ESAD-UK 19 8613611 8613611 single base substitution A C downstream_gene_variant ESAD-UK 19 8613611 8613611 single base substitution A C intron_variant ESAD-UK 19 8613611 8613611 single base substitution A C upstream_gene_variant ESAD-UK 19 8613896 8613896 single base substitution G A downstream_gene_variant ESAD-UK 19 8613896 8613896 single base substitution G A intron_variant ESAD-UK 19 8613896 8613896 single base substitution G A upstream_gene_variant ESAD-UK 19 8614562 8614562 single base substitution A G downstream_gene_variant ESAD-UK 19 8614562 8614562 single base substitution A G exon_variant ESAD-UK 19 8614562 8614562 single base substitution A G intron_variant ESAD-UK 19 8614562 8614562 single base substitution A G upstream_gene_variant ESAD-UK 19 8616338 8616338 single base substitution C A downstream_gene_variant ESAD-UK 19 8616338 8616338 single base substitution C A exon_variant ESAD-UK 19 8616338 8616338 single base substitution C A intron_variant ESAD-UK 19 8616338 8616338 single base substitution C A upstream_gene_variant ESAD-UK 19 8616613 8616613 single base substitution C A downstream_gene_variant ESAD-UK 19 8616613 8616613 single base substitution C A exon_variant ESAD-UK 19 8616613 8616613 single base substitution C A intron_variant ESAD-UK 19 8616613 8616613 single base substitution C A upstream_gene_variant ESAD-UK 19 8617577 8617577 deletion of <=200bp T - downstream_gene_variant ESAD-UK 19 8617577 8617577 deletion of <=200bp T - intron_variant ESAD-UK 19 8617577 8617577 deletion of <=200bp T - upstream_gene_variant ESAD-UK 19 8617788 8617788 single base substitution C A downstream_gene_variant ESAD-UK 19 8617788 8617788 single base substitution C A intron_variant ESAD-UK 19 8617788 8617788 single base substitution C A upstream_gene_variant ESAD-UK 19 8620097 8620097 single base substitution C A downstream_gene_variant ESAD-UK 19 8620097 8620097 single base substitution C A intron_variant ESAD-UK 19 8620097 8620097 single base substitution C A upstream_gene_variant ESAD-UK 19 8620597 8620597 single base substitution G A exon_variant ESAD-UK 19 8620597 8620597 single base substitution G A synonymous_variant T29T 87C>T ESAD-UK 19 8620597 8620597 single base substitution G A upstream_gene_variant ESAD-UK 19 8620668 8620668 single base substitution G A exon_variant ESAD-UK 19 8620668 8620668 single base substitution G A missense_variant R6C 16C>T ESAD-UK 19 8620668 8620668 single base substitution G A upstream_gene_variant ESAD-UK 19 8621643 8621643 single base substitution T C intron_variant ESAD-UK 19 8621643 8621643 single base substitution T C upstream_gene_variant ESAD-UK 19 8623223 8623223 insertion of <=200bp - T intron_variant ESAD-UK 19 8623223 8623223 insertion of <=200bp - T upstream_gene_variant ESAD-UK 19 8624520 8624520 single base substitution C T intron_variant ESAD-UK 19 8624520 8624520 single base substitution C T upstream_gene_variant ESAD-UK 19 8625747 8625747 single base substitution C T intron_variant ESAD-UK 19 8628541 8628541 single base substitution C G intron_variant ESAD-UK 19 8629334 8629334 single base substitution T G intron_variant ESAD-UK 19 8631297 8631297 single base substitution C T intron_variant ESAD-UK 19 8631366 8631366 single base substitution A T intron_variant ESAD-UK 19 8631440 8631440 single base substitution C G intron_variant ESAD-UK 19 8633796 8633796 single base substitution C T intron_variant ESAD-UK 19 8634073 8634073 single base substitution A G intron_variant ESAD-UK 19 8634958 8634958 single base substitution T G intron_variant ESAD-UK 19 8637255 8637255 single base substitution G A downstream_gene_variant ESAD-UK 19 8637255 8637255 single base substitution G A intron_variant ESAD-UK 19 8637303 8637303 single base substitution C G downstream_gene_variant ESAD-UK 19 8637303 8637303 single base substitution C G intron_variant ESAD-UK 19 8638583 8638583 single base substitution A T downstream_gene_variant ESAD-UK 19 8638583 8638583 single base substitution A T intron_variant ESAD-UK 19 8638838 8638838 single base substitution C G downstream_gene_variant ESAD-UK 19 8638838 8638838 single base substitution C G intron_variant ESAD-UK 19 8639017 8639017 single base substitution C T downstream_gene_variant ESAD-UK 19 8639017 8639017 single base substitution C T intron_variant ESAD-UK 19 8640017 8640017 single base substitution A G downstream_gene_variant ESAD-UK 19 8640017 8640017 single base substitution A G intron_variant ESAD-UK 19 8643237 8643237 single base substitution G A upstream_gene_variant ESAD-UK 19 8643667 8643667 single base substitution G T upstream_gene_variant ESAD-UK 19 8644112 8644112 single base substitution G A upstream_gene_variant ESAD-UK 19 8645979 8645979 single base substitution C T upstream_gene_variant ESAD-UK 19 8647075 8647075 single base substitution C T upstream_gene_variant ESCA-CN 19 8587342 8587342 single base substitution G A downstream_gene_variant ESCA-CN 19 8587342 8587342 single base substitution G A missense_variant R1047W 3139C>T ESCA-CN 19 8587528 8587528 single base substitution C T downstream_gene_variant ESCA-CN 19 8587528 8587528 single base substitution C T missense_variant G1014S 3040G>A ESCA-CN 19 8587694 8587694 single base substitution C A downstream_gene_variant ESCA-CN 19 8587694 8587694 single base substitution C A exon_variant ESCA-CN 19 8587694 8587694 single base substitution C A synonymous_variant V958V 2874G>T ESCA-CN 19 8595119 8595119 single base substitution G T exon_variant ESCA-CN 19 8595119 8595119 single base substitution G T missense_variant D763E 2289C>A ESCA-CN 19 8595119 8595119 single base substitution G T upstream_gene_variant GBM-US 19 8616651 8616651 single base substitution G A downstream_gene_variant GBM-US 19 8616651 8616651 single base substitution G A exon_variant GBM-US 19 8616651 8616651 single base substitution G A synonymous_variant D248D 744C>T GBM-US 19 8616651 8616651 single base substitution G A upstream_gene_variant KIRC-US 19 8592225 8592225 single base substitution A T 3_prime_UTR_variant KIRC-US 19 8592225 8592225 single base substitution A T downstream_gene_variant KIRC-US 19 8592225 8592225 single base substitution A T exon_variant KIRC-US 19 8592225 8592225 single base substitution A T missense_variant L824H 2471T>A KIRC-US 19 8592225 8592225 single base substitution A T upstream_gene_variant KIRC-US 19 8595162 8595162 single base substitution C T exon_variant KIRC-US 19 8595162 8595162 single base substitution C T missense_variant R749Q 2246G>A KIRC-US 19 8595162 8595162 single base substitution C T upstream_gene_variant KIRC-US 19 8606866 8606866 single base substitution C T downstream_gene_variant KIRC-US 19 8606866 8606866 single base substitution C T exon_variant KIRC-US 19 8606866 8606866 single base substitution C T missense_variant D512N 1534G>A KIRC-US 19 8606866 8606866 single base substitution C T upstream_gene_variant KIRC-US 19 8612963 8612963 single base substitution T A downstream_gene_variant KIRC-US 19 8612963 8612963 single base substitution T A exon_variant KIRC-US 19 8612963 8612963 single base substitution T A missense_variant K409M 1226A>T KIRC-US 19 8612963 8612963 single base substitution T A upstream_gene_variant KIRP-US 19 8604865 8604865 single base substitution T G downstream_gene_variant KIRP-US 19 8604865 8604865 single base substitution T G exon_variant KIRP-US 19 8604865 8604865 single base substitution T G missense_variant K553T 1658A>C KIRP-US 19 8609279 8609279 single base substitution C A downstream_gene_variant KIRP-US 19 8609279 8609279 single base substitution C A exon_variant KIRP-US 19 8609279 8609279 single base substitution C A missense_variant D476Y 1426G>T KIRP-US 19 8609279 8609279 single base substitution C A upstream_gene_variant KIRP-US 19 8642191 8642191 single base substitution C G exon_variant KIRP-US 19 8642191 8642191 single base substitution C G splice_region_variant KIRP-US 19 8642191 8642191 single base substitution C G start_lost M1I 3G>C LAML-KR 19 8581293 8581293 single base substitution G T downstream_gene_variant LAML-KR 19 8585674 8585674 single base substitution C T 3_prime_UTR_variant LAML-KR 19 8585674 8585674 single base substitution C T downstream_gene_variant LAML-KR 19 8598277 8598277 single base substitution C T intron_variant LAML-KR 19 8598277 8598277 single base substitution C T upstream_gene_variant LAML-KR 19 8598278 8598278 single base substitution G T intron_variant LAML-KR 19 8598278 8598278 single base substitution G T upstream_gene_variant LAML-KR 19 8608583 8608583 single base substitution G C downstream_gene_variant LAML-KR 19 8608583 8608583 single base substitution G C intron_variant LAML-KR 19 8608583 8608583 single base substitution G C upstream_gene_variant LAML-KR 19 8608751 8608751 single base substitution C G downstream_gene_variant LAML-KR 19 8608751 8608751 single base substitution C G intron_variant LAML-KR 19 8608751 8608751 single base substitution C G upstream_gene_variant LAML-KR 19 8608925 8608925 single base substitution C G downstream_gene_variant LAML-KR 19 8608925 8608925 single base substitution C G intron_variant LAML-KR 19 8608925 8608925 single base substitution C G upstream_gene_variant LAML-KR 19 8609472 8609472 single base substitution T G downstream_gene_variant LAML-KR 19 8609472 8609472 single base substitution T G intron_variant LAML-KR 19 8609472 8609472 single base substitution T G upstream_gene_variant LAML-KR 19 8616215 8616215 single base substitution T C downstream_gene_variant LAML-KR 19 8616215 8616215 single base substitution T C intron_variant LAML-KR 19 8616215 8616215 single base substitution T C upstream_gene_variant LAML-KR 19 8616216 8616216 single base substitution G T downstream_gene_variant LAML-KR 19 8616216 8616216 single base substitution G T intron_variant LAML-KR 19 8616216 8616216 single base substitution G T upstream_gene_variant LAML-KR 19 8616267 8616267 single base substitution A C downstream_gene_variant LAML-KR 19 8616267 8616267 single base substitution A C intron_variant LAML-KR 19 8616267 8616267 single base substitution A C upstream_gene_variant LAML-KR 19 8644424 8644424 single base substitution A C upstream_gene_variant LGG-US 19 8601249 8601249 single base substitution G A downstream_gene_variant LGG-US 19 8601249 8601249 single base substitution G A exon_variant LGG-US 19 8601249 8601249 single base substitution G A missense_variant R644W 1930C>T LGG-US 19 8617006 8617006 single base substitution C G downstream_gene_variant LGG-US 19 8617006 8617006 single base substitution C G exon_variant LGG-US 19 8617006 8617006 single base substitution C G missense_variant D183H 547G>C LGG-US 19 8617006 8617006 single base substitution C G upstream_gene_variant LGG-US 19 8620581 8620581 single base substitution C T exon_variant LGG-US 19 8620581 8620581 single base substitution C T missense_variant A35T 103G>A LGG-US 19 8620581 8620581 single base substitution C T upstream_gene_variant LICA-FR 19 8586455 8586455 single base substitution C A downstream_gene_variant LICA-FR 19 8586455 8586455 single base substitution C A missense_variant G1085V 3254G>T LICA-FR 19 8587587 8587587 single base substitution C G downstream_gene_variant LICA-FR 19 8587587 8587587 single base substitution C G missense_variant R994P 2981G>C LICA-FR 19 8601206 8601206 single base substitution C T downstream_gene_variant LICA-FR 19 8601206 8601206 single base substitution C T exon_variant LICA-FR 19 8601206 8601206 single base substitution C T missense_variant R658Q 1973G>A LICA-FR 19 8624231 8624231 single base substitution G T intron_variant LICA-FR 19 8624231 8624231 single base substitution G T upstream_gene_variant LICA-FR 19 8631943 8631943 deletion of <=200bp T - intron_variant LICA-FR 19 8639461 8639461 single base substitution T C downstream_gene_variant LICA-FR 19 8639461 8639461 single base substitution T C intron_variant LIHC-US 19 8619381 8619395 deletion of <=200bp CTCACAGTCGATAAG - 3_prime_UTR_variant LIHC-US 19 8619381 8619395 deletion of <=200bp CTCACAGTCGATAAG - downstream_gene_variant LIHC-US 19 8619381 8619395 deletion of <=200bp CTCACAGTCGATAAG - exon_variant LIHC-US 19 8619381 8619395 deletion of <=200bp CTCACAGTCGATAAG - inframe_deletion LIDCE94 LIHC-US 19 8619381 8619395 deletion of <=200bp CTCACAGTCGATAAG - inframe_deletion LIDCE98 LIHC-US 19 8619381 8619395 deletion of <=200bp CTCACAGTCGATAAG - upstream_gene_variant LINC-JP 19 8586482 8586482 single base substitution G A downstream_gene_variant LINC-JP 19 8586482 8586482 single base substitution G A missense_variant S1076L 3227C>T LINC-JP 19 8587197 8587197 single base substitution C T downstream_gene_variant LINC-JP 19 8587197 8587197 single base substitution C T intron_variant LINC-JP 19 8593184 8593184 single base substitution G A downstream_gene_variant LINC-JP 19 8593184 8593184 single base substitution G A intron_variant LINC-JP 19 8593184 8593184 single base substitution G A upstream_gene_variant LINC-JP 19 8595107 8595107 single base substitution C T exon_variant LINC-JP 19 8595107 8595107 single base substitution C T synonymous_variant S767S 2301G>A LINC-JP 19 8595107 8595107 single base substitution C T upstream_gene_variant LINC-JP 19 8616954 8616954 single base substitution T G downstream_gene_variant LINC-JP 19 8616954 8616954 single base substitution T G exon_variant LINC-JP 19 8616954 8616954 single base substitution T G missense_variant Q200P 599A>C LINC-JP 19 8616954 8616954 single base substitution T G upstream_gene_variant LINC-JP 19 8618612 8618612 single base substitution C T downstream_gene_variant LINC-JP 19 8618612 8618612 single base substitution C T intron_variant LINC-JP 19 8618612 8618612 single base substitution C T upstream_gene_variant LINC-JP 19 8628995 8628995 single base substitution C T intron_variant LIRI-JP 19 8583296 8583296 single base substitution G C downstream_gene_variant LIRI-JP 19 8588078 8588078 single base substitution G A downstream_gene_variant LIRI-JP 19 8588078 8588078 single base substitution G A intron_variant LIRI-JP 19 8591337 8591337 single base substitution T A 3_prime_UTR_variant LIRI-JP 19 8591337 8591337 single base substitution T A downstream_gene_variant LIRI-JP 19 8591337 8591337 single base substitution T A splice_region_variant LIRI-JP 19 8591337 8591337 single base substitution T A stop_gained K924* 2770A>T LIRI-JP 19 8596884 8596884 single base substitution C A intron_variant LIRI-JP 19 8596884 8596884 single base substitution C A upstream_gene_variant LIRI-JP 19 8599405 8599405 single base substitution G A intron_variant LIRI-JP 19 8599405 8599405 single base substitution G A upstream_gene_variant LIRI-JP 19 8602487 8602487 single base substitution G A downstream_gene_variant LIRI-JP 19 8602487 8602487 single base substitution G A intron_variant LIRI-JP 19 8603049 8603049 single base substitution C T downstream_gene_variant LIRI-JP 19 8603049 8603049 single base substitution C T intron_variant LIRI-JP 19 8605979 8605979 single base substitution T C downstream_gene_variant LIRI-JP 19 8605979 8605979 single base substitution T C intron_variant LIRI-JP 19 8605979 8605979 single base substitution T C upstream_gene_variant LIRI-JP 19 8607895 8607895 single base substitution C T downstream_gene_variant LIRI-JP 19 8607895 8607895 single base substitution C T intron_variant LIRI-JP 19 8607895 8607895 single base substitution C T upstream_gene_variant LIRI-JP 19 8607896 8607896 single base substitution T G downstream_gene_variant LIRI-JP 19 8607896 8607896 single base substitution T G intron_variant LIRI-JP 19 8607896 8607896 single base substitution T G upstream_gene_variant LIRI-JP 19 8612064 8612064 single base substitution G A downstream_gene_variant LIRI-JP 19 8612064 8612064 single base substitution G A intron_variant LIRI-JP 19 8612064 8612064 single base substitution G A upstream_gene_variant LIRI-JP 19 8613205 8613205 single base substitution C T downstream_gene_variant LIRI-JP 19 8613205 8613205 single base substitution C T intron_variant LIRI-JP 19 8613205 8613205 single base substitution C T splice_region_variant LIRI-JP 19 8613205 8613205 single base substitution C T upstream_gene_variant LIRI-JP 19 8615188 8615190 deletion of <=200bp CTC - downstream_gene_variant LIRI-JP 19 8615188 8615190 deletion of <=200bp CTC - exon_variant LIRI-JP 19 8615188 8615190 deletion of <=200bp CTC - inframe_deletion E319 LIRI-JP 19 8615188 8615190 deletion of <=200bp CTC - upstream_gene_variant LIRI-JP 19 8619181 8619181 single base substitution T G downstream_gene_variant LIRI-JP 19 8619181 8619181 single base substitution T G intron_variant LIRI-JP 19 8619181 8619181 single base substitution T G upstream_gene_variant LIRI-JP 19 8620464 8620464 single base substitution C T exon_variant LIRI-JP 19 8620464 8620464 single base substitution C T intron_variant LIRI-JP 19 8620464 8620464 single base substitution C T upstream_gene_variant LIRI-JP 19 8622975 8622975 deletion of <=200bp C - intron_variant LIRI-JP 19 8622975 8622975 deletion of <=200bp C - upstream_gene_variant LIRI-JP 19 8623465 8623465 single base substitution A G intron_variant LIRI-JP 19 8623465 8623465 single base substitution A G upstream_gene_variant LIRI-JP 19 8626763 8626763 single base substitution G T intron_variant LIRI-JP 19 8627790 8627790 single base substitution G A intron_variant LIRI-JP 19 8631979 8631979 single base substitution T C intron_variant LIRI-JP 19 8633740 8633740 single base substitution G T intron_variant LIRI-JP 19 8634874 8634874 single base substitution T C intron_variant LIRI-JP 19 8635667 8635667 single base substitution C A intron_variant LIRI-JP 19 8640108 8640108 single base substitution G A downstream_gene_variant LIRI-JP 19 8640108 8640108 single base substitution G A intron_variant LIRI-JP 19 8644540 8644540 single base substitution C T upstream_gene_variant LUSC-KR 19 8582188 8582188 single base substitution C G downstream_gene_variant LUSC-KR 19 8583226 8583226 single base substitution G C downstream_gene_variant LUSC-KR 19 8584892 8584892 single base substitution G T downstream_gene_variant LUSC-KR 19 8585706 8585706 single base substitution G T 3_prime_UTR_variant LUSC-KR 19 8585706 8585706 single base substitution G T downstream_gene_variant LUSC-KR 19 8587036 8587036 single base substitution A T downstream_gene_variant LUSC-KR 19 8587036 8587036 single base substitution A T intron_variant LUSC-KR 19 8587066 8587066 single base substitution C T downstream_gene_variant LUSC-KR 19 8587066 8587066 single base substitution C T intron_variant LUSC-KR 19 8587079 8587079 single base substitution T C downstream_gene_variant LUSC-KR 19 8587079 8587079 single base substitution T C intron_variant LUSC-KR 19 8588605 8588605 single base substitution C G downstream_gene_variant LUSC-KR 19 8588605 8588605 single base substitution C G intron_variant LUSC-KR 19 8589611 8589611 single base substitution G C downstream_gene_variant LUSC-KR 19 8589611 8589611 single base substitution G C intron_variant LUSC-KR 19 8590542 8590542 single base substitution C G downstream_gene_variant LUSC-KR 19 8590542 8590542 single base substitution C G intron_variant LUSC-KR 19 8594054 8594054 single base substitution G T downstream_gene_variant LUSC-KR 19 8594054 8594054 single base substitution G T intron_variant LUSC-KR 19 8594054 8594054 single base substitution G T upstream_gene_variant LUSC-KR 19 8596589 8596589 single base substitution G C intron_variant LUSC-KR 19 8596589 8596589 single base substitution G C upstream_gene_variant LUSC-KR 19 8600801 8600801 single base substitution G A downstream_gene_variant LUSC-KR 19 8600801 8600801 single base substitution G A intron_variant LUSC-KR 19 8608583 8608583 single base substitution G C downstream_gene_variant LUSC-KR 19 8608583 8608583 single base substitution G C intron_variant LUSC-KR 19 8608583 8608583 single base substitution G C upstream_gene_variant LUSC-KR 19 8608724 8608724 single base substitution G C downstream_gene_variant LUSC-KR 19 8608724 8608724 single base substitution G C intron_variant LUSC-KR 19 8608724 8608724 single base substitution G C upstream_gene_variant LUSC-KR 19 8608772 8608772 single base substitution G C downstream_gene_variant LUSC-KR 19 8608772 8608772 single base substitution G C intron_variant LUSC-KR 19 8608772 8608772 single base substitution G C upstream_gene_variant LUSC-KR 19 8608931 8608931 single base substitution G C downstream_gene_variant LUSC-KR 19 8608931 8608931 single base substitution G C intron_variant LUSC-KR 19 8608931 8608931 single base substitution G C upstream_gene_variant LUSC-KR 19 8616216 8616216 single base substitution G T downstream_gene_variant LUSC-KR 19 8616216 8616216 single base substitution G T intron_variant LUSC-KR 19 8616216 8616216 single base substitution G T upstream_gene_variant LUSC-KR 19 8618815 8618815 single base substitution T C downstream_gene_variant LUSC-KR 19 8618815 8618815 single base substitution T C intron_variant LUSC-KR 19 8618815 8618815 single base substitution T C upstream_gene_variant LUSC-KR 19 8618871 8618871 single base substitution C T downstream_gene_variant LUSC-KR 19 8618871 8618871 single base substitution C T intron_variant LUSC-KR 19 8618871 8618871 single base substitution C T upstream_gene_variant LUSC-KR 19 8626310 8626310 single base substitution T C intron_variant LUSC-KR 19 8627161 8627161 single base substitution A T intron_variant LUSC-KR 19 8635633 8635633 single base substitution C T intron_variant LUSC-KR 19 8639552 8639552 single base substitution T C downstream_gene_variant LUSC-KR 19 8639552 8639552 single base substitution T C intron_variant LUSC-KR 19 8639979 8639979 single base substitution G T downstream_gene_variant LUSC-KR 19 8639979 8639979 single base substitution G T intron_variant LUSC-KR 19 8642414 8642414 single base substitution G A 5_prime_UTR_variant LUSC-KR 19 8642414 8642414 single base substitution G A upstream_gene_variant LUSC-KR 19 8644098 8644098 single base substitution T A upstream_gene_variant LUSC-KR 19 8644658 8644658 single base substitution C A upstream_gene_variant LUSC-KR 19 8646484 8646484 single base substitution C A upstream_gene_variant LUSC-US 19 8586456 8586456 single base substitution C T downstream_gene_variant LUSC-US 19 8586456 8586456 single base substitution C T missense_variant G1085S 3253G>A LUSC-US 19 8595157 8595157 single base substitution C T exon_variant LUSC-US 19 8595157 8595157 single base substitution C T missense_variant E751K 2251G>A LUSC-US 19 8595157 8595157 single base substitution C T upstream_gene_variant LUSC-US 19 8595448 8595448 single base substitution G T exon_variant LUSC-US 19 8595448 8595448 single base substitution G T missense_variant L685M 2053C>A LUSC-US 19 8595448 8595448 single base substitution G T upstream_gene_variant LUSC-US 19 8601411 8601411 single base substitution G T downstream_gene_variant LUSC-US 19 8601411 8601411 single base substitution G T exon_variant LUSC-US 19 8601411 8601411 single base substitution G T missense_variant R624S 1870C>A LUSC-US 19 8601932 8601932 single base substitution G T downstream_gene_variant LUSC-US 19 8601932 8601932 single base substitution G T exon_variant LUSC-US 19 8601932 8601932 single base substitution G T missense_variant A567D 1700C>A LUSC-US 19 8609217 8609217 single base substitution C T downstream_gene_variant LUSC-US 19 8609217 8609217 single base substitution C T exon_variant LUSC-US 19 8609217 8609217 single base substitution C T stop_gained W496* 1488G>A LUSC-US 19 8609217 8609217 single base substitution C T upstream_gene_variant MALY-DE 19 8582439 8582440 deletion of <=200bp TG - downstream_gene_variant MALY-DE 19 8591234 8591235 deletion of <=200bp TC - downstream_gene_variant MALY-DE 19 8591234 8591235 deletion of <=200bp TC - intron_variant MALY-DE 19 8595116 8595116 single base substitution G A exon_variant MALY-DE 19 8595116 8595116 single base substitution G A synonymous_variant F764F 2292C>T MALY-DE 19 8595116 8595116 single base substitution G A upstream_gene_variant MALY-DE 19 8601052 8601053 deletion of <=200bp TC - downstream_gene_variant MALY-DE 19 8601052 8601053 deletion of <=200bp TC - intron_variant MALY-DE 19 8611041 8611041 single base substitution C T downstream_gene_variant MALY-DE 19 8611041 8611041 single base substitution C T intron_variant MALY-DE 19 8611041 8611041 single base substitution C T upstream_gene_variant MALY-DE 19 8613714 8613714 single base substitution C T downstream_gene_variant MALY-DE 19 8613714 8613714 single base substitution C T intron_variant MALY-DE 19 8613714 8613714 single base substitution C T upstream_gene_variant MALY-DE 19 8615718 8615718 single base substitution C T downstream_gene_variant MALY-DE 19 8615718 8615718 single base substitution C T intron_variant MALY-DE 19 8615718 8615718 single base substitution C T upstream_gene_variant MALY-DE 19 8627591 8627591 single base substitution T A intron_variant MALY-DE 19 8629419 8629419 single base substitution C T intron_variant MALY-DE 19 8635257 8635257 deletion of <=200bp T - intron_variant MALY-DE 19 8636194 8636194 single base substitution C A intron_variant MALY-DE 19 8636306 8636306 deletion of <=200bp T - intron_variant MALY-DE 19 8640913 8640914 deletion of <=200bp CT - downstream_gene_variant MALY-DE 19 8640913 8640914 deletion of <=200bp CT - intron_variant MALY-DE 19 8644963 8644963 single base substitution G A upstream_gene_variant MALY-DE 19 8645745 8645745 single base substitution C T upstream_gene_variant MELA-AU 19 8580721 8580721 single base substitution C T downstream_gene_variant MELA-AU 19 8580815 8580815 single base substitution C T downstream_gene_variant MELA-AU 19 8581033 8581033 single base substitution C T downstream_gene_variant MELA-AU 19 8581411 8581411 single base substitution C T downstream_gene_variant MELA-AU 19 8581822 8581822 single base substitution G A downstream_gene_variant MELA-AU 19 8581897 8581897 single base substitution G A downstream_gene_variant MELA-AU 19 8583357 8583357 single base substitution C T downstream_gene_variant MELA-AU 19 8583524 8583524 single base substitution A T downstream_gene_variant MELA-AU 19 8583535 8583535 single base substitution C T downstream_gene_variant MELA-AU 19 8583592 8583592 single base substitution C T downstream_gene_variant MELA-AU 19 8583621 8583621 single base substitution C T downstream_gene_variant MELA-AU 19 8583733 8583733 single base substitution C T downstream_gene_variant MELA-AU 19 8584667 8584667 single base substitution G A downstream_gene_variant MELA-AU 19 8585592 8585592 single base substitution G A downstream_gene_variant MELA-AU 19 8585993 8585993 single base substitution T C 3_prime_UTR_variant MELA-AU 19 8585993 8585993 single base substitution T C downstream_gene_variant MELA-AU 19 8586275 8586275 single base substitution G A 3_prime_UTR_variant MELA-AU 19 8586275 8586275 single base substitution G A downstream_gene_variant MELA-AU 19 8586485 8586485 single base substitution G A downstream_gene_variant MELA-AU 19 8586485 8586485 single base substitution G A missense_variant P1075L 3224C>T MELA-AU 19 8586528 8586528 single base substitution C T downstream_gene_variant MELA-AU 19 8586528 8586528 single base substitution C T intron_variant MELA-AU 19 8586851 8586851 single base substitution C T downstream_gene_variant MELA-AU 19 8586851 8586851 single base substitution C T intron_variant MELA-AU 19 8586853 8586853 single base substitution C T downstream_gene_variant MELA-AU 19 8586853 8586853 single base substitution C T intron_variant MELA-AU 19 8586980 8586980 single base substitution C T downstream_gene_variant MELA-AU 19 8586980 8586980 single base substitution C T intron_variant MELA-AU 19 8587141 8587141 single base substitution C T downstream_gene_variant MELA-AU 19 8587141 8587141 single base substitution C T intron_variant MELA-AU 19 8587547 8587547 single base substitution G A downstream_gene_variant MELA-AU 19 8587547 8587547 single base substitution G A synonymous_variant F1007F 3021C>T MELA-AU 19 8587587 8587587 single base substitution C T downstream_gene_variant MELA-AU 19 8587587 8587587 single base substitution C T missense_variant R994Q 2981G>A MELA-AU 19 8588187 8588187 single base substitution G A downstream_gene_variant MELA-AU 19 8588187 8588187 single base substitution G A intron_variant MELA-AU 19 8588206 8588206 single base substitution C T downstream_gene_variant MELA-AU 19 8588206 8588206 single base substitution C T intron_variant MELA-AU 19 8588337 8588337 single base substitution C T downstream_gene_variant MELA-AU 19 8588337 8588337 single base substitution C T intron_variant MELA-AU 19 8588756 8588756 single base substitution G A downstream_gene_variant MELA-AU 19 8588756 8588756 single base substitution G A intron_variant MELA-AU 19 8589219 8589219 single base substitution G A downstream_gene_variant MELA-AU 19 8589219 8589219 single base substitution G A intron_variant MELA-AU 19 8589395 8589396 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 19 8589395 8589396 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 8589720 8589720 single base substitution G A downstream_gene_variant MELA-AU 19 8589720 8589720 single base substitution G A intron_variant MELA-AU 19 8590209 8590209 single base substitution C T downstream_gene_variant MELA-AU 19 8590209 8590209 single base substitution C T exon_variant MELA-AU 19 8590209 8590209 single base substitution C T intron_variant MELA-AU 19 8590624 8590624 single base substitution G A downstream_gene_variant MELA-AU 19 8590624 8590624 single base substitution G A intron_variant MELA-AU 19 8590817 8590817 single base substitution C T downstream_gene_variant MELA-AU 19 8590817 8590817 single base substitution C T intron_variant MELA-AU 19 8590854 8590854 single base substitution C T downstream_gene_variant MELA-AU 19 8590854 8590854 single base substitution C T intron_variant MELA-AU 19 8590858 8590858 single base substitution C T downstream_gene_variant MELA-AU 19 8590858 8590858 single base substitution C T intron_variant MELA-AU 19 8591315 8591315 single base substitution C T downstream_gene_variant MELA-AU 19 8591315 8591315 single base substitution C T intron_variant MELA-AU 19 8592868 8592868 single base substitution G A downstream_gene_variant MELA-AU 19 8592868 8592868 single base substitution G A intron_variant MELA-AU 19 8592868 8592868 single base substitution G A upstream_gene_variant MELA-AU 19 8593473 8593473 single base substitution G A downstream_gene_variant MELA-AU 19 8593473 8593473 single base substitution G A intron_variant MELA-AU 19 8593473 8593473 single base substitution G A upstream_gene_variant MELA-AU 19 8594435 8594435 single base substitution G A downstream_gene_variant MELA-AU 19 8594435 8594435 single base substitution G A intron_variant MELA-AU 19 8594435 8594435 single base substitution G A upstream_gene_variant MELA-AU 19 8594478 8594478 single base substitution C T downstream_gene_variant MELA-AU 19 8594478 8594478 single base substitution C T intron_variant MELA-AU 19 8594478 8594478 single base substitution C T upstream_gene_variant MELA-AU 19 8594907 8594907 single base substitution C T downstream_gene_variant MELA-AU 19 8594907 8594907 single base substitution C T intron_variant MELA-AU 19 8594907 8594907 single base substitution C T upstream_gene_variant MELA-AU 19 8594916 8594916 single base substitution C T downstream_gene_variant MELA-AU 19 8594916 8594916 single base substitution C T intron_variant MELA-AU 19 8594916 8594916 single base substitution C T upstream_gene_variant MELA-AU 19 8594979 8594979 single base substitution C T downstream_gene_variant MELA-AU 19 8594979 8594979 single base substitution C T exon_variant MELA-AU 19 8594979 8594979 single base substitution C T intron_variant MELA-AU 19 8594979 8594979 single base substitution C T upstream_gene_variant MELA-AU 19 8595107 8595107 single base substitution C T exon_variant MELA-AU 19 8595107 8595107 single base substitution C T synonymous_variant S767S 2301G>A MELA-AU 19 8595107 8595107 single base substitution C T upstream_gene_variant MELA-AU 19 8595191 8595191 single base substitution G A exon_variant MELA-AU 19 8595191 8595191 single base substitution G A synonymous_variant F739F 2217C>T MELA-AU 19 8595191 8595191 single base substitution G A upstream_gene_variant MELA-AU 19 8595261 8595261 single base substitution G A intron_variant MELA-AU 19 8595261 8595261 single base substitution G A upstream_gene_variant MELA-AU 19 8595275 8595275 single base substitution G A intron_variant MELA-AU 19 8595275 8595275 single base substitution G A upstream_gene_variant MELA-AU 19 8595422 8595422 single base substitution G A exon_variant MELA-AU 19 8595422 8595422 single base substitution G A synonymous_variant F693F 2079C>T MELA-AU 19 8595422 8595422 single base substitution G A upstream_gene_variant MELA-AU 19 8595445 8595445 single base substitution C T exon_variant MELA-AU 19 8595445 8595445 single base substitution C T missense_variant E686K 2056G>A MELA-AU 19 8595445 8595445 single base substitution C T upstream_gene_variant MELA-AU 19 8595517 8595517 single base substitution C T intron_variant MELA-AU 19 8595517 8595517 single base substitution C T upstream_gene_variant MELA-AU 19 8595981 8595981 single base substitution C A intron_variant MELA-AU 19 8595981 8595981 single base substitution C A upstream_gene_variant MELA-AU 19 8596950 8596950 single base substitution G A intron_variant MELA-AU 19 8596950 8596950 single base substitution G A upstream_gene_variant MELA-AU 19 8597000 8597000 single base substitution C T intron_variant MELA-AU 19 8597000 8597000 single base substitution C T upstream_gene_variant MELA-AU 19 8597205 8597205 single base substitution C T intron_variant MELA-AU 19 8597205 8597205 single base substitution C T upstream_gene_variant MELA-AU 19 8597664 8597664 single base substitution C T intron_variant MELA-AU 19 8597664 8597664 single base substitution C T upstream_gene_variant MELA-AU 19 8597888 8597888 single base substitution C T intron_variant MELA-AU 19 8597888 8597888 single base substitution C T upstream_gene_variant MELA-AU 19 8597931 8597931 single base substitution C T intron_variant MELA-AU 19 8597931 8597931 single base substitution C T upstream_gene_variant MELA-AU 19 8598077 8598077 single base substitution A T intron_variant MELA-AU 19 8598077 8598077 single base substitution A T upstream_gene_variant MELA-AU 19 8598723 8598723 single base substitution G A intron_variant MELA-AU 19 8598723 8598723 single base substitution G A upstream_gene_variant MELA-AU 19 8598868 8598868 single base substitution G A intron_variant MELA-AU 19 8598868 8598868 single base substitution G A upstream_gene_variant MELA-AU 19 8599673 8599673 single base substitution C G intron_variant MELA-AU 19 8599673 8599673 single base substitution C G upstream_gene_variant MELA-AU 19 8600015 8600015 single base substitution C T intron_variant MELA-AU 19 8600015 8600015 single base substitution C T upstream_gene_variant MELA-AU 19 8600654 8600654 single base substitution C T downstream_gene_variant MELA-AU 19 8600654 8600654 single base substitution C T intron_variant MELA-AU 19 8601290 8601290 single base substitution G A downstream_gene_variant MELA-AU 19 8601290 8601290 single base substitution G A intron_variant MELA-AU 19 8601717 8601717 single base substitution G A downstream_gene_variant MELA-AU 19 8601717 8601717 single base substitution G A intron_variant MELA-AU 19 8601853 8601853 single base substitution G A downstream_gene_variant MELA-AU 19 8601853 8601853 single base substitution G A exon_variant MELA-AU 19 8601853 8601853 single base substitution G A synonymous_variant P593P 1779C>T MELA-AU 19 8602006 8602006 single base substitution C T downstream_gene_variant MELA-AU 19 8602006 8602006 single base substitution C T intron_variant MELA-AU 19 8602542 8602542 single base substitution T A downstream_gene_variant MELA-AU 19 8602542 8602542 single base substitution T A intron_variant MELA-AU 19 8602622 8602622 single base substitution G A downstream_gene_variant MELA-AU 19 8602622 8602622 single base substitution G A intron_variant MELA-AU 19 8603273 8603273 single base substitution C T downstream_gene_variant MELA-AU 19 8603273 8603273 single base substitution C T intron_variant MELA-AU 19 8603451 8603452 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 19 8603451 8603452 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 8604096 8604096 single base substitution C T downstream_gene_variant MELA-AU 19 8604096 8604096 single base substitution C T intron_variant MELA-AU 19 8604205 8604205 single base substitution G A downstream_gene_variant MELA-AU 19 8604205 8604205 single base substitution G A intron_variant MELA-AU 19 8604819 8604819 single base substitution C T downstream_gene_variant MELA-AU 19 8604819 8604819 single base substitution C T intron_variant MELA-AU 19 8604834 8604834 single base substitution G A downstream_gene_variant MELA-AU 19 8604834 8604834 single base substitution G A exon_variant MELA-AU 19 8604834 8604834 single base substitution G A synonymous_variant I563I 1689C>T MELA-AU 19 8605088 8605088 single base substitution G A downstream_gene_variant MELA-AU 19 8605088 8605088 single base substitution G A intron_variant MELA-AU 19 8605088 8605088 single base substitution G A upstream_gene_variant MELA-AU 19 8605243 8605243 single base substitution C T 3_prime_UTR_variant MELA-AU 19 8605243 8605243 single base substitution C T downstream_gene_variant MELA-AU 19 8605243 8605243 single base substitution C T intron_variant MELA-AU 19 8605243 8605243 single base substitution C T upstream_gene_variant MELA-AU 19 8605255 8605255 single base substitution C T 3_prime_UTR_variant MELA-AU 19 8605255 8605255 single base substitution C T downstream_gene_variant MELA-AU 19 8605255 8605255 single base substitution C T intron_variant MELA-AU 19 8605255 8605255 single base substitution C T upstream_gene_variant MELA-AU 19 8605314 8605314 single base substitution C T 3_prime_UTR_variant MELA-AU 19 8605314 8605314 single base substitution C T downstream_gene_variant MELA-AU 19 8605314 8605314 single base substitution C T intron_variant MELA-AU 19 8605314 8605314 single base substitution C T upstream_gene_variant MELA-AU 19 8605770 8605770 single base substitution C T downstream_gene_variant MELA-AU 19 8605770 8605770 single base substitution C T intron_variant MELA-AU 19 8605770 8605770 single base substitution C T upstream_gene_variant MELA-AU 19 8605884 8605884 single base substitution T C downstream_gene_variant MELA-AU 19 8605884 8605884 single base substitution T C intron_variant MELA-AU 19 8605884 8605884 single base substitution T C upstream_gene_variant MELA-AU 19 8605992 8605992 single base substitution C T downstream_gene_variant MELA-AU 19 8605992 8605992 single base substitution C T intron_variant MELA-AU 19 8605992 8605992 single base substitution C T upstream_gene_variant MELA-AU 19 8606198 8606198 single base substitution C T downstream_gene_variant MELA-AU 19 8606198 8606198 single base substitution C T intron_variant MELA-AU 19 8606198 8606198 single base substitution C T upstream_gene_variant MELA-AU 19 8606202 8606202 single base substitution G A downstream_gene_variant MELA-AU 19 8606202 8606202 single base substitution G A intron_variant MELA-AU 19 8606202 8606202 single base substitution G A upstream_gene_variant MELA-AU 19 8606343 8606343 single base substitution C T downstream_gene_variant MELA-AU 19 8606343 8606343 single base substitution C T intron_variant MELA-AU 19 8606343 8606343 single base substitution C T upstream_gene_variant MELA-AU 19 8606351 8606351 single base substitution C T downstream_gene_variant MELA-AU 19 8606351 8606351 single base substitution C T intron_variant MELA-AU 19 8606351 8606351 single base substitution C T upstream_gene_variant MELA-AU 19 8606411 8606411 single base substitution C A downstream_gene_variant MELA-AU 19 8606411 8606411 single base substitution C A intron_variant MELA-AU 19 8606411 8606411 single base substitution C A upstream_gene_variant MELA-AU 19 8606567 8606568 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 19 8606567 8606568 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 8606567 8606568 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 8606986 8606986 single base substitution G A downstream_gene_variant MELA-AU 19 8606986 8606986 single base substitution G A intron_variant MELA-AU 19 8606986 8606986 single base substitution G A upstream_gene_variant MELA-AU 19 8607326 8607326 single base substitution G A downstream_gene_variant MELA-AU 19 8607326 8607326 single base substitution G A intron_variant MELA-AU 19 8607326 8607326 single base substitution G A upstream_gene_variant MELA-AU 19 8607346 8607346 single base substitution G A downstream_gene_variant MELA-AU 19 8607346 8607346 single base substitution G A intron_variant MELA-AU 19 8607346 8607346 single base substitution G A upstream_gene_variant MELA-AU 19 8607787 8607787 single base substitution C T downstream_gene_variant MELA-AU 19 8607787 8607787 single base substitution C T intron_variant MELA-AU 19 8607787 8607787 single base substitution C T upstream_gene_variant MELA-AU 19 8607984 8607984 single base substitution C T downstream_gene_variant MELA-AU 19 8607984 8607984 single base substitution C T intron_variant MELA-AU 19 8607984 8607984 single base substitution C T upstream_gene_variant MELA-AU 19 8608014 8608014 single base substitution C T downstream_gene_variant MELA-AU 19 8608014 8608014 single base substitution C T intron_variant MELA-AU 19 8608014 8608014 single base substitution C T upstream_gene_variant MELA-AU 19 8608231 8608231 single base substitution C T downstream_gene_variant MELA-AU 19 8608231 8608231 single base substitution C T intron_variant MELA-AU 19 8608231 8608231 single base substitution C T upstream_gene_variant MELA-AU 19 8608295 8608296 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 19 8608295 8608296 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 8608295 8608296 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 19 8608385 8608385 single base substitution G A downstream_gene_variant MELA-AU 19 8608385 8608385 single base substitution G A intron_variant MELA-AU 19 8608385 8608385 single base substitution G A upstream_gene_variant MELA-AU 19 8609284 8609284 single base substitution C T downstream_gene_variant MELA-AU 19 8609284 8609284 single base substitution C T exon_variant MELA-AU 19 8609284 8609284 single base substitution C T missense_variant G474E 1421G>A MELA-AU 19 8609284 8609284 single base substitution C T upstream_gene_variant MELA-AU 19 8609286 8609286 single base substitution C T downstream_gene_variant MELA-AU 19 8609286 8609286 single base substitution C T exon_variant MELA-AU 19 8609286 8609286 single base substitution C T synonymous_variant G473G 1419G>A MELA-AU 19 8609286 8609286 single base substitution C T upstream_gene_variant MELA-AU 19 8609343 8609343 single base substitution G C downstream_gene_variant MELA-AU 19 8609343 8609343 single base substitution G C exon_variant MELA-AU 19 8609343 8609343 single base substitution G C synonymous_variant P454P 1362C>G MELA-AU 19 8609343 8609343 single base substitution G C upstream_gene_variant MELA-AU 19 8609694 8609694 single base substitution C T downstream_gene_variant MELA-AU 19 8609694 8609694 single base substitution C T intron_variant MELA-AU 19 8609694 8609694 single base substitution C T upstream_gene_variant MELA-AU 19 8609881 8609881 single base substitution C T downstream_gene_variant MELA-AU 19 8609881 8609881 single base substitution C T intron_variant MELA-AU 19 8609881 8609881 single base substitution C T upstream_gene_variant MELA-AU 19 8609882 8609882 single base substitution G A downstream_gene_variant MELA-AU 19 8609882 8609882 single base substitution G A intron_variant MELA-AU 19 8609882 8609882 single base substitution G A upstream_gene_variant MELA-AU 19 8609898 8609898 single base substitution G A downstream_gene_variant MELA-AU 19 8609898 8609898 single base substitution G A intron_variant MELA-AU 19 8609898 8609898 single base substitution G A upstream_gene_variant MELA-AU 19 8610081 8610081 single base substitution C T downstream_gene_variant MELA-AU 19 8610081 8610081 single base substitution C T intron_variant MELA-AU 19 8610081 8610081 single base substitution C T upstream_gene_variant MELA-AU 19 8610091 8610091 single base substitution C T downstream_gene_variant MELA-AU 19 8610091 8610091 single base substitution C T intron_variant MELA-AU 19 8610091 8610091 single base substitution C T upstream_gene_variant MELA-AU 19 8610230 8610230 single base substitution C T downstream_gene_variant MELA-AU 19 8610230 8610230 single base substitution C T intron_variant MELA-AU 19 8610230 8610230 single base substitution C T upstream_gene_variant MELA-AU 19 8610551 8610551 single base substitution G A downstream_gene_variant MELA-AU 19 8610551 8610551 single base substitution G A exon_variant MELA-AU 19 8610551 8610551 single base substitution G A missense_variant L447F 1339C>T MELA-AU 19 8610551 8610551 single base substitution G A upstream_gene_variant MELA-AU 19 8611039 8611039 single base substitution C T downstream_gene_variant MELA-AU 19 8611039 8611039 single base substitution C T intron_variant MELA-AU 19 8611039 8611039 single base substitution C T upstream_gene_variant MELA-AU 19 8611104 8611104 single base substitution A C downstream_gene_variant MELA-AU 19 8611104 8611104 single base substitution A C intron_variant MELA-AU 19 8611104 8611104 single base substitution A C upstream_gene_variant MELA-AU 19 8611360 8611360 single base substitution C T downstream_gene_variant MELA-AU 19 8611360 8611360 single base substitution C T intron_variant MELA-AU 19 8611360 8611360 single base substitution C T upstream_gene_variant MELA-AU 19 8611558 8611558 single base substitution C T downstream_gene_variant MELA-AU 19 8611558 8611558 single base substitution C T intron_variant MELA-AU 19 8611558 8611558 single base substitution C T upstream_gene_variant MELA-AU 19 8611872 8611872 single base substitution C T downstream_gene_variant MELA-AU 19 8611872 8611872 single base substitution C T intron_variant MELA-AU 19 8611872 8611872 single base substitution C T upstream_gene_variant MELA-AU 19 8612202 8612202 single base substitution A C downstream_gene_variant MELA-AU 19 8612202 8612202 single base substitution A C intron_variant MELA-AU 19 8612202 8612202 single base substitution A C upstream_gene_variant MELA-AU 19 8612506 8612506 single base substitution C T downstream_gene_variant MELA-AU 19 8612506 8612506 single base substitution C T intron_variant MELA-AU 19 8612506 8612506 single base substitution C T upstream_gene_variant MELA-AU 19 8612507 8612507 single base substitution C T downstream_gene_variant MELA-AU 19 8612507 8612507 single base substitution C T intron_variant MELA-AU 19 8612507 8612507 single base substitution C T upstream_gene_variant MELA-AU 19 8612738 8612738 single base substitution G A downstream_gene_variant MELA-AU 19 8612738 8612738 single base substitution G A exon_variant MELA-AU 19 8612738 8612738 single base substitution G A intron_variant MELA-AU 19 8612738 8612738 single base substitution G A upstream_gene_variant MELA-AU 19 8612873 8612873 single base substitution C T downstream_gene_variant MELA-AU 19 8612873 8612873 single base substitution C T exon_variant MELA-AU 19 8612873 8612873 single base substitution C T intron_variant MELA-AU 19 8612873 8612873 single base substitution C T upstream_gene_variant MELA-AU 19 8613015 8613015 single base substitution G A downstream_gene_variant MELA-AU 19 8613015 8613015 single base substitution G A intron_variant MELA-AU 19 8613015 8613015 single base substitution G A upstream_gene_variant MELA-AU 19 8613321 8613321 single base substitution C T downstream_gene_variant MELA-AU 19 8613321 8613321 single base substitution C T intron_variant MELA-AU 19 8613321 8613321 single base substitution C T upstream_gene_variant MELA-AU 19 8613396 8613396 single base substitution G A downstream_gene_variant MELA-AU 19 8613396 8613396 single base substitution G A intron_variant MELA-AU 19 8613396 8613396 single base substitution G A upstream_gene_variant MELA-AU 19 8613646 8613646 single base substitution G A downstream_gene_variant MELA-AU 19 8613646 8613646 single base substitution G A intron_variant MELA-AU 19 8613646 8613646 single base substitution G A upstream_gene_variant MELA-AU 19 8613792 8613792 single base substitution C T downstream_gene_variant MELA-AU 19 8613792 8613792 single base substitution C T intron_variant MELA-AU 19 8613792 8613792 single base substitution C T upstream_gene_variant MELA-AU 19 8613938 8613938 single base substitution G A downstream_gene_variant MELA-AU 19 8613938 8613938 single base substitution G A intron_variant MELA-AU 19 8613938 8613938 single base substitution G A upstream_gene_variant MELA-AU 19 8613997 8613997 single base substitution G A downstream_gene_variant MELA-AU 19 8613997 8613997 single base substitution G A intron_variant MELA-AU 19 8613997 8613997 single base substitution G A upstream_gene_variant MELA-AU 19 8614028 8614028 single base substitution T C downstream_gene_variant MELA-AU 19 8614028 8614028 single base substitution T C intron_variant MELA-AU 19 8614028 8614028 single base substitution T C upstream_gene_variant MELA-AU 19 8614081 8614081 single base substitution C T downstream_gene_variant MELA-AU 19 8614081 8614081 single base substitution C T intron_variant MELA-AU 19 8614081 8614081 single base substitution C T upstream_gene_variant MELA-AU 19 8614132 8614132 single base substitution G A downstream_gene_variant MELA-AU 19 8614132 8614132 single base substitution G A intron_variant MELA-AU 19 8614132 8614132 single base substitution G A upstream_gene_variant MELA-AU 19 8614188 8614188 single base substitution G A downstream_gene_variant MELA-AU 19 8614188 8614188 single base substitution G A intron_variant MELA-AU 19 8614188 8614188 single base substitution G A upstream_gene_variant MELA-AU 19 8614266 8614266 single base substitution C T downstream_gene_variant MELA-AU 19 8614266 8614266 single base substitution C T intron_variant MELA-AU 19 8614266 8614266 single base substitution C T upstream_gene_variant MELA-AU 19 8614289 8614289 single base substitution G A downstream_gene_variant MELA-AU 19 8614289 8614289 single base substitution G A intron_variant MELA-AU 19 8614289 8614289 single base substitution G A upstream_gene_variant MELA-AU 19 8614417 8614417 single base substitution G A downstream_gene_variant MELA-AU 19 8614417 8614417 single base substitution G A intron_variant MELA-AU 19 8614417 8614417 single base substitution G A upstream_gene_variant MELA-AU 19 8614481 8614482 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 19 8614481 8614482 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 19 8614481 8614482 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 8614481 8614482 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 8614855 8614855 single base substitution G A downstream_gene_variant MELA-AU 19 8614855 8614855 single base substitution G A exon_variant MELA-AU 19 8614855 8614855 single base substitution G A intron_variant MELA-AU 19 8614855 8614855 single base substitution G A upstream_gene_variant MELA-AU 19 8614862 8614862 single base substitution C T downstream_gene_variant MELA-AU 19 8614862 8614862 single base substitution C T exon_variant MELA-AU 19 8614862 8614862 single base substitution C T intron_variant MELA-AU 19 8614862 8614862 single base substitution C T upstream_gene_variant MELA-AU 19 8615691 8615692 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 19 8615691 8615692 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 8615691 8615692 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 8615838 8615838 single base substitution C T downstream_gene_variant MELA-AU 19 8615838 8615838 single base substitution C T intron_variant MELA-AU 19 8615838 8615838 single base substitution C T upstream_gene_variant MELA-AU 19 8615849 8615849 single base substitution C T downstream_gene_variant MELA-AU 19 8615849 8615849 single base substitution C T intron_variant MELA-AU 19 8615849 8615849 single base substitution C T upstream_gene_variant MELA-AU 19 8615926 8615926 single base substitution G A downstream_gene_variant MELA-AU 19 8615926 8615926 single base substitution G A intron_variant MELA-AU 19 8615926 8615926 single base substitution G A upstream_gene_variant MELA-AU 19 8616162 8616162 single base substitution C G downstream_gene_variant MELA-AU 19 8616162 8616162 single base substitution C G intron_variant MELA-AU 19 8616162 8616162 single base substitution C G upstream_gene_variant MELA-AU 19 8616225 8616225 single base substitution C T downstream_gene_variant MELA-AU 19 8616225 8616225 single base substitution C T intron_variant MELA-AU 19 8616225 8616225 single base substitution C T upstream_gene_variant MELA-AU 19 8616345 8616345 single base substitution C T downstream_gene_variant MELA-AU 19 8616345 8616345 single base substitution C T exon_variant MELA-AU 19 8616345 8616345 single base substitution C T intron_variant MELA-AU 19 8616345 8616345 single base substitution C T upstream_gene_variant MELA-AU 19 8616358 8616358 single base substitution C T downstream_gene_variant MELA-AU 19 8616358 8616358 single base substitution C T exon_variant MELA-AU 19 8616358 8616358 single base substitution C T intron_variant MELA-AU 19 8616358 8616358 single base substitution C T upstream_gene_variant MELA-AU 19 8616529 8616529 single base substitution C T downstream_gene_variant MELA-AU 19 8616529 8616529 single base substitution C T exon_variant MELA-AU 19 8616529 8616529 single base substitution C T intron_variant MELA-AU 19 8616529 8616529 single base substitution C T upstream_gene_variant MELA-AU 19 8616663 8616663 single base substitution C T downstream_gene_variant MELA-AU 19 8616663 8616663 single base substitution C T exon_variant MELA-AU 19 8616663 8616663 single base substitution C T synonymous_variant V244V 732G>A MELA-AU 19 8616663 8616663 single base substitution C T upstream_gene_variant MELA-AU 19 8616722 8616722 single base substitution G T downstream_gene_variant MELA-AU 19 8616722 8616722 single base substitution G T exon_variant MELA-AU 19 8616722 8616722 single base substitution G T missense_variant L225M 673C>A MELA-AU 19 8616722 8616722 single base substitution G T upstream_gene_variant MELA-AU 19 8616728 8616728 single base substitution G A downstream_gene_variant MELA-AU 19 8616728 8616728 single base substitution G A exon_variant MELA-AU 19 8616728 8616728 single base substitution G A stop_gained Q223* 667C>T MELA-AU 19 8616728 8616728 single base substitution G A upstream_gene_variant MELA-AU 19 8616850 8616850 single base substitution A G downstream_gene_variant MELA-AU 19 8616850 8616850 single base substitution A G exon_variant MELA-AU 19 8616850 8616850 single base substitution A G intron_variant MELA-AU 19 8616850 8616850 single base substitution A G upstream_gene_variant MELA-AU 19 8616894 8616894 single base substitution C T downstream_gene_variant MELA-AU 19 8616894 8616894 single base substitution C T exon_variant MELA-AU 19 8616894 8616894 single base substitution C T intron_variant MELA-AU 19 8616894 8616894 single base substitution C T upstream_gene_variant MELA-AU 19 8616897 8616897 single base substitution C T downstream_gene_variant MELA-AU 19 8616897 8616897 single base substitution C T exon_variant MELA-AU 19 8616897 8616897 single base substitution C T intron_variant MELA-AU 19 8616897 8616897 single base substitution C T upstream_gene_variant MELA-AU 19 8616904 8616904 single base substitution C T downstream_gene_variant MELA-AU 19 8616904 8616904 single base substitution C T exon_variant MELA-AU 19 8616904 8616904 single base substitution C T intron_variant MELA-AU 19 8616904 8616904 single base substitution C T upstream_gene_variant MELA-AU 19 8617021 8617021 single base substitution G A downstream_gene_variant MELA-AU 19 8617021 8617021 single base substitution G A exon_variant MELA-AU 19 8617021 8617021 single base substitution G A stop_gained R178* 532C>T MELA-AU 19 8617021 8617021 single base substitution G A upstream_gene_variant MELA-AU 19 8617051 8617051 single base substitution G A downstream_gene_variant MELA-AU 19 8617051 8617051 single base substitution G A intron_variant MELA-AU 19 8617051 8617051 single base substitution G A splice_region_variant MELA-AU 19 8617051 8617051 single base substitution G A upstream_gene_variant MELA-AU 19 8617150 8617150 single base substitution C T downstream_gene_variant MELA-AU 19 8617150 8617150 single base substitution C T intron_variant MELA-AU 19 8617150 8617150 single base substitution C T upstream_gene_variant MELA-AU 19 8617227 8617227 single base substitution C T downstream_gene_variant MELA-AU 19 8617227 8617227 single base substitution C T intron_variant MELA-AU 19 8617227 8617227 single base substitution C T upstream_gene_variant MELA-AU 19 8617238 8617238 single base substitution G A downstream_gene_variant MELA-AU 19 8617238 8617238 single base substitution G A intron_variant MELA-AU 19 8617238 8617238 single base substitution G A upstream_gene_variant MELA-AU 19 8617241 8617241 single base substitution C T downstream_gene_variant MELA-AU 19 8617241 8617241 single base substitution C T intron_variant MELA-AU 19 8617241 8617241 single base substitution C T upstream_gene_variant MELA-AU 19 8617717 8617717 single base substitution G A downstream_gene_variant MELA-AU 19 8617717 8617717 single base substitution G A intron_variant MELA-AU 19 8617717 8617717 single base substitution G A upstream_gene_variant MELA-AU 19 8618357 8618357 single base substitution G A downstream_gene_variant MELA-AU 19 8618357 8618357 single base substitution G A intron_variant MELA-AU 19 8618357 8618357 single base substitution G A upstream_gene_variant MELA-AU 19 8618921 8618921 single base substitution C T downstream_gene_variant MELA-AU 19 8618921 8618921 single base substitution C T intron_variant MELA-AU 19 8618921 8618921 single base substitution C T upstream_gene_variant MELA-AU 19 8619135 8619135 single base substitution C T downstream_gene_variant MELA-AU 19 8619135 8619135 single base substitution C T intron_variant MELA-AU 19 8619135 8619135 single base substitution C T upstream_gene_variant MELA-AU 19 8619529 8619529 single base substitution C T downstream_gene_variant MELA-AU 19 8619529 8619529 single base substitution C T exon_variant MELA-AU 19 8619529 8619529 single base substitution C T intron_variant MELA-AU 19 8619529 8619529 single base substitution C T upstream_gene_variant MELA-AU 19 8619718 8619718 single base substitution C T downstream_gene_variant MELA-AU 19 8619718 8619718 single base substitution C T intron_variant MELA-AU 19 8619718 8619718 single base substitution C T upstream_gene_variant MELA-AU 19 8619977 8619977 single base substitution G A downstream_gene_variant MELA-AU 19 8619977 8619977 single base substitution G A intron_variant MELA-AU 19 8619977 8619977 single base substitution G A upstream_gene_variant MELA-AU 19 8619983 8619983 single base substitution C T downstream_gene_variant MELA-AU 19 8619983 8619983 single base substitution C T intron_variant MELA-AU 19 8619983 8619983 single base substitution C T upstream_gene_variant MELA-AU 19 8620311 8620311 single base substitution G T exon_variant MELA-AU 19 8620311 8620311 single base substitution G T intron_variant MELA-AU 19 8620311 8620311 single base substitution G T upstream_gene_variant MELA-AU 19 8620408 8620408 single base substitution C T exon_variant MELA-AU 19 8620408 8620408 single base substitution C T intron_variant MELA-AU 19 8620408 8620408 single base substitution C T upstream_gene_variant MELA-AU 19 8620800 8620800 single base substitution C T intron_variant MELA-AU 19 8620800 8620800 single base substitution C T upstream_gene_variant MELA-AU 19 8620818 8620818 single base substitution C T intron_variant MELA-AU 19 8620818 8620818 single base substitution C T upstream_gene_variant MELA-AU 19 8621089 8621089 single base substitution T G intron_variant MELA-AU 19 8621089 8621089 single base substitution T G upstream_gene_variant MELA-AU 19 8621323 8621323 single base substitution C T intron_variant MELA-AU 19 8621323 8621323 single base substitution C T upstream_gene_variant MELA-AU 19 8621359 8621360 multiple base substitution (>=2bp and <=200bp) CT TA intron_variant MELA-AU 19 8621359 8621360 multiple base substitution (>=2bp and <=200bp) CT TA upstream_gene_variant MELA-AU 19 8621540 8621540 single base substitution G A intron_variant MELA-AU 19 8621540 8621540 single base substitution G A upstream_gene_variant MELA-AU 19 8621543 8621543 single base substitution G A intron_variant MELA-AU 19 8621543 8621543 single base substitution G A upstream_gene_variant MELA-AU 19 8621551 8621551 single base substitution C T intron_variant MELA-AU 19 8621551 8621551 single base substitution C T upstream_gene_variant MELA-AU 19 8621698 8621698 single base substitution G A intron_variant MELA-AU 19 8621698 8621698 single base substitution G A upstream_gene_variant MELA-AU 19 8621739 8621739 single base substitution C T intron_variant MELA-AU 19 8621739 8621739 single base substitution C T upstream_gene_variant MELA-AU 19 8622340 8622340 single base substitution C T intron_variant MELA-AU 19 8622340 8622340 single base substitution C T upstream_gene_variant MELA-AU 19 8622413 8622413 single base substitution C T intron_variant MELA-AU 19 8622413 8622413 single base substitution C T upstream_gene_variant MELA-AU 19 8622425 8622425 single base substitution G A intron_variant MELA-AU 19 8622425 8622425 single base substitution G A upstream_gene_variant MELA-AU 19 8622702 8622702 single base substitution C T intron_variant MELA-AU 19 8622702 8622702 single base substitution C T upstream_gene_variant MELA-AU 19 8622827 8622827 single base substitution C T intron_variant MELA-AU 19 8622827 8622827 single base substitution C T upstream_gene_variant MELA-AU 19 8622833 8622833 single base substitution G A intron_variant MELA-AU 19 8622833 8622833 single base substitution G A upstream_gene_variant MELA-AU 19 8622916 8622916 single base substitution C T intron_variant MELA-AU 19 8622916 8622916 single base substitution C T upstream_gene_variant MELA-AU 19 8622928 8622928 single base substitution C T intron_variant MELA-AU 19 8622928 8622928 single base substitution C T upstream_gene_variant MELA-AU 19 8622993 8622993 single base substitution A C intron_variant MELA-AU 19 8622993 8622993 single base substitution A C upstream_gene_variant MELA-AU 19 8623072 8623072 single base substitution G A intron_variant MELA-AU 19 8623072 8623072 single base substitution G A upstream_gene_variant MELA-AU 19 8623318 8623318 single base substitution G A intron_variant MELA-AU 19 8623318 8623318 single base substitution G A upstream_gene_variant MELA-AU 19 8623380 8623380 single base substitution G A intron_variant MELA-AU 19 8623380 8623380 single base substitution G A upstream_gene_variant MELA-AU 19 8623450 8623450 single base substitution C T intron_variant MELA-AU 19 8623450 8623450 single base substitution C T upstream_gene_variant MELA-AU 19 8623626 8623627 multiple base substitution (>=2bp and <=200bp) CC TA intron_variant MELA-AU 19 8623626 8623627 multiple base substitution (>=2bp and <=200bp) CC TA upstream_gene_variant MELA-AU 19 8623660 8623660 single base substitution G T intron_variant MELA-AU 19 8623660 8623660 single base substitution G T upstream_gene_variant MELA-AU 19 8624057 8624057 single base substitution C T intron_variant MELA-AU 19 8624057 8624057 single base substitution C T upstream_gene_variant MELA-AU 19 8624076 8624076 single base substitution C T intron_variant MELA-AU 19 8624076 8624076 single base substitution C T upstream_gene_variant MELA-AU 19 8624098 8624098 single base substitution C T intron_variant MELA-AU 19 8624098 8624098 single base substitution C T upstream_gene_variant MELA-AU 19 8624574 8624574 single base substitution C T intron_variant MELA-AU 19 8624574 8624574 single base substitution C T upstream_gene_variant MELA-AU 19 8624702 8624702 single base substitution C T intron_variant MELA-AU 19 8624702 8624702 single base substitution C T upstream_gene_variant MELA-AU 19 8624728 8624728 single base substitution G A intron_variant MELA-AU 19 8624728 8624728 single base substitution G A upstream_gene_variant MELA-AU 19 8624809 8624809 single base substitution G A intron_variant MELA-AU 19 8624809 8624809 single base substitution G A upstream_gene_variant MELA-AU 19 8624997 8624997 single base substitution C T intron_variant MELA-AU 19 8624997 8624997 single base substitution C T upstream_gene_variant MELA-AU 19 8625343 8625343 single base substitution T A intron_variant MELA-AU 19 8625343 8625343 single base substitution T A upstream_gene_variant MELA-AU 19 8625445 8625445 single base substitution G A intron_variant MELA-AU 19 8625445 8625445 single base substitution G A upstream_gene_variant MELA-AU 19 8625503 8625503 single base substitution G A intron_variant MELA-AU 19 8625503 8625503 single base substitution G A upstream_gene_variant MELA-AU 19 8625718 8625718 single base substitution G A intron_variant MELA-AU 19 8625816 8625816 single base substitution T A intron_variant MELA-AU 19 8626374 8626374 single base substitution C T intron_variant MELA-AU 19 8626545 8626545 single base substitution C T intron_variant MELA-AU 19 8626692 8626692 single base substitution C T intron_variant MELA-AU 19 8626725 8626725 single base substitution C T intron_variant MELA-AU 19 8626800 8626800 single base substitution C G intron_variant MELA-AU 19 8626897 8626897 single base substitution C T intron_variant MELA-AU 19 8626907 8626907 single base substitution C T intron_variant MELA-AU 19 8627187 8627188 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 8627251 8627251 single base substitution G A intron_variant MELA-AU 19 8627659 8627659 single base substitution C A intron_variant MELA-AU 19 8627816 8627816 single base substitution G A intron_variant MELA-AU 19 8627872 8627872 single base substitution C T intron_variant MELA-AU 19 8627910 8627910 single base substitution C T intron_variant MELA-AU 19 8628097 8628097 single base substitution G A intron_variant MELA-AU 19 8628102 8628102 single base substitution C T intron_variant MELA-AU 19 8628103 8628103 single base substitution C T intron_variant MELA-AU 19 8628459 8628459 single base substitution C T intron_variant MELA-AU 19 8628502 8628502 single base substitution C T intron_variant MELA-AU 19 8628655 8628655 single base substitution C T intron_variant MELA-AU 19 8628721 8628721 single base substitution C T intron_variant MELA-AU 19 8628819 8628819 single base substitution C T intron_variant MELA-AU 19 8628921 8628921 single base substitution C T intron_variant MELA-AU 19 8629010 8629010 single base substitution A T intron_variant MELA-AU 19 8629091 8629091 single base substitution C T intron_variant MELA-AU 19 8629148 8629148 single base substitution C T intron_variant MELA-AU 19 8629162 8629162 single base substitution G A intron_variant MELA-AU 19 8629191 8629192 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 8629349 8629349 single base substitution G A intron_variant MELA-AU 19 8629462 8629462 single base substitution G A intron_variant MELA-AU 19 8629613 8629613 single base substitution C T intron_variant MELA-AU 19 8629621 8629621 single base substitution G A intron_variant MELA-AU 19 8629952 8629952 single base substitution C T intron_variant MELA-AU 19 8630242 8630242 single base substitution C T intron_variant MELA-AU 19 8630361 8630361 single base substitution G A intron_variant MELA-AU 19 8630568 8630568 single base substitution G A intron_variant MELA-AU 19 8630602 8630602 single base substitution G A intron_variant MELA-AU 19 8630648 8630648 single base substitution G A intron_variant MELA-AU 19 8630720 8630720 single base substitution C T intron_variant MELA-AU 19 8631292 8631292 single base substitution C T intron_variant MELA-AU 19 8631308 8631308 single base substitution C T intron_variant MELA-AU 19 8631320 8631320 single base substitution G A intron_variant MELA-AU 19 8631320 8631321 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 8632075 8632075 single base substitution C T intron_variant MELA-AU 19 8632191 8632191 single base substitution C T intron_variant MELA-AU 19 8632239 8632239 single base substitution G A intron_variant MELA-AU 19 8632561 8632561 single base substitution G A intron_variant MELA-AU 19 8632600 8632600 single base substitution G A intron_variant MELA-AU 19 8632743 8632743 single base substitution C T intron_variant MELA-AU 19 8632813 8632813 single base substitution C T intron_variant MELA-AU 19 8632911 8632911 single base substitution C T intron_variant MELA-AU 19 8632962 8632962 single base substitution C T intron_variant MELA-AU 19 8633196 8633197 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 8633364 8633364 single base substitution G A intron_variant MELA-AU 19 8633394 8633394 single base substitution G A intron_variant MELA-AU 19 8633395 8633395 single base substitution G A intron_variant MELA-AU 19 8633421 8633421 single base substitution G A intron_variant MELA-AU 19 8633508 8633508 single base substitution C T intron_variant MELA-AU 19 8633518 8633518 single base substitution G A intron_variant MELA-AU 19 8634114 8634114 single base substitution C T intron_variant MELA-AU 19 8634379 8634379 single base substitution G A intron_variant MELA-AU 19 8634399 8634399 single base substitution G A intron_variant MELA-AU 19 8634421 8634421 single base substitution C T intron_variant MELA-AU 19 8634422 8634422 single base substitution C T intron_variant MELA-AU 19 8634676 8634676 single base substitution C T intron_variant MELA-AU 19 8634957 8634957 single base substitution A T intron_variant MELA-AU 19 8634987 8634987 single base substitution T A intron_variant MELA-AU 19 8635077 8635077 single base substitution C T intron_variant MELA-AU 19 8635174 8635174 single base substitution G A intron_variant MELA-AU 19 8635719 8635719 single base substitution G A intron_variant MELA-AU 19 8635720 8635720 single base substitution G A intron_variant MELA-AU 19 8636251 8636251 single base substitution C T intron_variant MELA-AU 19 8636295 8636295 single base substitution C T intron_variant MELA-AU 19 8636389 8636389 single base substitution C T downstream_gene_variant MELA-AU 19 8636389 8636389 single base substitution C T intron_variant MELA-AU 19 8636602 8636602 single base substitution C T downstream_gene_variant MELA-AU 19 8636602 8636602 single base substitution C T intron_variant MELA-AU 19 8636953 8636953 single base substitution C T downstream_gene_variant MELA-AU 19 8636953 8636953 single base substitution C T intron_variant MELA-AU 19 8637113 8637113 single base substitution C A downstream_gene_variant MELA-AU 19 8637113 8637113 single base substitution C A intron_variant MELA-AU 19 8637242 8637242 single base substitution C T downstream_gene_variant MELA-AU 19 8637242 8637242 single base substitution C T intron_variant MELA-AU 19 8637255 8637255 single base substitution G A downstream_gene_variant MELA-AU 19 8637255 8637255 single base substitution G A intron_variant MELA-AU 19 8637393 8637393 single base substitution C T downstream_gene_variant MELA-AU 19 8637393 8637393 single base substitution C T intron_variant MELA-AU 19 8637489 8637489 single base substitution C T downstream_gene_variant MELA-AU 19 8637489 8637489 single base substitution C T intron_variant MELA-AU 19 8637839 8637839 single base substitution C A downstream_gene_variant MELA-AU 19 8637839 8637839 single base substitution C A intron_variant MELA-AU 19 8637983 8637983 single base substitution G A downstream_gene_variant MELA-AU 19 8637983 8637983 single base substitution G A intron_variant MELA-AU 19 8638205 8638205 single base substitution G A downstream_gene_variant MELA-AU 19 8638205 8638205 single base substitution G A intron_variant MELA-AU 19 8638254 8638254 single base substitution G A downstream_gene_variant MELA-AU 19 8638254 8638254 single base substitution G A intron_variant MELA-AU 19 8638414 8638414 single base substitution C T downstream_gene_variant MELA-AU 19 8638414 8638414 single base substitution C T intron_variant MELA-AU 19 8638627 8638627 single base substitution G A downstream_gene_variant MELA-AU 19 8638627 8638627 single base substitution G A intron_variant MELA-AU 19 8638892 8638892 single base substitution C T downstream_gene_variant MELA-AU 19 8638892 8638892 single base substitution C T intron_variant MELA-AU 19 8639242 8639242 single base substitution C T downstream_gene_variant MELA-AU 19 8639242 8639242 single base substitution C T intron_variant MELA-AU 19 8639365 8639365 single base substitution G A downstream_gene_variant MELA-AU 19 8639365 8639365 single base substitution G A intron_variant MELA-AU 19 8639489 8639489 single base substitution C T downstream_gene_variant MELA-AU 19 8639489 8639489 single base substitution C T intron_variant MELA-AU 19 8639553 8639553 single base substitution C T downstream_gene_variant MELA-AU 19 8639553 8639553 single base substitution C T intron_variant MELA-AU 19 8639661 8639661 single base substitution A G downstream_gene_variant MELA-AU 19 8639661 8639661 single base substitution A G intron_variant MELA-AU 19 8639688 8639688 single base substitution G A downstream_gene_variant MELA-AU 19 8639688 8639688 single base substitution G A intron_variant MELA-AU 19 8639873 8639873 single base substitution C T downstream_gene_variant MELA-AU 19 8639873 8639873 single base substitution C T intron_variant MELA-AU 19 8639881 8639881 single base substitution C T downstream_gene_variant MELA-AU 19 8639881 8639881 single base substitution C T intron_variant MELA-AU 19 8640194 8640194 single base substitution C T downstream_gene_variant MELA-AU 19 8640194 8640194 single base substitution C T intron_variant MELA-AU 19 8640328 8640328 single base substitution G A downstream_gene_variant MELA-AU 19 8640328 8640328 single base substitution G A intron_variant MELA-AU 19 8640581 8640581 single base substitution C T downstream_gene_variant MELA-AU 19 8640581 8640581 single base substitution C T intron_variant MELA-AU 19 8640687 8640687 single base substitution C T downstream_gene_variant MELA-AU 19 8640687 8640687 single base substitution C T intron_variant MELA-AU 19 8640774 8640774 single base substitution G A downstream_gene_variant MELA-AU 19 8640774 8640774 single base substitution G A intron_variant MELA-AU 19 8640892 8640892 single base substitution C T downstream_gene_variant MELA-AU 19 8640892 8640892 single base substitution C T intron_variant MELA-AU 19 8641091 8641091 single base substitution C T downstream_gene_variant MELA-AU 19 8641091 8641091 single base substitution C T intron_variant MELA-AU 19 8641153 8641153 single base substitution G A downstream_gene_variant MELA-AU 19 8641153 8641153 single base substitution G A intron_variant MELA-AU 19 8641533 8641533 single base substitution C T exon_variant MELA-AU 19 8641533 8641533 single base substitution C T intron_variant MELA-AU 19 8641679 8641679 single base substitution C T exon_variant MELA-AU 19 8641679 8641679 single base substitution C T intron_variant MELA-AU 19 8641785 8641785 single base substitution G A exon_variant MELA-AU 19 8641785 8641785 single base substitution G A intron_variant MELA-AU 19 8641924 8641924 single base substitution C T exon_variant MELA-AU 19 8641924 8641924 single base substitution C T intron_variant MELA-AU 19 8642027 8642027 single base substitution G A exon_variant MELA-AU 19 8642027 8642027 single base substitution G A intron_variant MELA-AU 19 8642109 8642109 single base substitution C T exon_variant MELA-AU 19 8642109 8642109 single base substitution C T intron_variant MELA-AU 19 8642125 8642125 single base substitution G A exon_variant MELA-AU 19 8642125 8642125 single base substitution G A intron_variant MELA-AU 19 8642447 8642447 single base substitution G T 5_prime_UTR_variant MELA-AU 19 8642447 8642447 single base substitution G T upstream_gene_variant MELA-AU 19 8642501 8642501 single base substitution C T upstream_gene_variant MELA-AU 19 8642682 8642682 single base substitution G A upstream_gene_variant MELA-AU 19 8642840 8642840 single base substitution G A upstream_gene_variant MELA-AU 19 8643176 8643176 single base substitution C T upstream_gene_variant MELA-AU 19 8643292 8643292 single base substitution G A upstream_gene_variant MELA-AU 19 8643514 8643514 single base substitution C T upstream_gene_variant MELA-AU 19 8643671 8643671 single base substitution G A upstream_gene_variant MELA-AU 19 8643674 8643674 single base substitution C T upstream_gene_variant MELA-AU 19 8643793 8643793 single base substitution G A upstream_gene_variant MELA-AU 19 8643898 8643898 single base substitution G A upstream_gene_variant MELA-AU 19 8644055 8644056 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 19 8644242 8644242 single base substitution C T upstream_gene_variant MELA-AU 19 8644342 8644343 multiple base substitution (>=2bp and <=200bp) TC AA upstream_gene_variant MELA-AU 19 8644414 8644414 single base substitution C T upstream_gene_variant MELA-AU 19 8644879 8644879 single base substitution C T upstream_gene_variant MELA-AU 19 8645000 8645000 single base substitution G A upstream_gene_variant MELA-AU 19 8645001 8645001 single base substitution G A upstream_gene_variant MELA-AU 19 8645169 8645169 single base substitution C T upstream_gene_variant MELA-AU 19 8645280 8645280 single base substitution C T upstream_gene_variant MELA-AU 19 8645363 8645363 single base substitution G A upstream_gene_variant MELA-AU 19 8645502 8645502 single base substitution G A upstream_gene_variant MELA-AU 19 8645503 8645503 single base substitution G A upstream_gene_variant MELA-AU 19 8645516 8645516 single base substitution C T upstream_gene_variant MELA-AU 19 8645523 8645523 single base substitution C T upstream_gene_variant MELA-AU 19 8645682 8645682 single base substitution C T upstream_gene_variant MELA-AU 19 8645774 8645774 single base substitution C T upstream_gene_variant MELA-AU 19 8645813 8645813 single base substitution G A upstream_gene_variant MELA-AU 19 8645848 8645848 single base substitution C T upstream_gene_variant MELA-AU 19 8646158 8646158 single base substitution G A upstream_gene_variant MELA-AU 19 8646458 8646458 single base substitution C T upstream_gene_variant MELA-AU 19 8646495 8646495 single base substitution G A upstream_gene_variant MELA-AU 19 8647327 8647327 single base substitution G A upstream_gene_variant ORCA-IN 19 8587578 8587578 single base substitution G T downstream_gene_variant ORCA-IN 19 8587578 8587578 single base substitution G T missense_variant A997E 2990C>A ORCA-IN 19 8599987 8599987 single base substitution G A intron_variant ORCA-IN 19 8599987 8599987 single base substitution G A upstream_gene_variant ORCA-IN 19 8604694 8604694 single base substitution C T downstream_gene_variant ORCA-IN 19 8604694 8604694 single base substitution C T intron_variant ORCA-IN 19 8616737 8616737 single base substitution C A downstream_gene_variant ORCA-IN 19 8616737 8616737 single base substitution C A exon_variant ORCA-IN 19 8616737 8616737 single base substitution C A stop_gained E220* 658G>T ORCA-IN 19 8616737 8616737 single base substitution C A upstream_gene_variant ORCA-IN 19 8621298 8621298 single base substitution G A intron_variant ORCA-IN 19 8621298 8621298 single base substitution G A upstream_gene_variant ORCA-IN 19 8639894 8639894 single base substitution C A downstream_gene_variant ORCA-IN 19 8639894 8639894 single base substitution C A intron_variant ORCA-IN 19 8643212 8643212 single base substitution G A upstream_gene_variant ORCA-IN 19 8646744 8646744 deletion of <=200bp C - upstream_gene_variant OV-AU 19 8584893 8584893 single base substitution C T downstream_gene_variant OV-AU 19 8584986 8584986 single base substitution G T downstream_gene_variant OV-AU 19 8586495 8586495 single base substitution G T downstream_gene_variant OV-AU 19 8586495 8586495 single base substitution G T intron_variant OV-AU 19 8586590 8586590 single base substitution A G downstream_gene_variant OV-AU 19 8586590 8586590 single base substitution A G intron_variant OV-AU 19 8589897 8589897 single base substitution C T downstream_gene_variant OV-AU 19 8589897 8589897 single base substitution C T intron_variant OV-AU 19 8597949 8597949 single base substitution A T intron_variant OV-AU 19 8597949 8597949 single base substitution A T upstream_gene_variant OV-AU 19 8599675 8599675 single base substitution A C intron_variant OV-AU 19 8599675 8599675 single base substitution A C upstream_gene_variant OV-AU 19 8606086 8606086 single base substitution A T downstream_gene_variant OV-AU 19 8606086 8606086 single base substitution A T intron_variant OV-AU 19 8606086 8606086 single base substitution A T upstream_gene_variant OV-AU 19 8616187 8616187 single base substitution C T downstream_gene_variant OV-AU 19 8616187 8616187 single base substitution C T intron_variant OV-AU 19 8616187 8616187 single base substitution C T upstream_gene_variant OV-AU 19 8616940 8616940 single base substitution T G downstream_gene_variant OV-AU 19 8616940 8616940 single base substitution T G exon_variant OV-AU 19 8616940 8616940 single base substitution T G synonymous_variant R205R 613A>C OV-AU 19 8616940 8616940 single base substitution T G upstream_gene_variant OV-AU 19 8616975 8616975 single base substitution T A downstream_gene_variant OV-AU 19 8616975 8616975 single base substitution T A exon_variant OV-AU 19 8616975 8616975 single base substitution T A missense_variant E193V 578A>T OV-AU 19 8616975 8616975 single base substitution T A upstream_gene_variant OV-AU 19 8617780 8617780 single base substitution C T downstream_gene_variant OV-AU 19 8617780 8617780 single base substitution C T intron_variant OV-AU 19 8617780 8617780 single base substitution C T upstream_gene_variant OV-AU 19 8621890 8621890 single base substitution C T intron_variant OV-AU 19 8621890 8621890 single base substitution C T upstream_gene_variant OV-AU 19 8625707 8625707 single base substitution C G intron_variant OV-AU 19 8626869 8626869 single base substitution G A intron_variant OV-AU 19 8633874 8633874 single base substitution C T intron_variant OV-AU 19 8634384 8634384 single base substitution G A intron_variant OV-AU 19 8635254 8635254 single base substitution A T intron_variant OV-AU 19 8639258 8639258 single base substitution A G downstream_gene_variant OV-AU 19 8639258 8639258 single base substitution A G intron_variant OV-AU 19 8639471 8639471 single base substitution C T downstream_gene_variant OV-AU 19 8639471 8639471 single base substitution C T intron_variant OV-AU 19 8643945 8643945 single base substitution G C upstream_gene_variant OV-AU 19 8646978 8646978 single base substitution T C upstream_gene_variant OV-US 19 8587323 8587323 single base substitution A G downstream_gene_variant OV-US 19 8587323 8587323 single base substitution A G missense_variant V1053A 3158T>C OV-US 19 8620639 8620639 single base substitution C G exon_variant OV-US 19 8620639 8620639 single base substitution C G missense_variant K15N 45G>C OV-US 19 8620639 8620639 single base substitution C G upstream_gene_variant PACA-AU 19 8582316 8582316 single base substitution C T downstream_gene_variant PACA-AU 19 8585428 8585428 single base substitution C T downstream_gene_variant PACA-AU 19 8589752 8589752 single base substitution G A downstream_gene_variant PACA-AU 19 8589752 8589752 single base substitution G A intron_variant PACA-AU 19 8591234 8591235 deletion of <=200bp TC - downstream_gene_variant PACA-AU 19 8591234 8591235 deletion of <=200bp TC - intron_variant PACA-AU 19 8595352 8595352 single base substitution G A exon_variant PACA-AU 19 8595352 8595352 single base substitution G A missense_variant R717W 2149C>T PACA-AU 19 8595352 8595352 single base substitution G A upstream_gene_variant PACA-AU 19 8596145 8596145 single base substitution C T intron_variant PACA-AU 19 8596145 8596145 single base substitution C T upstream_gene_variant PACA-AU 19 8599754 8599754 single base substitution T G intron_variant PACA-AU 19 8599754 8599754 single base substitution T G upstream_gene_variant PACA-AU 19 8609318 8609318 single base substitution C T downstream_gene_variant PACA-AU 19 8609318 8609318 single base substitution C T exon_variant PACA-AU 19 8609318 8609318 single base substitution C T missense_variant D463N 1387G>A PACA-AU 19 8609318 8609318 single base substitution C T upstream_gene_variant PACA-AU 19 8609540 8609540 deletion of <=200bp A - downstream_gene_variant PACA-AU 19 8609540 8609540 deletion of <=200bp A - intron_variant PACA-AU 19 8609540 8609540 deletion of <=200bp A - upstream_gene_variant PACA-AU 19 8614093 8614093 single base substitution C T downstream_gene_variant PACA-AU 19 8614093 8614093 single base substitution C T intron_variant PACA-AU 19 8614093 8614093 single base substitution C T upstream_gene_variant PACA-AU 19 8614249 8614249 single base substitution G A downstream_gene_variant PACA-AU 19 8614249 8614249 single base substitution G A intron_variant PACA-AU 19 8614249 8614249 single base substitution G A upstream_gene_variant PACA-AU 19 8617160 8617160 single base substitution T C downstream_gene_variant PACA-AU 19 8617160 8617160 single base substitution T C intron_variant PACA-AU 19 8617160 8617160 single base substitution T C upstream_gene_variant PACA-AU 19 8618200 8618200 single base substitution G A downstream_gene_variant PACA-AU 19 8618200 8618200 single base substitution G A exon_variant PACA-AU 19 8618200 8618200 single base substitution G A intron_variant PACA-AU 19 8618200 8618200 single base substitution G A upstream_gene_variant PACA-AU 19 8620908 8620908 single base substitution A T intron_variant PACA-AU 19 8620908 8620908 single base substitution A T upstream_gene_variant PACA-AU 19 8623321 8623321 single base substitution A T intron_variant PACA-AU 19 8623321 8623321 single base substitution A T upstream_gene_variant PACA-AU 19 8625347 8625347 single base substitution C A intron_variant PACA-AU 19 8625347 8625347 single base substitution C A upstream_gene_variant PACA-AU 19 8627053 8627053 single base substitution T C intron_variant PACA-AU 19 8628328 8628328 single base substitution T C intron_variant PACA-AU 19 8628686 8628686 single base substitution G A intron_variant PACA-AU 19 8631366 8631366 single base substitution A T intron_variant PACA-AU 19 8632971 8632971 single base substitution G T intron_variant PACA-AU 19 8633180 8633180 single base substitution G A intron_variant PACA-AU 19 8634053 8634053 single base substitution C G intron_variant PACA-AU 19 8638029 8638029 deletion of <=200bp A - downstream_gene_variant PACA-AU 19 8638029 8638029 deletion of <=200bp A - intron_variant PACA-AU 19 8645249 8645249 single base substitution C T upstream_gene_variant PACA-CA 19 8581734 8581734 single base substitution G A downstream_gene_variant PACA-CA 19 8583224 8583224 single base substitution C G downstream_gene_variant PACA-CA 19 8587153 8587153 single base substitution G A downstream_gene_variant PACA-CA 19 8587153 8587153 single base substitution G A intron_variant PACA-CA 19 8591239 8591239 single base substitution C G downstream_gene_variant PACA-CA 19 8591239 8591239 single base substitution C G intron_variant PACA-CA 19 8593021 8593021 single base substitution G A downstream_gene_variant PACA-CA 19 8593021 8593021 single base substitution G A intron_variant PACA-CA 19 8593021 8593021 single base substitution G A upstream_gene_variant PACA-CA 19 8593745 8593745 single base substitution G A downstream_gene_variant PACA-CA 19 8593745 8593745 single base substitution G A intron_variant PACA-CA 19 8593745 8593745 single base substitution G A upstream_gene_variant PACA-CA 19 8594679 8594679 single base substitution T G downstream_gene_variant PACA-CA 19 8594679 8594679 single base substitution T G intron_variant PACA-CA 19 8594679 8594679 single base substitution T G upstream_gene_variant PACA-CA 19 8595323 8595323 single base substitution G A intron_variant PACA-CA 19 8595323 8595323 single base substitution G A upstream_gene_variant PACA-CA 19 8596671 8596671 single base substitution C A intron_variant PACA-CA 19 8596671 8596671 single base substitution C A upstream_gene_variant PACA-CA 19 8597613 8597613 single base substitution T C intron_variant PACA-CA 19 8597613 8597613 single base substitution T C upstream_gene_variant PACA-CA 19 8598415 8598415 insertion of <=200bp - T intron_variant PACA-CA 19 8598415 8598415 insertion of <=200bp - T upstream_gene_variant PACA-CA 19 8600659 8600659 single base substitution G T downstream_gene_variant PACA-CA 19 8600659 8600659 single base substitution G T intron_variant PACA-CA 19 8600868 8600868 single base substitution G A downstream_gene_variant PACA-CA 19 8600868 8600868 single base substitution G A intron_variant PACA-CA 19 8601302 8601304 deletion of <=200bp GTG - downstream_gene_variant PACA-CA 19 8601302 8601304 deletion of <=200bp GTG - intron_variant PACA-CA 19 8602751 8602751 single base substitution T C downstream_gene_variant PACA-CA 19 8602751 8602751 single base substitution T C intron_variant PACA-CA 19 8603014 8603014 single base substitution T A downstream_gene_variant PACA-CA 19 8603014 8603014 single base substitution T A intron_variant PACA-CA 19 8603021 8603021 single base substitution T A downstream_gene_variant PACA-CA 19 8603021 8603021 single base substitution T A intron_variant PACA-CA 19 8604912 8604912 single base substitution C T downstream_gene_variant PACA-CA 19 8604912 8604912 single base substitution C T exon_variant PACA-CA 19 8604912 8604912 single base substitution C T splice_region_variant PACA-CA 19 8604934 8604934 single base substitution A G downstream_gene_variant PACA-CA 19 8604934 8604934 single base substitution A G exon_variant PACA-CA 19 8604934 8604934 single base substitution A G intron_variant PACA-CA 19 8606269 8606269 single base substitution C A downstream_gene_variant PACA-CA 19 8606269 8606269 single base substitution C A intron_variant PACA-CA 19 8606269 8606269 single base substitution C A upstream_gene_variant PACA-CA 19 8606840 8606840 single base substitution G T downstream_gene_variant PACA-CA 19 8606840 8606840 single base substitution G T exon_variant PACA-CA 19 8606840 8606840 single base substitution G T missense_variant N520K 1560C>A PACA-CA 19 8606840 8606840 single base substitution G T upstream_gene_variant PACA-CA 19 8607057 8607057 single base substitution C T downstream_gene_variant PACA-CA 19 8607057 8607057 single base substitution C T intron_variant PACA-CA 19 8607057 8607057 single base substitution C T upstream_gene_variant PACA-CA 19 8609560 8609560 single base substitution G A downstream_gene_variant PACA-CA 19 8609560 8609560 single base substitution G A intron_variant PACA-CA 19 8609560 8609560 single base substitution G A upstream_gene_variant PACA-CA 19 8610592 8610592 single base substitution C T downstream_gene_variant PACA-CA 19 8610592 8610592 single base substitution C T exon_variant PACA-CA 19 8610592 8610592 single base substitution C T stop_gained W433* 1298G>A PACA-CA 19 8610592 8610592 single base substitution C T upstream_gene_variant PACA-CA 19 8612127 8612127 single base substitution G C downstream_gene_variant PACA-CA 19 8612127 8612127 single base substitution G C intron_variant PACA-CA 19 8612127 8612127 single base substitution G C upstream_gene_variant PACA-CA 19 8613803 8613803 single base substitution G T downstream_gene_variant PACA-CA 19 8613803 8613803 single base substitution G T intron_variant PACA-CA 19 8613803 8613803 single base substitution G T upstream_gene_variant PACA-CA 19 8613951 8613951 single base substitution C G downstream_gene_variant PACA-CA 19 8613951 8613951 single base substitution C G intron_variant PACA-CA 19 8613951 8613951 single base substitution C G upstream_gene_variant PACA-CA 19 8613996 8613996 single base substitution G A downstream_gene_variant PACA-CA 19 8613996 8613996 single base substitution G A intron_variant PACA-CA 19 8613996 8613996 single base substitution G A upstream_gene_variant PACA-CA 19 8617583 8617583 insertion of <=200bp - C downstream_gene_variant PACA-CA 19 8617583 8617583 insertion of <=200bp - C intron_variant PACA-CA 19 8617583 8617583 insertion of <=200bp - C upstream_gene_variant PACA-CA 19 8618046 8618046 single base substitution G A downstream_gene_variant PACA-CA 19 8618046 8618046 single base substitution G A exon_variant PACA-CA 19 8618046 8618046 single base substitution G A missense_variant R161C 481C>T PACA-CA 19 8618046 8618046 single base substitution G A upstream_gene_variant PACA-CA 19 8618606 8618606 single base substitution A G downstream_gene_variant PACA-CA 19 8618606 8618606 single base substitution A G intron_variant PACA-CA 19 8618606 8618606 single base substitution A G upstream_gene_variant PACA-CA 19 8618912 8618912 single base substitution C T downstream_gene_variant PACA-CA 19 8618912 8618912 single base substitution C T intron_variant PACA-CA 19 8618912 8618912 single base substitution C T upstream_gene_variant PACA-CA 19 8619004 8619004 single base substitution C T downstream_gene_variant PACA-CA 19 8619004 8619004 single base substitution C T intron_variant PACA-CA 19 8619004 8619004 single base substitution C T upstream_gene_variant PACA-CA 19 8621354 8621354 single base substitution C T intron_variant PACA-CA 19 8621354 8621354 single base substitution C T upstream_gene_variant PACA-CA 19 8622158 8622158 insertion of <=200bp - A intron_variant PACA-CA 19 8622158 8622158 insertion of <=200bp - A upstream_gene_variant PACA-CA 19 8623221 8623221 single base substitution A C intron_variant PACA-CA 19 8623221 8623221 single base substitution A C upstream_gene_variant PACA-CA 19 8627174 8627174 single base substitution C T intron_variant PACA-CA 19 8627541 8627541 single base substitution C T intron_variant PACA-CA 19 8628479 8628479 single base substitution G A intron_variant PACA-CA 19 8632244 8632244 single base substitution C T intron_variant PACA-CA 19 8632799 8632799 single base substitution A G intron_variant PACA-CA 19 8633896 8633896 single base substitution C T intron_variant PACA-CA 19 8635110 8635110 single base substitution C T intron_variant PACA-CA 19 8635442 8635442 single base substitution G T intron_variant PACA-CA 19 8635498 8635498 single base substitution G A intron_variant PACA-CA 19 8636728 8636728 single base substitution G A downstream_gene_variant PACA-CA 19 8636728 8636728 single base substitution G A intron_variant PACA-CA 19 8637068 8637068 single base substitution A G downstream_gene_variant PACA-CA 19 8637068 8637068 single base substitution A G intron_variant PACA-CA 19 8637703 8637703 single base substitution C A downstream_gene_variant PACA-CA 19 8637703 8637703 single base substitution C A intron_variant PACA-CA 19 8637833 8637833 single base substitution G A downstream_gene_variant PACA-CA 19 8637833 8637833 single base substitution G A intron_variant PACA-CA 19 8639658 8639658 single base substitution G T downstream_gene_variant PACA-CA 19 8639658 8639658 single base substitution G T intron_variant PACA-CA 19 8642643 8642643 single base substitution C T upstream_gene_variant PACA-CA 19 8643260 8643260 single base substitution T C upstream_gene_variant PACA-CA 19 8644142 8644142 single base substitution G A upstream_gene_variant PAEN-AU 19 8591848 8591848 single base substitution T G downstream_gene_variant PAEN-AU 19 8591848 8591848 single base substitution T G intron_variant PAEN-AU 19 8591848 8591848 single base substitution T G upstream_gene_variant PAEN-IT 19 8588820 8588820 single base substitution T C downstream_gene_variant PAEN-IT 19 8588820 8588820 single base substitution T C intron_variant PAEN-IT 19 8630847 8630847 single base substitution G T intron_variant PAEN-IT 19 8639253 8639253 single base substitution C A downstream_gene_variant PAEN-IT 19 8639253 8639253 single base substitution C A intron_variant PBCA-DE 19 8590595 8590595 single base substitution C A downstream_gene_variant PBCA-DE 19 8590595 8590595 single base substitution C A intron_variant PBCA-DE 19 8592149 8592149 single base substitution C T downstream_gene_variant PBCA-DE 19 8592149 8592149 single base substitution C T intron_variant PBCA-DE 19 8592149 8592149 single base substitution C T upstream_gene_variant PBCA-DE 19 8597040 8597040 insertion of <=200bp - A intron_variant PBCA-DE 19 8597040 8597040 insertion of <=200bp - A upstream_gene_variant PBCA-DE 19 8597595 8597595 single base substitution C T intron_variant PBCA-DE 19 8597595 8597595 single base substitution C T upstream_gene_variant PBCA-DE 19 8601650 8601650 single base substitution T G downstream_gene_variant PBCA-DE 19 8601650 8601650 single base substitution T G intron_variant PBCA-DE 19 8602183 8602183 single base substitution G A downstream_gene_variant PBCA-DE 19 8602183 8602183 single base substitution G A intron_variant PBCA-DE 19 8603060 8603060 single base substitution G A downstream_gene_variant PBCA-DE 19 8603060 8603060 single base substitution G A intron_variant PBCA-DE 19 8604325 8604325 insertion of <=200bp - TT downstream_gene_variant PBCA-DE 19 8604325 8604325 insertion of <=200bp - TT intron_variant PBCA-DE 19 8605877 8605877 deletion of <=200bp T - downstream_gene_variant PBCA-DE 19 8605877 8605877 deletion of <=200bp T - intron_variant PBCA-DE 19 8605877 8605877 deletion of <=200bp T - upstream_gene_variant PBCA-DE 19 8607652 8607652 deletion of <=200bp T - downstream_gene_variant PBCA-DE 19 8607652 8607652 deletion of <=200bp T - intron_variant PBCA-DE 19 8607652 8607652 deletion of <=200bp T - upstream_gene_variant PBCA-DE 19 8613844 8613844 insertion of <=200bp - T downstream_gene_variant PBCA-DE 19 8613844 8613844 insertion of <=200bp - T intron_variant PBCA-DE 19 8613844 8613844 insertion of <=200bp - T upstream_gene_variant PBCA-DE 19 8618628 8618628 single base substitution C T downstream_gene_variant PBCA-DE 19 8618628 8618628 single base substitution C T intron_variant PBCA-DE 19 8618628 8618628 single base substitution C T upstream_gene_variant PBCA-DE 19 8622159 8622159 insertion of <=200bp - A intron_variant PBCA-DE 19 8622159 8622159 insertion of <=200bp - A upstream_gene_variant PBCA-DE 19 8625226 8625226 single base substitution G A intron_variant PBCA-DE 19 8625226 8625226 single base substitution G A upstream_gene_variant PBCA-DE 19 8627383 8627383 single base substitution C A intron_variant PBCA-DE 19 8627444 8627444 single base substitution G T intron_variant PBCA-DE 19 8628986 8628986 single base substitution C T intron_variant PBCA-DE 19 8630255 8630255 single base substitution C T intron_variant PBCA-DE 19 8632260 8632260 deletion of <=200bp T - intron_variant PBCA-DE 19 8633674 8633674 single base substitution G A intron_variant PBCA-DE 19 8635773 8635773 single base substitution T G intron_variant PBCA-DE 19 8636447 8636447 single base substitution C T downstream_gene_variant PBCA-DE 19 8636447 8636447 single base substitution C T intron_variant PBCA-DE 19 8636542 8636542 single base substitution C T downstream_gene_variant PBCA-DE 19 8636542 8636542 single base substitution C T intron_variant PRAD-CA 19 8583226 8583226 single base substitution G C downstream_gene_variant PRAD-CA 19 8585674 8585674 single base substitution C T 3_prime_UTR_variant PRAD-CA 19 8585674 8585674 single base substitution C T downstream_gene_variant PRAD-CA 19 8597787 8597787 single base substitution T C intron_variant PRAD-CA 19 8597787 8597787 single base substitution T C upstream_gene_variant PRAD-CA 19 8614555 8614555 single base substitution C T downstream_gene_variant PRAD-CA 19 8614555 8614555 single base substitution C T exon_variant PRAD-CA 19 8614555 8614555 single base substitution C T intron_variant PRAD-CA 19 8614555 8614555 single base substitution C T upstream_gene_variant PRAD-CA 19 8631374 8631374 single base substitution T A intron_variant PRAD-CA 19 8641600 8641600 single base substitution C T exon_variant PRAD-CA 19 8641600 8641600 single base substitution C T intron_variant PRAD-CA 19 8645249 8645249 single base substitution C T upstream_gene_variant PRAD-UK 19 8601249 8601249 single base substitution G A downstream_gene_variant PRAD-UK 19 8601249 8601249 single base substitution G A exon_variant PRAD-UK 19 8601249 8601249 single base substitution G A missense_variant R644W 1930C>T PRAD-UK 19 8608195 8608195 single base substitution G A downstream_gene_variant PRAD-UK 19 8608195 8608195 single base substitution G A intron_variant PRAD-UK 19 8608195 8608195 single base substitution G A upstream_gene_variant PRAD-UK 19 8610006 8610006 single base substitution C G downstream_gene_variant PRAD-UK 19 8610006 8610006 single base substitution C G intron_variant PRAD-UK 19 8610006 8610006 single base substitution C G upstream_gene_variant PRAD-UK 19 8612371 8612371 single base substitution C G downstream_gene_variant PRAD-UK 19 8612371 8612371 single base substitution C G intron_variant PRAD-UK 19 8612371 8612371 single base substitution C G upstream_gene_variant PRAD-UK 19 8616063 8616063 single base substitution G C downstream_gene_variant PRAD-UK 19 8616063 8616063 single base substitution G C intron_variant PRAD-UK 19 8616063 8616063 single base substitution G C upstream_gene_variant PRAD-UK 19 8616982 8616982 single base substitution A C downstream_gene_variant PRAD-UK 19 8616982 8616982 single base substitution A C exon_variant PRAD-UK 19 8616982 8616982 single base substitution A C missense_variant L191V 571T>G PRAD-UK 19 8616982 8616982 single base substitution A C upstream_gene_variant PRAD-UK 19 8618779 8618779 insertion of <=200bp - CACACACACACTCTCT downstream_gene_variant PRAD-UK 19 8618779 8618779 insertion of <=200bp - CACACACACACTCTCT intron_variant PRAD-UK 19 8618779 8618779 insertion of <=200bp - CACACACACACTCTCT upstream_gene_variant PRAD-UK 19 8626252 8626252 single base substitution C T intron_variant PRAD-UK 19 8630011 8630011 single base substitution G A intron_variant PRAD-US 19 8604860 8604860 single base substitution G A downstream_gene_variant PRAD-US 19 8604860 8604860 single base substitution G A exon_variant PRAD-US 19 8604860 8604860 single base substitution G A missense_variant R555C 1663C>T PRAD-US 19 8612974 8612974 single base substitution G A downstream_gene_variant PRAD-US 19 8612974 8612974 single base substitution G A exon_variant PRAD-US 19 8612974 8612974 single base substitution G A synonymous_variant F405F 1215C>T PRAD-US 19 8612974 8612974 single base substitution G A upstream_gene_variant READ-US 19 8595385 8595385 single base substitution G A exon_variant READ-US 19 8595385 8595385 single base substitution G A missense_variant R706C 2116C>T READ-US 19 8595385 8595385 single base substitution G A upstream_gene_variant READ-US 19 8606858 8606858 single base substitution G A downstream_gene_variant READ-US 19 8606858 8606858 single base substitution G A exon_variant READ-US 19 8606858 8606858 single base substitution G A synonymous_variant S514S 1542C>T READ-US 19 8606858 8606858 single base substitution G A upstream_gene_variant READ-US 19 8615058 8615058 single base substitution C T downstream_gene_variant READ-US 19 8615058 8615058 single base substitution C T exon_variant READ-US 19 8615058 8615058 single base substitution C T missense_variant D363N 1087G>A READ-US 19 8615058 8615058 single base substitution C T upstream_gene_variant RECA-EU 19 8619111 8619111 single base substitution G A downstream_gene_variant RECA-EU 19 8619111 8619111 single base substitution G A intron_variant RECA-EU 19 8619111 8619111 single base substitution G A upstream_gene_variant RECA-EU 19 8634328 8634328 single base substitution G A intron_variant RECA-EU 19 8642239 8642239 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant RECA-EU 19 8642239 8642239 single base substitution G A exon_variant RECA-EU 19 8644234 8644234 single base substitution G T upstream_gene_variant SKCA-BR 19 8581152 8581152 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 19 8583226 8583226 single base substitution G C downstream_gene_variant SKCA-BR 19 8587546 8587546 single base substitution G A downstream_gene_variant SKCA-BR 19 8587546 8587546 single base substitution G A missense_variant L1008F 3022C>T SKCA-BR 19 8587547 8587547 single base substitution G A downstream_gene_variant SKCA-BR 19 8587547 8587547 single base substitution G A synonymous_variant F1007F 3021C>T SKCA-BR 19 8589779 8589779 single base substitution G A downstream_gene_variant SKCA-BR 19 8589779 8589779 single base substitution G A intron_variant SKCA-BR 19 8596025 8596025 single base substitution A G intron_variant SKCA-BR 19 8596025 8596025 single base substitution A G upstream_gene_variant SKCA-BR 19 8597784 8597787 deletion of <=200bp AAAT - intron_variant SKCA-BR 19 8597784 8597787 deletion of <=200bp AAAT - upstream_gene_variant SKCA-BR 19 8598217 8598217 insertion of <=200bp - ATTC intron_variant SKCA-BR 19 8598217 8598217 insertion of <=200bp - ATTC upstream_gene_variant SKCA-BR 19 8599290 8599290 single base substitution C T intron_variant SKCA-BR 19 8599290 8599290 single base substitution C T upstream_gene_variant SKCA-BR 19 8603995 8603995 single base substitution C T downstream_gene_variant SKCA-BR 19 8603995 8603995 single base substitution C T intron_variant SKCA-BR 19 8605585 8605585 single base substitution G A downstream_gene_variant SKCA-BR 19 8605585 8605585 single base substitution G A intron_variant SKCA-BR 19 8605585 8605585 single base substitution G A upstream_gene_variant SKCA-BR 19 8605788 8605788 single base substitution T C downstream_gene_variant SKCA-BR 19 8605788 8605788 single base substitution T C intron_variant SKCA-BR 19 8605788 8605788 single base substitution T C upstream_gene_variant SKCA-BR 19 8606287 8606287 insertion of <=200bp - TTG downstream_gene_variant SKCA-BR 19 8606287 8606287 insertion of <=200bp - TTG intron_variant SKCA-BR 19 8606287 8606287 insertion of <=200bp - TTG upstream_gene_variant SKCA-BR 19 8606287 8606289 deletion of <=200bp TTG - downstream_gene_variant SKCA-BR 19 8606287 8606289 deletion of <=200bp TTG - intron_variant SKCA-BR 19 8606287 8606289 deletion of <=200bp TTG - upstream_gene_variant SKCA-BR 19 8606309 8606311 deletion of <=200bp GTT - downstream_gene_variant SKCA-BR 19 8606309 8606311 deletion of <=200bp GTT - intron_variant SKCA-BR 19 8606309 8606311 deletion of <=200bp GTT - upstream_gene_variant SKCA-BR 19 8608781 8608781 single base substitution C G downstream_gene_variant SKCA-BR 19 8608781 8608781 single base substitution C G intron_variant SKCA-BR 19 8608781 8608781 single base substitution C G upstream_gene_variant SKCA-BR 19 8610306 8610306 single base substitution C T downstream_gene_variant SKCA-BR 19 8610306 8610306 single base substitution C T intron_variant SKCA-BR 19 8610306 8610306 single base substitution C T upstream_gene_variant SKCA-BR 19 8612528 8612528 single base substitution C T downstream_gene_variant SKCA-BR 19 8612528 8612528 single base substitution C T intron_variant SKCA-BR 19 8612528 8612528 single base substitution C T upstream_gene_variant SKCA-BR 19 8612873 8612873 single base substitution C T downstream_gene_variant SKCA-BR 19 8612873 8612873 single base substitution C T exon_variant SKCA-BR 19 8612873 8612873 single base substitution C T intron_variant SKCA-BR 19 8612873 8612873 single base substitution C T upstream_gene_variant SKCA-BR 19 8614418 8614418 single base substitution A G downstream_gene_variant SKCA-BR 19 8614418 8614418 single base substitution A G intron_variant SKCA-BR 19 8614418 8614418 single base substitution A G upstream_gene_variant SKCA-BR 19 8614520 8614520 single base substitution C T downstream_gene_variant SKCA-BR 19 8614520 8614520 single base substitution C T exon_variant SKCA-BR 19 8614520 8614520 single base substitution C T intron_variant SKCA-BR 19 8614520 8614520 single base substitution C T upstream_gene_variant SKCA-BR 19 8615497 8615497 single base substitution T C downstream_gene_variant SKCA-BR 19 8615497 8615497 single base substitution T C exon_variant SKCA-BR 19 8615497 8615497 single base substitution T C missense_variant N285D 853A>G SKCA-BR 19 8615497 8615497 single base substitution T C upstream_gene_variant SKCA-BR 19 8615512 8615512 single base substitution T C downstream_gene_variant SKCA-BR 19 8615512 8615512 single base substitution T C exon_variant SKCA-BR 19 8615512 8615512 single base substitution T C missense_variant I280V 838A>G SKCA-BR 19 8615512 8615512 single base substitution T C upstream_gene_variant SKCA-BR 19 8617564 8617564 single base substitution G A downstream_gene_variant SKCA-BR 19 8617564 8617564 single base substitution G A intron_variant SKCA-BR 19 8617564 8617564 single base substitution G A upstream_gene_variant SKCA-BR 19 8617722 8617722 single base substitution G A downstream_gene_variant SKCA-BR 19 8617722 8617722 single base substitution G A intron_variant SKCA-BR 19 8617722 8617722 single base substitution G A upstream_gene_variant SKCA-BR 19 8618776 8618776 insertion of <=200bp - ACTCTCT downstream_gene_variant SKCA-BR 19 8618776 8618776 insertion of <=200bp - ACTCTCT intron_variant SKCA-BR 19 8618776 8618776 insertion of <=200bp - ACTCTCT upstream_gene_variant SKCA-BR 19 8619417 8619417 single base substitution C T 3_prime_UTR_variant SKCA-BR 19 8619417 8619417 single base substitution C T downstream_gene_variant SKCA-BR 19 8619417 8619417 single base substitution C T exon_variant SKCA-BR 19 8619417 8619417 single base substitution C T synonymous_variant T86T 258G>A SKCA-BR 19 8619417 8619417 single base substitution C T synonymous_variant T90T 270G>A SKCA-BR 19 8619417 8619417 single base substitution C T upstream_gene_variant SKCA-BR 19 8620766 8620766 single base substitution T C intron_variant SKCA-BR 19 8620766 8620766 single base substitution T C upstream_gene_variant SKCA-BR 19 8621941 8621941 single base substitution G A intron_variant SKCA-BR 19 8621941 8621941 single base substitution G A upstream_gene_variant SKCA-BR 19 8622125 8622125 single base substitution C T intron_variant SKCA-BR 19 8622125 8622125 single base substitution C T upstream_gene_variant SKCA-BR 19 8623309 8623309 single base substitution C A intron_variant SKCA-BR 19 8623309 8623309 single base substitution C A upstream_gene_variant SKCA-BR 19 8626354 8626356 deletion of <=200bp CTT - intron_variant SKCA-BR 19 8626704 8626704 single base substitution G A intron_variant SKCA-BR 19 8627744 8627744 single base substitution C T intron_variant SKCA-BR 19 8628496 8628496 single base substitution G A intron_variant SKCA-BR 19 8628931 8628931 single base substitution T C intron_variant SKCA-BR 19 8630530 8630530 single base substitution C T intron_variant SKCA-BR 19 8630810 8630810 insertion of <=200bp - CA intron_variant SKCA-BR 19 8634422 8634422 single base substitution C T intron_variant SKCA-BR 19 8634813 8634813 single base substitution T G intron_variant SKCA-BR 19 8635924 8635924 single base substitution G A intron_variant SKCA-BR 19 8636385 8636385 single base substitution A C downstream_gene_variant SKCA-BR 19 8636385 8636385 single base substitution A C intron_variant SKCA-BR 19 8637075 8637075 single base substitution C T downstream_gene_variant SKCA-BR 19 8637075 8637075 single base substitution C T intron_variant SKCA-BR 19 8639414 8639414 insertion of <=200bp - CCTTTCTTTCTTT downstream_gene_variant SKCA-BR 19 8639414 8639414 insertion of <=200bp - CCTTTCTTTCTTT intron_variant SKCA-BR 19 8639414 8639414 insertion of <=200bp - CCTTTCTTT downstream_gene_variant SKCA-BR 19 8639414 8639414 insertion of <=200bp - CCTTTCTTT intron_variant SKCA-BR 19 8639465 8639465 single base substitution C T downstream_gene_variant SKCA-BR 19 8639465 8639465 single base substitution C T intron_variant SKCA-BR 19 8639985 8639985 single base substitution G A downstream_gene_variant SKCA-BR 19 8639985 8639985 single base substitution G A intron_variant SKCA-BR 19 8641275 8641275 single base substitution A C downstream_gene_variant SKCA-BR 19 8641275 8641275 single base substitution A C intron_variant SKCA-BR 19 8643089 8643089 single base substitution C G upstream_gene_variant SKCA-BR 19 8643158 8643158 single base substitution G A upstream_gene_variant SKCA-BR 19 8644857 8644857 single base substitution T A upstream_gene_variant SKCA-BR 19 8645538 8645538 insertion of <=200bp - AG upstream_gene_variant SKCM-US 19 8586485 8586485 single base substitution G A downstream_gene_variant SKCM-US 19 8586485 8586485 single base substitution G A missense_variant P1075L 3224C>T SKCM-US 19 8587285 8587285 single base substitution C T downstream_gene_variant SKCM-US 19 8587285 8587285 single base substitution C T missense_variant E1066K 3196G>A SKCM-US 19 8587408 8587408 single base substitution C T downstream_gene_variant SKCM-US 19 8587408 8587408 single base substitution C T missense_variant G1025R 3073G>A SKCM-US 19 8587587 8587587 single base substitution C T downstream_gene_variant SKCM-US 19 8587587 8587587 single base substitution C T missense_variant R994Q 2981G>A SKCM-US 19 8590392 8590392 single base substitution G A downstream_gene_variant SKCM-US 19 8590392 8590392 single base substitution G A exon_variant SKCM-US 19 8590392 8590392 single base substitution G A missense_variant P942L 2825C>T SKCM-US 19 8590433 8590433 single base substitution C T downstream_gene_variant SKCM-US 19 8590433 8590433 single base substitution C T exon_variant SKCM-US 19 8590433 8590433 single base substitution C T synonymous_variant K928K 2784G>A SKCM-US 19 8591470 8591470 single base substitution C T 3_prime_UTR_variant SKCM-US 19 8591470 8591470 single base substitution C T downstream_gene_variant SKCM-US 19 8591470 8591470 single base substitution C T exon_variant SKCM-US 19 8591470 8591470 single base substitution C T synonymous_variant V879V 2637G>A SKCM-US 19 8591700 8591700 single base substitution C T 3_prime_UTR_variant SKCM-US 19 8591700 8591700 single base substitution C T downstream_gene_variant SKCM-US 19 8591700 8591700 single base substitution C T exon_variant SKCM-US 19 8591700 8591700 single base substitution C T missense_variant R865K 2594G>A SKCM-US 19 8591700 8591700 single base substitution C T upstream_gene_variant SKCM-US 19 8592300 8592300 single base substitution T G downstream_gene_variant SKCM-US 19 8592300 8592300 single base substitution T G exon_variant SKCM-US 19 8592300 8592300 single base substitution T G missense_variant K799T 2396A>C SKCM-US 19 8592300 8592300 single base substitution T G upstream_gene_variant SKCM-US 19 8595250 8595250 single base substitution C T splice_acceptor_variant SKCM-US 19 8595250 8595250 single base substitution C T upstream_gene_variant SKCM-US 19 8595349 8595349 single base substitution C T exon_variant SKCM-US 19 8595349 8595349 single base substitution C T missense_variant E718K 2152G>A SKCM-US 19 8595349 8595349 single base substitution C T upstream_gene_variant SKCM-US 19 8601135 8601135 single base substitution C T downstream_gene_variant SKCM-US 19 8601135 8601135 single base substitution C T splice_donor_variant SKCM-US 19 8601239 8601239 single base substitution C T downstream_gene_variant SKCM-US 19 8601239 8601239 single base substitution C T exon_variant SKCM-US 19 8601239 8601239 single base substitution C T missense_variant G647E 1940G>A SKCM-US 19 8604837 8604837 single base substitution C T downstream_gene_variant SKCM-US 19 8604837 8604837 single base substitution C T exon_variant SKCM-US 19 8604837 8604837 single base substitution C T synonymous_variant K562K 1686G>A SKCM-US 19 8604855 8604855 single base substitution G A downstream_gene_variant SKCM-US 19 8604855 8604855 single base substitution G A exon_variant SKCM-US 19 8604855 8604855 single base substitution G A synonymous_variant P556P 1668C>T SKCM-US 19 8604862 8604862 single base substitution C T downstream_gene_variant SKCM-US 19 8604862 8604862 single base substitution C T exon_variant SKCM-US 19 8604862 8604862 single base substitution C T missense_variant G554E 1661G>A SKCM-US 19 8604875 8604875 single base substitution C T downstream_gene_variant SKCM-US 19 8604875 8604875 single base substitution C T exon_variant SKCM-US 19 8604875 8604875 single base substitution C T missense_variant G550R 1648G>A SKCM-US 19 8606848 8606848 single base substitution C T downstream_gene_variant SKCM-US 19 8606848 8606848 single base substitution C T exon_variant SKCM-US 19 8606848 8606848 single base substitution C T missense_variant E518K 1552G>A SKCM-US 19 8606848 8606848 single base substitution C T upstream_gene_variant SKCM-US 19 8606866 8606866 single base substitution C T downstream_gene_variant SKCM-US 19 8606866 8606866 single base substitution C T exon_variant SKCM-US 19 8606866 8606866 single base substitution C T missense_variant D512N 1534G>A SKCM-US 19 8606866 8606866 single base substitution C T upstream_gene_variant SKCM-US 19 8609209 8609209 single base substitution C T downstream_gene_variant SKCM-US 19 8609209 8609209 single base substitution C T exon_variant SKCM-US 19 8609209 8609209 single base substitution C T missense_variant G499D 1496G>A SKCM-US 19 8609209 8609209 single base substitution C T upstream_gene_variant SKCM-US 19 8609249 8609249 single base substitution C T downstream_gene_variant SKCM-US 19 8609249 8609249 single base substitution C T exon_variant SKCM-US 19 8609249 8609249 single base substitution C T missense_variant A486T 1456G>A SKCM-US 19 8609249 8609249 single base substitution C T upstream_gene_variant SKCM-US 19 8609284 8609284 single base substitution C T downstream_gene_variant SKCM-US 19 8609284 8609284 single base substitution C T exon_variant SKCM-US 19 8609284 8609284 single base substitution C T missense_variant G474E 1421G>A SKCM-US 19 8609284 8609284 single base substitution C T upstream_gene_variant SKCM-US 19 8609287 8609287 single base substitution C T downstream_gene_variant SKCM-US 19 8609287 8609287 single base substitution C T exon_variant SKCM-US 19 8609287 8609287 single base substitution C T missense_variant G473E 1418G>A SKCM-US 19 8609287 8609287 single base substitution C T upstream_gene_variant SKCM-US 19 8610545 8610545 single base substitution C T downstream_gene_variant SKCM-US 19 8610545 8610545 single base substitution C T exon_variant SKCM-US 19 8610545 8610545 single base substitution C T missense_variant E449K 1345G>A SKCM-US 19 8610545 8610545 single base substitution C T upstream_gene_variant SKCM-US 19 8610561 8610561 single base substitution G A downstream_gene_variant SKCM-US 19 8610561 8610561 single base substitution G A exon_variant SKCM-US 19 8610561 8610561 single base substitution G A synonymous_variant V443V 1329C>T SKCM-US 19 8610561 8610561 single base substitution G A upstream_gene_variant SKCM-US 19 8610586 8610586 single base substitution G A downstream_gene_variant SKCM-US 19 8610586 8610586 single base substitution G A exon_variant SKCM-US 19 8610586 8610586 single base substitution G A missense_variant P435L 1304C>T SKCM-US 19 8610586 8610586 single base substitution G A upstream_gene_variant SKCM-US 19 8610589 8610589 single base substitution G A downstream_gene_variant SKCM-US 19 8610589 8610589 single base substitution G A exon_variant SKCM-US 19 8610589 8610589 single base substitution G A missense_variant T434I 1301C>T SKCM-US 19 8610589 8610589 single base substitution G A upstream_gene_variant SKCM-US 19 8615459 8615459 single base substitution C T downstream_gene_variant SKCM-US 19 8615459 8615459 single base substitution C T exon_variant SKCM-US 19 8615459 8615459 single base substitution C T synonymous_variant V297V 891G>A SKCM-US 19 8615459 8615459 single base substitution C T upstream_gene_variant SKCM-US 19 8615533 8615533 single base substitution C T downstream_gene_variant SKCM-US 19 8615533 8615533 single base substitution C T exon_variant SKCM-US 19 8615533 8615533 single base substitution C T missense_variant V273I 817G>A SKCM-US 19 8615533 8615533 single base substitution C T upstream_gene_variant SKCM-US 19 8615558 8615558 single base substitution C T downstream_gene_variant SKCM-US 19 8615558 8615558 single base substitution C T exon_variant SKCM-US 19 8615558 8615558 single base substitution C T synonymous_variant G264G 792G>A SKCM-US 19 8615558 8615558 single base substitution C T upstream_gene_variant SKCM-US 19 8616642 8616642 single base substitution G A downstream_gene_variant SKCM-US 19 8616642 8616642 single base substitution G A exon_variant SKCM-US 19 8616642 8616642 single base substitution G A synonymous_variant S251S 753C>T SKCM-US 19 8616642 8616642 single base substitution G A upstream_gene_variant SKCM-US 19 8618077 8618077 single base substitution C T downstream_gene_variant SKCM-US 19 8618077 8618077 single base substitution C T exon_variant SKCM-US 19 8618077 8618077 single base substitution C T synonymous_variant L150L 450G>A SKCM-US 19 8618077 8618077 single base substitution C T upstream_gene_variant SKCM-US 19 8618261 8618261 single base substitution C T 3_prime_UTR_variant SKCM-US 19 8618261 8618261 single base substitution C T downstream_gene_variant SKCM-US 19 8618261 8618261 single base substitution C T exon_variant SKCM-US 19 8618261 8618261 single base substitution C T synonymous_variant K125K 375G>A SKCM-US 19 8618261 8618261 single base substitution C T synonymous_variant K129K 387G>A SKCM-US 19 8618261 8618261 single base substitution C T upstream_gene_variant SKCM-US 19 8618320 8618320 single base substitution C T downstream_gene_variant SKCM-US 19 8618320 8618320 single base substitution C T missense_variant G106R 316G>A SKCM-US 19 8618320 8618320 single base substitution C T missense_variant G110R 328G>A SKCM-US 19 8618320 8618320 single base substitution C T splice_region_variant SKCM-US 19 8618320 8618320 single base substitution C T upstream_gene_variant SKCM-US 19 8619417 8619417 single base substitution C T 3_prime_UTR_variant SKCM-US 19 8619417 8619417 single base substitution C T downstream_gene_variant SKCM-US 19 8619417 8619417 single base substitution C T exon_variant SKCM-US 19 8619417 8619417 single base substitution C T synonymous_variant T86T 258G>A SKCM-US 19 8619417 8619417 single base substitution C T synonymous_variant T90T 270G>A SKCM-US 19 8619417 8619417 single base substitution C T upstream_gene_variant SKCM-US 19 8620543 8620543 single base substitution G A exon_variant SKCM-US 19 8620543 8620543 single base substitution G A splice_region_variant SKCM-US 19 8620543 8620543 single base substitution G A synonymous_variant F47F 141C>T SKCM-US 19 8620543 8620543 single base substitution G A upstream_gene_variant SKCM-US 19 8620596 8620596 single base substitution C T exon_variant SKCM-US 19 8620596 8620596 single base substitution C T missense_variant E30K 88G>A SKCM-US 19 8620596 8620596 single base substitution C T upstream_gene_variant SKCM-US 19 8620608 8620608 single base substitution G A exon_variant SKCM-US 19 8620608 8620608 single base substitution G A missense_variant P26S 76C>T SKCM-US 19 8620608 8620608 single base substitution G A upstream_gene_variant SKCM-US 19 8620618 8620618 single base substitution C T exon_variant SKCM-US 19 8620618 8620618 single base substitution C T missense_variant M22I 66G>A SKCM-US 19 8620618 8620618 single base substitution C T upstream_gene_variant SKCM-US 19 8645813 8645813 single base substitution G A upstream_gene_variant SKCM-US 19 8645836 8645836 single base substitution G A upstream_gene_variant SKCM-US 19 8645854 8645854 single base substitution G A upstream_gene_variant STAD-US 19 8592285 8592285 deletion of <=200bp C - 3_prime_UTR_variant STAD-US 19 8592285 8592285 deletion of <=200bp C - downstream_gene_variant STAD-US 19 8592285 8592285 deletion of <=200bp C - frameshift_variant G804 STAD-US 19 8592285 8592285 deletion of <=200bp C - upstream_gene_variant STAD-US 19 8595116 8595116 single base substitution G A exon_variant STAD-US 19 8595116 8595116 single base substitution G A synonymous_variant F764F 2292C>T STAD-US 19 8595116 8595116 single base substitution G A upstream_gene_variant STAD-US 19 8595150 8595150 single base substitution C T exon_variant STAD-US 19 8595150 8595150 single base substitution C T missense_variant R753H 2258G>A STAD-US 19 8595150 8595150 single base substitution C T upstream_gene_variant STAD-US 19 8595190 8595190 single base substitution C T exon_variant STAD-US 19 8595190 8595190 single base substitution C T missense_variant V740I 2218G>A STAD-US 19 8595190 8595190 single base substitution C T upstream_gene_variant STAD-US 19 8595204 8595204 single base substitution A T exon_variant STAD-US 19 8595204 8595204 single base substitution A T missense_variant I735N 2204T>A STAD-US 19 8595204 8595204 single base substitution A T upstream_gene_variant STAD-US 19 8595214 8595214 single base substitution G A exon_variant STAD-US 19 8595214 8595214 single base substitution G A missense_variant R732C 2194C>T STAD-US 19 8595214 8595214 single base substitution G A upstream_gene_variant STAD-US 19 8595407 8595407 single base substitution T C exon_variant STAD-US 19 8595407 8595407 single base substitution T C synonymous_variant R698R 2094A>G STAD-US 19 8595407 8595407 single base substitution T C upstream_gene_variant STAD-US 19 8601234 8601234 single base substitution C T downstream_gene_variant STAD-US 19 8601234 8601234 single base substitution C T exon_variant STAD-US 19 8601234 8601234 single base substitution C T missense_variant E649K 1945G>A STAD-US 19 8604860 8604860 single base substitution G A downstream_gene_variant STAD-US 19 8604860 8604860 single base substitution G A exon_variant STAD-US 19 8604860 8604860 single base substitution G A missense_variant R555C 1663C>T STAD-US 19 8609190 8609190 single base substitution G A downstream_gene_variant STAD-US 19 8609190 8609190 single base substitution G A exon_variant STAD-US 19 8609190 8609190 single base substitution G A synonymous_variant Y505Y 1515C>T STAD-US 19 8609190 8609190 single base substitution G A upstream_gene_variant STAD-US 19 8609213 8609213 single base substitution C T downstream_gene_variant STAD-US 19 8609213 8609213 single base substitution C T exon_variant STAD-US 19 8609213 8609213 single base substitution C T missense_variant A498T 1492G>A STAD-US 19 8609213 8609213 single base substitution C T upstream_gene_variant STAD-US 19 8609255 8609255 single base substitution G A downstream_gene_variant STAD-US 19 8609255 8609255 single base substitution G A exon_variant STAD-US 19 8609255 8609255 single base substitution G A stop_gained Q484* 1450C>T STAD-US 19 8609255 8609255 single base substitution G A upstream_gene_variant STAD-US 19 8609293 8609293 single base substitution G A downstream_gene_variant STAD-US 19 8609293 8609293 single base substitution G A exon_variant STAD-US 19 8609293 8609293 single base substitution G A missense_variant T471M 1412C>T STAD-US 19 8609293 8609293 single base substitution G A upstream_gene_variant STAD-US 19 8609306 8609306 single base substitution T C downstream_gene_variant STAD-US 19 8609306 8609306 single base substitution T C exon_variant STAD-US 19 8609306 8609306 single base substitution T C missense_variant T467A 1399A>G STAD-US 19 8609306 8609306 single base substitution T C upstream_gene_variant STAD-US 19 8609309 8609309 single base substitution C T downstream_gene_variant STAD-US 19 8609309 8609309 single base substitution C T exon_variant STAD-US 19 8609309 8609309 single base substitution C T missense_variant A466T 1396G>A STAD-US 19 8609309 8609309 single base substitution C T upstream_gene_variant STAD-US 19 8612926 8612926 single base substitution G A downstream_gene_variant STAD-US 19 8612926 8612926 single base substitution G A exon_variant STAD-US 19 8612926 8612926 single base substitution G A synonymous_variant A421A 1263C>T STAD-US 19 8612926 8612926 single base substitution G A upstream_gene_variant STAD-US 19 8612995 8612995 single base substitution G A downstream_gene_variant STAD-US 19 8612995 8612995 single base substitution G A exon_variant STAD-US 19 8612995 8612995 single base substitution G A synonymous_variant F398F 1194C>T STAD-US 19 8612995 8612995 single base substitution G A upstream_gene_variant STAD-US 19 8613002 8613002 deletion of <=200bp T - downstream_gene_variant STAD-US 19 8613002 8613002 deletion of <=200bp T - exon_variant STAD-US 19 8613002 8613002 deletion of <=200bp T - frameshift_variant N396 STAD-US 19 8613002 8613002 deletion of <=200bp T - upstream_gene_variant STAD-US 19 8613174 8613174 single base substitution G C downstream_gene_variant STAD-US 19 8613174 8613174 single base substitution G C exon_variant STAD-US 19 8613174 8613174 single base substitution G C missense_variant Q377E 1129C>G STAD-US 19 8613174 8613174 single base substitution G C upstream_gene_variant STAD-US 19 8613192 8613192 single base substitution G A downstream_gene_variant STAD-US 19 8613192 8613192 single base substitution G A exon_variant STAD-US 19 8613192 8613192 single base substitution G A missense_variant R371C 1111C>T STAD-US 19 8613192 8613192 single base substitution G A upstream_gene_variant STAD-US 19 8616964 8616964 single base substitution C T downstream_gene_variant STAD-US 19 8616964 8616964 single base substitution C T exon_variant STAD-US 19 8616964 8616964 single base substitution C T missense_variant V197M 589G>A STAD-US 19 8616964 8616964 single base substitution C T upstream_gene_variant STAD-US 19 8618058 8618058 single base substitution C T downstream_gene_variant STAD-US 19 8618058 8618058 single base substitution C T exon_variant STAD-US 19 8618058 8618058 single base substitution C T missense_variant A157T 469G>A STAD-US 19 8618058 8618058 single base substitution C T upstream_gene_variant STAD-US 19 8618252 8618252 single base substitution G A 3_prime_UTR_variant STAD-US 19 8618252 8618252 single base substitution G A downstream_gene_variant STAD-US 19 8618252 8618252 single base substitution G A exon_variant STAD-US 19 8618252 8618252 single base substitution G A synonymous_variant G128G 384C>T STAD-US 19 8618252 8618252 single base substitution G A synonymous_variant G132G 396C>T STAD-US 19 8618252 8618252 single base substitution G A upstream_gene_variant STAD-US 19 8619539 8619539 single base substitution G A downstream_gene_variant STAD-US 19 8619539 8619539 single base substitution G A exon_variant STAD-US 19 8619539 8619539 single base substitution G A missense_variant A73V 218C>T STAD-US 19 8619539 8619539 single base substitution G A missense_variant A77V 230C>T STAD-US 19 8619539 8619539 single base substitution G A splice_region_variant STAD-US 19 8619539 8619539 single base substitution G A upstream_gene_variant STAD-US 19 8619568 8619568 single base substitution G A downstream_gene_variant STAD-US 19 8619568 8619568 single base substitution G A exon_variant STAD-US 19 8619568 8619568 single base substitution G A synonymous_variant T63T 189C>T STAD-US 19 8619568 8619568 single base substitution G A synonymous_variant T67T 201C>T STAD-US 19 8619568 8619568 single base substitution G A upstream_gene_variant STAD-US 19 8620591 8620591 single base substitution G A exon_variant STAD-US 19 8620591 8620591 single base substitution G A synonymous_variant D31D 93C>T STAD-US 19 8620591 8620591 single base substitution G A upstream_gene_variant STAD-US 19 8620596 8620596 single base substitution C T exon_variant STAD-US 19 8620596 8620596 single base substitution C T missense_variant E30K 88G>A STAD-US 19 8620596 8620596 single base substitution C T upstream_gene_variant UCEC-US 19 8586482 8586482 single base substitution G A downstream_gene_variant UCEC-US 19 8586482 8586482 single base substitution G A missense_variant S1076L 3227C>T UCEC-US 19 8595108 8595108 single base substitution G A exon_variant UCEC-US 19 8595108 8595108 single base substitution G A missense_variant S767L 2300C>T UCEC-US 19 8595108 8595108 single base substitution G A upstream_gene_variant UCEC-US 19 8595116 8595116 single base substitution G A exon_variant UCEC-US 19 8595116 8595116 single base substitution G A synonymous_variant F764F 2292C>T UCEC-US 19 8595116 8595116 single base substitution G A upstream_gene_variant UCEC-US 19 8595163 8595163 single base substitution G A exon_variant UCEC-US 19 8595163 8595163 single base substitution G A missense_variant R749W 2245C>T UCEC-US 19 8595163 8595163 single base substitution G A upstream_gene_variant UCEC-US 19 8595191 8595191 single base substitution G A exon_variant UCEC-US 19 8595191 8595191 single base substitution G A synonymous_variant F739F 2217C>T UCEC-US 19 8595191 8595191 single base substitution G A upstream_gene_variant UCEC-US 19 8595220 8595220 single base substitution G A exon_variant UCEC-US 19 8595220 8595220 single base substitution G A missense_variant R730W 2188C>T UCEC-US 19 8595220 8595220 single base substitution G A upstream_gene_variant UCEC-US 19 8595362 8595362 single base substitution G A exon_variant UCEC-US 19 8595362 8595362 single base substitution G A synonymous_variant Y713Y 2139C>T UCEC-US 19 8595362 8595362 single base substitution G A upstream_gene_variant UCEC-US 19 8595422 8595422 single base substitution G A exon_variant UCEC-US 19 8595422 8595422 single base substitution G A synonymous_variant F693F 2079C>T UCEC-US 19 8595422 8595422 single base substitution G A upstream_gene_variant UCEC-US 19 8604848 8604848 single base substitution C T downstream_gene_variant UCEC-US 19 8604848 8604848 single base substitution C T exon_variant UCEC-US 19 8604848 8604848 single base substitution C T missense_variant A559T 1675G>A UCEC-US 19 8609298 8609298 single base substitution G A downstream_gene_variant UCEC-US 19 8609298 8609298 single base substitution G A exon_variant UCEC-US 19 8609298 8609298 single base substitution G A synonymous_variant H469H 1407C>T UCEC-US 19 8609298 8609298 single base substitution G A upstream_gene_variant UCEC-US 19 8612926 8612926 single base substitution G A downstream_gene_variant UCEC-US 19 8612926 8612926 single base substitution G A exon_variant UCEC-US 19 8612926 8612926 single base substitution G A synonymous_variant A421A 1263C>T UCEC-US 19 8612926 8612926 single base substitution G A upstream_gene_variant UCEC-US 19 8612974 8612974 single base substitution G A downstream_gene_variant UCEC-US 19 8612974 8612974 single base substitution G A exon_variant UCEC-US 19 8612974 8612974 single base substitution G A synonymous_variant F405F 1215C>T UCEC-US 19 8612974 8612974 single base substitution G A upstream_gene_variant UCEC-US 19 8612994 8612994 single base substitution C T downstream_gene_variant UCEC-US 19 8612994 8612994 single base substitution C T exon_variant UCEC-US 19 8612994 8612994 single base substitution C T missense_variant E399K 1195G>A UCEC-US 19 8612994 8612994 single base substitution C T upstream_gene_variant UCEC-US 19 8612995 8612995 single base substitution G A downstream_gene_variant UCEC-US 19 8612995 8612995 single base substitution G A exon_variant UCEC-US 19 8612995 8612995 single base substitution G A synonymous_variant F398F 1194C>T UCEC-US 19 8612995 8612995 single base substitution G A upstream_gene_variant UCEC-US 19 8613157 8613157 single base substitution G A downstream_gene_variant UCEC-US 19 8613157 8613157 single base substitution G A exon_variant UCEC-US 19 8613157 8613157 single base substitution G A synonymous_variant I382I 1146C>T UCEC-US 19 8613157 8613157 single base substitution G A upstream_gene_variant UCEC-US 19 8615058 8615058 single base substitution C T downstream_gene_variant UCEC-US 19 8615058 8615058 single base substitution C T exon_variant UCEC-US 19 8615058 8615058 single base substitution C T missense_variant D363N 1087G>A UCEC-US 19 8615058 8615058 single base substitution C T upstream_gene_variant UCEC-US 19 8615148 8615148 single base substitution G A downstream_gene_variant UCEC-US 19 8615148 8615148 single base substitution G A exon_variant UCEC-US 19 8615148 8615148 single base substitution G A missense_variant R333C 997C>T UCEC-US 19 8615148 8615148 single base substitution G A upstream_gene_variant UCEC-US 19 8615468 8615468 single base substitution G A downstream_gene_variant UCEC-US 19 8615468 8615468 single base substitution G A exon_variant UCEC-US 19 8615468 8615468 single base substitution G A synonymous_variant Y294Y 882C>T UCEC-US 19 8615468 8615468 single base substitution G A upstream_gene_variant UCEC-US 19 8615486 8615486 single base substitution G A downstream_gene_variant UCEC-US 19 8615486 8615486 single base substitution G A exon_variant UCEC-US 19 8615486 8615486 single base substitution G A synonymous_variant F288F 864C>T UCEC-US 19 8615486 8615486 single base substitution G A upstream_gene_variant UCEC-US 19 8616642 8616642 single base substitution G A downstream_gene_variant UCEC-US 19 8616642 8616642 single base substitution G A exon_variant UCEC-US 19 8616642 8616642 single base substitution G A synonymous_variant S251S 753C>T UCEC-US 19 8616642 8616642 single base substitution G A upstream_gene_variant UCEC-US 19 8618046 8618046 single base substitution G A downstream_gene_variant UCEC-US 19 8618046 8618046 single base substitution G A exon_variant UCEC-US 19 8618046 8618046 single base substitution G A missense_variant R161C 481C>T UCEC-US 19 8618046 8618046 single base substitution G A upstream_gene_variant UCEC-US 19 8618065 8618065 single base substitution G A downstream_gene_variant UCEC-US 19 8618065 8618065 single base substitution G A exon_variant UCEC-US 19 8618065 8618065 single base substitution G A synonymous_variant F154F 462C>T UCEC-US 19 8618065 8618065 single base substitution G A upstream_gene_variant UCEC-US 19 8618081 8618081 single base substitution G A downstream_gene_variant UCEC-US 19 8618081 8618081 single base substitution G A exon_variant UCEC-US 19 8618081 8618081 single base substitution G A missense_variant P149L 446C>T UCEC-US 19 8618081 8618081 single base substitution G A upstream_gene_variant UCEC-US 19 8618246 8618246 single base substitution G A 3_prime_UTR_variant UCEC-US 19 8618246 8618246 single base substitution G A downstream_gene_variant UCEC-US 19 8618246 8618246 single base substitution G A exon_variant UCEC-US 19 8618246 8618246 single base substitution G A synonymous_variant G130G 390C>T UCEC-US 19 8618246 8618246 single base substitution G A synonymous_variant G134G 402C>T UCEC-US 19 8618246 8618246 single base substitution G A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand BD165T COSM4704929 c.2313C>T p.Y771Y Substitution - coding silent 19:8530211-8530211 - TCGA-AA-3966-01 COSM272988 c.231G>A p.A77A Substitution - coding silent 19:8554654-8554654 - TCGA-EE-A29D-06 COSM3541654 c.2784G>A p.K928K Substitution - coding silent 19:8525549-8525549 - Pat_76_B COSM5857171 c.238T>C p.Y80H Substitution - Missense 19:8554565-8554565 - pfg043T COSM4749621 c.221A>G p.Y74C Substitution - Missense 19:8554664-8554664 - TCGA-46-3767-01 COSM715608 c.1488G>A p.W496* Substitution - Nonsense 19:8544333-8544333 - TCGA-D9-A1JX-06 COSM3541654 c.2784G>A p.K928K Substitution - coding silent 19:8525549-8525549 - TCGA-F4-6856-01 COSM1397798 c.141+1G>A p.? Unknown 19:8555658-8555658 - HCC94T COSM1003548 c.3227C>T p.S1076L Substitution - Missense 19:8521598-8521598 - RK256_C01 COSM4945751 c.2770A>T p.K924* Substitution - Nonsense 19:8526453-8526453 - TCGA-BR-6452-01 COSM4083066 c.2194C>T p.R732C Substitution - Missense 19:8530330-8530330 - cSCCP1 COSM135807 c.2969G>A p.G990E Substitution - Missense 19:8522715-8522715 - TCGA-D3-A51G-06 COSM3541660 c.1661G>A p.G554E Substitution - Missense 19:8539978-8539978 - ESCC_BICR_016T COSM5439539 c.2289C>A p.D763E Substitution - Missense 19:8530235-8530235 - HCT15 COSM1680593 c.586C>T p.R196C Substitution - Missense 19:8552083-8552083 - TCGA-BS-A0UF-01 COSM1003561 c.1146C>T p.I382I Substitution - coding silent 19:8548273-8548273 - TCGA-GN-A268-06 COSM3541651 c.3196G>A p.E1066K Substitution - Missense 19:8522401-8522401 - CSCC-17-T COSM4516929 c.2529_2530GG>AA p.E844K Substitution - Missense 19:8526880-8526881 - TCGA-CM-4743-01 COSM1397792 c.289A>G p.M97V Substitution - Missense 19:8554514-8554514 - TCGA-BR-7707-01 COSM4083064 c.2258G>A p.R753H Substitution - Missense 19:8530266-8530266 - TCGA-J9-A52C-01 COSM1003559 c.1215C>T p.F405F Substitution - coding silent 19:8548090-8548090 - TCGA-AZ-6598-01 COSM1397783 c.2899delC p.L967fs*94 Deletion - Frameshift 19:8522785-8522785 - TCGA-GF-A6C9-06 COSM4903604 c.328G>A p.G110R Substitution - Missense 19:8553436-8553436 - RW2982 COSM4649632 c.1288G>A p.G430S Substitution - Missense 19:8545718-8545718 - TCGA-AA-3510-01 COSM1397791 c.528C>T p.F176F Substitution - coding silent 19:8552141-8552141 - DLD1 COSM1680593 c.586C>T p.R196C Substitution - Missense 19:8552083-8552083 - TCGA-BR-8284-01 COSM3693250 c.88G>A p.E30K Substitution - Missense 19:8555712-8555712 - TCGA-CD-A4MI-01 COSM4083070 c.1450C>T p.Q484* Substitution - Nonsense 19:8544371-8544371 - SH-0622 COSM5018174 c.1792_1794delGAG p.E598delE Deletion - In frame 19:8536954-8536956 - Gp2D COSM2730510 c.1983C>T p.N661N Substitution - coding silent 19:8536312-8536312 - CHC155T COSM3668397 c.2981G>C p.R994P Substitution - Missense 19:8522703-8522703 - TCGA-EE-A3AA-06 COSM3541650 c.3224C>T p.P1075L Substitution - Missense 19:8521601-8521601 - 61 COSM5741394 c.1777C>T p.P593S Substitution - Missense 19:8536971-8536971 - PD9842a COSM1286451 c.1976C>T p.A659V Substitution - Missense 19:8536319-8536319 - TTC466 COSM4581600 c.3065G>A p.R1022H Substitution - Missense 19:8522532-8522532 - TCGA-B5-A0JY-01 COSM1003565 c.864C>T p.F288F Substitution - coding silent 19:8550602-8550602 - TCGA-CD-A4MG-01 COSM4083072 c.1399A>G p.T467A Substitution - Missense 19:8544422-8544422 - TCGA-C5-A2LX-01 COSM4827325 c.2871G>T p.G957G Substitution - coding silent 19:8522813-8522813 - pfg220T COSM4749620 c.943G>A p.G315R Substitution - Missense 19:8550318-8550318 - BN24T COSM1613113 c.2301G>A p.S767S Substitution - coding silent 19:8530223-8530223 - S02244 COSM5678188 c.2885C>T p.A962V Substitution - Missense 19:8522799-8522799 - TCGA-BR-8059-01 COSM1003558 c.1263C>T p.A421A Substitution - coding silent 19:8548042-8548042 - 430 COSM4433364 c.2150G>A p.R717Q Substitution - Missense 19:8530467-8530467 - TCGA-D3-A5GO-06 COSM3541664 c.1418G>A p.G473E Substitution - Missense 19:8544403-8544403 - TCGA-HU-A4GT-01 COSM1258540 c.1515C>T p.Y505Y Substitution - coding silent 19:8544306-8544306 - 4_PRE-TREATMENT COSM1724148 c.1787G>A p.W596* Substitution - Nonsense 19:8536961-8536961 - TCGA-BH-A0E6-01 COSM440692 c.2355G>A p.T785T Substitution - coding silent 19:8527457-8527457 - TCGA-A8-A07E-01 COSM440694 c.874G>A p.G292R Substitution - Missense 19:8550592-8550592 - TCGA-CZ-5457-01 COSM475509 c.2246G>A p.R749Q Substitution - Missense 19:8530278-8530278 - TCGA-AP-A051-01 COSM1003551 c.2245C>T p.R749W Substitution - Missense 19:8530279-8530279 - 12T COSM107013 c.1632C>T p.F544F Substitution - coding silent 19:8540007-8540007 - TCGA-EE-A3JD-06 COSM4396985 c.2159-1G>A p.? Unknown 19:8530366-8530366 - ML_103_T_01 COSM5033962 c.853A>G p.N285D Substitution - Missense 19:8550613-8550613 - TCGA-AZ-4315-01 COSM1003555 c.2079C>T p.F693F Substitution - coding silent 19:8530538-8530538 - T578 COSM4704930 c.2022C>A p.V674V Substitution - coding silent 19:8536273-8536273 - TCGA-BR-7959-01 COSM4083077 c.469G>A p.A157T Substitution - Missense 19:8553174-8553174 - CHEWS001 COSM4581602 c.873C>T p.D291D Substitution - coding silent 19:8550593-8550593 - TCGA-EE-A2GC-06 COSM3541658 c.1686G>A p.K562K Substitution - coding silent 19:8539953-8539953 - TCGA-IH-A3EA-01 COSM3541655 c.2637G>A p.V879V Substitution - coding silent 19:8526586-8526586 - TCGA-CM-6675-01 COSM1003561 c.1146C>T p.I382I Substitution - coding silent 19:8548273-8548273 - 1_RESISTANT COSM1719596 c.2007G>T p.M669I Substitution - Missense 19:8536288-8536288 - 2492721 COSM3541650 c.3224C>T p.P1075L Substitution - Missense 19:8521601-8521601 - CSB1 COSM5028467 c.1173G>A p.E391E Substitution - coding silent 19:8548246-8548246 - S02245 COSM1003569 c.446C>T p.P149L Substitution - Missense 19:8553197-8553197 - PTC-14C COSM4132813 c.1100A>C p.E367A Substitution - Missense 19:8550161-8550161 - TCGA-HU-A4GQ-01 COSM4083065 c.2204T>A p.I735N Substitution - Missense 19:8530320-8530320 - T3152 COSM4704928 c.2518G>A p.D840N Substitution - Missense 19:8526892-8526892 - TCGA-BR-8360-01 COSM4083080 c.201C>T p.T67T Substitution - coding silent 19:8554684-8554684 - ORL-48 COSM4596641 c.3223C>G p.P1075A Substitution - Missense 19:8521602-8521602 - TCGA-D3-A1Q6-06 COSM3541671 c.66G>A p.M22I Substitution - Missense 19:8555734-8555734 - TCGA-AR-A1AR-01 COSM440693 c.1917C>T p.P639P Substitution - coding silent 19:8536378-8536378 - 0006_CRUK_PC_0006_T4_DNA COSM3849590 c.571T>G p.L191V Substitution - Missense 19:8552098-8552098 - YUKAT COSM5391214 c.544C>G p.P182A Substitution - Missense 19:8552125-8552125 - TCGA-EK-A3GJ-01 COSM4852420 c.2140G>A p.E714K Substitution - Missense 19:8530477-8530477 - TCGA-BS-A0UV-01 COSM1003552 c.2217C>T p.F739F Substitution - coding silent 19:8530307-8530307 - HCC2998 COSM1003553 c.2188C>T p.R730W Substitution - Missense 19:8530336-8530336 - 2492720 COSM3541650 c.3224C>T p.P1075L Substitution - Missense 19:8521601-8521601 - TCGA-FW-A3R5-06 COSM3893956 c.2594G>A p.R865K Substitution - Missense 19:8526816-8526816 - CSCC-29-T COSM4536208 c.2277G>A p.R759R Substitution - coding silent 19:8530247-8530247 - C135 COSM4618012 c.1455G>T p.A485A Substitution - coding silent 19:8544366-8544366 - TCGA-ER-A42K-06 COSM3541657 c.2152G>A p.E718K Substitution - Missense 19:8530465-8530465 - CSCC-40-T COSM3541662 c.1552G>A p.E518K Substitution - Missense 19:8541964-8541964 - BRC47 COSM2730556 c.533G>A p.R178Q Substitution - Missense 19:8552136-8552136 - HCC2998 COSM1003553 c.2188C>T p.R730W Substitution - Missense 19:8530336-8530336 - PCSI_0009_Pa_X COSM3378898 c.1298G>A p.W433* Substitution - Nonsense 19:8545708-8545708 - 4436_PT COSM5755528 c.2780G>A p.R927Q Substitution - Missense 19:8525553-8525553 - BN24 COSM1613113 c.2301G>A p.S767S Substitution - coding silent 19:8530223-8530223 - AOCS-079-1-1 COSM4128015 c.613A>C p.R205R Substitution - coding silent 19:8552056-8552056 - TCGA-ER-A193-06 COSM3541670 c.141C>T p.F47F Substitution - coding silent 19:8555659-8555659 - 6P2-2 COSM3734366 c.2354C>G p.T785R Substitution - Missense 19:8527458-8527458 - TCGA-D3-A1Q7-06 COSM3541653 c.2981G>A p.R994Q Substitution - Missense 19:8522703-8522703 - 8016470 COSM3389525 c.2149C>T p.R717W Substitution - Missense 19:8530468-8530468 - TCGA-C4-A0F6-01 COSM418704 c.2888G>C p.R963T Substitution - Missense 19:8522796-8522796 - TCGA-DA-A1I1-06 COSM3893962 c.387G>A p.K129K Substitution - coding silent 19:8553377-8553377 - 53M COSM5594944 c.2913C>T p.I971I Substitution - coding silent 19:8522771-8522771 - TCGA-EE-A3AA-06 COSM2730527 c.1421G>A p.G474E Substitution - Missense 19:8544400-8544400 - sysucc-1315T COSM5480121 c.1269+6C>T p.? Unknown 19:8548030-8548030 - CSCC-5-T COSM4522193 c.114G>A p.R38R Substitution - coding silent 19:8555686-8555686 - B59-Tumor COSM1751279 c.535G>A p.G179S Substitution - Missense 19:8552134-8552134 - TCGA-HU-A4G9-01 COSM4083068 c.1945G>A p.E649K Substitution - Missense 19:8536350-8536350 - 587342 COSM1216387 c.1060G>T p.A354S Substitution - Missense 19:8550201-8550201 - TCGA-G4-6588-01 COSM1397786 c.1869C>T p.Y623Y Substitution - coding silent 19:8536528-8536528 - 443 COSM4434764 c.262G>A p.A88T Substitution - Missense 19:8554541-8554541 - TCGA-D3-A3MV-06 COSM475511 c.1534G>A p.D512N Substitution - Missense 19:8541982-8541982 - ME050T COSM230777 c.3101G>A p.R1034Q Substitution - Missense 19:8522496-8522496 - TCGA-HF-7132-01 COSM1003550 c.2292C>T p.F764F Substitution - coding silent 19:8530232-8530232 - DLD1 COSM4624176 c.2993G>A p.R998H Substitution - Missense 19:8522691-8522691 - T84 COSM2730564 c.207T>C p.R69R Substitution - coding silent 19:8554678-8554678 - TCGA-D1-A103-01 COSM1003566 c.753C>T p.S251S Substitution - coding silent 19:8551758-8551758 - 2492722 COSM5722808 c.1239C>T p.I413I Substitution - coding silent 19:8548066-8548066 - TCGA-P5-A5EV-01 COSM4420451 c.547G>C p.D183H Substitution - Missense 19:8552122-8552122 - 8057726 COSM2730530 c.1387G>A p.D463N Substitution - Missense 19:8544434-8544434 - 0006_CRUK_PC_0006_T1_DNA COSM3849590 c.571T>G p.L191V Substitution - Missense 19:8552098-8552098 - PT15_1 COSM5898009 c.2107G>A p.A703T Substitution - Missense 19:8530510-8530510 - PT49 COSM5936502 c.1246G>A p.E416K Substitution - Missense 19:8548059-8548059 - TCGA-CA-6717-01 COSM1397796 c.213C>T p.I71I Substitution - coding silent 19:8554672-8554672 - NB-1092 COSM1286453 c.3140G>A p.R1047Q Substitution - Missense 19:8522457-8522457 - T1154 COSM4704927 c.2927delG p.G976fs*85 Deletion - Frameshift 19:8522757-8522757 - TCGA-EB-A3XD-01 COSM3541652 c.3073G>A p.G1025R Substitution - Missense 19:8522524-8522524 - AOCS-137-3-7 COSM4128016 c.578A>T p.E193V Substitution - Missense 19:8552091-8552091 - TCGA-HU-A4HD-01 COSM4083073 c.1396G>A p.A466T Substitution - Missense 19:8544425-8544425 - TCGA-A4-A48D-01 COSM3990422 c.3G>C p.M1I Substitution - Missense 19:8577307-8577307 - ESCC_131 COSM5642216 c.107A>C p.N36T Substitution - Missense 19:8555693-8555693 - CSCC-40-T COSM4471865 c.1746C>T p.I582I Substitution - coding silent 19:8537002-8537002 - TCGA-EE-A3J7-06 COSM3893964 c.76C>T p.P26S Substitution - Missense 19:8555724-8555724 - 3N57-VS-3T57 COSM4983961 c.1623G>A p.R541R Substitution - coding silent 19:8540016-8540016 - CSCC-27-T COSM4495698 c.459C>T p.A153A Substitution - coding silent 19:8553184-8553184 - TCGA-B5-A11Y-01 COSM1003562 c.1087G>A p.D363N Substitution - Missense 19:8550174-8550174 - TCGA-EE-A2GJ-06 COSM3541666 c.1304C>T p.P435L Substitution - Missense 19:8545702-8545702 - PD4971a COSM5788314 c.1582C>T p.L528F Substitution - Missense 19:8541934-8541934 - HDC101 COSM4636010 c.941G>T p.S314I Substitution - Missense 19:8550320-8550320 - CHC155T COSM3668397 c.2981G>C p.R994P Substitution - Missense 19:8522703-8522703 - TCGA-AZ-4615-01 COSM5139701 c.1187_1188insA p.N396fs*13 Insertion - Frameshift 19:8548117-8548118 - TCGA-HT-8564-01 COSM3971390 c.1930C>T p.R644W Substitution - Missense 19:8536365-8536365 - TCGA-B5-A0JY-01 COSM1003568 c.462C>T p.F154F Substitution - coding silent 19:8553181-8553181 - 6T COSM3734366 c.2354C>G p.T785R Substitution - Missense 19:8527458-8527458 - PDA_034 COSM4999831 c.1937G>T p.R646L Substitution - Missense 19:8536358-8536358 - TCGA-D1-A17M-01 COSM1003570 c.402C>T p.G134G Substitution - coding silent 19:8553362-8553362 - 1_PRE-TREATMENT COSM1719596 c.2007G>T p.M669I Substitution - Missense 19:8536288-8536288 - CHC1211T COSM4954962 c.3254G>T p.G1085V Substitution - Missense 19:8521571-8521571 - HCT8 COSM4624176 c.2993G>A p.R998H Substitution - Missense 19:8522691-8522691 - Pat_31_B COSM5857166 c.2140delG p.E714fs*12 Deletion - Frameshift 19:8530477-8530477 - SC_9008 COSM1003561 c.1146C>T p.I382I Substitution - coding silent 19:8548273-8548273 - TCGA-33-4586-01 COSM715613 c.3253G>A p.G1085S Substitution - Missense 19:8521572-8521572 - CHEWS031 COSM4581601 c.1710G>A p.L570L Substitution - coding silent 19:8537038-8537038 - CSCC-56-T COSM230777 c.3101G>A p.R1034Q Substitution - Missense 19:8522496-8522496 - TCGA-AP-A056-01 COSM1003555 c.2079C>T p.F693F Substitution - coding silent 19:8530538-8530538 - CSCC-32-T COSM4455373 c.748A>C p.R250R Substitution - coding silent 19:8551763-8551763 - TCGA-RP-A694-06 COSM4894294 c.1301C>T p.T434I Substitution - Missense 19:8545705-8545705 - YULETA COSM3893962 c.387G>A p.K129K Substitution - coding silent 19:8553377-8553377 - LUAD-F00121 COSM365724 c.112C>A p.R38R Substitution - coding silent 19:8555688-8555688 - CSCC-10-T COSM4542950 c.3286G>A p.E1096K Substitution - Missense 19:8521539-8521539 - TCGA-FW-A3R5-06 COSM3893957 c.2043+1G>A p.? Unknown 19:8536251-8536251 - TCGA-24-1426-01 COSM119805 c.3158T>C p.V1053A Substitution - Missense 19:8522439-8522439 - TCGA-B8-4153-01 COSM475513 c.566A>G p.N189S Substitution - Missense 19:8552103-8552103 - PCSI_0528_Pa_P_526 COSM1003567 c.481C>T p.R161C Substitution - Missense 19:8553162-8553162 - T2944 COSM4704932 c.1657_1659delAAG p.K553delK Deletion - In frame 19:8539980-8539982 - YUSPO COSM5391212 c.1429C>A p.Q477K Substitution - Missense 19:8544392-8544392 - TCGA-BR-4184-01 COSM4083078 c.396C>T p.G132G Substitution - coding silent 19:8553368-8553368 - TCGA-39-5028-01 COSM715610 c.1870C>A p.R624S Substitution - Missense 19:8536527-8536527 - pfg007T COSM1641278 c.1864G>A p.A622T Substitution - Missense 19:8536533-8536533 - TCGA-EE-A181-06 COSM3541663 c.1496G>A p.G499D Substitution - Missense 19:8544325-8544325 - H_KA-426980-S_15631 COSM158646 c.1610+1G>A p.? Unknown 19:8541905-8541905 - TCGA-QB-A6FS-06 COSM3693250 c.88G>A p.E30K Substitution - Missense 19:8555712-8555712 - TCGA-22-4601-01 COSM715609 c.1700C>A p.A567D Substitution - Missense 19:8537048-8537048 - T3535 COSM4704934 c.1165G>A p.G389S Substitution - Missense 19:8548254-8548254 - TCGA-AY-6197-01 COSM715612 c.2251G>A p.E751K Substitution - Missense 19:8530273-8530273 - TCGA-A5-A0VP-01 COSM1003556 c.1675G>A p.A559T Substitution - Missense 19:8539964-8539964 - WA12 COSM237796 c.129C>T p.D43D Substitution - coding silent 19:8555671-8555671 - 2492720 COSM5722808 c.1239C>T p.I413I Substitution - coding silent 19:8548066-8548066 - 426980 COSM158646 c.1610+1G>A p.? Unknown 19:8541905-8541905 - TCGA-AA-3510-01 COSM283058 c.1194C>T p.F398F Substitution - coding silent 19:8548111-8548111 - TCGA-AO-A129-01 COSM440695 c.108C>A p.N36K Substitution - Missense 19:8555692-8555692 - ESO-539 COSM1258540 c.1515C>T p.Y505Y Substitution - coding silent 19:8544306-8544306 - TCGA-EE-A2GE-06 COSM3541662 c.1552G>A p.E518K Substitution - Missense 19:8541964-8541964 - CHC1055T COSM2730512 c.1973G>A p.R658Q Substitution - Missense 19:8536322-8536322 - 587238 COSM1216385 c.2116C>T p.R706C Substitution - Missense 19:8530501-8530501 - TCGA-BR-8372-01 COSM4083071 c.1412C>T p.T471M Substitution - Missense 19:8544409-8544409 - T3094 COSM4704935 c.852delG p.N285fs*37 Deletion - Frameshift 19:8550614-8550614 - Pat_15_B COSM5857167 c.2090C>T p.A697V Substitution - Missense 19:8530527-8530527 - T3024 COSM4704936 c.833C>T p.A278V Substitution - Missense 19:8550633-8550633 - T3502 COSM4704926 c.2980C>T p.R994* Substitution - Nonsense 19:8522704-8522704 - TCGA-CD-8531-01 COSM4083075 c.1129C>G p.Q377E Substitution - Missense 19:8548290-8548290 - ESCC-129T COSM3938390 c.2874G>T p.V958V Substitution - coding silent 19:8522810-8522810 - TCGA-HU-A4H3-01 COSM4083081 c.93C>T p.D31D Substitution - coding silent 19:8555707-8555707 - CSCC-1-T COSM4470037 c.1635C>T p.P545P Substitution - coding silent 19:8540004-8540004 - LUAD-S01315 COSM344757 c.1074T>C p.Y358Y Substitution - coding silent 19:8550187-8550187 - TCGA-EE-A2MR-06 COSM3541668 c.817G>A p.V273I Substitution - Missense 19:8550649-8550649 - TCGA-B0-5119-01 COSM475508 c.2471T>A p.L824H Substitution - Missense 19:8527341-8527341 - TCGA-BS-A0UJ-01 COSM1003560 c.1195G>A p.E399K Substitution - Missense 19:8548110-8548110 - TCGA-BR-4184-01 COSM1129669 c.1663C>T p.R555C Substitution - Missense 19:8539976-8539976 - TCGA-EE-A2MR-06 COSM3541666 c.1304C>T p.P435L Substitution - Missense 19:8545702-8545702 - TCGA-CD-A4MI-01 COSM4083079 c.230C>T p.A77V Substitution - Missense 19:8554655-8554655 - sysucc-1397T COSM5474255 c.231+6G>A p.? Unknown 19:8554648-8554648 - B59 COSM1751279 c.535G>A p.G179S Substitution - Missense 19:8552134-8552134 - sysucc-880T COSM5462932 c.1565A>G p.D522G Substitution - Missense 19:8541951-8541951 - BD110T COSM5514345 c.740C>T p.T247M Substitution - Missense 19:8551771-8551771 - TCGA-AC-A23H-01 COSM3836204 c.852G>A p.G284G Substitution - coding silent 19:8550614-8550614 - LP6005334-DNA_A04 COSM4412193 c.3055C>A p.Q1019K Substitution - Missense 19:8522542-8522542 - S02255 COSM5680636 c.1522A>G p.K508E Substitution - Missense 19:8544299-8544299 - TCGA-B5-A11E-01 COSM1003567 c.481C>T p.R161C Substitution - Missense 19:8553162-8553162 - 4_RESISTANT COSM1724148 c.1787G>A p.W596* Substitution - Nonsense 19:8536961-8536961 - 40M COSM5585852 c.615G>A p.R205R Substitution - coding silent 19:8552054-8552054 - TCGA-CJ-5671-01 COSM475510 c.1796A>G p.N599S Substitution - Missense 19:8536952-8536952 - 587316 COSM1216386 c.2381G>A p.R794Q Substitution - Missense 19:8527431-8527431 - CRC-19T COSM5481578 c.1922C>T p.T641M Substitution - Missense 19:8536373-8536373 - CSCC-17-T COSM4475075 c.1960C>T p.Q654* Substitution - Nonsense 19:8536335-8536335 - TCGA-AA-3663-01 COSM1397794 c.266T>C p.L89P Substitution - Missense 19:8554537-8554537 - B89-4 COSM1751278 c.2296G>A p.D766N Substitution - Missense 19:8530228-8530228 - TCGA-BR-8591-01 COSM3693250 c.88G>A p.E30K Substitution - Missense 19:8555712-8555712 - LUAD-S01413 COSM347121 c.1307T>A p.I436N Substitution - Missense 19:8545699-8545699 - TCGA-EB-A5UN-06 COSM3541661 c.1648G>A p.G550R Substitution - Missense 19:8539991-8539991 - HCC94 COSM1003548 c.3227C>T p.S1076L Substitution - Missense 19:8521598-8521598 - TCGA-18-3409-01 COSM715612 c.2251G>A p.E751K Substitution - Missense 19:8530273-8530273 - PD7067a COSM2730568 c.118C>T p.R40C Substitution - Missense 19:8555682-8555682 - PCSI_0021_Pa_X COSM3378897 c.1611G>A p.Q537Q Substitution - coding silent 19:8540028-8540028 - TCGA-A5-A0VP-01 COSM1003564 c.882C>T p.Y294Y Substitution - coding silent 19:8550584-8550584 - ESO-0103 COSM1258541 c.589G>A p.V197M Substitution - Missense 19:8552080-8552080 - ESCC_129 COSM5641833 c.2065C>A p.R689R Substitution - coding silent 19:8530552-8530552 - TCGA-AX-A0J1-01 COSM1003558 c.1263C>T p.A421A Substitution - coding silent 19:8548042-8548042 - TCGA-EI-7002-01 COSM1003562 c.1087G>A p.D363N Substitution - Missense 19:8550174-8550174 - TCGA-B5-A11E-01 COSM1003553 c.2188C>T p.R730W Substitution - Missense 19:8530336-8530336 - TCGA-FW-A3R5-06 COSM3893960 c.1329C>T p.V443V Substitution - coding silent 19:8545677-8545677 - QC2-25-T2 COSM5653385 c.141+10G>T p.? Unknown 19:8555649-8555649 - CSCC-27-T COSM4458464 c.1086C>T p.F362F Substitution - coding silent 19:8550175-8550175 - TCGA-K4-A3WU-01 COSM3797717 c.2506G>C p.E836Q Substitution - Missense 19:8526904-8526904 - TARGET-30-PARMPP COSM1286451 c.1976C>T p.A659V Substitution - Missense 19:8536319-8536319 - CDGLIV0707A0251_T COSM5041725 c.434T>A p.L145Q Substitution - Missense 19:8553209-8553209 - TCGA-G2-A3IE-01 COSM1305328 c.876G>A p.G292G Substitution - coding silent 19:8550590-8550590 - ESO-717 COSM1242549 c.1704C>T p.N568N Substitution - coding silent 19:8537044-8537044 - TCGA-EE-A181-06 COSM1003566 c.753C>T p.S251S Substitution - coding silent 19:8551758-8551758 - 2492723 COSM5722808 c.1239C>T p.I413I Substitution - coding silent 19:8548066-8548066 - 49M COSM4704925 c.3270C>T p.F1090F Substitution - coding silent 19:8521555-8521555 - CSCC-19-T COSM4563528 c.978G>A p.M326I Substitution - Missense 19:8550283-8550283 - OSCC-GB_00690111 COSM4887097 c.2990C>A p.A997E Substitution - Missense 19:8522694-8522694 - TCGA-76-6661-01 COSM180084 c.744C>T p.D248D Substitution - coding silent 19:8551767-8551767 - TCGA-EJ-5532-01 COSM1129669 c.1663C>T p.R555C Substitution - Missense 19:8539976-8539976 - PD6422a COSM1613112 c.2721C>A p.G907G Substitution - coding silent 19:8526502-8526502 - TARGET-30-PASTCN COSM1286452 c.2010G>C p.G670G Substitution - coding silent 19:8536285-8536285 - TCGA-BR-8680-01 COSM283058 c.1194C>T p.F398F Substitution - coding silent 19:8548111-8548111 - BN45T COSM1613112 c.2721C>A p.G907G Substitution - coding silent 19:8526502-8526502 - HCT15 COSM4624176 c.2993G>A p.R998H Substitution - Missense 19:8522691-8522691 - 2296_T COSM3960727 c.2116C>G p.R706G Substitution - Missense 19:8530501-8530501 - CSCC-62-T COSM4484554 c.2823C>T p.A941A Substitution - coding silent 19:8525510-8525510 - TCGA-HT-7855-01 COSM3971391 c.103G>A p.A35T Substitution - Missense 19:8555697-8555697 - TCGA-AA-3502-01 COSM3693249 c.1096G>A p.V366M Substitution - Missense 19:8550165-8550165 - TCGA-BP-4992-01 COSM475511 c.1534G>A p.D512N Substitution - Missense 19:8541982-8541982 - OSCC-GB_00270111 COSM3713101 c.658G>T p.E220* Substitution - Nonsense 19:8551853-8551853 - 2492721 COSM5722808 c.1239C>T p.I413I Substitution - coding silent 19:8548066-8548066 - TCGA-BR-8360-01 COSM1258541 c.589G>A p.V197M Substitution - Missense 19:8552080-8552080 - TCGA-EV-5902-01 COSM3990420 c.1426G>T p.D476Y Substitution - Missense 19:8544395-8544395 - 631052 COSM321890 c.1363C>A p.P455T Substitution - Missense 19:8544458-8544458 - 4436_CLM COSM5755528 c.2780G>A p.R927Q Substitution - Missense 19:8525553-8525553 - HCC46T COSM3707548 c.599A>C p.Q200P Substitution - Missense 19:8552070-8552070 - TCGA-BS-A0UV-01 COSM283058 c.1194C>T p.F398F Substitution - coding silent 19:8548111-8548111 - RK308_C01 COSM3743209 c.1102-4G>A p.? Unknown 19:8548321-8548321 - KM12 COSM2730485 c.2809A>C p.R937R Substitution - coding silent 19:8525524-8525524 - WA17 COSM240801 c.1748G>A p.R583H Substitution - Missense 19:8537000-8537000 - HCT-15 COSM1680593 c.586C>T p.R196C Substitution - Missense 19:8552083-8552083 - TCGA-G4-6298-01 COSM1003551 c.2245C>T p.R749W Substitution - Missense 19:8530279-8530279 - TCGA-BG-A0MQ-01 COSM1003557 c.1407C>T p.H469H Substitution - coding silent 19:8544414-8544414 - CHC1211T COSM4954962 c.3254G>T p.G1085V Substitution - Missense 19:8521571-8521571 - ESCC_BICR_031T COSM5441080 c.3040G>A p.G1014S Substitution - Missense 19:8522644-8522644 - CSCC-30-T COSM1397793 c.284G>A p.R95Q Substitution - Missense 19:8554519-8554519 - TCGA-CA-6717-01 COSM1003550 c.2292C>T p.F764F Substitution - coding silent 19:8530232-8530232 - T3498 COSM4704931 c.1973G>T p.R658L Substitution - Missense 19:8536322-8536322 - 2159 COSM5013358 c.3119G>T p.R1040L Substitution - Missense 19:8522478-8522478 - PD11336a COSM2730520 c.1767G>A p.E589E Substitution - coding silent 19:8536981-8536981 - T578 COSM4704925 c.3270C>T p.F1090F Substitution - coding silent 19:8521555-8521555 - TCGA-AA-3663-01 COSM1397782 c.3138C>T p.C1046C Substitution - coding silent 19:8522459-8522459 - LC_S45 COSM1189819 c.1289G>T p.G430V Substitution - Missense 19:8545717-8545717 - TCGA-DM-A28M-01 COSM3693248 c.1854A>C p.R618S Substitution - Missense 19:8536543-8536543 - ESCC_4 COSM5622823 c.2028C>G p.V676V Substitution - coding silent 19:8536267-8536267 - 35M COSM5581785 c.2287G>A p.D763N Substitution - Missense 19:8530237-8530237 - TCGA-B5-A11E-01 COSM1003554 c.2139C>T p.Y713Y Substitution - coding silent 19:8530478-8530478 - TCGA-C5-A1MH-01 COSM4820829 c.130G>A p.D44N Substitution - Missense 19:8555670-8555670 - GHE0415 COSM5480121 c.1269+6C>T p.? Unknown 19:8548030-8548030 - TCGA-AD-6889-01 COSM1397797 c.151G>A p.G51S Substitution - Missense 19:8554734-8554734 - TCGA-AP-A056-01 COSM1003559 c.1215C>T p.F405F Substitution - coding silent 19:8548090-8548090 - CHEWS025 COSM4581599 c.3126T>C p.H1042H Substitution - coding silent 19:8522471-8522471 - TCGA-AB-2815-03 COSM1318226 c.1001G>T p.S334I Substitution - Missense 19:8550260-8550260 - PT35 COSM5914142 c.2059G>A p.E687K Substitution - Missense 19:8530558-8530558 - 0081_CRUK_PC_0081_T1_DNA COSM3971390 c.1930C>T p.R644W Substitution - Missense 19:8536365-8536365 - MN-298 COSM1578779 c.250C>T p.P84S Substitution - Missense 19:8554553-8554553 - S00936 COSM313058 c.946C>T p.R316* Substitution - Nonsense 19:8550315-8550315 - TCGA-CM-6171-01 COSM1397795 c.251delC p.P84fs*145 Deletion - Frameshift 19:8554552-8554552 - TCGA-FW-A3R5-06 COSM3893955 c.2825C>T p.P942L Substitution - Missense 19:8525508-8525508 - TCGA-BQ-5889-01 COSM3990419 c.1658A>C p.K553T Substitution - Missense 19:8539981-8539981 - TCGA-F1-6177-01 COSM4083069 c.1492G>A p.A498T Substitution - Missense 19:8544329-8544329 - 21 COSM4557876 c.745G>A p.D249N Substitution - Missense 19:8551766-8551766 - TCGA-FW-A3R5-06 COSM3893961 c.792G>A p.G264G Substitution - coding silent 19:8550674-8550674 - SNUH_G47_S1 COSM4001059 c.232-6T>C p.? Unknown 19:8554577-8554577 - Pat_45_B COSM5857165 c.2185G>A p.E729K Substitution - Missense 19:8530339-8530339 - 27T COSM3713101 c.658G>T p.E220* Substitution - Nonsense 19:8551853-8551853 - ESO-1670 COSM1258542 c.1327G>A p.V443I Substitution - Missense 19:8545679-8545679 - TCGA-23-1123-01 COSM75532 c.45G>C p.K15N Substitution - Missense 19:8555755-8555755 - LP6005334-DNA_C03 COSM1258540 c.1515C>T p.Y505Y Substitution - coding silent 19:8544306-8544306 - B89-4-Tumor COSM1751278 c.2296G>A p.D766N Substitution - Missense 19:8530228-8530228 - HT115 COSM2730568 c.118C>T p.R40C Substitution - Missense 19:8555682-8555682 - CSCC-55-T COSM4289030 c.1881C>T p.F627F Substitution - coding silent 19:8536516-8536516 - YURAY COSM5391213 c.585C>T p.S195S Substitution - coding silent 19:8552084-8552084 - TCGA-BR-4184-01 COSM4083067 c.2094A>G p.R698R Substitution - coding silent 19:8530523-8530523 - NB-1744 COSM1286450 c.1026C>T p.N342N Substitution - coding silent 19:8550235-8550235 - TCGA-EI-6917-01 COSM3423372 c.1542C>T p.S514S Substitution - coding silent 19:8541974-8541974 - LP6007404-DNA_A01 COSM4416429 c.1537G>A p.V513I Substitution - Missense 19:8541979-8541979 - ESO-0023 COSM1258540 c.1515C>T p.Y505Y Substitution - coding silent 19:8544306-8544306 - 2492723 COSM3541650 c.3224C>T p.P1075L Substitution - Missense 19:8521601-8521601 - HCT15 COSM2730543 c.920C>T p.A307V Substitution - Missense 19:8550341-8550341 - TCGA-FW-A3R5-06 COSM3893959 c.1456G>A p.A486T Substitution - Missense 19:8544365-8544365 - TCGA-BP-4352-01 COSM3363088 c.1226A>T p.K409M Substitution - Missense 19:8548079-8548079 - sysucc-882T COSM1258541 c.589G>A p.V197M Substitution - Missense 19:8552080-8552080 - SNUH_G76_S1 COSM4001059 c.232-6T>C p.? Unknown 19:8554577-8554577 - CHC1055T COSM2730512 c.1973G>A p.R658Q Substitution - Missense 19:8536322-8536322 - T2944 COSM1258541 c.589G>A p.V197M Substitution - Missense 19:8552080-8552080 - TCGA-24-1604-01 COSM82256 c.726C>T p.Y242Y Substitution - coding silent 19:8551785-8551785 - TCGA-DK-A3IQ-01 COSM1305329 c.517G>C p.E173Q Substitution - Missense 19:8552152-8552152 - HCC46 COSM3707548 c.599A>C p.Q200P Substitution - Missense 19:8552070-8552070 - TCGA-BR-8367-01 COSM4083076 c.1111C>T p.R371C Substitution - Missense 19:8548308-8548308 - TCGA-BS-A0UF-01 COSM1003563 c.997C>T p.R333C Substitution - Missense 19:8550264-8550264 - TCGA-FW-A3R5-06 COSM3893958 c.1940G>A p.G647E Substitution - Missense 19:8536355-8536355 - sysucc-880T COSM5462933 c.1483A>G p.S495G Substitution - Missense 19:8544338-8544338 - TCGA-G4-6302-01 COSM3693250 c.88G>A p.E30K Substitution - Missense 19:8555712-8555712 - ZZUFHECRKL-G047T COSM5433875 c.3139C>T p.R1047W Substitution - Missense 19:8522458-8522458 - TCGA-FW-A3R5-06 COSM3893963 c.270G>A p.T90T Substitution - coding silent 19:8554533-8554533 - Pat_40_B COSM4704926 c.2980C>T p.R994* Substitution - Nonsense 19:8522704-8522704 - TCGA-B5-A0JY-01 COSM1003549 c.2300C>T p.S767L Substitution - Missense 19:8530224-8530224 - TCGA-FJ-A3ZE-01 COSM3797718 c.1380C>T p.V460V Substitution - coding silent 19:8544441-8544441 - TCGA-66-2763-01 COSM715611 c.2053C>A p.L685M Substitution - Missense 19:8530564-8530564 - TCGA-D3-A3MU-06 COSM3541656 c.2396A>C p.K799T Substitution - Missense 19:8527416-8527416 - 227 COSM4425971 c.1378G>A p.V460I Substitution - Missense 19:8544443-8544443 - Gp5D COSM2730510 c.1983C>T p.N661N Substitution - coding silent 19:8536312-8536312 - CSCC-62-T COSM2730560 c.403G>A p.E135K Substitution - Missense 19:8553361-8553361 - TCGA-EE-A29D-06 COSM3541659 c.1668C>T p.P556P Substitution - coding silent 19:8539971-8539971 - PA285 COSM1163210 c.1612G>A p.A538T Substitution - Missense 19:8540027-8540027 - TCGA-B5-A11N-01 COSM1003550 c.2292C>T p.F764F Substitution - coding silent 19:8530232-8530232 - T578 COSM1003567 c.481C>T p.R161C Substitution - Missense 19:8553162-8553162 - 1517_PT COSM5755529 c.1034A>G p.Q345R Substitution - Missense 19:8550227-8550227 - T3225 COSM4704933 c.1417G>A p.G473R Substitution - Missense 19:8544404-8544404 - LP6005935-DNA_F01 COSM4879766 c.2318G>A p.R773H Substitution - Missense 19:8530206-8530206 - TCGA-AB-3002-03 COSM158646 c.1610+1G>A p.? Unknown 19:8541905-8541905 - TCGA-DM-A282-01 COSM1397784 c.2527C>A p.L843M Substitution - Missense 19:8526883-8526883 - TCGA-EE-A3J5-06 COSM3541665 c.1345G>A p.E449K Substitution - Missense 19:8545661-8545661 - TCGA-EJ-7125-01 COSM3673057 c.2052C>A p.L684L Substitution - coding silent 19:8530565-8530565 - TCGA-CM-4743-01 COSM1397793 c.284G>A p.R95Q Substitution - Missense 19:8554519-8554519 - TCGA-AA-A010-01 COSM283058 c.1194C>T p.F398F Substitution - coding silent 19:8548111-8548111 - TCGA-D3-A1Q5-06 COSM3541657 c.2152G>A p.E718K Substitution - Missense 19:8530465-8530465 - S02139 COSM5674308 c.2919T>A p.S973S Substitution - coding silent 19:8522765-8522765 - CSCC-20-T COSM4557876 c.745G>A p.D249N Substitution - Missense 19:8551766-8551766 - Pat_24_A COSM5857169 c.886C>T p.R296* Substitution - Nonsense 19:8550580-8550580 - T2417 COSM4704929 c.2313C>T p.Y771Y Substitution - coding silent 19:8530211-8530211 - TCGA-DS-A1OC-01 COSM1293920 c.930G>T p.L310L Substitution - coding silent 19:8550331-8550331 - Pat_63_B COSM5857170 c.271G>A p.D91N Substitution - Missense 19:8554532-8554532 - BD152T COSM5506523 c.1027G>A p.V343M Substitution - Missense 19:8550234-8550234 - B37-Tumor COSM1751277 c.2506G>A p.E836K Substitution - Missense 19:8526904-8526904 - TCGA-DM-A1HA-01 COSM1397787 c.1454C>T p.A485V Substitution - Missense 19:8544367-8544367 - TCGA-F5-6814-01 COSM1216385 c.2116C>T p.R706C Substitution - Missense 19:8530501-8530501 - TCGA-IR-A3LH-01 COSM4832995 c.643G>T p.E215* Substitution - Nonsense 19:8551868-8551868 - ESO-717 COSM1242550 c.1992C>T p.P664P Substitution - coding silent 19:8536303-8536303 - PT37 COSM3990419 c.1658A>C p.K553T Substitution - Missense 19:8539981-8539981 - B37 COSM1751277 c.2506G>A p.E836K Substitution - Missense 19:8526904-8526904 - Pat_63_B COSM5857168 c.1927C>T p.P643S Substitution - Missense 19:8536368-8536368 - AOCS-080-1-9 COSM4128014 c.3221-7C>A p.? Unknown 19:8521611-8521611 - C086 COSM5535078 c.331G>A p.E111K Substitution - Missense 19:8553433-8553433 - TCGA-AP-A0LM-01 COSM1003569 c.446C>T p.P149L Substitution - Missense 19:8553197-8553197 - TCGA-FP-A4BE-01 COSM2730500 c.2218G>A p.V740I Substitution - Missense 19:8530306-8530306 - CSB2 COSM5028468 c.717G>A p.S239S Substitution - coding silent 19:8551794-8551794 - TCGA-E9-A1R4-01 COSM1481691 c.2969G>C p.G990A Substitution - Missense 19:8522715-8522715 - T3048 COSM1003564 c.882C>T p.Y294Y Substitution - coding silent 19:8550584-8550584 - 1N56-VS-1T56 COSM4977199 c.834G>A p.A278A Substitution - coding silent 19:8550632-8550632 - TCGA-D3-A3MR-06 COSM3541667 c.891G>A p.V297V Substitution - coding silent 19:8550575-8550575 - 6P2-1 COSM3734366 c.2354C>G p.T785R Substitution - Missense 19:8527458-8527458 - T3174 COSM4433364 c.2150G>A p.R717Q Substitution - Missense 19:8530467-8530467 - TCGA-AP-A056-01 COSM1003561 c.1146C>T p.I382I Substitution - coding silent 19:8548273-8548273 - YUGEMA COSM5391211 c.1644G>A p.L548L Substitution - coding silent 19:8539995-8539995 - TCGA-EE-A3J5-06 COSM3541669 c.450G>A p.L150L Substitution - coding silent 19:8553193-8553193 - HCT8 COSM1680593 c.586C>T p.R196C Substitution - Missense 19:8552083-8552083 - TCGA-AP-A059-01 COSM1003548 c.3227C>T p.S1076L Substitution - Missense 19:8521598-8521598 - PD9571a COSM5795157 c.1295G>A p.R432H Substitution - Missense 19:8545711-8545711 - YUROG COSM3541653 c.2981G>A p.R994Q Substitution - Missense 19:8522703-8522703 - 509LT COSM4382237 c.500G>A p.R167H Substitution - Missense 19:8553143-8553143 - SC_9093 COSM5570455 c.2777C>T p.T926M Substitution - Missense 19:8525556-8525556 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.465813;Hs.465818 19p13.3-p13.2 601480 1532696|dbSNP|BC028071|C/T|non-coding||3605|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.L989P c.2966T>C 19 8587602 CM A G Missense p.V1053A c.3158T>C 19 8587323 OV A G Synonymous p.F696F c.2088T>C 19 8595413 LUAD A T Missense p.C577S c.1729T>A 19 8601903 CM A T Missense p.L824H c.2471T>A 19 8592225 RCCC C A Missense p.R730L c.2189G>T 19 8595219 LUAD CC TT Missense p.E686K c.2055_2056delinsAA 19 8595445 CM CC TT Missense p.V244M c.729_730delinsAA 19 8616665 CM C G Missense p.E173Q c.517G>C 19 8617036 BLCA C G Missense p.E204Q c.610G>C 19 8616943 HNSC C G Missense p.E70D c.210G>C 19 8619559 LUAD C G Missense p.G990A c.2969G>C 19 8587599 BRCA C G Missense p.K15N c.45G>C 19 8620639 OV C G Missense p.R618T c.1853G>C 19 8601428 HNSC C G Missense p.R963T c.2888G>C 19 8587680 BLCA C G Synonymous p.G670G c.2010G>C 19 8601169 NB C G Synonymous p.L531L c.1593G>C 19 8606807 HNSC C G Synonymous p.V118V c.354G>C 19 8618294 HNSC C T Missense p.A498T c.1492G>A 19 8609213 STAD C T Missense p.A559T c.1675G>A 19 8604848 UCEC C T Missense p.A622T c.1864G>A 19 8601417 STAD C T Missense p.D249N c.745G>A 19 8616650 CM C T Missense p.D512N c.1534G>A 19 8606866 CM C T Missense p.D512N c.1534G>A 19 8606866 RCCC C T Missense p.E1002K c.3004G>A 19 8587564 CM C T Missense p.E1002K c.3004G>A 19 8587564 HNSC C T Missense p.E1059K c.3175G>A 19 8587306 CM C T Missense p.E1066K c.3196G>A 19 8587285 CM C T Missense p.E449K c.1345G>A 19 8610545 CM C T Missense p.E518K c.1552G>A 19 8606848 CM C T Missense p.E640K c.1918G>A 19 8601261 CM C T Missense p.E718K c.2152G>A 19 8595349 CM C T Missense p.E81K c.241G>A 19 8619446 HNSC C T Missense p.G1085S c.3253G>A 19 8586456 LUSC C T Missense p.G264E c.791G>A 19 8615559 CM C T Missense p.G292R c.874G>A 19 8615476 BRCA C T Missense p.G474E c.1421G>A 19 8609284 CM C T Missense p.G499D c.1496G>A 19 8609209 CM C T Missense p.G800R c.2398G>A 19 8592298 CM C T Missense p.G804S c.2410G>A 19 8592286 CM C T Missense p.G908S c.2722G>A 19 8591385 LUAD C T Missense p.M22I c.66G>A 19 8620618 CM C T Missense p.R1047Q c.3140G>A 19 8587341 NB C T Missense p.R178Q c.533G>A 19 8617020 BRCA C T Missense p.R205K c.614G>A 19 8616939 CM C T Missense p.R749Q c.2246G>A 19 8595162 RCCC C T Missense p.R761Q c.2282G>A 19 8595126 MM C T Missense p.R994Q c.2981G>A 19 8587587 CM C T Missense p.V197M c.589G>A 19 8616964 ESCA C T Missense p.V443I c.1327G>A 19 8610563 ESCA C T Nonsense p.W496* c.1488G>A 19 8609217 LUSC C T SpliceAcceptorSNV . c.2159-1G>A 19 8595250 CM C T SpliceDonorSNV . c.1610+1G>A 19 8606789 AML C T Synonymous p.E391E c.1173G>A 19 8613130 BRCA C T Synonymous p.E718E c.2154G>A 19 8595347 CM C T Synonymous p.G292G c.876G>A 19 8615474 BLCA C T Synonymous p.K129K c.387G>A 19 8618261 CM C T Synonymous p.K562K c.1686G>A 19 8604837 CM C T Synonymous p.K677K c.2031G>A 19 8601148 CM C T Synonymous p.K928K c.2784G>A 19 8590433 CM C T Synonymous p.L150L c.450G>A 19 8618077 CM C T Synonymous p.S239S c.717G>A 19 8616678 BRCA C T Synonymous p.T785T c.2355G>A 19 8592341 BRCA C T Synonymous p.V297V c.891G>A 19 8615459 CM C T Synonymous p.V879V c.2637G>A 19 8591470 CM G A Missense p.A659V c.1976C>T 19 8601203 NB G A Missense p.P1075L c.3224C>T 19 8586485 CM G A Missense p.P26S c.76C>T 19 8620608 CM G A Missense p.P435L c.1304C>T 19 8610586 CM G A Missense p.R555C c.1663C>T 19 8604860 PRAD G A Missense p.T256I c.767C>T 19 8616628 CM G A Nonsense p.R316* c.946C>T 19 8615199 SCLC G A Synonymous p.D245D c.735C>T 19 8616660 HNSC G A Synonymous p.D248D c.744C>T 19 8616651 GBM G A Synonymous p.F154F c.462C>T 19 8618065 HNSC G A Synonymous p.F405F c.1215C>T 19 8612974 CM G A Synonymous p.F47F c.141C>T 19 8620543 CM G A Synonymous p.G134G c.402C>T 19 8618246 UCEC G A Synonymous p.H469H c.1407C>T 19 8609298 UCEC G A Synonymous p.L276L c.828C>T 19 8615522 CM G A Synonymous p.N1063N c.3189C>T 19 8587292 LUAD G A Synonymous p.N342N c.1026C>T 19 8615119 NB G A Synonymous p.P639P c.1917C>T 19 8601262 BRCA G A Synonymous p.S251S c.753C>T 19 8616642 CM G A Synonymous p.Y242Y c.726C>T 19 8616669 OV G A Synonymous p.Y294Y c.882C>T 19 8615468 UCEC GG AA Missense p.R432C c.1293_1294delinsTT 19 8610596 CM G T Missense p.A567D c.1700C>A 19 8601932 LUSC G T Missense p.L685M c.2053C>A 19 8595448 LUSC G T Missense p.N36K c.108C>A 19 8620576 BRCA G T Missense p.P455T c.1363C>A 19 8609342 SCLC G T Missense p.P959T c.2875C>A 19 8587693 BRCA G T Missense p.R624S c.1870C>A 19 8601411 LUSC G T Synonymous p.R594R c.1780C>A 19 8601852 LUAD T A Missense p.K409M c.1226A>T 19 8612963 RCCC T A Missense p.T926S c.2776A>T 19 8590441 LUAD T G 5-UTRSNV . c.1-3A>C 19 8642196 CM T G Missense p.K799T c.2396A>C 19 8592300 CM T G Synonymous p.R615R c.1843A>C 19 8601438 LUAD