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 5 176638620 176638620 + Missense_Mutation SNP C C T TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr5:176638620C>T c.3220C>T c.(3220-3222)Cgt>Tgt p.R1074C ACC 5 176687121 176687121 + Nonsense_Mutation SNP C C T TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr5:176687121C>T c.5098C>T c.(5098-5100)Cga>Tga p.R1700* ACC 5 176722232 176722233 + In_Frame_Ins INS - - CAA TCGA-OR-A5J7-01A-11D-A29I-10 TCGA-OR-A5J7-10A-01D-A29L-10 g.chr5:176722232_176722233insCAA c.7863_7864insCAA c.(7864-7866)caa>CAAcaa p.2622_2622Q>QQ BLCA 5 176562542 176562542 + Silent SNP C C T TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr5:176562542C>T c.438C>T c.(436-438)atC>atT p.I146I BLCA 5 176562564 176562564 + Missense_Mutation SNP G G C TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr5:176562564G>C c.460G>C c.(460-462)Gag>Cag p.E154Q BLCA 5 176562585 176562585 + Missense_Mutation SNP G G A TCGA-DK-AA76-01A-11D-A391-08 TCGA-DK-AA76-10A-01D-A394-08 g.chr5:176562585G>A c.481G>A c.(481-483)Gat>Aat p.D161N BLCA 5 176562709 176562709 + Missense_Mutation SNP G G A TCGA-CU-A0YR-01A-12D-A10S-08 TCGA-CU-A0YR-10A-01D-A10S-08 g.chr5:176562709G>A c.605G>A c.(604-606)gGt>gAt p.G202D BLCA 5 176636970 176636970 + Missense_Mutation SNP G G A TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr5:176636970G>A c.1570G>A c.(1570-1572)Gaa>Aaa p.E524K BLCA 5 176637121 176637122 + Frame_Shift_Ins INS - - A TCGA-XF-AAMJ-01A-11D-A42E-08 TCGA-XF-AAMJ-10A-01D-A42H-08 g.chr5:176637121_176637122insA c.1721_1722insA c.(1720-1725)ggaaaafs p.GK574fs BLCA 5 176637349 176637349 + Missense_Mutation SNP A A G TCGA-KQ-A41N-01A-11D-A339-08 TCGA-KQ-A41N-10D-01D-A339-08 g.chr5:176637349A>G c.1949A>G c.(1948-1950)gAt>gGt p.D650G BLCA 5 176637515 176637516 + Frame_Shift_Ins INS - - A TCGA-XF-A9T2-01A-11D-A42E-08 TCGA-XF-A9T2-10A-01D-A42H-08 g.chr5:176637515_176637516insA c.2115_2116insA c.(2116-2118)aacfs p.N706fs BLCA 5 176637763 176637763 + Missense_Mutation SNP G G C TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr5:176637763G>C c.2363G>C c.(2362-2364)cGa>cCa p.R788P BLCA 5 176637917 176637917 + Silent SNP G G A TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr5:176637917G>A c.2517G>A c.(2515-2517)ctG>ctA p.L839L BLCA 5 176638319 176638319 + Missense_Mutation SNP G G C TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr5:176638319G>C c.2919G>C c.(2917-2919)caG>caC p.Q973H BLCA 5 176638752 176638752 + Missense_Mutation SNP G G A TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr5:176638752G>A c.3352G>A c.(3352-3354)Gat>Aat p.D1118N BLCA 5 176638788 176638788 + Missense_Mutation SNP G G C TCGA-G2-A2EL-01A-12D-A18F-08 TCGA-G2-A2EL-10A-01D-A18F-08 g.chr5:176638788G>C c.3388G>C c.(3388-3390)Gaa>Caa p.E1130Q BLCA 5 176639086 176639086 + Missense_Mutation SNP C C T TCGA-FD-A6TD-01A-51D-A339-08 TCGA-FD-A6TD-10A-21D-A339-08 g.chr5:176639086C>T c.3686C>T c.(3685-3687)tCa>tTa p.S1229L BLCA 5 176665484 176665484 + Missense_Mutation SNP G G C TCGA-FD-A3SP-01A-31D-A22Z-08 TCGA-FD-A3SP-10A-01D-A22Z-08 g.chr5:176665484G>C c.4168G>C c.(4168-4170)Gag>Cag p.E1390Q BLCA 5 176666836 176666836 + Silent SNP C C G TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr5:176666836C>G c.4272C>G c.(4270-4272)ccC>ccG p.P1424P BLCA 5 176684035 176684035 + Missense_Mutation SNP G G A TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr5:176684035G>A c.4849G>A c.(4849-4851)Gaa>Aaa p.E1617K BLCA 5 176684067 176684068 + Frame_Shift_Ins INS - - A TCGA-ZF-A9R9-01A-11D-A38G-08 TCGA-ZF-A9R9-10A-01D-A38J-08 g.chr5:176684067_176684068insA c.4881_4882insA c.(4882-4884)atgfs p.M1628fs BLCA 5 176694604 176694604 + Missense_Mutation SNP C C A TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr5:176694604C>A c.5188C>A c.(5188-5190)Cat>Aat p.H1730N BLCA 5 176696618 176696618 + Missense_Mutation SNP G G C TCGA-DK-A3IQ-01A-31D-A20D-08 TCGA-DK-A3IQ-10A-01D-A20D-08 g.chr5:176696618G>C c.5319G>C c.(5317-5319)gaG>gaC p.E1773D BLCA 5 176696774 176696774 + Missense_Mutation SNP G G C TCGA-XF-A9SM-01A-11D-A42E-08 TCGA-XF-A9SM-10A-01D-A42H-08 g.chr5:176696774G>C c.5475G>C c.(5473-5475)aaG>aaC p.K1825N BLCA 5 176707662 176707662 + Missense_Mutation SNP A A G TCGA-DK-A1A7-01A-11D-A13W-08 TCGA-DK-A1A7-10A-01D-A13W-08 g.chr5:176707662A>G c.5719A>G c.(5719-5721)Ata>Gta p.I1907V BLCA 5 176709524 176709524 + Missense_Mutation SNP G G T TCGA-DK-A1AE-01A-11D-A13W-08 TCGA-DK-A1AE-10A-01D-A13W-08 g.chr5:176709524G>T c.5951G>T c.(5950-5952)cGa>cTa p.R1984L BLCA 5 176721219 176721219 + Missense_Mutation SNP G G C TCGA-BT-A20T-01A-11D-A14W-08 TCGA-BT-A20T-11A-11D-A14W-08 g.chr5:176721219G>C c.6850G>C c.(6850-6852)Gag>Cag p.E2284Q BLCA 5 176721473 176721473 + Silent SNP C C G TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr5:176721473C>G c.7104C>G c.(7102-7104)gcC>gcG p.A2368A BLCA 5 176721872 176721872 + Silent SNP G G T TCGA-4Z-AA7W-01A-11D-A391-08 TCGA-4Z-AA7W-10A-01D-A394-08 g.chr5:176721872G>T c.7503G>T c.(7501-7503)ccG>ccT p.P2501P BLCA 5 176722164 176722164 + Missense_Mutation SNP T T G TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr5:176722164T>G c.7795T>G c.(7795-7797)Tct>Gct p.S2599A BLCA 5 176722266 176722266 + Missense_Mutation SNP C C T TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr5:176722266C>T c.7897C>T c.(7897-7899)Cgg>Tgg p.R2633W BRCA 5 176562116 176562116 + Silent SNP C C T TCGA-AR-A256-01A-11D-A167-09 TCGA-AR-A256-10A-01D-A167-09 g.chr5:176562116C>T c.12C>T c.(10-12)acC>acT p.T4T BRCA 5 176562130 176562130 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr5:176562130G>A c.26G>A c.(25-27)aGa>aAa p.R9K BRCA 5 176562356 176562356 + Silent SNP A A G TCGA-A8-A0AD-01A-11W-A071-09 TCGA-A8-A0AD-10A-01W-A071-09 g.chr5:176562356A>G c.252A>G c.(250-252)gtA>gtG p.V84V BRCA 5 176637364 176637364 + Missense_Mutation SNP G G A TCGA-A7-A26G-01A-21D-A167-09 TCGA-A7-A26G-10A-01D-A167-09 g.chr5:176637364G>A c.1964G>A c.(1963-1965)aGc>aAc p.S655N BRCA 5 176637903 176637903 + Missense_Mutation SNP G G T TCGA-D8-A27P-01A-11D-A16D-09 TCGA-D8-A27P-10A-01D-A16D-09 g.chr5:176637903G>T c.2503G>T c.(2503-2505)Ggt>Tgt p.G835C BRCA 5 176638368 176638368 + Nonsense_Mutation SNP G G T TCGA-E9-A54Y-01A-11D-A25Q-09 TCGA-E9-A54Y-10A-01D-A25Q-09 g.chr5:176638368G>T c.2968G>T c.(2968-2970)Gag>Tag p.E990* BRCA 5 176638917 176638917 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr5:176638917C>T c.3517C>T c.(3517-3519)Cgc>Tgc p.R1173C BRCA 5 176666775 176666775 + Missense_Mutation SNP G G A TCGA-AC-A2B8-01A-11D-A17D-09 TCGA-AC-A2B8-10A-01D-A17D-09 g.chr5:176666775G>A c.4211G>A c.(4210-4212)cGt>cAt p.R1404H BRCA 5 176678835 176678835 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr5:176678835C>G c.4746C>G c.(4744-4746)atC>atG p.I1582M BRCA 5 176707706 176707706 + Missense_Mutation SNP C C G TCGA-E2-A2P5-01A-11D-A19Y-09 TCGA-E2-A2P5-10B-01D-A19Y-09 g.chr5:176707706C>G c.5763C>G c.(5761-5763)caC>caG p.H1921Q BRCA 5 176709505 176709505 + Missense_Mutation SNP G G A TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chr5:176709505G>A c.5932G>A c.(5932-5934)Gaa>Aaa p.E1978K BRCA 5 176719060 176719060 + Missense_Mutation SNP T T G TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr5:176719060T>G c.6364T>G c.(6364-6366)Ttt>Gtt p.F2122V BRCA 5 176719136 176719136 + Missense_Mutation SNP T T G TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr5:176719136T>G c.6440T>G c.(6439-6441)cTc>cGc p.L2147R BRCA 5 176720848 176720848 + Missense_Mutation SNP C C T TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr5:176720848C>T c.6479C>T c.(6478-6480)cCg>cTg p.P2160L BRCA 5 176721023 176721023 + Silent SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr5:176721023C>T c.6654C>T c.(6652-6654)atC>atT p.I2218I BRCA 5 176721686 176721686 + Silent SNP G G A TCGA-BH-A18V-01A-11D-A12B-09 TCGA-BH-A18V-11A-52D-A12B-09 g.chr5:176721686G>A c.7317G>A c.(7315-7317)ctG>ctA p.L2439L BRCA 5 176721812 176721812 + Silent SNP G G A TCGA-BH-A0HY-01A-11W-A071-09 TCGA-BH-A0HY-10A-02W-A071-09 g.chr5:176721812G>A c.7443G>A c.(7441-7443)gaG>gaA p.E2481E CESC 5 176562465 176562465 + Missense_Mutation SNP C C G TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr5:176562465C>G c.361C>G c.(361-363)Cct>Gct p.P121A CESC 5 176562700 176562700 + Missense_Mutation SNP C C T TCGA-JX-A3PZ-01A-11D-A21Q-09 TCGA-JX-A3PZ-10A-01D-A21Q-09 g.chr5:176562700C>T c.596C>T c.(595-597)tCa>tTa p.S199L CESC 5 176636673 176636673 + Missense_Mutation SNP G G T TCGA-C5-A0TN-01A-21D-A14W-08 TCGA-C5-A0TN-10B-01D-A14W-08 g.chr5:176636673G>T c.1273G>T c.(1273-1275)Gtt>Ttt p.V425F CESC 5 176636850 176636850 + Missense_Mutation SNP G G C TCGA-C5-A7UH-01A-11D-A351-09 TCGA-C5-A7UH-10A-01D-A351-09 g.chr5:176636850G>C c.1450G>C c.(1450-1452)Gaa>Caa p.E484Q CESC 5 176636899 176636899 + Missense_Mutation SNP G G C TCGA-C5-A7UH-01A-11D-A351-09 TCGA-C5-A7UH-10A-01D-A351-09 g.chr5:176636899G>C c.1499G>C c.(1498-1500)aGa>aCa p.R500T CESC 5 176637093 176637093 + Missense_Mutation SNP C C G TCGA-C5-A2LZ-01A-11D-A20U-09 TCGA-C5-A2LZ-10B-01D-A20U-09 g.chr5:176637093C>G c.1693C>G c.(1693-1695)Cca>Gca p.P565A CESC 5 176637274 176637274 + Missense_Mutation SNP G G C TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr5:176637274G>C c.1874G>C c.(1873-1875)gGa>gCa p.G625A CESC 5 176637327 176637327 + Missense_Mutation SNP G G A TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr5:176637327G>A c.1927G>A c.(1927-1929)Gat>Aat p.D643N CESC 5 176637330 176637330 + Missense_Mutation SNP G G A TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr5:176637330G>A c.1930G>A c.(1930-1932)Gat>Aat p.D644N CESC 5 176637357 176637357 + Missense_Mutation SNP G G A TCGA-C5-A7UH-01A-11D-A351-09 TCGA-C5-A7UH-10A-01D-A351-09 g.chr5:176637357G>A c.1957G>A c.(1957-1959)Gaa>Aaa p.E653K CESC 5 176637417 176637417 + Missense_Mutation SNP G G C TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr5:176637417G>C c.2017G>C c.(2017-2019)Gag>Cag p.E673Q CESC 5 176637601 176637601 + Missense_Mutation SNP A A G TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr5:176637601A>G c.2201A>G c.(2200-2202)aAg>aGg p.K734R CESC 5 176637740 176637740 + Silent SNP G G C TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr5:176637740G>C c.2340G>C c.(2338-2340)tcG>tcC p.S780S CESC 5 176637930 176637930 + Frame_Shift_Del DEL G G - TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr5:176637930delG c.2530delG c.(2530-2532)gagfs p.E844fs CESC 5 176637932 176637932 + Silent SNP G G A TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr5:176637932G>A c.2532G>A c.(2530-2532)gaG>gaA p.E844E CESC 5 176637992 176637992 + Silent SNP G G A TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr5:176637992G>A c.2592G>A c.(2590-2592)ttG>ttA p.L864L CESC 5 176638298 176638298 + Silent SNP G G A TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr5:176638298G>A c.2898G>A c.(2896-2898)gaG>gaA p.E966E CESC 5 176638806 176638806 + Missense_Mutation SNP G G A TCGA-C5-A7UH-01A-11D-A351-09 TCGA-C5-A7UH-10A-01D-A351-09 g.chr5:176638806G>A c.3406G>A c.(3406-3408)Gag>Aag p.E1136K CESC 5 176638817 176638817 + Silent SNP T T A TCGA-C5-A7UH-01A-11D-A351-09 TCGA-C5-A7UH-10A-01D-A351-09 g.chr5:176638817T>A c.3417T>A c.(3415-3417)tcT>tcA p.S1139S CESC 5 176638839 176638839 + Missense_Mutation SNP G G A TCGA-C5-A7UH-01A-11D-A351-09 TCGA-C5-A7UH-10A-01D-A351-09 g.chr5:176638839G>A c.3439G>A c.(3439-3441)Gaa>Aaa p.E1147K CESC 5 176638922 176638922 + Missense_Mutation SNP G G A TCGA-EK-A2PG-01A-11D-A18J-09 TCGA-EK-A2PG-10A-01D-A18J-09 g.chr5:176638922G>A c.3522G>A c.(3520-3522)atG>atA p.M1174I CESC 5 176639054 176639054 + Silent SNP G G A TCGA-EK-A2PG-01A-11D-A18J-09 TCGA-EK-A2PG-10A-01D-A18J-09 g.chr5:176639054G>A c.3654G>A c.(3652-3654)ctG>ctA p.L1218L CESC 5 176662835 176662835 + Silent SNP G G A TCGA-C5-A2LZ-01A-11D-A20U-09 TCGA-C5-A2LZ-10B-01D-A20U-09 g.chr5:176662835G>A c.3810G>A c.(3808-3810)gaG>gaA p.E1270E CESC 5 176687059 176687059 + Nonsense_Mutation SNP C C A TCGA-EK-A2RC-01A-11D-A18J-09 TCGA-EK-A2RC-10A-01D-A18J-09 g.chr5:176687059C>A c.5036C>A c.(5035-5037)tCa>tAa p.S1679* CESC 5 176687059 176687059 + Nonsense_Mutation SNP C C G TCGA-EA-A1QT-01A-11D-A14W-08 TCGA-EA-A1QT-10A-01D-A14W-08 g.chr5:176687059C>G c.5036C>G c.(5035-5037)tCa>tGa p.S1679* CESC 5 176687130 176687130 + Missense_Mutation SNP G G C TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr5:176687130G>C c.5107G>C c.(5107-5109)Gag>Cag p.E1703Q CESC 5 176721266 176721266 + Silent SNP C C T TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr5:176721266C>T c.6897C>T c.(6895-6897)ctC>ctT p.L2299L CHOL 5 176709524 176709524 + Missense_Mutation SNP G G T TCGA-W5-AA34-01A-11D-A417-09 TCGA-W5-AA34-10A-01D-A41A-09 g.chr5:176709524G>T c.5951G>T c.(5950-5952)cGa>cTa p.R1984L CHOL 5 176721680 176721680 + Silent SNP A A G TCGA-W5-AA30-01A-31D-A417-09 TCGA-W5-AA30-10A-01D-A41A-09 g.chr5:176721680A>G c.7311A>G c.(7309-7311)aaA>aaG p.K2437K COAD 5 176562133 176562133 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:176562133G>T c.29G>T c.(28-30)aGa>aTa p.R10I COAD 5 176562813 176562813 + Frame_Shift_Del DEL A A - TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr5:176562813delA c.709delA c.(709-711)aaafs p.K237fs COAD 5 176618976 176618976 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:176618976G>T c.1019G>T c.(1018-1020)aGg>aTg p.R340M COAD 5 176631233 176631233 + Silent SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr5:176631233C>T c.1176C>T c.(1174-1176)ttC>ttT p.F392F COAD 5 176631233 176631233 + Silent SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr5:176631233C>T c.1176C>T c.(1174-1176)ttC>ttT p.F392F COAD 5 176636719 176636719 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr5:176636719G>A c.1319G>A c.(1318-1320)cGa>cAa p.R440Q COAD 5 176637583 176637583 + Missense_Mutation SNP T T C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr5:176637583T>C c.2183T>C c.(2182-2184)gTt>gCt p.V728A COAD 5 176637845 176637845 + Silent SNP C C T TCGA-CM-5863-01A-21D-1835-10 TCGA-CM-5863-10A-01D-1835-10 g.chr5:176637845C>T c.2445C>T c.(2443-2445)tgC>tgT p.C815C COAD 5 176638117 176638117 + Missense_Mutation SNP A A C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr5:176638117A>C c.2717A>C c.(2716-2718)aAa>aCa p.K906T COAD 5 176638196 176638196 + Missense_Mutation SNP C C G TCGA-DM-A28C-01A-11D-A16V-10 TCGA-DM-A28C-10A-01D-A16V-10 g.chr5:176638196C>G c.2796C>G c.(2794-2796)aaC>aaG p.N932K COAD 5 176638222 176638222 + Missense_Mutation SNP G G A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr5:176638222G>A c.2822G>A c.(2821-2823)cGt>cAt p.R941H COAD 5 176638303 176638303 + Missense_Mutation SNP A A G TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr5:176638303A>G c.2903A>G c.(2902-2904)aAg>aGg p.K968R COAD 5 176638455 176638455 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr5:176638455C>T c.3055C>T c.(3055-3057)Cgc>Tgc p.R1019C COAD 5 176639039 176639039 + Missense_Mutation SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:176639039A>G c.3639A>G c.(3637-3639)atA>atG p.I1213M COAD 5 176662835 176662835 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:176662835G>T c.3810G>T c.(3808-3810)gaG>gaT p.E1270D COAD 5 176665317 176665317 + Missense_Mutation SNP C C A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr5:176665317C>A c.4001C>A c.(4000-4002)tCt>tAt p.S1334Y COAD 5 176665479 176665479 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:176665479A>C c.4163A>C c.(4162-4164)gAg>gCg p.E1388A COAD 5 176673712 176673712 + Missense_Mutation SNP G G A TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr5:176673712G>A c.4412G>A c.(4411-4413)cGa>cAa p.R1471Q COAD 5 176675253 176675253 + Silent SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr5:176675253C>T c.4569C>T c.(4567-4569)ccC>ccT p.P1523P COAD 5 176687051 176687051 + Silent SNP T T C TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr5:176687051T>C c.5028T>C c.(5026-5028)gcT>gcC p.A1676A COAD 5 176687162 176687162 + Silent SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr5:176687162C>T c.5139C>T c.(5137-5139)tgC>tgT p.C1713C COAD 5 176694670 176694670 + Frame_Shift_Del DEL A A - TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr5:176694670delA c.5254delA c.(5254-5256)aaafs p.K1753fs COAD 5 176700695 176700695 + Missense_Mutation SNP G G C TCGA-DM-A1D8-01A-11D-A152-10 TCGA-DM-A1D8-10A-01D-A152-10 g.chr5:176700695G>C c.5532G>C c.(5530-5532)agG>agC p.R1844S COAD 5 176709529 176709529 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr5:176709529C>T c.5956C>T c.(5956-5958)Cgc>Tgc p.R1986C COAD 5 176709569 176709570 + Missense_Mutation DNP TC TC GT TCGA-AA-3971-01A-01W-0995-10 TCGA-AA-3971-10A-01W-0999-10 g.chr5:176709569_176709570TC>GT c.5996_5997TC>GT c.(5995-5997)cTC>cGT p.L1999R COAD 5 176718994 176718996 + In_Frame_Del DEL AAG AAG - TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr5:176718994_176718996delAAG c.6298_6300delAAG c.(6298-6300)aagdel p.K2102del COAD 5 176719032 176719032 + Silent SNP A A G TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr5:176719032A>G c.6336A>G c.(6334-6336)gaA>gaG p.E2112E COAD 5 176719126 176719126 + Missense_Mutation SNP G G A TCGA-DM-A0XD-01A-12D-A152-10 TCGA-DM-A0XD-10A-01D-A152-10 g.chr5:176719126G>A c.6430G>A c.(6430-6432)Gca>Aca p.A2144T COAD 5 176721069 176721069 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr5:176721069A>G c.6700A>G c.(6700-6702)Act>Gct p.T2234A COAD 5 176721107 176721107 + Missense_Mutation SNP G G T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr5:176721107G>T c.6738G>T c.(6736-6738)caG>caT p.Q2246H COAD 5 176721368 176721368 + Silent SNP C C A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr5:176721368C>A c.6999C>A c.(6997-6999)ccC>ccA p.P2333P COAD 5 176721627 176721627 + Missense_Mutation SNP C C T TCGA-D5-6929-01A-31D-1924-10 TCGA-D5-6929-10A-01D-1924-10 g.chr5:176721627C>T c.7258C>T c.(7258-7260)Cct>Tct p.P2420S COAD 5 176721629 176721629 + Silent SNP T T C TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr5:176721629T>C c.7260T>C c.(7258-7260)ccT>ccC p.P2420P COAD 5 176721629 176721629 + Silent SNP T T C TCGA-CM-5863-01A-21D-1835-10 TCGA-CM-5863-10A-01D-1835-10 g.chr5:176721629T>C c.7260T>C c.(7258-7260)ccT>ccC p.P2420P COADREAD 5 176562133 176562133 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:176562133G>T c.29G>T c.(28-30)aGa>aTa p.R10I COADREAD 5 176562813 176562813 + Frame_Shift_Del DEL A A - TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr5:176562813delA c.709delA c.(709-711)aaafs p.K237fs COADREAD 5 176562826 176562826 + Missense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr5:176562826G>T c.722G>T c.(721-723)aGa>aTa p.R241I COADREAD 5 176618976 176618976 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:176618976G>T c.1019G>T c.(1018-1020)aGg>aTg p.R340M COADREAD 5 176631233 176631233 + Silent SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr5:176631233C>T c.1176C>T c.(1174-1176)ttC>ttT p.F392F COADREAD 5 176631233 176631233 + Silent SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr5:176631233C>T c.1176C>T c.(1174-1176)ttC>ttT p.F392F COADREAD 5 176636719 176636719 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr5:176636719G>A c.1319G>A c.(1318-1320)cGa>cAa p.R440Q COADREAD 5 176637583 176637583 + Missense_Mutation SNP T T C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr5:176637583T>C c.2183T>C c.(2182-2184)gTt>gCt p.V728A COADREAD 5 176637845 176637845 + Silent SNP C C T TCGA-CM-5863-01A-21D-1835-10 TCGA-CM-5863-10A-01D-1835-10 g.chr5:176637845C>T c.2445C>T c.(2443-2445)tgC>tgT p.C815C COADREAD 5 176638117 176638117 + Missense_Mutation SNP A A C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr5:176638117A>C c.2717A>C c.(2716-2718)aAa>aCa p.K906T COADREAD 5 176638196 176638196 + Missense_Mutation SNP C C G TCGA-DM-A28C-01A-11D-A16V-10 TCGA-DM-A28C-10A-01D-A16V-10 g.chr5:176638196C>G c.2796C>G c.(2794-2796)aaC>aaG p.N932K COADREAD 5 176638222 176638222 + Missense_Mutation SNP G G A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr5:176638222G>A c.2822G>A c.(2821-2823)cGt>cAt p.R941H COADREAD 5 176638303 176638303 + Missense_Mutation SNP A A G TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr5:176638303A>G c.2903A>G c.(2902-2904)aAg>aGg p.K968R COADREAD 5 176638455 176638455 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr5:176638455C>T c.3055C>T c.(3055-3057)Cgc>Tgc p.R1019C COADREAD 5 176639039 176639039 + Missense_Mutation SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:176639039A>G c.3639A>G c.(3637-3639)atA>atG p.I1213M COADREAD 5 176662835 176662835 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:176662835G>T c.3810G>T c.(3808-3810)gaG>gaT p.E1270D COADREAD 5 176665317 176665317 + Missense_Mutation SNP C C A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr5:176665317C>A c.4001C>A c.(4000-4002)tCt>tAt p.S1334Y COADREAD 5 176665479 176665479 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:176665479A>C c.4163A>C c.(4162-4164)gAg>gCg p.E1388A COADREAD 5 176665503 176665503 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:176665503C>T c.4187C>T c.(4186-4188)aCg>aTg p.T1396M COADREAD 5 176671259 176671259 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:176671259G>T c.4366G>T c.(4366-4368)Gat>Tat p.D1456Y COADREAD 5 176673712 176673712 + Missense_Mutation SNP G G A TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr5:176673712G>A c.4412G>A c.(4411-4413)cGa>cAa p.R1471Q COADREAD 5 176675253 176675253 + Silent SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr5:176675253C>T c.4569C>T c.(4567-4569)ccC>ccT p.P1523P COADREAD 5 176687051 176687051 + Silent SNP T T C TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr5:176687051T>C c.5028T>C c.(5026-5028)gcT>gcC p.A1676A COADREAD 5 176687162 176687162 + Silent SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr5:176687162C>T c.5139C>T c.(5137-5139)tgC>tgT p.C1713C COADREAD 5 176694670 176694670 + Frame_Shift_Del DEL A A - TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr5:176694670delA c.5254delA c.(5254-5256)aaafs p.K1753fs COADREAD 5 176696731 176696731 + Missense_Mutation SNP G G A TCGA-AH-6644-01A-21D-1826-10 TCGA-AH-6644-10A-01D-1826-10 g.chr5:176696731G>A c.5432G>A c.(5431-5433)cGa>cAa p.R1811Q COADREAD 5 176700695 176700695 + Missense_Mutation SNP G G C TCGA-DM-A1D8-01A-11D-A152-10 TCGA-DM-A1D8-10A-01D-A152-10 g.chr5:176700695G>C c.5532G>C c.(5530-5532)agG>agC p.R1844S COADREAD 5 176709529 176709529 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr5:176709529C>T c.5956C>T c.(5956-5958)Cgc>Tgc p.R1986C COADREAD 5 176709569 176709570 + Missense_Mutation DNP TC TC GT TCGA-AA-3971-01A-01W-0995-10 TCGA-AA-3971-10A-01W-0999-10 g.chr5:176709569_176709570TC>GT c.5996_5997TC>GT c.(5995-5997)cTC>cGT p.L1999R COADREAD 5 176718994 176718996 + In_Frame_Del DEL AAG AAG - TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr5:176718994_176718996delAAG c.6298_6300delAAG c.(6298-6300)aagdel p.K2102del COADREAD 5 176719032 176719032 + Silent SNP A A G TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr5:176719032A>G c.6336A>G c.(6334-6336)gaA>gaG p.E2112E COADREAD 5 176719126 176719126 + Missense_Mutation SNP G G A TCGA-DM-A0XD-01A-12D-A152-10 TCGA-DM-A0XD-10A-01D-A152-10 g.chr5:176719126G>A c.6430G>A c.(6430-6432)Gca>Aca p.A2144T COADREAD 5 176721069 176721069 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr5:176721069A>G c.6700A>G c.(6700-6702)Act>Gct p.T2234A COADREAD 5 176721107 176721107 + Missense_Mutation SNP G G T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr5:176721107G>T c.6738G>T c.(6736-6738)caG>caT p.Q2246H COADREAD 5 176721368 176721368 + Silent SNP C C A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr5:176721368C>A c.6999C>A c.(6997-6999)ccC>ccA p.P2333P COADREAD 5 176721627 176721627 + Missense_Mutation SNP C C T TCGA-D5-6929-01A-31D-1924-10 TCGA-D5-6929-10A-01D-1924-10 g.chr5:176721627C>T c.7258C>T c.(7258-7260)Cct>Tct p.P2420S COADREAD 5 176721629 176721629 + Silent SNP T T C TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr5:176721629T>C c.7260T>C c.(7258-7260)ccT>ccC p.P2420P COADREAD 5 176721629 176721629 + Silent SNP T T C TCGA-CM-5863-01A-21D-1835-10 TCGA-CM-5863-10A-01D-1835-10 g.chr5:176721629T>C c.7260T>C c.(7258-7260)ccT>ccC p.P2420P COADREAD 5 176721629 176721629 + Silent SNP T T C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr5:176721629T>C c.7260T>C c.(7258-7260)ccT>ccC p.P2420P COADREAD 5 176721701 176721701 + Silent SNP G G A TCGA-AG-A014-01A-02W-A00K-09 TCGA-AG-A014-10A-01W-A00K-09 g.chr5:176721701G>A c.7332G>A c.(7330-7332)caG>caA p.Q2444Q DLBC 5 176637471 176637471 + Missense_Mutation SNP G G A TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr5:176637471G>A c.2071G>A c.(2071-2073)Gcc>Acc p.A691T DLBC 5 176638506 176638506 + Missense_Mutation SNP G G C TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr5:176638506G>C c.3106G>C c.(3106-3108)Gcc>Ccc p.A1036P DLBC 5 176721879 176721879 + Missense_Mutation SNP G G A TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr5:176721879G>A c.7510G>A c.(7510-7512)Gtt>Att p.V2504I ESCA 5 176562826 176562826 + Missense_Mutation SNP G G T TCGA-L5-A8NE-01A-11D-A37C-09 TCGA-L5-A8NE-11A-11D-A37F-09 g.chr5:176562826G>T c.722G>T c.(721-723)aGa>aTa p.R241I ESCA 5 176618958 176618958 + Missense_Mutation SNP G G T TCGA-LN-A5U6-01A-11D-A28B-09 TCGA-LN-A5U6-10A-01D-A28E-09 g.chr5:176618958G>T c.1001G>T c.(1000-1002)cGc>cTc p.R334L ESCA 5 176638741 176638741 + Missense_Mutation SNP T T A TCGA-L5-A43I-01A-11D-A247-09 TCGA-L5-A43I-11A-11D-A247-09 g.chr5:176638741T>A c.3341T>A c.(3340-3342)gTt>gAt p.V1114D ESCA 5 176638912 176638912 + Missense_Mutation SNP G G T TCGA-JY-A93D-01A-11D-A387-09 TCGA-JY-A93D-10A-01D-A38A-09 g.chr5:176638912G>T c.3512G>T c.(3511-3513)cGt>cTt p.R1171L ESCA 5 176678794 176678794 + Nonsense_Mutation SNP G G T TCGA-IC-A6RF-01A-13D-A33E-09 TCGA-IC-A6RF-10A-21D-A33H-09 g.chr5:176678794G>T c.4705G>T c.(4705-4707)Gag>Tag p.E1569* ESCA 5 176683973 176683973 + Missense_Mutation SNP G G T TCGA-LN-A4A6-01A-11D-A27G-09 TCGA-LN-A4A6-10A-01D-A27G-09 g.chr5:176683973G>T c.4787G>T c.(4786-4788)tGt>tTt p.C1596F ESCA 5 176694593 176694593 + Missense_Mutation SNP C C T TCGA-JY-A93F-01A-21D-A37C-09 TCGA-JY-A93F-10A-01D-A37F-09 g.chr5:176694593C>T c.5177C>T c.(5176-5178)cCt>cTt p.P1726L ESCA 5 176696681 176696681 + Frame_Shift_Del DEL C C - TCGA-V5-AASV-01A-11D-A387-09 TCGA-V5-AASV-10A-01D-A38A-09 g.chr5:176696681delC c.5382delC c.(5380-5382)ttcfs p.F1794fs ESCA 5 176709465 176709465 + Splice_Site SNP G G A TCGA-JY-A93F-01A-21D-A37C-09 TCGA-JY-A93F-10A-01D-A37F-09 g.chr5:176709465G>A c.e19-1 ESCA 5 176709523 176709523 + Nonsense_Mutation SNP C C T TCGA-IC-A6RF-01A-13D-A33E-09 TCGA-IC-A6RF-10A-21D-A33H-09 g.chr5:176709523C>T c.5950C>T c.(5950-5952)Cga>Tga p.R1984* ESCA 5 176719030 176719030 + Missense_Mutation SNP G G A TCGA-JY-A93D-01A-11D-A387-09 TCGA-JY-A93D-10A-01D-A38A-09 g.chr5:176719030G>A c.6334G>A c.(6334-6336)Gaa>Aaa p.E2112K ESCA 5 176719054 176719054 + Nonsense_Mutation SNP G G T TCGA-LN-A4MR-01A-11D-A28B-09 TCGA-LN-A4MR-10A-01D-A28E-09 g.chr5:176719054G>T c.6358G>T c.(6358-6360)Gag>Tag p.E2120* ESCA 5 176721015 176721015 + Frame_Shift_Del DEL G G - TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr5:176721015delG c.6646delG c.(6646-6648)gggfs p.G2216fs ESCA 5 176721258 176721258 + Missense_Mutation SNP A A G TCGA-KH-A6WC-01A-11D-A33E-09 TCGA-KH-A6WC-10B-01D-A33H-09 g.chr5:176721258A>G c.6889A>G c.(6889-6891)Aga>Gga p.R2297G ESCA 5 176721680 176721680 + Silent SNP A A G TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr5:176721680A>G c.7311A>G c.(7309-7311)aaA>aaG p.K2437K ESCA 5 176722172 176722172 + Missense_Mutation SNP G G T TCGA-LN-A8I1-01A-11D-A36J-09 TCGA-LN-A8I1-10A-01D-A36M-09 g.chr5:176722172G>T c.7803G>T c.(7801-7803)agG>agT p.R2601S GBM 5 176638305 176638305 + Missense_Mutation SNP G G A TCGA-06-2563-01A-01D-1494-08 TCGA-06-2563-10A-01D-1494-08 g.chr5:176638305G>A c.2905G>A c.(2905-2907)Gga>Aga p.G969R GBMLGG 5 176638305 176638305 + Missense_Mutation SNP G G A TCGA-06-2563-01A-01D-1494-08 TCGA-06-2563-10A-01D-1494-08 g.chr5:176638305G>A c.2905G>A c.(2905-2907)Gga>Aga p.G969R GBMLGG 5 176638615 176638615 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:176638615G>A c.3215G>A c.(3214-3216)cGa>cAa p.R1072Q GBMLGG 5 176638954 176638954 + Missense_Mutation SNP G G T TCGA-S9-A6WG-01A-11D-A33T-08 TCGA-S9-A6WG-10A-01D-A33W-08 g.chr5:176638954G>T c.3554G>T c.(3553-3555)tGt>tTt p.C1185F GBMLGG 5 176707732 176707732 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:176707732G>A c.5789G>A c.(5788-5790)cGc>cAc p.R1930H GBMLGG 5 176722240 176722240 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:176722240C>A c.7871C>A c.(7870-7872)cCc>cAc p.P2624H HNSC 5 176562391 176562391 + Missense_Mutation SNP C C G TCGA-CV-6961-01A-21D-1912-08 TCGA-CV-6961-10A-01D-1912-08 g.chr5:176562391C>G c.287C>G c.(286-288)tCc>tGc p.S96C HNSC 5 176618931 176618931 + Missense_Mutation SNP A A T TCGA-CV-6441-01A-11D-1683-08 TCGA-CV-6441-11A-01D-1683-08 g.chr5:176618931A>T c.974A>T c.(973-975)gAt>gTt p.D325V HNSC 5 176631153 176631153 + Missense_Mutation SNP G G T TCGA-D6-8569-01A-11D-2394-08 TCGA-D6-8569-10A-01D-2394-08 g.chr5:176631153G>T c.1096G>T c.(1096-1098)Gtg>Ttg p.V366L HNSC 5 176636700 176636700 + Missense_Mutation SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr5:176636700C>T c.1300C>T c.(1300-1302)Ccc>Tcc p.P434S HNSC 5 176636701 176636701 + Missense_Mutation SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr5:176636701C>T c.1301C>T c.(1300-1302)cCc>cTc p.P434L HNSC 5 176637097 176637097 + Missense_Mutation SNP G G A TCGA-UF-A71B-01A-12D-A34J-08 TCGA-UF-A71B-10B-01D-A34M-08 g.chr5:176637097G>A c.1697G>A c.(1696-1698)gGa>gAa p.G566E HNSC 5 176637167 176637168 + Frame_Shift_Del DEL TT TT - TCGA-CN-4730-01A-01D-1434-08 TCGA-CN-4730-10A-01D-1434-08 g.chr5:176637167_176637168delTT c.1767_1768delTT c.(1765-1770)tctttafs p.L591fs HNSC 5 176637201 176637201 + Nonsense_Mutation SNP A A T TCGA-CV-A45Z-01A-21D-A25D-08 TCGA-CV-A45Z-10A-01D-A25E-08 g.chr5:176637201A>T c.1801A>T c.(1801-1803)Aag>Tag p.K601* HNSC 5 176637435 176637435 + Nonsense_Mutation SNP C C T TCGA-CQ-7072-01A-21D-A30E-08 TCGA-CQ-7072-10A-01D-A30H-08 g.chr5:176637435C>T c.2035C>T c.(2035-2037)Cag>Tag p.Q679* HNSC 5 176637520 176637520 + Nonsense_Mutation SNP C C G TCGA-BA-6869-01A-11D-1870-08 TCGA-BA-6869-10A-01D-1870-08 g.chr5:176637520C>G c.2120C>G c.(2119-2121)tCa>tGa p.S707* HNSC 5 176637567 176637567 + Missense_Mutation SNP A A T TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr5:176637567A>T c.2167A>T c.(2167-2169)Acc>Tcc p.T723S HNSC 5 176637631 176637631 + Nonsense_Mutation SNP C C G TCGA-CN-5360-01A-01D-1434-08 TCGA-CN-5360-10A-01D-1434-08 g.chr5:176637631C>G c.2231C>G c.(2230-2232)tCa>tGa p.S744* HNSC 5 176637659 176637659 + Frame_Shift_Del DEL A A - TCGA-D6-A74Q-01A-11D-A34J-08 TCGA-D6-A74Q-10A-02D-A34M-08 g.chr5:176637659delA c.2259delA c.(2257-2259)ccafs p.P753fs HNSC 5 176637762 176637762 + Nonsense_Mutation SNP C C T TCGA-BA-5555-01A-01D-1512-08 TCGA-BA-5555-10A-01D-1512-08 g.chr5:176637762C>T c.2362C>T c.(2362-2364)Cga>Tga p.R788* HNSC 5 176637762 176637762 + Nonsense_Mutation SNP C C T TCGA-QK-AA3J-01A-11D-A391-08 TCGA-QK-AA3J-10A-01D-A394-08 g.chr5:176637762C>T c.2362C>T c.(2362-2364)Cga>Tga p.R788* HNSC 5 176637776 176637776 + Nonsense_Mutation SNP C C A TCGA-CV-7440-01A-11D-2129-08 TCGA-CV-7440-10A-01D-2129-08 g.chr5:176637776C>A c.2376C>A c.(2374-2376)tgC>tgA p.C792* HNSC 5 176638165 176638165 + Frame_Shift_Del DEL C C - TCGA-UF-A71D-01A-12D-A34J-08 TCGA-UF-A71D-10B-01D-A34M-08 g.chr5:176638165delC c.2765delC c.(2764-2766)acgfs p.T922fs HNSC 5 176638275 176638275 + Nonsense_Mutation SNP G G T TCGA-CN-4727-01A-01D-1434-08 TCGA-CN-4727-10A-01D-1434-08 g.chr5:176638275G>T c.2875G>T c.(2875-2877)Gga>Tga p.G959* HNSC 5 176638343 176638344 + Frame_Shift_Ins INS - - G TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr5:176638343_176638344insG c.2943_2944insG c.(2944-2946)gggfs p.G982fs HNSC 5 176638368 176638368 + Nonsense_Mutation SNP G G T TCGA-BB-7870-01A-11D-2229-08 TCGA-BB-7870-10A-01D-2229-08 g.chr5:176638368G>T c.2968G>T c.(2968-2970)Gag>Tag p.E990* HNSC 5 176638400 176638400 + Silent SNP C C T TCGA-CN-A6V3-01A-12D-A34J-08 TCGA-CN-A6V3-10A-01D-A34M-08 g.chr5:176638400C>T c.3000C>T c.(2998-3000)tcC>tcT p.S1000S HNSC 5 176638614 176638614 + Nonsense_Mutation SNP C C T TCGA-BA-A6DL-01A-21D-A30E-08 TCGA-BA-A6DL-10A-01D-A30H-08 g.chr5:176638614C>T c.3214C>T c.(3214-3216)Cga>Tga p.R1072* HNSC 5 176638656 176638662 + Frame_Shift_Del DEL AGTAAAG AGTAAAG - TCGA-CV-7253-01A-11D-2012-08 TCGA-CV-7253-10A-01D-2013-08 g.chr5:176638656_176638662delAGTAAAG c.3256_3262delAGTAAAG c.(3256-3264)agtaaagagfs p.SKE1086fs HNSC 5 176638682 176638682 + Frame_Shift_Del DEL G G - TCGA-F7-7848-01A-11D-2129-08 TCGA-F7-7848-10A-01D-2129-08 g.chr5:176638682delG c.3282delG c.(3280-3282)atgfs p.M1094fs HNSC 5 176638683 176638693 + Frame_Shift_Del DEL GGCCACTTAAC GGCCACTTAAC - TCGA-BB-A5HZ-01A-21D-A28R-08 TCGA-BB-A5HZ-10A-01D-A28U-08 g.chr5:176638683_176638693delGGCCACTTAAC c.3283_3293delGGCCACTTAAC c.(3283-3294)ggccacttaacafs p.GHLT1095fs HNSC 5 176638879 176638879 + Nonsense_Mutation SNP G G A TCGA-CN-A63W-01A-11D-A30E-08 TCGA-CN-A63W-10A-01D-A30H-08 g.chr5:176638879G>A c.3479G>A c.(3478-3480)tGg>tAg p.W1160* HNSC 5 176638999 176639006 + Frame_Shift_Del DEL GGGATGAG GGGATGAG - TCGA-BA-A6DL-01A-21D-A30E-08 TCGA-BA-A6DL-10A-01D-A30H-08 g.chr5:176638999_176639006delGGGATGAG c.3599_3606delGGGATGAG c.(3598-3606)cgggatgagfs p.RDE1200fs HNSC 5 176662896 176662897 + Frame_Shift_Ins INS - - T TCGA-BB-A5HZ-01A-21D-A28R-08 TCGA-BB-A5HZ-10A-01D-A28U-08 g.chr5:176662896_176662897insT c.3871_3872insT c.(3871-3873)atafs p.I1291fs HNSC 5 176665274 176665274 + Nonsense_Mutation SNP C C T TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr5:176665274C>T c.3958C>T c.(3958-3960)Cga>Tga p.R1320* HNSC 5 176665392 176665392 + Nonsense_Mutation SNP C C A TCGA-CV-7250-01A-11D-2012-08 TCGA-CV-7250-10A-01D-2013-08 g.chr5:176665392C>A c.4076C>A c.(4075-4077)tCa>tAa p.S1359* HNSC 5 176665487 176665487 + Nonsense_Mutation SNP G G T TCGA-CN-A497-01A-11D-A24D-08 TCGA-CN-A497-10A-01D-A24F-08 g.chr5:176665487G>T c.4171G>T c.(4171-4173)Gaa>Taa p.E1391* HNSC 5 176666861 176666861 + Nonsense_Mutation SNP A A T TCGA-CN-5356-01A-01D-1434-08 TCGA-CN-5356-10A-01D-1434-08 g.chr5:176666861A>T c.4297A>T c.(4297-4299)Aaa>Taa p.K1433* HNSC 5 176673717 176673717 + Nonsense_Mutation SNP C C T TCGA-CV-6941-01A-11D-1912-08 TCGA-CV-6941-10A-01D-1912-08 g.chr5:176673717C>T c.4417C>T c.(4417-4419)Cga>Tga p.R1473* HNSC 5 176673765 176673765 + Missense_Mutation SNP G G A TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr5:176673765G>A c.4465G>A c.(4465-4467)Gat>Aat p.D1489N HNSC 5 176675185 176675185 + Nonsense_Mutation SNP G G T TCGA-CN-A63U-01A-11D-A30E-08 TCGA-CN-A63U-10A-01D-A30H-08 g.chr5:176675185G>T c.4501G>T c.(4501-4503)Gaa>Taa p.E1501* HNSC 5 176675230 176675230 + Nonsense_Mutation SNP G G T TCGA-P3-A6T6-01A-11D-A34J-08 TCGA-P3-A6T6-10A-01D-A34M-08 g.chr5:176675230G>T c.4546G>T c.(4546-4548)Gag>Tag p.E1516* HNSC 5 176675242 176675242 + Missense_Mutation SNP G G A TCGA-F7-A623-01A-11D-A28R-08 TCGA-F7-A623-10A-01D-A28U-08 g.chr5:176675242G>A c.4558G>A c.(4558-4560)Gaa>Aaa p.E1520K HNSC 5 176675254 176675254 + Frame_Shift_Del DEL G G - TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr5:176675254delG c.4570delG c.(4570-4572)gggfs p.G1524fs HNSC 5 176675267 176675267 + Missense_Mutation SNP C C A TCGA-UF-A719-01A-12D-A34J-08 TCGA-UF-A719-10A-01D-A34M-08 g.chr5:176675267C>A c.4583C>A c.(4582-4584)tCt>tAt p.S1528Y HNSC 5 176675268 176675269 + Frame_Shift_Ins INS - - A TCGA-CR-7398-01A-11D-2012-08 TCGA-CR-7398-10A-01D-2013-08 g.chr5:176675268_176675269insA c.4584_4585insA c.(4585-4587)aaafs p.K1529fs HNSC 5 176675284 176675284 + Nonsense_Mutation SNP G G T TCGA-CV-7245-01A-11D-2012-08 TCGA-CV-7245-10A-01D-2013-08 g.chr5:176675284G>T c.4600G>T c.(4600-4602)Gaa>Taa p.E1534* HNSC 5 176678812 176678812 + Nonsense_Mutation SNP G G T TCGA-BA-A6DE-01A-22D-A31L-08 TCGA-BA-A6DE-10A-01D-A31J-08 g.chr5:176678812G>T c.4723G>T c.(4723-4725)Gag>Tag p.E1575* HNSC 5 176684032 176684032 + Missense_Mutation SNP C C T TCGA-KU-A66S-01A-21D-A30E-08 TCGA-KU-A66S-10A-01D-A30H-08 g.chr5:176684032C>T c.4846C>T c.(4846-4848)Cat>Tat p.H1616Y HNSC 5 176684042 176684042 + Missense_Mutation SNP G G C TCGA-CV-7440-01A-11D-2129-08 TCGA-CV-7440-10A-01D-2129-08 g.chr5:176684042G>C c.4856G>C c.(4855-4857)tGt>tCt p.C1619S HNSC 5 176684087 176684087 + Missense_Mutation SNP G G A TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr5:176684087G>A c.4901G>A c.(4900-4902)cGg>cAg p.R1634Q HNSC 5 176687015 176687017 + In_Frame_Del DEL TCC TCC - TCGA-H7-A6C5-01A-11D-A30E-08 TCGA-H7-A6C5-10A-01D-A30H-08 g.chr5:176687015_176687017delTCC c.4992_4994delTCC c.(4990-4995)tgtcct>tgt p.P1665del HNSC 5 176687017 176687017 + Missense_Mutation SNP C C T TCGA-BA-A4IF-01A-11D-A25Y-08 TCGA-BA-A4IF-10A-01D-A25Y-08 g.chr5:176687017C>T c.4994C>T c.(4993-4995)cCt>cTt p.P1665L HNSC 5 176687055 176687055 + Missense_Mutation SNP G G T TCGA-CV-6960-01A-41D-2012-08 TCGA-CV-6960-10A-01D-2013-08 g.chr5:176687055G>T c.5032G>T c.(5032-5034)Ggg>Tgg p.G1678W HNSC 5 176687121 176687121 + Nonsense_Mutation SNP C C T TCGA-CR-7385-01A-11D-2012-08 TCGA-CR-7385-10A-01D-2013-08 g.chr5:176687121C>T c.5098C>T c.(5098-5100)Cga>Tga p.R1700* HNSC 5 176687152 176687152 + Missense_Mutation SNP G G A TCGA-CN-A6V3-01A-12D-A34J-08 TCGA-CN-A6V3-10A-01D-A34M-08 g.chr5:176687152G>A c.5129G>A c.(5128-5130)tGc>tAc p.C1710Y HNSC 5 176687152 176687152 + Missense_Mutation SNP G G C TCGA-CN-4739-01A-02D-1512-08 TCGA-CN-4739-10A-01D-1512-08 g.chr5:176687152G>C c.5129G>C c.(5128-5130)tGc>tCc p.C1710S HNSC 5 176694686 176694686 + Frame_Shift_Del DEL G G - TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr5:176694686delG c.5270delG c.(5269-5271)aggfs p.R1757fs HNSC 5 176696606 176696606 + Missense_Mutation SNP G G T TCGA-CN-A6V3-01A-12D-A34J-08 TCGA-CN-A6V3-10A-01D-A34M-08 g.chr5:176696606G>T c.5307G>T c.(5305-5307)tgG>tgT p.W1769C HNSC 5 176696801 176696802 + Frame_Shift_Ins INS - - A TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr5:176696801_176696802insA c.5502_5503insA c.(5503-5505)aaafs p.K1835fs HNSC 5 176700720 176700720 + Nonsense_Mutation SNP G G T TCGA-UF-A7JF-01A-11D-A34J-08 TCGA-UF-A7JF-10A-01D-A34M-08 g.chr5:176700720G>T c.5557G>T c.(5557-5559)Gag>Tag p.E1853* HNSC 5 176700778 176700779 + Frame_Shift_Del DEL AT AT - TCGA-CV-5441-01A-01D-1512-08 TCGA-CV-5441-11A-01D-1512-08 g.chr5:176700778_176700779delAT c.5615_5616delAT c.(5614-5616)catfs p.H1872fs HNSC 5 176700778 176700779 + Frame_Shift_Del DEL AT AT - TCGA-QK-A8Z8-01A-11D-A391-08 TCGA-QK-A8Z8-10A-01D-A394-08 g.chr5:176700778_176700779delAT c.5615_5616delAT c.(5614-5616)catfs p.H1872fs HNSC 5 176707633 176707633 + Missense_Mutation SNP G G T TCGA-CN-A641-01A-11D-A30E-08 TCGA-CN-A641-10A-01D-A30H-08 g.chr5:176707633G>T c.5690G>T c.(5689-5691)tGt>tTt p.C1897F HNSC 5 176707725 176707725 + Nonsense_Mutation SNP G G T TCGA-CN-4727-01A-01D-1434-08 TCGA-CN-4727-10A-01D-1434-08 g.chr5:176707725G>T c.5782G>T c.(5782-5784)Gga>Tga p.G1928* HNSC 5 176707765 176707766 + Frame_Shift_Ins INS - - T TCGA-CV-A6JU-01A-11D-A31L-08 TCGA-CV-A6JU-10A-01D-A31J-08 g.chr5:176707765_176707766insT c.5822_5823insT c.(5821-5826)tatccafs p.P1942fs HNSC 5 176707779 176707780 + Frame_Shift_Ins INS - - T TCGA-CN-A641-01A-11D-A30E-08 TCGA-CN-A641-10A-01D-A30H-08 g.chr5:176707779_176707780insT c.5836_5837insT c.(5836-5838)attfs p.I1946fs HNSC 5 176707785 176707785 + Missense_Mutation SNP C C A TCGA-CN-A641-01A-11D-A30E-08 TCGA-CN-A641-10A-01D-A30H-08 g.chr5:176707785C>A c.5842C>A c.(5842-5844)Cgc>Agc p.R1948S HNSC 5 176707786 176707786 + Missense_Mutation SNP G G T TCGA-CN-A641-01A-11D-A30E-08 TCGA-CN-A641-10A-01D-A30H-08 g.chr5:176707786G>T c.5843G>T c.(5842-5844)cGc>cTc p.R1948L HNSC 5 176707798 176707798 + Frame_Shift_Del DEL G G - TCGA-KU-A66S-01A-21D-A30E-08 TCGA-KU-A66S-10A-01D-A30H-08 g.chr5:176707798delG c.5855delG c.(5854-5856)cggfs p.R1952fs HNSC 5 176709482 176709482 + Missense_Mutation SNP A A C TCGA-CN-A63T-01A-11D-A28R-08 TCGA-CN-A63T-10A-01D-A28U-08 g.chr5:176709482A>C c.5909A>C c.(5908-5910)gAg>gCg p.E1970A HNSC 5 176709508 176709508 + Nonsense_Mutation SNP G G T TCGA-CR-7364-01A-11D-2012-08 TCGA-CR-7364-10A-01D-2013-08 g.chr5:176709508G>T c.5935G>T c.(5935-5937)Gaa>Taa p.E1979* HNSC 5 176709523 176709523 + Nonsense_Mutation SNP C C T TCGA-CV-6956-01A-21D-2012-08 TCGA-CV-6956-10A-01D-2013-08 g.chr5:176709523C>T c.5950C>T c.(5950-5952)Cga>Tga p.R1984* HNSC 5 176709538 176709538 + Nonsense_Mutation SNP C C T TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr5:176709538C>T c.5965C>T c.(5965-5967)Caa>Taa p.Q1989* HNSC 5 176709547 176709547 + Missense_Mutation SNP G G C TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr5:176709547G>C c.5974G>C c.(5974-5976)Gat>Cat p.D1992H HNSC 5 176709563 176709563 + Missense_Mutation SNP A A G TCGA-CR-5247-01A-01D-2012-08 TCGA-CR-5247-10A-01D-2013-08 g.chr5:176709563A>G c.5990A>G c.(5989-5991)tAt>tGt p.Y1997C HNSC 5 176709577 176709577 + Missense_Mutation SNP G G C TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr5:176709577G>C c.6004G>C c.(6004-6006)Gac>Cac p.D2002H HNSC 5 176710792 176710792 + Missense_Mutation SNP G G A TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chr5:176710792G>A c.6014G>A c.(6013-6015)cGa>cAa p.R2005Q HNSC 5 176710803 176710803 + Missense_Mutation SNP G G A TCGA-CV-7242-01A-11D-2012-08 TCGA-CV-7242-10A-01D-2013-08 g.chr5:176710803G>A c.6025G>A c.(6025-6027)Gct>Act p.A2009T HNSC 5 176710861 176710861 + Frame_Shift_Del DEL A A - TCGA-D6-A6EO-01A-11D-A31L-08 TCGA-D6-A6EO-10A-01D-A31J-08 g.chr5:176710861delA c.6083delA c.(6082-6084)gaafs p.E2028fs HNSC 5 176710873 176710873 + Nonsense_Mutation SNP G G A TCGA-CN-A497-01A-11D-A24D-08 TCGA-CN-A497-10A-01D-A24F-08 g.chr5:176710873G>A c.6095G>A c.(6094-6096)tGg>tAg p.W2032* HNSC 5 176715829 176715829 + Missense_Mutation SNP T T G TCGA-CR-7395-01A-11D-2012-08 TCGA-CR-7395-10A-01D-2013-08 g.chr5:176715829T>G c.6161T>G c.(6160-6162)cTt>cGt p.L2054R HNSC 5 176719160 176719160 + Splice_Site SNP G G A TCGA-CN-A63T-01A-11D-A28R-08 TCGA-CN-A63T-10A-01D-A28U-08 g.chr5:176719160G>A c.e22+1 HNSC 5 176721512 176721512 + Silent SNP C C A TCGA-CV-7440-01A-11D-2129-08 TCGA-CV-7440-10A-01D-2129-08 g.chr5:176721512C>A c.7143C>A c.(7141-7143)ccC>ccA p.P2381P HNSC 5 176721768 176721768 + Missense_Mutation SNP G G C TCGA-CV-6942-01A-21D-2012-08 TCGA-CV-6942-10A-01D-2013-08 g.chr5:176721768G>C c.7399G>C c.(7399-7401)Gag>Cag p.E2467Q HNSC 5 176722361 176722361 + Frame_Shift_Del DEL T T - TCGA-P3-A6T8-01A-11D-A34J-08 TCGA-P3-A6T8-10A-01D-A34M-08 g.chr5:176722361delT c.7992delT c.(7990-7992)tctfs p.S2664fs KIPAN 5 176562309 176562309 + Missense_Mutation SNP T T C TCGA-CJ-4912-01A-01D-1429-08 TCGA-CJ-4912-11A-01D-1429-08 g.chr5:176562309T>C c.205T>C c.(205-207)Tac>Cac p.Y69H KIPAN 5 176562399 176562399 + Missense_Mutation SNP G G A TCGA-B8-5552-01B-11D-1669-08 TCGA-B8-5552-10A-01D-1669-08 g.chr5:176562399G>A c.295G>A c.(295-297)Gac>Aac p.D99N KIPAN 5 176562915 176562915 + Missense_Mutation SNP T T G TCGA-GL-A59T-01A-21D-A28G-10 TCGA-GL-A59T-10A-01D-A28G-10 g.chr5:176562915T>G c.811T>G c.(811-813)Tta>Gta p.L271V KIPAN 5 176631295 176631295 + Splice_Site SNP T T C TCGA-CJ-6031-01A-11D-1669-08 TCGA-CJ-6031-11A-01D-1669-08 g.chr5:176631295T>C c.e4+2 KIPAN 5 176636690 176636690 + Silent SNP G G A TCGA-B0-4712-01A-01D-1501-10 TCGA-B0-4712-11A-02D-1501-10 g.chr5:176636690G>A c.1290G>A c.(1288-1290)caG>caA p.Q430Q KIPAN 5 176637152 176637152 + Frame_Shift_Del DEL T T - TCGA-B0-5084-01A-01D-1462-08 TCGA-B0-5084-11A-01D-1462-08 g.chr5:176637152delT c.1752delT c.(1750-1752)actfs p.T584fs KIPAN 5 176637818 176637818 + Silent SNP A A C TCGA-BP-4988-01A-01D-1462-08 TCGA-BP-4988-11A-01D-1462-08 g.chr5:176637818A>C c.2418A>C c.(2416-2418)atA>atC p.I806I KIPAN 5 176637880 176637880 + Frame_Shift_Del DEL T T - TCGA-BQ-7060-01A-11D-1961-08 TCGA-BQ-7060-11A-01D-1961-08 g.chr5:176637880delT c.2480delT c.(2479-2481)attfs p.I827fs KIPAN 5 176639042 176639042 + Silent SNP T T C TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr5:176639042T>C c.3642T>C c.(3640-3642)ctT>ctC p.L1214L KIPAN 5 176665505 176665505 + Missense_Mutation SNP C C G TCGA-B2-4099-01A-02D-1251-10 TCGA-B2-4099-11A-01D-1251-10 g.chr5:176665505C>G c.4189C>G c.(4189-4191)Cca>Gca p.P1397A KIPAN 5 176684057 176684057 + Missense_Mutation SNP C C A TCGA-B4-5838-01A-11D-1669-08 TCGA-B4-5838-10A-01D-1669-08 g.chr5:176684057C>A c.4871C>A c.(4870-4872)cCa>cAa p.P1624Q KIPAN 5 176696648 176696648 + Silent SNP C C T TCGA-A4-7585-01A-11D-2136-08 TCGA-A4-7585-11A-01D-2136-08 g.chr5:176696648C>T c.5349C>T c.(5347-5349)aaC>aaT p.N1783N KIPAN 5 176709581 176709584 + Splice_Site DEL AAGT AAGT - TCGA-MH-A55W-01A-11D-A26P-10 TCGA-MH-A55W-10A-01D-A26P-10 g.chr5:176709581_176709584delAAGT c.6008_6009delAAGT c.(6007-6009)aaa>a p.K2003fs KIPAN 5 176720945 176720945 + Silent SNP C C T TCGA-CJ-6030-01A-11D-1669-08 TCGA-CJ-6030-11A-01D-1669-08 g.chr5:176720945C>T c.6576C>T c.(6574-6576)ttC>ttT p.F2192F KIPAN 5 176721020 176721020 + Missense_Mutation SNP G G T TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr5:176721020G>T c.6651G>T c.(6649-6651)gaG>gaT p.E2217D KIRC 5 176562309 176562309 + Missense_Mutation SNP T T C TCGA-CJ-4912-01A-01D-1429-08 TCGA-CJ-4912-11A-01D-1429-08 g.chr5:176562309T>C c.205T>C c.(205-207)Tac>Cac p.Y69H KIRC 5 176562399 176562399 + Missense_Mutation SNP G G A TCGA-B8-5552-01B-11D-1669-08 TCGA-B8-5552-10A-01D-1669-08 g.chr5:176562399G>A c.295G>A c.(295-297)Gac>Aac p.D99N KIRC 5 176631295 176631295 + Splice_Site SNP T T C TCGA-CJ-6031-01A-11D-1669-08 TCGA-CJ-6031-11A-01D-1669-08 g.chr5:176631295T>C c.e4+2 KIRC 5 176636690 176636690 + Silent SNP G G A TCGA-B0-4712-01A-01D-1501-10 TCGA-B0-4712-11A-02D-1501-10 g.chr5:176636690G>A c.1290G>A c.(1288-1290)caG>caA p.Q430Q KIRC 5 176637152 176637152 + Frame_Shift_Del DEL T T - TCGA-B0-5084-01A-01D-1462-08 TCGA-B0-5084-11A-01D-1462-08 g.chr5:176637152delT c.1752delT c.(1750-1752)actfs p.T584fs KIRC 5 176637818 176637818 + Silent SNP A A C TCGA-BP-4988-01A-01D-1462-08 TCGA-BP-4988-11A-01D-1462-08 g.chr5:176637818A>C c.2418A>C c.(2416-2418)atA>atC p.I806I KIRC 5 176665505 176665505 + Missense_Mutation SNP C C G TCGA-B2-4099-01A-02D-1251-10 TCGA-B2-4099-11A-01D-1251-10 g.chr5:176665505C>G c.4189C>G c.(4189-4191)Cca>Gca p.P1397A KIRC 5 176684057 176684057 + Missense_Mutation SNP C C A TCGA-B4-5838-01A-11D-1669-08 TCGA-B4-5838-10A-01D-1669-08 g.chr5:176684057C>A c.4871C>A c.(4870-4872)cCa>cAa p.P1624Q KIRC 5 176720945 176720945 + Silent SNP C C T TCGA-CJ-6030-01A-11D-1669-08 TCGA-CJ-6030-11A-01D-1669-08 g.chr5:176720945C>T c.6576C>T c.(6574-6576)ttC>ttT p.F2192F KIRP 5 176562915 176562915 + Missense_Mutation SNP T T G TCGA-GL-A59T-01A-21D-A28G-10 TCGA-GL-A59T-10A-01D-A28G-10 g.chr5:176562915T>G c.811T>G c.(811-813)Tta>Gta p.L271V KIRP 5 176637880 176637880 + Frame_Shift_Del DEL T T - TCGA-BQ-7060-01A-11D-1961-08 TCGA-BQ-7060-11A-01D-1961-08 g.chr5:176637880delT c.2480delT c.(2479-2481)attfs p.I827fs KIRP 5 176639042 176639042 + Silent SNP T T C TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr5:176639042T>C c.3642T>C c.(3640-3642)ctT>ctC p.L1214L KIRP 5 176696648 176696648 + Silent SNP C C T TCGA-A4-7585-01A-11D-2136-08 TCGA-A4-7585-11A-01D-2136-08 g.chr5:176696648C>T c.5349C>T c.(5347-5349)aaC>aaT p.N1783N KIRP 5 176709581 176709584 + Splice_Site DEL AAGT AAGT - TCGA-MH-A55W-01A-11D-A26P-10 TCGA-MH-A55W-10A-01D-A26P-10 g.chr5:176709581_176709584delAAGT c.6008_6009delAAGT c.(6007-6009)aaa>a p.K2003fs KIRP 5 176721020 176721020 + Missense_Mutation SNP G G T TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr5:176721020G>T c.6651G>T c.(6649-6651)gaG>gaT p.E2217D LGG 5 176638615 176638615 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:176638615G>A c.3215G>A c.(3214-3216)cGa>cAa p.R1072Q LGG 5 176638954 176638954 + Missense_Mutation SNP G G T TCGA-S9-A6WG-01A-11D-A33T-08 TCGA-S9-A6WG-10A-01D-A33W-08 g.chr5:176638954G>T c.3554G>T c.(3553-3555)tGt>tTt p.C1185F LGG 5 176707732 176707732 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:176707732G>A c.5789G>A c.(5788-5790)cGc>cAc p.R1930H LGG 5 176722240 176722240 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:176722240C>A c.7871C>A c.(7870-7872)cCc>cAc p.P2624H LIHC 5 176562164 176562164 + Silent SNP G G A TCGA-EP-A26S-01A-11D-A16V-10 TCGA-EP-A26S-10A-01D-A16V-10 g.chr5:176562164G>A c.60G>A c.(58-60)gtG>gtA p.V20V LIHC 5 176562395 176562395 + Missense_Mutation SNP T T G TCGA-G3-A5SJ-01A-11D-A27I-10 TCGA-G3-A5SJ-10A-01D-A27I-10 g.chr5:176562395T>G c.291T>G c.(289-291)ttT>ttG p.F97L LIHC 5 176637954 176637954 + Missense_Mutation SNP A A G TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr5:176637954A>G c.2554A>G c.(2554-2556)Ata>Gta p.I852V LIHC 5 176638499 176638499 + Frame_Shift_Del DEL T T - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr5:176638499delT c.3099delT c.(3097-3099)gctfs p.A1033fs LIHC 5 176721059 176721059 + Silent SNP A A G TCGA-2Y-A9H1-01A-11D-A382-10 TCGA-2Y-A9H1-10A-01D-A385-10 g.chr5:176721059A>G c.6690A>G c.(6688-6690)ccA>ccG p.P2230P LIHC 5 176721088 176721088 + Nonsense_Mutation SNP C C A TCGA-G3-A5SK-01A-11D-A27I-10 TCGA-G3-A5SK-10A-01D-A27I-10 g.chr5:176721088C>A c.6719C>A c.(6718-6720)tCa>tAa p.S2240* LIHC 5 176721162 176721162 + Missense_Mutation SNP T T C TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr5:176721162T>C c.6793T>C c.(6793-6795)Tcc>Ccc p.S2265P LIHC 5 176721807 176721807 + Missense_Mutation SNP G G A TCGA-CC-A8HV-01A-11D-A35Z-10 TCGA-CC-A8HV-10A-01D-A35Z-10 g.chr5:176721807G>A c.7438G>A c.(7438-7440)Gat>Aat p.D2480N LIHC 5 176722236 176722236 + Missense_Mutation SNP A A C TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr5:176722236A>C c.7867A>C c.(7867-7869)Agt>Cgt p.S2623R LIHC 5 176722361 176722361 + Silent SNP T T C TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr5:176722361T>C c.7992T>C c.(7990-7992)tcT>tcC p.S2664S LIHC 5 176722371 176722371 + Missense_Mutation SNP G G A TCGA-2Y-A9H3-01A-11D-A382-10 TCGA-2Y-A9H3-10A-01D-A385-10 g.chr5:176722371G>A c.8002G>A c.(8002-8004)Ggg>Agg p.G2668R LUAD 5 176562339 176562339 + Missense_Mutation SNP G G T TCGA-91-A4BC-01A-11D-A24D-08 TCGA-91-A4BC-10A-01D-A24F-08 g.chr5:176562339G>T c.235G>T c.(235-237)Gcc>Tcc p.A79S LUAD 5 176562359 176562359 + Missense_Mutation SNP G G T TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr5:176562359G>T c.255G>T c.(253-255)gaG>gaT p.E85D LUAD 5 176562677 176562677 + Silent SNP C C T TCGA-55-8085-01A-11D-2238-08 TCGA-55-8085-10A-01D-2238-08 g.chr5:176562677C>T c.573C>T c.(571-573)gcC>gcT p.A191A LUAD 5 176562850 176562850 + Frame_Shift_Del DEL A A - TCGA-44-7671-01A-11D-2063-08 TCGA-44-7671-10A-01D-2063-08 g.chr5:176562850delA c.746delA c.(745-747)gaafs p.E249fs LUAD 5 176636857 176636857 + Missense_Mutation SNP C C G TCGA-49-6745-01A-11D-1855-08 TCGA-49-6745-11A-01D-1855-08 g.chr5:176636857C>G c.1457C>G c.(1456-1458)tCt>tGt p.S486C LUAD 5 176637018 176637018 + Missense_Mutation SNP G G T TCGA-55-7903-01A-11D-2167-08 TCGA-55-7903-10A-01D-2167-08 g.chr5:176637018G>T c.1618G>T c.(1618-1620)Ggg>Tgg p.G540W LUAD 5 176637041 176637041 + Silent SNP C C T TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr5:176637041C>T c.1641C>T c.(1639-1641)gcC>gcT p.A547A LUAD 5 176637183 176637183 + Missense_Mutation SNP G G A TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr5:176637183G>A c.1783G>A c.(1783-1785)Gag>Aag p.E595K LUAD 5 176637325 176637325 + Missense_Mutation SNP C C T TCGA-55-6968-01A-11D-1945-08 TCGA-55-6968-11A-01D-1945-08 g.chr5:176637325C>T c.1925C>T c.(1924-1926)tCt>tTt p.S642F LUAD 5 176637505 176637505 + Missense_Mutation SNP C C A TCGA-80-5611-01A-01D-1625-08 TCGA-80-5611-10A-01D-1625-08 g.chr5:176637505C>A c.2105C>A c.(2104-2106)cCt>cAt p.P702H LUAD 5 176637951 176637951 + Missense_Mutation SNP G G C TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr5:176637951G>C c.2551G>C c.(2551-2553)Gac>Cac p.D851H LUAD 5 176638942 176638942 + Missense_Mutation SNP A A T TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr5:176638942A>T c.3542A>T c.(3541-3543)gAa>gTa p.E1181V LUAD 5 176638954 176638954 + Missense_Mutation SNP G G T TCGA-17-Z016-01A-01W-0746-08 TCGA-17-Z016-11A-01W-0746-08 g.chr5:176638954G>T c.3554G>T c.(3553-3555)tGt>tTt p.C1185F LUAD 5 176665401 176665401 + Missense_Mutation SNP G G C TCGA-05-4249-01A-01D-1105-08 TCGA-05-4249-10A-01D-1105-08 g.chr5:176665401G>C c.4085G>C c.(4084-4086)gGa>gCa p.G1362A LUAD 5 176671224 176671224 + Missense_Mutation SNP G G A TCGA-17-Z059-01A-01W-0747-08 TCGA-17-Z059-11A-01W-0747-08 g.chr5:176671224G>A c.4331G>A c.(4330-4332)gGc>gAc p.G1444D LUAD 5 176673678 176673678 + Splice_Site SNP G G T TCGA-78-8660-01A-11D-2393-08 TCGA-78-8660-10A-01D-2393-08 g.chr5:176673678G>T c.e10-1 LUAD 5 176673679 176673679 + Splice_Site SNP G G T TCGA-78-8660-01A-11D-2393-08 TCGA-78-8660-10A-01D-2393-08 g.chr5:176673679G>T c.4379G>T c.(4378-4380)gGc>gTc p.G1460V LUAD 5 176696757 176696757 + Missense_Mutation SNP G G A TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr5:176696757G>A c.5458G>A c.(5458-5460)Gtg>Atg p.V1820M LUAD 5 176707624 176707624 + Missense_Mutation SNP G G T TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr5:176707624G>T c.5681G>T c.(5680-5682)cGt>cTt p.R1894L LUAD 5 176707799 176707799 + Silent SNP G G T TCGA-91-6848-01A-11D-1945-08 TCGA-91-6848-11A-01D-1945-08 g.chr5:176707799G>T c.5856G>T c.(5854-5856)cgG>cgT p.R1952R LUAD 5 176709559 176709559 + Missense_Mutation SNP T T A TCGA-17-Z000-01A-01W-0746-08 TCGA-17-Z000-11A-01W-0746-08 g.chr5:176709559T>A c.5986T>A c.(5986-5988)Ttc>Atc p.F1996I LUAD 5 176710798 176710798 + Missense_Mutation SNP T T C TCGA-50-5946-01A-11D-1753-08 TCGA-50-5946-10A-01D-1753-08 g.chr5:176710798T>C c.6020T>C c.(6019-6021)aTt>aCt p.I2007T LUAD 5 176710860 176710860 + Missense_Mutation SNP G G A TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr5:176710860G>A c.6082G>A c.(6082-6084)Gaa>Aaa p.E2028K LUAD 5 176710903 176710903 + Frame_Shift_Del DEL T T - TCGA-17-Z050-01A-01W-0747-08 TCGA-17-Z050-11A-01W-0747-08 g.chr5:176710903delT c.6125delT c.(6124-6126)cttfs p.L2042fs LUAD 5 176721186 176721186 + Missense_Mutation SNP T T G TCGA-05-4430-01A-02D-1265-08 TCGA-05-4430-10A-01D-1265-08 g.chr5:176721186T>G c.6817T>G c.(6817-6819)Tgt>Ggt p.C2273G LUAD 5 176721339 176721339 + Missense_Mutation SNP G G A TCGA-17-Z056-01A-01W-0747-08 TCGA-17-Z056-11A-01W-0747-08 g.chr5:176721339G>A c.6970G>A c.(6970-6972)Gga>Aga p.G2324R LUAD 5 176721900 176721900 + Missense_Mutation SNP G G C TCGA-97-A4M5-01A-11D-A24P-08 TCGA-97-A4M5-10A-01D-A24P-08 g.chr5:176721900G>C c.7531G>C c.(7531-7533)Gat>Cat p.D2511H LUAD 5 176722109 176722109 + Silent SNP G G A TCGA-91-8499-01A-11D-2393-08 TCGA-91-8499-10A-01D-2393-08 g.chr5:176722109G>A c.7740G>A c.(7738-7740)gcG>gcA p.A2580A LUAD 5 176722250 176722250 + Silent SNP G G T TCGA-86-7954-01A-11D-2184-08 TCGA-86-7954-10A-01D-2184-08 g.chr5:176722250G>T c.7881G>T c.(7879-7881)ctG>ctT p.L2627L LUSC 5 176637166 176637166 + Missense_Mutation SNP C C G TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr5:176637166C>G c.1766C>G c.(1765-1767)tCt>tGt p.S589C LUSC 5 176637416 176637416 + Silent SNP A A T TCGA-18-4721-01A-01D-1441-08 TCGA-18-4721-11A-01D-1441-08 g.chr5:176637416A>T c.2016A>T c.(2014-2016)acA>acT p.T672T LUSC 5 176638020 176638020 + Nonsense_Mutation SNP G G T TCGA-34-5231-01A-21D-1817-08 TCGA-34-5231-10A-01D-1817-08 g.chr5:176638020G>T c.2620G>T c.(2620-2622)Gag>Tag p.E874* LUSC 5 176638319 176638319 + Missense_Mutation SNP G G C TCGA-22-4595-01A-01D-1267-08 TCGA-22-4595-11A-01D-1267-08 g.chr5:176638319G>C c.2919G>C c.(2917-2919)caG>caC p.Q973H LUSC 5 176638381 176638381 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr5:176638381C>T c.2981C>T c.(2980-2982)tCc>tTc p.S994F LUSC 5 176638561 176638561 + Missense_Mutation SNP G G C TCGA-21-5782-01A-01D-1632-08 TCGA-21-5782-10A-01D-1632-08 g.chr5:176638561G>C c.3161G>C c.(3160-3162)aGa>aCa p.R1054T LUSC 5 176673711 176673711 + Nonsense_Mutation SNP C C T TCGA-66-2786-01A-01D-1522-08 TCGA-66-2786-11A-01D-1522-08 g.chr5:176673711C>T c.4411C>T c.(4411-4413)Cga>Tga p.R1471* LUSC 5 176678730 176678730 + Splice_Site SNP G G C TCGA-60-2724-01A-01D-1522-08 TCGA-60-2724-11A-01D-1522-08 g.chr5:176678730G>C c.e12-1 LUSC 5 176684105 176684105 + Missense_Mutation SNP G G C TCGA-46-6026-01A-11D-1817-08 TCGA-46-6026-10A-01D-1817-08 g.chr5:176684105G>C c.4919G>C c.(4918-4920)tGt>tCt p.C1640S LUSC 5 176696631 176696631 + Nonsense_Mutation SNP C C T TCGA-34-5927-01A-11D-1817-08 TCGA-34-5927-10A-01D-1817-08 g.chr5:176696631C>T c.5332C>T c.(5332-5334)Cga>Tga p.R1778* LUSC 5 176710800 176710800 + Missense_Mutation SNP G G A TCGA-34-5929-01A-11D-1817-08 TCGA-34-5929-11A-01D-1817-08 g.chr5:176710800G>A c.6022G>A c.(6022-6024)Gat>Aat p.D2008N OV 5 176562394 176562394 + Missense_Mutation SNP T T A TCGA-29-1777-01A-01W-0639-09 TCGA-29-1777-10A-01W-0639-09 g.chr5:176562394T>A c.290T>A c.(289-291)tTt>tAt p.F97Y OV 5 176665275 176665275 + Missense_Mutation SNP G G A TCGA-29-2432-01A-01D-1526-09 TCGA-29-2432-10A-01D-1526-09 g.chr5:176665275G>A c.3959G>A c.(3958-3960)cGa>cAa p.R1320Q OV 5 176687050 176687050 + Missense_Mutation SNP C C A TCGA-24-0980-01A-01W-0421-09 TCGA-24-0980-10A-01W-0421-09 g.chr5:176687050C>A c.5027C>A c.(5026-5028)gCt>gAt p.A1676D OV 5 176715818 176715818 + Splice_Site SNP A A C TCGA-29-1691-01A-01W-0633-09 TCGA-29-1691-10A-01W-0633-09 g.chr5:176715818A>C c.e21-1 OV 5 176721628 176721628 + Missense_Mutation SNP C C G TCGA-24-1422-01A-01W-0545-08 TCGA-24-1422-10A-01W-0545-08 g.chr5:176721628C>G c.7259C>G c.(7258-7260)cCt>cGt p.P2420R PAAD 5 176562201 176562201 + Missense_Mutation SNP G G T TCGA-HZ-A77Q-01A-11D-A36O-08 TCGA-HZ-A77Q-10A-01D-A367-08 g.chr5:176562201G>T c.97G>T c.(97-99)Ggt>Tgt p.G33C PAAD 5 176562809 176562809 + Silent SNP A A G TCGA-IB-A5SQ-01A-11D-A32N-08 TCGA-IB-A5SQ-10A-01D-A32N-08 g.chr5:176562809A>G c.705A>G c.(703-705)acA>acG p.T235T PAAD 5 176562876 176562876 + Missense_Mutation SNP T T C TCGA-2L-AAQI-01A-12D-A397-08 TCGA-2L-AAQI-11A-11D-A39A-08 g.chr5:176562876T>C c.772T>C c.(772-774)Ttt>Ctt p.F258L PAAD 5 176638654 176638654 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr5:176638654C>A c.3254C>A c.(3253-3255)cCt>cAt p.P1085H PAAD 5 176639155 176639155 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr5:176639155G>A c.3755G>A c.(3754-3756)gGa>gAa p.G1252E PAAD 5 176687011 176687011 + Missense_Mutation SNP G G A TCGA-IB-AAUR-01A-21D-A38G-08 TCGA-IB-AAUR-10A-01D-A38J-08 g.chr5:176687011G>A c.4988G>A c.(4987-4989)cGc>cAc p.R1663H PAAD 5 176710903 176710903 + Frame_Shift_Del DEL T T - TCGA-3A-A9IR-01A-11D-A38G-08 TCGA-3A-A9IR-10A-01D-A38J-08 g.chr5:176710903delT c.6125delT c.(6124-6126)cttfs p.L2042fs PAAD 5 176722104 176722104 + Nonsense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr5:176722104C>T c.7735C>T c.(7735-7737)Cag>Tag p.Q2579* PRAD 5 176636871 176636871 + Missense_Mutation SNP G G A TCGA-EJ-5496-01A-01D-1576-08 TCGA-EJ-5496-10A-01D-1577-08 g.chr5:176636871G>A c.1471G>A c.(1471-1473)Gaa>Aaa p.E491K PRAD 5 176638166 176638166 + Silent SNP G G A TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr5:176638166G>A c.2766G>A c.(2764-2766)acG>acA p.T922T PRAD 5 176696757 176696757 + Missense_Mutation SNP G G A TCGA-VP-A87B-01A-11D-A34U-08 TCGA-VP-A87B-10A-01D-A34X-08 g.chr5:176696757G>A c.5458G>A c.(5458-5460)Gtg>Atg p.V1820M PRAD 5 176707813 176707813 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr5:176707813G>A c.5870G>A c.(5869-5871)cGg>cAg p.R1957Q PRAD 5 176719086 176719086 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr5:176719086C>T c.6390C>T c.(6388-6390)ctC>ctT p.L2130L PRAD 5 176720970 176720970 + Missense_Mutation SNP T T C TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr5:176720970T>C c.6601T>C c.(6601-6603)Tct>Cct p.S2201P PRAD 5 176720972 176720972 + Silent SNP T T A TCGA-G9-7521-01A-11D-2260-08 TCGA-G9-7521-10A-01D-2260-08 g.chr5:176720972T>A c.6603T>A c.(6601-6603)tcT>tcA p.S2201S READ 5 176562826 176562826 + Missense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr5:176562826G>T c.722G>T c.(721-723)aGa>aTa p.R241I READ 5 176665503 176665503 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:176665503C>T c.4187C>T c.(4186-4188)aCg>aTg p.T1396M READ 5 176671259 176671259 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:176671259G>T c.4366G>T c.(4366-4368)Gat>Tat p.D1456Y READ 5 176696731 176696731 + Missense_Mutation SNP G G A TCGA-AH-6644-01A-21D-1826-10 TCGA-AH-6644-10A-01D-1826-10 g.chr5:176696731G>A c.5432G>A c.(5431-5433)cGa>cAa p.R1811Q READ 5 176721629 176721629 + Silent SNP T T C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr5:176721629T>C c.7260T>C c.(7258-7260)ccT>ccC p.P2420P READ 5 176721701 176721701 + Silent SNP G G A TCGA-AG-A014-01A-02W-A00K-09 TCGA-AG-A014-10A-01W-A00K-09 g.chr5:176721701G>A c.7332G>A c.(7330-7332)caG>caA p.Q2444Q SARC 5 176638415 176638415 + Silent SNP C C T TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr5:176638415C>T c.3015C>T c.(3013-3015)ctC>ctT p.L1005L SARC 5 176721767 176721767 + Silent SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr5:176721767G>A c.7398G>A c.(7396-7398)aaG>aaA p.K2466K SKCM 5 176562160 176562160 + Missense_Mutation SNP C C T TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr5:176562160C>T c.56C>T c.(55-57)cCa>cTa p.P19L SKCM 5 176562207 176562207 + Missense_Mutation SNP G G A TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr5:176562207G>A c.103G>A c.(103-105)Ggt>Agt p.G35S SKCM 5 176562432 176562432 + Missense_Mutation SNP C C T TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr5:176562432C>T c.328C>T c.(328-330)Cca>Tca p.P110S SKCM 5 176562927 176562927 + Missense_Mutation SNP A A C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr5:176562927A>C c.823A>C c.(823-825)Aat>Cat p.N275H SKCM 5 176631248 176631248 + Silent SNP C C T TCGA-D9-A6EA-06A-11D-A30X-08 TCGA-D9-A6EA-10A-01D-A30X-08 g.chr5:176631248C>T c.1191C>T c.(1189-1191)gtC>gtT p.V397V SKCM 5 176636777 176636777 + Silent SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr5:176636777C>T c.1377C>T c.(1375-1377)gaC>gaT p.D459D SKCM 5 176637091 176637091 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr5:176637091C>T c.1691C>T c.(1690-1692)gCc>gTc p.A564V SKCM 5 176637326 176637326 + Silent SNP T T A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr5:176637326T>A c.1926T>A c.(1924-1926)tcT>tcA p.S642S SKCM 5 176637511 176637511 + Missense_Mutation SNP T T A TCGA-FS-A1ZC-06A-11D-A197-08 TCGA-FS-A1ZC-10A-01D-A199-08 g.chr5:176637511T>A c.2111T>A c.(2110-2112)aTt>aAt p.I704N SKCM 5 176638012 176638012 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr5:176638012C>T c.2612C>T c.(2611-2613)tCc>tTc p.S871F SKCM 5 176638258 176638258 + Missense_Mutation SNP C C T TCGA-EE-A3J4-06A-11D-A20D-08 TCGA-EE-A3J4-10A-01D-A20D-08 g.chr5:176638258C>T c.2858C>T c.(2857-2859)tCt>tTt p.S953F SKCM 5 176638265 176638265 + Silent SNP T T C TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr5:176638265T>C c.2865T>C c.(2863-2865)gtT>gtC p.V955V SKCM 5 176638324 176638324 + Missense_Mutation SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr5:176638324C>T c.2924C>T c.(2923-2925)tCc>tTc p.S975F SKCM 5 176638325 176638325 + Silent SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr5:176638325C>T c.2925C>T c.(2923-2925)tcC>tcT p.S975S SKCM 5 176638709 176638709 + Silent SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr5:176638709C>T c.3309C>T c.(3307-3309)gaC>gaT p.D1103D SKCM 5 176638794 176638794 + Missense_Mutation SNP G G A TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr5:176638794G>A c.3394G>A c.(3394-3396)Gga>Aga p.G1132R SKCM 5 176638795 176638795 + Missense_Mutation SNP G G A TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr5:176638795G>A c.3395G>A c.(3394-3396)gGa>gAa p.G1132E SKCM 5 176696688 176696688 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr5:176696688C>T c.5389C>T c.(5389-5391)Ctc>Ttc p.L1797F SKCM 5 176696738 176696738 + Silent SNP C C T TCGA-FR-A3YN-06A-11D-A23B-08 TCGA-FR-A3YN-10A-01D-A23B-08 g.chr5:176696738C>T c.5439C>T c.(5437-5439)ttC>ttT p.F1813F SKCM 5 176696740 176696740 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr5:176696740C>T c.5441C>T c.(5440-5442)cCt>cTt p.P1814L SKCM 5 176696747 176696747 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr5:176696747G>A c.5448G>A c.(5446-5448)atG>atA p.M1816I SKCM 5 176700722 176700722 + Silent SNP G G A TCGA-RP-A694-06A-11D-A30X-08 TCGA-RP-A694-10A-01D-A30X-08 g.chr5:176700722G>A c.5559G>A c.(5557-5559)gaG>gaA p.E1853E SKCM 5 176707784 176707784 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr5:176707784C>T c.5841C>T c.(5839-5841)ttC>ttT p.F1947F SKCM 5 176709573 176709573 + Silent SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr5:176709573C>T c.6000C>T c.(5998-6000)acC>acT p.T2000T SKCM 5 176710809 176710809 + Missense_Mutation SNP C C T TCGA-FR-A3YO-06A-11D-A23B-08 TCGA-FR-A3YO-10A-01D-A23B-08 g.chr5:176710809C>T c.6031C>T c.(6031-6033)Ccc>Tcc p.P2011S SKCM 5 176719072 176719072 + Missense_Mutation SNP G G C TCGA-GF-A6C8-06A-12D-A30X-08 TCGA-GF-A6C8-10A-01D-A30X-08 g.chr5:176719072G>C c.6376G>C c.(6376-6378)Gat>Cat p.D2126H SKCM 5 176719085 176719085 + Missense_Mutation SNP T T C TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr5:176719085T>C c.6389T>C c.(6388-6390)cTc>cCc p.L2130P SKCM 5 176719086 176719086 + Silent SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr5:176719086C>T c.6390C>T c.(6388-6390)ctC>ctT p.L2130L SKCM 5 176721287 176721287 + Silent SNP C C T TCGA-EE-A29T-06A-11D-A197-08 TCGA-EE-A29T-10A-01D-A199-08 g.chr5:176721287C>T c.6918C>T c.(6916-6918)tcC>tcT p.S2306S SKCM 5 176721292 176721292 + Missense_Mutation SNP C C T TCGA-GN-A265-06A-21D-A197-08 TCGA-GN-A265-10A-01D-A199-08 g.chr5:176721292C>T c.6923C>T c.(6922-6924)tCc>tTc p.S2308F SKCM 5 176721426 176721426 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr5:176721426C>T c.7057C>T c.(7057-7059)Cct>Tct p.P2353S SKCM 5 176721888 176721888 + Missense_Mutation SNP G G A TCGA-D3-A3CF-06A-11D-A196-08 TCGA-D3-A3CF-10A-01D-A198-08 g.chr5:176721888G>A c.7519G>A c.(7519-7521)Ggc>Agc p.G2507S SKCM 5 176721950 176721950 + Nonsense_Mutation SNP G G A TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr5:176721950G>A c.7581G>A c.(7579-7581)tgG>tgA p.W2527*

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 5 176562880 176562880 single base substitution C T downstream_gene_variant BLCA-CN 5 176562880 176562880 single base substitution C T exon_variant BLCA-CN 5 176562880 176562880 single base substitution C T intron_variant BLCA-CN 5 176562880 176562880 single base substitution C T missense_variant S259L 776C>T BLCA-CN 5 176637883 176637883 single base substitution C T downstream_gene_variant BLCA-CN 5 176637883 176637883 single base substitution C T missense_variant S559F 1676C>T BLCA-CN 5 176637883 176637883 single base substitution C T missense_variant S725F 2174C>T BLCA-CN 5 176637883 176637883 single base substitution C T missense_variant S828F 2483C>T BLCA-CN 5 176637883 176637883 single base substitution C T upstream_gene_variant BLCA-CN 5 176638676 176638676 single base substitution G C downstream_gene_variant BLCA-CN 5 176638676 176638676 single base substitution G C missense_variant Q1092H 3276G>C BLCA-CN 5 176638676 176638676 single base substitution G C missense_variant Q823H 2469G>C BLCA-CN 5 176638676 176638676 single base substitution G C missense_variant Q989H 2967G>C BLCA-CN 5 176638676 176638676 single base substitution G C upstream_gene_variant BLCA-CN 5 176662943 176662943 single base substitution C G 3_prime_UTR_variant BLCA-CN 5 176662943 176662943 single base substitution C G missense_variant H1037Q 3111C>G BLCA-CN 5 176662943 176662943 single base substitution C G missense_variant H1203Q 3609C>G BLCA-CN 5 176662943 176662943 single base substitution C G missense_variant H1306Q 3918C>G BLCA-CN 5 176721151 176721151 single base substitution T C downstream_gene_variant BLCA-CN 5 176721151 176721151 single base substitution T C missense_variant M1992T 5975T>C BLCA-CN 5 176721151 176721151 single base substitution T C missense_variant M2158T 6473T>C BLCA-CN 5 176721151 176721151 single base substitution T C missense_variant M2261T 6782T>C BLCA-CN 5 176721872 176721872 single base substitution G A downstream_gene_variant BLCA-CN 5 176721872 176721872 single base substitution G A synonymous_variant P2232P 6696G>A BLCA-CN 5 176721872 176721872 single base substitution G A synonymous_variant P2398P 7194G>A BLCA-CN 5 176721872 176721872 single base substitution G A synonymous_variant P2501P 7503G>A BLCA-CN 5 176722109 176722109 single base substitution G A downstream_gene_variant BLCA-CN 5 176722109 176722109 single base substitution G A synonymous_variant A2311A 6933G>A BLCA-CN 5 176722109 176722109 single base substitution G A synonymous_variant A2477A 7431G>A BLCA-CN 5 176722109 176722109 single base substitution G A synonymous_variant A2580A 7740G>A BLCA-CN 5 176729751 176729751 single base substitution A C downstream_gene_variant BLCA-US 5 176637917 176637917 single base substitution G A downstream_gene_variant BLCA-US 5 176637917 176637917 single base substitution G A synonymous_variant L570L 1710G>A BLCA-US 5 176637917 176637917 single base substitution G A synonymous_variant L736L 2208G>A BLCA-US 5 176637917 176637917 single base substitution G A synonymous_variant L839L 2517G>A BLCA-US 5 176637917 176637917 single base substitution G A upstream_gene_variant BLCA-US 5 176721473 176721473 single base substitution C G downstream_gene_variant BLCA-US 5 176721473 176721473 single base substitution C G synonymous_variant A2099A 6297C>G BLCA-US 5 176721473 176721473 single base substitution C G synonymous_variant A2265A 6795C>G BLCA-US 5 176721473 176721473 single base substitution C G synonymous_variant A2368A 7104C>G BLCA-US 5 176730193 176730193 single base substitution G C downstream_gene_variant BRCA-EU 5 176558336 176558337 deletion of <=200bp TT - upstream_gene_variant BRCA-EU 5 176559738 176559738 single base substitution G T upstream_gene_variant BRCA-EU 5 176559744 176559744 single base substitution A T upstream_gene_variant BRCA-EU 5 176560124 176560124 single base substitution G A 5_prime_UTR_variant BRCA-EU 5 176560124 176560124 single base substitution G A exon_variant BRCA-EU 5 176560124 176560124 single base substitution G A upstream_gene_variant BRCA-EU 5 176560715 176560715 single base substitution G A intron_variant BRCA-EU 5 176560715 176560715 single base substitution G A upstream_gene_variant BRCA-EU 5 176560715 176560715 single base substitution G C intron_variant BRCA-EU 5 176560715 176560715 single base substitution G C upstream_gene_variant BRCA-EU 5 176561372 176561372 single base substitution C T intron_variant BRCA-EU 5 176561372 176561372 single base substitution C T upstream_gene_variant BRCA-EU 5 176561742 176561742 single base substitution C G intron_variant BRCA-EU 5 176561742 176561742 single base substitution C G upstream_gene_variant BRCA-EU 5 176562738 176562738 single base substitution G C downstream_gene_variant BRCA-EU 5 176562738 176562738 single base substitution G C exon_variant BRCA-EU 5 176562738 176562738 single base substitution G C intron_variant BRCA-EU 5 176562738 176562738 single base substitution G C missense_variant D212H 634G>C BRCA-EU 5 176563895 176563895 single base substitution C T downstream_gene_variant BRCA-EU 5 176563895 176563895 single base substitution C T intron_variant BRCA-EU 5 176563895 176563895 single base substitution C T missense_variant P48S 142C>T BRCA-EU 5 176565032 176565032 single base substitution C T downstream_gene_variant BRCA-EU 5 176565032 176565032 single base substitution C T intron_variant BRCA-EU 5 176568219 176568219 single base substitution C T downstream_gene_variant BRCA-EU 5 176568219 176568219 single base substitution C T intron_variant BRCA-EU 5 176569127 176569127 single base substitution G A downstream_gene_variant BRCA-EU 5 176569127 176569127 single base substitution G A intron_variant BRCA-EU 5 176569364 176569364 single base substitution G T downstream_gene_variant BRCA-EU 5 176569364 176569364 single base substitution G T intron_variant BRCA-EU 5 176571898 176571898 single base substitution G A intron_variant BRCA-EU 5 176571928 176571928 deletion of <=200bp A - intron_variant BRCA-EU 5 176574491 176574495 multiple base substitution (>=2bp and <=200bp) AGTCA AG intron_variant BRCA-EU 5 176574496 176574496 single base substitution T G intron_variant BRCA-EU 5 176576016 176576016 single base substitution C T intron_variant BRCA-EU 5 176576116 176576116 single base substitution G A intron_variant BRCA-EU 5 176576417 176576417 single base substitution C T intron_variant BRCA-EU 5 176576430 176576430 single base substitution A T intron_variant BRCA-EU 5 176577054 176577054 single base substitution C A intron_variant BRCA-EU 5 176577351 176577351 single base substitution C G intron_variant BRCA-EU 5 176577615 176577615 single base substitution C G intron_variant BRCA-EU 5 176577710 176577710 single base substitution A G intron_variant BRCA-EU 5 176578419 176578419 single base substitution C T intron_variant BRCA-EU 5 176580439 176580439 single base substitution A G intron_variant BRCA-EU 5 176581679 176581679 single base substitution C G intron_variant BRCA-EU 5 176583002 176583002 single base substitution G C intron_variant BRCA-EU 5 176583651 176583651 single base substitution T A intron_variant BRCA-EU 5 176583805 176583805 single base substitution G A intron_variant BRCA-EU 5 176584643 176584643 single base substitution C T intron_variant BRCA-EU 5 176584948 176584948 single base substitution T A intron_variant BRCA-EU 5 176586899 176586899 single base substitution T A intron_variant BRCA-EU 5 176588074 176588074 single base substitution T C intron_variant BRCA-EU 5 176589088 176589088 single base substitution C G intron_variant BRCA-EU 5 176589620 176589620 single base substitution C T intron_variant BRCA-EU 5 176590373 176590373 single base substitution A G intron_variant BRCA-EU 5 176591907 176591907 single base substitution G T intron_variant BRCA-EU 5 176592283 176592283 single base substitution C T intron_variant BRCA-EU 5 176594238 176594238 single base substitution C G intron_variant BRCA-EU 5 176595938 176595938 single base substitution A C intron_variant BRCA-EU 5 176597288 176597288 deletion of <=200bp T - intron_variant BRCA-EU 5 176597550 176597550 single base substitution C T intron_variant BRCA-EU 5 176597871 176597871 single base substitution A T intron_variant BRCA-EU 5 176598137 176598137 single base substitution C T intron_variant BRCA-EU 5 176598634 176598634 single base substitution C T intron_variant BRCA-EU 5 176600719 176600719 single base substitution C T intron_variant BRCA-EU 5 176600962 176600962 single base substitution C T intron_variant BRCA-EU 5 176601716 176601716 single base substitution C T intron_variant BRCA-EU 5 176602030 176602030 single base substitution G A intron_variant BRCA-EU 5 176602123 176602123 single base substitution C T intron_variant BRCA-EU 5 176603105 176603105 single base substitution G A intron_variant BRCA-EU 5 176603938 176603938 single base substitution C G intron_variant BRCA-EU 5 176604349 176604349 single base substitution C T intron_variant BRCA-EU 5 176604767 176604767 single base substitution G C intron_variant BRCA-EU 5 176604894 176604894 single base substitution A T intron_variant BRCA-EU 5 176604999 176604999 single base substitution G A intron_variant BRCA-EU 5 176606373 176606373 single base substitution C T intron_variant BRCA-EU 5 176607793 176607793 single base substitution C T intron_variant BRCA-EU 5 176609434 176609434 single base substitution G A intron_variant BRCA-EU 5 176610969 176610969 single base substitution C G intron_variant BRCA-EU 5 176611500 176611500 single base substitution A G intron_variant BRCA-EU 5 176611934 176611934 single base substitution G A intron_variant BRCA-EU 5 176614450 176614450 single base substitution C T intron_variant BRCA-EU 5 176615096 176615096 single base substitution C G intron_variant BRCA-EU 5 176615303 176615303 single base substitution C G intron_variant BRCA-EU 5 176615683 176615683 deletion of <=200bp T - intron_variant BRCA-EU 5 176615846 176615846 single base substitution A T intron_variant BRCA-EU 5 176616368 176616368 single base substitution C T intron_variant BRCA-EU 5 176617328 176617328 single base substitution C T intron_variant BRCA-EU 5 176617342 176617342 single base substitution G A intron_variant BRCA-EU 5 176618858 176618858 single base substitution G C intron_variant BRCA-EU 5 176618888 176618888 single base substitution C T intron_variant BRCA-EU 5 176618888 176618888 single base substitution C T stop_gained Q311* 931C>T BRCA-EU 5 176618888 176618888 single base substitution C T stop_gained Q42* 124C>T BRCA-EU 5 176622008 176622008 single base substitution A C intron_variant BRCA-EU 5 176624020 176624020 single base substitution C G intron_variant BRCA-EU 5 176626203 176626203 single base substitution A G intron_variant BRCA-EU 5 176628546 176628546 single base substitution C G intron_variant BRCA-EU 5 176629296 176629296 single base substitution A T intron_variant BRCA-EU 5 176629311 176629311 single base substitution C G intron_variant BRCA-EU 5 176629719 176629719 single base substitution C G intron_variant BRCA-EU 5 176630436 176630436 single base substitution C G intron_variant BRCA-EU 5 176630535 176630535 single base substitution A G intron_variant BRCA-EU 5 176631303 176631303 single base substitution G A downstream_gene_variant BRCA-EU 5 176631303 176631303 single base substitution G A intron_variant BRCA-EU 5 176631437 176631437 single base substitution C A downstream_gene_variant BRCA-EU 5 176631437 176631437 single base substitution C A intron_variant BRCA-EU 5 176631786 176631787 deletion of <=200bp TG - downstream_gene_variant BRCA-EU 5 176631786 176631787 deletion of <=200bp TG - intron_variant BRCA-EU 5 176633488 176633488 single base substitution C T downstream_gene_variant BRCA-EU 5 176633488 176633488 single base substitution C T intron_variant BRCA-EU 5 176633791 176633791 single base substitution C G downstream_gene_variant BRCA-EU 5 176633791 176633791 single base substitution C G intron_variant BRCA-EU 5 176634229 176634229 single base substitution G C downstream_gene_variant BRCA-EU 5 176634229 176634229 single base substitution G C intron_variant BRCA-EU 5 176634229 176634229 single base substitution G C upstream_gene_variant BRCA-EU 5 176637762 176637762 single base substitution C G downstream_gene_variant BRCA-EU 5 176637762 176637762 single base substitution C G missense_variant R519G 1555C>G BRCA-EU 5 176637762 176637762 single base substitution C G missense_variant R685G 2053C>G BRCA-EU 5 176637762 176637762 single base substitution C G missense_variant R788G 2362C>G BRCA-EU 5 176637762 176637762 single base substitution C G upstream_gene_variant BRCA-EU 5 176638350 176638350 single base substitution G A downstream_gene_variant BRCA-EU 5 176638350 176638350 single base substitution G A missense_variant D715N 2143G>A BRCA-EU 5 176638350 176638350 single base substitution G A missense_variant D881N 2641G>A BRCA-EU 5 176638350 176638350 single base substitution G A missense_variant D984N 2950G>A BRCA-EU 5 176638350 176638350 single base substitution G A upstream_gene_variant BRCA-EU 5 176640373 176640373 single base substitution C T downstream_gene_variant BRCA-EU 5 176640373 176640373 single base substitution C T intron_variant BRCA-EU 5 176640494 176640494 single base substitution A C downstream_gene_variant BRCA-EU 5 176640494 176640494 single base substitution A C intron_variant BRCA-EU 5 176643679 176643679 single base substitution T G intron_variant BRCA-EU 5 176644040 176644040 deletion of <=200bp A - intron_variant BRCA-EU 5 176644134 176644134 single base substitution T A intron_variant BRCA-EU 5 176644382 176644382 single base substitution G A intron_variant BRCA-EU 5 176649311 176649311 single base substitution G A intron_variant BRCA-EU 5 176652673 176652673 single base substitution T C intron_variant BRCA-EU 5 176652744 176652744 single base substitution T C intron_variant BRCA-EU 5 176652978 176652978 deletion of <=200bp T - intron_variant BRCA-EU 5 176654426 176654426 single base substitution C T intron_variant BRCA-EU 5 176654528 176654528 single base substitution A G intron_variant BRCA-EU 5 176654985 176654985 insertion of <=200bp - T intron_variant BRCA-EU 5 176655571 176655571 deletion of <=200bp T - intron_variant BRCA-EU 5 176656471 176656471 single base substitution T C intron_variant BRCA-EU 5 176656972 176656972 single base substitution C T intron_variant BRCA-EU 5 176656978 176656978 single base substitution C T intron_variant BRCA-EU 5 176658365 176658365 single base substitution C T intron_variant BRCA-EU 5 176658578 176658578 single base substitution G A intron_variant BRCA-EU 5 176658745 176658745 single base substitution G A intron_variant BRCA-EU 5 176659344 176659344 single base substitution C A intron_variant BRCA-EU 5 176661229 176661229 single base substitution C T intron_variant BRCA-EU 5 176662704 176662704 single base substitution C G intron_variant BRCA-EU 5 176662842 176662844 deletion of <=200bp CGC - 3_prime_UTR_variant BRCA-EU 5 176662842 176662844 deletion of <=200bp CGC - inframe_deletion R1004 BRCA-EU 5 176662842 176662844 deletion of <=200bp CGC - inframe_deletion R1170 BRCA-EU 5 176662842 176662844 deletion of <=200bp CGC - inframe_deletion R1273 BRCA-EU 5 176662900 176662900 single base substitution T G 3_prime_UTR_variant BRCA-EU 5 176662900 176662900 single base substitution T G missense_variant F1023C 3068T>G BRCA-EU 5 176662900 176662900 single base substitution T G missense_variant F1189C 3566T>G BRCA-EU 5 176662900 176662900 single base substitution T G missense_variant F1292C 3875T>G BRCA-EU 5 176664035 176664035 single base substitution T C intron_variant BRCA-EU 5 176664778 176664778 single base substitution C T intron_variant BRCA-EU 5 176665545 176665545 single base substitution A T intron_variant BRCA-EU 5 176666236 176666236 single base substitution G C intron_variant BRCA-EU 5 176666486 176666486 single base substitution C T intron_variant BRCA-EU 5 176667383 176667383 single base substitution T A downstream_gene_variant BRCA-EU 5 176667383 176667383 single base substitution T A intron_variant BRCA-EU 5 176667976 176667976 single base substitution C T downstream_gene_variant BRCA-EU 5 176667976 176667976 single base substitution C T intron_variant BRCA-EU 5 176668258 176668258 single base substitution G A downstream_gene_variant BRCA-EU 5 176668258 176668258 single base substitution G A intron_variant BRCA-EU 5 176668875 176668875 single base substitution G A downstream_gene_variant BRCA-EU 5 176668875 176668875 single base substitution G A intron_variant BRCA-EU 5 176669119 176669119 single base substitution T C downstream_gene_variant BRCA-EU 5 176669119 176669119 single base substitution T C intron_variant BRCA-EU 5 176669335 176669335 single base substitution G C downstream_gene_variant BRCA-EU 5 176669335 176669335 single base substitution G C intron_variant BRCA-EU 5 176670938 176670938 single base substitution C A downstream_gene_variant BRCA-EU 5 176670938 176670938 single base substitution C A intron_variant BRCA-EU 5 176671610 176671610 single base substitution A T downstream_gene_variant BRCA-EU 5 176671610 176671610 single base substitution A T intron_variant BRCA-EU 5 176672442 176672442 single base substitution T C intron_variant BRCA-EU 5 176674271 176674271 single base substitution C T intron_variant BRCA-EU 5 176677439 176677439 single base substitution T C intron_variant BRCA-EU 5 176677767 176677787 deletion of <=200bp AAGCTGTCCTGTTTTTTATTT - intron_variant BRCA-EU 5 176677862 176677862 single base substitution T G intron_variant BRCA-EU 5 176681197 176681197 single base substitution C A intron_variant BRCA-EU 5 176682448 176682448 single base substitution C G intron_variant BRCA-EU 5 176682512 176682512 single base substitution C G intron_variant BRCA-EU 5 176682862 176682862 single base substitution G A intron_variant BRCA-EU 5 176682866 176682866 single base substitution C G intron_variant BRCA-EU 5 176683002 176683002 single base substitution G C intron_variant BRCA-EU 5 176683054 176683054 single base substitution G A intron_variant BRCA-EU 5 176683382 176683382 single base substitution C G intron_variant BRCA-EU 5 176683535 176683535 single base substitution C T intron_variant BRCA-EU 5 176683784 176683784 single base substitution C G intron_variant BRCA-EU 5 176684158 176684158 single base substitution G T splice_region_variant BRCA-EU 5 176684339 176684339 single base substitution C G intron_variant BRCA-EU 5 176685881 176685881 single base substitution C T intron_variant BRCA-EU 5 176688225 176688225 single base substitution C T intron_variant BRCA-EU 5 176688225 176688225 single base substitution C T upstream_gene_variant BRCA-EU 5 176688878 176688878 single base substitution G A intron_variant BRCA-EU 5 176688878 176688878 single base substitution G A upstream_gene_variant BRCA-EU 5 176689901 176689901 single base substitution C G intron_variant BRCA-EU 5 176689901 176689901 single base substitution C G upstream_gene_variant BRCA-EU 5 176694221 176694221 single base substitution C T intron_variant BRCA-EU 5 176694492 176694492 single base substitution A G intron_variant BRCA-EU 5 176696126 176696126 single base substitution A G intron_variant BRCA-EU 5 176696515 176696515 single base substitution G A intron_variant BRCA-EU 5 176699460 176699460 single base substitution G C downstream_gene_variant BRCA-EU 5 176699460 176699460 single base substitution G C intron_variant BRCA-EU 5 176699594 176699594 single base substitution A C downstream_gene_variant BRCA-EU 5 176699594 176699594 single base substitution A C intron_variant BRCA-EU 5 176700430 176700430 single base substitution T G downstream_gene_variant BRCA-EU 5 176700430 176700430 single base substitution T G intron_variant BRCA-EU 5 176700533 176700533 single base substitution C A downstream_gene_variant BRCA-EU 5 176700533 176700533 single base substitution C A intron_variant BRCA-EU 5 176700920 176700920 single base substitution G C downstream_gene_variant BRCA-EU 5 176700920 176700920 single base substitution G C intron_variant BRCA-EU 5 176701439 176701439 single base substitution C G downstream_gene_variant BRCA-EU 5 176701439 176701439 single base substitution C G intron_variant BRCA-EU 5 176703956 176703956 single base substitution A G downstream_gene_variant BRCA-EU 5 176703956 176703956 single base substitution A G intron_variant BRCA-EU 5 176707741 176707741 single base substitution A G downstream_gene_variant BRCA-EU 5 176707741 176707741 single base substitution A G missense_variant N1664S 4991A>G BRCA-EU 5 176707741 176707741 single base substitution A G missense_variant N1830S 5489A>G BRCA-EU 5 176707741 176707741 single base substitution A G missense_variant N1933S 5798A>G BRCA-EU 5 176709091 176709091 single base substitution G C downstream_gene_variant BRCA-EU 5 176709091 176709091 single base substitution G C intron_variant BRCA-EU 5 176709396 176709396 single base substitution A T downstream_gene_variant BRCA-EU 5 176709396 176709396 single base substitution A T intron_variant BRCA-EU 5 176712260 176712260 single base substitution C T downstream_gene_variant BRCA-EU 5 176712260 176712260 single base substitution C T intron_variant BRCA-EU 5 176712260 176712260 single base substitution C T upstream_gene_variant BRCA-EU 5 176712533 176712533 single base substitution C G downstream_gene_variant BRCA-EU 5 176712533 176712533 single base substitution C G intron_variant BRCA-EU 5 176712533 176712533 single base substitution C G upstream_gene_variant BRCA-EU 5 176713191 176713191 single base substitution C T intron_variant BRCA-EU 5 176713191 176713191 single base substitution C T upstream_gene_variant BRCA-EU 5 176713429 176713434 deletion of <=200bp GGAATG - intron_variant BRCA-EU 5 176713429 176713434 deletion of <=200bp GGAATG - upstream_gene_variant BRCA-EU 5 176714998 176714998 single base substitution G C intron_variant BRCA-EU 5 176714998 176714998 single base substitution G C upstream_gene_variant BRCA-EU 5 176715263 176715263 single base substitution C G intron_variant BRCA-EU 5 176715263 176715263 single base substitution C G upstream_gene_variant BRCA-EU 5 176715855 176715855 single base substitution C T exon_variant BRCA-EU 5 176715855 176715855 single base substitution C T missense_variant L1794F 5380C>T BRCA-EU 5 176715855 176715855 single base substitution C T missense_variant L1960F 5878C>T BRCA-EU 5 176715855 176715855 single base substitution C T missense_variant L2063F 6187C>T BRCA-EU 5 176716319 176716319 single base substitution C T intron_variant BRCA-EU 5 176716779 176716779 single base substitution T C intron_variant BRCA-EU 5 176717201 176717201 single base substitution G A intron_variant BRCA-EU 5 176719239 176719239 single base substitution A G downstream_gene_variant BRCA-EU 5 176719239 176719239 single base substitution A G intron_variant BRCA-EU 5 176719240 176719240 single base substitution A T downstream_gene_variant BRCA-EU 5 176719240 176719240 single base substitution A T intron_variant BRCA-EU 5 176722590 176722590 single base substitution C T 3_prime_UTR_variant BRCA-EU 5 176722590 176722590 single base substitution C T downstream_gene_variant BRCA-EU 5 176723365 176723365 single base substitution T C 3_prime_UTR_variant BRCA-EU 5 176723365 176723365 single base substitution T C downstream_gene_variant BRCA-EU 5 176724147 176724147 single base substitution G T 3_prime_UTR_variant BRCA-EU 5 176724147 176724147 single base substitution G T downstream_gene_variant BRCA-EU 5 176724148 176724148 single base substitution A G 3_prime_UTR_variant BRCA-EU 5 176724148 176724148 single base substitution A G downstream_gene_variant BRCA-EU 5 176724419 176724419 single base substitution A G 3_prime_UTR_variant BRCA-EU 5 176724419 176724419 single base substitution A G downstream_gene_variant BRCA-EU 5 176725967 176725969 deletion of <=200bp AGA - 3_prime_UTR_variant BRCA-EU 5 176725967 176725969 deletion of <=200bp AGA - downstream_gene_variant BRCA-EU 5 176728431 176728431 single base substitution A G downstream_gene_variant BRCA-EU 5 176729375 176729375 single base substitution C A downstream_gene_variant BRCA-EU 5 176731250 176731250 single base substitution G T downstream_gene_variant BRCA-EU 5 176731339 176731339 single base substitution C A downstream_gene_variant BRCA-FR 5 176569364 176569364 single base substitution G T downstream_gene_variant BRCA-FR 5 176569364 176569364 single base substitution G T intron_variant BRCA-FR 5 176571002 176571002 single base substitution C G intron_variant BRCA-FR 5 176577063 176577063 single base substitution G A intron_variant BRCA-FR 5 176577615 176577615 single base substitution C G intron_variant BRCA-FR 5 176583805 176583805 single base substitution G A intron_variant BRCA-FR 5 176584643 176584643 single base substitution C T intron_variant BRCA-FR 5 176589088 176589088 single base substitution C G intron_variant BRCA-FR 5 176590373 176590373 single base substitution A G intron_variant BRCA-FR 5 176591907 176591907 single base substitution G T intron_variant BRCA-FR 5 176597871 176597871 single base substitution A T intron_variant BRCA-FR 5 176598137 176598137 single base substitution C T intron_variant BRCA-FR 5 176600962 176600962 single base substitution C T intron_variant BRCA-FR 5 176603938 176603938 single base substitution C G intron_variant BRCA-FR 5 176604349 176604349 single base substitution C T intron_variant BRCA-FR 5 176625203 176625203 single base substitution T A intron_variant BRCA-FR 5 176640585 176640585 single base substitution C T downstream_gene_variant BRCA-FR 5 176640585 176640585 single base substitution C T intron_variant BRCA-FR 5 176642002 176642002 single base substitution G A intron_variant BRCA-FR 5 176643679 176643679 single base substitution T G intron_variant BRCA-FR 5 176649311 176649311 single base substitution G A intron_variant BRCA-FR 5 176656978 176656978 single base substitution C T intron_variant BRCA-FR 5 176668258 176668258 single base substitution G A downstream_gene_variant BRCA-FR 5 176668258 176668258 single base substitution G A intron_variant BRCA-FR 5 176668875 176668875 single base substitution G A downstream_gene_variant BRCA-FR 5 176668875 176668875 single base substitution G A intron_variant BRCA-FR 5 176671610 176671610 single base substitution A T downstream_gene_variant BRCA-FR 5 176671610 176671610 single base substitution A T intron_variant BRCA-FR 5 176682866 176682866 single base substitution C G intron_variant BRCA-FR 5 176682936 176682936 single base substitution T C intron_variant BRCA-FR 5 176694221 176694221 single base substitution C T intron_variant BRCA-FR 5 176700233 176700233 single base substitution G T downstream_gene_variant BRCA-FR 5 176700233 176700233 single base substitution G T intron_variant BRCA-FR 5 176700920 176700920 single base substitution G C downstream_gene_variant BRCA-FR 5 176700920 176700920 single base substitution G C intron_variant BRCA-FR 5 176708427 176708427 single base substitution C T downstream_gene_variant BRCA-FR 5 176708427 176708427 single base substitution C T intron_variant BRCA-FR 5 176725823 176725823 single base substitution C G 3_prime_UTR_variant BRCA-FR 5 176725823 176725823 single base substitution C G downstream_gene_variant BRCA-FR 5 176728692 176728692 single base substitution C G downstream_gene_variant BRCA-FR 5 176729375 176729375 single base substitution C A downstream_gene_variant BRCA-UK 5 176583651 176583651 single base substitution T A intron_variant BRCA-UK 5 176638508 176638508 single base substitution C G downstream_gene_variant BRCA-UK 5 176638508 176638508 single base substitution C G synonymous_variant A1036A 3108C>G BRCA-UK 5 176638508 176638508 single base substitution C G synonymous_variant A767A 2301C>G BRCA-UK 5 176638508 176638508 single base substitution C G synonymous_variant A933A 2799C>G BRCA-UK 5 176638508 176638508 single base substitution C G upstream_gene_variant BRCA-UK 5 176652673 176652673 single base substitution T C intron_variant BRCA-UK 5 176672442 176672442 single base substitution T C intron_variant BRCA-UK 5 176703803 176703803 single base substitution C G downstream_gene_variant BRCA-UK 5 176703803 176703803 single base substitution C G intron_variant BRCA-US 5 176562116 176562116 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 5 176562116 176562116 single base substitution C T exon_variant BRCA-US 5 176562116 176562116 single base substitution C T synonymous_variant T4T 12C>T BRCA-US 5 176562130 176562130 single base substitution G A 5_prime_UTR_variant BRCA-US 5 176562130 176562130 single base substitution G A exon_variant BRCA-US 5 176562130 176562130 single base substitution G A missense_variant R9K 26G>A BRCA-US 5 176562356 176562356 single base substitution A G exon_variant BRCA-US 5 176562356 176562356 single base substitution A G intron_variant BRCA-US 5 176562356 176562356 single base substitution A G synonymous_variant V84V 252A>G BRCA-US 5 176637364 176637364 single base substitution G A downstream_gene_variant BRCA-US 5 176637364 176637364 single base substitution G A missense_variant S386N 1157G>A BRCA-US 5 176637364 176637364 single base substitution G A missense_variant S552N 1655G>A BRCA-US 5 176637364 176637364 single base substitution G A missense_variant S655N 1964G>A BRCA-US 5 176637364 176637364 single base substitution G A upstream_gene_variant BRCA-US 5 176637449 176637449 single base substitution G T downstream_gene_variant BRCA-US 5 176637449 176637449 single base substitution G T missense_variant K414N 1242G>T BRCA-US 5 176637449 176637449 single base substitution G T missense_variant K580N 1740G>T BRCA-US 5 176637449 176637449 single base substitution G T missense_variant K683N 2049G>T BRCA-US 5 176637449 176637449 single base substitution G T upstream_gene_variant BRCA-US 5 176637903 176637903 single base substitution G T downstream_gene_variant BRCA-US 5 176637903 176637903 single base substitution G T missense_variant G566C 1696G>T BRCA-US 5 176637903 176637903 single base substitution G T missense_variant G732C 2194G>T BRCA-US 5 176637903 176637903 single base substitution G T missense_variant G835C 2503G>T BRCA-US 5 176637903 176637903 single base substitution G T upstream_gene_variant BRCA-US 5 176638368 176638368 single base substitution G T downstream_gene_variant BRCA-US 5 176638368 176638368 single base substitution G T stop_gained E721* 2161G>T BRCA-US 5 176638368 176638368 single base substitution G T stop_gained E887* 2659G>T BRCA-US 5 176638368 176638368 single base substitution G T stop_gained E990* 2968G>T BRCA-US 5 176638368 176638368 single base substitution G T upstream_gene_variant BRCA-US 5 176638917 176638917 single base substitution C T downstream_gene_variant BRCA-US 5 176638917 176638917 single base substitution C T missense_variant R1070C 3208C>T BRCA-US 5 176638917 176638917 single base substitution C T missense_variant R1173C 3517C>T BRCA-US 5 176638917 176638917 single base substitution C T missense_variant R904C 2710C>T BRCA-US 5 176638917 176638917 single base substitution C T upstream_gene_variant BRCA-US 5 176666775 176666775 single base substitution G A 3_prime_UTR_variant BRCA-US 5 176666775 176666775 single base substitution G A missense_variant R1135H 3404G>A BRCA-US 5 176666775 176666775 single base substitution G A missense_variant R1301H 3902G>A BRCA-US 5 176666775 176666775 single base substitution G A missense_variant R1404H 4211G>A BRCA-US 5 176678835 176678835 single base substitution C G missense_variant I1313M 3939C>G BRCA-US 5 176678835 176678835 single base substitution C G missense_variant I1479M 4437C>G BRCA-US 5 176678835 176678835 single base substitution C G missense_variant I1582M 4746C>G BRCA-US 5 176707706 176707706 single base substitution C G downstream_gene_variant BRCA-US 5 176707706 176707706 single base substitution C G missense_variant H1652Q 4956C>G BRCA-US 5 176707706 176707706 single base substitution C G missense_variant H1818Q 5454C>G BRCA-US 5 176707706 176707706 single base substitution C G missense_variant H1921Q 5763C>G BRCA-US 5 176709505 176709505 single base substitution G A downstream_gene_variant BRCA-US 5 176709505 176709505 single base substitution G A missense_variant E1709K 5125G>A BRCA-US 5 176709505 176709505 single base substitution G A missense_variant E1875K 5623G>A BRCA-US 5 176709505 176709505 single base substitution G A missense_variant E1978K 5932G>A BRCA-US 5 176719060 176719060 single base substitution T G exon_variant BRCA-US 5 176719060 176719060 single base substitution T G missense_variant F1853V 5557T>G BRCA-US 5 176719060 176719060 single base substitution T G missense_variant F2019V 6055T>G BRCA-US 5 176719060 176719060 single base substitution T G missense_variant F2122V 6364T>G BRCA-US 5 176719136 176719136 single base substitution T G downstream_gene_variant BRCA-US 5 176719136 176719136 single base substitution T G missense_variant L1878R 5633T>G BRCA-US 5 176719136 176719136 single base substitution T G missense_variant L2044R 6131T>G BRCA-US 5 176719136 176719136 single base substitution T G missense_variant L2147R 6440T>G BRCA-US 5 176720848 176720848 single base substitution C T downstream_gene_variant BRCA-US 5 176720848 176720848 single base substitution C T missense_variant P1891L 5672C>T BRCA-US 5 176720848 176720848 single base substitution C T missense_variant P2057L 6170C>T BRCA-US 5 176720848 176720848 single base substitution C T missense_variant P2160L 6479C>T BRCA-US 5 176721023 176721023 single base substitution C T downstream_gene_variant BRCA-US 5 176721023 176721023 single base substitution C T synonymous_variant I1949I 5847C>T BRCA-US 5 176721023 176721023 single base substitution C T synonymous_variant I2115I 6345C>T BRCA-US 5 176721023 176721023 single base substitution C T synonymous_variant I2218I 6654C>T BRCA-US 5 176721686 176721686 single base substitution G A downstream_gene_variant BRCA-US 5 176721686 176721686 single base substitution G A synonymous_variant L2170L 6510G>A BRCA-US 5 176721686 176721686 single base substitution G A synonymous_variant L2336L 7008G>A BRCA-US 5 176721686 176721686 single base substitution G A synonymous_variant L2439L 7317G>A BRCA-US 5 176729805 176729805 single base substitution C A downstream_gene_variant BTCA-JP 5 176562322 176562322 single base substitution G A exon_variant BTCA-JP 5 176562322 176562322 single base substitution G A intron_variant BTCA-JP 5 176562322 176562322 single base substitution G A missense_variant R73Q 218G>A BTCA-JP 5 176562491 176562491 single base substitution A T downstream_gene_variant BTCA-JP 5 176562491 176562491 single base substitution A T exon_variant BTCA-JP 5 176562491 176562491 single base substitution A T intron_variant BTCA-JP 5 176562491 176562491 single base substitution A T missense_variant E129D 387A>T BTCA-JP 5 176631082 176631082 single base substitution C G intron_variant BTCA-JP 5 176631141 176631141 single base substitution C T intron_variant BTCA-JP 5 176631141 176631141 single base substitution C T missense_variant R362W 1084C>T BTCA-JP 5 176631141 176631141 single base substitution C T missense_variant R93W 277C>T BTCA-JP 5 176637438 176637438 single base substitution A C downstream_gene_variant BTCA-JP 5 176637438 176637438 single base substitution A C missense_variant K411Q 1231A>C BTCA-JP 5 176637438 176637438 single base substitution A C missense_variant K577Q 1729A>C BTCA-JP 5 176637438 176637438 single base substitution A C missense_variant K680Q 2038A>C BTCA-JP 5 176637438 176637438 single base substitution A C upstream_gene_variant BTCA-JP 5 176707731 176707731 single base substitution C T downstream_gene_variant BTCA-JP 5 176707731 176707731 single base substitution C T missense_variant R1661C 4981C>T BTCA-JP 5 176707731 176707731 single base substitution C T missense_variant R1827C 5479C>T BTCA-JP 5 176707731 176707731 single base substitution C T missense_variant R1930C 5788C>T BTCA-JP 5 176721609 176721609 single base substitution T G downstream_gene_variant BTCA-JP 5 176721609 176721609 single base substitution T G missense_variant L2145V 6433T>G BTCA-JP 5 176721609 176721609 single base substitution T G missense_variant L2311V 6931T>G BTCA-JP 5 176721609 176721609 single base substitution T G missense_variant L2414V 7240T>G BTCA-JP 5 176728795 176728795 single base substitution C T downstream_gene_variant BTCA-JP 5 176729006 176729006 single base substitution G C downstream_gene_variant BTCA-JP 5 176730125 176730125 deletion of <=200bp C - downstream_gene_variant BTCA-JP 5 176731547 176731547 single base substitution G C downstream_gene_variant BTCA-JP 5 176731875 176731875 single base substitution C T downstream_gene_variant CESC-US 5 176562465 176562465 single base substitution C G downstream_gene_variant CESC-US 5 176562465 176562465 single base substitution C G exon_variant CESC-US 5 176562465 176562465 single base substitution C G intron_variant CESC-US 5 176562465 176562465 single base substitution C G missense_variant P121A 361C>G CESC-US 5 176562700 176562700 single base substitution C T downstream_gene_variant CESC-US 5 176562700 176562700 single base substitution C T exon_variant CESC-US 5 176562700 176562700 single base substitution C T intron_variant CESC-US 5 176562700 176562700 single base substitution C T missense_variant S199L 596C>T CESC-US 5 176636673 176636673 single base substitution G T missense_variant V156F 466G>T CESC-US 5 176636673 176636673 single base substitution G T missense_variant V322F 964G>T CESC-US 5 176636673 176636673 single base substitution G T missense_variant V425F 1273G>T CESC-US 5 176636673 176636673 single base substitution G T synonymous_variant ?156 CESC-US 5 176636673 176636673 single base substitution G T upstream_gene_variant CESC-US 5 176636850 176636850 single base substitution G C downstream_gene_variant CESC-US 5 176636850 176636850 single base substitution G C missense_variant E215Q 643G>C CESC-US 5 176636850 176636850 single base substitution G C missense_variant E381Q 1141G>C CESC-US 5 176636850 176636850 single base substitution G C missense_variant E484Q 1450G>C CESC-US 5 176636850 176636850 single base substitution G C upstream_gene_variant CESC-US 5 176636899 176636899 single base substitution G C downstream_gene_variant CESC-US 5 176636899 176636899 single base substitution G C missense_variant R231T 692G>C CESC-US 5 176636899 176636899 single base substitution G C missense_variant R397T 1190G>C CESC-US 5 176636899 176636899 single base substitution G C missense_variant R500T 1499G>C CESC-US 5 176636899 176636899 single base substitution G C upstream_gene_variant CESC-US 5 176637093 176637093 single base substitution C G downstream_gene_variant CESC-US 5 176637093 176637093 single base substitution C G missense_variant P296A 886C>G CESC-US 5 176637093 176637093 single base substitution C G missense_variant P462A 1384C>G CESC-US 5 176637093 176637093 single base substitution C G missense_variant P565A 1693C>G CESC-US 5 176637093 176637093 single base substitution C G upstream_gene_variant CESC-US 5 176637274 176637274 single base substitution G C downstream_gene_variant CESC-US 5 176637274 176637274 single base substitution G C missense_variant G356A 1067G>C CESC-US 5 176637274 176637274 single base substitution G C missense_variant G522A 1565G>C CESC-US 5 176637274 176637274 single base substitution G C missense_variant G625A 1874G>C CESC-US 5 176637274 176637274 single base substitution G C upstream_gene_variant CESC-US 5 176637327 176637327 single base substitution G A downstream_gene_variant CESC-US 5 176637327 176637327 single base substitution G A missense_variant D374N 1120G>A CESC-US 5 176637327 176637327 single base substitution G A missense_variant D540N 1618G>A CESC-US 5 176637327 176637327 single base substitution G A missense_variant D643N 1927G>A CESC-US 5 176637327 176637327 single base substitution G A upstream_gene_variant CESC-US 5 176637330 176637330 single base substitution G A downstream_gene_variant CESC-US 5 176637330 176637330 single base substitution G A missense_variant D375N 1123G>A CESC-US 5 176637330 176637330 single base substitution G A missense_variant D541N 1621G>A CESC-US 5 176637330 176637330 single base substitution G A missense_variant D644N 1930G>A CESC-US 5 176637330 176637330 single base substitution G A upstream_gene_variant CESC-US 5 176637357 176637357 single base substitution G A downstream_gene_variant CESC-US 5 176637357 176637357 single base substitution G A missense_variant E384K 1150G>A CESC-US 5 176637357 176637357 single base substitution G A missense_variant E550K 1648G>A CESC-US 5 176637357 176637357 single base substitution G A missense_variant E653K 1957G>A CESC-US 5 176637357 176637357 single base substitution G A upstream_gene_variant CESC-US 5 176637417 176637417 single base substitution G C downstream_gene_variant CESC-US 5 176637417 176637417 single base substitution G C missense_variant E404Q 1210G>C CESC-US 5 176637417 176637417 single base substitution G C missense_variant E570Q 1708G>C CESC-US 5 176637417 176637417 single base substitution G C missense_variant E673Q 2017G>C CESC-US 5 176637417 176637417 single base substitution G C upstream_gene_variant CESC-US 5 176637601 176637601 single base substitution A G downstream_gene_variant CESC-US 5 176637601 176637601 single base substitution A G missense_variant K465R 1394A>G CESC-US 5 176637601 176637601 single base substitution A G missense_variant K631R 1892A>G CESC-US 5 176637601 176637601 single base substitution A G missense_variant K734R 2201A>G CESC-US 5 176637601 176637601 single base substitution A G upstream_gene_variant CESC-US 5 176637740 176637740 single base substitution G C downstream_gene_variant CESC-US 5 176637740 176637740 single base substitution G C synonymous_variant S511S 1533G>C CESC-US 5 176637740 176637740 single base substitution G C synonymous_variant S677S 2031G>C CESC-US 5 176637740 176637740 single base substitution G C synonymous_variant S780S 2340G>C CESC-US 5 176637740 176637740 single base substitution G C upstream_gene_variant CESC-US 5 176637930 176637930 deletion of <=200bp G - downstream_gene_variant CESC-US 5 176637930 176637930 deletion of <=200bp G - frameshift_variant E575 CESC-US 5 176637930 176637930 deletion of <=200bp G - frameshift_variant E741 CESC-US 5 176637930 176637930 deletion of <=200bp G - frameshift_variant E844 CESC-US 5 176637930 176637930 deletion of <=200bp G - upstream_gene_variant CESC-US 5 176637932 176637932 single base substitution G A downstream_gene_variant CESC-US 5 176637932 176637932 single base substitution G A synonymous_variant E575E 1725G>A CESC-US 5 176637932 176637932 single base substitution G A synonymous_variant E741E 2223G>A CESC-US 5 176637932 176637932 single base substitution G A synonymous_variant E844E 2532G>A CESC-US 5 176637932 176637932 single base substitution G A upstream_gene_variant CESC-US 5 176637992 176637992 single base substitution G A downstream_gene_variant CESC-US 5 176637992 176637992 single base substitution G A synonymous_variant L595L 1785G>A CESC-US 5 176637992 176637992 single base substitution G A synonymous_variant L761L 2283G>A CESC-US 5 176637992 176637992 single base substitution G A synonymous_variant L864L 2592G>A CESC-US 5 176637992 176637992 single base substitution G A upstream_gene_variant CESC-US 5 176638298 176638298 single base substitution G A downstream_gene_variant CESC-US 5 176638298 176638298 single base substitution G A synonymous_variant E697E 2091G>A CESC-US 5 176638298 176638298 single base substitution G A synonymous_variant E863E 2589G>A CESC-US 5 176638298 176638298 single base substitution G A synonymous_variant E966E 2898G>A CESC-US 5 176638298 176638298 single base substitution G A upstream_gene_variant CESC-US 5 176638806 176638806 single base substitution G A downstream_gene_variant CESC-US 5 176638806 176638806 single base substitution G A missense_variant E1033K 3097G>A CESC-US 5 176638806 176638806 single base substitution G A missense_variant E1136K 3406G>A CESC-US 5 176638806 176638806 single base substitution G A missense_variant E867K 2599G>A CESC-US 5 176638806 176638806 single base substitution G A upstream_gene_variant CESC-US 5 176638817 176638817 single base substitution T A downstream_gene_variant CESC-US 5 176638817 176638817 single base substitution T A synonymous_variant S1036S 3108T>A CESC-US 5 176638817 176638817 single base substitution T A synonymous_variant S1139S 3417T>A CESC-US 5 176638817 176638817 single base substitution T A synonymous_variant S870S 2610T>A CESC-US 5 176638817 176638817 single base substitution T A upstream_gene_variant CESC-US 5 176638839 176638839 single base substitution G A downstream_gene_variant CESC-US 5 176638839 176638839 single base substitution G A missense_variant E1044K 3130G>A CESC-US 5 176638839 176638839 single base substitution G A missense_variant E1147K 3439G>A CESC-US 5 176638839 176638839 single base substitution G A missense_variant E878K 2632G>A CESC-US 5 176638839 176638839 single base substitution G A upstream_gene_variant CESC-US 5 176638922 176638922 single base substitution G A downstream_gene_variant CESC-US 5 176638922 176638922 single base substitution G A missense_variant M1071I 3213G>A CESC-US 5 176638922 176638922 single base substitution G A missense_variant M1174I 3522G>A CESC-US 5 176638922 176638922 single base substitution G A missense_variant M905I 2715G>A CESC-US 5 176638922 176638922 single base substitution G A upstream_gene_variant CESC-US 5 176639054 176639054 single base substitution G A downstream_gene_variant CESC-US 5 176639054 176639054 single base substitution G A synonymous_variant L1115L 3345G>A CESC-US 5 176639054 176639054 single base substitution G A synonymous_variant L1218L 3654G>A CESC-US 5 176639054 176639054 single base substitution G A synonymous_variant L949L 2847G>A CESC-US 5 176639054 176639054 single base substitution G A upstream_gene_variant CESC-US 5 176662835 176662835 single base substitution G A 3_prime_UTR_variant CESC-US 5 176662835 176662835 single base substitution G A synonymous_variant E1001E 3003G>A CESC-US 5 176662835 176662835 single base substitution G A synonymous_variant E1167E 3501G>A CESC-US 5 176662835 176662835 single base substitution G A synonymous_variant E1270E 3810G>A CESC-US 5 176687059 176687059 single base substitution C A stop_gained S1410* 4229C>A CESC-US 5 176687059 176687059 single base substitution C A stop_gained S1576* 4727C>A CESC-US 5 176687059 176687059 single base substitution C A stop_gained S1679* 5036C>A CESC-US 5 176687059 176687059 single base substitution C G stop_gained S1410* 4229C>G CESC-US 5 176687059 176687059 single base substitution C G stop_gained S1576* 4727C>G CESC-US 5 176687059 176687059 single base substitution C G stop_gained S1679* 5036C>G CESC-US 5 176687130 176687130 single base substitution G C missense_variant E1434Q 4300G>C CESC-US 5 176687130 176687130 single base substitution G C missense_variant E1600Q 4798G>C CESC-US 5 176687130 176687130 single base substitution G C missense_variant E1703Q 5107G>C CESC-US 5 176721266 176721266 single base substitution C T downstream_gene_variant CESC-US 5 176721266 176721266 single base substitution C T synonymous_variant L2030L 6090C>T CESC-US 5 176721266 176721266 single base substitution C T synonymous_variant L2196L 6588C>T CESC-US 5 176721266 176721266 single base substitution C T synonymous_variant L2299L 6897C>T CESC-US 5 176730095 176730095 single base substitution G A downstream_gene_variant CLLE-ES 5 176586533 176586533 single base substitution C T intron_variant CLLE-ES 5 176608868 176608868 single base substitution A T intron_variant CLLE-ES 5 176618222 176618222 single base substitution C G intron_variant CLLE-ES 5 176645799 176645799 single base substitution T C intron_variant CLLE-ES 5 176666540 176666540 single base substitution C T intron_variant CLLE-ES 5 176677983 176677983 single base substitution G C intron_variant CLLE-ES 5 176701731 176701731 deletion of <=200bp G - downstream_gene_variant CLLE-ES 5 176701731 176701731 deletion of <=200bp G - intron_variant CLLE-ES 5 176710863 176710863 single base substitution A G downstream_gene_variant CLLE-ES 5 176710863 176710863 single base substitution A G missense_variant T1760A 5278A>G CLLE-ES 5 176710863 176710863 single base substitution A G missense_variant T1926A 5776A>G CLLE-ES 5 176710863 176710863 single base substitution A G missense_variant T2029A 6085A>G CLLE-ES 5 176710863 176710863 single base substitution A G upstream_gene_variant CLLE-ES 5 176714360 176714360 single base substitution G A intron_variant CLLE-ES 5 176714360 176714360 single base substitution G A upstream_gene_variant CLLE-ES 5 176720535 176720535 single base substitution G C downstream_gene_variant CLLE-ES 5 176720535 176720535 single base substitution G C intron_variant CLLE-ES 5 176721157 176721157 single base substitution C T downstream_gene_variant CLLE-ES 5 176721157 176721157 single base substitution C T missense_variant S1994L 5981C>T CLLE-ES 5 176721157 176721157 single base substitution C T missense_variant S2160L 6479C>T CLLE-ES 5 176721157 176721157 single base substitution C T missense_variant S2263L 6788C>T COAD-US 5 176562786 176562786 single base substitution C G downstream_gene_variant COAD-US 5 176562786 176562786 single base substitution C G exon_variant COAD-US 5 176562786 176562786 single base substitution C G intron_variant COAD-US 5 176562786 176562786 single base substitution C G missense_variant P228A 682C>G COAD-US 5 176562813 176562813 deletion of <=200bp A - downstream_gene_variant COAD-US 5 176562813 176562813 deletion of <=200bp A - exon_variant COAD-US 5 176562813 176562813 deletion of <=200bp A - frameshift_variant K237 COAD-US 5 176562813 176562813 deletion of <=200bp A - intron_variant COAD-US 5 176631233 176631233 single base substitution C T intron_variant COAD-US 5 176631233 176631233 single base substitution C T synonymous_variant F123F 369C>T COAD-US 5 176631233 176631233 single base substitution C T synonymous_variant F392F 1176C>T COAD-US 5 176636719 176636719 single base substitution G A downstream_gene_variant COAD-US 5 176636719 176636719 single base substitution G A missense_variant R171Q 512G>A COAD-US 5 176636719 176636719 single base substitution G A missense_variant R337Q 1010G>A COAD-US 5 176636719 176636719 single base substitution G A missense_variant R440Q 1319G>A COAD-US 5 176636719 176636719 single base substitution G A upstream_gene_variant COAD-US 5 176638196 176638196 single base substitution C G downstream_gene_variant COAD-US 5 176638196 176638196 single base substitution C G missense_variant N663K 1989C>G COAD-US 5 176638196 176638196 single base substitution C G missense_variant N829K 2487C>G COAD-US 5 176638196 176638196 single base substitution C G missense_variant N932K 2796C>G COAD-US 5 176638196 176638196 single base substitution C G upstream_gene_variant COAD-US 5 176665317 176665317 single base substitution C A intron_variant COAD-US 5 176665317 176665317 single base substitution C A missense_variant S1065Y 3194C>A COAD-US 5 176665317 176665317 single base substitution C A missense_variant S1231Y 3692C>A COAD-US 5 176665317 176665317 single base substitution C A missense_variant S1334Y 4001C>A COAD-US 5 176675253 176675253 single base substitution C T synonymous_variant P1254P 3762C>T COAD-US 5 176675253 176675253 single base substitution C T synonymous_variant P1420P 4260C>T COAD-US 5 176675253 176675253 single base substitution C T synonymous_variant P1523P 4569C>T COAD-US 5 176687162 176687162 single base substitution C T synonymous_variant C1444C 4332C>T COAD-US 5 176687162 176687162 single base substitution C T synonymous_variant C1610C 4830C>T COAD-US 5 176687162 176687162 single base substitution C T synonymous_variant C1713C 5139C>T COAD-US 5 176700695 176700695 single base substitution G C downstream_gene_variant COAD-US 5 176700695 176700695 single base substitution G C missense_variant R1575S 4725G>C COAD-US 5 176700695 176700695 single base substitution G C missense_variant R1741S 5223G>C COAD-US 5 176700695 176700695 single base substitution G C missense_variant R1844S 5532G>C COAD-US 5 176700695 176700695 single base substitution G C missense_variant R58S 174G>C COAD-US 5 176700728 176700728 single base substitution A T downstream_gene_variant COAD-US 5 176700728 176700728 single base substitution A T missense_variant R1586S 4758A>T COAD-US 5 176700728 176700728 single base substitution A T missense_variant R1752S 5256A>T COAD-US 5 176700728 176700728 single base substitution A T missense_variant R1855S 5565A>T COAD-US 5 176700728 176700728 single base substitution A T missense_variant R69S 207A>T COAD-US 5 176709523 176709523 single base substitution C T downstream_gene_variant COAD-US 5 176709523 176709523 single base substitution C T stop_gained R1715* 5143C>T COAD-US 5 176709523 176709523 single base substitution C T stop_gained R1881* 5641C>T COAD-US 5 176709523 176709523 single base substitution C T stop_gained R1984* 5950C>T COAD-US 5 176719126 176719126 single base substitution G A exon_variant COAD-US 5 176719126 176719126 single base substitution G A missense_variant A1875T 5623G>A COAD-US 5 176719126 176719126 single base substitution G A missense_variant A2041T 6121G>A COAD-US 5 176719126 176719126 single base substitution G A missense_variant A2144T 6430G>A COAD-US 5 176721031 176721031 single base substitution A G downstream_gene_variant COAD-US 5 176721031 176721031 single base substitution A G missense_variant Y1952C 5855A>G COAD-US 5 176721031 176721031 single base substitution A G missense_variant Y2118C 6353A>G COAD-US 5 176721031 176721031 single base substitution A G missense_variant Y2221C 6662A>G COAD-US 5 176721107 176721107 single base substitution G T downstream_gene_variant COAD-US 5 176721107 176721107 single base substitution G T missense_variant Q1977H 5931G>T COAD-US 5 176721107 176721107 single base substitution G T missense_variant Q2143H 6429G>T COAD-US 5 176721107 176721107 single base substitution G T missense_variant Q2246H 6738G>T COAD-US 5 176729434 176729434 single base substitution G A downstream_gene_variant COCA-CN 5 176562969 176562969 single base substitution T G downstream_gene_variant COCA-CN 5 176562969 176562969 single base substitution T G exon_variant COCA-CN 5 176562969 176562969 single base substitution T G missense_variant L20V 58T>G COCA-CN 5 176562969 176562969 single base substitution T G missense_variant L289V 865T>G COCA-CN 5 176565099 176565099 single base substitution C A downstream_gene_variant COCA-CN 5 176565099 176565099 single base substitution C A intron_variant COCA-CN 5 176579360 176579360 single base substitution A T intron_variant COCA-CN 5 176591167 176591167 single base substitution C T intron_variant COCA-CN 5 176621603 176621603 single base substitution T A intron_variant COCA-CN 5 176622760 176622760 single base substitution C T intron_variant COCA-CN 5 176631072 176631072 single base substitution G T intron_variant COCA-CN 5 176631206 176631206 single base substitution C T intron_variant COCA-CN 5 176631206 176631206 single base substitution C T synonymous_variant I114I 342C>T COCA-CN 5 176631206 176631206 single base substitution C T synonymous_variant I383I 1149C>T COCA-CN 5 176631352 176631352 single base substitution A C downstream_gene_variant COCA-CN 5 176631352 176631352 single base substitution A C intron_variant COCA-CN 5 176631787 176631787 single base substitution G T downstream_gene_variant COCA-CN 5 176631787 176631787 single base substitution G T intron_variant COCA-CN 5 176633950 176633950 single base substitution C T downstream_gene_variant COCA-CN 5 176633950 176633950 single base substitution C T intron_variant COCA-CN 5 176636953 176636953 single base substitution T A downstream_gene_variant COCA-CN 5 176636953 176636953 single base substitution T A missense_variant F249Y 746T>A COCA-CN 5 176636953 176636953 single base substitution T A missense_variant F415Y 1244T>A COCA-CN 5 176636953 176636953 single base substitution T A missense_variant F518Y 1553T>A COCA-CN 5 176636953 176636953 single base substitution T A upstream_gene_variant COCA-CN 5 176636974 176636974 single base substitution G A downstream_gene_variant COCA-CN 5 176636974 176636974 single base substitution G A missense_variant R256Q 767G>A COCA-CN 5 176636974 176636974 single base substitution G A missense_variant R422Q 1265G>A COCA-CN 5 176636974 176636974 single base substitution G A missense_variant R525Q 1574G>A COCA-CN 5 176636974 176636974 single base substitution G A upstream_gene_variant COCA-CN 5 176638001 176638001 single base substitution C A downstream_gene_variant COCA-CN 5 176638001 176638001 single base substitution C A synonymous_variant L598L 1794C>A COCA-CN 5 176638001 176638001 single base substitution C A synonymous_variant L764L 2292C>A COCA-CN 5 176638001 176638001 single base substitution C A synonymous_variant L867L 2601C>A COCA-CN 5 176638001 176638001 single base substitution C A upstream_gene_variant COCA-CN 5 176638833 176638833 single base substitution A C downstream_gene_variant COCA-CN 5 176638833 176638833 single base substitution A C missense_variant N1042H 3124A>C COCA-CN 5 176638833 176638833 single base substitution A C missense_variant N1145H 3433A>C COCA-CN 5 176638833 176638833 single base substitution A C missense_variant N876H 2626A>C COCA-CN 5 176638833 176638833 single base substitution A C upstream_gene_variant COCA-CN 5 176638875 176638875 single base substitution C T downstream_gene_variant COCA-CN 5 176638875 176638875 single base substitution C T missense_variant R1056W 3166C>T COCA-CN 5 176638875 176638875 single base substitution C T missense_variant R1159W 3475C>T COCA-CN 5 176638875 176638875 single base substitution C T missense_variant R890W 2668C>T COCA-CN 5 176638875 176638875 single base substitution C T upstream_gene_variant COCA-CN 5 176639486 176639486 single base substitution C T downstream_gene_variant COCA-CN 5 176639486 176639486 single base substitution C T intron_variant COCA-CN 5 176654229 176654229 single base substitution A C intron_variant COCA-CN 5 176665317 176665317 single base substitution C A intron_variant COCA-CN 5 176665317 176665317 single base substitution C A missense_variant S1065Y 3194C>A COCA-CN 5 176665317 176665317 single base substitution C A missense_variant S1231Y 3692C>A COCA-CN 5 176665317 176665317 single base substitution C A missense_variant S1334Y 4001C>A COCA-CN 5 176672975 176672975 single base substitution A T intron_variant COCA-CN 5 176672978 176672978 single base substitution T A intron_variant COCA-CN 5 176676457 176676457 single base substitution A T intron_variant COCA-CN 5 176676465 176676465 single base substitution T A intron_variant COCA-CN 5 176683940 176683940 single base substitution T G intron_variant COCA-CN 5 176684218 176684218 single base substitution C T intron_variant COCA-CN 5 176684226 176684226 single base substitution T C intron_variant COCA-CN 5 176684841 176684841 single base substitution T A intron_variant COCA-CN 5 176684843 176684843 single base substitution A T intron_variant COCA-CN 5 176691279 176691279 single base substitution T G intron_variant COCA-CN 5 176691279 176691279 single base substitution T G upstream_gene_variant COCA-CN 5 176693051 176693051 single base substitution G A intron_variant COCA-CN 5 176693051 176693051 single base substitution G A upstream_gene_variant COCA-CN 5 176693182 176693182 single base substitution G A intron_variant COCA-CN 5 176693182 176693182 single base substitution G A upstream_gene_variant COCA-CN 5 176710796 176710796 single base substitution C A downstream_gene_variant COCA-CN 5 176710796 176710796 single base substitution C A synonymous_variant I1737I 5211C>A COCA-CN 5 176710796 176710796 single base substitution C A synonymous_variant I1903I 5709C>A COCA-CN 5 176710796 176710796 single base substitution C A synonymous_variant I2006I 6018C>A COCA-CN 5 176710796 176710796 single base substitution C A upstream_gene_variant COCA-CN 5 176721931 176721931 single base substitution C T downstream_gene_variant COCA-CN 5 176721931 176721931 single base substitution C T missense_variant A2252V 6755C>T COCA-CN 5 176721931 176721931 single base substitution C T missense_variant A2418V 7253C>T COCA-CN 5 176721931 176721931 single base substitution C T missense_variant A2521V 7562C>T COCA-CN 5 176723213 176723213 single base substitution C T 3_prime_UTR_variant COCA-CN 5 176723213 176723213 single base substitution C T downstream_gene_variant COCA-CN 5 176729737 176729737 single base substitution C A downstream_gene_variant COCA-CN 5 176731143 176731143 single base substitution C A downstream_gene_variant ESAD-UK 5 176559267 176559267 single base substitution A G upstream_gene_variant ESAD-UK 5 176559489 176559489 single base substitution C T upstream_gene_variant ESAD-UK 5 176566959 176566959 single base substitution G T downstream_gene_variant ESAD-UK 5 176566959 176566959 single base substitution G T intron_variant ESAD-UK 5 176568849 176568849 single base substitution C T downstream_gene_variant ESAD-UK 5 176568849 176568849 single base substitution C T intron_variant ESAD-UK 5 176572459 176572459 single base substitution T G intron_variant ESAD-UK 5 176572640 176572640 single base substitution G A intron_variant ESAD-UK 5 176573711 176573711 single base substitution T G intron_variant ESAD-UK 5 176573935 176573935 single base substitution G A intron_variant ESAD-UK 5 176574693 176574693 single base substitution C T intron_variant ESAD-UK 5 176575493 176575493 single base substitution C G intron_variant ESAD-UK 5 176576417 176576417 single base substitution C T intron_variant ESAD-UK 5 176585303 176585303 deletion of <=200bp T - intron_variant ESAD-UK 5 176586898 176586898 single base substitution T A intron_variant ESAD-UK 5 176586900 176586900 single base substitution T A intron_variant ESAD-UK 5 176586902 176586902 single base substitution T A intron_variant ESAD-UK 5 176587347 176587347 single base substitution G A intron_variant ESAD-UK 5 176590960 176590960 single base substitution T C intron_variant ESAD-UK 5 176591456 176591456 single base substitution G A intron_variant ESAD-UK 5 176592996 176592996 single base substitution C T intron_variant ESAD-UK 5 176595311 176595311 single base substitution A C intron_variant ESAD-UK 5 176596163 176596163 deletion of <=200bp T - intron_variant ESAD-UK 5 176596390 176596390 single base substitution C T intron_variant ESAD-UK 5 176598172 176598172 single base substitution T C intron_variant ESAD-UK 5 176599394 176599394 single base substitution C A intron_variant ESAD-UK 5 176601041 176601041 insertion of <=200bp - T intron_variant ESAD-UK 5 176601164 176601164 single base substitution G A intron_variant ESAD-UK 5 176604981 176604981 single base substitution C T intron_variant ESAD-UK 5 176609949 176609949 insertion of <=200bp - T intron_variant ESAD-UK 5 176613317 176613317 single base substitution C T intron_variant ESAD-UK 5 176613464 176613464 single base substitution T A intron_variant ESAD-UK 5 176615845 176615845 single base substitution T A intron_variant ESAD-UK 5 176616506 176616506 single base substitution A G intron_variant ESAD-UK 5 176619402 176619402 single base substitution T A intron_variant ESAD-UK 5 176620683 176620683 single base substitution C G intron_variant ESAD-UK 5 176621885 176621885 single base substitution C T intron_variant ESAD-UK 5 176622761 176622761 single base substitution G A intron_variant ESAD-UK 5 176623314 176623314 single base substitution G A intron_variant ESAD-UK 5 176626787 176626787 single base substitution G T intron_variant ESAD-UK 5 176627600 176627600 deletion of <=200bp T - intron_variant ESAD-UK 5 176628169 176628187 deletion of <=200bp TGAGCCACTGTGTCCAACC - intron_variant ESAD-UK 5 176629194 176629194 single base substitution A T intron_variant ESAD-UK 5 176629815 176629815 single base substitution T G intron_variant ESAD-UK 5 176631013 176631013 single base substitution T C intron_variant ESAD-UK 5 176632268 176632268 single base substitution G A downstream_gene_variant ESAD-UK 5 176632268 176632268 single base substitution G A intron_variant ESAD-UK 5 176632346 176632346 single base substitution A C downstream_gene_variant ESAD-UK 5 176632346 176632346 single base substitution A C intron_variant ESAD-UK 5 176633932 176633932 single base substitution C A downstream_gene_variant ESAD-UK 5 176633932 176633932 single base substitution C A intron_variant ESAD-UK 5 176639097 176639097 single base substitution C T downstream_gene_variant ESAD-UK 5 176639097 176639097 single base substitution C T missense_variant R1130W 3388C>T ESAD-UK 5 176639097 176639097 single base substitution C T missense_variant R1233W 3697C>T ESAD-UK 5 176639097 176639097 single base substitution C T missense_variant R964W 2890C>T ESAD-UK 5 176639097 176639097 single base substitution C T upstream_gene_variant ESAD-UK 5 176639794 176639794 single base substitution C T downstream_gene_variant ESAD-UK 5 176639794 176639794 single base substitution C T intron_variant ESAD-UK 5 176642548 176642548 single base substitution A T intron_variant ESAD-UK 5 176646226 176646226 single base substitution C T intron_variant ESAD-UK 5 176648016 176648016 single base substitution C T intron_variant ESAD-UK 5 176649232 176649232 single base substitution C T intron_variant ESAD-UK 5 176650254 176650254 single base substitution A T intron_variant ESAD-UK 5 176650602 176650602 single base substitution C T intron_variant ESAD-UK 5 176650791 176650791 single base substitution G A intron_variant ESAD-UK 5 176651445 176651445 single base substitution G T intron_variant ESAD-UK 5 176653822 176653822 single base substitution T A intron_variant ESAD-UK 5 176653931 176653931 single base substitution G T intron_variant ESAD-UK 5 176654455 176654455 insertion of <=200bp - A intron_variant ESAD-UK 5 176659959 176659959 single base substitution A C intron_variant ESAD-UK 5 176660182 176660182 single base substitution C A intron_variant ESAD-UK 5 176660503 176660503 single base substitution C T intron_variant ESAD-UK 5 176668992 176668992 single base substitution C T downstream_gene_variant ESAD-UK 5 176668992 176668992 single base substitution C T intron_variant ESAD-UK 5 176671063 176671063 single base substitution T G downstream_gene_variant ESAD-UK 5 176671063 176671063 single base substitution T G intron_variant ESAD-UK 5 176672978 176672978 single base substitution T A intron_variant ESAD-UK 5 176672980 176672980 single base substitution T A intron_variant ESAD-UK 5 176674734 176674734 single base substitution G A intron_variant ESAD-UK 5 176677765 176677765 single base substitution T G intron_variant ESAD-UK 5 176679511 176679511 single base substitution T G intron_variant ESAD-UK 5 176680359 176680359 single base substitution G A intron_variant ESAD-UK 5 176680548 176680548 single base substitution G A intron_variant ESAD-UK 5 176682085 176682085 single base substitution T A intron_variant ESAD-UK 5 176685918 176685918 single base substitution G C intron_variant ESAD-UK 5 176687133 176687133 single base substitution C T missense_variant H1435Y 4303C>T ESAD-UK 5 176687133 176687133 single base substitution C T missense_variant H1601Y 4801C>T ESAD-UK 5 176687133 176687133 single base substitution C T missense_variant H1704Y 5110C>T ESAD-UK 5 176689914 176689914 single base substitution G T intron_variant ESAD-UK 5 176689914 176689914 single base substitution G T upstream_gene_variant ESAD-UK 5 176692622 176692622 single base substitution G T 5_prime_UTR_variant ESAD-UK 5 176692622 176692622 single base substitution G T intron_variant ESAD-UK 5 176692622 176692622 single base substitution G T upstream_gene_variant ESAD-UK 5 176694382 176694382 single base substitution G A intron_variant ESAD-UK 5 176695689 176695689 single base substitution C A intron_variant ESAD-UK 5 176698250 176698250 single base substitution A T downstream_gene_variant ESAD-UK 5 176698250 176698250 single base substitution A T intron_variant ESAD-UK 5 176699179 176699179 single base substitution G A downstream_gene_variant ESAD-UK 5 176699179 176699179 single base substitution G A intron_variant ESAD-UK 5 176701850 176701850 single base substitution G A downstream_gene_variant ESAD-UK 5 176701850 176701850 single base substitution G A intron_variant ESAD-UK 5 176703211 176703211 single base substitution C T downstream_gene_variant ESAD-UK 5 176703211 176703211 single base substitution C T intron_variant ESAD-UK 5 176710116 176710116 single base substitution G A downstream_gene_variant ESAD-UK 5 176710116 176710116 single base substitution G A intron_variant ESAD-UK 5 176710856 176710856 single base substitution C T downstream_gene_variant ESAD-UK 5 176710856 176710856 single base substitution C T synonymous_variant N1757N 5271C>T ESAD-UK 5 176710856 176710856 single base substitution C T synonymous_variant N1923N 5769C>T ESAD-UK 5 176710856 176710856 single base substitution C T synonymous_variant N2026N 6078C>T ESAD-UK 5 176710856 176710856 single base substitution C T upstream_gene_variant ESAD-UK 5 176712336 176712336 single base substitution G T downstream_gene_variant ESAD-UK 5 176712336 176712336 single base substitution G T intron_variant ESAD-UK 5 176712336 176712336 single base substitution G T upstream_gene_variant ESAD-UK 5 176713499 176713499 single base substitution G T intron_variant ESAD-UK 5 176713499 176713499 single base substitution G T upstream_gene_variant ESAD-UK 5 176713912 176713912 single base substitution C T intron_variant ESAD-UK 5 176713912 176713912 single base substitution C T upstream_gene_variant ESAD-UK 5 176714245 176714245 single base substitution A G intron_variant ESAD-UK 5 176714245 176714245 single base substitution A G upstream_gene_variant ESAD-UK 5 176716634 176716634 single base substitution G A intron_variant ESAD-UK 5 176717071 176717071 single base substitution C T intron_variant ESAD-UK 5 176718976 176718976 single base substitution G A exon_variant ESAD-UK 5 176718976 176718976 single base substitution G A missense_variant E1825K 5473G>A ESAD-UK 5 176718976 176718976 single base substitution G A missense_variant E1991K 5971G>A ESAD-UK 5 176718976 176718976 single base substitution G A missense_variant E2094K 6280G>A ESAD-UK 5 176719939 176719939 single base substitution T C downstream_gene_variant ESAD-UK 5 176719939 176719939 single base substitution T C intron_variant ESAD-UK 5 176720311 176720311 insertion of <=200bp - CTGAT downstream_gene_variant ESAD-UK 5 176720311 176720311 insertion of <=200bp - CTGAT intron_variant ESAD-UK 5 176721436 176721436 single base substitution C T downstream_gene_variant ESAD-UK 5 176721436 176721436 single base substitution C T missense_variant T2087M 6260C>T ESAD-UK 5 176721436 176721436 single base substitution C T missense_variant T2253M 6758C>T ESAD-UK 5 176721436 176721436 single base substitution C T missense_variant T2356M 7067C>T ESAD-UK 5 176726871 176726871 single base substitution G A 3_prime_UTR_variant ESAD-UK 5 176726871 176726871 single base substitution G A downstream_gene_variant ESAD-UK 5 176731056 176731056 deletion of <=200bp C - downstream_gene_variant ESAD-UK 5 176731057 176731057 single base substitution A G downstream_gene_variant ESAD-UK 5 176731934 176731934 single base substitution G C downstream_gene_variant ESAD-UK 5 176732184 176732184 single base substitution C T downstream_gene_variant ESCA-CN 5 176562239 176562239 single base substitution G C exon_variant ESCA-CN 5 176562239 176562239 single base substitution G C intron_variant ESCA-CN 5 176562239 176562239 single base substitution G C synonymous_variant G45G 135G>C ESCA-CN 5 176562880 176562880 single base substitution C T downstream_gene_variant ESCA-CN 5 176562880 176562880 single base substitution C T exon_variant ESCA-CN 5 176562880 176562880 single base substitution C T intron_variant ESCA-CN 5 176562880 176562880 single base substitution C T missense_variant S259L 776C>T ESCA-CN 5 176637149 176637149 single base substitution G A downstream_gene_variant ESCA-CN 5 176637149 176637149 single base substitution G A synonymous_variant E314E 942G>A ESCA-CN 5 176637149 176637149 single base substitution G A synonymous_variant E480E 1440G>A ESCA-CN 5 176637149 176637149 single base substitution G A synonymous_variant E583E 1749G>A ESCA-CN 5 176637149 176637149 single base substitution G A upstream_gene_variant ESCA-CN 5 176637240 176637240 single base substitution G T downstream_gene_variant ESCA-CN 5 176637240 176637240 single base substitution G T missense_variant V345L 1033G>T ESCA-CN 5 176637240 176637240 single base substitution G T missense_variant V511L 1531G>T ESCA-CN 5 176637240 176637240 single base substitution G T missense_variant V614L 1840G>T ESCA-CN 5 176637240 176637240 single base substitution G T upstream_gene_variant ESCA-CN 5 176707669 176707669 single base substitution C G downstream_gene_variant ESCA-CN 5 176707669 176707669 single base substitution C G missense_variant S1640C 4919C>G ESCA-CN 5 176707669 176707669 single base substitution C G missense_variant S1806C 5417C>G ESCA-CN 5 176707669 176707669 single base substitution C G missense_variant S1909C 5726C>G ESCA-CN 5 176709489 176709489 single base substitution G C downstream_gene_variant ESCA-CN 5 176709489 176709489 single base substitution G C synonymous_variant V1703V 5109G>C ESCA-CN 5 176709489 176709489 single base substitution G C synonymous_variant V1869V 5607G>C ESCA-CN 5 176709489 176709489 single base substitution G C synonymous_variant V1972V 5916G>C ESCA-CN 5 176710801 176710801 single base substitution A T downstream_gene_variant ESCA-CN 5 176710801 176710801 single base substitution A T missense_variant D1739V 5216A>T ESCA-CN 5 176710801 176710801 single base substitution A T missense_variant D1905V 5714A>T ESCA-CN 5 176710801 176710801 single base substitution A T missense_variant D2008V 6023A>T ESCA-CN 5 176710801 176710801 single base substitution A T upstream_gene_variant ESCA-CN 5 176718958 176718958 single base substitution C T exon_variant ESCA-CN 5 176718958 176718958 single base substitution C T stop_gained Q1819* 5455C>T ESCA-CN 5 176718958 176718958 single base substitution C T stop_gained Q1985* 5953C>T ESCA-CN 5 176718958 176718958 single base substitution C T stop_gained Q2088* 6262C>T ESCA-CN 5 176721372 176721372 single base substitution C G downstream_gene_variant ESCA-CN 5 176721372 176721372 single base substitution C G missense_variant P2066A 6196C>G ESCA-CN 5 176721372 176721372 single base substitution C G missense_variant P2232A 6694C>G ESCA-CN 5 176721372 176721372 single base substitution C G missense_variant P2335A 7003C>G GBM-US 5 176638305 176638305 single base substitution G A downstream_gene_variant GBM-US 5 176638305 176638305 single base substitution G A missense_variant G700R 2098G>A GBM-US 5 176638305 176638305 single base substitution G A missense_variant G866R 2596G>A GBM-US 5 176638305 176638305 single base substitution G A missense_variant G969R 2905G>A GBM-US 5 176638305 176638305 single base substitution G A upstream_gene_variant GBM-US 5 176729179 176729179 single base substitution T C downstream_gene_variant KIRC-US 5 176562309 176562309 single base substitution T C exon_variant KIRC-US 5 176562309 176562309 single base substitution T C intron_variant KIRC-US 5 176562309 176562309 single base substitution T C missense_variant Y69H 205T>C KIRC-US 5 176562399 176562399 single base substitution G A exon_variant KIRC-US 5 176562399 176562399 single base substitution G A intron_variant KIRC-US 5 176562399 176562399 single base substitution G A missense_variant D99N 295G>A KIRC-US 5 176631295 176631295 single base substitution T C downstream_gene_variant KIRC-US 5 176631295 176631295 single base substitution T C intron_variant KIRC-US 5 176631295 176631295 single base substitution T C splice_donor_variant KIRC-US 5 176636690 176636690 single base substitution G A downstream_gene_variant KIRC-US 5 176636690 176636690 single base substitution G A synonymous_variant Q161Q 483G>A KIRC-US 5 176636690 176636690 single base substitution G A synonymous_variant Q327Q 981G>A KIRC-US 5 176636690 176636690 single base substitution G A synonymous_variant Q430Q 1290G>A KIRC-US 5 176636690 176636690 single base substitution G A upstream_gene_variant KIRC-US 5 176637818 176637818 single base substitution A C downstream_gene_variant KIRC-US 5 176637818 176637818 single base substitution A C synonymous_variant I537I 1611A>C KIRC-US 5 176637818 176637818 single base substitution A C synonymous_variant I703I 2109A>C KIRC-US 5 176637818 176637818 single base substitution A C synonymous_variant I806I 2418A>C KIRC-US 5 176637818 176637818 single base substitution A C upstream_gene_variant KIRC-US 5 176665505 176665505 single base substitution C G intron_variant KIRC-US 5 176665505 176665505 single base substitution C G missense_variant P1128A 3382C>G KIRC-US 5 176665505 176665505 single base substitution C G missense_variant P1294A 3880C>G KIRC-US 5 176665505 176665505 single base substitution C G missense_variant P1397A 4189C>G KIRC-US 5 176720945 176720945 single base substitution C T downstream_gene_variant KIRC-US 5 176720945 176720945 single base substitution C T synonymous_variant F1923F 5769C>T KIRC-US 5 176720945 176720945 single base substitution C T synonymous_variant F2089F 6267C>T KIRC-US 5 176720945 176720945 single base substitution C T synonymous_variant F2192F 6576C>T KIRC-US 5 176728925 176728925 single base substitution C T downstream_gene_variant KIRC-US 5 176728945 176728945 single base substitution A G downstream_gene_variant KIRC-US 5 176729429 176729429 single base substitution C A downstream_gene_variant KIRC-US 5 176729440 176729440 single base substitution G A downstream_gene_variant KIRC-US 5 176731056 176731056 single base substitution C A downstream_gene_variant KIRP-US 5 176562915 176562915 single base substitution T G downstream_gene_variant KIRP-US 5 176562915 176562915 single base substitution T G exon_variant KIRP-US 5 176562915 176562915 single base substitution T G intron_variant KIRP-US 5 176562915 176562915 single base substitution T G missense_variant L271V 811T>G KIRP-US 5 176637880 176637880 deletion of <=200bp T - downstream_gene_variant KIRP-US 5 176637880 176637880 deletion of <=200bp T - frameshift_variant I558 KIRP-US 5 176637880 176637880 deletion of <=200bp T - frameshift_variant I724 KIRP-US 5 176637880 176637880 deletion of <=200bp T - frameshift_variant I827 KIRP-US 5 176637880 176637880 deletion of <=200bp T - upstream_gene_variant KIRP-US 5 176639042 176639042 single base substitution T C downstream_gene_variant KIRP-US 5 176639042 176639042 single base substitution T C synonymous_variant L1111L 3333T>C KIRP-US 5 176639042 176639042 single base substitution T C synonymous_variant L1214L 3642T>C KIRP-US 5 176639042 176639042 single base substitution T C synonymous_variant L945L 2835T>C KIRP-US 5 176639042 176639042 single base substitution T C upstream_gene_variant KIRP-US 5 176696648 176696648 single base substitution C T 5_prime_UTR_variant KIRP-US 5 176696648 176696648 single base substitution C T synonymous_variant N1514N 4542C>T KIRP-US 5 176696648 176696648 single base substitution C T synonymous_variant N1680N 5040C>T KIRP-US 5 176696648 176696648 single base substitution C T synonymous_variant N1783N 5349C>T KIRP-US 5 176709581 176709584 deletion of <=200bp AAGT - downstream_gene_variant KIRP-US 5 176709581 176709584 deletion of <=200bp AAGT - frameshift_variant K1734 KIRP-US 5 176709581 176709584 deletion of <=200bp AAGT - frameshift_variant K1900 KIRP-US 5 176709581 176709584 deletion of <=200bp AAGT - frameshift_variant K2003 KIRP-US 5 176721020 176721020 single base substitution G T downstream_gene_variant KIRP-US 5 176721020 176721020 single base substitution G T missense_variant E1948D 5844G>T KIRP-US 5 176721020 176721020 single base substitution G T missense_variant E2114D 6342G>T KIRP-US 5 176721020 176721020 single base substitution G T missense_variant E2217D 6651G>T KIRP-US 5 176729807 176729807 single base substitution C G downstream_gene_variant LAML-CN 5 176562217 176562217 single base substitution A G exon_variant LAML-CN 5 176562217 176562217 single base substitution A G intron_variant LAML-CN 5 176562217 176562217 single base substitution A G missense_variant N38S 113A>G LAML-KR 5 176576009 176576009 single base substitution A G intron_variant LAML-KR 5 176581818 176581818 single base substitution A T intron_variant LAML-KR 5 176586286 176586286 single base substitution G T intron_variant LAML-KR 5 176597377 176597377 single base substitution A G intron_variant LAML-KR 5 176597382 176597382 single base substitution C T intron_variant LAML-KR 5 176600492 176600492 single base substitution G T intron_variant LAML-KR 5 176639105 176639105 single base substitution T C downstream_gene_variant LAML-KR 5 176639105 176639105 single base substitution T C synonymous_variant N1132N 3396T>C LAML-KR 5 176639105 176639105 single base substitution T C synonymous_variant N1235N 3705T>C LAML-KR 5 176639105 176639105 single base substitution T C synonymous_variant N966N 2898T>C LAML-KR 5 176639105 176639105 single base substitution T C upstream_gene_variant LAML-KR 5 176642301 176642301 single base substitution T C intron_variant LAML-KR 5 176643691 176643691 single base substitution A T intron_variant LAML-KR 5 176658554 176658554 single base substitution G T intron_variant LAML-KR 5 176663102 176663102 single base substitution T C intron_variant LAML-KR 5 176684249 176684249 single base substitution G T intron_variant LAML-KR 5 176712589 176712589 single base substitution T A intron_variant LAML-KR 5 176712589 176712589 single base substitution T A upstream_gene_variant LICA-CN 5 176709533 176709533 single base substitution A G downstream_gene_variant LICA-CN 5 176709533 176709533 single base substitution A G missense_variant Y1718C 5153A>G LICA-CN 5 176709533 176709533 single base substitution A G missense_variant Y1884C 5651A>G LICA-CN 5 176709533 176709533 single base substitution A G missense_variant Y1987C 5960A>G LICA-CN 5 176728977 176728977 single base substitution G A downstream_gene_variant LICA-CN 5 176730012 176730012 single base substitution A G downstream_gene_variant LICA-FR 5 176563358 176563358 single base substitution G C downstream_gene_variant LICA-FR 5 176563358 176563358 single base substitution G C intron_variant LICA-FR 5 176578690 176578690 deletion of <=200bp T - intron_variant LICA-FR 5 176592912 176592912 deletion of <=200bp T - intron_variant LICA-FR 5 176596813 176596813 single base substitution A G intron_variant LICA-FR 5 176607106 176607106 single base substitution T A intron_variant LICA-FR 5 176631176 176631176 single base substitution T A intron_variant LICA-FR 5 176631176 176631176 single base substitution T A synonymous_variant S104S 312T>A LICA-FR 5 176631176 176631176 single base substitution T A synonymous_variant S373S 1119T>A LICA-FR 5 176638291 176638291 single base substitution A G downstream_gene_variant LICA-FR 5 176638291 176638291 single base substitution A G missense_variant N695S 2084A>G LICA-FR 5 176638291 176638291 single base substitution A G missense_variant N861S 2582A>G LICA-FR 5 176638291 176638291 single base substitution A G missense_variant N964S 2891A>G LICA-FR 5 176638291 176638291 single base substitution A G upstream_gene_variant LICA-FR 5 176639058 176639058 single base substitution G C downstream_gene_variant LICA-FR 5 176639058 176639058 single base substitution G C missense_variant E1117Q 3349G>C LICA-FR 5 176639058 176639058 single base substitution G C missense_variant E1220Q 3658G>C LICA-FR 5 176639058 176639058 single base substitution G C missense_variant E951Q 2851G>C LICA-FR 5 176639058 176639058 single base substitution G C upstream_gene_variant LICA-FR 5 176643672 176643672 deletion of <=200bp T - intron_variant LICA-FR 5 176647688 176647688 single base substitution A T intron_variant LICA-FR 5 176647746 176647746 single base substitution C G intron_variant LICA-FR 5 176648241 176648241 single base substitution C T intron_variant LICA-FR 5 176649555 176649555 single base substitution C T intron_variant LICA-FR 5 176649746 176649746 single base substitution C G intron_variant LICA-FR 5 176649877 176649877 single base substitution C T intron_variant LICA-FR 5 176674449 176674449 single base substitution C T intron_variant LICA-FR 5 176674567 176674567 deletion of <=200bp A - intron_variant LICA-FR 5 176686973 176686982 deletion of <=200bp TGATTTTCCT - splice_region_variant LICA-FR 5 176688591 176688591 single base substitution A T intron_variant LICA-FR 5 176688591 176688591 single base substitution A T upstream_gene_variant LICA-FR 5 176710822 176710822 single base substitution A G downstream_gene_variant LICA-FR 5 176710822 176710822 single base substitution A G missense_variant Y1746C 5237A>G LICA-FR 5 176710822 176710822 single base substitution A G missense_variant Y1912C 5735A>G LICA-FR 5 176710822 176710822 single base substitution A G missense_variant Y2015C 6044A>G LICA-FR 5 176710822 176710822 single base substitution A G upstream_gene_variant LICA-FR 5 176728619 176728619 insertion of <=200bp - GC downstream_gene_variant LICA-FR 5 176729737 176729738 deletion of <=200bp CC - downstream_gene_variant LIHC-US 5 176562164 176562164 single base substitution G A 5_prime_UTR_variant LIHC-US 5 176562164 176562164 single base substitution G A exon_variant LIHC-US 5 176562164 176562164 single base substitution G A synonymous_variant V20V 60G>A LIHC-US 5 176562319 176562319 single base substitution T G exon_variant LIHC-US 5 176562319 176562319 single base substitution T G intron_variant LIHC-US 5 176562319 176562319 single base substitution T G missense_variant L72R 215T>G LIHC-US 5 176562395 176562395 single base substitution T G exon_variant LIHC-US 5 176562395 176562395 single base substitution T G intron_variant LIHC-US 5 176562395 176562395 single base substitution T G missense_variant F97L 291T>G LIHC-US 5 176637954 176637954 single base substitution A G downstream_gene_variant LIHC-US 5 176637954 176637954 single base substitution A G missense_variant I583V 1747A>G LIHC-US 5 176637954 176637954 single base substitution A G missense_variant I749V 2245A>G LIHC-US 5 176637954 176637954 single base substitution A G missense_variant I852V 2554A>G LIHC-US 5 176637954 176637954 single base substitution A G upstream_gene_variant LIHC-US 5 176675231 176675231 single base substitution A G missense_variant E1247G 3740A>G LIHC-US 5 176675231 176675231 single base substitution A G missense_variant E1413G 4238A>G LIHC-US 5 176675231 176675231 single base substitution A G missense_variant E1516G 4547A>G LIHC-US 5 176721088 176721088 single base substitution C A downstream_gene_variant LIHC-US 5 176721088 176721088 single base substitution C A stop_gained S1971* 5912C>A LIHC-US 5 176721088 176721088 single base substitution C A stop_gained S2137* 6410C>A LIHC-US 5 176721088 176721088 single base substitution C A stop_gained S2240* 6719C>A LIHC-US 5 176722236 176722236 single base substitution A C downstream_gene_variant LIHC-US 5 176722236 176722236 single base substitution A C missense_variant S2354R 7060A>C LIHC-US 5 176722236 176722236 single base substitution A C missense_variant S2520R 7558A>C LIHC-US 5 176722236 176722236 single base substitution A C missense_variant S2623R 7867A>C LIHC-US 5 176722361 176722361 single base substitution T C downstream_gene_variant LIHC-US 5 176722361 176722361 single base substitution T C synonymous_variant S2395S 7185T>C LIHC-US 5 176722361 176722361 single base substitution T C synonymous_variant S2561S 7683T>C LIHC-US 5 176722361 176722361 single base substitution T C synonymous_variant S2664S 7992T>C LIHC-US 5 176728924 176728924 single base substitution A G downstream_gene_variant LIHC-US 5 176731012 176731012 single base substitution G T downstream_gene_variant LINC-JP 5 176559867 176559867 single base substitution C T upstream_gene_variant LINC-JP 5 176564657 176564657 single base substitution A G downstream_gene_variant LINC-JP 5 176564657 176564657 single base substitution A G intron_variant LINC-JP 5 176570138 176570138 single base substitution A C intron_variant LINC-JP 5 176571627 176571627 single base substitution A G intron_variant LINC-JP 5 176572759 176572759 single base substitution A G intron_variant LINC-JP 5 176594665 176594665 single base substitution C T intron_variant LINC-JP 5 176598831 176598831 single base substitution A C intron_variant LINC-JP 5 176600579 176600579 single base substitution A G intron_variant LINC-JP 5 176610331 176610331 single base substitution A G intron_variant LINC-JP 5 176612492 176612492 single base substitution G A intron_variant LINC-JP 5 176616435 176616435 single base substitution A G intron_variant LINC-JP 5 176622287 176622287 single base substitution C T intron_variant LINC-JP 5 176628527 176628527 single base substitution G A intron_variant LINC-JP 5 176635891 176635891 single base substitution T G downstream_gene_variant LINC-JP 5 176635891 176635891 single base substitution T G intron_variant LINC-JP 5 176635891 176635891 single base substitution T G upstream_gene_variant LINC-JP 5 176643692 176643692 single base substitution A T intron_variant LINC-JP 5 176646405 176646405 single base substitution C T intron_variant LINC-JP 5 176657082 176657082 single base substitution A G intron_variant LINC-JP 5 176677900 176677900 single base substitution A T intron_variant LINC-JP 5 176678769 176678769 single base substitution T G synonymous_variant A1291A 3873T>G LINC-JP 5 176678769 176678769 single base substitution T G synonymous_variant A1457A 4371T>G LINC-JP 5 176678769 176678769 single base substitution T G synonymous_variant A1560A 4680T>G LINC-JP 5 176678880 176678880 single base substitution C A intron_variant LINC-JP 5 176687403 176687403 single base substitution T A intron_variant LINC-JP 5 176694822 176694822 single base substitution A G intron_variant LINC-JP 5 176694971 176694971 single base substitution T A intron_variant LINC-JP 5 176701227 176701227 single base substitution A G downstream_gene_variant LINC-JP 5 176701227 176701227 single base substitution A G intron_variant LINC-JP 5 176702498 176702498 single base substitution G A downstream_gene_variant LINC-JP 5 176702498 176702498 single base substitution G A intron_variant LINC-JP 5 176704259 176704259 single base substitution G C downstream_gene_variant LINC-JP 5 176704259 176704259 single base substitution G C intron_variant LINC-JP 5 176709649 176709649 single base substitution A G downstream_gene_variant LINC-JP 5 176709649 176709649 single base substitution A G intron_variant LINC-JP 5 176721593 176721593 single base substitution C T downstream_gene_variant LINC-JP 5 176721593 176721593 single base substitution C T synonymous_variant D2139D 6417C>T LINC-JP 5 176721593 176721593 single base substitution C T synonymous_variant D2305D 6915C>T LINC-JP 5 176721593 176721593 single base substitution C T synonymous_variant D2408D 7224C>T LINC-JP 5 176721609 176721609 single base substitution T G downstream_gene_variant LINC-JP 5 176721609 176721609 single base substitution T G missense_variant L2145V 6433T>G LINC-JP 5 176721609 176721609 single base substitution T G missense_variant L2311V 6931T>G LINC-JP 5 176721609 176721609 single base substitution T G missense_variant L2414V 7240T>G LINC-JP 5 176729808 176729809 deletion of <=200bp AT - downstream_gene_variant LINC-JP 5 176731204 176731204 single base substitution A T downstream_gene_variant LINC-JP 5 176731292 176731292 single base substitution A G downstream_gene_variant LINC-JP 5 176731558 176731558 single base substitution T A downstream_gene_variant LINC-JP 5 176731843 176731843 single base substitution C T downstream_gene_variant LIRI-JP 5 176555818 176555818 single base substitution G A upstream_gene_variant LIRI-JP 5 176562841 176562841 single base substitution G A downstream_gene_variant LIRI-JP 5 176562841 176562841 single base substitution G A exon_variant LIRI-JP 5 176562841 176562841 single base substitution G A intron_variant LIRI-JP 5 176562841 176562841 single base substitution G A missense_variant G246D 737G>A LIRI-JP 5 176563123 176563123 single base substitution G A downstream_gene_variant LIRI-JP 5 176563123 176563123 single base substitution G A exon_variant LIRI-JP 5 176563123 176563123 single base substitution G A intron_variant LIRI-JP 5 176564177 176564177 single base substitution G T 3_prime_UTR_variant LIRI-JP 5 176564177 176564177 single base substitution G T downstream_gene_variant LIRI-JP 5 176564177 176564177 single base substitution G T intron_variant LIRI-JP 5 176565154 176565154 single base substitution A T downstream_gene_variant LIRI-JP 5 176565154 176565154 single base substitution A T intron_variant LIRI-JP 5 176566622 176566622 single base substitution T C downstream_gene_variant LIRI-JP 5 176566622 176566622 single base substitution T C intron_variant LIRI-JP 5 176566689 176566689 single base substitution C G downstream_gene_variant LIRI-JP 5 176566689 176566689 single base substitution C G intron_variant LIRI-JP 5 176571187 176571187 single base substitution A G intron_variant LIRI-JP 5 176573680 176573680 single base substitution A G intron_variant LIRI-JP 5 176577438 176577438 single base substitution A G intron_variant LIRI-JP 5 176580730 176580730 insertion of <=200bp - TAAA intron_variant LIRI-JP 5 176580808 176580808 single base substitution C A intron_variant LIRI-JP 5 176581524 176581524 single base substitution G T intron_variant LIRI-JP 5 176585631 176585631 single base substitution A G intron_variant LIRI-JP 5 176587896 176587896 single base substitution A G intron_variant LIRI-JP 5 176589876 176589876 single base substitution G T intron_variant LIRI-JP 5 176593474 176593474 single base substitution G A intron_variant LIRI-JP 5 176593869 176593869 single base substitution A G intron_variant LIRI-JP 5 176594800 176594800 single base substitution A G intron_variant LIRI-JP 5 176595689 176595689 single base substitution T A intron_variant LIRI-JP 5 176597391 176597391 single base substitution G A intron_variant LIRI-JP 5 176599835 176599835 single base substitution A G intron_variant LIRI-JP 5 176601944 176601944 single base substitution C T intron_variant LIRI-JP 5 176603640 176603640 single base substitution A G intron_variant LIRI-JP 5 176604098 176604098 single base substitution C G intron_variant LIRI-JP 5 176606625 176606625 single base substitution G T intron_variant LIRI-JP 5 176607584 176607584 single base substitution C A intron_variant LIRI-JP 5 176607640 176607640 single base substitution C T intron_variant LIRI-JP 5 176607914 176607914 single base substitution C G intron_variant LIRI-JP 5 176608679 176608679 single base substitution G A intron_variant LIRI-JP 5 176609892 176609892 single base substitution G T intron_variant LIRI-JP 5 176610990 176610990 single base substitution A G intron_variant LIRI-JP 5 176611406 176611406 single base substitution C T intron_variant LIRI-JP 5 176613448 176613448 single base substitution C A intron_variant LIRI-JP 5 176618129 176618129 single base substitution C A intron_variant LIRI-JP 5 176618705 176618705 single base substitution A G intron_variant LIRI-JP 5 176622594 176622594 single base substitution A T intron_variant LIRI-JP 5 176626463 176626463 single base substitution G T intron_variant LIRI-JP 5 176628897 176628897 single base substitution G T intron_variant LIRI-JP 5 176630913 176630913 single base substitution C G intron_variant LIRI-JP 5 176633888 176633888 single base substitution G T downstream_gene_variant LIRI-JP 5 176633888 176633888 single base substitution G T intron_variant LIRI-JP 5 176636895 176636895 single base substitution G C downstream_gene_variant LIRI-JP 5 176636895 176636895 single base substitution G C missense_variant A230P 688G>C LIRI-JP 5 176636895 176636895 single base substitution G C missense_variant A396P 1186G>C LIRI-JP 5 176636895 176636895 single base substitution G C missense_variant A499P 1495G>C LIRI-JP 5 176636895 176636895 single base substitution G C upstream_gene_variant LIRI-JP 5 176640494 176640494 single base substitution A G downstream_gene_variant LIRI-JP 5 176640494 176640494 single base substitution A G intron_variant LIRI-JP 5 176641541 176641541 single base substitution G A downstream_gene_variant LIRI-JP 5 176641541 176641541 single base substitution G A intron_variant LIRI-JP 5 176642384 176642384 single base substitution C A intron_variant LIRI-JP 5 176642784 176642784 single base substitution G A intron_variant LIRI-JP 5 176642876 176642876 single base substitution T A intron_variant LIRI-JP 5 176643395 176643395 single base substitution C T intron_variant LIRI-JP 5 176644083 176644083 single base substitution T A intron_variant LIRI-JP 5 176644908 176644908 single base substitution A G intron_variant LIRI-JP 5 176648113 176648113 single base substitution A T intron_variant LIRI-JP 5 176648416 176648416 single base substitution A G intron_variant LIRI-JP 5 176650929 176650929 single base substitution A G intron_variant LIRI-JP 5 176651466 176651466 single base substitution C T intron_variant LIRI-JP 5 176652407 176652407 single base substitution G C intron_variant LIRI-JP 5 176653132 176653132 single base substitution T C intron_variant LIRI-JP 5 176653569 176653569 single base substitution C T intron_variant LIRI-JP 5 176655867 176655867 single base substitution A G intron_variant LIRI-JP 5 176655888 176655888 single base substitution A G intron_variant LIRI-JP 5 176656804 176656804 single base substitution G T exon_variant LIRI-JP 5 176656804 176656804 single base substitution G T intron_variant LIRI-JP 5 176656962 176656962 single base substitution C A intron_variant LIRI-JP 5 176659430 176659430 single base substitution A G intron_variant LIRI-JP 5 176662291 176662291 single base substitution T C intron_variant LIRI-JP 5 176663814 176663814 single base substitution A T intron_variant LIRI-JP 5 176664835 176664835 single base substitution A G intron_variant LIRI-JP 5 176664946 176664946 single base substitution A G intron_variant LIRI-JP 5 176666022 176666022 single base substitution A G intron_variant LIRI-JP 5 176666353 176666353 single base substitution A T intron_variant LIRI-JP 5 176669428 176669428 single base substitution G T downstream_gene_variant LIRI-JP 5 176669428 176669428 single base substitution G T intron_variant LIRI-JP 5 176670675 176670675 single base substitution C G downstream_gene_variant LIRI-JP 5 176670675 176670675 single base substitution C G intron_variant LIRI-JP 5 176672254 176672254 single base substitution A G intron_variant LIRI-JP 5 176673302 176673302 single base substitution T G intron_variant LIRI-JP 5 176674522 176674522 single base substitution T G intron_variant LIRI-JP 5 176675570 176675570 single base substitution A G intron_variant LIRI-JP 5 176675575 176675575 single base substitution T A intron_variant LIRI-JP 5 176675592 176675592 single base substitution A C intron_variant LIRI-JP 5 176685747 176685747 single base substitution G A intron_variant LIRI-JP 5 176688819 176688819 single base substitution T C intron_variant LIRI-JP 5 176688819 176688819 single base substitution T C upstream_gene_variant LIRI-JP 5 176690701 176690701 single base substitution C T intron_variant LIRI-JP 5 176690701 176690701 single base substitution C T upstream_gene_variant LIRI-JP 5 176692061 176692061 single base substitution A T intron_variant LIRI-JP 5 176692061 176692061 single base substitution A T upstream_gene_variant LIRI-JP 5 176692876 176692876 single base substitution G A intron_variant LIRI-JP 5 176692876 176692876 single base substitution G A upstream_gene_variant LIRI-JP 5 176693652 176693652 single base substitution T G 5_prime_UTR_premature_start_codon_gain_variant LIRI-JP 5 176693652 176693652 single base substitution T G intron_variant LIRI-JP 5 176693771 176693771 single base substitution A G intron_variant LIRI-JP 5 176698854 176698854 single base substitution A G downstream_gene_variant LIRI-JP 5 176698854 176698854 single base substitution A G intron_variant LIRI-JP 5 176701159 176701159 single base substitution A C downstream_gene_variant LIRI-JP 5 176701159 176701159 single base substitution A C intron_variant LIRI-JP 5 176702123 176702123 single base substitution C T downstream_gene_variant LIRI-JP 5 176702123 176702123 single base substitution C T intron_variant LIRI-JP 5 176702569 176702569 single base substitution G A downstream_gene_variant LIRI-JP 5 176702569 176702569 single base substitution G A intron_variant LIRI-JP 5 176702971 176702971 single base substitution A G downstream_gene_variant LIRI-JP 5 176702971 176702971 single base substitution A G intron_variant LIRI-JP 5 176705820 176705820 single base substitution T A intron_variant LIRI-JP 5 176706553 176706553 single base substitution A C intron_variant LIRI-JP 5 176707059 176707059 single base substitution G A intron_variant LIRI-JP 5 176707191 176707191 single base substitution G C intron_variant LIRI-JP 5 176710119 176710119 single base substitution T G downstream_gene_variant LIRI-JP 5 176710119 176710119 single base substitution T G intron_variant LIRI-JP 5 176710266 176710266 single base substitution A T downstream_gene_variant LIRI-JP 5 176710266 176710266 single base substitution A T intron_variant LIRI-JP 5 176711865 176711865 single base substitution G T downstream_gene_variant LIRI-JP 5 176711865 176711865 single base substitution G T intron_variant LIRI-JP 5 176711865 176711865 single base substitution G T upstream_gene_variant LIRI-JP 5 176712852 176712852 single base substitution A T intron_variant LIRI-JP 5 176712852 176712852 single base substitution A T upstream_gene_variant LIRI-JP 5 176713877 176713877 single base substitution C A intron_variant LIRI-JP 5 176713877 176713877 single base substitution C A upstream_gene_variant LIRI-JP 5 176714055 176714055 single base substitution G A intron_variant LIRI-JP 5 176714055 176714055 single base substitution G A upstream_gene_variant LIRI-JP 5 176717731 176717731 single base substitution A T intron_variant LIRI-JP 5 176725258 176725258 single base substitution C G 3_prime_UTR_variant LIRI-JP 5 176725258 176725258 single base substitution C G downstream_gene_variant LIRI-JP 5 176725387 176725387 single base substitution G A 3_prime_UTR_variant LIRI-JP 5 176725387 176725387 single base substitution G A downstream_gene_variant LIRI-JP 5 176730683 176730683 single base substitution A G downstream_gene_variant LUSC-KR 5 176556356 176556356 single base substitution G C upstream_gene_variant LUSC-KR 5 176572299 176572299 single base substitution G T intron_variant LUSC-KR 5 176572843 176572843 single base substitution A G intron_variant LUSC-KR 5 176577701 176577701 single base substitution G T intron_variant LUSC-KR 5 176578287 176578287 single base substitution G A intron_variant LUSC-KR 5 176583091 176583091 single base substitution G A intron_variant LUSC-KR 5 176590842 176590842 single base substitution G T intron_variant LUSC-KR 5 176590843 176590843 single base substitution G T intron_variant LUSC-KR 5 176594309 176594309 single base substitution G T intron_variant LUSC-KR 5 176602353 176602353 single base substitution G C intron_variant LUSC-KR 5 176619482 176619482 single base substitution C T intron_variant LUSC-KR 5 176633639 176633639 single base substitution G C downstream_gene_variant LUSC-KR 5 176633639 176633639 single base substitution G C intron_variant LUSC-KR 5 176634030 176634030 single base substitution T C downstream_gene_variant LUSC-KR 5 176634030 176634030 single base substitution T C intron_variant LUSC-KR 5 176638261 176638261 single base substitution A T downstream_gene_variant LUSC-KR 5 176638261 176638261 single base substitution A T missense_variant K685M 2054A>T LUSC-KR 5 176638261 176638261 single base substitution A T missense_variant K851M 2552A>T LUSC-KR 5 176638261 176638261 single base substitution A T missense_variant K954M 2861A>T LUSC-KR 5 176638261 176638261 single base substitution A T upstream_gene_variant LUSC-KR 5 176639163 176639163 single base substitution A T downstream_gene_variant LUSC-KR 5 176639163 176639163 single base substitution A T exon_variant LUSC-KR 5 176639163 176639163 single base substitution A T missense_variant S1152C 3454A>T LUSC-KR 5 176639163 176639163 single base substitution A T missense_variant S1255C 3763A>T LUSC-KR 5 176639163 176639163 single base substitution A T missense_variant S986C 2956A>T LUSC-KR 5 176644686 176644686 single base substitution G T intron_variant LUSC-KR 5 176651087 176651087 single base substitution G C intron_variant LUSC-KR 5 176654994 176654994 single base substitution G T intron_variant LUSC-KR 5 176668645 176668645 single base substitution G T downstream_gene_variant LUSC-KR 5 176668645 176668645 single base substitution G T intron_variant LUSC-KR 5 176679460 176679460 single base substitution A T intron_variant LUSC-KR 5 176681565 176681565 single base substitution T A intron_variant LUSC-KR 5 176689788 176689788 single base substitution G A intron_variant LUSC-KR 5 176689788 176689788 single base substitution G A upstream_gene_variant LUSC-KR 5 176693054 176693054 single base substitution G T intron_variant LUSC-KR 5 176693054 176693054 single base substitution G T upstream_gene_variant LUSC-KR 5 176698905 176698905 single base substitution A G downstream_gene_variant LUSC-KR 5 176698905 176698905 single base substitution A G intron_variant LUSC-KR 5 176707985 176707985 single base substitution T C downstream_gene_variant LUSC-KR 5 176707985 176707985 single base substitution T C intron_variant LUSC-KR 5 176721686 176721686 single base substitution G A downstream_gene_variant LUSC-KR 5 176721686 176721686 single base substitution G A synonymous_variant L2170L 6510G>A LUSC-KR 5 176721686 176721686 single base substitution G A synonymous_variant L2336L 7008G>A LUSC-KR 5 176721686 176721686 single base substitution G A synonymous_variant L2439L 7317G>A LUSC-US 5 176637166 176637166 single base substitution C G downstream_gene_variant LUSC-US 5 176637166 176637166 single base substitution C G missense_variant S320C 959C>G LUSC-US 5 176637166 176637166 single base substitution C G missense_variant S486C 1457C>G LUSC-US 5 176637166 176637166 single base substitution C G missense_variant S589C 1766C>G LUSC-US 5 176637166 176637166 single base substitution C G upstream_gene_variant LUSC-US 5 176637416 176637416 single base substitution A T downstream_gene_variant LUSC-US 5 176637416 176637416 single base substitution A T synonymous_variant T403T 1209A>T LUSC-US 5 176637416 176637416 single base substitution A T synonymous_variant T569T 1707A>T LUSC-US 5 176637416 176637416 single base substitution A T synonymous_variant T672T 2016A>T LUSC-US 5 176637416 176637416 single base substitution A T upstream_gene_variant LUSC-US 5 176638020 176638020 single base substitution G T downstream_gene_variant LUSC-US 5 176638020 176638020 single base substitution G T stop_gained E605* 1813G>T LUSC-US 5 176638020 176638020 single base substitution G T stop_gained E771* 2311G>T LUSC-US 5 176638020 176638020 single base substitution G T stop_gained E874* 2620G>T LUSC-US 5 176638020 176638020 single base substitution G T upstream_gene_variant LUSC-US 5 176638319 176638319 single base substitution G C downstream_gene_variant LUSC-US 5 176638319 176638319 single base substitution G C missense_variant Q704H 2112G>C LUSC-US 5 176638319 176638319 single base substitution G C missense_variant Q870H 2610G>C LUSC-US 5 176638319 176638319 single base substitution G C missense_variant Q973H 2919G>C LUSC-US 5 176638319 176638319 single base substitution G C upstream_gene_variant LUSC-US 5 176638381 176638381 single base substitution C T downstream_gene_variant LUSC-US 5 176638381 176638381 single base substitution C T missense_variant S725F 2174C>T LUSC-US 5 176638381 176638381 single base substitution C T missense_variant S891F 2672C>T LUSC-US 5 176638381 176638381 single base substitution C T missense_variant S994F 2981C>T LUSC-US 5 176638381 176638381 single base substitution C T upstream_gene_variant LUSC-US 5 176638561 176638561 single base substitution G C downstream_gene_variant LUSC-US 5 176638561 176638561 single base substitution G C missense_variant R1054T 3161G>C LUSC-US 5 176638561 176638561 single base substitution G C missense_variant R785T 2354G>C LUSC-US 5 176638561 176638561 single base substitution G C missense_variant R951T 2852G>C LUSC-US 5 176638561 176638561 single base substitution G C upstream_gene_variant LUSC-US 5 176673711 176673711 single base substitution C T stop_gained R1202* 3604C>T LUSC-US 5 176673711 176673711 single base substitution C T stop_gained R1368* 4102C>T LUSC-US 5 176673711 176673711 single base substitution C T stop_gained R1471* 4411C>T LUSC-US 5 176678730 176678730 single base substitution G C splice_acceptor_variant LUSC-US 5 176684105 176684105 single base substitution G C missense_variant C1371S 4112G>C LUSC-US 5 176684105 176684105 single base substitution G C missense_variant C1537S 4610G>C LUSC-US 5 176684105 176684105 single base substitution G C missense_variant C1640S 4919G>C LUSC-US 5 176696631 176696631 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant LUSC-US 5 176696631 176696631 single base substitution C T stop_gained R1509* 4525C>T LUSC-US 5 176696631 176696631 single base substitution C T stop_gained R1675* 5023C>T LUSC-US 5 176696631 176696631 single base substitution C T stop_gained R1778* 5332C>T LUSC-US 5 176710800 176710800 single base substitution G A downstream_gene_variant LUSC-US 5 176710800 176710800 single base substitution G A missense_variant D1739N 5215G>A LUSC-US 5 176710800 176710800 single base substitution G A missense_variant D1905N 5713G>A LUSC-US 5 176710800 176710800 single base substitution G A missense_variant D2008N 6022G>A LUSC-US 5 176710800 176710800 single base substitution G A upstream_gene_variant MALY-DE 5 176558532 176558532 single base substitution G T upstream_gene_variant MALY-DE 5 176563780 176563780 single base substitution C T downstream_gene_variant MALY-DE 5 176563780 176563780 single base substitution C T intron_variant MALY-DE 5 176567968 176567968 single base substitution C T downstream_gene_variant MALY-DE 5 176567968 176567968 single base substitution C T intron_variant MALY-DE 5 176574598 176574598 insertion of <=200bp - T intron_variant MALY-DE 5 176576070 176576070 single base substitution T G intron_variant MALY-DE 5 176583963 176583964 deletion of <=200bp CT - intron_variant MALY-DE 5 176585087 176585087 single base substitution T G intron_variant MALY-DE 5 176586682 176586682 single base substitution C T intron_variant MALY-DE 5 176586900 176586900 single base substitution T A intron_variant MALY-DE 5 176588661 176588661 single base substitution T A intron_variant MALY-DE 5 176593921 176593921 single base substitution A C intron_variant MALY-DE 5 176603147 176603147 single base substitution G A intron_variant MALY-DE 5 176604998 176604998 single base substitution T G intron_variant MALY-DE 5 176618081 176618081 insertion of <=200bp - TC intron_variant MALY-DE 5 176618968 176618968 single base substitution G A intron_variant MALY-DE 5 176618968 176618968 single base substitution G A stop_gained W337* 1011G>A MALY-DE 5 176618968 176618968 single base substitution G A stop_gained W68* 204G>A MALY-DE 5 176622644 176622644 single base substitution T G intron_variant MALY-DE 5 176626023 176626023 single base substitution A G intron_variant MALY-DE 5 176626259 176626259 single base substitution A T intron_variant MALY-DE 5 176634907 176634908 deletion of <=200bp GT - downstream_gene_variant MALY-DE 5 176634907 176634908 deletion of <=200bp GT - intron_variant MALY-DE 5 176634907 176634908 deletion of <=200bp GT - upstream_gene_variant MALY-DE 5 176651390 176651390 single base substitution T A intron_variant MALY-DE 5 176653463 176653463 single base substitution T A intron_variant MALY-DE 5 176653519 176653519 single base substitution T C intron_variant MALY-DE 5 176658267 176658267 single base substitution G A intron_variant MALY-DE 5 176660221 176660221 single base substitution C G intron_variant MALY-DE 5 176665407 176665407 single base substitution G A intron_variant MALY-DE 5 176665407 176665407 single base substitution G A missense_variant G1095E 3284G>A MALY-DE 5 176665407 176665407 single base substitution G A missense_variant G1261E 3782G>A MALY-DE 5 176665407 176665407 single base substitution G A missense_variant G1364E 4091G>A MALY-DE 5 176665789 176665789 single base substitution C T intron_variant MALY-DE 5 176686527 176686527 single base substitution T C intron_variant MALY-DE 5 176686990 176686990 single base substitution G T missense_variant G1387V 4160G>T MALY-DE 5 176686990 176686990 single base substitution G T missense_variant G1553V 4658G>T MALY-DE 5 176686990 176686990 single base substitution G T missense_variant G1656V 4967G>T MALY-DE 5 176689524 176689524 insertion of <=200bp - A intron_variant MALY-DE 5 176689524 176689524 insertion of <=200bp - A upstream_gene_variant MALY-DE 5 176691532 176691532 single base substitution G T intron_variant MALY-DE 5 176691532 176691532 single base substitution G T upstream_gene_variant MALY-DE 5 176692755 176692755 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MALY-DE 5 176692755 176692755 single base substitution G A intron_variant MALY-DE 5 176692755 176692755 single base substitution G A upstream_gene_variant MALY-DE 5 176698198 176698198 single base substitution T A downstream_gene_variant MALY-DE 5 176698198 176698198 single base substitution T A intron_variant MALY-DE 5 176701699 176701700 deletion of <=200bp TG - downstream_gene_variant MALY-DE 5 176701699 176701700 deletion of <=200bp TG - intron_variant MALY-DE 5 176704004 176704004 deletion of <=200bp C - downstream_gene_variant MALY-DE 5 176704004 176704004 deletion of <=200bp C - intron_variant MALY-DE 5 176709196 176709196 single base substitution G A downstream_gene_variant MALY-DE 5 176709196 176709196 single base substitution G A intron_variant MALY-DE 5 176715021 176715021 single base substitution G A intron_variant MALY-DE 5 176715021 176715021 single base substitution G A upstream_gene_variant MALY-DE 5 176716904 176716904 single base substitution C T intron_variant MALY-DE 5 176719370 176719370 single base substitution T C downstream_gene_variant MALY-DE 5 176719370 176719370 single base substitution T C intron_variant MELA-AU 5 176555213 176555213 single base substitution C T upstream_gene_variant MELA-AU 5 176555316 176555317 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 5 176555660 176555660 single base substitution G A upstream_gene_variant MELA-AU 5 176556159 176556159 single base substitution G A upstream_gene_variant MELA-AU 5 176557380 176557380 single base substitution C T upstream_gene_variant MELA-AU 5 176557410 176557410 single base substitution C T upstream_gene_variant MELA-AU 5 176558523 176558524 multiple base substitution (>=2bp and <=200bp) CC GT upstream_gene_variant MELA-AU 5 176559183 176559183 single base substitution C T upstream_gene_variant MELA-AU 5 176559537 176559537 single base substitution T G upstream_gene_variant MELA-AU 5 176560089 176560089 single base substitution G A 5_prime_UTR_variant MELA-AU 5 176560089 176560089 single base substitution G A exon_variant MELA-AU 5 176560089 176560089 single base substitution G A upstream_gene_variant MELA-AU 5 176560262 176560262 single base substitution G A intron_variant MELA-AU 5 176560262 176560262 single base substitution G A upstream_gene_variant MELA-AU 5 176560274 176560274 single base substitution C T intron_variant MELA-AU 5 176560274 176560274 single base substitution C T upstream_gene_variant MELA-AU 5 176561685 176561685 single base substitution G A intron_variant MELA-AU 5 176561685 176561685 single base substitution G A upstream_gene_variant MELA-AU 5 176561714 176561714 single base substitution C T intron_variant MELA-AU 5 176561714 176561714 single base substitution C T upstream_gene_variant MELA-AU 5 176561871 176561871 single base substitution G C intron_variant MELA-AU 5 176561871 176561871 single base substitution G C upstream_gene_variant MELA-AU 5 176562127 176562127 single base substitution C T 5_prime_UTR_variant MELA-AU 5 176562127 176562127 single base substitution C T exon_variant MELA-AU 5 176562127 176562127 single base substitution C T missense_variant P8L 23C>T MELA-AU 5 176563369 176563369 single base substitution C T downstream_gene_variant MELA-AU 5 176563369 176563369 single base substitution C T intron_variant MELA-AU 5 176563790 176563790 single base substitution T C downstream_gene_variant MELA-AU 5 176563790 176563790 single base substitution T C intron_variant MELA-AU 5 176564627 176564627 single base substitution C T downstream_gene_variant MELA-AU 5 176564627 176564627 single base substitution C T intron_variant MELA-AU 5 176565380 176565380 single base substitution C T downstream_gene_variant MELA-AU 5 176565380 176565380 single base substitution C T intron_variant MELA-AU 5 176567226 176567227 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 5 176567226 176567227 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 176567736 176567736 single base substitution G A downstream_gene_variant MELA-AU 5 176567736 176567736 single base substitution G A intron_variant MELA-AU 5 176569558 176569558 single base substitution C T intron_variant MELA-AU 5 176569671 176569671 single base substitution C T intron_variant MELA-AU 5 176569867 176569867 single base substitution T A intron_variant MELA-AU 5 176570713 176570713 single base substitution C T intron_variant MELA-AU 5 176571034 176571034 single base substitution C T intron_variant MELA-AU 5 176572939 176572939 single base substitution C T intron_variant MELA-AU 5 176573422 176573422 single base substitution G A intron_variant MELA-AU 5 176573833 176573833 single base substitution C T intron_variant MELA-AU 5 176573898 176573898 single base substitution C T intron_variant MELA-AU 5 176573900 176573900 single base substitution C T intron_variant MELA-AU 5 176574848 176574849 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 176575454 176575454 single base substitution C T intron_variant MELA-AU 5 176575625 176575625 single base substitution C T intron_variant MELA-AU 5 176575763 176575764 multiple base substitution (>=2bp and <=200bp) TC GT intron_variant MELA-AU 5 176575832 176575832 single base substitution T A intron_variant MELA-AU 5 176576085 176576085 single base substitution C T intron_variant MELA-AU 5 176576698 176576698 single base substitution C T intron_variant MELA-AU 5 176577165 176577165 single base substitution C T intron_variant MELA-AU 5 176577424 176577424 single base substitution C T intron_variant MELA-AU 5 176578126 176578126 single base substitution C T intron_variant MELA-AU 5 176578539 176578539 single base substitution G A intron_variant MELA-AU 5 176579155 176579155 single base substitution C T intron_variant MELA-AU 5 176579545 176579545 single base substitution C T intron_variant MELA-AU 5 176579836 176579836 single base substitution C T intron_variant MELA-AU 5 176579981 176579981 single base substitution C T intron_variant MELA-AU 5 176580044 176580044 single base substitution C T intron_variant MELA-AU 5 176580327 176580327 single base substitution T C intron_variant MELA-AU 5 176580734 176580734 single base substitution G A intron_variant MELA-AU 5 176581306 176581306 single base substitution G A intron_variant MELA-AU 5 176582223 176582223 single base substitution C T intron_variant MELA-AU 5 176582247 176582247 single base substitution C T intron_variant MELA-AU 5 176582905 176582905 single base substitution C T intron_variant MELA-AU 5 176585939 176585939 single base substitution G A intron_variant MELA-AU 5 176585948 176585948 single base substitution C T intron_variant MELA-AU 5 176586772 176586772 single base substitution T G intron_variant MELA-AU 5 176586919 176586919 single base substitution C T intron_variant MELA-AU 5 176587150 176587150 single base substitution C T intron_variant MELA-AU 5 176587160 176587160 single base substitution G A intron_variant MELA-AU 5 176587307 176587307 single base substitution T A intron_variant MELA-AU 5 176587471 176587471 single base substitution T C intron_variant MELA-AU 5 176588100 176588100 single base substitution A T intron_variant MELA-AU 5 176588211 176588211 single base substitution C T intron_variant MELA-AU 5 176588633 176588633 single base substitution C T intron_variant MELA-AU 5 176590986 176590986 single base substitution G A intron_variant MELA-AU 5 176591251 176591251 single base substitution G A intron_variant MELA-AU 5 176592561 176592561 single base substitution C T intron_variant MELA-AU 5 176592710 176592710 single base substitution C T intron_variant MELA-AU 5 176593032 176593032 deletion of <=200bp T - intron_variant MELA-AU 5 176593034 176593035 multiple base substitution (>=2bp and <=200bp) CC GT intron_variant MELA-AU 5 176593423 176593423 single base substitution C T intron_variant MELA-AU 5 176593468 176593468 single base substitution G A intron_variant MELA-AU 5 176593771 176593771 single base substitution G A intron_variant MELA-AU 5 176594341 176594341 single base substitution C T intron_variant MELA-AU 5 176594979 176594979 single base substitution C T intron_variant MELA-AU 5 176594980 176594980 single base substitution C T intron_variant MELA-AU 5 176595393 176595393 single base substitution C T intron_variant MELA-AU 5 176595808 176595808 single base substitution T C intron_variant MELA-AU 5 176597442 176597442 single base substitution C T intron_variant MELA-AU 5 176597545 176597545 single base substitution G A intron_variant MELA-AU 5 176597605 176597605 single base substitution C T intron_variant MELA-AU 5 176597800 176597800 single base substitution C T intron_variant MELA-AU 5 176597827 176597827 single base substitution C T intron_variant MELA-AU 5 176598147 176598147 single base substitution C T intron_variant MELA-AU 5 176598300 176598300 single base substitution C T intron_variant MELA-AU 5 176598365 176598365 single base substitution C T intron_variant MELA-AU 5 176598729 176598729 single base substitution G A intron_variant MELA-AU 5 176599103 176599103 single base substitution C T intron_variant MELA-AU 5 176600671 176600671 single base substitution C T intron_variant MELA-AU 5 176601439 176601440 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 176601565 176601565 single base substitution T A intron_variant MELA-AU 5 176601732 176601732 single base substitution C T intron_variant MELA-AU 5 176601747 176601747 single base substitution A T intron_variant MELA-AU 5 176602406 176602406 single base substitution C T intron_variant MELA-AU 5 176602719 176602719 single base substitution C T intron_variant MELA-AU 5 176603190 176603190 single base substitution C T intron_variant MELA-AU 5 176603253 176603253 single base substitution C T intron_variant MELA-AU 5 176603982 176603982 single base substitution G A intron_variant MELA-AU 5 176607322 176607322 single base substitution G T intron_variant MELA-AU 5 176607364 176607365 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 176607892 176607892 single base substitution C T intron_variant MELA-AU 5 176608070 176608070 single base substitution C T intron_variant MELA-AU 5 176609107 176609107 single base substitution C T intron_variant MELA-AU 5 176609545 176609545 single base substitution G A intron_variant MELA-AU 5 176609603 176609603 single base substitution C T intron_variant MELA-AU 5 176610067 176610067 single base substitution C T intron_variant MELA-AU 5 176610611 176610611 single base substitution T G intron_variant MELA-AU 5 176611218 176611218 single base substitution T C intron_variant MELA-AU 5 176611507 176611507 single base substitution C T intron_variant MELA-AU 5 176612347 176612347 single base substitution C T intron_variant MELA-AU 5 176613284 176613284 single base substitution C A intron_variant MELA-AU 5 176613787 176613787 single base substitution C T intron_variant MELA-AU 5 176614761 176614762 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 176614887 176614887 single base substitution C T intron_variant MELA-AU 5 176616043 176616043 single base substitution C A intron_variant MELA-AU 5 176616064 176616064 single base substitution C T intron_variant MELA-AU 5 176616926 176616926 single base substitution C T intron_variant MELA-AU 5 176619241 176619241 single base substitution C T intron_variant MELA-AU 5 176620035 176620035 single base substitution T C intron_variant MELA-AU 5 176620522 176620522 single base substitution C T intron_variant MELA-AU 5 176620891 176620891 single base substitution G A intron_variant MELA-AU 5 176620968 176620969 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 176621958 176621958 single base substitution G T intron_variant MELA-AU 5 176621960 176621960 single base substitution G A intron_variant MELA-AU 5 176622455 176622456 deletion of <=200bp TC - intron_variant MELA-AU 5 176622617 176622617 single base substitution C T intron_variant MELA-AU 5 176623138 176623138 single base substitution C T intron_variant MELA-AU 5 176623248 176623248 single base substitution A C intron_variant MELA-AU 5 176623541 176623541 single base substitution C T intron_variant MELA-AU 5 176624155 176624155 single base substitution C T intron_variant MELA-AU 5 176624682 176624682 single base substitution A G intron_variant MELA-AU 5 176625389 176625389 single base substitution C T intron_variant MELA-AU 5 176625992 176625992 single base substitution C T intron_variant MELA-AU 5 176626017 176626017 single base substitution G A intron_variant MELA-AU 5 176626256 176626256 single base substitution C T intron_variant MELA-AU 5 176626723 176626723 single base substitution C T intron_variant MELA-AU 5 176627035 176627035 single base substitution C T intron_variant MELA-AU 5 176627381 176627381 single base substitution C T intron_variant MELA-AU 5 176627519 176627519 single base substitution C T intron_variant MELA-AU 5 176630846 176630846 single base substitution C T intron_variant MELA-AU 5 176631654 176631654 single base substitution C T downstream_gene_variant MELA-AU 5 176631654 176631654 single base substitution C T intron_variant MELA-AU 5 176631726 176631726 single base substitution C T downstream_gene_variant MELA-AU 5 176631726 176631726 single base substitution C T intron_variant MELA-AU 5 176632604 176632604 single base substitution A T downstream_gene_variant MELA-AU 5 176632604 176632604 single base substitution A T intron_variant MELA-AU 5 176632636 176632636 single base substitution C T downstream_gene_variant MELA-AU 5 176632636 176632636 single base substitution C T intron_variant MELA-AU 5 176632853 176632853 single base substitution C T downstream_gene_variant MELA-AU 5 176632853 176632853 single base substitution C T intron_variant MELA-AU 5 176633243 176633243 single base substitution C T downstream_gene_variant MELA-AU 5 176633243 176633243 single base substitution C T intron_variant MELA-AU 5 176633632 176633632 single base substitution T G downstream_gene_variant MELA-AU 5 176633632 176633632 single base substitution T G intron_variant MELA-AU 5 176634924 176634924 single base substitution C T downstream_gene_variant MELA-AU 5 176634924 176634924 single base substitution C T intron_variant MELA-AU 5 176634924 176634924 single base substitution C T upstream_gene_variant MELA-AU 5 176635219 176635219 single base substitution C T downstream_gene_variant MELA-AU 5 176635219 176635219 single base substitution C T intron_variant MELA-AU 5 176635219 176635219 single base substitution C T upstream_gene_variant MELA-AU 5 176635230 176635230 single base substitution C T downstream_gene_variant MELA-AU 5 176635230 176635230 single base substitution C T intron_variant MELA-AU 5 176635230 176635230 single base substitution C T upstream_gene_variant MELA-AU 5 176636605 176636605 single base substitution A G intron_variant MELA-AU 5 176636605 176636605 single base substitution A G upstream_gene_variant MELA-AU 5 176637822 176637822 single base substitution G A downstream_gene_variant MELA-AU 5 176637822 176637822 single base substitution G A missense_variant E539K 1615G>A MELA-AU 5 176637822 176637822 single base substitution G A missense_variant E705K 2113G>A MELA-AU 5 176637822 176637822 single base substitution G A missense_variant E808K 2422G>A MELA-AU 5 176637822 176637822 single base substitution G A upstream_gene_variant MELA-AU 5 176638324 176638325 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 5 176638324 176638325 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant S706F 2117CC>TT MELA-AU 5 176638324 176638325 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant S872F 2615CC>TT MELA-AU 5 176638324 176638325 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant S975F 2924CC>TT MELA-AU 5 176638324 176638325 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 5 176638997 176638997 single base substitution G C downstream_gene_variant MELA-AU 5 176638997 176638997 single base substitution G C synonymous_variant G1096G 3288G>C MELA-AU 5 176638997 176638997 single base substitution G C synonymous_variant G1199G 3597G>C MELA-AU 5 176638997 176638997 single base substitution G C synonymous_variant G930G 2790G>C MELA-AU 5 176638997 176638997 single base substitution G C upstream_gene_variant MELA-AU 5 176639272 176639272 single base substitution C T downstream_gene_variant MELA-AU 5 176639272 176639272 single base substitution C T intron_variant MELA-AU 5 176639428 176639428 single base substitution C T downstream_gene_variant MELA-AU 5 176639428 176639428 single base substitution C T intron_variant MELA-AU 5 176639672 176639672 single base substitution C T downstream_gene_variant MELA-AU 5 176639672 176639672 single base substitution C T intron_variant MELA-AU 5 176639886 176639886 single base substitution C T downstream_gene_variant MELA-AU 5 176639886 176639886 single base substitution C T intron_variant MELA-AU 5 176640424 176640424 single base substitution C T downstream_gene_variant MELA-AU 5 176640424 176640424 single base substitution C T intron_variant MELA-AU 5 176640511 176640511 single base substitution C T downstream_gene_variant MELA-AU 5 176640511 176640511 single base substitution C T intron_variant MELA-AU 5 176640561 176640561 single base substitution C T downstream_gene_variant MELA-AU 5 176640561 176640561 single base substitution C T intron_variant MELA-AU 5 176641309 176641309 single base substitution A G downstream_gene_variant MELA-AU 5 176641309 176641309 single base substitution A G intron_variant MELA-AU 5 176641653 176641653 single base substitution C G downstream_gene_variant MELA-AU 5 176641653 176641653 single base substitution C G intron_variant MELA-AU 5 176642842 176642842 single base substitution C T intron_variant MELA-AU 5 176643016 176643016 single base substitution C T intron_variant MELA-AU 5 176643345 176643345 single base substitution T C intron_variant MELA-AU 5 176643599 176643599 single base substitution C T intron_variant MELA-AU 5 176644096 176644096 single base substitution G A intron_variant MELA-AU 5 176644156 176644156 single base substitution C T intron_variant MELA-AU 5 176644289 176644289 single base substitution C T intron_variant MELA-AU 5 176645163 176645163 single base substitution C T intron_variant MELA-AU 5 176646510 176646510 single base substitution C T intron_variant MELA-AU 5 176646533 176646533 single base substitution C T intron_variant MELA-AU 5 176648339 176648339 single base substitution C T intron_variant MELA-AU 5 176648630 176648630 single base substitution C A intron_variant MELA-AU 5 176648738 176648738 single base substitution G A intron_variant MELA-AU 5 176649364 176649364 single base substitution C T intron_variant MELA-AU 5 176649791 176649791 single base substitution T A intron_variant MELA-AU 5 176650724 176650724 single base substitution C T intron_variant MELA-AU 5 176652264 176652264 single base substitution C G intron_variant MELA-AU 5 176652439 176652439 single base substitution C T intron_variant MELA-AU 5 176652769 176652769 single base substitution T C intron_variant MELA-AU 5 176653001 176653001 single base substitution C T intron_variant MELA-AU 5 176653277 176653277 single base substitution C T intron_variant MELA-AU 5 176653340 176653340 single base substitution G A intron_variant MELA-AU 5 176654233 176654233 single base substitution C T intron_variant MELA-AU 5 176655428 176655428 single base substitution G T intron_variant MELA-AU 5 176655500 176655500 single base substitution G A intron_variant MELA-AU 5 176655810 176655810 single base substitution C T intron_variant MELA-AU 5 176656929 176656929 single base substitution G A intron_variant MELA-AU 5 176657567 176657567 single base substitution C T intron_variant MELA-AU 5 176657671 176657671 single base substitution C T intron_variant MELA-AU 5 176657672 176657672 single base substitution C T intron_variant MELA-AU 5 176658485 176658485 single base substitution G A intron_variant MELA-AU 5 176659201 176659201 single base substitution T C intron_variant MELA-AU 5 176659254 176659254 single base substitution G T intron_variant MELA-AU 5 176661225 176661225 single base substitution G T intron_variant MELA-AU 5 176661466 176661466 single base substitution C T intron_variant MELA-AU 5 176661707 176661707 insertion of <=200bp - C intron_variant MELA-AU 5 176662264 176662265 deletion of <=200bp TG - intron_variant MELA-AU 5 176662626 176662627 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 176663028 176663028 single base substitution G A intron_variant MELA-AU 5 176663818 176663818 single base substitution C T intron_variant MELA-AU 5 176664146 176664146 single base substitution C T intron_variant MELA-AU 5 176664185 176664185 single base substitution C T intron_variant MELA-AU 5 176664234 176664234 single base substitution T C intron_variant MELA-AU 5 176664266 176664266 single base substitution C T intron_variant MELA-AU 5 176665265 176665265 single base substitution C T intron_variant MELA-AU 5 176665265 176665265 single base substitution C T missense_variant L1048F 3142C>T MELA-AU 5 176665265 176665265 single base substitution C T missense_variant L1214F 3640C>T MELA-AU 5 176665265 176665265 single base substitution C T missense_variant L1317F 3949C>T MELA-AU 5 176665379 176665379 single base substitution C T intron_variant MELA-AU 5 176665379 176665379 single base substitution C T missense_variant P1086S 3256C>T MELA-AU 5 176665379 176665379 single base substitution C T missense_variant P1252S 3754C>T MELA-AU 5 176665379 176665379 single base substitution C T missense_variant P1355S 4063C>T MELA-AU 5 176665499 176665499 single base substitution A G intron_variant MELA-AU 5 176665499 176665499 single base substitution A G missense_variant K1126E 3376A>G MELA-AU 5 176665499 176665499 single base substitution A G missense_variant K1292E 3874A>G MELA-AU 5 176665499 176665499 single base substitution A G missense_variant K1395E 4183A>G MELA-AU 5 176666125 176666126 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 176666184 176666184 single base substitution C T intron_variant MELA-AU 5 176666944 176666944 single base substitution T C downstream_gene_variant MELA-AU 5 176666944 176666944 single base substitution T C intron_variant MELA-AU 5 176667095 176667095 single base substitution T A downstream_gene_variant MELA-AU 5 176667095 176667095 single base substitution T A intron_variant MELA-AU 5 176667099 176667099 single base substitution T A downstream_gene_variant MELA-AU 5 176667099 176667099 single base substitution T A intron_variant MELA-AU 5 176667510 176667510 single base substitution C T downstream_gene_variant MELA-AU 5 176667510 176667510 single base substitution C T intron_variant MELA-AU 5 176668854 176668854 single base substitution C T downstream_gene_variant MELA-AU 5 176668854 176668854 single base substitution C T intron_variant MELA-AU 5 176669420 176669420 single base substitution A C downstream_gene_variant MELA-AU 5 176669420 176669420 single base substitution A C intron_variant MELA-AU 5 176669823 176669823 single base substitution C T downstream_gene_variant MELA-AU 5 176669823 176669823 single base substitution C T intron_variant MELA-AU 5 176670212 176670212 single base substitution T C downstream_gene_variant MELA-AU 5 176670212 176670212 single base substitution T C intron_variant MELA-AU 5 176670276 176670277 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 5 176670276 176670277 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 176670848 176670848 single base substitution C T downstream_gene_variant MELA-AU 5 176670848 176670848 single base substitution C T intron_variant MELA-AU 5 176671019 176671019 single base substitution C T downstream_gene_variant MELA-AU 5 176671019 176671019 single base substitution C T intron_variant MELA-AU 5 176671164 176671164 single base substitution C T downstream_gene_variant MELA-AU 5 176671164 176671164 single base substitution C T intron_variant MELA-AU 5 176671512 176671512 single base substitution T G downstream_gene_variant MELA-AU 5 176671512 176671512 single base substitution T G intron_variant MELA-AU 5 176672046 176672046 single base substitution C T intron_variant MELA-AU 5 176672327 176672327 single base substitution C T intron_variant MELA-AU 5 176672379 176672379 single base substitution C T intron_variant MELA-AU 5 176672563 176672563 single base substitution C T intron_variant MELA-AU 5 176672637 176672637 single base substitution T C intron_variant MELA-AU 5 176672976 176672976 single base substitution T A intron_variant MELA-AU 5 176674058 176674058 single base substitution C T intron_variant MELA-AU 5 176674305 176674305 single base substitution C T intron_variant MELA-AU 5 176674382 176674382 single base substitution C T intron_variant MELA-AU 5 176674554 176674554 single base substitution C T intron_variant MELA-AU 5 176675055 176675055 single base substitution C T intron_variant MELA-AU 5 176675311 176675311 single base substitution G A missense_variant E1274K 3820G>A MELA-AU 5 176675311 176675311 single base substitution G A missense_variant E1440K 4318G>A MELA-AU 5 176675311 176675311 single base substitution G A missense_variant E1543K 4627G>A MELA-AU 5 176675673 176675673 single base substitution G A intron_variant MELA-AU 5 176675998 176675998 single base substitution C T intron_variant MELA-AU 5 176676480 176676480 single base substitution A T intron_variant MELA-AU 5 176676496 176676496 single base substitution C T intron_variant MELA-AU 5 176676979 176676979 single base substitution G A intron_variant MELA-AU 5 176677351 176677351 single base substitution C T intron_variant MELA-AU 5 176677696 176677696 single base substitution C G intron_variant MELA-AU 5 176678160 176678160 single base substitution C T intron_variant MELA-AU 5 176678391 176678391 single base substitution C T intron_variant MELA-AU 5 176678484 176678484 single base substitution C T intron_variant MELA-AU 5 176679418 176679418 single base substitution T A intron_variant MELA-AU 5 176679496 176679496 single base substitution C T intron_variant MELA-AU 5 176680624 176680624 single base substitution C T intron_variant MELA-AU 5 176680639 176680639 single base substitution C T intron_variant MELA-AU 5 176680648 176680648 single base substitution C T intron_variant MELA-AU 5 176680952 176680952 single base substitution C T intron_variant MELA-AU 5 176681869 176681869 deletion of <=200bp T - intron_variant MELA-AU 5 176682352 176682352 single base substitution C T intron_variant MELA-AU 5 176682440 176682440 single base substitution G A intron_variant MELA-AU 5 176682564 176682564 single base substitution T A intron_variant MELA-AU 5 176682903 176682903 single base substitution G A intron_variant MELA-AU 5 176682938 176682938 single base substitution C T intron_variant MELA-AU 5 176682986 176682986 single base substitution C T intron_variant MELA-AU 5 176683577 176683577 single base substitution C T intron_variant MELA-AU 5 176683621 176683621 single base substitution C A intron_variant MELA-AU 5 176684084 176684084 single base substitution T A missense_variant F1364Y 4091T>A MELA-AU 5 176684084 176684084 single base substitution T A missense_variant F1530Y 4589T>A MELA-AU 5 176684084 176684084 single base substitution T A missense_variant F1633Y 4898T>A MELA-AU 5 176684098 176684098 single base substitution C T missense_variant H1369Y 4105C>T MELA-AU 5 176684098 176684098 single base substitution C T missense_variant H1535Y 4603C>T MELA-AU 5 176684098 176684098 single base substitution C T missense_variant H1638Y 4912C>T MELA-AU 5 176685347 176685347 single base substitution G A intron_variant MELA-AU 5 176685778 176685778 single base substitution C T intron_variant MELA-AU 5 176686511 176686511 single base substitution C T intron_variant MELA-AU 5 176686693 176686693 single base substitution C T intron_variant MELA-AU 5 176686864 176686864 single base substitution T G intron_variant MELA-AU 5 176687103 176687103 single base substitution A T missense_variant T1425S 4273A>T MELA-AU 5 176687103 176687103 single base substitution A T missense_variant T1591S 4771A>T MELA-AU 5 176687103 176687103 single base substitution A T missense_variant T1694S 5080A>T MELA-AU 5 176687388 176687389 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 176687390 176687390 single base substitution C T intron_variant MELA-AU 5 176687996 176687996 single base substitution T C intron_variant MELA-AU 5 176687996 176687996 single base substitution T C upstream_gene_variant MELA-AU 5 176688231 176688231 single base substitution C T intron_variant MELA-AU 5 176688231 176688231 single base substitution C T upstream_gene_variant MELA-AU 5 176689114 176689114 single base substitution C T intron_variant MELA-AU 5 176689114 176689114 single base substitution C T upstream_gene_variant MELA-AU 5 176690042 176690043 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 176690042 176690043 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 5 176690527 176690527 single base substitution C T intron_variant MELA-AU 5 176690527 176690527 single base substitution C T upstream_gene_variant MELA-AU 5 176690578 176690578 single base substitution C T intron_variant MELA-AU 5 176690578 176690578 single base substitution C T upstream_gene_variant MELA-AU 5 176690614 176690614 single base substitution A G intron_variant MELA-AU 5 176690614 176690614 single base substitution A G upstream_gene_variant MELA-AU 5 176690905 176690905 single base substitution C T intron_variant MELA-AU 5 176690905 176690905 single base substitution C T upstream_gene_variant MELA-AU 5 176691066 176691066 single base substitution C T intron_variant MELA-AU 5 176691066 176691066 single base substitution C T upstream_gene_variant MELA-AU 5 176693422 176693422 single base substitution C T 5_prime_UTR_variant MELA-AU 5 176693422 176693422 single base substitution C T intron_variant MELA-AU 5 176693422 176693422 single base substitution C T upstream_gene_variant MELA-AU 5 176693806 176693806 single base substitution C T intron_variant MELA-AU 5 176694200 176694200 single base substitution A C intron_variant MELA-AU 5 176694480 176694480 insertion of <=200bp - AT intron_variant MELA-AU 5 176695525 176695525 single base substitution G A intron_variant MELA-AU 5 176695533 176695533 single base substitution A T intron_variant MELA-AU 5 176696050 176696050 single base substitution C T intron_variant MELA-AU 5 176696453 176696453 single base substitution T C intron_variant MELA-AU 5 176696549 176696549 single base substitution C T intron_variant MELA-AU 5 176696640 176696640 single base substitution C T 5_prime_UTR_variant MELA-AU 5 176696640 176696640 single base substitution C T missense_variant P1512S 4534C>T MELA-AU 5 176696640 176696640 single base substitution C T missense_variant P1678S 5032C>T MELA-AU 5 176696640 176696640 single base substitution C T missense_variant P1781S 5341C>T MELA-AU 5 176697780 176697780 single base substitution G A downstream_gene_variant MELA-AU 5 176697780 176697780 single base substitution G A intron_variant MELA-AU 5 176700678 176700678 single base substitution C T downstream_gene_variant MELA-AU 5 176700678 176700678 single base substitution C T stop_gained Q1570* 4708C>T MELA-AU 5 176700678 176700678 single base substitution C T stop_gained Q1736* 5206C>T MELA-AU 5 176700678 176700678 single base substitution C T stop_gained Q1839* 5515C>T MELA-AU 5 176700678 176700678 single base substitution C T stop_gained Q53* 157C>T MELA-AU 5 176700678 176700678 single base substitution C T synonymous_variant ?53 MELA-AU 5 176701164 176701164 single base substitution G A downstream_gene_variant MELA-AU 5 176701164 176701164 single base substitution G A intron_variant MELA-AU 5 176701476 176701476 single base substitution C T downstream_gene_variant MELA-AU 5 176701476 176701476 single base substitution C T intron_variant MELA-AU 5 176702294 176702294 single base substitution C T downstream_gene_variant MELA-AU 5 176702294 176702294 single base substitution C T intron_variant MELA-AU 5 176703331 176703331 single base substitution T C downstream_gene_variant MELA-AU 5 176703331 176703331 single base substitution T C intron_variant MELA-AU 5 176703647 176703647 single base substitution C T downstream_gene_variant MELA-AU 5 176703647 176703647 single base substitution C T intron_variant MELA-AU 5 176703651 176703651 single base substitution C T downstream_gene_variant MELA-AU 5 176703651 176703651 single base substitution C T intron_variant MELA-AU 5 176703689 176703689 single base substitution C T downstream_gene_variant MELA-AU 5 176703689 176703689 single base substitution C T intron_variant MELA-AU 5 176704414 176704414 single base substitution G C downstream_gene_variant MELA-AU 5 176704414 176704414 single base substitution G C intron_variant MELA-AU 5 176705941 176705941 single base substitution G T intron_variant MELA-AU 5 176705970 176705970 single base substitution T C intron_variant MELA-AU 5 176706060 176706060 single base substitution G A intron_variant MELA-AU 5 176706506 176706506 single base substitution G A intron_variant MELA-AU 5 176706654 176706654 single base substitution C T intron_variant MELA-AU 5 176706961 176706961 single base substitution C T intron_variant MELA-AU 5 176707725 176707725 single base substitution G A downstream_gene_variant MELA-AU 5 176707725 176707725 single base substitution G A missense_variant G1659R 4975G>A MELA-AU 5 176707725 176707725 single base substitution G A missense_variant G1825R 5473G>A MELA-AU 5 176707725 176707725 single base substitution G A missense_variant G1928R 5782G>A MELA-AU 5 176707726 176707726 single base substitution G T downstream_gene_variant MELA-AU 5 176707726 176707726 single base substitution G T missense_variant G1659V 4976G>T MELA-AU 5 176707726 176707726 single base substitution G T missense_variant G1825V 5474G>T MELA-AU 5 176707726 176707726 single base substitution G T missense_variant G1928V 5783G>T MELA-AU 5 176708643 176708643 single base substitution G A downstream_gene_variant MELA-AU 5 176708643 176708643 single base substitution G A intron_variant MELA-AU 5 176709010 176709010 single base substitution C T downstream_gene_variant MELA-AU 5 176709010 176709010 single base substitution C T intron_variant MELA-AU 5 176709426 176709426 single base substitution C T downstream_gene_variant MELA-AU 5 176709426 176709426 single base substitution C T intron_variant MELA-AU 5 176709690 176709690 single base substitution C T downstream_gene_variant MELA-AU 5 176709690 176709690 single base substitution C T intron_variant MELA-AU 5 176709822 176709822 single base substitution T C downstream_gene_variant MELA-AU 5 176709822 176709822 single base substitution T C intron_variant MELA-AU 5 176710180 176710180 single base substitution C T downstream_gene_variant MELA-AU 5 176710180 176710180 single base substitution C T intron_variant MELA-AU 5 176710676 176710676 single base substitution G A downstream_gene_variant MELA-AU 5 176710676 176710676 single base substitution G A intron_variant MELA-AU 5 176710676 176710676 single base substitution G A upstream_gene_variant MELA-AU 5 176711092 176711092 single base substitution C T downstream_gene_variant MELA-AU 5 176711092 176711092 single base substitution C T intron_variant MELA-AU 5 176711092 176711092 single base substitution C T upstream_gene_variant MELA-AU 5 176712920 176712920 single base substitution G A intron_variant MELA-AU 5 176712920 176712920 single base substitution G A upstream_gene_variant MELA-AU 5 176713591 176713591 single base substitution C T intron_variant MELA-AU 5 176713591 176713591 single base substitution C T upstream_gene_variant MELA-AU 5 176713640 176713640 single base substitution C T intron_variant MELA-AU 5 176713640 176713640 single base substitution C T upstream_gene_variant MELA-AU 5 176713694 176713694 single base substitution C T intron_variant MELA-AU 5 176713694 176713694 single base substitution C T upstream_gene_variant MELA-AU 5 176714502 176714502 single base substitution T A intron_variant MELA-AU 5 176714502 176714502 single base substitution T A upstream_gene_variant MELA-AU 5 176716183 176716183 single base substitution G A intron_variant MELA-AU 5 176717422 176717422 single base substitution T G intron_variant MELA-AU 5 176717687 176717687 single base substitution G A intron_variant MELA-AU 5 176718314 176718314 single base substitution T C intron_variant MELA-AU 5 176718647 176718647 single base substitution C T intron_variant MELA-AU 5 176719403 176719403 single base substitution C T downstream_gene_variant MELA-AU 5 176719403 176719403 single base substitution C T intron_variant MELA-AU 5 176720077 176720077 single base substitution G A downstream_gene_variant MELA-AU 5 176720077 176720077 single base substitution G A intron_variant MELA-AU 5 176720283 176720283 single base substitution C T downstream_gene_variant MELA-AU 5 176720283 176720283 single base substitution C T intron_variant MELA-AU 5 176721287 176721287 single base substitution C T downstream_gene_variant MELA-AU 5 176721287 176721287 single base substitution C T synonymous_variant S2037S 6111C>T MELA-AU 5 176721287 176721287 single base substitution C T synonymous_variant S2203S 6609C>T MELA-AU 5 176721287 176721287 single base substitution C T synonymous_variant S2306S 6918C>T MELA-AU 5 176721351 176721351 single base substitution C A downstream_gene_variant MELA-AU 5 176721351 176721351 single base substitution C A missense_variant Q2059K 6175C>A MELA-AU 5 176721351 176721351 single base substitution C A missense_variant Q2225K 6673C>A MELA-AU 5 176721351 176721351 single base substitution C A missense_variant Q2328K 6982C>A MELA-AU 5 176721429 176721429 single base substitution C T downstream_gene_variant MELA-AU 5 176721429 176721429 single base substitution C T synonymous_variant L2085L 6253C>T MELA-AU 5 176721429 176721429 single base substitution C T synonymous_variant L2251L 6751C>T MELA-AU 5 176721429 176721429 single base substitution C T synonymous_variant L2354L 7060C>T MELA-AU 5 176721432 176721433 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 5 176721432 176721433 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant G2086K 6256GG>AA MELA-AU 5 176721432 176721433 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant G2252K 6754GG>AA MELA-AU 5 176721432 176721433 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant G2355K 7063GG>AA MELA-AU 5 176722710 176722711 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 5 176722710 176722711 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 5 176722811 176722811 single base substitution C T 3_prime_UTR_variant MELA-AU 5 176722811 176722811 single base substitution C T downstream_gene_variant MELA-AU 5 176723547 176723547 single base substitution C T 3_prime_UTR_variant MELA-AU 5 176723547 176723547 single base substitution C T downstream_gene_variant MELA-AU 5 176724053 176724053 single base substitution A T 3_prime_UTR_variant MELA-AU 5 176724053 176724053 single base substitution A T downstream_gene_variant MELA-AU 5 176724324 176724324 single base substitution G A 3_prime_UTR_variant MELA-AU 5 176724324 176724324 single base substitution G A downstream_gene_variant MELA-AU 5 176724480 176724480 single base substitution C T 3_prime_UTR_variant MELA-AU 5 176724480 176724480 single base substitution C T downstream_gene_variant MELA-AU 5 176724743 176724743 single base substitution G A 3_prime_UTR_variant MELA-AU 5 176724743 176724743 single base substitution G A downstream_gene_variant MELA-AU 5 176724951 176724951 single base substitution A G 3_prime_UTR_variant MELA-AU 5 176724951 176724951 single base substitution A G downstream_gene_variant MELA-AU 5 176724961 176724961 single base substitution C T 3_prime_UTR_variant MELA-AU 5 176724961 176724961 single base substitution C T downstream_gene_variant MELA-AU 5 176725164 176725164 single base substitution G A 3_prime_UTR_variant MELA-AU 5 176725164 176725164 single base substitution G A downstream_gene_variant MELA-AU 5 176725882 176725882 single base substitution T A 3_prime_UTR_variant MELA-AU 5 176725882 176725882 single base substitution T A downstream_gene_variant MELA-AU 5 176726410 176726410 single base substitution G A 3_prime_UTR_variant MELA-AU 5 176726410 176726410 single base substitution G A downstream_gene_variant MELA-AU 5 176726752 176726752 single base substitution C T 3_prime_UTR_variant MELA-AU 5 176726752 176726752 single base substitution C T downstream_gene_variant MELA-AU 5 176727307 176727307 single base substitution C T downstream_gene_variant MELA-AU 5 176727445 176727445 single base substitution G A downstream_gene_variant MELA-AU 5 176728200 176728200 single base substitution C G downstream_gene_variant MELA-AU 5 176728683 176728683 single base substitution G A downstream_gene_variant MELA-AU 5 176729614 176729614 single base substitution T C downstream_gene_variant MELA-AU 5 176730694 176730694 single base substitution C T downstream_gene_variant MELA-AU 5 176730712 176730713 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant ORCA-IN 5 176563331 176563331 deletion of <=200bp A - downstream_gene_variant ORCA-IN 5 176563331 176563331 deletion of <=200bp A - exon_variant ORCA-IN 5 176563331 176563331 deletion of <=200bp A - intron_variant ORCA-IN 5 176563608 176563608 deletion of <=200bp T - downstream_gene_variant ORCA-IN 5 176563608 176563608 deletion of <=200bp T - intron_variant ORCA-IN 5 176566256 176566256 deletion of <=200bp A - downstream_gene_variant ORCA-IN 5 176566256 176566256 deletion of <=200bp A - intron_variant ORCA-IN 5 176570785 176570786 deletion of <=200bp TT - intron_variant ORCA-IN 5 176572283 176572283 deletion of <=200bp T - intron_variant ORCA-IN 5 176577251 176577251 single base substitution C T intron_variant ORCA-IN 5 176581997 176581997 single base substitution A T intron_variant ORCA-IN 5 176585302 176585302 single base substitution C T intron_variant ORCA-IN 5 176586032 176586033 deletion of <=200bp AT - intron_variant ORCA-IN 5 176586594 176586594 insertion of <=200bp - T intron_variant ORCA-IN 5 176588375 176588375 single base substitution C T intron_variant ORCA-IN 5 176590143 176590143 insertion of <=200bp - T intron_variant ORCA-IN 5 176591948 176591948 deletion of <=200bp A - intron_variant ORCA-IN 5 176593546 176593546 deletion of <=200bp A - intron_variant ORCA-IN 5 176593745 176593745 deletion of <=200bp T - intron_variant ORCA-IN 5 176593745 176593746 deletion of <=200bp TT - intron_variant ORCA-IN 5 176595452 176595452 deletion of <=200bp T - intron_variant ORCA-IN 5 176598308 176598308 deletion of <=200bp A - intron_variant ORCA-IN 5 176602671 176602671 single base substitution C G intron_variant ORCA-IN 5 176603427 176603427 deletion of <=200bp T - intron_variant ORCA-IN 5 176608044 176608044 deletion of <=200bp T - intron_variant ORCA-IN 5 176611751 176611751 single base substitution G C intron_variant ORCA-IN 5 176617675 176617675 deletion of <=200bp T - intron_variant ORCA-IN 5 176619202 176619202 insertion of <=200bp - T intron_variant ORCA-IN 5 176619203 176619203 deletion of <=200bp T - intron_variant ORCA-IN 5 176624270 176624270 deletion of <=200bp A - intron_variant ORCA-IN 5 176627901 176627901 deletion of <=200bp T - intron_variant ORCA-IN 5 176628563 176628563 insertion of <=200bp - T intron_variant ORCA-IN 5 176636550 176636550 insertion of <=200bp - A intron_variant ORCA-IN 5 176636550 176636550 insertion of <=200bp - A upstream_gene_variant ORCA-IN 5 176636949 176636949 single base substitution C T downstream_gene_variant ORCA-IN 5 176636949 176636949 single base substitution C T stop_gained Q248* 742C>T ORCA-IN 5 176636949 176636949 single base substitution C T stop_gained Q414* 1240C>T ORCA-IN 5 176636949 176636949 single base substitution C T stop_gained Q517* 1549C>T ORCA-IN 5 176636949 176636949 single base substitution C T upstream_gene_variant ORCA-IN 5 176638273 176638273 single base substitution C T downstream_gene_variant ORCA-IN 5 176638273 176638273 single base substitution C T missense_variant S689L 2066C>T ORCA-IN 5 176638273 176638273 single base substitution C T missense_variant S855L 2564C>T ORCA-IN 5 176638273 176638273 single base substitution C T missense_variant S958L 2873C>T ORCA-IN 5 176638273 176638273 single base substitution C T upstream_gene_variant ORCA-IN 5 176643671 176643671 insertion of <=200bp - T intron_variant ORCA-IN 5 176645501 176645501 insertion of <=200bp - T intron_variant ORCA-IN 5 176650083 176650083 deletion of <=200bp T - intron_variant ORCA-IN 5 176654984 176654984 insertion of <=200bp - T intron_variant ORCA-IN 5 176655267 176655267 deletion of <=200bp T - intron_variant ORCA-IN 5 176657828 176657828 deletion of <=200bp A - intron_variant ORCA-IN 5 176668344 176668344 deletion of <=200bp A - downstream_gene_variant ORCA-IN 5 176668344 176668344 deletion of <=200bp A - intron_variant ORCA-IN 5 176672976 176672976 single base substitution T A intron_variant ORCA-IN 5 176672978 176672978 single base substitution T A intron_variant ORCA-IN 5 176674566 176674566 insertion of <=200bp - T intron_variant ORCA-IN 5 176674567 176674567 deletion of <=200bp A - intron_variant ORCA-IN 5 176678191 176678191 deletion of <=200bp A - intron_variant ORCA-IN 5 176679796 176679796 deletion of <=200bp C - intron_variant ORCA-IN 5 176696730 176696730 single base substitution C T downstream_gene_variant ORCA-IN 5 176696730 176696730 single base substitution C T stop_gained R1542* 4624C>T ORCA-IN 5 176696730 176696730 single base substitution C T stop_gained R1708* 5122C>T ORCA-IN 5 176696730 176696730 single base substitution C T stop_gained R1811* 5431C>T ORCA-IN 5 176696730 176696730 single base substitution C T stop_gained R25* 73C>T ORCA-IN 5 176700314 176700314 insertion of <=200bp - T downstream_gene_variant ORCA-IN 5 176700314 176700314 insertion of <=200bp - T intron_variant ORCA-IN 5 176703325 176703325 deletion of <=200bp T - downstream_gene_variant ORCA-IN 5 176703325 176703325 deletion of <=200bp T - intron_variant ORCA-IN 5 176703338 176703338 single base substitution C T downstream_gene_variant ORCA-IN 5 176703338 176703338 single base substitution C T intron_variant ORCA-IN 5 176706570 176706570 single base substitution G A intron_variant ORCA-IN 5 176707166 176707166 single base substitution G A intron_variant ORCA-IN 5 176707675 176707675 single base substitution G T downstream_gene_variant ORCA-IN 5 176707675 176707675 single base substitution G T missense_variant C1642F 4925G>T ORCA-IN 5 176707675 176707675 single base substitution G T missense_variant C1808F 5423G>T ORCA-IN 5 176707675 176707675 single base substitution G T missense_variant C1911F 5732G>T ORCA-IN 5 176711457 176711457 deletion of <=200bp T - downstream_gene_variant ORCA-IN 5 176711457 176711457 deletion of <=200bp T - intron_variant ORCA-IN 5 176711457 176711457 deletion of <=200bp T - upstream_gene_variant ORCA-IN 5 176711868 176711868 single base substitution G A downstream_gene_variant ORCA-IN 5 176711868 176711868 single base substitution G A intron_variant ORCA-IN 5 176711868 176711868 single base substitution G A upstream_gene_variant ORCA-IN 5 176712949 176712949 single base substitution T G intron_variant ORCA-IN 5 176712949 176712949 single base substitution T G upstream_gene_variant ORCA-IN 5 176717410 176717410 deletion of <=200bp T - intron_variant ORCA-IN 5 176727976 176727976 single base substitution G C downstream_gene_variant ORCA-IN 5 176729958 176729958 single base substitution C T downstream_gene_variant OV-AU 5 176556415 176556415 single base substitution C G upstream_gene_variant OV-AU 5 176562049 176562049 single base substitution C G intron_variant OV-AU 5 176562049 176562049 single base substitution C G upstream_gene_variant OV-AU 5 176565758 176565758 single base substitution A G downstream_gene_variant OV-AU 5 176565758 176565758 single base substitution A G intron_variant OV-AU 5 176566470 176566470 single base substitution A T downstream_gene_variant OV-AU 5 176566470 176566470 single base substitution A T intron_variant OV-AU 5 176566603 176566603 single base substitution A C downstream_gene_variant OV-AU 5 176566603 176566603 single base substitution A C intron_variant OV-AU 5 176572217 176572217 single base substitution C T intron_variant OV-AU 5 176572697 176572697 single base substitution G A intron_variant OV-AU 5 176573789 176573789 single base substitution G A intron_variant OV-AU 5 176574169 176574169 single base substitution G A intron_variant OV-AU 5 176593106 176593106 single base substitution G C intron_variant OV-AU 5 176594267 176594267 single base substitution G A intron_variant OV-AU 5 176597303 176597303 single base substitution T C intron_variant OV-AU 5 176598339 176598339 single base substitution G A intron_variant OV-AU 5 176611987 176611987 single base substitution T G intron_variant OV-AU 5 176617340 176617340 single base substitution G C intron_variant OV-AU 5 176637996 176637996 single base substitution G C downstream_gene_variant OV-AU 5 176637996 176637996 single base substitution G C missense_variant E597Q 1789G>C OV-AU 5 176637996 176637996 single base substitution G C missense_variant E763Q 2287G>C OV-AU 5 176637996 176637996 single base substitution G C missense_variant E866Q 2596G>C OV-AU 5 176637996 176637996 single base substitution G C upstream_gene_variant OV-AU 5 176641212 176641212 single base substitution A T downstream_gene_variant OV-AU 5 176641212 176641212 single base substitution A T intron_variant OV-AU 5 176644908 176644908 single base substitution A G intron_variant OV-AU 5 176646918 176646918 single base substitution A T intron_variant OV-AU 5 176649002 176649002 single base substitution G A intron_variant OV-AU 5 176650511 176650511 single base substitution T G intron_variant OV-AU 5 176655960 176655960 single base substitution A G intron_variant OV-AU 5 176667971 176667971 single base substitution G C downstream_gene_variant OV-AU 5 176667971 176667971 single base substitution G C intron_variant OV-AU 5 176673209 176673209 single base substitution G A intron_variant OV-AU 5 176676465 176676465 single base substitution T A intron_variant OV-AU 5 176682029 176682029 single base substitution A T intron_variant OV-AU 5 176683188 176683188 single base substitution G A intron_variant OV-AU 5 176690270 176690270 single base substitution A G intron_variant OV-AU 5 176690270 176690270 single base substitution A G upstream_gene_variant OV-AU 5 176692768 176692768 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant OV-AU 5 176692768 176692768 single base substitution C G intron_variant OV-AU 5 176692768 176692768 single base substitution C G upstream_gene_variant OV-AU 5 176697994 176697994 single base substitution G A downstream_gene_variant OV-AU 5 176697994 176697994 single base substitution G A intron_variant OV-AU 5 176699668 176699668 single base substitution A C downstream_gene_variant OV-AU 5 176699668 176699668 single base substitution A C intron_variant OV-AU 5 176706288 176706288 single base substitution C T intron_variant OV-AU 5 176711676 176711676 single base substitution G A downstream_gene_variant OV-AU 5 176711676 176711676 single base substitution G A intron_variant OV-AU 5 176711676 176711676 single base substitution G A upstream_gene_variant OV-AU 5 176712869 176712869 single base substitution G C intron_variant OV-AU 5 176712869 176712869 single base substitution G C upstream_gene_variant OV-AU 5 176728342 176728342 single base substitution A G downstream_gene_variant OV-US 5 176687050 176687050 single base substitution C A missense_variant A1407D 4220C>A OV-US 5 176687050 176687050 single base substitution C A missense_variant A1573D 4718C>A OV-US 5 176687050 176687050 single base substitution C A missense_variant A1676D 5027C>A PACA-AU 5 176564789 176564789 single base substitution A T downstream_gene_variant PACA-AU 5 176564789 176564789 single base substitution A T intron_variant PACA-AU 5 176565085 176565085 single base substitution A C downstream_gene_variant PACA-AU 5 176565085 176565085 single base substitution A C intron_variant PACA-AU 5 176565092 176565095 deletion of <=200bp AAAA - downstream_gene_variant PACA-AU 5 176565092 176565095 deletion of <=200bp AAAA - intron_variant PACA-AU 5 176565411 176565411 single base substitution C T downstream_gene_variant PACA-AU 5 176565411 176565411 single base substitution C T intron_variant PACA-AU 5 176568470 176568470 single base substitution T C downstream_gene_variant PACA-AU 5 176568470 176568470 single base substitution T C intron_variant PACA-AU 5 176584135 176584135 single base substitution G C intron_variant PACA-AU 5 176586899 176586899 single base substitution T A intron_variant PACA-AU 5 176586901 176586901 single base substitution T A intron_variant PACA-AU 5 176589892 176589892 insertion of <=200bp - ATGA intron_variant PACA-AU 5 176592201 176592201 single base substitution C G intron_variant PACA-AU 5 176597031 176597031 single base substitution C T intron_variant PACA-AU 5 176597225 176597225 single base substitution C T intron_variant PACA-AU 5 176598490 176598490 single base substitution G T intron_variant PACA-AU 5 176602353 176602353 single base substitution G C intron_variant PACA-AU 5 176608480 176608480 single base substitution G T intron_variant PACA-AU 5 176613037 176613037 single base substitution A T intron_variant PACA-AU 5 176618574 176618574 single base substitution C T intron_variant PACA-AU 5 176619385 176619385 insertion of <=200bp - T intron_variant PACA-AU 5 176626537 176626537 single base substitution C T intron_variant PACA-AU 5 176627580 176627580 single base substitution T C intron_variant PACA-AU 5 176632025 176632025 single base substitution G T downstream_gene_variant PACA-AU 5 176632025 176632025 single base substitution G T intron_variant PACA-AU 5 176632283 176632283 single base substitution C T downstream_gene_variant PACA-AU 5 176632283 176632283 single base substitution C T intron_variant PACA-AU 5 176634223 176634237 deletion of <=200bp ACAGGCGTGAGCCAC - downstream_gene_variant PACA-AU 5 176634223 176634237 deletion of <=200bp ACAGGCGTGAGCCAC - intron_variant PACA-AU 5 176634223 176634237 deletion of <=200bp ACAGGCGTGAGCCAC - upstream_gene_variant PACA-AU 5 176648473 176648473 single base substitution T C intron_variant PACA-AU 5 176649280 176649280 single base substitution C T intron_variant PACA-AU 5 176651603 176651603 deletion of <=200bp T - intron_variant PACA-AU 5 176658610 176658610 single base substitution C T intron_variant PACA-AU 5 176660272 176660272 single base substitution G A intron_variant PACA-AU 5 176665804 176665804 single base substitution A G intron_variant PACA-AU 5 176667183 176667183 single base substitution A G downstream_gene_variant PACA-AU 5 176667183 176667183 single base substitution A G intron_variant PACA-AU 5 176669282 176669282 single base substitution A T downstream_gene_variant PACA-AU 5 176669282 176669282 single base substitution A T intron_variant PACA-AU 5 176674238 176674238 single base substitution C T intron_variant PACA-AU 5 176676457 176676457 single base substitution A T intron_variant PACA-AU 5 176681479 176681479 single base substitution C A intron_variant PACA-AU 5 176686997 176686997 single base substitution G A synonymous_variant L1389L 4167G>A PACA-AU 5 176686997 176686997 single base substitution G A synonymous_variant L1555L 4665G>A PACA-AU 5 176686997 176686997 single base substitution G A synonymous_variant L1658L 4974G>A PACA-AU 5 176690821 176690821 single base substitution A G intron_variant PACA-AU 5 176690821 176690821 single base substitution A G upstream_gene_variant PACA-AU 5 176692219 176692219 single base substitution A C intron_variant PACA-AU 5 176692219 176692219 single base substitution A C upstream_gene_variant PACA-AU 5 176692556 176692556 single base substitution C T 5_prime_UTR_variant PACA-AU 5 176692556 176692556 single base substitution C T intron_variant PACA-AU 5 176692556 176692556 single base substitution C T upstream_gene_variant PACA-AU 5 176702784 176702784 single base substitution T G downstream_gene_variant PACA-AU 5 176702784 176702784 single base substitution T G intron_variant PACA-AU 5 176710608 176710608 deletion of <=200bp A - downstream_gene_variant PACA-AU 5 176710608 176710608 deletion of <=200bp A - intron_variant PACA-AU 5 176710608 176710608 deletion of <=200bp A - upstream_gene_variant PACA-AU 5 176711953 176711953 single base substitution A T downstream_gene_variant PACA-AU 5 176711953 176711953 single base substitution A T intron_variant PACA-AU 5 176711953 176711953 single base substitution A T upstream_gene_variant PACA-AU 5 176715500 176715500 single base substitution T A intron_variant PACA-AU 5 176715500 176715500 single base substitution T A upstream_gene_variant PACA-AU 5 176718344 176718344 single base substitution G C intron_variant PACA-AU 5 176728283 176728283 single base substitution T G downstream_gene_variant PACA-AU 5 176728798 176728798 single base substitution G A downstream_gene_variant PACA-CA 5 176556498 176556498 single base substitution G T upstream_gene_variant PACA-CA 5 176560117 176560117 single base substitution G A 5_prime_UTR_variant PACA-CA 5 176560117 176560117 single base substitution G A exon_variant PACA-CA 5 176560117 176560117 single base substitution G A upstream_gene_variant PACA-CA 5 176560394 176560394 single base substitution G A intron_variant PACA-CA 5 176560394 176560394 single base substitution G A upstream_gene_variant PACA-CA 5 176563279 176563279 single base substitution T A downstream_gene_variant PACA-CA 5 176563279 176563279 single base substitution T A exon_variant PACA-CA 5 176563279 176563279 single base substitution T A intron_variant PACA-CA 5 176565500 176565500 single base substitution G A downstream_gene_variant PACA-CA 5 176565500 176565500 single base substitution G A intron_variant PACA-CA 5 176570743 176570743 single base substitution T A intron_variant PACA-CA 5 176579083 176579083 single base substitution G A intron_variant PACA-CA 5 176580894 176580894 single base substitution A C intron_variant PACA-CA 5 176581588 176581589 deletion of <=200bp TT - intron_variant PACA-CA 5 176582014 176582014 single base substitution C G intron_variant PACA-CA 5 176585303 176585303 deletion of <=200bp T - intron_variant PACA-CA 5 176585330 176585330 deletion of <=200bp T - intron_variant PACA-CA 5 176591470 176591470 single base substitution G T intron_variant PACA-CA 5 176596851 176596851 single base substitution A C intron_variant PACA-CA 5 176605827 176605827 deletion of <=200bp A - intron_variant PACA-CA 5 176609183 176609183 single base substitution T C intron_variant PACA-CA 5 176610722 176610722 deletion of <=200bp T - intron_variant PACA-CA 5 176613364 176613364 single base substitution T C intron_variant PACA-CA 5 176615845 176615845 single base substitution T A intron_variant PACA-CA 5 176622133 176622133 single base substitution C T intron_variant PACA-CA 5 176624283 176624283 single base substitution T A intron_variant PACA-CA 5 176626005 176626005 single base substitution T C intron_variant PACA-CA 5 176628592 176628592 single base substitution C T intron_variant PACA-CA 5 176632651 176632651 single base substitution A G downstream_gene_variant PACA-CA 5 176632651 176632651 single base substitution A G intron_variant PACA-CA 5 176632775 176632775 deletion of <=200bp T - downstream_gene_variant PACA-CA 5 176632775 176632775 deletion of <=200bp T - intron_variant PACA-CA 5 176633791 176633791 single base substitution C G downstream_gene_variant PACA-CA 5 176633791 176633791 single base substitution C G intron_variant PACA-CA 5 176633950 176633950 single base substitution C T downstream_gene_variant PACA-CA 5 176633950 176633950 single base substitution C T intron_variant PACA-CA 5 176634924 176634924 single base substitution C T downstream_gene_variant PACA-CA 5 176634924 176634924 single base substitution C T intron_variant PACA-CA 5 176634924 176634924 single base substitution C T upstream_gene_variant PACA-CA 5 176637709 176637709 single base substitution G A downstream_gene_variant PACA-CA 5 176637709 176637709 single base substitution G A missense_variant G501D 1502G>A PACA-CA 5 176637709 176637709 single base substitution G A missense_variant G667D 2000G>A PACA-CA 5 176637709 176637709 single base substitution G A missense_variant G770D 2309G>A PACA-CA 5 176637709 176637709 single base substitution G A upstream_gene_variant PACA-CA 5 176641092 176641092 single base substitution G A downstream_gene_variant PACA-CA 5 176641092 176641092 single base substitution G A intron_variant PACA-CA 5 176649919 176649919 single base substitution A C intron_variant PACA-CA 5 176651458 176651458 single base substitution A G intron_variant PACA-CA 5 176652038 176652038 deletion of <=200bp T - intron_variant PACA-CA 5 176654696 176654696 single base substitution C T intron_variant PACA-CA 5 176658245 176658245 single base substitution C T intron_variant PACA-CA 5 176667402 176667402 single base substitution G A downstream_gene_variant PACA-CA 5 176667402 176667402 single base substitution G A intron_variant PACA-CA 5 176679522 176679522 single base substitution G A intron_variant PACA-CA 5 176690756 176690756 single base substitution A G intron_variant PACA-CA 5 176690756 176690756 single base substitution A G upstream_gene_variant PACA-CA 5 176690943 176690976 deletion of <=200bp ATTGGATCATGGTAGTATTAATAAATGTGATTTT - intron_variant PACA-CA 5 176690943 176690976 deletion of <=200bp ATTGGATCATGGTAGTATTAATAAATGTGATTTT - upstream_gene_variant PACA-CA 5 176691711 176691711 single base substitution A C intron_variant PACA-CA 5 176691711 176691711 single base substitution A C upstream_gene_variant PACA-CA 5 176691922 176691922 single base substitution G A intron_variant PACA-CA 5 176691922 176691922 single base substitution G A upstream_gene_variant PACA-CA 5 176693421 176693421 single base substitution C T 5_prime_UTR_variant PACA-CA 5 176693421 176693421 single base substitution C T intron_variant PACA-CA 5 176693421 176693421 single base substitution C T upstream_gene_variant PACA-CA 5 176694545 176694545 insertion of <=200bp - T intron_variant PACA-CA 5 176695440 176695440 single base substitution C T intron_variant PACA-CA 5 176698765 176698765 single base substitution A T downstream_gene_variant PACA-CA 5 176698765 176698765 single base substitution A T intron_variant PACA-CA 5 176700669 176700669 single base substitution A C downstream_gene_variant PACA-CA 5 176700669 176700669 single base substitution A C intron_variant PACA-CA 5 176700669 176700669 single base substitution A C splice_region_variant PACA-CA 5 176706684 176706684 single base substitution C T intron_variant PACA-CA 5 176710254 176710254 single base substitution C T downstream_gene_variant PACA-CA 5 176710254 176710254 single base substitution C T intron_variant PACA-CA 5 176710419 176710419 single base substitution T C downstream_gene_variant PACA-CA 5 176710419 176710419 single base substitution T C intron_variant PACA-CA 5 176714800 176714800 single base substitution C T intron_variant PACA-CA 5 176714800 176714800 single base substitution C T upstream_gene_variant PACA-CA 5 176715735 176715736 deletion of <=200bp TT - exon_variant PACA-CA 5 176715735 176715736 deletion of <=200bp TT - intron_variant PACA-CA 5 176716442 176716442 single base substitution G T intron_variant PACA-CA 5 176722021 176722021 single base substitution C A downstream_gene_variant PACA-CA 5 176722021 176722021 single base substitution C A missense_variant P2282Q 6845C>A PACA-CA 5 176722021 176722021 single base substitution C A missense_variant P2448Q 7343C>A PACA-CA 5 176722021 176722021 single base substitution C A missense_variant P2551Q 7652C>A PACA-CA 5 176723108 176723108 single base substitution C T 3_prime_UTR_variant PACA-CA 5 176723108 176723108 single base substitution C T downstream_gene_variant PACA-CA 5 176723133 176723133 single base substitution C T 3_prime_UTR_variant PACA-CA 5 176723133 176723133 single base substitution C T downstream_gene_variant PACA-CA 5 176723689 176723689 single base substitution G A 3_prime_UTR_variant PACA-CA 5 176723689 176723689 single base substitution G A downstream_gene_variant PACA-CA 5 176724356 176724356 single base substitution G C 3_prime_UTR_variant PACA-CA 5 176724356 176724356 single base substitution G C downstream_gene_variant PACA-CA 5 176725743 176725743 single base substitution G T 3_prime_UTR_variant PACA-CA 5 176725743 176725743 single base substitution G T downstream_gene_variant PACA-CA 5 176729908 176729918 deletion of <=200bp TATGAGAAATG - downstream_gene_variant PACA-CA 5 176731019 176731019 single base substitution C G downstream_gene_variant PACA-CA 5 176731479 176731487 deletion of <=200bp ACTCTGGTT - downstream_gene_variant PAEN-AU 5 176579324 176579324 single base substitution A G intron_variant PAEN-AU 5 176606436 176606436 single base substitution G A intron_variant PAEN-AU 5 176643835 176643835 single base substitution G A intron_variant PAEN-AU 5 176676769 176676769 single base substitution T G intron_variant PAEN-AU 5 176695488 176695488 deletion of <=200bp A - intron_variant PAEN-AU 5 176723477 176723477 single base substitution G C 3_prime_UTR_variant PAEN-AU 5 176723477 176723477 single base substitution G C downstream_gene_variant PAEN-AU 5 176730178 176730178 single base substitution G A downstream_gene_variant PAEN-IT 5 176574132 176574132 single base substitution C T intron_variant PAEN-IT 5 176671603 176671603 single base substitution C A downstream_gene_variant PAEN-IT 5 176671603 176671603 single base substitution C A intron_variant PAEN-IT 5 176685493 176685493 single base substitution T G intron_variant PAEN-IT 5 176691456 176691456 single base substitution A G intron_variant PAEN-IT 5 176691456 176691456 single base substitution A G upstream_gene_variant PAEN-IT 5 176720215 176720215 single base substitution C G downstream_gene_variant PAEN-IT 5 176720215 176720215 single base substitution C G intron_variant PBCA-DE 5 176566311 176566311 deletion of <=200bp A - downstream_gene_variant PBCA-DE 5 176566311 176566311 deletion of <=200bp A - intron_variant PBCA-DE 5 176574726 176574726 single base substitution G A intron_variant PBCA-DE 5 176583972 176583972 insertion of <=200bp - TAAA intron_variant PBCA-DE 5 176585924 176585925 deletion of <=200bp TG - intron_variant PBCA-DE 5 176588475 176588475 single base substitution A G intron_variant PBCA-DE 5 176591967 176591967 single base substitution T A intron_variant PBCA-DE 5 176602740 176602740 single base substitution A T intron_variant PBCA-DE 5 176606226 176606226 insertion of <=200bp - T intron_variant PBCA-DE 5 176608504 176608504 single base substitution G A intron_variant PBCA-DE 5 176608936 176608936 insertion of <=200bp - CT intron_variant PBCA-DE 5 176610888 176610888 deletion of <=200bp A - intron_variant PBCA-DE 5 176613376 176613376 single base substitution G C intron_variant PBCA-DE 5 176622455 176622456 deletion of <=200bp TC - intron_variant PBCA-DE 5 176629359 176629359 single base substitution T A intron_variant PBCA-DE 5 176630723 176630723 insertion of <=200bp - T intron_variant PBCA-DE 5 176633339 176633339 single base substitution C A downstream_gene_variant PBCA-DE 5 176633339 176633339 single base substitution C A intron_variant PBCA-DE 5 176648099 176648099 deletion of <=200bp C - intron_variant PBCA-DE 5 176651775 176651775 single base substitution G T intron_variant PBCA-DE 5 176665713 176665713 single base substitution A G intron_variant PBCA-DE 5 176668327 176668327 single base substitution G A downstream_gene_variant PBCA-DE 5 176668327 176668327 single base substitution G A intron_variant PBCA-DE 5 176672731 176672731 deletion of <=200bp G - intron_variant PBCA-DE 5 176679815 176679815 single base substitution C T intron_variant PBCA-DE 5 176687465 176687465 single base substitution A G intron_variant PBCA-DE 5 176691030 176691033 deletion of <=200bp TTTT - intron_variant PBCA-DE 5 176691030 176691033 deletion of <=200bp TTTT - upstream_gene_variant PBCA-DE 5 176692209 176692209 single base substitution G A intron_variant PBCA-DE 5 176692209 176692209 single base substitution G A upstream_gene_variant PBCA-DE 5 176701699 176701700 deletion of <=200bp TG - downstream_gene_variant PBCA-DE 5 176701699 176701700 deletion of <=200bp TG - intron_variant PBCA-DE 5 176709943 176709943 single base substitution A T downstream_gene_variant PBCA-DE 5 176709943 176709943 single base substitution A T intron_variant PBCA-DE 5 176709962 176709962 single base substitution A T downstream_gene_variant PBCA-DE 5 176709962 176709962 single base substitution A T intron_variant PBCA-DE 5 176713584 176713584 single base substitution C T intron_variant PBCA-DE 5 176713584 176713584 single base substitution C T upstream_gene_variant PBCA-DE 5 176715832 176715832 insertion of <=200bp - TTCC exon_variant PBCA-DE 5 176715832 176715832 insertion of <=200bp - TTCC frameshift_variant T1786IP? PBCA-DE 5 176715832 176715832 insertion of <=200bp - TTCC frameshift_variant T1952IP? PBCA-DE 5 176715832 176715832 insertion of <=200bp - TTCC frameshift_variant T2055IP? PBCA-DE 5 176719015 176719015 insertion of <=200bp - GAGAA exon_variant PBCA-DE 5 176719015 176719015 insertion of <=200bp - GAGAA frameshift_variant R1838EN? PBCA-DE 5 176719015 176719015 insertion of <=200bp - GAGAA frameshift_variant R2004EN? PBCA-DE 5 176719015 176719015 insertion of <=200bp - GAGAA frameshift_variant R2107EN? PBCA-DE 5 176719048 176719048 single base substitution G A exon_variant PBCA-DE 5 176719048 176719048 single base substitution G A missense_variant E1849K 5545G>A PBCA-DE 5 176719048 176719048 single base substitution G A missense_variant E2015K 6043G>A PBCA-DE 5 176719048 176719048 single base substitution G A missense_variant E2118K 6352G>A PBCA-DE 5 176719113 176719113 insertion of <=200bp - AGGG exon_variant PBCA-DE 5 176719113 176719113 insertion of <=200bp - AGGG frameshift_variant P1870PG? PBCA-DE 5 176719113 176719113 insertion of <=200bp - AGGG frameshift_variant P2036PG? PBCA-DE 5 176719113 176719113 insertion of <=200bp - AGGG frameshift_variant P2139PG? PBCA-DE 5 176719114 176719114 insertion of <=200bp - GGG exon_variant PBCA-DE 5 176719114 176719114 insertion of <=200bp - GGG inframe_insertion K1871GK PBCA-DE 5 176719114 176719114 insertion of <=200bp - GGG inframe_insertion K2037GK PBCA-DE 5 176719114 176719114 insertion of <=200bp - GGG inframe_insertion K2140GK PBCA-DE 5 176719115 176719115 insertion of <=200bp - G exon_variant PBCA-DE 5 176719115 176719115 insertion of <=200bp - G frameshift_variant K1871R? PBCA-DE 5 176719115 176719115 insertion of <=200bp - G frameshift_variant K2037R? PBCA-DE 5 176719115 176719115 insertion of <=200bp - G frameshift_variant K2140R? PBCA-DE 5 176724679 176724679 single base substitution G C 3_prime_UTR_variant PBCA-DE 5 176724679 176724679 single base substitution G C downstream_gene_variant PRAD-CA 5 176598285 176598285 single base substitution C T intron_variant PRAD-CA 5 176603198 176603198 single base substitution T G intron_variant PRAD-CA 5 176613938 176613938 single base substitution A G intron_variant PRAD-CA 5 176618629 176618629 single base substitution C G intron_variant PRAD-CA 5 176641515 176641515 single base substitution A C downstream_gene_variant PRAD-CA 5 176641515 176641515 single base substitution A C intron_variant PRAD-CA 5 176654571 176654571 single base substitution C T intron_variant PRAD-CA 5 176680357 176680357 single base substitution T C intron_variant PRAD-CA 5 176697688 176697688 single base substitution A G downstream_gene_variant PRAD-CA 5 176697688 176697688 single base substitution A G intron_variant PRAD-CA 5 176708353 176708353 single base substitution A T downstream_gene_variant PRAD-CA 5 176708353 176708353 single base substitution A T intron_variant PRAD-CA 5 176712302 176712302 single base substitution C T downstream_gene_variant PRAD-CA 5 176712302 176712302 single base substitution C T intron_variant PRAD-CA 5 176712302 176712302 single base substitution C T upstream_gene_variant PRAD-CA 5 176731360 176731360 single base substitution T G downstream_gene_variant PRAD-UK 5 176563789 176563789 deletion of <=200bp T - downstream_gene_variant PRAD-UK 5 176563789 176563789 deletion of <=200bp T - intron_variant PRAD-UK 5 176574601 176574601 single base substitution T G intron_variant PRAD-UK 5 176581917 176581917 single base substitution G A intron_variant PRAD-UK 5 176595316 176595316 single base substitution T C intron_variant PRAD-UK 5 176606367 176606367 single base substitution C G intron_variant PRAD-UK 5 176608561 176608561 single base substitution G T intron_variant PRAD-UK 5 176615846 176615846 single base substitution A T intron_variant PRAD-UK 5 176616723 176616726 deletion of <=200bp ATTT - intron_variant PRAD-UK 5 176647911 176647911 single base substitution G A intron_variant PRAD-UK 5 176667766 176667766 single base substitution G A downstream_gene_variant PRAD-UK 5 176667766 176667766 single base substitution G A intron_variant PRAD-UK 5 176683741 176683741 single base substitution T C intron_variant PRAD-UK 5 176690512 176690516 multiple base substitution (>=2bp and <=200bp) AAAGC AGTG intron_variant PRAD-UK 5 176690512 176690516 multiple base substitution (>=2bp and <=200bp) AAAGC AGTG upstream_gene_variant PRAD-UK 5 176690513 176690513 single base substitution A G intron_variant PRAD-UK 5 176690513 176690513 single base substitution A G upstream_gene_variant PRAD-UK 5 176690514 176690514 single base substitution A T intron_variant PRAD-UK 5 176690514 176690514 single base substitution A T upstream_gene_variant PRAD-UK 5 176693794 176693794 single base substitution C T intron_variant PRAD-UK 5 176708385 176708385 single base substitution G T downstream_gene_variant PRAD-UK 5 176708385 176708385 single base substitution G T intron_variant PRAD-UK 5 176709396 176709396 single base substitution A T downstream_gene_variant PRAD-UK 5 176709396 176709396 single base substitution A T intron_variant PRAD-UK 5 176709541 176709541 single base substitution G C downstream_gene_variant PRAD-UK 5 176709541 176709541 single base substitution G C missense_variant E1721Q 5161G>C PRAD-UK 5 176709541 176709541 single base substitution G C missense_variant E1887Q 5659G>C PRAD-UK 5 176709541 176709541 single base substitution G C missense_variant E1990Q 5968G>C PRAD-UK 5 176723297 176723297 single base substitution G A 3_prime_UTR_variant PRAD-UK 5 176723297 176723297 single base substitution G A downstream_gene_variant PRAD-UK 5 176723558 176723558 single base substitution G T 3_prime_UTR_variant PRAD-UK 5 176723558 176723558 single base substitution G T downstream_gene_variant PRAD-US 5 176636871 176636871 single base substitution G A downstream_gene_variant PRAD-US 5 176636871 176636871 single base substitution G A missense_variant E222K 664G>A PRAD-US 5 176636871 176636871 single base substitution G A missense_variant E388K 1162G>A PRAD-US 5 176636871 176636871 single base substitution G A missense_variant E491K 1471G>A PRAD-US 5 176636871 176636871 single base substitution G A upstream_gene_variant PRAD-US 5 176638166 176638166 single base substitution G A downstream_gene_variant PRAD-US 5 176638166 176638166 single base substitution G A synonymous_variant T653T 1959G>A PRAD-US 5 176638166 176638166 single base substitution G A synonymous_variant T819T 2457G>A PRAD-US 5 176638166 176638166 single base substitution G A synonymous_variant T922T 2766G>A PRAD-US 5 176638166 176638166 single base substitution G A upstream_gene_variant PRAD-US 5 176720972 176720972 single base substitution T A downstream_gene_variant PRAD-US 5 176720972 176720972 single base substitution T A synonymous_variant S1932S 5796T>A PRAD-US 5 176720972 176720972 single base substitution T A synonymous_variant S2098S 6294T>A PRAD-US 5 176720972 176720972 single base substitution T A synonymous_variant S2201S 6603T>A PRAD-US 5 176731691 176731691 single base substitution G A downstream_gene_variant READ-US 5 176638937 176638937 single base substitution G T downstream_gene_variant READ-US 5 176638937 176638937 single base substitution G T missense_variant E1076D 3228G>T READ-US 5 176638937 176638937 single base substitution G T missense_variant E1179D 3537G>T READ-US 5 176638937 176638937 single base substitution G T missense_variant E910D 2730G>T READ-US 5 176638937 176638937 single base substitution G T upstream_gene_variant READ-US 5 176687042 176687042 single base substitution T G missense_variant F1404L 4212T>G READ-US 5 176687042 176687042 single base substitution T G missense_variant F1570L 4710T>G READ-US 5 176687042 176687042 single base substitution T G missense_variant F1673L 5019T>G READ-US 5 176687145 176687145 single base substitution A T missense_variant S1439C 4315A>T READ-US 5 176687145 176687145 single base substitution A T missense_variant S1605C 4813A>T READ-US 5 176687145 176687145 single base substitution A T missense_variant S1708C 5122A>T READ-US 5 176696731 176696731 single base substitution G A downstream_gene_variant READ-US 5 176696731 176696731 single base substitution G A missense_variant R1542Q 4625G>A READ-US 5 176696731 176696731 single base substitution G A missense_variant R1708Q 5123G>A READ-US 5 176696731 176696731 single base substitution G A missense_variant R1811Q 5432G>A READ-US 5 176696731 176696731 single base substitution G A missense_variant R25Q 74G>A RECA-EU 5 176557066 176557066 single base substitution C G upstream_gene_variant RECA-EU 5 176575889 176575889 single base substitution G C intron_variant RECA-EU 5 176577315 176577315 single base substitution A C intron_variant RECA-EU 5 176577818 176577818 single base substitution G C intron_variant RECA-EU 5 176580449 176580449 single base substitution T A intron_variant RECA-EU 5 176599051 176599051 single base substitution G A intron_variant RECA-EU 5 176599721 176599721 single base substitution A C intron_variant RECA-EU 5 176601074 176601074 single base substitution A C intron_variant RECA-EU 5 176608548 176608548 single base substitution T G intron_variant RECA-EU 5 176617249 176617249 single base substitution G A intron_variant RECA-EU 5 176628380 176628380 single base substitution G A intron_variant RECA-EU 5 176630234 176630234 single base substitution T C intron_variant RECA-EU 5 176633637 176633637 single base substitution T C downstream_gene_variant RECA-EU 5 176633637 176633637 single base substitution T C intron_variant RECA-EU 5 176634750 176634750 single base substitution T A downstream_gene_variant RECA-EU 5 176634750 176634750 single base substitution T A intron_variant RECA-EU 5 176634750 176634750 single base substitution T A upstream_gene_variant RECA-EU 5 176642112 176642112 single base substitution C T intron_variant RECA-EU 5 176644461 176644461 single base substitution A T intron_variant RECA-EU 5 176652947 176652947 single base substitution C G intron_variant RECA-EU 5 176653222 176653222 single base substitution A G intron_variant RECA-EU 5 176662597 176662597 single base substitution A G intron_variant RECA-EU 5 176663907 176663907 single base substitution G T intron_variant RECA-EU 5 176669225 176669225 single base substitution C A downstream_gene_variant RECA-EU 5 176669225 176669225 single base substitution C A intron_variant RECA-EU 5 176670093 176670093 single base substitution A T downstream_gene_variant RECA-EU 5 176670093 176670093 single base substitution A T intron_variant RECA-EU 5 176684233 176684233 single base substitution T C intron_variant RECA-EU 5 176690145 176690145 single base substitution G T intron_variant RECA-EU 5 176690145 176690145 single base substitution G T upstream_gene_variant RECA-EU 5 176700470 176700470 single base substitution A C downstream_gene_variant RECA-EU 5 176700470 176700470 single base substitution A C intron_variant RECA-EU 5 176705001 176705001 single base substitution T C downstream_gene_variant RECA-EU 5 176705001 176705001 single base substitution T C intron_variant RECA-EU 5 176727520 176727520 single base substitution A C downstream_gene_variant RECA-EU 5 176729582 176729582 single base substitution T A downstream_gene_variant SKCA-BR 5 176555268 176555268 single base substitution A G upstream_gene_variant SKCA-BR 5 176559230 176559230 single base substitution G A upstream_gene_variant SKCA-BR 5 176559366 176559366 single base substitution C T upstream_gene_variant SKCA-BR 5 176559367 176559367 single base substitution C T upstream_gene_variant SKCA-BR 5 176560844 176560844 single base substitution A G exon_variant SKCA-BR 5 176560844 176560844 single base substitution A G intron_variant SKCA-BR 5 176560844 176560844 single base substitution A G upstream_gene_variant SKCA-BR 5 176560851 176560851 single base substitution T G exon_variant SKCA-BR 5 176560851 176560851 single base substitution T G intron_variant SKCA-BR 5 176560851 176560851 single base substitution T G upstream_gene_variant SKCA-BR 5 176561338 176561338 single base substitution A G intron_variant SKCA-BR 5 176561338 176561338 single base substitution A G upstream_gene_variant SKCA-BR 5 176562343 176562343 single base substitution C T exon_variant SKCA-BR 5 176562343 176562343 single base substitution C T intron_variant SKCA-BR 5 176562343 176562343 single base substitution C T missense_variant S80F 239C>T SKCA-BR 5 176563577 176563577 single base substitution C T downstream_gene_variant SKCA-BR 5 176563577 176563577 single base substitution C T intron_variant SKCA-BR 5 176564245 176564245 single base substitution A T 3_prime_UTR_variant SKCA-BR 5 176564245 176564245 single base substitution A T downstream_gene_variant SKCA-BR 5 176564245 176564245 single base substitution A T intron_variant SKCA-BR 5 176565091 176565091 single base substitution C A downstream_gene_variant SKCA-BR 5 176565091 176565091 single base substitution C A intron_variant SKCA-BR 5 176565465 176565465 single base substitution C T downstream_gene_variant SKCA-BR 5 176565465 176565465 single base substitution C T intron_variant SKCA-BR 5 176566942 176566942 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 5 176566942 176566942 insertion of <=200bp - CA intron_variant SKCA-BR 5 176567990 176567990 single base substitution C T downstream_gene_variant SKCA-BR 5 176567990 176567990 single base substitution C T intron_variant SKCA-BR 5 176569724 176569724 single base substitution C T intron_variant SKCA-BR 5 176569994 176569994 single base substitution C T intron_variant SKCA-BR 5 176570695 176570695 single base substitution C T intron_variant SKCA-BR 5 176573206 176573207 deletion of <=200bp GT - intron_variant SKCA-BR 5 176576713 176576713 single base substitution T C intron_variant SKCA-BR 5 176577354 176577354 single base substitution A C intron_variant SKCA-BR 5 176579477 176579478 deletion of <=200bp CT - intron_variant SKCA-BR 5 176582313 176582313 single base substitution A T intron_variant SKCA-BR 5 176583150 176583150 single base substitution C T intron_variant SKCA-BR 5 176584128 176584128 single base substitution G A intron_variant SKCA-BR 5 176585238 176585238 insertion of <=200bp - ATTTCTTTC intron_variant SKCA-BR 5 176585294 176585294 insertion of <=200bp - CTTTCTTTTCTTTTCT intron_variant SKCA-BR 5 176585298 176585298 insertion of <=200bp - CTTTCT intron_variant SKCA-BR 5 176585298 176585303 deletion of <=200bp CTTTCT - intron_variant SKCA-BR 5 176591103 176591103 single base substitution G T intron_variant SKCA-BR 5 176591167 176591167 single base substitution C T intron_variant SKCA-BR 5 176595469 176595469 single base substitution C T intron_variant SKCA-BR 5 176601975 176601975 single base substitution C T intron_variant SKCA-BR 5 176604947 176604947 single base substitution G A intron_variant SKCA-BR 5 176605324 176605324 single base substitution T G intron_variant SKCA-BR 5 176607925 176607925 single base substitution A C intron_variant SKCA-BR 5 176608428 176608428 insertion of <=200bp - GT intron_variant SKCA-BR 5 176609287 176609287 single base substitution C T intron_variant SKCA-BR 5 176610097 176610097 single base substitution T G intron_variant SKCA-BR 5 176610680 176610680 single base substitution T A intron_variant SKCA-BR 5 176610681 176610681 single base substitution G A intron_variant SKCA-BR 5 176622592 176622592 single base substitution C T intron_variant SKCA-BR 5 176624042 176624042 single base substitution C G intron_variant SKCA-BR 5 176630000 176630000 single base substitution C T intron_variant SKCA-BR 5 176635541 176635541 single base substitution C T downstream_gene_variant SKCA-BR 5 176635541 176635541 single base substitution C T intron_variant SKCA-BR 5 176635541 176635541 single base substitution C T upstream_gene_variant SKCA-BR 5 176643225 176643225 single base substitution C T intron_variant SKCA-BR 5 176647764 176647764 single base substitution G T intron_variant SKCA-BR 5 176649777 176649777 single base substitution C T intron_variant SKCA-BR 5 176660236 176660236 single base substitution T A intron_variant SKCA-BR 5 176663797 176663797 single base substitution G A intron_variant SKCA-BR 5 176664532 176664532 insertion of <=200bp - CTT intron_variant SKCA-BR 5 176668178 176668178 single base substitution G A downstream_gene_variant SKCA-BR 5 176668178 176668178 single base substitution G A intron_variant SKCA-BR 5 176668389 176668389 single base substitution C T downstream_gene_variant SKCA-BR 5 176668389 176668389 single base substitution C T intron_variant SKCA-BR 5 176672633 176672633 insertion of <=200bp - CT intron_variant SKCA-BR 5 176672975 176672975 single base substitution A T intron_variant SKCA-BR 5 176676498 176676498 single base substitution C T intron_variant SKCA-BR 5 176678421 176678421 single base substitution G T intron_variant SKCA-BR 5 176678845 176678845 single base substitution T G missense_variant C1317G 3949T>G SKCA-BR 5 176678845 176678845 single base substitution T G missense_variant C1483G 4447T>G SKCA-BR 5 176678845 176678845 single base substitution T G missense_variant C1586G 4756T>G SKCA-BR 5 176684225 176684225 single base substitution C T intron_variant SKCA-BR 5 176684818 176684818 insertion of <=200bp - TTTTTA intron_variant SKCA-BR 5 176688551 176688551 single base substitution C T intron_variant SKCA-BR 5 176688551 176688551 single base substitution C T upstream_gene_variant SKCA-BR 5 176694971 176694971 single base substitution T A intron_variant SKCA-BR 5 176706612 176706612 single base substitution T A intron_variant SKCA-BR 5 176707449 176707449 single base substitution T C intron_variant SKCA-BR 5 176712118 176712118 single base substitution G T downstream_gene_variant SKCA-BR 5 176712118 176712118 single base substitution G T intron_variant SKCA-BR 5 176712118 176712118 single base substitution G T upstream_gene_variant SKCA-BR 5 176712151 176712151 single base substitution T C downstream_gene_variant SKCA-BR 5 176712151 176712151 single base substitution T C intron_variant SKCA-BR 5 176712151 176712151 single base substitution T C upstream_gene_variant SKCA-BR 5 176713008 176713008 single base substitution T A intron_variant SKCA-BR 5 176713008 176713008 single base substitution T A upstream_gene_variant SKCA-BR 5 176716377 176716377 single base substitution A T intron_variant SKCA-BR 5 176717022 176717022 single base substitution G T intron_variant SKCA-BR 5 176721272 176721272 single base substitution G C downstream_gene_variant SKCA-BR 5 176721272 176721272 single base substitution G C synonymous_variant G2032G 6096G>C SKCA-BR 5 176721272 176721272 single base substitution G C synonymous_variant G2198G 6594G>C SKCA-BR 5 176721272 176721272 single base substitution G C synonymous_variant G2301G 6903G>C SKCA-BR 5 176722971 176722971 single base substitution C G 3_prime_UTR_variant SKCA-BR 5 176722971 176722971 single base substitution C G downstream_gene_variant SKCA-BR 5 176724669 176724669 single base substitution C G 3_prime_UTR_variant SKCA-BR 5 176724669 176724669 single base substitution C G downstream_gene_variant SKCA-BR 5 176727401 176727401 single base substitution C T downstream_gene_variant SKCA-BR 5 176727456 176727456 single base substitution T G downstream_gene_variant SKCA-BR 5 176732215 176732215 single base substitution G T downstream_gene_variant SKCM-US 5 176562160 176562160 single base substitution C T 5_prime_UTR_variant SKCM-US 5 176562160 176562160 single base substitution C T exon_variant SKCM-US 5 176562160 176562160 single base substitution C T missense_variant P19L 56C>T SKCM-US 5 176562207 176562207 single base substitution G A exon_variant SKCM-US 5 176562207 176562207 single base substitution G A missense_variant G35S 103G>A SKCM-US 5 176562207 176562207 single base substitution G A splice_region_variant SKCM-US 5 176562432 176562432 single base substitution C T downstream_gene_variant SKCM-US 5 176562432 176562432 single base substitution C T exon_variant SKCM-US 5 176562432 176562432 single base substitution C T intron_variant SKCM-US 5 176562432 176562432 single base substitution C T missense_variant P110S 328C>T SKCM-US 5 176562927 176562927 single base substitution A C downstream_gene_variant SKCM-US 5 176562927 176562927 single base substitution A C exon_variant SKCM-US 5 176562927 176562927 single base substitution A C intron_variant SKCM-US 5 176562927 176562927 single base substitution A C missense_variant N275H 823A>C SKCM-US 5 176631248 176631248 single base substitution C T downstream_gene_variant SKCM-US 5 176631248 176631248 single base substitution C T intron_variant SKCM-US 5 176631248 176631248 single base substitution C T synonymous_variant V128V 384C>T SKCM-US 5 176631248 176631248 single base substitution C T synonymous_variant V397V 1191C>T SKCM-US 5 176636777 176636777 single base substitution C T downstream_gene_variant SKCM-US 5 176636777 176636777 single base substitution C T synonymous_variant D190D 570C>T SKCM-US 5 176636777 176636777 single base substitution C T synonymous_variant D356D 1068C>T SKCM-US 5 176636777 176636777 single base substitution C T synonymous_variant D459D 1377C>T SKCM-US 5 176636777 176636777 single base substitution C T upstream_gene_variant SKCM-US 5 176637091 176637091 single base substitution C T downstream_gene_variant SKCM-US 5 176637091 176637091 single base substitution C T missense_variant A295V 884C>T SKCM-US 5 176637091 176637091 single base substitution C T missense_variant A461V 1382C>T SKCM-US 5 176637091 176637091 single base substitution C T missense_variant A564V 1691C>T SKCM-US 5 176637091 176637091 single base substitution C T upstream_gene_variant SKCM-US 5 176637326 176637326 single base substitution T A downstream_gene_variant SKCM-US 5 176637326 176637326 single base substitution T A synonymous_variant S373S 1119T>A SKCM-US 5 176637326 176637326 single base substitution T A synonymous_variant S539S 1617T>A SKCM-US 5 176637326 176637326 single base substitution T A synonymous_variant S642S 1926T>A SKCM-US 5 176637326 176637326 single base substitution T A upstream_gene_variant SKCM-US 5 176637511 176637511 single base substitution T A downstream_gene_variant SKCM-US 5 176637511 176637511 single base substitution T A missense_variant I435N 1304T>A SKCM-US 5 176637511 176637511 single base substitution T A missense_variant I601N 1802T>A SKCM-US 5 176637511 176637511 single base substitution T A missense_variant I704N 2111T>A SKCM-US 5 176637511 176637511 single base substitution T A upstream_gene_variant SKCM-US 5 176638012 176638012 single base substitution C T downstream_gene_variant SKCM-US 5 176638012 176638012 single base substitution C T missense_variant S602F 1805C>T SKCM-US 5 176638012 176638012 single base substitution C T missense_variant S768F 2303C>T SKCM-US 5 176638012 176638012 single base substitution C T missense_variant S871F 2612C>T SKCM-US 5 176638012 176638012 single base substitution C T upstream_gene_variant SKCM-US 5 176638258 176638258 single base substitution C T downstream_gene_variant SKCM-US 5 176638258 176638258 single base substitution C T missense_variant S684F 2051C>T SKCM-US 5 176638258 176638258 single base substitution C T missense_variant S850F 2549C>T SKCM-US 5 176638258 176638258 single base substitution C T missense_variant S953F 2858C>T SKCM-US 5 176638258 176638258 single base substitution C T upstream_gene_variant SKCM-US 5 176638265 176638265 single base substitution T C downstream_gene_variant SKCM-US 5 176638265 176638265 single base substitution T C synonymous_variant V686V 2058T>C SKCM-US 5 176638265 176638265 single base substitution T C synonymous_variant V852V 2556T>C SKCM-US 5 176638265 176638265 single base substitution T C synonymous_variant V955V 2865T>C SKCM-US 5 176638265 176638265 single base substitution T C upstream_gene_variant SKCM-US 5 176638665 176638665 single base substitution G A downstream_gene_variant SKCM-US 5 176638665 176638665 single base substitution G A missense_variant D1089N 3265G>A SKCM-US 5 176638665 176638665 single base substitution G A missense_variant D820N 2458G>A SKCM-US 5 176638665 176638665 single base substitution G A missense_variant D986N 2956G>A SKCM-US 5 176638665 176638665 single base substitution G A upstream_gene_variant SKCM-US 5 176638709 176638709 single base substitution C T downstream_gene_variant SKCM-US 5 176638709 176638709 single base substitution C T synonymous_variant D1000D 3000C>T SKCM-US 5 176638709 176638709 single base substitution C T synonymous_variant D1103D 3309C>T SKCM-US 5 176638709 176638709 single base substitution C T synonymous_variant D834D 2502C>T SKCM-US 5 176638709 176638709 single base substitution C T upstream_gene_variant SKCM-US 5 176696688 176696688 single base substitution C T downstream_gene_variant SKCM-US 5 176696688 176696688 single base substitution C T missense_variant L11F 31C>T SKCM-US 5 176696688 176696688 single base substitution C T missense_variant L1528F 4582C>T SKCM-US 5 176696688 176696688 single base substitution C T missense_variant L1694F 5080C>T SKCM-US 5 176696688 176696688 single base substitution C T missense_variant L1797F 5389C>T SKCM-US 5 176696738 176696738 single base substitution C T downstream_gene_variant SKCM-US 5 176696738 176696738 single base substitution C T synonymous_variant F1544F 4632C>T SKCM-US 5 176696738 176696738 single base substitution C T synonymous_variant F1710F 5130C>T SKCM-US 5 176696738 176696738 single base substitution C T synonymous_variant F1813F 5439C>T SKCM-US 5 176696738 176696738 single base substitution C T synonymous_variant F27F 81C>T SKCM-US 5 176696740 176696740 single base substitution C T downstream_gene_variant SKCM-US 5 176696740 176696740 single base substitution C T missense_variant P1545L 4634C>T SKCM-US 5 176696740 176696740 single base substitution C T missense_variant P1711L 5132C>T SKCM-US 5 176696740 176696740 single base substitution C T missense_variant P1814L 5441C>T SKCM-US 5 176696740 176696740 single base substitution C T missense_variant P28L 83C>T SKCM-US 5 176696747 176696747 single base substitution G A downstream_gene_variant SKCM-US 5 176696747 176696747 single base substitution G A missense_variant M1547I 4641G>A SKCM-US 5 176696747 176696747 single base substitution G A missense_variant M1713I 5139G>A SKCM-US 5 176696747 176696747 single base substitution G A missense_variant M1816I 5448G>A SKCM-US 5 176696747 176696747 single base substitution G A missense_variant M30I 90G>A SKCM-US 5 176700722 176700722 single base substitution G A downstream_gene_variant SKCM-US 5 176700722 176700722 single base substitution G A synonymous_variant E1584E 4752G>A SKCM-US 5 176700722 176700722 single base substitution G A synonymous_variant E1750E 5250G>A SKCM-US 5 176700722 176700722 single base substitution G A synonymous_variant E1853E 5559G>A SKCM-US 5 176700722 176700722 single base substitution G A synonymous_variant E67E 201G>A SKCM-US 5 176707784 176707784 single base substitution C T downstream_gene_variant SKCM-US 5 176707784 176707784 single base substitution C T synonymous_variant F1678F 5034C>T SKCM-US 5 176707784 176707784 single base substitution C T synonymous_variant F1844F 5532C>T SKCM-US 5 176707784 176707784 single base substitution C T synonymous_variant F1947F 5841C>T SKCM-US 5 176709573 176709573 single base substitution C T downstream_gene_variant SKCM-US 5 176709573 176709573 single base substitution C T synonymous_variant T1731T 5193C>T SKCM-US 5 176709573 176709573 single base substitution C T synonymous_variant T1897T 5691C>T SKCM-US 5 176709573 176709573 single base substitution C T synonymous_variant T2000T 6000C>T SKCM-US 5 176710809 176710809 single base substitution C T downstream_gene_variant SKCM-US 5 176710809 176710809 single base substitution C T missense_variant P1742S 5224C>T SKCM-US 5 176710809 176710809 single base substitution C T missense_variant P1908S 5722C>T SKCM-US 5 176710809 176710809 single base substitution C T missense_variant P2011S 6031C>T SKCM-US 5 176710809 176710809 single base substitution C T upstream_gene_variant SKCM-US 5 176719072 176719072 single base substitution G C exon_variant SKCM-US 5 176719072 176719072 single base substitution G C missense_variant D1857H 5569G>C SKCM-US 5 176719072 176719072 single base substitution G C missense_variant D2023H 6067G>C SKCM-US 5 176719072 176719072 single base substitution G C missense_variant D2126H 6376G>C SKCM-US 5 176721292 176721292 single base substitution C T downstream_gene_variant SKCM-US 5 176721292 176721292 single base substitution C T missense_variant S2039F 6116C>T SKCM-US 5 176721292 176721292 single base substitution C T missense_variant S2205F 6614C>T SKCM-US 5 176721292 176721292 single base substitution C T missense_variant S2308F 6923C>T SKCM-US 5 176721376 176721376 single base substitution T G downstream_gene_variant SKCM-US 5 176721376 176721376 single base substitution T G missense_variant V2067G 6200T>G SKCM-US 5 176721376 176721376 single base substitution T G missense_variant V2233G 6698T>G SKCM-US 5 176721376 176721376 single base substitution T G missense_variant V2336G 7007T>G SKCM-US 5 176721426 176721426 single base substitution C T downstream_gene_variant SKCM-US 5 176721426 176721426 single base substitution C T missense_variant P2084S 6250C>T SKCM-US 5 176721426 176721426 single base substitution C T missense_variant P2250S 6748C>T SKCM-US 5 176721426 176721426 single base substitution C T missense_variant P2353S 7057C>T SKCM-US 5 176721888 176721888 single base substitution G A downstream_gene_variant SKCM-US 5 176721888 176721888 single base substitution G A missense_variant G2238S 6712G>A SKCM-US 5 176721888 176721888 single base substitution G A missense_variant G2404S 7210G>A SKCM-US 5 176721888 176721888 single base substitution G A missense_variant G2507S 7519G>A SKCM-US 5 176721950 176721950 single base substitution G A downstream_gene_variant SKCM-US 5 176721950 176721950 single base substitution G A stop_gained W2258* 6774G>A SKCM-US 5 176721950 176721950 single base substitution G A stop_gained W2424* 7272G>A SKCM-US 5 176721950 176721950 single base substitution G A stop_gained W2527* 7581G>A SKCM-US 5 176731688 176731688 single base substitution C T downstream_gene_variant STAD-US 5 176562872 176562872 single base substitution C T downstream_gene_variant STAD-US 5 176562872 176562872 single base substitution C T exon_variant STAD-US 5 176562872 176562872 single base substitution C T intron_variant STAD-US 5 176562872 176562872 single base substitution C T synonymous_variant A256A 768C>T STAD-US 5 176636805 176636805 single base substitution G T downstream_gene_variant STAD-US 5 176636805 176636805 single base substitution G T missense_variant D200Y 598G>T STAD-US 5 176636805 176636805 single base substitution G T missense_variant D366Y 1096G>T STAD-US 5 176636805 176636805 single base substitution G T missense_variant D469Y 1405G>T STAD-US 5 176636805 176636805 single base substitution G T upstream_gene_variant STAD-US 5 176637132 176637132 single base substitution G T downstream_gene_variant STAD-US 5 176637132 176637132 single base substitution G T missense_variant A309S 925G>T STAD-US 5 176637132 176637132 single base substitution G T missense_variant A475S 1423G>T STAD-US 5 176637132 176637132 single base substitution G T missense_variant A578S 1732G>T STAD-US 5 176637132 176637132 single base substitution G T upstream_gene_variant STAD-US 5 176638327 176638327 single base substitution C A downstream_gene_variant STAD-US 5 176638327 176638327 single base substitution C A missense_variant A707D 2120C>A STAD-US 5 176638327 176638327 single base substitution C A missense_variant A873D 2618C>A STAD-US 5 176638327 176638327 single base substitution C A missense_variant A976D 2927C>A STAD-US 5 176638327 176638327 single base substitution C A upstream_gene_variant STAD-US 5 176638555 176638555 single base substitution G A downstream_gene_variant STAD-US 5 176638555 176638555 single base substitution G A missense_variant R1052H 3155G>A STAD-US 5 176638555 176638555 single base substitution G A missense_variant R783H 2348G>A STAD-US 5 176638555 176638555 single base substitution G A missense_variant R949H 2846G>A STAD-US 5 176638555 176638555 single base substitution G A upstream_gene_variant STAD-US 5 176638979 176638979 single base substitution T C downstream_gene_variant STAD-US 5 176638979 176638979 single base substitution T C synonymous_variant S1090S 3270T>C STAD-US 5 176638979 176638979 single base substitution T C synonymous_variant S1193S 3579T>C STAD-US 5 176638979 176638979 single base substitution T C synonymous_variant S924S 2772T>C STAD-US 5 176638979 176638979 single base substitution T C upstream_gene_variant STAD-US 5 176638998 176638998 single base substitution C T downstream_gene_variant STAD-US 5 176638998 176638998 single base substitution C T missense_variant R1097W 3289C>T STAD-US 5 176638998 176638998 single base substitution C T missense_variant R1200W 3598C>T STAD-US 5 176638998 176638998 single base substitution C T missense_variant R931W 2791C>T STAD-US 5 176638998 176638998 single base substitution C T upstream_gene_variant STAD-US 5 176639130 176639130 single base substitution A G downstream_gene_variant STAD-US 5 176639130 176639130 single base substitution A G exon_variant STAD-US 5 176639130 176639130 single base substitution A G missense_variant I1141V 3421A>G STAD-US 5 176639130 176639130 single base substitution A G missense_variant I1244V 3730A>G STAD-US 5 176639130 176639130 single base substitution A G missense_variant I975V 2923A>G STAD-US 5 176665366 176665366 single base substitution G A intron_variant STAD-US 5 176665366 176665366 single base substitution G A synonymous_variant P1081P 3243G>A STAD-US 5 176665366 176665366 single base substitution G A synonymous_variant P1247P 3741G>A STAD-US 5 176665366 176665366 single base substitution G A synonymous_variant P1350P 4050G>A STAD-US 5 176665443 176665443 single base substitution C A intron_variant STAD-US 5 176665443 176665443 single base substitution C A missense_variant P1107H 3320C>A STAD-US 5 176665443 176665443 single base substitution C A missense_variant P1273H 3818C>A STAD-US 5 176665443 176665443 single base substitution C A missense_variant P1376H 4127C>A STAD-US 5 176671259 176671259 single base substitution G T downstream_gene_variant STAD-US 5 176671259 176671259 single base substitution G T missense_variant D1187Y 3559G>T STAD-US 5 176671259 176671259 single base substitution G T missense_variant D1353Y 4057G>T STAD-US 5 176671259 176671259 single base substitution G T missense_variant D1456Y 4366G>T STAD-US 5 176673695 176673695 single base substitution T C synonymous_variant F1196F 3588T>C STAD-US 5 176673695 176673695 single base substitution T C synonymous_variant F1362F 4086T>C STAD-US 5 176673695 176673695 single base substitution T C synonymous_variant F1465F 4395T>C STAD-US 5 176673750 176673750 deletion of <=200bp A - frameshift_variant K1215 STAD-US 5 176673750 176673750 deletion of <=200bp A - frameshift_variant K1381 STAD-US 5 176673750 176673750 deletion of <=200bp A - frameshift_variant K1484 STAD-US 5 176673788 176673788 single base substitution A G synonymous_variant P1227P 3681A>G STAD-US 5 176673788 176673788 single base substitution A G synonymous_variant P1393P 4179A>G STAD-US 5 176673788 176673788 single base substitution A G synonymous_variant P1496P 4488A>G STAD-US 5 176678848 176678848 single base substitution C T missense_variant R1318C 3952C>T STAD-US 5 176678848 176678848 single base substitution C T missense_variant R1484C 4450C>T STAD-US 5 176678848 176678848 single base substitution C T missense_variant R1587C 4759C>T STAD-US 5 176687028 176687028 single base substitution C T missense_variant H1400Y 4198C>T STAD-US 5 176687028 176687028 single base substitution C T missense_variant H1566Y 4696C>T STAD-US 5 176687028 176687028 single base substitution C T missense_variant H1669Y 5005C>T STAD-US 5 176694615 176694615 single base substitution C T 5_prime_UTR_variant STAD-US 5 176694615 176694615 single base substitution C T synonymous_variant C1464C 4392C>T STAD-US 5 176694615 176694615 single base substitution C T synonymous_variant C1630C 4890C>T STAD-US 5 176694615 176694615 single base substitution C T synonymous_variant C1733C 5199C>T STAD-US 5 176694686 176694686 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 5 176694686 176694686 single base substitution G T missense_variant R1488M 4463G>T STAD-US 5 176694686 176694686 single base substitution G T missense_variant R1654M 4961G>T STAD-US 5 176694686 176694686 single base substitution G T missense_variant R1757M 5270G>T STAD-US 5 176696802 176696802 deletion of <=200bp A - downstream_gene_variant STAD-US 5 176696802 176696802 deletion of <=200bp A - frameshift_variant K1566 STAD-US 5 176696802 176696802 deletion of <=200bp A - frameshift_variant K1732 STAD-US 5 176696802 176696802 deletion of <=200bp A - frameshift_variant K1835 STAD-US 5 176696802 176696802 deletion of <=200bp A - frameshift_variant K49 STAD-US 5 176700715 176700715 deletion of <=200bp A - downstream_gene_variant STAD-US 5 176700715 176700715 deletion of <=200bp A - frameshift_variant Q1582 STAD-US 5 176700715 176700715 deletion of <=200bp A - frameshift_variant Q1748 STAD-US 5 176700715 176700715 deletion of <=200bp A - frameshift_variant Q1851 STAD-US 5 176700715 176700715 deletion of <=200bp A - frameshift_variant Q65 STAD-US 5 176707623 176707623 single base substitution C T downstream_gene_variant STAD-US 5 176707623 176707623 single base substitution C T missense_variant R1625C 4873C>T STAD-US 5 176707623 176707623 single base substitution C T missense_variant R1791C 5371C>T STAD-US 5 176707623 176707623 single base substitution C T missense_variant R1894C 5680C>T STAD-US 5 176707797 176707797 single base substitution C T downstream_gene_variant STAD-US 5 176707797 176707797 single base substitution C T missense_variant R1683W 5047C>T STAD-US 5 176707797 176707797 single base substitution C T missense_variant R1849W 5545C>T STAD-US 5 176707797 176707797 single base substitution C T missense_variant R1952W 5854C>T STAD-US 5 176710894 176710894 single base substitution G A downstream_gene_variant STAD-US 5 176710894 176710894 single base substitution G A missense_variant R1770H 5309G>A STAD-US 5 176710894 176710894 single base substitution G A missense_variant R1936H 5807G>A STAD-US 5 176710894 176710894 single base substitution G A missense_variant R2039H 6116G>A STAD-US 5 176710894 176710894 single base substitution G A upstream_gene_variant STAD-US 5 176719013 176719013 single base substitution A T exon_variant STAD-US 5 176719013 176719013 single base substitution A T missense_variant K1837M 5510A>T STAD-US 5 176719013 176719013 single base substitution A T missense_variant K2003M 6008A>T STAD-US 5 176719013 176719013 single base substitution A T missense_variant K2106M 6317A>T STAD-US 5 176719126 176719126 single base substitution G A exon_variant STAD-US 5 176719126 176719126 single base substitution G A missense_variant A1875T 5623G>A STAD-US 5 176719126 176719126 single base substitution G A missense_variant A2041T 6121G>A STAD-US 5 176719126 176719126 single base substitution G A missense_variant A2144T 6430G>A STAD-US 5 176720831 176720831 single base substitution A G downstream_gene_variant STAD-US 5 176720831 176720831 single base substitution A G splice_acceptor_variant STAD-US 5 176721436 176721436 single base substitution C T downstream_gene_variant STAD-US 5 176721436 176721436 single base substitution C T missense_variant T2087M 6260C>T STAD-US 5 176721436 176721436 single base substitution C T missense_variant T2253M 6758C>T STAD-US 5 176721436 176721436 single base substitution C T missense_variant T2356M 7067C>T STAD-US 5 176721549 176721549 single base substitution A G downstream_gene_variant STAD-US 5 176721549 176721549 single base substitution A G missense_variant I2125V 6373A>G STAD-US 5 176721549 176721549 single base substitution A G missense_variant I2291V 6871A>G STAD-US 5 176721549 176721549 single base substitution A G missense_variant I2394V 7180A>G STAD-US 5 176721771 176721771 single base substitution C T downstream_gene_variant STAD-US 5 176721771 176721771 single base substitution C T missense_variant R2199W 6595C>T STAD-US 5 176721771 176721771 single base substitution C T missense_variant R2365W 7093C>T STAD-US 5 176721771 176721771 single base substitution C T missense_variant R2468W 7402C>T STAD-US 5 176722004 176722004 single base substitution G T downstream_gene_variant STAD-US 5 176722004 176722004 single base substitution G T missense_variant K2276N 6828G>T STAD-US 5 176722004 176722004 single base substitution G T missense_variant K2442N 7326G>T STAD-US 5 176722004 176722004 single base substitution G T missense_variant K2545N 7635G>T STAD-US 5 176730061 176730061 single base substitution G A downstream_gene_variant THCA-SA 5 176729443 176729443 single base substitution T A downstream_gene_variant THCA-US 5 176636938 176636938 single base substitution A G downstream_gene_variant THCA-US 5 176636938 176636938 single base substitution A G missense_variant K244R 731A>G THCA-US 5 176636938 176636938 single base substitution A G missense_variant K410R 1229A>G THCA-US 5 176636938 176636938 single base substitution A G missense_variant K513R 1538A>G THCA-US 5 176636938 176636938 single base substitution A G upstream_gene_variant THCA-US 5 176673763 176673763 single base substitution A G missense_variant N1219S 3656A>G THCA-US 5 176673763 176673763 single base substitution A G missense_variant N1385S 4154A>G THCA-US 5 176673763 176673763 single base substitution A G missense_variant N1488S 4463A>G THCA-US 5 176721551 176721551 insertion of <=200bp - A downstream_gene_variant THCA-US 5 176721551 176721551 insertion of <=200bp - A frameshift_variant I2125I? THCA-US 5 176721551 176721551 insertion of <=200bp - A frameshift_variant I2291I? THCA-US 5 176721551 176721551 insertion of <=200bp - A frameshift_variant I2394I? UCEC-US 5 176562201 176562201 single base substitution G A exon_variant UCEC-US 5 176562201 176562201 single base substitution G A missense_variant G33S 97G>A UCEC-US 5 176562201 176562201 single base substitution G A splice_region_variant UCEC-US 5 176562745 176562745 single base substitution C T downstream_gene_variant UCEC-US 5 176562745 176562745 single base substitution C T exon_variant UCEC-US 5 176562745 176562745 single base substitution C T intron_variant UCEC-US 5 176562745 176562745 single base substitution C T missense_variant T214I 641C>T UCEC-US 5 176562916 176562916 single base substitution T C downstream_gene_variant UCEC-US 5 176562916 176562916 single base substitution T C exon_variant UCEC-US 5 176562916 176562916 single base substitution T C intron_variant UCEC-US 5 176562916 176562916 single base substitution T C missense_variant L271S 812T>C UCEC-US 5 176562924 176562924 single base substitution A C downstream_gene_variant UCEC-US 5 176562924 176562924 single base substitution A C exon_variant UCEC-US 5 176562924 176562924 single base substitution A C intron_variant UCEC-US 5 176562924 176562924 single base substitution A C missense_variant I274L 820A>C UCEC-US 5 176563067 176563067 single base substitution A G downstream_gene_variant UCEC-US 5 176563067 176563067 single base substitution A G exon_variant UCEC-US 5 176563067 176563067 single base substitution A G intron_variant UCEC-US 5 176618958 176618958 single base substitution G A intron_variant UCEC-US 5 176618958 176618958 single base substitution G A missense_variant R334H 1001G>A UCEC-US 5 176618958 176618958 single base substitution G A missense_variant R65H 194G>A UCEC-US 5 176631233 176631233 single base substitution C T intron_variant UCEC-US 5 176631233 176631233 single base substitution C T synonymous_variant F123F 369C>T UCEC-US 5 176631233 176631233 single base substitution C T synonymous_variant F392F 1176C>T UCEC-US 5 176636852 176636852 single base substitution A G downstream_gene_variant UCEC-US 5 176636852 176636852 single base substitution A G synonymous_variant E215E 645A>G UCEC-US 5 176636852 176636852 single base substitution A G synonymous_variant E381E 1143A>G UCEC-US 5 176636852 176636852 single base substitution A G synonymous_variant E484E 1452A>G UCEC-US 5 176636852 176636852 single base substitution A G upstream_gene_variant UCEC-US 5 176636883 176636883 single base substitution G A downstream_gene_variant UCEC-US 5 176636883 176636883 single base substitution G A missense_variant A226T 676G>A UCEC-US 5 176636883 176636883 single base substitution G A missense_variant A392T 1174G>A UCEC-US 5 176636883 176636883 single base substitution G A missense_variant A495T 1483G>A UCEC-US 5 176636883 176636883 single base substitution G A upstream_gene_variant UCEC-US 5 176636892 176636892 single base substitution C T downstream_gene_variant UCEC-US 5 176636892 176636892 single base substitution C T stop_gained R229* 685C>T UCEC-US 5 176636892 176636892 single base substitution C T stop_gained R395* 1183C>T UCEC-US 5 176636892 176636892 single base substitution C T stop_gained R498* 1492C>T UCEC-US 5 176636892 176636892 single base substitution C T upstream_gene_variant UCEC-US 5 176637034 176637034 single base substitution C T downstream_gene_variant UCEC-US 5 176637034 176637034 single base substitution C T missense_variant T276M 827C>T UCEC-US 5 176637034 176637034 single base substitution C T missense_variant T442M 1325C>T UCEC-US 5 176637034 176637034 single base substitution C T missense_variant T545M 1634C>T UCEC-US 5 176637034 176637034 single base substitution C T upstream_gene_variant UCEC-US 5 176637232 176637232 single base substitution G T downstream_gene_variant UCEC-US 5 176637232 176637232 single base substitution G T missense_variant R342L 1025G>T UCEC-US 5 176637232 176637232 single base substitution G T missense_variant R508L 1523G>T UCEC-US 5 176637232 176637232 single base substitution G T missense_variant R611L 1832G>T UCEC-US 5 176637232 176637232 single base substitution G T upstream_gene_variant UCEC-US 5 176637237 176637237 single base substitution C A downstream_gene_variant UCEC-US 5 176637237 176637237 single base substitution C A missense_variant L344M 1030C>A UCEC-US 5 176637237 176637237 single base substitution C A missense_variant L510M 1528C>A UCEC-US 5 176637237 176637237 single base substitution C A missense_variant L613M 1837C>A UCEC-US 5 176637237 176637237 single base substitution C A upstream_gene_variant UCEC-US 5 176637407 176637407 single base substitution C T downstream_gene_variant UCEC-US 5 176637407 176637407 single base substitution C T synonymous_variant F400F 1200C>T UCEC-US 5 176637407 176637407 single base substitution C T synonymous_variant F566F 1698C>T UCEC-US 5 176637407 176637407 single base substitution C T synonymous_variant F669F 2007C>T UCEC-US 5 176637407 176637407 single base substitution C T upstream_gene_variant UCEC-US 5 176637697 176637697 single base substitution C T downstream_gene_variant UCEC-US 5 176637697 176637697 single base substitution C T missense_variant S497L 1490C>T UCEC-US 5 176637697 176637697 single base substitution C T missense_variant S663L 1988C>T UCEC-US 5 176637697 176637697 single base substitution C T missense_variant S766L 2297C>T UCEC-US 5 176637697 176637697 single base substitution C T upstream_gene_variant UCEC-US 5 176638202 176638202 single base substitution C A downstream_gene_variant UCEC-US 5 176638202 176638202 single base substitution C A synonymous_variant V665V 1995C>A UCEC-US 5 176638202 176638202 single base substitution C A synonymous_variant V831V 2493C>A UCEC-US 5 176638202 176638202 single base substitution C A synonymous_variant V934V 2802C>A UCEC-US 5 176638202 176638202 single base substitution C A upstream_gene_variant UCEC-US 5 176638500 176638500 single base substitution T G downstream_gene_variant UCEC-US 5 176638500 176638500 single base substitution T G missense_variant F1034V 3100T>G UCEC-US 5 176638500 176638500 single base substitution T G missense_variant F765V 2293T>G UCEC-US 5 176638500 176638500 single base substitution T G missense_variant F931V 2791T>G UCEC-US 5 176638500 176638500 single base substitution T G upstream_gene_variant UCEC-US 5 176638605 176638605 single base substitution C T downstream_gene_variant UCEC-US 5 176638605 176638605 single base substitution C T stop_gained Q1069* 3205C>T UCEC-US 5 176638605 176638605 single base substitution C T stop_gained Q800* 2398C>T UCEC-US 5 176638605 176638605 single base substitution C T stop_gained Q966* 2896C>T UCEC-US 5 176638605 176638605 single base substitution C T upstream_gene_variant UCEC-US 5 176638766 176638766 single base substitution T G downstream_gene_variant UCEC-US 5 176638766 176638766 single base substitution T G missense_variant I1019M 3057T>G UCEC-US 5 176638766 176638766 single base substitution T G missense_variant I1122M 3366T>G UCEC-US 5 176638766 176638766 single base substitution T G missense_variant I853M 2559T>G UCEC-US 5 176638766 176638766 single base substitution T G upstream_gene_variant UCEC-US 5 176638830 176638830 single base substitution G A downstream_gene_variant UCEC-US 5 176638830 176638830 single base substitution G A missense_variant E1041K 3121G>A UCEC-US 5 176638830 176638830 single base substitution G A missense_variant E1144K 3430G>A UCEC-US 5 176638830 176638830 single base substitution G A missense_variant E875K 2623G>A UCEC-US 5 176638830 176638830 single base substitution G A upstream_gene_variant UCEC-US 5 176638884 176638884 single base substitution C T downstream_gene_variant UCEC-US 5 176638884 176638884 single base substitution C T missense_variant R1059C 3175C>T UCEC-US 5 176638884 176638884 single base substitution C T missense_variant R1162C 3484C>T UCEC-US 5 176638884 176638884 single base substitution C T missense_variant R893C 2677C>T UCEC-US 5 176638884 176638884 single base substitution C T upstream_gene_variant UCEC-US 5 176638935 176638935 single base substitution G T downstream_gene_variant UCEC-US 5 176638935 176638935 single base substitution G T stop_gained E1076* 3226G>T UCEC-US 5 176638935 176638935 single base substitution G T stop_gained E1179* 3535G>T UCEC-US 5 176638935 176638935 single base substitution G T stop_gained E910* 2728G>T UCEC-US 5 176638935 176638935 single base substitution G T upstream_gene_variant UCEC-US 5 176639147 176639147 single base substitution G T downstream_gene_variant UCEC-US 5 176639147 176639147 single base substitution G T exon_variant UCEC-US 5 176639147 176639147 single base substitution G T missense_variant K1146N 3438G>T UCEC-US 5 176639147 176639147 single base substitution G T missense_variant K1249N 3747G>T UCEC-US 5 176639147 176639147 single base substitution G T missense_variant K980N 2940G>T UCEC-US 5 176662842 176662842 single base substitution C T 3_prime_UTR_variant UCEC-US 5 176662842 176662842 single base substitution C T missense_variant R1004C 3010C>T UCEC-US 5 176662842 176662842 single base substitution C T missense_variant R1170C 3508C>T UCEC-US 5 176662842 176662842 single base substitution C T missense_variant R1273C 3817C>T UCEC-US 5 176665281 176665281 single base substitution G A intron_variant UCEC-US 5 176665281 176665281 single base substitution G A missense_variant R1053Q 3158G>A UCEC-US 5 176665281 176665281 single base substitution G A missense_variant R1219Q 3656G>A UCEC-US 5 176665281 176665281 single base substitution G A missense_variant R1322Q 3965G>A UCEC-US 5 176673767 176673767 single base substitution T C synonymous_variant D1220D 3660T>C UCEC-US 5 176673767 176673767 single base substitution T C synonymous_variant D1386D 4158T>C UCEC-US 5 176673767 176673767 single base substitution T C synonymous_variant D1489D 4467T>C UCEC-US 5 176675287 176675287 single base substitution C T missense_variant R1266C 3796C>T UCEC-US 5 176675287 176675287 single base substitution C T missense_variant R1432C 4294C>T UCEC-US 5 176675287 176675287 single base substitution C T missense_variant R1535C 4603C>T UCEC-US 5 176675305 176675305 single base substitution C G missense_variant L1272V 3814C>G UCEC-US 5 176675305 176675305 single base substitution C G missense_variant L1438V 4312C>G UCEC-US 5 176675305 176675305 single base substitution C G missense_variant L1541V 4621C>G UCEC-US 5 176683967 176683967 single base substitution T G missense_variant F1325C 3974T>G UCEC-US 5 176683967 176683967 single base substitution T G missense_variant F1491C 4472T>G UCEC-US 5 176683967 176683967 single base substitution T G missense_variant F1594C 4781T>G UCEC-US 5 176684042 176684042 single base substitution G A missense_variant C1350Y 4049G>A UCEC-US 5 176684042 176684042 single base substitution G A missense_variant C1516Y 4547G>A UCEC-US 5 176684042 176684042 single base substitution G A missense_variant C1619Y 4856G>A UCEC-US 5 176684064 176684064 single base substitution T G synonymous_variant T1357T 4071T>G UCEC-US 5 176684064 176684064 single base substitution T G synonymous_variant T1523T 4569T>G UCEC-US 5 176684064 176684064 single base substitution T G synonymous_variant T1626T 4878T>G UCEC-US 5 176687066 176687066 single base substitution C A synonymous_variant I1412I 4236C>A UCEC-US 5 176687066 176687066 single base substitution C A synonymous_variant I1578I 4734C>A UCEC-US 5 176687066 176687066 single base substitution C A synonymous_variant I1681I 5043C>A UCEC-US 5 176696722 176696722 single base substitution A G downstream_gene_variant UCEC-US 5 176696722 176696722 single base substitution A G missense_variant H1539R 4616A>G UCEC-US 5 176696722 176696722 single base substitution A G missense_variant H1705R 5114A>G UCEC-US 5 176696722 176696722 single base substitution A G missense_variant H1808R 5423A>G UCEC-US 5 176696722 176696722 single base substitution A G missense_variant H22R 65A>G UCEC-US 5 176700767 176700767 single base substitution A G downstream_gene_variant UCEC-US 5 176700767 176700767 single base substitution A G synonymous_variant P1599P 4797A>G UCEC-US 5 176700767 176700767 single base substitution A G synonymous_variant P1765P 5295A>G UCEC-US 5 176700767 176700767 single base substitution A G synonymous_variant P1868P 5604A>G UCEC-US 5 176700767 176700767 single base substitution A G synonymous_variant P82P 246A>G UCEC-US 5 176700780 176700780 single base substitution A G downstream_gene_variant UCEC-US 5 176700780 176700780 single base substitution A G missense_variant I1604V 4810A>G UCEC-US 5 176700780 176700780 single base substitution A G missense_variant I1770V 5308A>G UCEC-US 5 176700780 176700780 single base substitution A G missense_variant I1873V 5617A>G UCEC-US 5 176700780 176700780 single base substitution A G missense_variant I87V 259A>G UCEC-US 5 176707683 176707683 single base substitution C T downstream_gene_variant UCEC-US 5 176707683 176707683 single base substitution C T missense_variant R1645C 4933C>T UCEC-US 5 176707683 176707683 single base substitution C T missense_variant R1811C 5431C>T UCEC-US 5 176707683 176707683 single base substitution C T missense_variant R1914C 5740C>T UCEC-US 5 176709473 176709473 single base substitution T G downstream_gene_variant UCEC-US 5 176709473 176709473 single base substitution T G missense_variant F1698C 5093T>G UCEC-US 5 176709473 176709473 single base substitution T G missense_variant F1864C 5591T>G UCEC-US 5 176709473 176709473 single base substitution T G missense_variant F1967C 5900T>G UCEC-US 5 176709530 176709530 single base substitution G A downstream_gene_variant UCEC-US 5 176709530 176709530 single base substitution G A missense_variant R1717H 5150G>A UCEC-US 5 176709530 176709530 single base substitution G A missense_variant R1883H 5648G>A UCEC-US 5 176709530 176709530 single base substitution G A missense_variant R1986H 5957G>A UCEC-US 5 176709555 176709555 single base substitution T G downstream_gene_variant UCEC-US 5 176709555 176709555 single base substitution T G synonymous_variant T1725T 5175T>G UCEC-US 5 176709555 176709555 single base substitution T G synonymous_variant T1891T 5673T>G UCEC-US 5 176709555 176709555 single base substitution T G synonymous_variant T1994T 5982T>G UCEC-US 5 176710828 176710828 single base substitution G A downstream_gene_variant UCEC-US 5 176710828 176710828 single base substitution G A missense_variant R1748Q 5243G>A UCEC-US 5 176710828 176710828 single base substitution G A missense_variant R1914Q 5741G>A UCEC-US 5 176710828 176710828 single base substitution G A missense_variant R2017Q 6050G>A UCEC-US 5 176710828 176710828 single base substitution G A upstream_gene_variant UCEC-US 5 176719076 176719076 single base substitution C T exon_variant UCEC-US 5 176719076 176719076 single base substitution C T missense_variant A1858V 5573C>T UCEC-US 5 176719076 176719076 single base substitution C T missense_variant A2024V 6071C>T UCEC-US 5 176719076 176719076 single base substitution C T missense_variant A2127V 6380C>T UCEC-US 5 176720989 176720989 single base substitution C A downstream_gene_variant UCEC-US 5 176720989 176720989 single base substitution C A missense_variant P1938H 5813C>A UCEC-US 5 176720989 176720989 single base substitution C A missense_variant P2104H 6311C>A UCEC-US 5 176720989 176720989 single base substitution C A missense_variant P2207H 6620C>A UCEC-US 5 176721424 176721424 single base substitution G T downstream_gene_variant UCEC-US 5 176721424 176721424 single base substitution G T missense_variant R2083I 6248G>T UCEC-US 5 176721424 176721424 single base substitution G T missense_variant R2249I 6746G>T UCEC-US 5 176721424 176721424 single base substitution G T missense_variant R2352I 7055G>T UCEC-US 5 176721760 176721760 single base substitution G A downstream_gene_variant UCEC-US 5 176721760 176721760 single base substitution G A missense_variant R2195H 6584G>A UCEC-US 5 176721760 176721760 single base substitution G A missense_variant R2361H 7082G>A UCEC-US 5 176721760 176721760 single base substitution G A missense_variant R2464H 7391G>A UCEC-US 5 176721858 176721858 single base substitution C A downstream_gene_variant UCEC-US 5 176721858 176721858 single base substitution C A missense_variant L2228M 6682C>A UCEC-US 5 176721858 176721858 single base substitution C A missense_variant L2394M 7180C>A UCEC-US 5 176721858 176721858 single base substitution C A missense_variant L2497M 7489C>A UCEC-US 5 176722138 176722138 single base substitution C T downstream_gene_variant UCEC-US 5 176722138 176722138 single base substitution C T missense_variant P2321L 6962C>T UCEC-US 5 176722138 176722138 single base substitution C T missense_variant P2487L 7460C>T UCEC-US 5 176722138 176722138 single base substitution C T missense_variant P2590L 7769C>T UCEC-US 5 176722277 176722277 single base substitution C G downstream_gene_variant UCEC-US 5 176722277 176722277 single base substitution C G synonymous_variant L2367L 7101C>G UCEC-US 5 176722277 176722277 single base substitution C G synonymous_variant L2533L 7599C>G UCEC-US 5 176722277 176722277 single base substitution C G synonymous_variant L2636L 7908C>G UCEC-US 5 176728799 176728799 single base substitution C T downstream_gene_variant UCEC-US 5 176729180 176729180 single base substitution C A downstream_gene_variant UCEC-US 5 176729476 176729476 single base substitution C T downstream_gene_variant UCEC-US 5 176729583 176729583 single base substitution C T downstream_gene_variant UCEC-US 5 176729591 176729591 single base substitution C T downstream_gene_variant UCEC-US 5 176729796 176729796 single base substitution A T downstream_gene_variant UCEC-US 5 176729812 176729812 single base substitution C T downstream_gene_variant UCEC-US 5 176730032 176730032 single base substitution C T downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand ID06 COSM1166660 c.1589C>T p.P530L Substitution - Missense 5:177209988-177209988 + PD6987a COSM4384058 c.1906A>G p.I636V Substitution - Missense 5:177210305-177210305 + CSCC-55-T COSM4554083 c.6107G>A p.G2036E Substitution - Missense 5:177283884-177283884 + TCGA-21-5782-01 COSM737603 c.3161G>C p.R1054T Substitution - Missense 5:177211560-177211560 + 587332 COSM1217940 c.4707G>T p.E1569D Substitution - Missense 5:177251795-177251795 + TCGA-66-2773-01 COSM737613 c.1766C>G p.S589C Substitution - Missense 5:177210165-177210165 + PTC-7C COSM4159760 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + cSCCP6 COSM136514 c.6542C>T p.S2181F Substitution - Missense 5:177293910-177293910 + U87 COSM3341117 c.3380T>G p.L1127R Substitution - Missense 5:177211779-177211779 + TCGA-A7-A26G-01 COSM1486627 c.1964G>A p.S655N Substitution - Missense 5:177210363-177210363 + TCGA-AZ-6598-01 COSM1436275 c.5139C>T p.C1713C Substitution - coding silent 5:177260161-177260161 + Gp2D COSM3341126 c.3717A>G p.K1239K Substitution - coding silent 5:177212116-177212116 + 193 COSM1741807 c.4794G>C p.Q1598H Substitution - Missense 5:177256979-177256979 + TCGA-BR-6452-01 COSM3853947 c.768C>T p.A256A Substitution - coding silent 5:177135871-177135871 + SH-7166 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-CD-A4MG-01 COSM3853958 c.3730A>G p.I1244V Substitution - Missense 5:177212129-177212129 + B109-Tumor COSM1754201 c.3918C>G p.H1306Q Substitution - Missense 5:177235942-177235942 + TCGA-DK-A3IQ-01 COSM1311010 c.5319G>C p.E1773D Substitution - Missense 5:177269617-177269617 + sysucc-1163T COSM5459190 c.865T>G p.L289V Substitution - Missense 5:177135968-177135968 + SC_9047 COSM5561001 c.114T>A p.N38K Substitution - Missense 5:177135217-177135217 + PT23_1 COSM5902745 c.2183T>G p.V728G Substitution - Missense 5:177210582-177210582 + BD22T COSM5508822 c.2038A>C p.K680Q Substitution - Missense 5:177210437-177210437 + PD6829a COSM4384048 c.946T>G p.S316A Substitution - Missense 5:177191902-177191902 + 453 COSM3341097 c.3091C>T p.R1031* Substitution - Nonsense 5:177211490-177211490 + TCGA-UB-A7MB-01 COSM4932079 c.2554A>G p.I852V Substitution - Missense 5:177210953-177210953 + SNUH_G76_S1 COSM4416947 c.1840G>C p.V614L Substitution - Missense 5:177210239-177210239 + SH-3133 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-AP-A056-01 COSM1066193 c.812T>C p.L271S Substitution - Missense 5:177135915-177135915 + SJAMLM7011 COSM4776062 c.6656G>A p.R2219H Substitution - Missense 5:177294024-177294024 + TCGA-AX-A0J0-01 COSM1066282 c.5604A>G p.P1868P Substitution - coding silent 5:177273766-177273766 + TCGA-EE-A3J4-06 COSM3919743 c.2858C>T p.S953F Substitution - Missense 5:177211257-177211257 + PT08_1 COSM5893068 c.3133C>T p.R1045C Substitution - Missense 5:177211532-177211532 + SH-5693 COSM5019784 c.3705T>C p.N1235N Substitution - coding silent 5:177212104-177212104 + TCGA-AZ-4315-01 COSM1436256 c.1319G>A p.R440Q Substitution - Missense 5:177209718-177209718 + SH-9771 COSM4419701 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + 587332 COSM1217941 c.4707G>T p.E1569D Substitution - Missense 5:177251795-177251795 + PD6201a COSM4384041 c.20T>C p.L7P Substitution - Missense 5:177135123-177135123 + 2P3 COSM3733671 c.6431C>T p.A2144V Substitution - Missense 5:177292126-177292126 + TCGA-AN-A046-01 COSM3827751 c.3517C>T p.R1173C Substitution - Missense 5:177211916-177211916 + TCGA-60-2724-01 COSM737596 c.4642-1G>C p.? Unknown 5:177251729-177251729 + TCGA-DJ-A4UW-01 COSM3373814 c.4463A>G p.N1488S Substitution - Missense 5:177246762-177246762 + LUAD-NYU259 COSM371967 c.3010G>T p.D1004Y Substitution - Missense 5:177211409-177211409 + TCGA-FU-A2QG-01 COSM4849142 c.2592G>A p.L864L Substitution - coding silent 5:177210991-177210991 + RMS80_ COSM4987203 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + TCGA-34-5929-01 COSM737591 c.6022G>A p.D2008N Substitution - Missense 5:177283799-177283799 + TCGA-22-4595-01 COSM737606 c.2919G>C p.Q973H Substitution - Missense 5:177211318-177211318 + T46 COSM5065044 c.4444C>T p.Q1482* Substitution - Nonsense 5:177246743-177246743 + SH-2871 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + SH-8559 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + PT37 COSM5918715 c.1114C>T p.P372S Substitution - Missense 5:177204170-177204170 + 413LT COSM337161 c.2105C>A p.P702H Substitution - Missense 5:177210504-177210504 + PD6934a COSM4385618 c.166_167insA p.T56fs*37 Insertion - Frameshift 5:177135269-177135270 + LUAD-S00488 COSM395297 c.2049G>A p.K683K Substitution - coding silent 5:177210448-177210448 + TCGA-B0-4712-01 COSM482568 c.1290G>A p.Q430Q Substitution - coding silent 5:177209689-177209689 + TCGA-CJ-6030-01 COSM482577 c.6576C>T p.F2192F Substitution - coding silent 5:177293944-177293944 + TCGA-C5-A7UH-01 COSM4856840 c.3417T>A p.S1139S Substitution - coding silent 5:177211816-177211816 + SH-9771 COSM5020995 c.5781C>G p.A1927A Substitution - coding silent 5:177280723-177280723 + sysucc-1163T COSM5459191 c.3475C>T p.R1159W Substitution - Missense 5:177211874-177211874 + PT08_1 COSM5893067 c.3133C>T p.R1045C Substitution - Missense 5:177211532-177211532 + YUROC COSM5403156 c.5004C>T p.Y1668Y Substitution - coding silent 5:177260026-177260026 + RMS85_ COSM4988876 c.2071G>A p.A691T Substitution - Missense 5:177210470-177210470 + YUROC COSM5403157 c.5004C>T p.Y1668Y Substitution - coding silent 5:177260026-177260026 + RMS85_ COSM4418708 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + CLL044 COSM145694 c.6085A>G p.T2029A Substitution - Missense 5:177283862-177283862 + Pat_59_B COSM5868237 c.7936G>A p.A2646T Substitution - Missense 5:177295304-177295304 + ZZUFHECRKL-G045T COSM4987203 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + TCGA-B5-A0JY-01 COSM1066296 c.5982T>G p.T1994T Substitution - coding silent 5:177282554-177282554 + RKO COSM3341251 c.7130A>C p.K2377T Substitution - Missense 5:177294498-177294498 + TCGA-BR-7707-01 COSM1436283 c.6430G>A p.A2144T Substitution - Missense 5:177292125-177292125 + EGC15 COSM5060966 c.6047C>T p.A2016V Substitution - Missense 5:177283824-177283824 + Gp5D COSM3341126 c.3717A>G p.K1239K Substitution - coding silent 5:177212116-177212116 + TCGA-CG-4442-01 COSM3853956 c.3579T>C p.S1193S Substitution - coding silent 5:177211978-177211978 + PD6110a COSM4384089 c.6323delG p.T2109fs*41 Deletion - Frameshift 5:177292018-177292018 + TCGA-AC-A2B8-01 COSM3827753 c.4211G>A p.R1404H Substitution - Missense 5:177239774-177239774 + TCGA-GL-A59T-01 COSM3994205 c.811T>G p.L271V Substitution - Missense 5:177135914-177135914 + PD5755a COSM591563 c.1457C>G p.S486C Substitution - Missense 5:177209856-177209856 + SH-3133 COSM5019784 c.3705T>C p.N1235N Substitution - coding silent 5:177212104-177212104 + tumor_4149246 COSM5950214 c.4967G>T p.G1656V Substitution - Missense 5:177259989-177259989 + TCGA-EK-A2PG-01 COSM4819571 c.3654G>A p.L1218L Substitution - coding silent 5:177212053-177212053 + PD6788a COSM4384068 c.2893T>G p.S965A Substitution - Missense 5:177211292-177211292 + STC297 COSM5060963 c.5741G>A p.R1914H Substitution - Missense 5:177280683-177280683 + TCGA-BS-A0UF-01 COSM1066221 c.2007C>T p.F669F Substitution - coding silent 5:177210406-177210406 + PD6914a COSM4384052 c.1126G>T p.A376S Substitution - Missense 5:177204182-177204182 + Gp5D COSM3341162 c.4774A>G p.T1592A Substitution - Missense 5:177256959-177256959 + LP6005690-DNA_C02 COSM4411791 c.6078C>T p.N2026N Substitution - coding silent 5:177283855-177283855 + 3N62-VS-3T62 COSM4984476 c.1861C>T p.L621F Substitution - Missense 5:177210260-177210260 + ESCC_BICR_048T COSM5432379 c.6023A>T p.D2008V Substitution - Missense 5:177283800-177283800 + 1115154 COSM3341172 c.4961C>G p.S1654C Substitution - Missense 5:177257146-177257146 + BD236T COSM5518630 c.387A>T p.E129D Substitution - Missense 5:177135490-177135490 + Gp2D COSM3341127 c.3717A>G p.K1239K Substitution - coding silent 5:177212116-177212116 + HCT8 COSM1672148 c.7875G>T p.W2625C Substitution - Missense 5:177295243-177295243 + TCGA-A5-A0GP-01 COSM1066267 c.4781T>G p.F1594C Substitution - Missense 5:177256966-177256966 + TCGA-EE-A29V-06 COSM3614491 c.103G>A p.G35S Substitution - Missense 5:177135206-177135206 + ZZUFHECRKL-G045T COSM4987204 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + TCGA-FW-A3R5-06 COSM3919746 c.5841C>T p.F1947F Substitution - coding silent 5:177280783-177280783 + ESO-859 COSM1239635 c.2850A>G p.V950V Substitution - coding silent 5:177211249-177211249 + CSCC-62-T COSM4517884 c.4532_4533CC>TT p.P1511L Substitution - Missense 5:177248215-177248216 + RK156_C01 COSM3702785 c.1495G>C p.A499P Substitution - Missense 5:177209894-177209894 + RKO COSM3341112 c.3281T>C p.M1094T Substitution - Missense 5:177211680-177211680 + PD7367a COSM4384071 c.2912G>A p.G971D Substitution - Missense 5:177211311-177211311 + J76_T COSM3947306 c.3763A>T p.S1255C Substitution - Missense 5:177212162-177212162 + SC_9035 COSM3853976 c.5854C>T p.R1952W Substitution - Missense 5:177280796-177280796 + TCGA-D1-A103-01 COSM1066196 c.820A>C p.I274L Substitution - Missense 5:177135923-177135923 + TCGA-GN-A265-06 COSM3614516 c.6923C>T p.S2308F Substitution - Missense 5:177294291-177294291 + PD6050a COSM4385620 c.6795_6796insA p.A2268fs*13 Insertion - Frameshift 5:177294163-177294164 + RMS85_ COSM4988879 c.3106G>C p.A1036P Substitution - Missense 5:177211505-177211505 + TCGA-JX-A3PZ-01 COSM4823821 c.596C>T p.S199L Substitution - Missense 5:177135699-177135699 + TCGA-A8-A0AD-01 COSM449382 c.252A>G p.V84V Substitution - coding silent 5:177135355-177135355 + 8067240 COSM3784823 c.4974G>A p.L1658L Substitution - coding silent 5:177259996-177259996 + SH-9161 COSM4418709 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + TCGA-FU-A2QG-01 COSM4849033 c.1930G>A p.D644N Substitution - Missense 5:177210329-177210329 + TCGA-DM-A1D8-01 COSM1436278 c.5532G>C p.R1844S Substitution - Missense 5:177273694-177273694 + TCGA-FW-A3R5-06 COSM3919752 c.7057C>T p.P2353S Substitution - Missense 5:177294425-177294425 + PD6822a COSM4384093 c.6673C>T p.P2225S Substitution - Missense 5:177294041-177294041 + PD8934a COSM4384090 c.6418A>T p.K2140* Substitution - Nonsense 5:177292113-177292113 + B109 COSM1754200 c.3918C>G p.H1306Q Substitution - Missense 5:177235942-177235942 + SH-3458 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-AA-3811-01 COSM293772 c.6999C>A p.P2333P Substitution - coding silent 5:177294367-177294367 + TCGA-18-3409-01 COSM737604 c.2981C>T p.S994F Substitution - Missense 5:177211380-177211380 + 587228 COSM1217934 c.5785G>T p.G1929W Substitution - Missense 5:177280727-177280727 + TCGA-AM-5820-01 COSM3697160 c.6662A>G p.Y2221C Substitution - Missense 5:177294030-177294030 + CCC64 COSM3661732 c.7240T>G p.L2414V Substitution - Missense 5:177294608-177294608 + TCGA-D8-A27P-01 COSM1486630 c.2503G>T p.G835C Substitution - Missense 5:177210902-177210902 + 016-0040-02TD COSM1292097 c.6085A>G p.T2029A Substitution - Missense 5:177283862-177283862 + TCGA-EI-7002-01 COSM3429313 c.5122A>T p.S1708C Substitution - Missense 5:177260144-177260144 + Au2 COSM3341242 c.6924C>T p.S2308S Substitution - coding silent 5:177294292-177294292 + TCGA-AN-A046-01 COSM3827766 c.6654C>T p.I2218I Substitution - coding silent 5:177294022-177294022 + OSCC-GB_00020111 COSM3715046 c.2873C>T p.S958L Substitution - Missense 5:177211272-177211272 + TCGA-EV-5903-01 COSM3994207 c.3642T>C p.L1214L Substitution - coding silent 5:177212041-177212041 + PD6888a COSM4384073 c.3097G>A p.A1033T Substitution - Missense 5:177211496-177211496 + LUAD-S01315 COSM345736 c.6259-1G>C p.? Unknown 5:177291953-177291953 + TCGA-B0-5695-01 COSM482565 c.959A>G p.K320R Substitution - Missense 5:177191915-177191915 + TCGA-B0-4710-01 COSM482579 c.7980G>A p.Q2660Q Substitution - coding silent 5:177295348-177295348 + TCGA-CD-A4MG-01 COSM3853989 c.7635G>T p.K2545N Substitution - Missense 5:177295003-177295003 + TCGA-E2-A2P5-01 COSM3827756 c.5763C>G p.H1921Q Substitution - Missense 5:177280705-177280705 + PD6888a COSM4384072 c.3097G>A p.A1033T Substitution - Missense 5:177211496-177211496 + Pat_26_A COSM5868235 c.6796delA p.A2268fs*26 Deletion - Frameshift 5:177294164-177294164 + Pat_41_B COSM5868229 c.3613G>A p.E1205K Substitution - Missense 5:177212012-177212012 + 381 COSM4426524 c.4378+1_4378+4delGTGA p.? Unknown 5:177244271-177244274 + TCGA-29-2432-01 COSM1328887 c.3959G>A p.R1320Q Substitution - Missense 5:177238274-177238274 + TCGA-FV-A3R3-01 COSM4921834 c.4547A>G p.E1516G Substitution - Missense 5:177248230-177248230 + SH-1362 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + 587278 COSM1217937 c.4760G>A p.R1587H Substitution - Missense 5:177251848-177251848 + PCSI_0083_Pa_X COSM3381208 c.2309G>A p.G770D Substitution - Missense 5:177210708-177210708 + TCGA-DK-A3IQ-01 COSM1311011 c.5319G>C p.E1773D Substitution - Missense 5:177269617-177269617 + Gp2D COSM3341145 c.4347T>C p.C1449C Substitution - coding silent 5:177244239-177244239 + 38T COSM3715050 c.5732G>T p.C1911F Substitution - Missense 5:177280674-177280674 + RMS110_ COSM4418708 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + 12924 COSM5617278 c.4766-10G>A p.? Unknown 5:177256941-177256941 + CHC2103T COSM4952542 c.6044A>G p.Y2015C Substitution - Missense 5:177283821-177283821 + TCGA-AA-3971-01 COSM301463 c.5996_5997TC>GT p.L1999R Substitution - Missense 5:177282568-177282569 + CCK81 COSM3341070 c.2428T>C p.C810R Substitution - Missense 5:177210827-177210827 + PCSI_0083_Pa_P_526 COSM3381208 c.2309G>A p.G770D Substitution - Missense 5:177210708-177210708 + L02 COSM5368546 c.6986T>G p.L2329R Substitution - Missense 5:177294354-177294354 + 2492703 COSM3341243 c.6924C>T p.S2308S Substitution - coding silent 5:177294292-177294292 + LAU63 COSM232909 c.6794C>T p.S2265F Substitution - Missense 5:177294162-177294162 + TCGA-AC-A23H-01 COSM3827745 c.26G>A p.R9K Substitution - Missense 5:177135129-177135129 + SH-6055 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + PD4099a COSM163004 c.3108C>G p.A1036A Substitution - coding silent 5:177211507-177211507 + B47 COSM1754199 c.3276G>C p.Q1092H Substitution - Missense 5:177211675-177211675 + TCGA-DM-A0XD-01 COSM1436282 c.6430G>A p.A2144T Substitution - Missense 5:177292125-177292125 + PCSI_0083_Pa_P_526 COSM3381209 c.2309G>A p.G770D Substitution - Missense 5:177210708-177210708 + TCGA-BR-6452-01 COSM3853974 c.5680C>T p.R1894C Substitution - Missense 5:177280622-177280622 + PD6872a COSM4384078 c.3361A>G p.K1121E Substitution - Missense 5:177211760-177211760 + TCGA-AA-A00N-01 COSM276402 c.2183T>C p.V728A Substitution - Missense 5:177210582-177210582 + TCGA-FS-A1Z3-06 COSM3614501 c.2865T>C p.V955V Substitution - coding silent 5:177211264-177211264 + TCGA-AC-A2B8-01 COSM3827752 c.4211G>A p.R1404H Substitution - Missense 5:177239774-177239774 + J52_T COSM449383 c.7317G>A p.L2439L Substitution - coding silent 5:177294685-177294685 + 2492723 COSM5720516 c.6635C>T p.P2212L Substitution - Missense 5:177294003-177294003 + TCGA-AN-A0AK-01 COSM3827764 c.6479C>T p.P2160L Substitution - Missense 5:177293847-177293847 + 0071_CRUK_PC_0071_T1_DNA COSM4420957 c.5968G>C p.E1990Q Substitution - Missense 5:177282540-177282540 + TCGA-FS-A1Z3-06 COSM3614502 c.2865T>C p.V955V Substitution - coding silent 5:177211264-177211264 + 2521243 COSM5886419 c.5864G>T p.G1955V Substitution - Missense 5:177280806-177280806 + SH-102782 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + SH-9771 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + S07-39193-TP COSM4992297 c.4446_4447delGT p.C1483fs*1 Deletion - Frameshift 5:177246745-177246746 + TCGA-AM-5821-01 COSM3697156 c.682C>G p.P228A Substitution - Missense 5:177135785-177135785 + J88_T COSM3947304 c.2861A>T p.K954M Substitution - Missense 5:177211260-177211260 + TCGA-KK-A59V-01 COSM4708348 c.2766G>A p.T922T Substitution - coding silent 5:177211165-177211165 + TCGA-D1-A103-01 COSM1066242 c.3484C>T p.R1162C Substitution - Missense 5:177211883-177211883 + T3080 COSM4708354 c.5918G>A p.G1973D Substitution - Missense 5:177282490-177282490 + SNUH_G10_S1 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + S06-38853-TP COSM4992299 c.4487C>T p.P1496L Substitution - Missense 5:177246786-177246786 + SCMC_RM2_ COSM4418709 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + CHEWS032 COSM4585727 c.7696A>G p.T2566A Substitution - Missense 5:177295064-177295064 + SH-3458 COSM4159761 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + 11T COSM3715048 c.5431C>T p.R1811* Substitution - Nonsense 5:177269729-177269729 + CSCC-49-T COSM4556516 c.6949G>A p.D2317N Substitution - Missense 5:177294317-177294317 + TCGA-B5-A11E-01 COSM1066219 c.1837C>A p.L613M Substitution - Missense 5:177210236-177210236 + 345480 COSM3726246 c.6329A>T p.Q2110L Substitution - Missense 5:177292024-177292024 + ESO-859 COSM1239634 c.2850A>G p.V950V Substitution - coding silent 5:177211249-177211249 + TCGA-G3-A5SK-01 COSM4927453 c.6719C>A p.S2240* Substitution - Nonsense 5:177294087-177294087 + In-9 COSM144830 c.5177C>T p.P1726L Substitution - Missense 5:177267592-177267592 + TCGA-EJ-5496-01 COSM1132199 c.1471G>A p.E491K Substitution - Missense 5:177209870-177209870 + TCGA-BG-A18B-01 COSM1066306 c.6620C>A p.P2207H Substitution - Missense 5:177293988-177293988 + B106-Tumor COSM1754197 c.2483C>T p.S828F Substitution - Missense 5:177210882-177210882 + PCSI_0083_Pa_X COSM3381209 c.2309G>A p.G770D Substitution - Missense 5:177210708-177210708 + PD6782a COSM4384074 c.3104C>A p.S1035* Substitution - Nonsense 5:177211503-177211503 + SH-2871 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + MedB-1 COSM5621404 c.6451A>G p.K2151E Substitution - Missense 5:177292146-177292146 + T2950 COSM4708342 c.617C>T p.A206V Substitution - Missense 5:177135720-177135720 + PD6881a COSM4384094 c.6739G>A p.A2247T Substitution - Missense 5:177294107-177294107 + ID35 COSM1166638 c.5912A>G p.Y1971C Substitution - Missense 5:177282484-177282484 + CHLA-258 COSM4585725 c.3092G>A p.R1031Q Substitution - Missense 5:177211491-177211491 + PT08_1 COSM5893065 c.3132C>A p.N1044K Substitution - Missense 5:177211531-177211531 + S00501 COSM313374 c.6898G>A p.A2300T Substitution - Missense 5:177294266-177294266 + XHDG04C COSM4767676 c.7438G>A p.D2480N Substitution - Missense 5:177294806-177294806 + TCGA-GF-A6C8-06 COSM3919749 c.6376G>C p.D2126H Substitution - Missense 5:177292071-177292071 + TCGA-D1-A174-01 COSM1066210 c.1492C>T p.R498* Substitution - Nonsense 5:177209891-177209891 + SR COSM1672147 c.4552G>T p.G1518C Substitution - Missense 5:177248235-177248235 + TCGA-D8-A1XK-01 COSM3827760 c.6364T>G p.F2122V Substitution - Missense 5:177292059-177292059 + 394 COSM3722831 c.6094T>C p.W2032R Substitution - Missense 5:177283871-177283871 + TCGA-EE-A3JD-06 COSM4394923 c.6000C>T p.T2000T Substitution - coding silent 5:177282572-177282572 + TCGA-EB-A3Y7-01 COSM3919751 c.7007T>G p.V2336G Substitution - Missense 5:177294375-177294375 + TCGA-KK-A59V-01 COSM4708347 c.2766G>A p.T922T Substitution - coding silent 5:177211165-177211165 + SJAMLM7011 COSM4776062 c.6656G>A p.R2219H Substitution - Missense 5:177294024-177294024 + TCGA-34-5231-01 COSM737608 c.2620G>T p.E874* Substitution - Nonsense 5:177211019-177211019 + Pat_26_A COSM5868236 c.6796delA p.A2268fs*26 Deletion - Frameshift 5:177294164-177294164 + MedB-1 COSM5621403 c.508C>A p.P170T Substitution - Missense 5:177135611-177135611 + SA071 COSM213291 c.7900G>T p.A2634S Substitution - Missense 5:177295268-177295268 + 1346 COSM1644835 c.4289G>C p.G1430A Substitution - Missense 5:177239852-177239852 + T46 COSM5065043 c.4444C>T p.Q1482* Substitution - Nonsense 5:177246743-177246743 + TCGA-BS-A0TA-01 COSM1066278 c.5423A>G p.H1808R Substitution - Missense 5:177269721-177269721 + SH-1679 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + ZZUFHECRKL-G045T COSM4419035 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + BK0004 COSM4185517 c.1600G>C p.G534R Substitution - Missense 5:177209999-177209999 + 863TCS COSM673682 c.6653T>C p.I2218T Substitution - Missense 5:177294021-177294021 + CLL044 COSM1292097 c.6085A>G p.T2029A Substitution - Missense 5:177283862-177283862 + Pat_40_A COSM5868226 c.1196G>A p.R399K Substitution - Missense 5:177204252-177204252 + PT08_1 COSM5893066 c.3132C>A p.N1044K Substitution - Missense 5:177211531-177211531 + SH-3133 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + SH-7032 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + LAU63 COSM235065 c.6795C>T p.S2265S Substitution - coding silent 5:177294163-177294163 + CSCC-62-T COSM4517885 c.4532_4533CC>TT p.P1511L Substitution - Missense 5:177248215-177248216 + sysucc-1163T COSM5459189 c.865T>G p.L289V Substitution - Missense 5:177135968-177135968 + TCGA-G9-7521-01 COSM1471833 c.6603T>A p.S2201S Substitution - coding silent 5:177293971-177293971 + TCGA-CJ-4912-01 COSM482560 c.205T>C p.Y69H Substitution - Missense 5:177135308-177135308 + PR-04-194 COSM246117 c.4978C>T p.R1660C Substitution - Missense 5:177260000-177260000 + Pat_59_B COSM5868238 c.7936G>A p.A2646T Substitution - Missense 5:177295304-177295304 + ccRCC-66 COSM1659925 c.111C>A p.S37S Substitution - coding silent 5:177135214-177135214 + SH-9161 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + 2012-703:2012-1309-T COSM4605652 c.5892+1G>T p.? Unknown 5:177280835-177280835 + 489 COSM3697157 c.5950C>T p.R1984* Substitution - Nonsense 5:177282522-177282522 + S02-15015-TP COSM4992293 c.2226C>T p.P742P Substitution - coding silent 5:177210625-177210625 + TCGA-CU-A0YR-01 COSM420768 c.605G>A p.G202D Substitution - Missense 5:177135708-177135708 + 513 COSM1066299 c.6050G>A p.R2017Q Substitution - Missense 5:177283827-177283827 + SH-3133 COSM4419702 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + Pat_36_B COSM5868232 c.4810delA p.R1605fs*37 Deletion - Frameshift 5:177256995-177256995 + TCGA-D1-A15Z-01 COSM1066260 c.4603C>T p.R1535C Substitution - Missense 5:177248286-177248286 + PT48 COSM5931695 c.6559C>T p.R2187* Substitution - Nonsense 5:177293927-177293927 + TCGA-D3-A3CF-06 COSM3614517 c.7519G>A p.G2507S Substitution - Missense 5:177294887-177294887 + Pat_40_A COSM5868225 c.1196G>A p.R399K Substitution - Missense 5:177204252-177204252 + PD6782a COSM4384075 c.3104C>A p.S1035* Substitution - Nonsense 5:177211503-177211503 + TCGA-BR-4184-01 COSM3853955 c.3155G>A p.R1052H Substitution - Missense 5:177211554-177211554 + 2218465 COSM4421340 c.5842C>T p.R1948C Substitution - Missense 5:177280784-177280784 + 4_PRE-TREATMENT COSM1724163 c.5628C>T p.N1876N Substitution - coding silent 5:177280570-177280570 + TCGA-FS-A1ZC-06 COSM3614497 c.2111T>A p.I704N Substitution - Missense 5:177210510-177210510 + RMS85_ COSM4988881 c.6750G>A p.M2250I Substitution - Missense 5:177294118-177294118 + PT34 COSM5910461 c.2428T>A p.C810S Substitution - Missense 5:177210827-177210827 + tumor_4188879 COSM5949173 c.1011G>A p.W337* Substitution - Nonsense 5:177191967-177191967 + S09-31237-TP COSM4992301 c.5382C>T p.F1794F Substitution - coding silent 5:177269680-177269680 + LIM2405 COSM4642984 c.5580C>T p.D1860D Substitution - coding silent 5:177273742-177273742 + 2011-2311:2012-362-T COSM4605165 c.3394G>T p.G1132* Substitution - Nonsense 5:177211793-177211793 + TCGA-G4-6322-01 COSM3697158 c.5950C>T p.R1984* Substitution - Nonsense 5:177282522-177282522 + TCGA-JX-A3PZ-01 COSM4823822 c.596C>T p.S199L Substitution - Missense 5:177135699-177135699 + TCGA-EB-A3Y7-01 COSM3919750 c.7007T>G p.V2336G Substitution - Missense 5:177294375-177294375 + TCGA-AP-A0LM-01 COSM1066318 c.7769C>T p.P2590L Substitution - Missense 5:177295137-177295137 + TCGA-B5-A0JY-01 COSM1066297 c.5982T>G p.T1994T Substitution - coding silent 5:177282554-177282554 + TCGA-BP-4988-01 COSM482571 c.2418A>C p.I806I Substitution - coding silent 5:177210817-177210817 + 6115219 COSM5563361 c.5552A>G p.Q1851R Substitution - Missense 5:177273714-177273714 + TCGA-AP-A0LM-01 COSM1066248 c.3747G>T p.K1249N Substitution - Missense 5:177212146-177212146 + cSCCP1 COSM134102 c.7322C>T p.P2441L Substitution - Missense 5:177294690-177294690 + TCGA-D1-A103-01 COSM1066207 c.1483G>A p.A495T Substitution - Missense 5:177209882-177209882 + TCGA-29-2432-01 COSM1328888 c.3959G>A p.R1320Q Substitution - Missense 5:177238274-177238274 + TCGA-A6-6141-01 COSM1436267 c.4001C>A p.S1334Y Substitution - Missense 5:177238316-177238316 + RMS88_ COSM4005988 c.6782T>C p.M2261T Substitution - Missense 5:177294150-177294150 + SH-9161 COSM4419034 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + 2011-2280:2012-366-T COSM4605277 c.3921+2T>C p.? Unknown 5:177235947-177235947 + SH-9161 COSM4987204 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + TCGA-GF-A6C9-06 COSM4899496 c.1377C>T p.D459D Substitution - coding silent 5:177209776-177209776 + 2492722 COSM5720515 c.6635C>T p.P2212L Substitution - Missense 5:177294003-177294003 + TCGA-BP-4988-01 COSM482570 c.2418A>C p.I806I Substitution - coding silent 5:177210817-177210817 + TCGA-EE-A29M-06 COSM3614509 c.5441C>T p.P1814L Substitution - Missense 5:177269739-177269739 + TCGA-EE-A3JI-06 COSM3614520 c.7581G>A p.W2527* Substitution - Nonsense 5:177294949-177294949 + tumor_4144951 COSM5948811 c.4091G>A p.G1364E Substitution - Missense 5:177238406-177238406 + TCGA-06-2563-01 COSM2152855 c.2905G>A p.G969R Substitution - Missense 5:177211304-177211304 + ESCC-153T COSM3941259 c.7003C>G p.P2335A Substitution - Missense 5:177294371-177294371 + sysucc-311T COSM4585723 c.1149C>T p.I383I Substitution - coding silent 5:177204205-177204205 + SH-9771 COSM5019785 c.3705T>C p.N1235N Substitution - coding silent 5:177212104-177212104 + TCGA-BR-4361-01 COSM3853977 c.5854C>T p.R1952W Substitution - Missense 5:177280796-177280796 + ESO-859 COSM1239637 c.4966+2T>C p.? Unknown 5:177257153-177257153 + TCGA-FU-A2QG-01 COSM4849165 c.2017G>C p.E673Q Substitution - Missense 5:177210416-177210416 + PD6984a COSM4384064 c.2625T>A p.D875E Substitution - Missense 5:177211024-177211024 + PD23578a COSM5795102 c.2362C>G p.R788G Substitution - Missense 5:177210761-177210761 + 2492702 COSM3341243 c.6924C>T p.S2308S Substitution - coding silent 5:177294292-177294292 + TCGA-CJ-6030-01 COSM482576 c.6576C>T p.F2192F Substitution - coding silent 5:177293944-177293944 + TCGA-E3-A3DZ-01 COSM3373812 c.1538A>G p.K513R Substitution - Missense 5:177209937-177209937 + 587278 COSM1217938 c.7897C>T p.R2633W Substitution - Missense 5:177295265-177295265 + ESO-913 COSM1259602 c.6118G>A p.V2040I Substitution - Missense 5:177283895-177283895 + 3765_T COSM3947301 c.1433C>G p.S478* Substitution - Nonsense 5:177209832-177209832 + S06-38853-TP COSM4992295 c.3930C>T p.S1310S Substitution - coding silent 5:177238245-177238245 + TCGA-E9-A54Y-01 COSM3827749 c.2968G>T p.E990* Substitution - Nonsense 5:177211367-177211367 + TCGA-C5-A7UH-01 COSM4856841 c.3417T>A p.S1139S Substitution - coding silent 5:177211816-177211816 + SH-7282 COSM4419035 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + LUAD-NYU259 COSM371966 c.3010G>T p.D1004Y Substitution - Missense 5:177211409-177211409 + EGC15 COSM5060965 c.6047C>T p.A2016V Substitution - Missense 5:177283824-177283824 + TCGA-AA-3713-01 COSM1436286 c.6738G>T p.Q2246H Substitution - Missense 5:177294106-177294106 + 3498_T COSM3947308 c.6476G>C p.C2159S Substitution - Missense 5:177293844-177293844 + TCGA-BG-A0LX-01 COSM1066321 c.7908C>G p.L2636L Substitution - coding silent 5:177295276-177295276 + TCGA-A5-A0GP-01 COSM1066300 c.6050G>A p.R2017Q Substitution - Missense 5:177283827-177283827 + J52_T COSM449384 c.7317G>A p.L2439L Substitution - coding silent 5:177294685-177294685 + TCGA-B0-4712-01 COSM482569 c.1290G>A p.Q430Q Substitution - coding silent 5:177209689-177209689 + TCGA-FS-A1ZZ-06 COSM3614506 c.3309C>T p.D1103D Substitution - coding silent 5:177211708-177211708 + 3498_T COSM3947307 c.6476G>C p.C2159S Substitution - Missense 5:177293844-177293844 + 2011-2292:2012-324-T COSM4603938 c.5391_5392insT p.G1800fs*3 Insertion - Frameshift 5:177269689-177269690 + T3724 COSM4708343 c.1345T>A p.L449M Substitution - Missense 5:177209744-177209744 + TCGA-C5-A7UH-01 COSM4856673 c.1499G>C p.R500T Substitution - Missense 5:177209898-177209898 + TCGA-GN-A265-06 COSM3614515 c.6923C>T p.S2308F Substitution - Missense 5:177294291-177294291 + SH-1362 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + 2492720 COSM5720516 c.6635C>T p.P2212L Substitution - Missense 5:177294003-177294003 + PD4962a COSM5788263 c.4966+6G>T p.? Unknown 5:177257157-177257157 + TCGA-A5-A0GA-01 COSM1066239 c.3430G>A p.E1144K Substitution - Missense 5:177211829-177211829 + LUAD-E00918 COSM365338 c.5458G>A p.V1820M Substitution - Missense 5:177269756-177269756 + TCGA-D1-A103-01 COSM1066187 c.97G>A p.G33S Substitution - Missense 5:177135200-177135200 + PD6518a COSM4384047 c.796A>G p.T266A Substitution - Missense 5:177135899-177135899 + TCGA-G4-6304-01 COSM1436255 c.709delA p.N238fs*23 Deletion - Frameshift 5:177135812-177135812 + 2492730 COSM5729309 c.1367C>T p.P456L Substitution - Missense 5:177209766-177209766 + C135 COSM4618500 c.3273T>G p.L1091L Substitution - coding silent 5:177211672-177211672 + PT48 COSM5931696 c.6559C>T p.R2187* Substitution - Nonsense 5:177293927-177293927 + TCGA-RC-A7SF-01 COSM4923148 c.215T>G p.L72R Substitution - Missense 5:177135318-177135318 + S02-15015-TP COSM4992294 c.2226C>T p.P742P Substitution - coding silent 5:177210625-177210625 + TCGA-FU-A2QG-01 COSM4849076 c.2340G>C p.S780S Substitution - coding silent 5:177210739-177210739 + 2011-2335:2012-1340-T COSM4603827 c.6470delG p.E2158fs*136 Deletion - Frameshift 5:177293838-177293838 + YURAY COSM5403152 c.4001C>T p.S1334F Substitution - Missense 5:177238316-177238316 + TCGA-BR-6452-01 COSM3853946 c.768C>T p.A256A Substitution - coding silent 5:177135871-177135871 + 38T COSM3715051 c.5732G>T p.C1911F Substitution - Missense 5:177280674-177280674 + SH-9248 COSM4419034 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + PT34 COSM5910464 c.2427G>T p.E809D Substitution - Missense 5:177210826-177210826 + 11T COSM3715049 c.5431C>T p.R1811* Substitution - Nonsense 5:177269729-177269729 + D28 COSM5545443 c.6224C>G p.P2075R Substitution - Missense 5:177288891-177288891 + TCGA-BS-A0UV-01 COSM1066228 c.2802C>A p.V934V Substitution - coding silent 5:177211201-177211201 + 11T COSM3715044 c.1549C>T p.Q517* Substitution - Nonsense 5:177209948-177209948 + TCGA-BG-A0LX-01 COSM1066320 c.7908C>G p.L2636L Substitution - coding silent 5:177295276-177295276 + ESO-859 COSM1239636 c.4966+2T>C p.? Unknown 5:177257153-177257153 + TCGA-EE-A29M-06 COSM3614510 c.5441C>T p.P1814L Substitution - Missense 5:177269739-177269739 + TCGA-GL-A59T-01 COSM3994204 c.811T>G p.L271V Substitution - Missense 5:177135914-177135914 + 2011-2315:2012-358-T COSM4604565 c.1828C>T p.Q610* Substitution - Nonsense 5:177210227-177210227 + 2011-2315:2012-358-T COSM4604564 c.1828C>T p.Q610* Substitution - Nonsense 5:177210227-177210227 + pfg008T COSM1642693 c.5887delA p.K1964fs*5 Deletion - Frameshift 5:177280829-177280829 + HCT-15 COSM1672149 c.7875G>T p.W2625C Substitution - Missense 5:177295243-177295243 + ID06 COSM1166659 c.1589C>T p.P530L Substitution - Missense 5:177209988-177209988 + TCGA-DK-A1A7-01 COSM420766 c.5719A>G p.I1907V Substitution - Missense 5:177280661-177280661 + 2012-701:2012-1307-T COSM4603810 c.4359delT p.S1454fs*33 Deletion - Frameshift 5:177244251-177244251 + SNUH_G76_S1 COSM4418709 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + SH-0348 COSM4159760 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + SA071 COSM213290 c.7900G>T p.A2634S Substitution - Missense 5:177295268-177295268 + S02339 COSM4386946 c.3140C>G p.A1047G Substitution - Missense 5:177211539-177211539 + TCGA-BR-4184-01 COSM3853954 c.3155G>A p.R1052H Substitution - Missense 5:177211554-177211554 + 390 COSM4427850 c.5965C>A p.Q1989K Substitution - Missense 5:177282537-177282537 + TCGA-AP-A056-01 COSM276400 c.1176C>T p.F392F Substitution - coding silent 5:177204232-177204232 + ESCC-153T COSM3941260 c.7003C>G p.P2335A Substitution - Missense 5:177294371-177294371 + Gp2D COSM3341144 c.4347T>C p.C1449C Substitution - coding silent 5:177244239-177244239 + PD6967a COSM4384084 c.4858G>A p.V1620I Substitution - Missense 5:177257043-177257043 + TCGA-EP-A2KA-01 COSM4917451 c.7867A>C p.S2623R Substitution - Missense 5:177295235-177295235 + RMS88_ COSM4988877 c.2071G>A p.A691T Substitution - Missense 5:177210470-177210470 + T3105 COSM4708348 c.2766G>A p.T922T Substitution - coding silent 5:177211165-177211165 + PT08_2 COSM5893067 c.3133C>T p.R1045C Substitution - Missense 5:177211532-177211532 + PT08_2 COSM5893066 c.3132C>A p.N1044K Substitution - Missense 5:177211531-177211531 + TCGA-AP-A056-01 COSM276401 c.1176C>T p.F392F Substitution - coding silent 5:177204232-177204232 + S02248 COSM5679755 c.3359G>T p.G1120V Substitution - Missense 5:177211758-177211758 + RMS88_ COSM4988876 c.2071G>A p.A691T Substitution - Missense 5:177210470-177210470 + PD6780a COSM4384042 c.388C>T p.P130S Substitution - Missense 5:177135491-177135491 + PD6862a COSM4384081 c.3698G>A p.R1233Q Substitution - Missense 5:177212097-177212097 + SH-1679 COSM4419702 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + 0071_CRUK_PC_0071_T1_DNA COSM4420956 c.5968G>C p.E1990Q Substitution - Missense 5:177282540-177282540 + tumor_4188879 COSM5949172 c.1011G>A p.W337* Substitution - Nonsense 5:177191967-177191967 + L02 COSM5368547 c.6986T>G p.L2329R Substitution - Missense 5:177294354-177294354 + TCGA-D3-A5GO-06 COSM3614493 c.328C>T p.P110S Substitution - Missense 5:177135431-177135431 + TCGA-C5-A7UH-01 COSM4856761 c.1957G>A p.E653K Substitution - Missense 5:177210356-177210356 + PD6862a COSM4384080 c.3698G>A p.R1233Q Substitution - Missense 5:177212097-177212097 + Pat_36_B COSM5868231 c.4810delA p.R1605fs*37 Deletion - Frameshift 5:177256995-177256995 + SH-3327 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + SH-5693 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-66-2786-01 COSM737598 c.4411C>T p.R1471* Substitution - Nonsense 5:177246710-177246710 + YURAY COSM5403153 c.4001C>T p.S1334F Substitution - Missense 5:177238316-177238316 + LIM1899 COSM4640655 c.2133C>T p.H711H Substitution - coding silent 5:177210532-177210532 + CHC2113T COSM4788380 c.1119T>A p.S373S Substitution - coding silent 5:177204175-177204175 + TCGA-C5-A7UH-01 COSM4856730 c.1450G>C p.E484Q Substitution - Missense 5:177209849-177209849 + LUAD-E00918 COSM365337 c.5458G>A p.V1820M Substitution - Missense 5:177269756-177269756 + TCGA-B5-A11E-01 COSM1066218 c.1837C>A p.L613M Substitution - Missense 5:177210236-177210236 + B89-12-Tumor COSM4005985 c.776C>T p.S259L Substitution - Missense 5:177135879-177135879 + I2L-P19Ta-Tumor-Biopsy COSM4585723 c.1149C>T p.I383I Substitution - coding silent 5:177204205-177204205 + TCGA-FU-A2QG-01 COSM4849079 c.1927G>A p.D643N Substitution - Missense 5:177210326-177210326 + S02-14875-TP COSM4992308 c.7568C>T p.S2523L Substitution - Missense 5:177294936-177294936 + LUAD-S01315 COSM345735 c.6259-1G>C p.? Unknown 5:177291953-177291953 + TCGA-C5-A7UH-01 COSM4856608 c.3439G>A p.E1147K Substitution - Missense 5:177211838-177211838 + SH-5693 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + ESCC-159T COSM3941258 c.5726C>G p.S1909C Substitution - Missense 5:177280668-177280668 + CSCC-30-T COSM4505418 c.6924C>A p.S2308S Substitution - coding silent 5:177294292-177294292 + 61 COSM5737438 c.4748G>A p.C1583Y Substitution - Missense 5:177251836-177251836 + SH-3327 COSM4159760 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + pfg008T COSM1642692 c.5887delA p.K1964fs*5 Deletion - Frameshift 5:177280829-177280829 + CSCC-7-T COSM4571112 c.3862T>A p.Y1288N Substitution - Missense 5:177235886-177235886 + Gp5D COSM3341145 c.4347T>C p.C1449C Substitution - coding silent 5:177244239-177244239 + TCGA-AO-A03M-01 COSM3827759 c.5932G>A p.E1978K Substitution - Missense 5:177282504-177282504 + TCGA-CG-4442-01 COSM3853957 c.3579T>C p.S1193S Substitution - coding silent 5:177211978-177211978 + TCGA-P4-A5EB-01 COSM3994211 c.6651G>T p.E2217D Substitution - Missense 5:177294019-177294019 + PD8934a COSM4384086 c.5198G>A p.C1733Y Substitution - Missense 5:177267613-177267613 + TCGA-EP-A26S-01 COSM4913547 c.60G>A p.V20V Substitution - coding silent 5:177135163-177135163 + TCGA-B5-A0JR-01 COSM1066311 c.7391G>A p.R2464H Substitution - Missense 5:177294759-177294759 + PT37 COSM5918714 c.1114C>T p.P372S Substitution - Missense 5:177204170-177204170 + SNUH_G76_S1 COSM4418708 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + 2492702 COSM3341242 c.6924C>T p.S2308S Substitution - coding silent 5:177294292-177294292 + 2218465 COSM4421341 c.5842C>T p.R1948C Substitution - Missense 5:177280784-177280784 + 587228 COSM1217935 c.5785G>T p.G1929W Substitution - Missense 5:177280727-177280727 + TCGA-EE-A3J4-06 COSM3919742 c.2858C>T p.S953F Substitution - Missense 5:177211257-177211257 + TCGA-F4-6570-01 COSM3696843 c.5565A>T p.R1855S Substitution - Missense 5:177273727-177273727 + SJACT001_D COSM4967907 c.361C>T p.P121S Substitution - Missense 5:177135464-177135464 + TCGA-BR-6565-01 COSM3853951 c.1732G>T p.A578S Substitution - Missense 5:177210131-177210131 + SW480 COSM4655942 c.3018T>A p.P1006P Substitution - coding silent 5:177211417-177211417 + TCGA-DK-A1AC-01 COSM1311004 c.460G>C p.E154Q Substitution - Missense 5:177135563-177135563 + 1346 COSM1644834 c.4289G>C p.G1430A Substitution - Missense 5:177239852-177239852 + OSCC-GB_00110111 COSM3715045 c.1549C>T p.Q517* Substitution - Nonsense 5:177209948-177209948 + 2296_T COSM3947299 c.628G>C p.E210Q Substitution - Missense 5:177135731-177135731 + SH-9771 COSM4419702 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + 30997 COSM5038862 c.6664_6665ins18 p.P2230_G2231insPVPLPP Insertion - In frame 5:177294032-177294033 + 381 COSM4426525 c.4378+1_4378+4delGTGA p.? Unknown 5:177244271-177244274 + TCGA-FU-A2QG-01 COSM4849032 c.1930G>A p.D644N Substitution - Missense 5:177210329-177210329 + SH-1641 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + YUKAT COSM5403159 c.5770G>A p.V1924M Substitution - Missense 5:177280712-177280712 + SNUH_G76_S1 COSM4419035 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + TCGA-BS-A0UV-01 COSM1066227 c.2802C>A p.V934V Substitution - coding silent 5:177211201-177211201 + LC_S51 COSM1186910 c.3706G>A p.V1236I Substitution - Missense 5:177212105-177212105 + TCGA-AR-A256-01 COSM1486626 c.12C>T p.T4T Substitution - coding silent 5:177135115-177135115 + HCC2998 COSM3341131 c.3844T>G p.L1282V Substitution - Missense 5:177235868-177235868 + TCGA-FP-7829-01 COSM3853953 c.2927C>A p.A976D Substitution - Missense 5:177211326-177211326 + CSCC-29-T COSM4518629 c.7244_7245CC>TT p.S2415F Substitution - Missense 5:177294612-177294613 + TCGA-FU-A2QG-01 COSM4849129 c.2532G>A p.E844E Substitution - coding silent 5:177210931-177210931 + CN-AML-CR-63-Dx COSM5019785 c.3705T>C p.N1235N Substitution - coding silent 5:177212104-177212104 + ESCC-128T COSM3941255 c.135G>C p.G45G Substitution - coding silent 5:177135238-177135238 + TCGA-AX-A0J0-01 COSM1066225 c.2297C>T p.S766L Substitution - Missense 5:177210696-177210696 + TCGA-BR-4184-01 COSM3341123 c.3598C>T p.R1200W Substitution - Missense 5:177211997-177211997 + TCGA-B2-4099-01 COSM482572 c.4189C>G p.P1397A Substitution - Missense 5:177238504-177238504 + TCGA-BR-8680-01 COSM3853949 c.1405G>T p.D469Y Substitution - Missense 5:177209804-177209804 + S00501 COSM313373 c.6898G>A p.A2300T Substitution - Missense 5:177294266-177294266 + SH-1641 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + RMS80_ COSM4418709 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + TCGA-D1-A17Q-01 COSM1066308 c.7055G>T p.R2352I Substitution - Missense 5:177294423-177294423 + Pat_41_B COSM5868233 c.6649G>A p.E2217K Substitution - Missense 5:177294017-177294017 + TCGA-BS-A0UF-01 COSM1066222 c.2007C>T p.F669F Substitution - coding silent 5:177210406-177210406 + BD199T COSM3661732 c.7240T>G p.L2414V Substitution - Missense 5:177294608-177294608 + 016-0040-02TD COSM145694 c.6085A>G p.T2029A Substitution - Missense 5:177283862-177283862 + CCK81 COSM3341071 c.2428T>C p.C810R Substitution - Missense 5:177210827-177210827 + YUFIT COSM5403154 c.4153_4154CC>TT p.P1385F Substitution - Missense 5:177238468-177238469 + S06-19548-TP COSM4992305 c.7443G>C p.E2481D Substitution - Missense 5:177294811-177294811 + SC_9047 COSM5561000 c.114T>A p.N38K Substitution - Missense 5:177135217-177135217 + TCGA-29-1691-01 COSM1328885 c.6152-2A>C p.? Unknown 5:177288817-177288817 + 2011-2318:2012-356-T COSM4603761 c.2400delG p.A801fs*6 Deletion - Frameshift 5:177210799-177210799 + 587376 COSM1217947 c.3742G>A p.E1248K Substitution - Missense 5:177212141-177212141 + DLBCL793 COSM1581357 c.2203G>A p.A735T Substitution - Missense 5:177210602-177210602 + PD6962a COSM4384098 c.7367T>C p.M2456T Substitution - Missense 5:177294735-177294735 + XHDG04 COSM4767675 c.7438G>A p.D2480N Substitution - Missense 5:177294806-177294806 + TCGA-A5-A0VP-01 COSM1066252 c.3817C>T p.R1273C Substitution - Missense 5:177235841-177235841 + TCGA-B5-A11R-01 COSM1066190 c.641C>T p.T214I Substitution - Missense 5:177135744-177135744 + TCGA-BR-6452-01 COSM3853975 c.5680C>T p.R1894C Substitution - Missense 5:177280622-177280622 + RMS88_ COSM4988879 c.3106G>C p.A1036P Substitution - Missense 5:177211505-177211505 + S22_post COSM5574825 c.7163C>T p.P2388L Substitution - Missense 5:177294531-177294531 + tumor_4149246 COSM5950213 c.4967G>T p.G1656V Substitution - Missense 5:177259989-177259989 + TCGA-29-1777-01 COSM1328890 c.290T>A p.F97Y Substitution - Missense 5:177135393-177135393 + SH-0348 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-EE-A2GC-06 COSM3614512 c.5448G>A p.M1816I Substitution - Missense 5:177269746-177269746 + B35-Tumor COSM1754202 c.7503G>A p.P2501P Substitution - coding silent 5:177294871-177294871 + SH-3776 COSM4159760 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + BN33T COSM1620094 c.7224C>T p.D2408D Substitution - coding silent 5:177294592-177294592 + TCGA-A5-A0GA-01 COSM1066240 c.3430G>A p.E1144K Substitution - Missense 5:177211829-177211829 + SS6003109 COSM3965625 c.6280G>A p.E2094K Substitution - Missense 5:177291975-177291975 + SH-9161 COSM4418708 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + LUAD-S00488 COSM395298 c.2049G>A p.K683K Substitution - coding silent 5:177210448-177210448 + TCGA-D1-A17Q-01 COSM1066309 c.7055G>T p.R2352I Substitution - Missense 5:177294423-177294423 + HCC118T COSM1620092 c.3920A>C p.K1307T Substitution - Missense 5:177235944-177235944 + PD8936a COSM4384083 c.4049C>T p.P1350L Substitution - Missense 5:177238364-177238364 + TCGA-EP-A2KA-01 COSM4917374 c.7992T>C p.S2664S Substitution - coding silent 5:177295360-177295360 + TCGA-BR-8363-01 COSM3341247 c.7067C>T p.T2356M Substitution - Missense 5:177294435-177294435 + SH-9248 COSM4419035 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + TCGA-AN-A046-01 COSM3827767 c.6654C>T p.I2218I Substitution - coding silent 5:177294022-177294022 + PD6278a COSM4384056 c.1558G>A p.A520T Substitution - Missense 5:177209957-177209957 + ESCC-159T COSM3941257 c.5726C>G p.S1909C Substitution - Missense 5:177280668-177280668 + 502635 COSM5702597 c.7147G>T p.G2383C Substitution - Missense 5:177294515-177294515 + TCGA-BR-4184-01 COSM3341139 c.4050G>A p.P1350P Substitution - coding silent 5:177238365-177238365 + I2L-P19Ta-Tumor-Organoid COSM4585723 c.1149C>T p.I383I Substitution - coding silent 5:177204205-177204205 + SH-9161 COSM4419702 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + SH-3133 COSM4419701 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + RMS88_ COSM4988880 c.6750G>A p.M2250I Substitution - Missense 5:177294118-177294118 + S00501 COSM313374 c.6898G>A p.A2300T Substitution - Missense 5:177294266-177294266 + TCGA-BR-8363-01 COSM3341246 c.7067C>T p.T2356M Substitution - Missense 5:177294435-177294435 + TCGA-FU-A2QG-01 COSM4849166 c.2017G>C p.E673Q Substitution - Missense 5:177210416-177210416 + TCGA-D9-A4Z3-01 COSM3614504 c.3265G>A p.D1089N Substitution - Missense 5:177211664-177211664 + TCGA-18-4721-01 COSM737610 c.2016A>T p.T672T Substitution - coding silent 5:177210415-177210415 + 2T COSM3715046 c.2873C>T p.S958L Substitution - Missense 5:177211272-177211272 + PD6914a COSM4384053 c.1126G>T p.A376S Substitution - Missense 5:177204182-177204182 + SH-7282 COSM4419702 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + CN-AML-CR-63-Dx COSM5019784 c.3705T>C p.N1235N Substitution - coding silent 5:177212104-177212104 + ESO-077 COSM1259598 c.255G>A p.E85E Substitution - coding silent 5:177135358-177135358 + 2492730 COSM5729308 c.1367C>T p.P456L Substitution - Missense 5:177209766-177209766 + TCGA-D1-A15X-01 COSM1066288 c.5740C>T p.R1914C Substitution - Missense 5:177280682-177280682 + TCGA-B5-A0JY-01 COSM1066230 c.3100T>G p.F1034V Substitution - Missense 5:177211499-177211499 + CHEWS024 COSM4585723 c.1149C>T p.I383I Substitution - coding silent 5:177204205-177204205 + TCGA-B4-5838-01 COSM1496038 c.4871C>A p.P1624Q Substitution - Missense 5:177257056-177257056 + 1N49-VS-1T49 COSM4976476 c.6013C>T p.R2005* Substitution - Nonsense 5:177283790-177283790 + TCGA-34-5927-01 COSM737592 c.5332C>T p.R1778* Substitution - Nonsense 5:177269630-177269630 + 2172 COSM5011555 c.5671G>T p.E1891* Substitution - Nonsense 5:177280613-177280613 + PD8934a COSM4384087 c.5198G>A p.C1733Y Substitution - Missense 5:177267613-177267613 + TCGA-AP-A0LM-01 COSM1066213 c.1634C>T p.T545M Substitution - Missense 5:177210033-177210033 + ccRCC-4 COSM1663152 c.5369A>G p.D1790G Substitution - Missense 5:177269667-177269667 + S08-41239-TP COSM4992292 c.1192C>T p.L398F Substitution - Missense 5:177204248-177204248 + GC8_T COSM150018 c.339C>T p.C113C Substitution - coding silent 5:177135442-177135442 + MD-289 COSM302776 c.5910G>C p.E1970D Substitution - Missense 5:177282482-177282482 + CCC64T COSM3661731 c.7240T>G p.L2414V Substitution - Missense 5:177294608-177294608 + 390 COSM4427849 c.5965C>A p.Q1989K Substitution - Missense 5:177282537-177282537 + PT48 COSM5931697 c.6542C>T p.S2181F Substitution - Missense 5:177293910-177293910 + PD6110a COSM4384088 c.6323delG p.T2109fs*41 Deletion - Frameshift 5:177292018-177292018 + pfg043T COSM4763646 c.2332T>G p.L778V Substitution - Missense 5:177210731-177210731 + PD6872a COSM4384079 c.3361A>G p.K1121E Substitution - Missense 5:177211760-177211760 + CSB1 COSM5026461 c.3781G>A p.E1261K Substitution - Missense 5:177212180-177212180 + TCGA-BR-8363-01 COSM3853987 c.7402C>T p.R2468W Substitution - Missense 5:177294770-177294770 + T3118 COSM4708349 c.3035G>A p.R1012H Substitution - Missense 5:177211434-177211434 + HX30T COSM3661730 c.4680T>G p.A1560A Substitution - coding silent 5:177251768-177251768 + TCGA-D1-A17M-01 COSM1066284 c.5617A>G p.I1873V Substitution - Missense 5:177273779-177273779 + TCGA-A5-A0GP-01 COSM1066299 c.6050G>A p.R2017Q Substitution - Missense 5:177283827-177283827 + 587376 COSM1217945 c.1025G>A p.C342Y Substitution - Missense 5:177191981-177191981 + ESO-077 COSM1259599 c.255G>A p.E85E Substitution - coding silent 5:177135358-177135358 + HT COSM1581353 c.1544A>T p.H515L Substitution - Missense 5:177209943-177209943 + T3225 COSM3341235 c.6595C>T p.R2199C Substitution - Missense 5:177293963-177293963 + TCGA-BR-8363-01 COSM3853986 c.7402C>T p.R2468W Substitution - Missense 5:177294770-177294770 + 385 COSM4427013 c.499G>C p.E167Q Substitution - Missense 5:177135602-177135602 + SW1222 COSM4654919 c.2715C>A p.Y905* Substitution - Nonsense 5:177211114-177211114 + TCGA-F5-6814-01 COSM3429309 c.3537G>T p.E1179D Substitution - Missense 5:177211936-177211936 + SH-1679 COSM4419701 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + SH-5693 COSM4419701 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + PD6788a COSM4384061 c.1976A>G p.D659G Substitution - Missense 5:177210375-177210375 + GHE0536 COSM5713881 c.6157G>A p.E2053K Substitution - Missense 5:177288824-177288824 + H650 COSM1194585 c.3331G>T p.D1111Y Substitution - Missense 5:177211730-177211730 + TCGA-DM-A28C-01 COSM1436260 c.2796C>G p.N932K Substitution - Missense 5:177211195-177211195 + TCGA-D9-A6EC-06 COSM4406162 c.823A>C p.N275H Substitution - Missense 5:177135926-177135926 + TCGA-66-2786-01 COSM737599 c.4411C>T p.R1471* Substitution - Nonsense 5:177246710-177246710 + TCGA-AH-6644-01 COSM1567766 c.5432G>A p.R1811Q Substitution - Missense 5:177269730-177269730 + Pat_41_B COSM5868234 c.6649G>A p.E2217K Substitution - Missense 5:177294017-177294017 + TCGA-B0-4710-01 COSM482578 c.7980G>A p.Q2660Q Substitution - coding silent 5:177295348-177295348 + HCC2998 COSM1672145 c.3363A>C p.K1121N Substitution - Missense 5:177211762-177211762 + PD7038a COSM4384097 c.6968C>T p.A2323V Substitution - Missense 5:177294336-177294336 + TCGA-JX-A3Q0-01 COSM4824356 c.6897C>T p.L2299L Substitution - coding silent 5:177294265-177294265 + SH-7329 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-BR-4201-01 COSM3853967 c.4759C>T p.R1587C Substitution - Missense 5:177251847-177251847 + TCGA-E2-A2P5-01 COSM3827757 c.5763C>G p.H1921Q Substitution - Missense 5:177280705-177280705 + TCGA-AP-A0LM-01 COSM1066255 c.3965G>A p.R1322Q Substitution - Missense 5:177238280-177238280 + CHC1754T COSM4792837 c.3658G>C p.E1220Q Substitution - Missense 5:177212057-177212057 + TCGA-D1-A15X-01 COSM1066287 c.5740C>T p.R1914C Substitution - Missense 5:177280682-177280682 + T3225 COSM3341234 c.6595C>T p.R2199C Substitution - Missense 5:177293963-177293963 + TCGA-D9-A6EA-06 COSM4397800 c.1191C>T p.V397V Substitution - coding silent 5:177204247-177204247 + ZZUFHECRKL-G045T COSM4419034 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + SH-7282 COSM4987203 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + B106 COSM1754196 c.2483C>T p.S828F Substitution - Missense 5:177210882-177210882 + TCGA-AZ-4315-01 COSM276400 c.1176C>T p.F392F Substitution - coding silent 5:177204232-177204232 + RMS85_ COSM4988878 c.3106G>C p.A1036P Substitution - Missense 5:177211505-177211505 + PD6965a COSM4384054 c.1544A>G p.H515R Substitution - Missense 5:177209943-177209943 + SH-3458 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + 2P3 COSM3733670 c.6431C>T p.A2144V Substitution - Missense 5:177292126-177292126 + PT27 COSM5905627 c.6010G>A p.D2004N Substitution - Missense 5:177283787-177283787 + HN_62739 COSM124865 c.5177C>A p.P1726H Substitution - Missense 5:177267592-177267592 + CHC2103T COSM4952543 c.6044A>G p.Y2015C Substitution - Missense 5:177283821-177283821 + TCGA-FU-A2QG-01 COSM4849143 c.2592G>A p.L864L Substitution - coding silent 5:177210991-177210991 + PT08_2 COSM5893068 c.3133C>T p.R1045C Substitution - Missense 5:177211532-177211532 + SCMC_RM2_ COSM4987203 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + Gp5D COSM3341144 c.4347T>C p.C1449C Substitution - coding silent 5:177244239-177244239 + TCGA-AA-A00N-01 COSM276403 c.2183T>C p.V728A Substitution - Missense 5:177210582-177210582 + PD6125a COSM4384077 c.3330C>A p.F1110L Substitution - Missense 5:177211729-177211729 + TCGA-B5-A0JZ-01 COSM1066302 c.6380C>T p.A2127V Substitution - Missense 5:177292075-177292075 + TCGA-AG-3892-01 COSM257563 c.722G>T p.R241I Substitution - Missense 5:177135825-177135825 + TCGA-HU-A4GT-01 COSM3853982 c.6464-2A>G p.? Unknown 5:177293830-177293830 + BD199T COSM3661731 c.7240T>G p.L2414V Substitution - Missense 5:177294608-177294608 + ccRCC-4 COSM1663151 c.5369A>G p.D1790G Substitution - Missense 5:177269667-177269667 + H650 COSM1194435 c.1954A>G p.I652V Substitution - Missense 5:177210353-177210353 + TCGA-EE-A29V-06 COSM3614492 c.103G>A p.G35S Substitution - Missense 5:177135206-177135206 + TCGA-D1-A167-01 COSM1066199 c.1001G>A p.R334H Substitution - Missense 5:177191957-177191957 + CHC205T COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + 863TCS COSM673683 c.6653T>C p.I2218T Substitution - Missense 5:177294021-177294021 + RMS88_ COSM4418709 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + TCGA-FW-A3R5-06 COSM3919744 c.5389C>T p.L1797F Substitution - Missense 5:177269687-177269687 + TCGA-AA-A010-01 COSM283396 c.4163A>C p.E1388A Substitution - Missense 5:177238478-177238478 + SH-7166 COSM4159760 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + TCGA-AZ-4315-01 COSM276401 c.1176C>T p.F392F Substitution - coding silent 5:177204232-177204232 + S10-44607-TP COSM4642984 c.5580C>T p.D1860D Substitution - coding silent 5:177273742-177273742 + TCGA-FU-A2QG-01 COSM4849037 c.2898G>A p.E966E Substitution - coding silent 5:177211297-177211297 + DLBCL1055 COSM1582040 c.5356_5360delAAGAT p.K1786fs*3 Deletion - Frameshift 5:177269654-177269658 + CSCC-44-T COSM4517578 c.3760_3761CC>TT p.P1254F Substitution - Missense 5:177212159-177212160 + SH-9161 COSM4987203 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + AOCS-164-1-7 COSM4422182 c.2596G>C p.E866Q Substitution - Missense 5:177210995-177210995 + ML_103_T_01 COSM4159760 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + TCGA-AC-A23H-01 COSM3827755 c.4746C>G p.I1582M Substitution - Missense 5:177251834-177251834 + TCGA-GN-A266-06 COSM3614499 c.2612C>T p.S871F Substitution - Missense 5:177211011-177211011 + TCGA-EE-A2GC-06 COSM3614511 c.5448G>A p.M1816I Substitution - Missense 5:177269746-177269746 + TCGA-B8-5546-01 COSM482575 c.5145A>G p.E1715E Substitution - coding silent 5:177260167-177260167 + TCGA-29-1691-01 COSM1328886 c.6152-2A>C p.? Unknown 5:177288817-177288817 + MedB-1 COSM5621405 c.6451A>G p.K2151E Substitution - Missense 5:177292146-177292146 + 108 COSM5016853 c.2781G>C p.L927F Substitution - Missense 5:177211180-177211180 + TCGA-AG-A002-01 COSM262473 c.4366G>T p.D1456Y Substitution - Missense 5:177244258-177244258 + T3236 COSM4708346 c.2586C>T p.S862S Substitution - coding silent 5:177210985-177210985 + PT32 COSM5907362 c.7097G>A p.G2366D Substitution - Missense 5:177294465-177294465 + HX30T COSM3661729 c.4680T>G p.A1560A Substitution - coding silent 5:177251768-177251768 + PD8936a COSM4384082 c.4049C>T p.P1350L Substitution - Missense 5:177238364-177238364 + YUKAT COSM5403150 c.3345G>A p.K1115K Substitution - coding silent 5:177211744-177211744 + PT08_2 COSM5893065 c.3132C>A p.N1044K Substitution - Missense 5:177211531-177211531 + B104-0 COSM1754205 c.7740G>A p.A2580A Substitution - coding silent 5:177295108-177295108 + HCT15 COSM1672148 c.7875G>T p.W2625C Substitution - Missense 5:177295243-177295243 + TCGA-AX-A0J0-01 COSM1066224 c.2297C>T p.S766L Substitution - Missense 5:177210696-177210696 + 2011-2311:2012-362-T COSM4605164 c.3394G>T p.G1132* Substitution - Nonsense 5:177211793-177211793 + PD2170a COSM26994 c.6879A>G p.L2293L Substitution - coding silent 5:177294247-177294247 + TCGA-AA-A010-01 COSM283389 c.29G>T p.R10I Substitution - Missense 5:177135132-177135132 + TCGA-A6-6781-01 COSM1436268 c.4569C>T p.P1523P Substitution - coding silent 5:177248252-177248252 + TCGA-A6-6781-01 COSM1436269 c.4569C>T p.P1523P Substitution - coding silent 5:177248252-177248252 + T3094 COSM4708355 c.6850G>T p.E2284* Substitution - Nonsense 5:177294218-177294218 + PT24_1 COSM5904252 c.4121C>T p.S1374F Substitution - Missense 5:177238436-177238436 + 587376 COSM1217944 c.1025G>A p.C342Y Substitution - Missense 5:177191981-177191981 + SH-102782 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + J88_T COSM3947303 c.2861A>T p.K954M Substitution - Missense 5:177211260-177211260 + 2T COSM3715047 c.2873C>T p.S958L Substitution - Missense 5:177211272-177211272 + SW480 COSM4655941 c.3018T>A p.P1006P Substitution - coding silent 5:177211417-177211417 + 385 COSM4427012 c.499G>C p.E167Q Substitution - Missense 5:177135602-177135602 + TCGA-G4-6304-01 COSM1436254 c.709delA p.N238fs*23 Deletion - Frameshift 5:177135812-177135812 + TCGA-BR-4368-01 COSM3853963 c.4395T>C p.F1465F Substitution - coding silent 5:177246694-177246694 + TCGA-HU-A4H3-01 COSM3853978 c.6116G>A p.R2039H Substitution - Missense 5:177283893-177283893 + 12924 COSM5617279 c.4766-10G>A p.? Unknown 5:177256941-177256941 + SH-7166 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + 2011-2280:2012-366-T COSM4605276 c.3921+2T>C p.? Unknown 5:177235947-177235947 + TCGA-24-1422-01 COSM71885 c.7259C>G p.P2420R Substitution - Missense 5:177294627-177294627 + 11T COSM3715045 c.1549C>T p.Q517* Substitution - Nonsense 5:177209948-177209948 + TCGA-AP-A056-01 COSM1066246 c.3535G>T p.E1179* Substitution - Nonsense 5:177211934-177211934 + TCGA-FU-A2QG-01 COSM4849078 c.1927G>A p.D643N Substitution - Missense 5:177210326-177210326 + SCC-9 COSM3341174 c.4966G>T p.G1656C Substitution - Missense 5:177257151-177257151 + LUAD-D01382 COSM337161 c.2105C>A p.P702H Substitution - Missense 5:177210504-177210504 + I2L-P19Ta-Tumor-Biopsy COSM4585724 c.1149C>T p.I383I Substitution - coding silent 5:177204205-177204205 + TCGA-AH-6644-01 COSM1567767 c.5432G>A p.R1811Q Substitution - Missense 5:177269730-177269730 + TCGA-DM-A0XD-01 COSM1436283 c.6430G>A p.A2144T Substitution - Missense 5:177292125-177292125 + HCC118T COSM1620091 c.3920A>C p.K1307T Substitution - Missense 5:177235944-177235944 + TCGA-B4-5838-01 COSM1496039 c.4871C>A p.P1624Q Substitution - Missense 5:177257056-177257056 + TCGA-EV-5903-01 COSM3994206 c.3642T>C p.L1214L Substitution - coding silent 5:177212041-177212041 + LUAD-D01382 COSM337162 c.2105C>A p.P702H Substitution - Missense 5:177210504-177210504 + SC_9008 COSM5548840 c.5180C>T p.A1727V Substitution - Missense 5:177267595-177267595 + EGC15 COSM5060968 c.6596G>A p.R2199H Substitution - Missense 5:177293964-177293964 + Pat_40_B COSM5868226 c.1196G>A p.R399K Substitution - Missense 5:177204252-177204252 + TCGA-FS-A1ZC-06 COSM3614498 c.2111T>A p.I704N Substitution - Missense 5:177210510-177210510 + TCGA-DK-A1A7-01 COSM420767 c.5719A>G p.I1907V Substitution - Missense 5:177280661-177280661 + SH-0348 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-BS-A0UV-01 COSM1066258 c.4467T>C p.D1489D Substitution - coding silent 5:177246766-177246766 + TCGA-B5-A0JR-01 COSM1066312 c.7391G>A p.R2464H Substitution - Missense 5:177294759-177294759 + LIM2405 COSM4642983 c.5580C>T p.D1860D Substitution - coding silent 5:177273742-177273742 + TCGA-BR-4201-01 COSM3853984 c.7180A>G p.I2394V Substitution - Missense 5:177294548-177294548 + TCGA-AX-A060-01 COSM1066263 c.4621C>G p.L1541V Substitution - Missense 5:177248304-177248304 + TCGA-C5-A7UH-01 COSM4856830 c.3406G>A p.E1136K Substitution - Missense 5:177211805-177211805 + TCGA-AA-A010-01 COSM283397 c.4163A>C p.E1388A Substitution - Missense 5:177238478-177238478 + SH-1679 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + C086 COSM5535718 c.4027C>T p.P1343S Substitution - Missense 5:177238342-177238342 + 2492700 COSM3341243 c.6924C>T p.S2308S Substitution - coding silent 5:177294292-177294292 + TCGA-F4-6570-01 COSM3696844 c.5565A>T p.R1855S Substitution - Missense 5:177273727-177273727 + TCGA-34-5231-01 COSM737609 c.2620G>T p.E874* Substitution - Nonsense 5:177211019-177211019 + TCGA-BR-8676-01 COSM3853981 c.6317A>T p.K2106M Substitution - Missense 5:177292012-177292012 + TCGA-AX-A05Z-01 COSM1066291 c.5900T>G p.F1967C Substitution - Missense 5:177282472-177282472 + PD6125a COSM4384076 c.3330C>A p.F1110L Substitution - Missense 5:177211729-177211729 + 587342 COSM1217942 c.6199A>G p.K2067E Substitution - Missense 5:177288866-177288866 + CSCC-55-T COSM4554082 c.6107G>A p.G2036E Substitution - Missense 5:177283884-177283884 + T2284 COSM4708351 c.3348A>G p.Q1116Q Substitution - coding silent 5:177211747-177211747 + TCGA-FU-A2QG-01 COSM4849112 c.1874G>C p.G625A Substitution - Missense 5:177210273-177210273 + TCGA-FU-A2QG-01 COSM4849102 c.2201A>G p.K734R Substitution - Missense 5:177210600-177210600 + TCGA-AX-A060-01 COSM1066264 c.4621C>G p.L1541V Substitution - Missense 5:177248304-177248304 + OSCC-GB_00110111 COSM3715049 c.5431C>T p.R1811* Substitution - Nonsense 5:177269729-177269729 + SH-3133 COSM4159760 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + RKO COSM3341250 c.7130A>C p.K2377T Substitution - Missense 5:177294498-177294498 + TCGA-D8-A1XK-01 COSM3827762 c.6440T>G p.L2147R Substitution - Missense 5:177292135-177292135 + TCGA-C5-A7UH-01 COSM4856731 c.1450G>C p.E484Q Substitution - Missense 5:177209849-177209849 + B86-Tumor COSM4005987 c.6782T>C p.M2261T Substitution - Missense 5:177294150-177294150 + TCGA-AO-A03M-01 COSM3827758 c.5932G>A p.E1978K Substitution - Missense 5:177282504-177282504 + TCGA-DM-A28C-01 COSM1436261 c.2796C>G p.N932K Substitution - Missense 5:177211195-177211195 + TCGA-CD-A4MI-01 COSM3853965 c.4488A>G p.P1496P Substitution - coding silent 5:177246787-177246787 + SH-9248 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + PDA_097 COSM5003315 c.4024C>A p.P1342T Substitution - Missense 5:177238339-177238339 + TCGA-CD-A4MG-01 COSM3853988 c.7635G>T p.K2545N Substitution - Missense 5:177295003-177295003 + Pat_41_B COSM5868227 c.1722delA p.N576fs*23 Deletion - Frameshift 5:177210121-177210121 + TCGA-FR-A3YO-06 COSM3614513 c.6031C>T p.P2011S Substitution - Missense 5:177283808-177283808 + HN_63095 COSM124866 c.5951G>A p.R1984Q Substitution - Missense 5:177282523-177282523 + SCC-9 COSM3341175 c.4966G>T p.G1656C Substitution - Missense 5:177257151-177257151 + TCGA-B5-A0JZ-01 COSM1066233 c.3205C>T p.Q1069* Substitution - Nonsense 5:177211604-177211604 + SH-1439 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + SH-1679 COSM4419035 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + TCGA-BS-A0UV-01 COSM1066257 c.4467T>C p.D1489D Substitution - coding silent 5:177246766-177246766 + RMS110_ COSM4987204 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + TCGA-RC-A7SF-01 COSM4923149 c.215T>G p.L72R Substitution - Missense 5:177135318-177135318 + Gp2D COSM3341163 c.4774A>G p.T1592A Substitution - Missense 5:177256959-177256959 + SH-4435 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + SH-7282 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + MedB-1 COSM5621402 c.508C>A p.P170T Substitution - Missense 5:177135611-177135611 + RKO COSM3341197 c.5392delT p.F1799fs*22 Deletion - Frameshift 5:177269690-177269690 + TCGA-A3-3374-01 COSM1496040 c.3032G>C p.S1011T Substitution - Missense 5:177211431-177211431 + TCGA-F5-6814-01 COSM3429308 c.3537G>T p.E1179D Substitution - Missense 5:177211936-177211936 + TCGA-AA-A010-01 COSM283393 c.3639A>G p.I1213M Substitution - Missense 5:177212038-177212038 + TCGA-BS-A0TA-01 COSM1066279 c.5423A>G p.H1808R Substitution - Missense 5:177269721-177269721 + CSB1 COSM5026460 c.3781G>A p.E1261K Substitution - Missense 5:177212180-177212180 + TCGA-BR-8676-01 COSM3853980 c.6317A>T p.K2106M Substitution - Missense 5:177292012-177292012 + TCGA-FR-A3YN-06 COSM3614508 c.5439C>T p.F1813F Substitution - coding silent 5:177269737-177269737 + ESCC-128T COSM3941256 c.135G>C p.G45G Substitution - coding silent 5:177135238-177135238 + 2012-703:2012-1309-T COSM4605653 c.5892+1G>T p.? Unknown 5:177280835-177280835 + TCGA-C5-A7UH-01 COSM4856760 c.1957G>A p.E653K Substitution - Missense 5:177210356-177210356 + pfg068T COSM4748092 c.5503delA p.A1837fs*12 Deletion - Frameshift 5:177269801-177269801 + T155 COSM1177185 c.1810C>T p.R604* Substitution - Nonsense 5:177210209-177210209 + PD6278a COSM4384057 c.1558G>A p.A520T Substitution - Missense 5:177209957-177209957 + S02339 COSM4386945 c.3140C>G p.A1047G Substitution - Missense 5:177211539-177211539 + GHE0536 COSM5713882 c.6157G>A p.E2053K Substitution - Missense 5:177288824-177288824 + ML_103_T_01 COSM4159761 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + RMS88_ COSM4005987 c.6782T>C p.M2261T Substitution - Missense 5:177294150-177294150 + RMS85_ COSM4005987 c.6782T>C p.M2261T Substitution - Missense 5:177294150-177294150 + RMS85_ COSM4988880 c.6750G>A p.M2250I Substitution - Missense 5:177294118-177294118 + CHEWS024 COSM4585724 c.1149C>T p.I383I Substitution - coding silent 5:177204205-177204205 + SC_9096 COSM1436262 c.2903A>G p.K968R Substitution - Missense 5:177211302-177211302 + T3105 COSM4708347 c.2766G>A p.T922T Substitution - coding silent 5:177211165-177211165 + 6115219 COSM5563362 c.5552A>G p.Q1851R Substitution - Missense 5:177273714-177273714 + B47-Tumor COSM1754198 c.3276G>C p.Q1092H Substitution - Missense 5:177211675-177211675 + TCGA-EJ-5496-01 COSM1132198 c.1471G>A p.E491K Substitution - Missense 5:177209870-177209870 + LP6005690-DNA_C02 COSM4411792 c.6078C>T p.N2026N Substitution - coding silent 5:177283855-177283855 + TCGA-FU-A2QG-01 COSM4849128 c.2532G>A p.E844E Substitution - coding silent 5:177210931-177210931 + TCGA-BG-A0M4-01 COSM1066203 c.1452A>G p.E484E Substitution - coding silent 5:177209851-177209851 + TCGA-18-4721-01 COSM737611 c.2016A>T p.T672T Substitution - coding silent 5:177210415-177210415 + TCGA-AP-A0LM-01 COSM1066317 c.7769C>T p.P2590L Substitution - Missense 5:177295137-177295137 + DLBCL793 COSM1581356 c.2203G>A p.A735T Substitution - Missense 5:177210602-177210602 + TCGA-EI-7002-01 COSM3429312 c.5122A>T p.S1708C Substitution - Missense 5:177260144-177260144 + TCGA-EE-A3JI-06 COSM3614519 c.7581G>A p.W2527* Substitution - Nonsense 5:177294949-177294949 + 30997 COSM5038863 c.6664_6665ins18 p.P2230_G2231insPVPLPP Insertion - In frame 5:177294032-177294033 + BK0002 COSM4185422 c.842A>G p.D281G Substitution - Missense 5:177135945-177135945 + 9227_T COSM5039403 c.5026G>A p.A1676T Substitution - Missense 5:177260048-177260048 + TCGA-AX-A0J0-01 COSM1066281 c.5604A>G p.P1868P Substitution - coding silent 5:177273766-177273766 + SW1222 COSM4654918 c.2715C>A p.Y905* Substitution - Nonsense 5:177211114-177211114 + TCGA-C5-A7UH-01 COSM4856607 c.3439G>A p.E1147K Substitution - Missense 5:177211838-177211838 + 587342 COSM1217943 c.6199A>G p.K2067E Substitution - Missense 5:177288866-177288866 + TCGA-CD-A4MG-01 COSM3853959 c.3730A>G p.I1244V Substitution - Missense 5:177212129-177212129 + TCGA-GF-A6C9-06 COSM4899495 c.1377C>T p.D459D Substitution - coding silent 5:177209776-177209776 + ESCC_BICR_001T COSM5440693 c.6262C>T p.Q2088* Substitution - Nonsense 5:177291957-177291957 + TCGA-BR-6565-01 COSM3853950 c.1732G>T p.A578S Substitution - Missense 5:177210131-177210131 + SJAMLM7011 COSM4776063 c.6656G>A p.R2219H Substitution - Missense 5:177294024-177294024 + PD6944a COSM4384044 c.638G>A p.S213N Substitution - Missense 5:177135741-177135741 + SH-1641 COSM5019444 c.3564G>C p.R1188S Substitution - Missense 5:177211963-177211963 + TCGA-AA-3713-01 COSM1436287 c.6738G>T p.Q2246H Substitution - Missense 5:177294106-177294106 + CHC1725T COSM4800691 c.2891A>G p.N964S Substitution - Missense 5:177211290-177211290 + TCGA-AA-A010-01 COSM283388 c.29G>T p.R10I Substitution - Missense 5:177135132-177135132 + AOCS-164-1-7 COSM4422181 c.2596G>C p.E866Q Substitution - Missense 5:177210995-177210995 + PT48 COSM136514 c.6542C>T p.S2181F Substitution - Missense 5:177293910-177293910 + DLD1 COSM1672148 c.7875G>T p.W2625C Substitution - Missense 5:177295243-177295243 + J76_T COSM3947305 c.3763A>T p.S1255C Substitution - Missense 5:177212162-177212162 + 1115154 COSM3341173 c.4961C>G p.S1654C Substitution - Missense 5:177257146-177257146 + SH-9248 COSM4419702 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + SNU-C4 COSM4653947 c.3058A>G p.N1020D Substitution - Missense 5:177211457-177211457 + SNU_09_S1 COSM4420027 c.3067C>A p.R1023R Substitution - coding silent 5:177211466-177211466 + TCGA-29-1777-01 COSM1328889 c.290T>A p.F97Y Substitution - Missense 5:177135393-177135393 + B104-0-Tumor COSM1754205 c.7740G>A p.A2580A Substitution - coding silent 5:177295108-177295108 + TCGA-AA-A010-01 COSM283391 c.1019G>T p.R340M Substitution - Missense 5:177191975-177191975 + TCGA-60-2724-01 COSM737597 c.4642-1G>C p.? Unknown 5:177251729-177251729 + PD7038a COSM4384096 c.6968C>T p.A2323V Substitution - Missense 5:177294336-177294336 + PT14_1 COSM5896768 c.2213T>C p.L738P Substitution - Missense 5:177210612-177210612 + PT36 COSM5915422 c.5147-7C>T p.? Unknown 5:177267555-177267555 + PT36 COSM5915423 c.5147-7C>T p.? Unknown 5:177267555-177267555 + TCGA-EI-6917-01 COSM3429310 c.5019T>G p.F1673L Substitution - Missense 5:177260041-177260041 + TCGA-CD-8536-01 COSM3853961 c.4127C>A p.P1376H Substitution - Missense 5:177238442-177238442 + PCSI_0161_Pa_P_526 COSM4965874 c.7652C>A p.P2551Q Substitution - Missense 5:177295020-177295020 + TCGA-BR-6452-01 COSM3853971 c.5199C>T p.C1733C Substitution - coding silent 5:177267614-177267614 + RMS110_ COSM4418709 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + 2011-2292:2012-324-T COSM4603937 c.5391_5392insT p.G1800fs*3 Insertion - Frameshift 5:177269689-177269690 + TCGA-BT-A20T-01 COSM420765 c.6850G>C p.E2284Q Substitution - Missense 5:177294218-177294218 + PD6967a COSM4384085 c.4858G>A p.V1620I Substitution - Missense 5:177257043-177257043 + TCGA-06-2563-01 COSM2152856 c.2905G>A p.G969R Substitution - Missense 5:177211304-177211304 + 489 COSM3697158 c.5950C>T p.R1984* Substitution - Nonsense 5:177282522-177282522 + SH-3133 COSM5019785 c.3705T>C p.N1235N Substitution - coding silent 5:177212104-177212104 + SH-1679 COSM4159761 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + TCGA-FU-A2QG-01 COSM4849038 c.2898G>A p.E966E Substitution - coding silent 5:177211297-177211297 + PD6965a COSM4384055 c.1544A>G p.H515R Substitution - Missense 5:177209943-177209943 + TCGA-D3-A5GO-06 COSM3614494 c.328C>T p.P110S Substitution - Missense 5:177135431-177135431 + TCGA-AM-5821-01 COSM3697155 c.682C>G p.P228A Substitution - Missense 5:177135785-177135785 + SS6003109 COSM3965624 c.6280G>A p.E2094K Substitution - Missense 5:177291975-177291975 + CML015T COSM5802638 c.113A>G p.N38S Substitution - Missense 5:177135216-177135216 + HN_00378 COSM127160 c.4192+1G>T p.? Unknown 5:177238508-177238508 + SH-7166 COSM5020618 c.4522G>T p.A1508S Substitution - Missense 5:177248205-177248205 + 17802 COSM5346171 c.4036delG p.E1346fs*26 Deletion - Frameshift 5:177238351-177238351 + TCGA-AP-A0LM-01 COSM1066249 c.3747G>T p.K1249N Substitution - Missense 5:177212146-177212146 + PD6822a COSM4384092 c.6673C>T p.P2225S Substitution - Missense 5:177294041-177294041 + SH-1679 COSM4987203 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + 2296_T COSM3947300 c.628G>C p.E210Q Substitution - Missense 5:177135731-177135731 + TCGA-G2-A2EL-01 COSM1311009 c.3388G>C p.E1130Q Substitution - Missense 5:177211787-177211787 + TCGA-AP-A0LM-01 COSM1066212 c.1634C>T p.T545M Substitution - Missense 5:177210033-177210033 + K176 COSM249593 c.3835A>C p.K1279Q Substitution - Missense 5:177235859-177235859 + B86-Tumor COSM4005988 c.6782T>C p.M2261T Substitution - Missense 5:177294150-177294150 + BD120T COSM5514635 c.1084C>T p.R362W Substitution - Missense 5:177204140-177204140 + TCGA-AP-A056-01 COSM1066194 c.812T>C p.L271S Substitution - Missense 5:177135915-177135915 + YUKAT COSM5403158 c.5770G>A p.V1924M Substitution - Missense 5:177280712-177280712 + pfg008T COSM1642693 c.5887delA p.K1964fs*5 Deletion - Frameshift 5:177280829-177280829 + TCGA-22-4595-01 COSM737607 c.2919G>C p.Q973H Substitution - Missense 5:177211318-177211318 + B89-12-Tumor COSM4005986 c.776C>T p.S259L Substitution - Missense 5:177135879-177135879 + TCGA-DK-A1AC-01 COSM1311015 c.7104C>G p.A2368A Substitution - coding silent 5:177294472-177294472 + TCGA-DK-A1AE-01 COSM1311012 c.5951G>T p.R1984L Substitution - Missense 5:177282523-177282523 + TCGA-D1-A103-01 COSM1066206 c.1483G>A p.A495T Substitution - Missense 5:177209882-177209882 + B104-0-Tumor COSM1754204 c.7740G>A p.A2580A Substitution - coding silent 5:177295108-177295108 + UM-SCC-17B COSM4598375 c.6062A>G p.H2021R Substitution - Missense 5:177283839-177283839 + LS411 COSM3341148 c.4421A>C p.Q1474P Substitution - Missense 5:177246720-177246720 + TCGA-EK-A2RC-01 COSM4848495 c.5036C>A p.S1679* Substitution - Nonsense 5:177260058-177260058 + TCGA-D8-A27P-01 COSM1486629 c.2503G>T p.G835C Substitution - Missense 5:177210902-177210902 + TCGA-EA-A1QT-01 COSM462002 c.5036C>G p.S1679* Substitution - Nonsense 5:177260058-177260058 + CHC1754T COSM4792836 c.3658G>C p.E1220Q Substitution - Missense 5:177212057-177212057 + ODG6 COSM5731424 c.4012A>G p.T1338A Substitution - Missense 5:177238327-177238327 + TCGA-A5-A0GP-01 COSM1066266 c.4781T>G p.F1594C Substitution - Missense 5:177256966-177256966 + TCGA-B5-A11E-01 COSM1066270 c.4856G>A p.C1619Y Substitution - Missense 5:177257041-177257041 + ODG6 COSM5731423 c.4012A>G p.T1338A Substitution - Missense 5:177238327-177238327 + OSCC-GB_00110111 COSM3715048 c.5431C>T p.R1811* Substitution - Nonsense 5:177269729-177269729 + 108 COSM5016854 c.2781G>C p.L927F Substitution - Missense 5:177211180-177211180 + TCGA-AG-3892-01 COSM257562 c.722G>T p.R241I Substitution - Missense 5:177135825-177135825 + CHC205T COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + SH-1679 COSM4159760 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + S10-44607-TP COSM4642983 c.5580C>T p.D1860D Substitution - coding silent 5:177273742-177273742 + TCGA-AA-3811-01 COSM293771 c.6999C>A p.P2333P Substitution - coding silent 5:177294367-177294367 + SR COSM1672146 c.4552G>T p.G1518C Substitution - Missense 5:177248235-177248235 + S10-44607-TP COSM4992304 c.5581C>T p.R1861* Substitution - Nonsense 5:177273743-177273743 + ESCC_BICR_034T COSM5443545 c.5916G>C p.V1972V Substitution - coding silent 5:177282488-177282488 + CHLA-258 COSM4585726 c.3092G>A p.R1031Q Substitution - Missense 5:177211491-177211491 + TCGA-BR-7851-01 COSM3853972 c.5270G>T p.R1757M Substitution - Missense 5:177267685-177267685 + BD120T COSM5514636 c.1084C>T p.R362W Substitution - Missense 5:177204140-177204140 + 8067240 COSM3784824 c.4974G>A p.L1658L Substitution - coding silent 5:177259996-177259996 + PD8939a COSM4384101 c.7817delC p.P2607fs*12 Deletion - Frameshift 5:177295185-177295185 + TCGA-D1-A103-01 COSM1066188 c.97G>A p.G33S Substitution - Missense 5:177135200-177135200 + BD236T COSM5518631 c.387A>T p.E129D Substitution - Missense 5:177135490-177135490 + TCGA-HU-A4GT-01 COSM3853983 c.6464-2A>G p.? Unknown 5:177293830-177293830 + HCC028T COSM5807738 c.5960A>G p.Y1987C Substitution - Missense 5:177282532-177282532 + SNUH_G10_S1 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-A5-A0VP-01 COSM1066251 c.3817C>T p.R1273C Substitution - Missense 5:177235841-177235841 + B104-0 COSM1754204 c.7740G>A p.A2580A Substitution - coding silent 5:177295108-177295108 + TCGA-A4-7585-01 COSM3994208 c.5349C>T p.N1783N Substitution - coding silent 5:177269647-177269647 + TCGA-UB-A7MB-01 COSM4932078 c.2554A>G p.I852V Substitution - Missense 5:177210953-177210953 + SH-7166 COSM4159761 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + SC_9035 COSM3853977 c.5854C>T p.R1952W Substitution - Missense 5:177280796-177280796 + S06-19548-TP COSM4992306 c.7443G>C p.E2481D Substitution - Missense 5:177294811-177294811 + MD-289 COSM302775 c.5910G>C p.E1970D Substitution - Missense 5:177282482-177282482 + PD6956a COSM4384054 c.1544A>G p.H515R Substitution - Missense 5:177209943-177209943 + CCC64T COSM3661732 c.7240T>G p.L2414V Substitution - Missense 5:177294608-177294608 + 2492700 COSM3341242 c.6924C>T p.S2308S Substitution - coding silent 5:177294292-177294292 + 400 COSM4429488 c.5237A>G p.N1746S Substitution - Missense 5:177267652-177267652 + TCGA-EE-A3JD-06 COSM4394922 c.6000C>T p.T2000T Substitution - coding silent 5:177282572-177282572 + TCGA-AA-A010-01 COSM283392 c.3639A>G p.I1213M Substitution - Missense 5:177212038-177212038 + PD6788a COSM4384069 c.2893T>G p.S965A Substitution - Missense 5:177211292-177211292 + TCGA-EI-6917-01 COSM3429311 c.5019T>G p.F1673L Substitution - Missense 5:177260041-177260041 + TCGA-CU-A0YR-01 COSM420769 c.605G>A p.G202D Substitution - Missense 5:177135708-177135708 + TCGA-C5-A0TN-01 COSM4856142 c.1273G>T p.V425F Substitution - Missense 5:177209672-177209672 + TCGA-G3-A5SJ-01 COSM4914990 c.291T>G p.F97L Substitution - Missense 5:177135394-177135394 + 587278 COSM1217936 c.4760G>A p.R1587H Substitution - Missense 5:177251848-177251848 + TCGA-BR-4361-01 COSM3853976 c.5854C>T p.R1952W Substitution - Missense 5:177280796-177280796 + TCGA-FW-A3R5-06 COSM3919753 c.7057C>T p.P2353S Substitution - Missense 5:177294425-177294425 + TCGA-B5-A11E-01 COSM1066269 c.4856G>A p.C1619Y Substitution - Missense 5:177257041-177257041 + TCGA-A6-6141-01 COSM1436266 c.4001C>A p.S1334Y Substitution - Missense 5:177238316-177238316 + TCGA-CD-A4MI-01 COSM3853964 c.4488A>G p.P1496P Substitution - coding silent 5:177246787-177246787 + SNUH_G76_S1 COSM4419702 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + CHC2103T COSM4952543 c.6044A>G p.Y2015C Substitution - Missense 5:177283821-177283821 + PT32 COSM5907361 c.7097G>A p.G2366D Substitution - Missense 5:177294465-177294465 + 1N49-VS-1T49 COSM4976475 c.6013C>T p.R2005* Substitution - Nonsense 5:177283790-177283790 + CSCC-29-T COSM4518628 c.7244_7245CC>TT p.S2415F Substitution - Missense 5:177294612-177294613 + 2492723 COSM5720515 c.6635C>T p.P2212L Substitution - Missense 5:177294003-177294003 + TCGA-B8-5546-01 COSM482574 c.5145A>G p.E1715E Substitution - coding silent 5:177260167-177260167 + 2172 COSM5011556 c.5671G>T p.E1891* Substitution - Nonsense 5:177280613-177280613 + S06-38853-TP COSM4992300 c.4487C>T p.P1496L Substitution - Missense 5:177246786-177246786 + 2492701 COSM3341243 c.6924C>T p.S2308S Substitution - coding silent 5:177294292-177294292 + Au2 COSM3341243 c.6924C>T p.S2308S Substitution - coding silent 5:177294292-177294292 + TCGA-46-6026-01 COSM737595 c.4919G>C p.C1640S Substitution - Missense 5:177257104-177257104 + PD11750a COSM5786567 c.634G>C p.D212H Substitution - Missense 5:177135737-177135737 + 4_PRE-TREATMENT COSM1724162 c.5628C>T p.N1876N Substitution - coding silent 5:177280570-177280570 + PD8939a COSM4384100 c.7817delC p.P2607fs*12 Deletion - Frameshift 5:177295185-177295185 + 394 COSM3722832 c.6094T>C p.W2032R Substitution - Missense 5:177283871-177283871 + BD236T COSM5518633 c.5788C>T p.R1930C Substitution - Missense 5:177280730-177280730 + SH-7032 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-D1-A17Q-01 COSM276401 c.1176C>T p.F392F Substitution - coding silent 5:177204232-177204232 + TCGA-AR-A256-01 COSM1486625 c.12C>T p.T4T Substitution - coding silent 5:177135115-177135115 + OSCC-GB_00020111 COSM3715047 c.2873C>T p.S958L Substitution - Missense 5:177211272-177211272 + TCGA-CD-8536-01 COSM3853960 c.4127C>A p.P1376H Substitution - Missense 5:177238442-177238442 + CHC2113T COSM4788380 c.1119T>A p.S373S Substitution - coding silent 5:177204175-177204175 + PT13 COSM1066209 c.1492C>T p.R498* Substitution - Nonsense 5:177209891-177209891 + K176 COSM249592 c.3835A>C p.K1279Q Substitution - Missense 5:177235859-177235859 + TCGA-BR-8680-01 COSM3853948 c.1405G>T p.D469Y Substitution - Missense 5:177209804-177209804 + T3118 COSM4708350 c.3035G>A p.R1012H Substitution - Missense 5:177211434-177211434 + TCGA-C5-A7UH-01 COSM4856831 c.3406G>A p.E1136K Substitution - Missense 5:177211805-177211805 + SH-1641 COSM5019443 c.3564G>C p.R1188S Substitution - Missense 5:177211963-177211963 + SH-7282 COSM4419701 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + HN_63021 COSM128640 c.3698delG p.L1234fs*1 Deletion - Frameshift 5:177212097-177212097 + TCGA-BH-A18V-01 COSM449383 c.7317G>A p.L2439L Substitution - coding silent 5:177294685-177294685 + SH-9248 COSM4418709 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + 2011-2311:2012-362-T COSM4605676 c.6050G>T p.R2017L Substitution - Missense 5:177283827-177283827 + B47-Tumor COSM1754199 c.3276G>C p.Q1092H Substitution - Missense 5:177211675-177211675 + ESO-610 COSM1259600 c.1446T>C p.D482D Substitution - coding silent 5:177209845-177209845 + RMS85_ COSM4988877 c.2071G>A p.A691T Substitution - Missense 5:177210470-177210470 + TCGA-AP-A0LM-01 COSM1066254 c.3965G>A p.R1322Q Substitution - Missense 5:177238280-177238280 + 2492721 COSM5720515 c.6635C>T p.P2212L Substitution - Missense 5:177294003-177294003 + PD6987a COSM4384059 c.1906A>G p.I636V Substitution - Missense 5:177210305-177210305 + 345480 COSM3726247 c.6329A>T p.Q2110L Substitution - Missense 5:177292024-177292024 + SH-3327 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-BR-4201-01 COSM3853985 c.7180A>G p.I2394V Substitution - Missense 5:177294548-177294548 + TCGA-AP-A056-01 COSM1066315 c.7489C>A p.L2497M Substitution - Missense 5:177294857-177294857 + TCGA-AA-A00N-01 COSM276401 c.1176C>T p.F392F Substitution - coding silent 5:177204232-177204232 + CHEWS032 COSM4585728 c.7696A>G p.T2566A Substitution - Missense 5:177295064-177295064 + HCC2998 COSM1672144 c.3363A>C p.K1121N Substitution - Missense 5:177211762-177211762 + S07-39193-TP COSM4992298 c.4446_4447delGT p.C1483fs*1 Deletion - Frameshift 5:177246745-177246746 + B106 COSM1754197 c.2483C>T p.S828F Substitution - Missense 5:177210882-177210882 + C709 COSM3341235 c.6595C>T p.R2199C Substitution - Missense 5:177293963-177293963 + EGC15 COSM5060967 c.6596G>A p.R2199H Substitution - Missense 5:177293964-177293964 + D28 COSM5545444 c.6224C>G p.P2075R Substitution - Missense 5:177288891-177288891 + TCGA-D1-A15Z-01 COSM1066261 c.4603C>T p.R1535C Substitution - Missense 5:177248286-177248286 + SC_9096 COSM1436263 c.2903A>G p.K968R Substitution - Missense 5:177211302-177211302 + PCSI_0161_Pa_P_526 COSM4965875 c.7652C>A p.P2551Q Substitution - Missense 5:177295020-177295020 + BD22T COSM5508823 c.2038A>C p.K680Q Substitution - Missense 5:177210437-177210437 + pfg008T COSM1642692 c.5887delA p.K1964fs*5 Deletion - Frameshift 5:177280829-177280829 + CSCC-30-T COSM4505417 c.6924C>A p.S2308S Substitution - coding silent 5:177294292-177294292 + TCGA-C5-A0TN-01 COSM4856141 c.1273G>T p.V425F Substitution - Missense 5:177209672-177209672 + U87 COSM3341116 c.3380T>G p.L1127R Substitution - Missense 5:177211779-177211779 + PT34 COSM5910462 c.2428T>A p.C810S Substitution - Missense 5:177210827-177210827 + sysucc-2215T COSM5765680 c.1574G>A p.R525Q Substitution - Missense 5:177209973-177209973 + T3080 COSM4708353 c.5918G>A p.G1973D Substitution - Missense 5:177282490-177282490 + TCGA-BR-7707-01 COSM1436282 c.6430G>A p.A2144T Substitution - Missense 5:177292125-177292125 + ATL071 COSM5709660 c.6169A>G p.N2057D Substitution - Missense 5:177288836-177288836 + 2492721 COSM5720516 c.6635C>T p.P2212L Substitution - Missense 5:177294003-177294003 + TCGA-FR-A3YN-06 COSM3614507 c.5439C>T p.F1813F Substitution - coding silent 5:177269737-177269737 + TCGA-CJ-4912-01 COSM482561 c.205T>C p.Y69H Substitution - Missense 5:177135308-177135308 + TCGA-CJ-6031-01 COSM482566 c.1236+2T>C p.? Unknown 5:177204294-177204294 + MEL-JWCI-WGS-22 COSM1167808 c.3468_3469insA p.R1159fs*11 Insertion - Frameshift 5:177211867-177211868 + TCGA-EK-A2RC-01 COSM4848496 c.5036C>A p.S1679* Substitution - Nonsense 5:177260058-177260058 + YUKAT COSM5403151 c.3345G>A p.K1115K Substitution - coding silent 5:177211744-177211744 + 61 COSM5737437 c.4748G>A p.C1583Y Substitution - Missense 5:177251836-177251836 + YUFIT COSM5403155 c.4153_4154CC>TT p.P1385F Substitution - Missense 5:177238468-177238469 + CHC2113T COSM4788379 c.1119T>A p.S373S Substitution - coding silent 5:177204175-177204175 + C135 COSM4618499 c.3273T>G p.L1091L Substitution - coding silent 5:177211672-177211672 + HT COSM1581352 c.1544A>T p.H515L Substitution - Missense 5:177209943-177209943 + TCGA-AG-A002-01 COSM262472 c.4366G>T p.D1456Y Substitution - Missense 5:177244258-177244258 + TCGA-D3-A5GO-06 COSM3614489 c.56C>T p.P19L Substitution - Missense 5:177135159-177135159 + T204 COSM4708358 c.7752C>T p.V2584V Substitution - coding silent 5:177295120-177295120 + TCGA-EK-A2PG-01 COSM4819889 c.3522G>A p.M1174I Substitution - Missense 5:177211921-177211921 + TCGA-EP-A2KA-01 COSM4917375 c.7992T>C p.S2664S Substitution - coding silent 5:177295360-177295360 + Pat_41_B COSM5868230 c.3613G>A p.E1205K Substitution - Missense 5:177212012-177212012 + TCGA-AA-A00N-01 COSM276400 c.1176C>T p.F392F Substitution - coding silent 5:177204232-177204232 + C086 COSM5535719 c.4027C>T p.P1343S Substitution - Missense 5:177238342-177238342 + SH-7329 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-BS-A0UF-01 COSM1066236 c.3366T>G p.I1122M Substitution - Missense 5:177211765-177211765 + TCGA-B8-5552-01 COSM482562 c.295G>A p.D99N Substitution - Missense 5:177135398-177135398 + LS411 COSM3341149 c.4421A>C p.Q1474P Substitution - Missense 5:177246720-177246720 + TCGA-DJ-A4UW-01 COSM3373815 c.4463A>G p.N1488S Substitution - Missense 5:177246762-177246762 + TCGA-AP-A056-01 COSM1066314 c.7489C>A p.L2497M Substitution - Missense 5:177294857-177294857 + TCGA-AM-5820-01 COSM3697159 c.6662A>G p.Y2221C Substitution - Missense 5:177294030-177294030 + RMS88_ COSM4988881 c.6750G>A p.M2250I Substitution - Missense 5:177294118-177294118 + TCGA-G3-A5SK-01 COSM4927454 c.6719C>A p.S2240* Substitution - Nonsense 5:177294087-177294087 + TCGA-BS-A0UF-01 COSM1066237 c.3366T>G p.I1122M Substitution - Missense 5:177211765-177211765 + SH-6055 COSM4159760 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + PD6873a COSM4384084 c.4858G>A p.V1620I Substitution - Missense 5:177257043-177257043 + sysucc-1163T COSM5459194 c.7562C>T p.A2521V Substitution - Missense 5:177294930-177294930 + CSCC-29-T COSM4506117 c.7116C>T p.P2372P Substitution - coding silent 5:177294484-177294484 + pfg001T COSM1642689 c.816C>T p.N272N Substitution - coding silent 5:177135919-177135919 + PD8934a COSM4384063 c.2068G>A p.A690T Substitution - Missense 5:177210467-177210467 + CHC2103T COSM4952542 c.6044A>G p.Y2015C Substitution - Missense 5:177283821-177283821 + CHC1754T COSM4792837 c.3658G>C p.E1220Q Substitution - Missense 5:177212057-177212057 + ME049T COSM230086 c.1990G>A p.E664K Substitution - Missense 5:177210389-177210389 + C709 COSM3341234 c.6595C>T p.R2199C Substitution - Missense 5:177293963-177293963 + RMS85_ COSM4005988 c.6782T>C p.M2261T Substitution - Missense 5:177294150-177294150 + pfg043T COSM4763645 c.2332T>G p.L778V Substitution - Missense 5:177210731-177210731 + TCGA-D1-A17Q-01 COSM276400 c.1176C>T p.F392F Substitution - coding silent 5:177204232-177204232 + 4_RESISTANT COSM1724162 c.5628C>T p.N1876N Substitution - coding silent 5:177280570-177280570 + RMS88_ COSM4988878 c.3106G>C p.A1036P Substitution - Missense 5:177211505-177211505 + TCGA-D1-A167-01 COSM1066200 c.1001G>A p.R334H Substitution - Missense 5:177191957-177191957 + CSCC-20-T COSM4507981 c.7627C>T p.P2543S Substitution - Missense 5:177294995-177294995 + TCGA-FW-A3R5-06 COSM3919747 c.5841C>T p.F1947F Substitution - coding silent 5:177280783-177280783 + TCGA-HU-A4H3-01 COSM3853979 c.6116G>A p.R2039H Substitution - Missense 5:177283893-177283893 + PD6984a COSM4384065 c.2625T>A p.D875E Substitution - Missense 5:177211024-177211024 + 513 COSM1066300 c.6050G>A p.R2017Q Substitution - Missense 5:177283827-177283827 + LAU63 COSM232910 c.6794C>T p.S2265F Substitution - Missense 5:177294162-177294162 + PT25 COSM4987204 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + 9227_T COSM5039404 c.5026G>A p.A1676T Substitution - Missense 5:177260048-177260048 + SH-3776 COSM4159761 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + S08-41239-TP COSM4992291 c.1192C>T p.L398F Substitution - Missense 5:177204248-177204248 + TCGA-D9-A6EC-06 COSM4406161 c.823A>C p.N275H Substitution - Missense 5:177135926-177135926 + TCGA-D3-A5GO-06 COSM3614490 c.56C>T p.P19L Substitution - Missense 5:177135159-177135159 + B35 COSM1754202 c.7503G>A p.P2501P Substitution - coding silent 5:177294871-177294871 + BN33 COSM1620094 c.7224C>T p.D2408D Substitution - coding silent 5:177294592-177294592 + LAU63 COSM235066 c.6795C>T p.S2265S Substitution - coding silent 5:177294163-177294163 + TCGA-D9-A4Z3-01 COSM3614503 c.3265G>A p.D1089N Substitution - Missense 5:177211664-177211664 + PD6788a COSM4384060 c.1976A>G p.D659G Substitution - Missense 5:177210375-177210375 + PD4099a COSM163003 c.3108C>G p.A1036A Substitution - coding silent 5:177211507-177211507 + TCGA-AZ-6598-01 COSM1436274 c.5139C>T p.C1713C Substitution - coding silent 5:177260161-177260161 + TCGA-AN-A046-01 COSM3827750 c.3517C>T p.R1173C Substitution - Missense 5:177211916-177211916 + PD8934a COSM4384062 c.2068G>A p.A690T Substitution - Missense 5:177210467-177210467 + S22_post COSM5574824 c.7163C>T p.P2388L Substitution - Missense 5:177294531-177294531 + TCGA-B5-A0JZ-01 COSM1066303 c.6380C>T p.A2127V Substitution - Missense 5:177292075-177292075 + TCGA-BG-A18B-01 COSM1066305 c.6620C>A p.P2207H Substitution - Missense 5:177293988-177293988 + BK0002 COSM4185423 c.842A>G p.D281G Substitution - Missense 5:177135945-177135945 + TCGA-E9-A54Y-01 COSM3827748 c.2968G>T p.E990* Substitution - Nonsense 5:177211367-177211367 + I2L-P19Ta-Tumor-Organoid COSM4585724 c.1149C>T p.I383I Substitution - coding silent 5:177204205-177204205 + TCGA-DK-A1AC-01 COSM1311014 c.7104C>G p.A2368A Substitution - coding silent 5:177294472-177294472 + TCGA-BR-4184-01 COSM3341122 c.3598C>T p.R1200W Substitution - Missense 5:177211997-177211997 + 587228 COSM1217933 c.3512G>A p.R1171H Substitution - Missense 5:177211911-177211911 + TCGA-FW-A3R5-06 COSM3919745 c.5389C>T p.L1797F Substitution - Missense 5:177269687-177269687 + TCGA-G2-A2EL-01 COSM1311008 c.3388G>C p.E1130Q Substitution - Missense 5:177211787-177211787 + PT23_1 COSM5902744 c.2183T>G p.V728G Substitution - Missense 5:177210582-177210582 + TCGA-B5-A0JR-01 COSM1066272 c.4878T>G p.T1626T Substitution - coding silent 5:177257063-177257063 + CHC1725T COSM4800691 c.2891A>G p.N964S Substitution - Missense 5:177211290-177211290 + SH-9161 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + XHDG04 COSM4767676 c.7438G>A p.D2480N Substitution - Missense 5:177294806-177294806 + S06-38853-TP COSM4992296 c.3930C>T p.S1310S Substitution - coding silent 5:177238245-177238245 + 2011-2315:2012-358-T COSM4603816 c.5090delG p.G1698fs*37 Deletion - Frameshift 5:177260112-177260112 + TCGA-D1-A174-01 COSM1066209 c.1492C>T p.R498* Substitution - Nonsense 5:177209891-177209891 + PT13 COSM1066210 c.1492C>T p.R498* Substitution - Nonsense 5:177209891-177209891 + 2492701 COSM3341242 c.6924C>T p.S2308S Substitution - coding silent 5:177294292-177294292 + TCGA-D8-A1XK-01 COSM3827763 c.6440T>G p.L2147R Substitution - Missense 5:177292135-177292135 + SNU-C4 COSM4653948 c.3058A>G p.N1020D Substitution - Missense 5:177211457-177211457 + SH-7282 COSM4987204 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + TCGA-AP-A056-01 COSM1066245 c.3535G>T p.E1179* Substitution - Nonsense 5:177211934-177211934 + BD72T COSM5512183 c.218G>A p.R73Q Substitution - Missense 5:177135321-177135321 + SH-7166 COSM5020617 c.4522G>T p.A1508S Substitution - Missense 5:177248205-177248205 + SJACT001_D COSM4967908 c.361C>T p.P121S Substitution - Missense 5:177135464-177135464 + TCGA-G2-A2EO-01 COSM1311006 c.2517G>A p.L839L Substitution - coding silent 5:177210916-177210916 + TCGA-AN-A0AK-01 COSM3827765 c.6479C>T p.P2160L Substitution - Missense 5:177293847-177293847 + TCGA-24-0980-01 COSM75655 c.5027C>A p.A1676D Substitution - Missense 5:177260049-177260049 + TCGA-FU-A2QG-01 COSM4849111 c.1874G>C p.G625A Substitution - Missense 5:177210273-177210273 + T3236 COSM4708345 c.2586C>T p.S862S Substitution - coding silent 5:177210985-177210985 + 17802 COSM5346170 c.4036delG p.E1346fs*26 Deletion - Frameshift 5:177238351-177238351 + 2492703 COSM3341242 c.6924C>T p.S2308S Substitution - coding silent 5:177294292-177294292 + pfg122T COSM4763650 c.6886G>C p.V2296L Substitution - Missense 5:177294254-177294254 + T204 COSM4708357 c.7752C>T p.V2584V Substitution - coding silent 5:177295120-177295120 + SM-4AX84 COSM3341247 c.7067C>T p.T2356M Substitution - Missense 5:177294435-177294435 + TCGA-FS-A1ZZ-06 COSM3614505 c.3309C>T p.D1103D Substitution - coding silent 5:177211708-177211708 + SH-9771 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + 3765_T COSM3947302 c.1433C>G p.S478* Substitution - Nonsense 5:177209832-177209832 + 273T COSM1727361 c.2465C>T p.S822F Substitution - Missense 5:177210864-177210864 + PT33 COSM5908528 c.1067C>T p.S356F Substitution - Missense 5:177204123-177204123 + SH-9161 COSM4419035 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + TCGA-BR-8680-01 COSM262472 c.4366G>T p.D1456Y Substitution - Missense 5:177244258-177244258 + tumor_4144951 COSM5948812 c.4091G>A p.G1364E Substitution - Missense 5:177238406-177238406 + HCT15 COSM1672149 c.7875G>T p.W2625C Substitution - Missense 5:177295243-177295243 + HCT8 COSM1672149 c.7875G>T p.W2625C Substitution - Missense 5:177295243-177295243 + GC8_T COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + TCGA-G4-6322-01 COSM3697157 c.5950C>T p.R1984* Substitution - Nonsense 5:177282522-177282522 + B109 COSM1754201 c.3918C>G p.H1306Q Substitution - Missense 5:177235942-177235942 + ID35 COSM1166637 c.5912A>G p.Y1971C Substitution - Missense 5:177282484-177282484 + PD6159a COSM4384085 c.4858G>A p.V1620I Substitution - Missense 5:177257043-177257043 + BK0004 COSM4185518 c.1600G>C p.G534R Substitution - Missense 5:177209999-177209999 + SH-3776 COSM150019 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + ESCC_BICR_034T COSM5443544 c.5916G>C p.V1972V Substitution - coding silent 5:177282488-177282488 + CHC2113T COSM4788379 c.1119T>A p.S373S Substitution - coding silent 5:177204175-177204175 + 587228 COSM1217932 c.3512G>A p.R1171H Substitution - Missense 5:177211911-177211911 + PD13310a COSM5767573 c.3875T>G p.F1292C Substitution - Missense 5:177235899-177235899 + TCGA-GF-A6C8-06 COSM3919748 c.6376G>C p.D2126H Substitution - Missense 5:177292071-177292071 + T3094 COSM4708356 c.6850G>T p.E2284* Substitution - Nonsense 5:177294218-177294218 + PD6962a COSM4384099 c.7367T>C p.M2456T Substitution - Missense 5:177294735-177294735 + PD6780a COSM4384043 c.388C>T p.P130S Substitution - Missense 5:177135491-177135491 + RMS88_ COSM4418708 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + HN_62686 COSM126839 c.5130C>A p.C1710* Substitution - Nonsense 5:177260152-177260152 + TCGA-FR-A3YO-06 COSM3614514 c.6031C>T p.P2011S Substitution - Missense 5:177283808-177283808 + pfg016T COSM1642691 c.1968_1969delAG p.E657fs*2 Deletion - Frameshift 5:177210367-177210368 + TCGA-AC-A23H-01 COSM3827744 c.26G>A p.R9K Substitution - Missense 5:177135129-177135129 + TCGA-G2-A2EO-01 COSM1311007 c.2517G>A p.L839L Substitution - coding silent 5:177210916-177210916 + UM-SCC-17B COSM4598376 c.6062A>G p.H2021R Substitution - Missense 5:177283839-177283839 + OSCC-GB_00380111 COSM3715050 c.5732G>T p.C1911F Substitution - Missense 5:177280674-177280674 + SH-7282 COSM4418708 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + TCGA-B2-4099-01 COSM482573 c.4189C>G p.P1397A Substitution - Missense 5:177238504-177238504 + TCGA-BS-A0UJ-01 COSM1066275 c.5043C>A p.I1681I Substitution - coding silent 5:177260065-177260065 + 587278 COSM1217939 c.7897C>T p.R2633W Substitution - Missense 5:177295265-177295265 + BN33T COSM1620093 c.7224C>T p.D2408D Substitution - coding silent 5:177294592-177294592 + SH-5693 COSM4419702 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + SH-6055 COSM4159761 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + CCC64 COSM3661731 c.7240T>G p.L2414V Substitution - Missense 5:177294608-177294608 + DLD1 COSM1672149 c.7875G>T p.W2625C Substitution - Missense 5:177295243-177295243 + pfg102T COSM4765491 c.1722_1723insA p.N576fs*8 Insertion - Frameshift 5:177210121-177210122 + TCGA-RP-A694-06 COSM4894474 c.5559G>A p.E1853E Substitution - coding silent 5:177273721-177273721 + ccRCC-66 COSM1659924 c.111C>A p.S37S Substitution - coding silent 5:177135214-177135214 + ESCC_BICR_017T COSM4005986 c.776C>T p.S259L Substitution - Missense 5:177135879-177135879 + TCGA-BR-6452-01 COSM3853970 c.5199C>T p.C1733C Substitution - coding silent 5:177267614-177267614 + PT34 COSM5910463 c.2427G>T p.E809D Substitution - Missense 5:177210826-177210826 + TCGA-06-2563 COSM2152856 c.2905G>A p.G969R Substitution - Missense 5:177211304-177211304 + HCC2998 COSM3341130 c.3844T>G p.L1282V Substitution - Missense 5:177235868-177235868 + TCGA-GN-A266-06 COSM3614496 c.1691C>T p.A564V Substitution - Missense 5:177210090-177210090 + PD6050a COSM4385619 c.6795_6796insA p.A2268fs*13 Insertion - Frameshift 5:177294163-177294164 + S02-14875-TP COSM4992307 c.7568C>T p.S2523L Substitution - Missense 5:177294936-177294936 + TCGA-34-5929-01 COSM737590 c.6022G>A p.D2008N Substitution - Missense 5:177283799-177283799 + SH-9771 COSM5020996 c.5781C>G p.A1927A Substitution - coding silent 5:177280723-177280723 + RMS85_ COSM4418709 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + TCGA-FV-A3R3-01 COSM4921833 c.4547A>G p.E1516G Substitution - Missense 5:177248230-177248230 + SH-7282 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + sysucc-1163T COSM5459192 c.3475C>T p.R1159W Substitution - Missense 5:177211874-177211874 + TCGA-E3-A3DZ-01 COSM3373813 c.1538A>G p.K513R Substitution - Missense 5:177209937-177209937 + 2011-2311:2012-362-T COSM4605677 c.6050G>T p.R2017L Substitution - Missense 5:177283827-177283827 + LIM1899 COSM4640654 c.2133C>T p.H711H Substitution - coding silent 5:177210532-177210532 + TCGA-21-5782-01 COSM737602 c.3161G>C p.R1054T Substitution - Missense 5:177211560-177211560 + pfg102T COSM4765492 c.1722_1723insA p.N576fs*8 Insertion - Frameshift 5:177210121-177210122 + TCGA-A7-A26J-01 COSM3827747 c.2049G>T p.K683N Substitution - Missense 5:177210448-177210448 + TCGA-BR-6566-01 COSM3853969 c.5005C>T p.H1669Y Substitution - Missense 5:177260027-177260027 + ESO-610 COSM1259601 c.1446T>C p.D482D Substitution - coding silent 5:177209845-177209845 + TCGA-A7-A26J-01 COSM3827746 c.2049G>T p.K683N Substitution - Missense 5:177210448-177210448 + TCGA-P4-A5EB-01 COSM3994210 c.6651G>T p.E2217D Substitution - Missense 5:177294019-177294019 + T2284 COSM4708352 c.3348A>G p.Q1116Q Substitution - coding silent 5:177211747-177211747 + TCGA-B5-A11R-01 COSM1066191 c.641C>T p.T214I Substitution - Missense 5:177135744-177135744 + 193 COSM1741806 c.4794G>C p.Q1598H Substitution - Missense 5:177256979-177256979 + Pat_40_B COSM5868225 c.1196G>A p.R399K Substitution - Missense 5:177204252-177204252 + 2492722 COSM5720516 c.6635C>T p.P2212L Substitution - Missense 5:177294003-177294003 + PT48 COSM5931693 c.4258C>T p.P1420S Substitution - Missense 5:177239821-177239821 + SH-1439 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + 273T COSM1727360 c.2465C>T p.S822F Substitution - Missense 5:177210864-177210864 + TCGA-B5-A11E-01 COSM1066294 c.5957G>A p.R1986H Substitution - Missense 5:177282529-177282529 + TCGA-AX-A05Z-01 COSM1066290 c.5900T>G p.F1967C Substitution - Missense 5:177282472-177282472 + PD6873a COSM4384085 c.4858G>A p.V1620I Substitution - Missense 5:177257043-177257043 + PDA_097 COSM5003316 c.4024C>A p.P1342T Substitution - Missense 5:177238339-177238339 + S02248 COSM5679756 c.3359G>T p.G1120V Substitution - Missense 5:177211758-177211758 + B109-Tumor COSM1754200 c.3918C>G p.H1306Q Substitution - Missense 5:177235942-177235942 + PD5740a COSM1166637 c.5912A>G p.Y1971C Substitution - Missense 5:177282484-177282484 + 193 COSM1741809 c.4966+6G>C p.? Unknown 5:177257157-177257157 + H650 COSM1194586 c.3331G>T p.D1111Y Substitution - Missense 5:177211730-177211730 + TCGA-A7-A26G-01 COSM1486628 c.1964G>A p.S655N Substitution - Missense 5:177210363-177210363 + OSCC-GB_00380111 COSM3715051 c.5732G>T p.C1911F Substitution - Missense 5:177280674-177280674 + 1N28-VS-1T28 COSM4973817 c.6275C>T p.T2092M Substitution - Missense 5:177291970-177291970 + PD8934a COSM4384091 c.6418A>T p.K2140* Substitution - Nonsense 5:177292113-177292113 + 453 COSM3341096 c.3091C>T p.R1031* Substitution - Nonsense 5:177211490-177211490 + B35-Tumor COSM1754203 c.7503G>A p.P2501P Substitution - coding silent 5:177294871-177294871 + SNUH_G76_S1 COSM4419701 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + TCGA-46-6026-01 COSM737594 c.4919G>C p.C1640S Substitution - Missense 5:177257104-177257104 + 1N28-VS-1T28 COSM4973818 c.6275C>T p.T2092M Substitution - Missense 5:177291970-177291970 + TCGA-EK-A2PG-01 COSM4819570 c.3654G>A p.L1218L Substitution - coding silent 5:177212053-177212053 + OSCC-GB_00110111 COSM3715044 c.1549C>T p.Q517* Substitution - Nonsense 5:177209948-177209948 + TCGA-AZ-4315-01 COSM1436257 c.1319G>A p.R440Q Substitution - Missense 5:177209718-177209718 + RKO COSM3341196 c.5392delT p.F1799fs*22 Deletion - Frameshift 5:177269690-177269690 + PD6194a COSM3341128 c.3778G>T p.A1260S Substitution - Missense 5:177212177-177212177 + 3N62-VS-3T62 COSM4984477 c.1861C>T p.L621F Substitution - Missense 5:177210260-177210260 + SCMC_RM2_ COSM4987204 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + RKO COSM3341113 c.3281T>C p.M1094T Substitution - Missense 5:177211680-177211680 + TCGA-D9-A6EC-06 COSM4400612 c.1926T>A p.S642S Substitution - coding silent 5:177210325-177210325 + TCGA-BR-8680-01 COSM262473 c.4366G>T p.D1456Y Substitution - Missense 5:177244258-177244258 + TCGA-AA-A010-01 COSM283390 c.1019G>T p.R340M Substitution - Missense 5:177191975-177191975 + S00501 COSM313373 c.6898G>A p.A2300T Substitution - Missense 5:177294266-177294266 + PD6934a COSM4385617 c.166_167insA p.T56fs*37 Insertion - Frameshift 5:177135269-177135270 + YUGURT COSM5403161 c.7387C>T p.P2463S Substitution - Missense 5:177294755-177294755 + S10-44607-TP COSM4992303 c.5581C>T p.R1861* Substitution - Nonsense 5:177273743-177273743 + TCGA-FU-A2QG-01 COSM4849103 c.2201A>G p.K734R Substitution - Missense 5:177210600-177210600 + TCGA-A8-A0AD-01 COSM449381 c.252A>G p.V84V Substitution - coding silent 5:177135355-177135355 + HN_62415 COSM124867 c.6371G>A p.C2124Y Substitution - Missense 5:177292066-177292066 + TCGA-BS-A0UJ-01 COSM1066276 c.5043C>A p.I1681I Substitution - coding silent 5:177260065-177260065 + T2950 COSM4708341 c.617C>T p.A206V Substitution - Missense 5:177135720-177135720 + STC297 COSM5060964 c.5741G>A p.R1914H Substitution - Missense 5:177280683-177280683 + ESCC_BICR_001T COSM5440694 c.6262C>T p.Q2088* Substitution - Nonsense 5:177291957-177291957 + pfg016T COSM1642690 c.1968_1969delAG p.E657fs*2 Deletion - Frameshift 5:177210367-177210368 + ESCC_BICR_017T COSM4005985 c.776C>T p.S259L Substitution - Missense 5:177135879-177135879 + SNUH_G76_S1 COSM4419034 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + SH-9248 COSM4987203 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + SH-1679 COSM4418709 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + B47 COSM1754198 c.3276G>C p.Q1092H Substitution - Missense 5:177211675-177211675 + TCGA-AP-A053-01 COSM1066215 c.1832G>T p.R611L Substitution - Missense 5:177210231-177210231 + CHC1725T COSM4800692 c.2891A>G p.N964S Substitution - Missense 5:177211290-177211290 + CSCC-49-T COSM4556515 c.6949G>A p.D2317N Substitution - Missense 5:177294317-177294317 + XHDG04C COSM4767675 c.7438G>A p.D2480N Substitution - Missense 5:177294806-177294806 + Gp2D COSM3341162 c.4774A>G p.T1592A Substitution - Missense 5:177256959-177256959 + CSCC-44-T COSM4517577 c.3760_3761CC>TT p.P1254F Substitution - Missense 5:177212159-177212160 + RMS80_ COSM4987204 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + SH-1679 COSM4987204 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + SH-3327 COSM4159761 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + TCGA-AC-A23H-01 COSM3827754 c.4746C>G p.I1582M Substitution - Missense 5:177251834-177251834 + CSCC-29-T COSM4506116 c.7116C>T p.P2372P Substitution - coding silent 5:177294484-177294484 + TCGA-BR-4201-01 COSM3853966 c.4759C>T p.R1587C Substitution - Missense 5:177251847-177251847 + SH-4435 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + A3 COSM5351180 c.5198G>T p.C1733F Substitution - Missense 5:177267613-177267613 + TCGA-DK-A1AE-01 COSM1311013 c.5951G>T p.R1984L Substitution - Missense 5:177282523-177282523 + SH-5693 COSM5019785 c.3705T>C p.N1235N Substitution - coding silent 5:177212104-177212104 + SH-0348 COSM4159761 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + T155 COSM1177184 c.1810C>T p.R604* Substitution - Nonsense 5:177210209-177210209 + PT14_1 COSM5896769 c.2213T>C p.L738P Substitution - Missense 5:177210612-177210612 + YUGURT COSM5403160 c.7387C>T p.P2463S Substitution - Missense 5:177294755-177294755 + TCGA-RP-A694-06 COSM4894475 c.5559G>A p.E1853E Substitution - coding silent 5:177273721-177273721 + sysucc-311T COSM4585724 c.1149C>T p.I383I Substitution - coding silent 5:177204205-177204205 + SH-9248 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + SH-3458 COSM4159760 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + DLBCL759 COSM1581355 c.2170G>A p.E724K Substitution - Missense 5:177210569-177210569 + Gp5D COSM3341127 c.3717A>G p.K1239K Substitution - coding silent 5:177212116-177212116 + PT27 COSM5905628 c.6010G>A p.D2004N Substitution - Missense 5:177283787-177283787 + MEL-JWCI-WGS-22 COSM1167807 c.3468_3469insA p.R1159fs*11 Insertion - Frameshift 5:177211867-177211868 + TCGA-DM-A1D8-01 COSM1436279 c.5532G>C p.R1844S Substitution - Missense 5:177273694-177273694 + SC_9008 COSM5548841 c.5180C>T p.A1727V Substitution - Missense 5:177267595-177267595 + sysucc-2215T COSM5765681 c.1574G>A p.R525Q Substitution - Missense 5:177209973-177209973 + SCMC_RM2_ COSM4418708 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + TCGA-D3-A3CF-06 COSM3614518 c.7519G>A p.G2507S Substitution - Missense 5:177294887-177294887 + SH-7282 COSM4419034 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + PD11750a COSM5786566 c.634G>C p.D212H Substitution - Missense 5:177135737-177135737 + HCC028T COSM5807737 c.5960A>G p.Y1987C Substitution - Missense 5:177282532-177282532 + PTC-7C COSM4159761 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + PD5740a COSM1166638 c.5912A>G p.Y1971C Substitution - Missense 5:177282484-177282484 + PD6944a COSM4384045 c.638G>A p.S213N Substitution - Missense 5:177135741-177135741 + PD6105a COSM4384067 c.2650C>T p.P884S Substitution - Missense 5:177211049-177211049 + TCGA-BR-4184-01 COSM3341138 c.4050G>A p.P1350P Substitution - coding silent 5:177238365-177238365 + 502635 COSM5702596 c.7147G>T p.G2383C Substitution - Missense 5:177294515-177294515 + PD6881a COSM4384095 c.6739G>A p.A2247T Substitution - Missense 5:177294107-177294107 + SH-1679 COSM4419034 c.1749G>A p.E583E Substitution - coding silent 5:177210148-177210148 + SH-3133 COSM4159761 c.6903G>C p.G2301G Substitution - coding silent 5:177294271-177294271 + SNUH_G76_S1 COSM4416946 c.1840G>C p.V614L Substitution - Missense 5:177210239-177210239 + ME049T COSM230085 c.1990G>A p.E664K Substitution - Missense 5:177210389-177210389 + TCGA-B5-A11E-01 COSM1066293 c.5957G>A p.R1986H Substitution - Missense 5:177282529-177282529 + DLBCL759 COSM1581354 c.2170G>A p.E724K Substitution - Missense 5:177210569-177210569 + PT24_1 COSM5904251 c.4121C>T p.S1374F Substitution - Missense 5:177238436-177238436 + 4_RESISTANT COSM1724163 c.5628C>T p.N1876N Substitution - coding silent 5:177280570-177280570 + TCGA-06-2563 COSM2152855 c.2905G>A p.G969R Substitution - Missense 5:177211304-177211304 + TCGA-FP-7829-01 COSM3853952 c.2927C>A p.A976D Substitution - Missense 5:177211326-177211326 + T3724 COSM4708344 c.1345T>A p.L449M Substitution - Missense 5:177209744-177209744 + TCGA-AA-A010-01 COSM283394 c.3810G>T p.E1270D Substitution - Missense 5:177235834-177235834 + TCGA-AP-A053-01 COSM1066216 c.1832G>T p.R611L Substitution - Missense 5:177210231-177210231 + TCGA-B5-A0JZ-01 COSM1066234 c.3205C>T p.Q1069* Substitution - Nonsense 5:177211604-177211604 + SM-4AX84 COSM3341246 c.7067C>T p.T2356M Substitution - Missense 5:177294435-177294435 + CHC1725T COSM4800692 c.2891A>G p.N964S Substitution - Missense 5:177211290-177211290 + PT33 COSM5908527 c.1067C>T p.S356F Substitution - Missense 5:177204123-177204123 + pfg122T COSM4763651 c.6886G>C p.V2296L Substitution - Missense 5:177294254-177294254 + TCGA-A4-7585-01 COSM3994209 c.5349C>T p.N1783N Substitution - coding silent 5:177269647-177269647 + TCGA-B5-A0JR-01 COSM1066273 c.4878T>G p.T1626T Substitution - coding silent 5:177257063-177257063 + SH-6055 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + PD6829a COSM4384049 c.946T>G p.S316A Substitution - Missense 5:177191902-177191902 + CSCC-7-T COSM4571111 c.3862T>A p.Y1288N Substitution - Missense 5:177235886-177235886 + RMS80_ COSM4418708 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + SH-9248 COSM4418708 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + 393-01-6TD COSM5419419 c.6788C>T p.S2263L Substitution - Missense 5:177294156-177294156 + SH-9161 COSM4419701 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + PD6057a COSM4384050 c.1079C>T p.P360L Substitution - Missense 5:177204135-177204135 + 016 COSM145694 c.6085A>G p.T2029A Substitution - Missense 5:177283862-177283862 + BN33 COSM1620093 c.7224C>T p.D2408D Substitution - coding silent 5:177294592-177294592 + TCGA-D8-A1XK-01 COSM3827761 c.6364T>G p.F2122V Substitution - Missense 5:177292059-177292059 + TCGA-G9-7521-01 COSM1471834 c.6603T>A p.S2201S Substitution - coding silent 5:177293971-177293971 + PD6201a COSM4384040 c.20T>C p.L7P Substitution - Missense 5:177135123-177135123 + TCGA-BT-A20T-01 COSM420764 c.6850G>C p.E2284Q Substitution - Missense 5:177294218-177294218 + 393-01-6TD COSM5419418 c.6788C>T p.S2263L Substitution - Missense 5:177294156-177294156 + TCGA-D9-A6EA-06 COSM4397799 c.1191C>T p.V397V Substitution - coding silent 5:177204247-177204247 + TCGA-DK-A1AC-01 COSM1311005 c.460G>C p.E154Q Substitution - Missense 5:177135563-177135563 + TCGA-C5-A7UH-01 COSM4856674 c.1499G>C p.R500T Substitution - Missense 5:177209898-177209898 + HCT-15 COSM1672148 c.7875G>T p.W2625C Substitution - Missense 5:177295243-177295243 + TCGA-B5-A0JY-01 COSM1066231 c.3100T>G p.F1034V Substitution - Missense 5:177211499-177211499 + TCGA-A3-3374-01 COSM1496041 c.3032G>C p.S1011T Substitution - Missense 5:177211431-177211431 + PD6057a COSM4384051 c.1079C>T p.P360L Substitution - Missense 5:177204135-177204135 + Pat_41_B COSM5868228 c.1722delA p.N576fs*23 Deletion - Frameshift 5:177210121-177210121 + B106-Tumor COSM1754196 c.2483C>T p.S828F Substitution - Missense 5:177210882-177210882 + RMS110_ COSM4987203 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + PD6194a COSM3341129 c.3778G>T p.A1260S Substitution - Missense 5:177212177-177212177 + PD6518a COSM4384046 c.796A>G p.T266A Substitution - Missense 5:177135899-177135899 + 2011-2315:2012-358-T COSM4603817 c.5090delG p.G1698fs*37 Deletion - Frameshift 5:177260112-177260112 + 2011-2318:2012-356-T COSM4603760 c.2400delG p.A801fs*6 Deletion - Frameshift 5:177210799-177210799 + 400 COSM4429487 c.5237A>G p.N1746S Substitution - Missense 5:177267652-177267652 + 2521243 COSM5886418 c.5864G>T p.G1955V Substitution - Missense 5:177280806-177280806 + TCGA-EK-A2PG-01 COSM4819888 c.3522G>A p.M1174I Substitution - Missense 5:177211921-177211921 + TCGA-CJ-6031-01 COSM482567 c.1236+2T>C p.? Unknown 5:177204294-177204294 + SH-1679 COSM4418708 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + SH-9248 COSM4987204 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + PD4962a COSM5788264 c.4966+6G>T p.? Unknown 5:177257157-177257157 + TCGA-B8-5552-01 COSM482563 c.295G>A p.D99N Substitution - Missense 5:177135398-177135398 + TCGA-EP-A26S-01 COSM4913548 c.60G>A p.V20V Substitution - coding silent 5:177135163-177135163 + SH-7282 COSM4418709 c.2176T>C p.S726P Substitution - Missense 5:177210575-177210575 + LC_S51 COSM1186909 c.3706G>A p.V1236I Substitution - Missense 5:177212105-177212105 + TCGA-FU-A2QG-01 COSM4849077 c.2340G>C p.S780S Substitution - coding silent 5:177210739-177210739 + CHC1754T COSM4792836 c.3658G>C p.E1220Q Substitution - Missense 5:177212057-177212057 + TCGA-BR-6566-01 COSM3853968 c.5005C>T p.H1669Y Substitution - Missense 5:177260027-177260027 + PD7367a COSM4384070 c.2912G>A p.G971D Substitution - Missense 5:177211311-177211311 + 193 COSM1741808 c.4966+6G>C p.? Unknown 5:177257157-177257157 + TCGA-BR-7851-01 COSM3853973 c.5270G>T p.R1757M Substitution - Missense 5:177267685-177267685 + PD6105a COSM4384066 c.2650C>T p.P884S Substitution - Missense 5:177211049-177211049 + pfg068T COSM4748091 c.5503delA p.A1837fs*12 Deletion - Frameshift 5:177269801-177269801 + TCGA-EA-A1QT-01 COSM462001 c.5036C>G p.S1679* Substitution - Nonsense 5:177260058-177260058 + Gp5D COSM3341163 c.4774A>G p.T1592A Substitution - Missense 5:177256959-177256959 + pfg001T COSM1642688 c.816C>T p.N272N Substitution - coding silent 5:177135919-177135919 + BD236T COSM5518632 c.5788C>T p.R1930C Substitution - Missense 5:177280730-177280730 + PD13310a COSM5767574 c.3875T>G p.F1292C Substitution - Missense 5:177235899-177235899 + 2011-2335:2012-1340-T COSM4603828 c.6470delG p.E2158fs*136 Deletion - Frameshift 5:177293838-177293838 + ATL071 COSM5709659 c.6169A>G p.N2057D Substitution - Missense 5:177288836-177288836 + CML015T COSM5802639 c.113A>G p.N38S Substitution - Missense 5:177135216-177135216 + SH-9771 COSM5019784 c.3705T>C p.N1235N Substitution - coding silent 5:177212104-177212104 + B35 COSM1754203 c.7503G>A p.P2501P Substitution - coding silent 5:177294871-177294871 + TCGA-AA-3971-01 COSM301464 c.5996_5997TC>GT p.L1999>? Complex 5:177282568-177282569 + PD6159a COSM4384084 c.4858G>A p.V1620I Substitution - Missense 5:177257043-177257043 + 413LT COSM337162 c.2105C>A p.P702H Substitution - Missense 5:177210504-177210504 + TCGA-D1-A103-01 COSM1066197 c.820A>C p.I274L Substitution - Missense 5:177135923-177135923 + 2492720 COSM5720515 c.6635C>T p.P2212L Substitution - Missense 5:177294003-177294003 + PD23578a COSM5795103 c.2362C>G p.R788G Substitution - Missense 5:177210761-177210761 + TCGA-D1-A103-01 COSM1066243 c.3484C>T p.R1162C Substitution - Missense 5:177211883-177211883 + PR-04-194 COSM246118 c.4978C>T p.R1660C Substitution - Missense 5:177260000-177260000 + TCGA-B0-5695-01 COSM482564 c.959A>G p.K320R Substitution - Missense 5:177191915-177191915 + HN_62897 COSM128701 c.5502_5503insA p.A1837fs*10 Insertion - Frameshift 5:177269800-177269801 + TCGA-BG-A0M4-01 COSM1066204 c.1452A>G p.E484E Substitution - coding silent 5:177209851-177209851 + PD6956a COSM4384055 c.1544A>G p.H515R Substitution - Missense 5:177209943-177209943 + DLBCL1055 COSM1582039 c.5356_5360delAAGAT p.K1786fs*3 Deletion - Frameshift 5:177269654-177269658 + SH-9248 COSM4419701 c.1482C>T p.C494C Substitution - coding silent 5:177209881-177209881 + CSCC-20-T COSM4507980 c.7627C>T p.P2543S Substitution - Missense 5:177294995-177294995 + H650 COSM1194436 c.1954A>G p.I652V Substitution - Missense 5:177210353-177210353 + TCGA-18-3409-01 COSM737605 c.2981C>T p.S994F Substitution - Missense 5:177211380-177211380 + BD72T COSM5512184 c.218G>A p.R73Q Substitution - Missense 5:177135321-177135321 + ESCC_BICR_048T COSM5432380 c.6023A>T p.D2008V Substitution - Missense 5:177283800-177283800 + PD5755a COSM591562 c.1457C>G p.S486C Substitution - Missense 5:177209856-177209856 + TCGA-BH-A18V-01 COSM449384 c.7317G>A p.L2439L Substitution - coding silent 5:177294685-177294685 + SJAMLM7011 COSM4776063 c.6656G>A p.R2219H Substitution - Missense 5:177294024-177294024 + TCGA-D1-A17M-01 COSM1066285 c.5617A>G p.I1873V Substitution - Missense 5:177273779-177273779 + TCGA-AA-A010-01 COSM283395 c.3810G>T p.E1270D Substitution - Missense 5:177235834-177235834 + SH-8559 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + SH-3776 COSM4003461 c.6829T>C p.L2277L Substitution - coding silent 5:177294197-177294197 + ESO-913 COSM1259603 c.6118G>A p.V2040I Substitution - Missense 5:177283895-177283895 + TCGA-D9-A6EC-06 COSM4400611 c.1926T>A p.S642S Substitution - coding silent 5:177210325-177210325 + 2012-701:2012-1307-T COSM4603809 c.4359delT p.S1454fs*33 Deletion - Frameshift 5:177244251-177244251 + TCGA-GN-A266-06 COSM3614500 c.2612C>T p.S871F Substitution - Missense 5:177211011-177211011 + TCGA-BR-4368-01 COSM3853962 c.4395T>C p.F1465F Substitution - coding silent 5:177246694-177246694 + PT25 COSM4987203 c.1840G>T p.V614L Substitution - Missense 5:177210239-177210239 + TCGA-EP-A2KA-01 COSM4917450 c.7867A>C p.S2623R Substitution - Missense 5:177295235-177295235 + A3 COSM5351179 c.5198G>T p.C1733F Substitution - Missense 5:177267613-177267613 + TCGA-G3-A5SJ-01 COSM4914991 c.291T>G p.F97L Substitution - Missense 5:177135394-177135394 + TCGA-JX-A3Q0-01 COSM4824355 c.6897C>T p.L2299L Substitution - coding silent 5:177294265-177294265 + TCGA-66-2773-01 COSM737612 c.1766C>G p.S589C Substitution - Missense 5:177210165-177210165 + RK156_C01 COSM3702784 c.1495G>C p.A499P Substitution - Missense 5:177209894-177209894 + TCGA-GN-A266-06 COSM3614495 c.1691C>T p.A564V Substitution - Missense 5:177210090-177210090 + TCGA-34-5927-01 COSM737593 c.5332C>T p.R1778* Substitution - Nonsense 5:177269630-177269630 + 587376 COSM1217946 c.3742G>A p.E1248K Substitution - Missense 5:177212141-177212141 + SNU_09_S1 COSM4420026 c.3067C>A p.R1023R Substitution - coding silent 5:177211466-177211466 + PT48 COSM5931694 c.4258C>T p.P1420S Substitution - Missense 5:177239821-177239821 + S09-31237-TP COSM4992302 c.5382C>T p.F1794F Substitution - coding silent 5:177269680-177269680 + sysucc-1163T COSM5459193 c.7562C>T p.A2521V Substitution - Missense 5:177294930-177294930 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.106861 5q35 606681

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Synonymous p.I806I c.2418A>C 5 176637818 RCCC A - Frameshift p.K1964Rfs*5 c.5891delA 5 176707830 STAD A - Frameshift p.M1531Cfs*43 c.4591delA 5 176675269 STAD - A Frameshift p.M1531Nfs*4 c.4591dupA 5 176675269 HNSC - A Frameshift p.R1159Afs*11 c.3473dupA 5 176638869 CM - A Frameshift p.T2395Nfs*2 c.7183dupA 5 176721552 THCA AG - Frameshift p.E657Vfs*2 c.1970_1971delAG 5 176637368 STAD A G Missense p.D2002G c.6005A>G 5 176709578 ALL A G Missense p.H1808R c.5423A>G 5 176696722 UCEC A G Missense p.I1873V c.5617A>G 5 176700780 UCEC A G Missense p.I1907V c.5719A>G 5 176707662 BLCA A G Missense p.I2394V c.7180A>G 5 176721549 STAD A G Missense p.K2067R c.6200A>G 5 176715868 MM A G Missense p.K513R c.1538A>G 5 176636938 THCA A G Missense p.T2029A c.6085A>G 5 176710863 CLL A G Missense p.Y1997C c.5990A>G 5 176709563 HNSC A G Synonymous p.E2112E c.6336A>G 5 176719032 COREAD A G Synonymous p.E243E c.729A>G 5 176562833 LUAD A G Synonymous p.E484E c.1452A>G 5 176636852 UCEC A G Synonymous p.V84V c.252A>G 5 176562356 BRCA A G Synonymous p.V950V c.2850A>G 5 176638250 ESCA AGTAAAG - Frameshift p.S1086Rfs*6 c.3258_3264delTAAAGAG 5 176638656 HNSC AT - Frameshift p.I1873Kfs*18 c.5618_5619delTA 5 176700778 HNSC A T IntronicSNV . c.5147-2502A>T 5 176692061 HC A T IntronicSNV . c.928-10017A>T 5 176608868 CLL A T Missense p.D325V c.974A>T 5 176618931 HNSC A T Nonsense p.K1433* c.4297A>T 5 176666861 HNSC A T Synonymous p.T672T c.2016A>T 5 176637416 LUSC C A Missense p.A1676D c.5027C>A 5 176687050 OV C A Missense p.P1726H c.5177C>A 5 176694593 HNSC C A Missense p.P2207H c.6620C>A 5 176720989 UCEC C A Missense p.P702H c.2105C>A 5 176637505 LUAD C A Nonsense p.C1710* c.5130C>A 5 176687153 HNSC C A Nonsense p.C792* c.2376C>A 5 176637776 HNSC C A Nonsense p.S1359* c.4076C>A 5 176665392 HNSC C A Nonsense p.S300* c.899C>A 5 176563003 BRCA C A Synonymous p.I183I c.549C>A 5 176562653 BRCA C A Synonymous p.P2381P c.7143C>A 5 176721512 HNSC CC TT Missense p.P1922L c.5765_5766delinsTT 5 176707708 CM CC TT Missense p.S975F c.2924_2925delinsTT 5 176638324 CM C - Frameshift p.P804Qfs*3 c.2411delC 5 176637807 HNSC C G Missense p.I2113M c.6339C>G 5 176719035 HNSC C G Missense p.L1541V c.4621C>G 5 176675305 UCEC C G Missense p.P1397A c.4189C>G 5 176665505 RCCC C G Missense p.P2420R c.7259C>G 5 176721628 OV C G Missense p.Q2246E c.6736C>G 5 176721105 BRCA C G Missense p.S37C c.110C>G 5 176562214 BRCA C G Missense p.S486C c.1457C>G 5 176636857 LUAD C G Missense p.S589C c.1766C>G 5 176637166 LUSC C G Missense p.S96C c.287C>G 5 176562391 HNSC C G Nonsense p.S707* c.2120C>G 5 176637520 HNSC C G Nonsense p.S744* c.2231C>G 5 176637631 HNSC C G Synonymous p.A1036A c.3108C>G 5 176638508 BRCA C G Synonymous p.L2636L c.7908C>G 5 176722277 UCEC C T 3-UTRSNV . c.8088+4177C>T 5 176726634 ALL C T IntronicSNV . c.927+23502C>T 5 176586533 CLL C T Missense p.A2127V c.6380C>T 5 176719076 UCEC C T Missense p.P1814L c.5441C>T 5 176696740 CM C T Missense p.P2292S c.6874C>T 5 176721243 CM C T Missense p.R1273C c.3817C>T 5 176662842 UCEC C T Missense p.R1535C c.4603C>T 5 176675287 UCEC C T Missense p.R1587C c.4759C>T 5 176678848 STAD C T Missense p.R1660C c.4978C>T 5 176687001 THCA C T Missense p.S1432F c.4295C>T 5 176666859 CM C T Missense p.S2194F c.6581C>T 5 176720950 CM C T Missense p.S2308F c.6923C>T 5 176721292 CM C T Missense p.S539F c.1616C>T 5 176637016 CM C T Missense p.S57F c.170C>T 5 176562274 BRCA C T Missense p.S953F c.2858C>T 5 176638258 CM C T Missense p.T1507M c.4520C>T 5 176675204 BRCA C T Missense p.T214I c.641C>T 5 176562745 UCEC C T Nonsense p.Q1069* c.3205C>T 5 176638605 UCEC C T Nonsense p.Q1153* c.3457C>T 5 176638857 HNSC C T Nonsense p.R1471* c.4411C>T 5 176673711 LUSC C T Nonsense p.R1473* c.4417C>T 5 176673717 HNSC C T Nonsense p.R1700* c.5098C>T 5 176687121 HNSC C T Nonsense p.R1778* c.5332C>T 5 176696631 LUSC C T Nonsense p.R1984* c.5950C>T 5 176709523 HNSC C T Nonsense p.R498* c.1492C>T 5 176636892 UCEC C T Nonsense p.R788* c.2362C>T 5 176637762 HNSC C T Synonymous p.A547A c.1641C>T 5 176637041 LUAD C T Synonymous p.D1103D c.3309C>T 5 176638709 CM C T Synonymous p.F2192F c.6576C>T 5 176720945 RCCC C T Synonymous p.F907F c.2721C>T 5 176638121 CM C T Synonymous p.L1262L c.3786C>T 5 176639186 CM C T Synonymous p.L1797L c.5391C>T 5 176696690 CM C T Synonymous p.L2603L c.7809C>T 5 176722178 CM C T Synonymous p.N272N c.816C>T 5 176562920 STAD C T Synonymous p.S2306S c.6918C>T 5 176721287 CM C T Synonymous p.T2000T c.6000C>T 5 176709573 CM C T Synonymous p.T2304T c.6912C>T 5 176721281 STAD C T Synonymous p.T4T c.12C>T 5 176562116 BRCA G A IntronicSNV . c.4766-10G>A 5 176683942 NSCLC G A IntronicSNV . c.5147-2354G>A 5 176692209 MB G A Missense p.A2009T c.6025G>A 5 176710803 HNSC G A Missense p.A2300T c.6898G>A 5 176721267 SCLC G A Missense p.C2124Y c.6371G>A 5 176719067 HNSC G A Missense p.D1489N c.4465G>A 5 176673765 HNSC G A Missense p.D2008N c.6022G>A 5 176710800 LUSC G A Missense p.D99N c.295G>A 5 176562399 RCCC G A Missense p.E1144K c.3430G>A 5 176638830 UCEC G A Missense p.E1261K c.3781G>A 5 176639181 BRCA G A Missense p.E491K c.1471G>A 5 176636871 PRAD G A Missense p.E664K c.1990G>A 5 176637390 CM G A Missense p.G202D c.605G>A 5 176562709 BLCA G A Missense p.G2324R c.6970G>A 5 176721339 LUAD G A Missense p.G2507S c.7519G>A 5 176721888 CM G A Missense p.G35S c.103G>A 5 176562207 CM G A Missense p.G969R c.2905G>A 5 176638305 GBM G A Missense p.G997S c.2989G>A 5 176638389 CM G A Missense p.M1481I c.4443G>A 5 176673743 MM G A Missense p.M1816I c.5448G>A 5 176696747 CM G A Missense p.R1984Q c.5951G>A 5 176709524 HNSC G A Missense p.R2017Q c.6050G>A 5 176710828 UCEC G A Missense p.R2464H c.7391G>A 5 176721760 STAD G A Missense p.R2464H c.7391G>A 5 176721760 UCEC G A Missense p.S2596N c.7787G>A 5 176722156 CM G A Missense p.S655N c.1964G>A 5 176637364 BRCA G A Missense p.V2040I c.6118G>A 5 176710896 ESCA G A Nonsense p.W2527* c.7581G>A 5 176721950 CM G A Synonymous p.E2481E c.7443G>A 5 176721812 BRCA G A Synonymous p.L2439L c.7317G>A 5 176721686 BRCA G A Synonymous p.L839L c.2517G>A 5 176637917 BLCA G A Synonymous p.Q2444Q c.7332G>A 5 176721701 COREAD G A Synonymous p.Q430Q c.1290G>A 5 176636690 RCCC G C Missense p.C1619S c.4856G>C 5 176684042 HNSC G C Missense p.C1640S c.4919G>C 5 176684105 LUSC G C Missense p.C1710S c.5129G>C 5 176687152 HNSC G C Missense p.D1992H c.5974G>C 5 176709547 HNSC G C Missense p.D2002H c.6004G>C 5 176709577 HNSC G C Missense p.E1130Q c.3388G>C 5 176638788 BLCA G C Missense p.E1773D c.5319G>C 5 176696618 BLCA G C Missense p.E2284Q c.6850G>C 5 176721219 BLCA G C Missense p.E2467Q c.7399G>C 5 176721768 HNSC G C Missense p.G1362A c.4085G>C 5 176665401 LUAD G C Missense p.Q973H c.2919G>C 5 176638319 LUSC G C Missense p.R1054T c.3161G>C 5 176638561 LUSC G C SpliceAcceptorSNV . c.4642-1G>C 5 176678730 LUSC G C Synonymous p.L613L c.1839G>C 5 176637239 CM G - Frameshift p.E1202Sfs*17 c.3604delG 5 176639004 HNSC G - Frameshift p.G1095Afs*3 c.3284delG 5 176638682 HNSC GG AA Missense p.G1132K c.3394_3395delinsAA 5 176638794 CM G T IntronicSNV . c.6152-14G>T 5 176715806 CM G T Missense p.A2634S c.7900G>T 5 176722269 BRCA G T Missense p.A578S c.1732G>T 5 176637132 STAD G T Missense p.C1185F c.3554G>T 5 176638954 LUAD G T Missense p.G1678W c.5032G>T 5 176687055 HNSC G T Missense p.G835C c.2503G>T 5 176637903 BRCA G T Missense p.R1984L c.5951G>T 5 176709524 BLCA G T Missense p.R611L c.1832G>T 5 176637232 UCEC G T Nonsense p.E1534* c.4600G>T 5 176675284 HNSC G T Nonsense p.E1979* c.5935G>T 5 176709508 HNSC G T Nonsense p.E874* c.2620G>T 5 176638020 LUSC G T Nonsense p.E990* c.2968G>T 5 176638368 HNSC G T Nonsense p.G1928* c.5782G>T 5 176707725 HNSC G T Nonsense p.G959* c.2875G>T 5 176638275 HNSC G T SpliceDonorSNV . c.4192+1G>T 5 176665509 HNSC - TAA IntronicInsertion . c.4641+1136_4641+1137insAAT 5 176676460 CLL T A Missense p.F1996I c.5986T>A 5 176709559 LUAD T A Missense p.I704N c.2111T>A 5 176637511 CM T A Missense p.L1431H c.4292T>A 5 176666856 CM T A Synonymous p.S2201S c.6603T>A 5 176720972 PRAD TC CT Missense p.L2130P c.6389_6390delinsCT 5 176719085 CM TC GT Missense p.L1999R c.5996_5997delinsGT 5 176709569 COREAD T C Missense p.F16L c.46T>C 5 176562150 CM T C Missense p.Y69H c.205T>C 5 176562309 RCCC T C SpliceDonorSNV . c.1236+2T>C 5 176631295 RCCC T C SpliceDonorSNV . c.4966+2T>C 5 176684154 ESCA T C Synonymous p.D482D c.1446T>C 5 176636846 ESCA T C Synonymous p.F1465F c.4395T>C 5 176673695 STAD T C Synonymous p.V955V c.2865T>C 5 176638265 CM T G Missense p.C2273G c.6817T>G 5 176721186 LUAD T G Missense p.F1594C c.4781T>G 5 176683967 UCEC T G Missense p.L2054R c.6161T>G 5 176715829 HNSC T G Synonymous p.T1626T c.4878T>G 5 176684064 UCEC TT - Frameshift p.L590Ifs*5 c.1768_1769delTT 5 176637167 HNSC