Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 19 38377735 38377735 single base substitution C G missense_variant M2153I 6459G>C BLCA-CN 19 38377735 38377735 single base substitution C G missense_variant M2192I 6576G>C BRCA-EU 19 38372960 38372960 single base substitution T A downstream_gene_variant BRCA-EU 19 38373267 38373267 single base substitution C T downstream_gene_variant BRCA-EU 19 38374042 38374042 single base substitution C T downstream_gene_variant BRCA-EU 19 38374251 38374251 single base substitution A C downstream_gene_variant BRCA-EU 19 38374988 38374988 single base substitution T G downstream_gene_variant BRCA-EU 19 38375135 38375135 single base substitution C T downstream_gene_variant BRCA-EU 19 38375481 38375481 single base substitution A G 3_prime_UTR_variant BRCA-EU 19 38375481 38375481 single base substitution A G downstream_gene_variant BRCA-EU 19 38376330 38376330 single base substitution G C missense_variant Q2622E 7864C>G BRCA-EU 19 38376330 38376330 single base substitution G C missense_variant Q2661E 7981C>G BRCA-EU 19 38376608 38376608 single base substitution C T missense_variant R2529H 7586G>A BRCA-EU 19 38376608 38376608 single base substitution C T missense_variant R2568H 7703G>A BRCA-EU 19 38377247 38377247 single base substitution T A missense_variant E2316V 6947A>T BRCA-EU 19 38377247 38377247 single base substitution T A missense_variant E2355V 7064A>T BRCA-EU 19 38379253 38379253 single base substitution T C synonymous_variant R1647R 4941A>G BRCA-EU 19 38379253 38379253 single base substitution T C synonymous_variant R1686R 5058A>G BRCA-EU 19 38379301 38379301 single base substitution G C synonymous_variant A1631A 4893C>G BRCA-EU 19 38379301 38379301 single base substitution G C synonymous_variant A1670A 5010C>G BRCA-EU 19 38379583 38379583 single base substitution C T synonymous_variant Q1537Q 4611G>A BRCA-EU 19 38379583 38379583 single base substitution C T synonymous_variant Q1576Q 4728G>A BRCA-EU 19 38380374 38380374 single base substitution G A stop_gained Q1274* 3820C>T BRCA-EU 19 38380374 38380374 single base substitution G A stop_gained Q1313* 3937C>T BRCA-EU 19 38380788 38380788 single base substitution C T missense_variant V1136I 3406G>A BRCA-EU 19 38380788 38380788 single base substitution C T missense_variant V1175I 3523G>A BRCA-EU 19 38381133 38381133 single base substitution G A intron_variant BRCA-EU 19 38381150 38381150 single base substitution G C intron_variant BRCA-EU 19 38381157 38381157 deletion of <=200bp T - intron_variant BRCA-EU 19 38382714 38382714 single base substitution C T downstream_gene_variant BRCA-EU 19 38382714 38382714 single base substitution C T intron_variant BRCA-EU 19 38383199 38383199 single base substitution G C downstream_gene_variant BRCA-EU 19 38383199 38383199 single base substitution G C intron_variant BRCA-EU 19 38383516 38383516 single base substitution C T downstream_gene_variant BRCA-EU 19 38383516 38383516 single base substitution C T missense_variant A904T 2710G>A BRCA-EU 19 38383516 38383516 single base substitution C T missense_variant A943T 2827G>A BRCA-EU 19 38383892 38383892 single base substitution A T downstream_gene_variant BRCA-EU 19 38383892 38383892 single base substitution A T synonymous_variant L778L 2334T>A BRCA-EU 19 38383892 38383892 single base substitution A T synonymous_variant L817L 2451T>A BRCA-EU 19 38383932 38383932 single base substitution T G downstream_gene_variant BRCA-EU 19 38383932 38383932 single base substitution T G missense_variant Q765P 2294A>C BRCA-EU 19 38383932 38383932 single base substitution T G missense_variant Q804P 2411A>C BRCA-EU 19 38384059 38384059 single base substitution G A downstream_gene_variant BRCA-EU 19 38384059 38384059 single base substitution G A missense_variant R723C 2167C>T BRCA-EU 19 38384059 38384059 single base substitution G A missense_variant R762C 2284C>T BRCA-EU 19 38384222 38384222 single base substitution G T downstream_gene_variant BRCA-EU 19 38384222 38384222 single base substitution G T missense_variant F668L 2004C>A BRCA-EU 19 38384222 38384222 single base substitution G T missense_variant F707L 2121C>A BRCA-EU 19 38384511 38384511 single base substitution G C downstream_gene_variant BRCA-EU 19 38384511 38384511 single base substitution G C missense_variant S572C 1715C>G BRCA-EU 19 38384511 38384511 single base substitution G C missense_variant S611C 1832C>G BRCA-EU 19 38384977 38384977 single base substitution G A downstream_gene_variant BRCA-EU 19 38384977 38384977 single base substitution G A stop_gained Q417* 1249C>T BRCA-EU 19 38384977 38384977 single base substitution G A stop_gained Q456* 1366C>T BRCA-EU 19 38387160 38387160 single base substitution C G intron_variant BRCA-EU 19 38387171 38387171 single base substitution C G intron_variant BRCA-EU 19 38387183 38387183 single base substitution A G intron_variant BRCA-EU 19 38387257 38387257 single base substitution C G intron_variant BRCA-EU 19 38388550 38388550 single base substitution A T intron_variant BRCA-EU 19 38388946 38388946 single base substitution C A intron_variant BRCA-EU 19 38389023 38389023 single base substitution T G intron_variant BRCA-EU 19 38389083 38389083 single base substitution A T intron_variant BRCA-EU 19 38392620 38392620 single base substitution T G intron_variant BRCA-EU 19 38393029 38393029 deletion of <=200bp T - intron_variant BRCA-EU 19 38393230 38393230 single base substitution G C intron_variant BRCA-EU 19 38394109 38394109 single base substitution A T intron_variant BRCA-EU 19 38394209 38394209 single base substitution A T intron_variant BRCA-EU 19 38395481 38395481 single base substitution C G intron_variant BRCA-EU 19 38395593 38395593 single base substitution G A intron_variant BRCA-EU 19 38397602 38397602 single base substitution G A upstream_gene_variant BRCA-EU 19 38397603 38397603 single base substitution G A upstream_gene_variant BRCA-EU 19 38397771 38397771 single base substitution C G upstream_gene_variant BRCA-EU 19 38397773 38397773 single base substitution G C upstream_gene_variant BRCA-EU 19 38397975 38397975 single base substitution G T upstream_gene_variant BRCA-EU 19 38398422 38398422 single base substitution G C upstream_gene_variant BRCA-EU 19 38399831 38399831 single base substitution C T upstream_gene_variant BRCA-FR 19 38381133 38381133 single base substitution G A intron_variant BRCA-FR 19 38382714 38382714 single base substitution C T downstream_gene_variant BRCA-FR 19 38382714 38382714 single base substitution C T intron_variant BRCA-FR 19 38393895 38393895 single base substitution G A intron_variant BRCA-FR 19 38395593 38395593 single base substitution G A intron_variant BRCA-FR 19 38397602 38397602 single base substitution G A upstream_gene_variant BRCA-FR 19 38397603 38397603 single base substitution G A upstream_gene_variant BRCA-FR 19 38397975 38397975 single base substitution G T upstream_gene_variant BRCA-FR 19 38398068 38398068 single base substitution G C upstream_gene_variant BRCA-FR 19 38398422 38398422 single base substitution G C upstream_gene_variant BRCA-KR 19 38384505 38384505 single base substitution T C downstream_gene_variant BRCA-KR 19 38384505 38384505 single base substitution T C missense_variant D574G 1721A>G BRCA-KR 19 38384505 38384505 single base substitution T C missense_variant D613G 1838A>G BRCA-UK 19 38373028 38373028 single base substitution C A downstream_gene_variant BRCA-UK 19 38376347 38376347 single base substitution G C missense_variant P2616R 7847C>G BRCA-UK 19 38376347 38376347 single base substitution G C missense_variant P2655R 7964C>G BRCA-UK 19 38383870 38383870 single base substitution G C downstream_gene_variant BRCA-UK 19 38383870 38383870 single base substitution G C missense_variant P786A 2356C>G BRCA-UK 19 38383870 38383870 single base substitution G C missense_variant P825A 2473C>G BRCA-UK 19 38384311 38384311 single base substitution G A downstream_gene_variant BRCA-UK 19 38384311 38384311 single base substitution G A missense_variant L639F 1915C>T BRCA-UK 19 38384311 38384311 single base substitution G A missense_variant L678F 2032C>T BRCA-UK 19 38392936 38392936 single base substitution C A intron_variant BRCA-UK 19 38397771 38397771 single base substitution C G upstream_gene_variant BRCA-UK 19 38397773 38397773 single base substitution G C upstream_gene_variant BRCA-US 19 38375769 38375769 deletion of <=200bp A - frameshift_variant C2809 BRCA-US 19 38375769 38375769 deletion of <=200bp A - frameshift_variant C2848 BRCA-US 19 38377679 38377679 single base substitution G C stop_gained S2172* 6515C>G BRCA-US 19 38377679 38377679 single base substitution G C stop_gained S2211* 6632C>G BRCA-US 19 38378199 38378199 single base substitution T G missense_variant T1999P 5995A>C BRCA-US 19 38378199 38378199 single base substitution T G missense_variant T2038P 6112A>C BRCA-US 19 38378957 38378957 single base substitution T A missense_variant K1746M 5237A>T BRCA-US 19 38378957 38378957 single base substitution T A missense_variant K1785M 5354A>T BRCA-US 19 38379529 38379529 single base substitution T A missense_variant E1555D 4665A>T BRCA-US 19 38379529 38379529 single base substitution T A missense_variant E1594D 4782A>T BRCA-US 19 38379723 38379723 single base substitution G T missense_variant Q1491K 4471C>A BRCA-US 19 38379723 38379723 single base substitution G T missense_variant Q1530K 4588C>A BRCA-US 19 38380122 38380122 single base substitution G A synonymous_variant L1358L 4072C>T BRCA-US 19 38380122 38380122 single base substitution G A synonymous_variant L1397L 4189C>T BRCA-US 19 38380336 38380336 single base substitution G C synonymous_variant L1286L 3858C>G BRCA-US 19 38380336 38380336 single base substitution G C synonymous_variant L1325L 3975C>G BRCA-US 19 38380339 38380339 single base substitution T C synonymous_variant E1285E 3855A>G BRCA-US 19 38380339 38380339 single base substitution T C synonymous_variant E1324E 3972A>G BRCA-US 19 38380480 38380480 single base substitution A G synonymous_variant D1238D 3714T>C BRCA-US 19 38380480 38380480 single base substitution A G synonymous_variant D1277D 3831T>C BRCA-US 19 38380661 38380661 single base substitution T G missense_variant K1178T 3533A>C BRCA-US 19 38380661 38380661 single base substitution T G missense_variant K1217T 3650A>C BRCA-US 19 38380815 38380815 single base substitution C T missense_variant A1127T 3379G>A BRCA-US 19 38380815 38380815 single base substitution C T missense_variant A1166T 3496G>A BRCA-US 19 38382389 38382389 single base substitution G C downstream_gene_variant BRCA-US 19 38382389 38382389 single base substitution G C missense_variant S1027C 3080C>G BRCA-US 19 38382389 38382389 single base substitution G C missense_variant S1066C 3197C>G BRCA-US 19 38382411 38382411 deletion of <=200bp C - downstream_gene_variant BRCA-US 19 38382411 38382411 deletion of <=200bp C - frameshift_variant A1020 BRCA-US 19 38382411 38382411 deletion of <=200bp C - frameshift_variant A1059 BRCA-US 19 38382421 38382421 single base substitution C A downstream_gene_variant BRCA-US 19 38382421 38382421 single base substitution C A synonymous_variant L1016L 3048G>T BRCA-US 19 38382421 38382421 single base substitution C A synonymous_variant L1055L 3165G>T BRCA-US 19 38383348 38383348 single base substitution C T downstream_gene_variant BRCA-US 19 38383348 38383348 single base substitution C T missense_variant A960T 2878G>A BRCA-US 19 38383348 38383348 single base substitution C T missense_variant A999T 2995G>A BRCA-US 19 38383735 38383735 single base substitution C T downstream_gene_variant BRCA-US 19 38383735 38383735 single base substitution C T missense_variant A831T 2491G>A BRCA-US 19 38383735 38383735 single base substitution C T missense_variant A870T 2608G>A BRCA-US 19 38383936 38383936 single base substitution A G downstream_gene_variant BRCA-US 19 38383936 38383936 single base substitution A G missense_variant Y764H 2290T>C BRCA-US 19 38383936 38383936 single base substitution A G missense_variant Y803H 2407T>C BRCA-US 19 38384389 38384389 single base substitution C A downstream_gene_variant BRCA-US 19 38384389 38384389 single base substitution C A missense_variant V613F 1837G>T BRCA-US 19 38384389 38384389 single base substitution C A missense_variant V652F 1954G>T BRCA-US 19 38385190 38385190 single base substitution C T downstream_gene_variant BRCA-US 19 38385190 38385190 single base substitution C T missense_variant E346K 1036G>A BRCA-US 19 38385190 38385190 single base substitution C T missense_variant E385K 1153G>A BRCA-US 19 38385971 38385971 single base substitution G T downstream_gene_variant BRCA-US 19 38385971 38385971 single base substitution G T stop_gained Y124* 372C>A BRCA-US 19 38385971 38385971 single base substitution G T stop_gained Y85* 255C>A BRCA-US 19 38386920 38386920 single base substitution A G exon_variant BRCA-US 19 38386920 38386920 single base substitution A G missense_variant L35P 104T>C BTCA-JP 19 38375483 38375483 deletion of <=200bp G - 3_prime_UTR_variant BTCA-JP 19 38375483 38375483 deletion of <=200bp G - downstream_gene_variant BTCA-JP 19 38377766 38377766 single base substitution T A missense_variant Q2143L 6428A>T BTCA-JP 19 38377766 38377766 single base substitution T A missense_variant Q2182L 6545A>T BTCA-JP 19 38378007 38378007 deletion of <=200bp T - frameshift_variant R2063 BTCA-JP 19 38378007 38378007 deletion of <=200bp T - frameshift_variant R2102 BTCA-JP 19 38378075 38378075 single base substitution C T missense_variant R2040K 6119G>A BTCA-JP 19 38378075 38378075 single base substitution C T missense_variant R2079K 6236G>A BTCA-JP 19 38378469 38378469 single base substitution G C missense_variant L1909V 5725C>G BTCA-JP 19 38378469 38378469 single base substitution G C missense_variant L1948V 5842C>G BTCA-JP 19 38378971 38378971 single base substitution T A missense_variant K1741N 5223A>T BTCA-JP 19 38378971 38378971 single base substitution T A missense_variant K1780N 5340A>T BTCA-JP 19 38380203 38380203 single base substitution C T missense_variant G1331S 3991G>A BTCA-JP 19 38380203 38380203 single base substitution C T missense_variant G1370S 4108G>A BTCA-JP 19 38382106 38382106 single base substitution C T downstream_gene_variant BTCA-JP 19 38382106 38382106 single base substitution C T intron_variant BTCA-JP 19 38383245 38383245 single base substitution T G downstream_gene_variant BTCA-JP 19 38383245 38383245 single base substitution T G missense_variant Q1033P 3098A>C BTCA-JP 19 38383245 38383245 single base substitution T G missense_variant Q994P 2981A>C BTCA-JP 19 38385130 38385130 single base substitution G A downstream_gene_variant BTCA-JP 19 38385130 38385130 single base substitution G A missense_variant P366S 1096C>T BTCA-JP 19 38385130 38385130 single base substitution G A missense_variant P405S 1213C>T BTCA-JP 19 38385720 38385720 single base substitution C A downstream_gene_variant BTCA-JP 19 38385720 38385720 single base substitution C A missense_variant G169V 506G>T BTCA-JP 19 38385720 38385720 single base substitution C A missense_variant G208V 623G>T CESC-US 19 38377309 38377309 single base substitution C A missense_variant K2295N 6885G>T CESC-US 19 38377309 38377309 single base substitution C A missense_variant K2334N 7002G>T CESC-US 19 38377815 38377815 single base substitution C T missense_variant E2127K 6379G>A CESC-US 19 38377815 38377815 single base substitution C T missense_variant E2166K 6496G>A CESC-US 19 38380396 38380396 single base substitution G A synonymous_variant N1266N 3798C>T CESC-US 19 38380396 38380396 single base substitution G A synonymous_variant N1305N 3915C>T CESC-US 19 38380730 38380730 single base substitution G A missense_variant S1155F 3464C>T CESC-US 19 38380730 38380730 single base substitution G A missense_variant S1194F 3581C>T CESC-US 19 38380843 38380843 single base substitution G C synonymous_variant L1117L 3351C>G CESC-US 19 38380843 38380843 single base substitution G C synonymous_variant L1156L 3468C>G CESC-US 19 38382241 38382241 single base substitution G C downstream_gene_variant CESC-US 19 38382241 38382241 single base substitution G C missense_variant I1076M 3228C>G CESC-US 19 38382241 38382241 single base substitution G C missense_variant I1115M 3345C>G CESC-US 19 38382299 38382299 single base substitution G C downstream_gene_variant CESC-US 19 38382299 38382299 single base substitution G C missense_variant S1057C 3170C>G CESC-US 19 38382299 38382299 single base substitution G C missense_variant S1096C 3287C>G CESC-US 19 38383943 38383943 single base substitution G A downstream_gene_variant CESC-US 19 38383943 38383943 single base substitution G A synonymous_variant L761L 2283C>T CESC-US 19 38383943 38383943 single base substitution G A synonymous_variant L800L 2400C>T CESC-US 19 38385384 38385384 single base substitution C T downstream_gene_variant CESC-US 19 38385384 38385384 single base substitution C T missense_variant R281Q 842G>A CESC-US 19 38385384 38385384 single base substitution C T missense_variant R320Q 959G>A CESC-US 19 38386878 38386878 single base substitution G T exon_variant CESC-US 19 38386878 38386878 single base substitution G T intron_variant CESC-US 19 38386878 38386878 single base substitution G T missense_variant S49Y 146C>A CLLE-ES 19 38394595 38394595 single base substitution C T intron_variant CLLE-ES 19 38395319 38395319 single base substitution T C intron_variant COAD-US 19 38375613 38375613 single base substitution G C missense_variant L2861V 8581C>G COAD-US 19 38375613 38375613 single base substitution G C missense_variant L2900V 8698C>G COAD-US 19 38375666 38375666 single base substitution C T missense_variant R2843Q 8528G>A COAD-US 19 38375666 38375666 single base substitution C T missense_variant R2882Q 8645G>A COAD-US 19 38375815 38375815 deletion of <=200bp T - frameshift_variant K2793 COAD-US 19 38375815 38375815 deletion of <=200bp T - frameshift_variant K2832 COAD-US 19 38375944 38375944 single base substitution C T stop_gained W2750* 8250G>A COAD-US 19 38375944 38375944 single base substitution C T stop_gained W2789* 8367G>A COAD-US 19 38376035 38376035 deletion of <=200bp T - frameshift_variant K2720 COAD-US 19 38376035 38376035 deletion of <=200bp T - frameshift_variant K2759 COAD-US 19 38376103 38376103 single base substitution A G synonymous_variant F2697F 8091T>C COAD-US 19 38376103 38376103 single base substitution A G synonymous_variant F2736F 8208T>C COAD-US 19 38376208 38376208 single base substitution T G missense_variant E2662D 7986A>C COAD-US 19 38376208 38376208 single base substitution T G missense_variant E2701D 8103A>C COAD-US 19 38376538 38376538 single base substitution C A synonymous_variant L2552L 7656G>T COAD-US 19 38376538 38376538 single base substitution C A synonymous_variant L2591L 7773G>T COAD-US 19 38377389 38377389 single base substitution T C missense_variant R2269G 6805A>G COAD-US 19 38377389 38377389 single base substitution T C missense_variant R2308G 6922A>G COAD-US 19 38377404 38377404 single base substitution C T missense_variant E2264K 6790G>A COAD-US 19 38377404 38377404 single base substitution C T missense_variant E2303K 6907G>A COAD-US 19 38377406 38377406 single base substitution C A missense_variant R2263M 6788G>T COAD-US 19 38377406 38377406 single base substitution C A missense_variant R2302M 6905G>T COAD-US 19 38377414 38377414 single base substitution C T synonymous_variant E2260E 6780G>A COAD-US 19 38377414 38377414 single base substitution C T synonymous_variant E2299E 6897G>A COAD-US 19 38377417 38377417 single base substitution C T synonymous_variant E2259E 6777G>A COAD-US 19 38377417 38377417 single base substitution C T synonymous_variant E2298E 6894G>A COAD-US 19 38377527 38377527 single base substitution C A stop_gained E2223* 6667G>T COAD-US 19 38377527 38377527 single base substitution C A stop_gained E2262* 6784G>T COAD-US 19 38377563 38377563 single base substitution C A stop_gained E2211* 6631G>T COAD-US 19 38377563 38377563 single base substitution C A stop_gained E2250* 6748G>T COAD-US 19 38377773 38377773 single base substitution G A missense_variant R2141W 6421C>T COAD-US 19 38377773 38377773 single base substitution G A missense_variant R2180W 6538C>T COAD-US 19 38377927 38377927 single base substitution T A missense_variant K2089N 6267A>T COAD-US 19 38377927 38377927 single base substitution T A missense_variant K2128N 6384A>T COAD-US 19 38378311 38378311 single base substitution C A missense_variant K1961N 5883G>T COAD-US 19 38378311 38378311 single base substitution C A missense_variant K2000N 6000G>T COAD-US 19 38378415 38378415 insertion of <=200bp - T frameshift_variant Q1927Q? COAD-US 19 38378415 38378415 insertion of <=200bp - T frameshift_variant Q1966Q? COAD-US 19 38378721 38378721 single base substitution C A stop_gained E1825* 5473G>T COAD-US 19 38378721 38378721 single base substitution C A stop_gained E1864* 5590G>T COAD-US 19 38379163 38379163 single base substitution C A missense_variant E1677D 5031G>T COAD-US 19 38379163 38379163 single base substitution C A missense_variant E1716D 5148G>T COAD-US 19 38379432 38379432 single base substitution G A stop_gained R1588* 4762C>T COAD-US 19 38379432 38379432 single base substitution G A stop_gained R1627* 4879C>T COAD-US 19 38379712 38379712 single base substitution C A missense_variant E1494D 4482G>T COAD-US 19 38379712 38379712 single base substitution C A missense_variant E1533D 4599G>T COAD-US 19 38380099 38380099 single base substitution C A synonymous_variant V1365V 4095G>T COAD-US 19 38380099 38380099 single base substitution C A synonymous_variant V1404V 4212G>T COAD-US 19 38380367 38380367 single base substitution A G missense_variant M1276T 3827T>C COAD-US 19 38380367 38380367 single base substitution A G missense_variant M1315T 3944T>C COAD-US 19 38380396 38380396 single base substitution G A synonymous_variant N1266N 3798C>T COAD-US 19 38380396 38380396 single base substitution G A synonymous_variant N1305N 3915C>T COAD-US 19 38380663 38380663 single base substitution G C missense_variant D1177E 3531C>G COAD-US 19 38380663 38380663 single base substitution G C missense_variant D1216E 3648C>G COAD-US 19 38382199 38382199 single base substitution T G downstream_gene_variant COAD-US 19 38382199 38382199 single base substitution T G missense_variant K1090N 3270A>C COAD-US 19 38382199 38382199 single base substitution T G missense_variant K1129N 3387A>C COAD-US 19 38382328 38382328 single base substitution C T downstream_gene_variant COAD-US 19 38382328 38382328 single base substitution C T synonymous_variant P1047P 3141G>A COAD-US 19 38382328 38382328 single base substitution C T synonymous_variant P1086P 3258G>A COAD-US 19 38383286 38383286 single base substitution C A downstream_gene_variant COAD-US 19 38383286 38383286 single base substitution C A missense_variant E1019D 3057G>T COAD-US 19 38383286 38383286 single base substitution C A missense_variant E980D 2940G>T COAD-US 19 38383422 38383422 single base substitution G A downstream_gene_variant COAD-US 19 38383422 38383422 single base substitution G A missense_variant P935L 2804C>T COAD-US 19 38383422 38383422 single base substitution G A missense_variant P974L 2921C>T COAD-US 19 38383489 38383489 single base substitution G T downstream_gene_variant COAD-US 19 38383489 38383489 single base substitution G T missense_variant Q913K 2737C>A COAD-US 19 38383489 38383489 single base substitution G T missense_variant Q952K 2854C>A COAD-US 19 38383508 38383508 single base substitution C T downstream_gene_variant COAD-US 19 38383508 38383508 single base substitution C T synonymous_variant G906G 2718G>A COAD-US 19 38383508 38383508 single base substitution C T synonymous_variant G945G 2835G>A COAD-US 19 38383626 38383626 single base substitution C T downstream_gene_variant COAD-US 19 38383626 38383626 single base substitution C T missense_variant R867Q 2600G>A COAD-US 19 38383626 38383626 single base substitution C T missense_variant R906Q 2717G>A COAD-US 19 38384098 38384098 single base substitution C T downstream_gene_variant COAD-US 19 38384098 38384098 single base substitution C T missense_variant V710M 2128G>A COAD-US 19 38384098 38384098 single base substitution C T missense_variant V749M 2245G>A COAD-US 19 38384105 38384105 single base substitution C T downstream_gene_variant COAD-US 19 38384105 38384105 single base substitution C T synonymous_variant V707V 2121G>A COAD-US 19 38384105 38384105 single base substitution C T synonymous_variant V746V 2238G>A COAD-US 19 38384841 38384841 single base substitution A G downstream_gene_variant COAD-US 19 38384841 38384841 single base substitution A G missense_variant M462T 1385T>C COAD-US 19 38384841 38384841 single base substitution A G missense_variant M501T 1502T>C COAD-US 19 38385470 38385470 single base substitution G A downstream_gene_variant COAD-US 19 38385470 38385470 single base substitution G A synonymous_variant S252S 756C>T COAD-US 19 38385470 38385470 single base substitution G A synonymous_variant S291S 873C>T COCA-CN 19 38375790 38375790 single base substitution G A missense_variant R2802W 8404C>T COCA-CN 19 38375790 38375790 single base substitution G A missense_variant R2841W 8521C>T COCA-CN 19 38376118 38376118 single base substitution C A missense_variant K2692N 8076G>T COCA-CN 19 38376118 38376118 single base substitution C A missense_variant K2731N 8193G>T COCA-CN 19 38376805 38376805 single base substitution C A missense_variant K2463N 7389G>T COCA-CN 19 38376805 38376805 single base substitution C A missense_variant K2502N 7506G>T COCA-CN 19 38377327 38377327 single base substitution C A missense_variant K2289N 6867G>T COCA-CN 19 38377327 38377327 single base substitution C A missense_variant K2328N 6984G>T COCA-CN 19 38377381 38377381 single base substitution C A missense_variant E2271D 6813G>T COCA-CN 19 38377381 38377381 single base substitution C A missense_variant E2310D 6930G>T COCA-CN 19 38377533 38377533 single base substitution C A stop_gained E2221* 6661G>T COCA-CN 19 38377533 38377533 single base substitution C A stop_gained E2260* 6778G>T COCA-CN 19 38377576 38377576 single base substitution A G synonymous_variant G2206G 6618T>C COCA-CN 19 38377576 38377576 single base substitution A G synonymous_variant G2245G 6735T>C COCA-CN 19 38377791 38377791 single base substitution C A missense_variant D2135Y 6403G>T COCA-CN 19 38377791 38377791 single base substitution C A missense_variant D2174Y 6520G>T COCA-CN 19 38377869 38377869 single base substitution G A missense_variant R2109C 6325C>T COCA-CN 19 38377869 38377869 single base substitution G A missense_variant R2148C 6442C>T COCA-CN 19 38378066 38378066 single base substitution C A missense_variant R2043I 6128G>T COCA-CN 19 38378066 38378066 single base substitution C A missense_variant R2082I 6245G>T COCA-CN 19 38378184 38378184 single base substitution C A stop_gained E2004* 6010G>T COCA-CN 19 38378184 38378184 single base substitution C A stop_gained E2043* 6127G>T COCA-CN 19 38378207 38378207 single base substitution C A missense_variant R1996M 5987G>T COCA-CN 19 38378207 38378207 single base substitution C A missense_variant R2035M 6104G>T COCA-CN 19 38378250 38378250 single base substitution C A stop_gained E1982* 5944G>T COCA-CN 19 38378250 38378250 single base substitution C A stop_gained E2021* 6061G>T COCA-CN 19 38378287 38378287 single base substitution T A missense_variant R1969S 5907A>T COCA-CN 19 38378287 38378287 single base substitution T A missense_variant R2008S 6024A>T COCA-CN 19 38379193 38379193 single base substitution C A missense_variant K1667N 5001G>T COCA-CN 19 38379193 38379193 single base substitution C A missense_variant K1706N 5118G>T COCA-CN 19 38379962 38379962 single base substitution C A missense_variant R1411I 4232G>T COCA-CN 19 38379962 38379962 single base substitution C A missense_variant R1450I 4349G>T COCA-CN 19 38379989 38379989 single base substitution T G missense_variant Q1402P 4205A>C COCA-CN 19 38379989 38379989 single base substitution T G missense_variant Q1441P 4322A>C COCA-CN 19 38380488 38380488 single base substitution C T missense_variant A1236T 3706G>A COCA-CN 19 38380488 38380488 single base substitution C T missense_variant A1275T 3823G>A COCA-CN 19 38380616 38380616 single base substitution T G missense_variant K1193T 3578A>C COCA-CN 19 38380616 38380616 single base substitution T G missense_variant K1232T 3695A>C COCA-CN 19 38380675 38380675 single base substitution C A missense_variant Q1173H 3519G>T COCA-CN 19 38380675 38380675 single base substitution C A missense_variant Q1212H 3636G>T COCA-CN 19 38380902 38380902 single base substitution G A missense_variant R1098W 3292C>T COCA-CN 19 38380902 38380902 single base substitution G A missense_variant R1137W 3409C>T COCA-CN 19 38381009 38381009 single base substitution A T intron_variant COCA-CN 19 38382196 38382196 single base substitution C A downstream_gene_variant COCA-CN 19 38382196 38382196 single base substitution C A missense_variant K1091N 3273G>T COCA-CN 19 38382196 38382196 single base substitution C A missense_variant K1130N 3390G>T COCA-CN 19 38382368 38382368 single base substitution A G downstream_gene_variant COCA-CN 19 38382368 38382368 single base substitution A G missense_variant L1034S 3101T>C COCA-CN 19 38382368 38382368 single base substitution A G missense_variant L1073S 3218T>C COCA-CN 19 38382415 38382415 single base substitution C T downstream_gene_variant COCA-CN 19 38382415 38382415 single base substitution C T missense_variant M1018I 3054G>A COCA-CN 19 38382415 38382415 single base substitution C T missense_variant M1057I 3171G>A COCA-CN 19 38382440 38382440 single base substitution T C downstream_gene_variant COCA-CN 19 38382440 38382440 single base substitution T C missense_variant E1010G 3029A>G COCA-CN 19 38382440 38382440 single base substitution T C missense_variant E1049G 3146A>G COCA-CN 19 38385237 38385237 single base substitution C T downstream_gene_variant COCA-CN 19 38385237 38385237 single base substitution C T missense_variant R330H 989G>A COCA-CN 19 38385237 38385237 single base substitution C T missense_variant R369H 1106G>A COCA-CN 19 38385931 38385931 single base substitution G A downstream_gene_variant COCA-CN 19 38385931 38385931 single base substitution G A missense_variant R138W 412C>T COCA-CN 19 38385931 38385931 single base substitution G A missense_variant R99W 295C>T EOPC-DE 19 38381959 38381959 single base substitution A C downstream_gene_variant EOPC-DE 19 38381959 38381959 single base substitution A C intron_variant ESAD-UK 19 38374067 38374067 insertion of <=200bp - TTTG downstream_gene_variant ESAD-UK 19 38374329 38374329 single base substitution T A downstream_gene_variant ESAD-UK 19 38375307 38375307 single base substitution A C downstream_gene_variant ESAD-UK 19 38376890 38376890 single base substitution T G missense_variant K2435T 7304A>C ESAD-UK 19 38376890 38376890 single base substitution T G missense_variant K2474T 7421A>C ESAD-UK 19 38376968 38376968 single base substitution G A missense_variant P2409L 7226C>T ESAD-UK 19 38376968 38376968 single base substitution G A missense_variant P2448L 7343C>T ESAD-UK 19 38377253 38377253 single base substitution C A missense_variant S2314I 6941G>T ESAD-UK 19 38377253 38377253 single base substitution C A missense_variant S2353I 7058G>T ESAD-UK 19 38378331 38378331 single base substitution C A missense_variant D1955Y 5863G>T ESAD-UK 19 38378331 38378331 single base substitution C A missense_variant D1994Y 5980G>T ESAD-UK 19 38378602 38378602 single base substitution T G missense_variant K1864N 5592A>C ESAD-UK 19 38378602 38378602 single base substitution T G missense_variant K1903N 5709A>C ESAD-UK 19 38378971 38378971 single base substitution T G missense_variant K1741N 5223A>C ESAD-UK 19 38378971 38378971 single base substitution T G missense_variant K1780N 5340A>C ESAD-UK 19 38379369 38379369 single base substitution A C missense_variant L1609V 4825T>G ESAD-UK 19 38379369 38379369 single base substitution A C missense_variant L1648V 4942T>G ESAD-UK 19 38380462 38380462 single base substitution G A synonymous_variant D1244D 3732C>T ESAD-UK 19 38380462 38380462 single base substitution G A synonymous_variant D1283D 3849C>T ESAD-UK 19 38380685 38380685 single base substitution T G missense_variant K1170T 3509A>C ESAD-UK 19 38380685 38380685 single base substitution T G missense_variant K1209T 3626A>C ESAD-UK 19 38381053 38381053 single base substitution A C intron_variant ESAD-UK 19 38381589 38381589 single base substitution T A intron_variant ESAD-UK 19 38381784 38381784 single base substitution T A downstream_gene_variant ESAD-UK 19 38381784 38381784 single base substitution T A intron_variant ESAD-UK 19 38381785 38381785 single base substitution C T downstream_gene_variant ESAD-UK 19 38381785 38381785 single base substitution C T intron_variant ESAD-UK 19 38382012 38382012 single base substitution C T downstream_gene_variant ESAD-UK 19 38382012 38382012 single base substitution C T intron_variant ESAD-UK 19 38382014 38382014 single base substitution G A downstream_gene_variant ESAD-UK 19 38382014 38382014 single base substitution G A intron_variant ESAD-UK 19 38383113 38383113 single base substitution G C downstream_gene_variant ESAD-UK 19 38383113 38383113 single base substitution G C intron_variant ESAD-UK 19 38383616 38383616 single base substitution C A downstream_gene_variant ESAD-UK 19 38383616 38383616 single base substitution C A synonymous_variant L870L 2610G>T ESAD-UK 19 38383616 38383616 single base substitution C A synonymous_variant L909L 2727G>T ESAD-UK 19 38384847 38384847 single base substitution T G downstream_gene_variant ESAD-UK 19 38384847 38384847 single base substitution T G missense_variant K460T 1379A>C ESAD-UK 19 38384847 38384847 single base substitution T G missense_variant K499T 1496A>C ESAD-UK 19 38386813 38386813 single base substitution G A exon_variant ESAD-UK 19 38386813 38386813 single base substitution G A intron_variant ESAD-UK 19 38386813 38386813 single base substitution G A missense_variant L71F 211C>T ESAD-UK 19 38387502 38387502 single base substitution C T intron_variant ESAD-UK 19 38387971 38387971 single base substitution C A intron_variant ESAD-UK 19 38389535 38389537 deletion of <=200bp AGA - intron_variant ESAD-UK 19 38390482 38390482 single base substitution C A intron_variant ESAD-UK 19 38390575 38390575 single base substitution C A intron_variant ESAD-UK 19 38391980 38391980 single base substitution G A intron_variant ESAD-UK 19 38393429 38393429 single base substitution A G intron_variant ESAD-UK 19 38393606 38393606 single base substitution T G intron_variant ESAD-UK 19 38393748 38393748 single base substitution C T intron_variant ESAD-UK 19 38394140 38394140 single base substitution G A intron_variant ESAD-UK 19 38397649 38397649 single base substitution C T upstream_gene_variant ESAD-UK 19 38401851 38401851 single base substitution T A upstream_gene_variant ESCA-CN 19 38376052 38376057 deletion of <=200bp CTGTGT - inframe_deletion TQ2713 ESCA-CN 19 38376052 38376057 deletion of <=200bp CTGTGT - inframe_deletion TQ2752 ESCA-CN 19 38376521 38376521 single base substitution G C stop_gained S2558* 7673C>G ESCA-CN 19 38376521 38376521 single base substitution G C stop_gained S2597* 7790C>G ESCA-CN 19 38377101 38377102 deletion of <=200bp TT - frameshift_variant ER2364 ESCA-CN 19 38377101 38377102 deletion of <=200bp TT - frameshift_variant ER2403 ESCA-CN 19 38378115 38378115 single base substitution C T missense_variant E2027K 6079G>A ESCA-CN 19 38378115 38378115 single base substitution C T missense_variant E2066K 6196G>A ESCA-CN 19 38378320 38378320 single base substitution C G missense_variant K1958N 5874G>C ESCA-CN 19 38378320 38378320 single base substitution C G missense_variant K1997N 5991G>C ESCA-CN 19 38379335 38379335 single base substitution T A missense_variant Y1620F 4859A>T ESCA-CN 19 38379335 38379335 single base substitution T A missense_variant Y1659F 4976A>T ESCA-CN 19 38382363 38382363 single base substitution C A downstream_gene_variant ESCA-CN 19 38382363 38382363 single base substitution C A stop_gained E1036* 3106G>T ESCA-CN 19 38382363 38382363 single base substitution C A stop_gained E1075* 3223G>T ESCA-CN 19 38383399 38383399 single base substitution C T downstream_gene_variant ESCA-CN 19 38383399 38383399 single base substitution C T missense_variant E943K 2827G>A ESCA-CN 19 38383399 38383399 single base substitution C T missense_variant E982K 2944G>A ESCA-CN 19 38383418 38383418 single base substitution C G downstream_gene_variant ESCA-CN 19 38383418 38383418 single base substitution C G synonymous_variant L936L 2808G>C ESCA-CN 19 38383418 38383418 single base substitution C G synonymous_variant L975L 2925G>C ESCA-CN 19 38383488 38383488 single base substitution T A downstream_gene_variant ESCA-CN 19 38383488 38383488 single base substitution T A missense_variant Q913L 2738A>T ESCA-CN 19 38383488 38383488 single base substitution T A missense_variant Q952L 2855A>T KIRC-US 19 38377432 38377432 single base substitution T C synonymous_variant E2254E 6762A>G KIRC-US 19 38377432 38377432 single base substitution T C synonymous_variant E2293E 6879A>G KIRC-US 19 38380084 38380084 single base substitution G A synonymous_variant G1370G 4110C>T KIRC-US 19 38380084 38380084 single base substitution G A synonymous_variant G1409G 4227C>T KIRC-US 19 38382417 38382417 single base substitution T A downstream_gene_variant KIRC-US 19 38382417 38382417 single base substitution T A missense_variant M1018L 3052A>T KIRC-US 19 38382417 38382417 single base substitution T A missense_variant M1057L 3169A>T KIRC-US 19 38383341 38383341 single base substitution C G downstream_gene_variant KIRC-US 19 38383341 38383341 single base substitution C G missense_variant G1001A 3002G>C KIRC-US 19 38383341 38383341 single base substitution C G missense_variant G962A 2885G>C KIRC-US 19 38383368 38383368 single base substitution T C downstream_gene_variant KIRC-US 19 38383368 38383368 single base substitution T C missense_variant H953R 2858A>G KIRC-US 19 38383368 38383368 single base substitution T C missense_variant H992R 2975A>G KIRC-US 19 38385920 38385920 single base substitution T G downstream_gene_variant KIRC-US 19 38385920 38385920 single base substitution T G missense_variant K102N 306A>C KIRC-US 19 38385920 38385920 single base substitution T G missense_variant K141N 423A>C KIRP-US 19 38385244 38385244 single base substitution G T downstream_gene_variant KIRP-US 19 38385244 38385244 single base substitution G T missense_variant Q328K 982C>A KIRP-US 19 38385244 38385244 single base substitution G T missense_variant Q367K 1099C>A LAML-KR 19 38375830 38375830 single base substitution G A synonymous_variant Y2788Y 8364C>T LAML-KR 19 38375830 38375830 single base substitution G A synonymous_variant Y2827Y 8481C>T LAML-KR 19 38387096 38387096 single base substitution C G intron_variant LICA-CN 19 38375753 38375753 single base substitution G T missense_variant T2814N 8441C>A LICA-CN 19 38375753 38375753 single base substitution G T missense_variant T2853N 8558C>A LICA-CN 19 38376929 38376929 single base substitution A T missense_variant V2422E 7265T>A LICA-CN 19 38376929 38376929 single base substitution A T missense_variant V2461E 7382T>A LICA-CN 19 38378038 38378038 single base substitution T A missense_variant L2052F 6156A>T LICA-CN 19 38378038 38378038 single base substitution T A missense_variant L2091F 6273A>T LICA-CN 19 38378072 38378072 single base substitution C T missense_variant G2041E 6122G>A LICA-CN 19 38378072 38378072 single base substitution C T missense_variant G2080E 6239G>A LICA-CN 19 38379369 38379369 single base substitution A T missense_variant L1609M 4825T>A LICA-CN 19 38379369 38379369 single base substitution A T missense_variant L1648M 4942T>A LICA-CN 19 38382301 38382301 single base substitution A T downstream_gene_variant LICA-CN 19 38382301 38382301 single base substitution A T synonymous_variant P1056P 3168T>A LICA-CN 19 38382301 38382301 single base substitution A T synonymous_variant P1095P 3285T>A LICA-CN 19 38383618 38383618 single base substitution G T downstream_gene_variant LICA-CN 19 38383618 38383618 single base substitution G T missense_variant L870M 2608C>A LICA-CN 19 38383618 38383618 single base substitution G T missense_variant L909M 2725C>A LICA-CN 19 38385056 38385056 single base substitution G T downstream_gene_variant LICA-CN 19 38385056 38385056 single base substitution G T synonymous_variant G390G 1170C>A LICA-CN 19 38385056 38385056 single base substitution G T synonymous_variant G429G 1287C>A LICA-CN 19 38385636 38385636 single base substitution G A downstream_gene_variant LICA-CN 19 38385636 38385636 single base substitution G A missense_variant T197M 590C>T LICA-CN 19 38385636 38385636 single base substitution G A missense_variant T236M 707C>T LICA-CN 19 38385926 38385926 single base substitution T G downstream_gene_variant LICA-CN 19 38385926 38385926 single base substitution T G synonymous_variant A100A 300A>C LICA-CN 19 38385926 38385926 single base substitution T G synonymous_variant A139A 417A>C LICA-FR 19 38370776 38370776 single base substitution G C downstream_gene_variant LICA-FR 19 38375694 38375694 single base substitution G A missense_variant R2834C 8500C>T LICA-FR 19 38375694 38375694 single base substitution G A missense_variant R2873C 8617C>T LICA-FR 19 38376087 38376087 single base substitution A C missense_variant F2703V 8107T>G LICA-FR 19 38376087 38376087 single base substitution A C missense_variant F2742V 8224T>G LICA-FR 19 38376199 38376199 single base substitution G T stop_gained Y2665* 7995C>A LICA-FR 19 38376199 38376199 single base substitution G T stop_gained Y2704* 8112C>A LICA-FR 19 38376704 38376704 single base substitution G A missense_variant P2497L 7490C>T LICA-FR 19 38376704 38376704 single base substitution G A missense_variant P2536L 7607C>T LICA-FR 19 38377356 38377356 single base substitution C A missense_variant V2280L 6838G>T LICA-FR 19 38377356 38377356 single base substitution C A missense_variant V2319L 6955G>T LICA-FR 19 38380667 38380667 single base substitution C A missense_variant R1176L 3527G>T LICA-FR 19 38380667 38380667 single base substitution C A missense_variant R1215L 3644G>T LICA-FR 19 38382196 38382196 single base substitution C T downstream_gene_variant LICA-FR 19 38382196 38382196 single base substitution C T synonymous_variant K1091K 3273G>A LICA-FR 19 38382196 38382196 single base substitution C T synonymous_variant K1130K 3390G>A LICA-FR 19 38382325 38382325 single base substitution A C downstream_gene_variant LICA-FR 19 38382325 38382325 single base substitution A C synonymous_variant A1048A 3144T>G LICA-FR 19 38382325 38382325 single base substitution A C synonymous_variant A1087A 3261T>G LICA-FR 19 38384308 38384308 single base substitution G A downstream_gene_variant LICA-FR 19 38384308 38384308 single base substitution G A missense_variant P640S 1918C>T LICA-FR 19 38384308 38384308 single base substitution G A missense_variant P679S 2035C>T LIHC-US 19 38377028 38377028 single base substitution G T missense_variant P2389H 7166C>A LIHC-US 19 38377028 38377028 single base substitution G T missense_variant P2428H 7283C>A LIHC-US 19 38377306 38377306 single base substitution C T synonymous_variant K2296K 6888G>A LIHC-US 19 38377306 38377306 single base substitution C T synonymous_variant K2335K 7005G>A LIHC-US 19 38378259 38378259 single base substitution C A stop_gained E1979* 5935G>T LIHC-US 19 38378259 38378259 single base substitution C A stop_gained E2018* 6052G>T LIHC-US 19 38378503 38378503 single base substitution C G missense_variant Q1897H 5691G>C LIHC-US 19 38378503 38378503 single base substitution C G missense_variant Q1936H 5808G>C LIHC-US 19 38378513 38378513 single base substitution T G missense_variant K1894T 5681A>C LIHC-US 19 38378513 38378513 single base substitution T G missense_variant K1933T 5798A>C LIHC-US 19 38378936 38378936 single base substitution T A missense_variant E1753V 5258A>T LIHC-US 19 38378936 38378936 single base substitution T A missense_variant E1792V 5375A>T LIHC-US 19 38380424 38380424 single base substitution G T missense_variant S1257Y 3770C>A LIHC-US 19 38380424 38380424 single base substitution G T missense_variant S1296Y 3887C>A LIHC-US 19 38382236 38382236 single base substitution G A downstream_gene_variant LIHC-US 19 38382236 38382236 single base substitution G A missense_variant P1078L 3233C>T LIHC-US 19 38382236 38382236 single base substitution G A missense_variant P1117L 3350C>T LIHC-US 19 38383656 38383656 single base substitution G A downstream_gene_variant LIHC-US 19 38383656 38383656 single base substitution G A missense_variant T857I 2570C>T LIHC-US 19 38383656 38383656 single base substitution G A missense_variant T896I 2687C>T LIHC-US 19 38383676 38383676 single base substitution C G downstream_gene_variant LIHC-US 19 38383676 38383676 single base substitution C G missense_variant M850I 2550G>C LIHC-US 19 38383676 38383676 single base substitution C G missense_variant M889I 2667G>C LIHC-US 19 38383818 38383818 single base substitution A T downstream_gene_variant LIHC-US 19 38383818 38383818 single base substitution A T missense_variant L803Q 2408T>A LIHC-US 19 38383818 38383818 single base substitution A T missense_variant L842Q 2525T>A LIHC-US 19 38384319 38384319 single base substitution A G downstream_gene_variant LIHC-US 19 38384319 38384319 single base substitution A G missense_variant L636S 1907T>C LIHC-US 19 38384319 38384319 single base substitution A G missense_variant L675S 2024T>C LIHC-US 19 38384931 38384931 single base substitution C T downstream_gene_variant LIHC-US 19 38384931 38384931 single base substitution C T missense_variant R432Q 1295G>A LIHC-US 19 38384931 38384931 single base substitution C T missense_variant R471Q 1412G>A LIHC-US 19 38385769 38385769 single base substitution T A downstream_gene_variant LIHC-US 19 38385769 38385769 single base substitution T A missense_variant M153L 457A>T LIHC-US 19 38385769 38385769 single base substitution T A missense_variant M192L 574A>T LINC-JP 19 38371608 38371608 single base substitution C A downstream_gene_variant LINC-JP 19 38371804 38371804 single base substitution T G downstream_gene_variant LINC-JP 19 38374884 38374884 single base substitution G T downstream_gene_variant LINC-JP 19 38376583 38376583 single base substitution C T synonymous_variant A2537A 7611G>A LINC-JP 19 38376583 38376583 single base substitution C T synonymous_variant A2576A 7728G>A LINC-JP 19 38377377 38377377 single base substitution C T missense_variant E2273K 6817G>A LINC-JP 19 38377377 38377377 single base substitution C T missense_variant E2312K 6934G>A LINC-JP 19 38377810 38377810 insertion of <=200bp - T frameshift_variant K2128K? LINC-JP 19 38377810 38377810 insertion of <=200bp - T frameshift_variant K2167K? LINC-JP 19 38377868 38377868 single base substitution C T missense_variant R2109H 6326G>A LINC-JP 19 38377868 38377868 single base substitution C T missense_variant R2148H 6443G>A LINC-JP 19 38379562 38379562 single base substitution C A synonymous_variant V1544V 4632G>T LINC-JP 19 38379562 38379562 single base substitution C A synonymous_variant V1583V 4749G>T LINC-JP 19 38380177 38380177 single base substitution G T missense_variant H1339Q 4017C>A LINC-JP 19 38380177 38380177 single base substitution G T missense_variant H1378Q 4134C>A LINC-JP 19 38380350 38380350 single base substitution G A missense_variant P1282S 3844C>T LINC-JP 19 38380350 38380350 single base substitution G A missense_variant P1321S 3961C>T LINC-JP 19 38382175 38382175 single base substitution G A downstream_gene_variant LINC-JP 19 38382175 38382175 single base substitution G A intron_variant LINC-JP 19 38383144 38383144 single base substitution G A downstream_gene_variant LINC-JP 19 38383144 38383144 single base substitution G A intron_variant LINC-JP 19 38383382 38383382 single base substitution T C downstream_gene_variant LINC-JP 19 38383382 38383382 single base substitution T C synonymous_variant L948L 2844A>G LINC-JP 19 38383382 38383382 single base substitution T C synonymous_variant L987L 2961A>G LINC-JP 19 38384956 38384956 single base substitution C T downstream_gene_variant LINC-JP 19 38384956 38384956 single base substitution C T missense_variant A424T 1270G>A LINC-JP 19 38384956 38384956 single base substitution C T missense_variant A463T 1387G>A LINC-JP 19 38390167 38390167 single base substitution C A intron_variant LIRI-JP 19 38370463 38370463 single base substitution T C downstream_gene_variant LIRI-JP 19 38371291 38371291 single base substitution A G downstream_gene_variant LIRI-JP 19 38371919 38371919 single base substitution G A downstream_gene_variant LIRI-JP 19 38372583 38372583 single base substitution A T downstream_gene_variant LIRI-JP 19 38373019 38373019 single base substitution C A downstream_gene_variant LIRI-JP 19 38373894 38373894 single base substitution T C downstream_gene_variant LIRI-JP 19 38375683 38375683 single base substitution A C synonymous_variant L2837L 8511T>G LIRI-JP 19 38375683 38375683 single base substitution A C synonymous_variant L2876L 8628T>G LIRI-JP 19 38376096 38376096 single base substitution T C missense_variant K2700E 8098A>G LIRI-JP 19 38376096 38376096 single base substitution T C missense_variant K2739E 8215A>G LIRI-JP 19 38376349 38376349 deletion of <=200bp T - frameshift_variant K2615 LIRI-JP 19 38376349 38376349 deletion of <=200bp T - frameshift_variant K2654 LIRI-JP 19 38376545 38376545 single base substitution C G missense_variant C2550S 7649G>C LIRI-JP 19 38376545 38376545 single base substitution C G missense_variant C2589S 7766G>C LIRI-JP 19 38376798 38376798 single base substitution A G missense_variant F2466L 7396T>C LIRI-JP 19 38376798 38376798 single base substitution A G missense_variant F2505L 7513T>C LIRI-JP 19 38377416 38377416 single base substitution C G missense_variant E2260Q 6778G>C LIRI-JP 19 38377416 38377416 single base substitution C G missense_variant E2299Q 6895G>C LIRI-JP 19 38378183 38378183 single base substitution T A missense_variant E2004V 6011A>T LIRI-JP 19 38378183 38378183 single base substitution T A missense_variant E2043V 6128A>T LIRI-JP 19 38379141 38379141 single base substitution T C missense_variant K1685E 5053A>G LIRI-JP 19 38379141 38379141 single base substitution T C missense_variant K1724E 5170A>G LIRI-JP 19 38381514 38381514 single base substitution A T intron_variant LIRI-JP 19 38381746 38381746 single base substitution G A downstream_gene_variant LIRI-JP 19 38381746 38381746 single base substitution G A intron_variant LIRI-JP 19 38387490 38387490 single base substitution C T intron_variant LIRI-JP 19 38388118 38388118 single base substitution G C intron_variant LIRI-JP 19 38388625 38388625 single base substitution C T intron_variant LIRI-JP 19 38389056 38389056 single base substitution C A intron_variant LIRI-JP 19 38391381 38391381 single base substitution T C intron_variant LIRI-JP 19 38393414 38393414 single base substitution T A intron_variant LIRI-JP 19 38393426 38393426 single base substitution T C intron_variant LIRI-JP 19 38397935 38397935 single base substitution C T upstream_gene_variant LIRI-JP 19 38398121 38398121 single base substitution G A upstream_gene_variant LIRI-JP 19 38400477 38400477 single base substitution T C upstream_gene_variant LIRI-JP 19 38401089 38401089 single base substitution T C upstream_gene_variant LIRI-JP 19 38402124 38402124 single base substitution G C upstream_gene_variant LUSC-KR 19 38371332 38371332 single base substitution T A downstream_gene_variant LUSC-KR 19 38375985 38375985 single base substitution G A missense_variant R2737W 8209C>T LUSC-KR 19 38375985 38375985 single base substitution G A missense_variant R2776W 8326C>T LUSC-KR 19 38378296 38378296 single base substitution T C synonymous_variant E1966E 5898A>G LUSC-KR 19 38378296 38378296 single base substitution T C synonymous_variant E2005E 6015A>G LUSC-KR 19 38379699 38379699 single base substitution C A missense_variant A1499S 4495G>T LUSC-KR 19 38379699 38379699 single base substitution C A missense_variant A1538S 4612G>T LUSC-KR 19 38381520 38381520 single base substitution C A intron_variant LUSC-KR 19 38381822 38381822 single base substitution G T downstream_gene_variant LUSC-KR 19 38381822 38381822 single base substitution G T intron_variant LUSC-KR 19 38385422 38385422 single base substitution G T downstream_gene_variant LUSC-KR 19 38385422 38385422 single base substitution G T synonymous_variant I268I 804C>A LUSC-KR 19 38385422 38385422 single base substitution G T synonymous_variant I307I 921C>A LUSC-KR 19 38392575 38392575 single base substitution C T intron_variant LUSC-KR 19 38394411 38394411 single base substitution C A intron_variant LUSC-KR 19 38395017 38395017 single base substitution G C intron_variant LUSC-KR 19 38395017 38395017 single base substitution G T intron_variant LUSC-KR 19 38397265 38397265 single base substitution C T 5_prime_UTR_variant LUSC-KR 19 38397265 38397265 single base substitution C T upstream_gene_variant LUSC-KR 19 38398651 38398651 single base substitution C T upstream_gene_variant MALY-DE 19 38372026 38372026 single base substitution A G downstream_gene_variant MALY-DE 19 38373119 38373119 deletion of <=200bp T - downstream_gene_variant MALY-DE 19 38374392 38374392 single base substitution G A downstream_gene_variant MALY-DE 19 38375183 38375183 single base substitution C T downstream_gene_variant MALY-DE 19 38377757 38377757 single base substitution A T missense_variant L2146Q 6437T>A MALY-DE 19 38377757 38377757 single base substitution A T missense_variant L2185Q 6554T>A MALY-DE 19 38389243 38389243 single base substitution G T intron_variant MALY-DE 19 38396850 38396850 single base substitution C T intron_variant MALY-DE 19 38399257 38399257 insertion of <=200bp - T upstream_gene_variant MALY-DE 19 38401891 38401892 deletion of <=200bp GT - upstream_gene_variant MELA-AU 19 38370514 38370514 single base substitution A G downstream_gene_variant MELA-AU 19 38370525 38370525 single base substitution C T downstream_gene_variant MELA-AU 19 38370645 38370645 single base substitution C T downstream_gene_variant MELA-AU 19 38370755 38370755 single base substitution A T downstream_gene_variant MELA-AU 19 38370807 38370807 single base substitution G A downstream_gene_variant MELA-AU 19 38370879 38370880 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 19 38370946 38370946 single base substitution C T downstream_gene_variant MELA-AU 19 38370965 38370965 single base substitution C T downstream_gene_variant MELA-AU 19 38371124 38371124 single base substitution G A downstream_gene_variant MELA-AU 19 38371286 38371286 single base substitution G A downstream_gene_variant MELA-AU 19 38371474 38371474 single base substitution G A downstream_gene_variant MELA-AU 19 38371590 38371590 single base substitution C T downstream_gene_variant MELA-AU 19 38372024 38372024 single base substitution G A downstream_gene_variant MELA-AU 19 38372057 38372057 single base substitution G A downstream_gene_variant MELA-AU 19 38372212 38372212 single base substitution G A downstream_gene_variant MELA-AU 19 38372256 38372256 single base substitution G A downstream_gene_variant MELA-AU 19 38372307 38372307 single base substitution C T downstream_gene_variant MELA-AU 19 38372438 38372438 single base substitution G A downstream_gene_variant MELA-AU 19 38372454 38372454 single base substitution T G downstream_gene_variant MELA-AU 19 38372574 38372574 single base substitution G A downstream_gene_variant MELA-AU 19 38372802 38372802 single base substitution G A downstream_gene_variant MELA-AU 19 38372803 38372803 single base substitution G A downstream_gene_variant MELA-AU 19 38372900 38372900 single base substitution C T downstream_gene_variant MELA-AU 19 38372997 38372997 single base substitution G A downstream_gene_variant MELA-AU 19 38373228 38373228 single base substitution G A downstream_gene_variant MELA-AU 19 38373247 38373247 single base substitution C T downstream_gene_variant MELA-AU 19 38373323 38373323 single base substitution G A downstream_gene_variant MELA-AU 19 38373382 38373382 single base substitution C T downstream_gene_variant MELA-AU 19 38373643 38373643 single base substitution G A downstream_gene_variant MELA-AU 19 38373918 38373918 single base substitution G A downstream_gene_variant MELA-AU 19 38374022 38374022 single base substitution G A downstream_gene_variant MELA-AU 19 38374158 38374158 single base substitution C T downstream_gene_variant MELA-AU 19 38374221 38374221 single base substitution C A downstream_gene_variant MELA-AU 19 38374494 38374494 single base substitution C T downstream_gene_variant MELA-AU 19 38374530 38374530 single base substitution C T downstream_gene_variant MELA-AU 19 38374676 38374676 single base substitution C G downstream_gene_variant MELA-AU 19 38374758 38374758 single base substitution C T downstream_gene_variant MELA-AU 19 38374770 38374770 single base substitution C T downstream_gene_variant MELA-AU 19 38374791 38374791 single base substitution G A downstream_gene_variant MELA-AU 19 38375007 38375007 single base substitution C T downstream_gene_variant MELA-AU 19 38375041 38375041 single base substitution G A downstream_gene_variant MELA-AU 19 38375092 38375092 single base substitution G A downstream_gene_variant MELA-AU 19 38375110 38375110 single base substitution G A downstream_gene_variant MELA-AU 19 38375222 38375222 single base substitution A G downstream_gene_variant MELA-AU 19 38375256 38375256 single base substitution T C downstream_gene_variant MELA-AU 19 38375258 38375258 single base substitution C T downstream_gene_variant MELA-AU 19 38375278 38375278 single base substitution G A downstream_gene_variant MELA-AU 19 38375287 38375287 single base substitution C T downstream_gene_variant MELA-AU 19 38375351 38375351 single base substitution C T downstream_gene_variant MELA-AU 19 38375475 38375475 single base substitution A T 3_prime_UTR_variant MELA-AU 19 38375475 38375475 single base substitution A T downstream_gene_variant MELA-AU 19 38375685 38375685 single base substitution G A missense_variant L2837F 8509C>T MELA-AU 19 38375685 38375685 single base substitution G A missense_variant L2876F 8626C>T MELA-AU 19 38375814 38375814 single base substitution C T missense_variant A2794T 8380G>A MELA-AU 19 38375814 38375814 single base substitution C T missense_variant A2833T 8497G>A MELA-AU 19 38375853 38375853 single base substitution G A missense_variant P2781S 8341C>T MELA-AU 19 38375853 38375853 single base substitution G A missense_variant P2820S 8458C>T MELA-AU 19 38375928 38375928 single base substitution G A stop_gained Q2756* 8266C>T MELA-AU 19 38375928 38375928 single base substitution G A stop_gained Q2795* 8383C>T MELA-AU 19 38376117 38376117 single base substitution C T missense_variant D2693N 8077G>A MELA-AU 19 38376117 38376117 single base substitution C T missense_variant D2732N 8194G>A MELA-AU 19 38376348 38376348 single base substitution G A missense_variant P2616S 7846C>T MELA-AU 19 38376348 38376348 single base substitution G A missense_variant P2655S 7963C>T MELA-AU 19 38376428 38376428 single base substitution G A missense_variant S2589L 7766C>T MELA-AU 19 38376428 38376428 single base substitution G A missense_variant S2628L 7883C>T MELA-AU 19 38376430 38376430 single base substitution G A synonymous_variant I2588I 7764C>T MELA-AU 19 38376430 38376430 single base substitution G A synonymous_variant I2627I 7881C>T MELA-AU 19 38376535 38376535 single base substitution G A synonymous_variant L2553L 7659C>T MELA-AU 19 38376535 38376535 single base substitution G A synonymous_variant L2592L 7776C>T MELA-AU 19 38376561 38376561 single base substitution C T missense_variant G2545S 7633G>A MELA-AU 19 38376561 38376561 single base substitution C T missense_variant G2584S 7750G>A MELA-AU 19 38376581 38376581 single base substitution C T missense_variant G2538E 7613G>A MELA-AU 19 38376581 38376581 single base substitution C T missense_variant G2577E 7730G>A MELA-AU 19 38376651 38376651 single base substitution C T missense_variant E2515K 7543G>A MELA-AU 19 38376651 38376651 single base substitution C T missense_variant E2554K 7660G>A MELA-AU 19 38376814 38376814 single base substitution C T synonymous_variant Q2460Q 7380G>A MELA-AU 19 38376814 38376814 single base substitution C T synonymous_variant Q2499Q 7497G>A MELA-AU 19 38376882 38376882 single base substitution C T missense_variant E2438K 7312G>A MELA-AU 19 38376882 38376882 single base substitution C T missense_variant E2477K 7429G>A MELA-AU 19 38376895 38376895 single base substitution C T missense_variant M2433I 7299G>A MELA-AU 19 38376895 38376895 single base substitution C T missense_variant M2472I 7416G>A MELA-AU 19 38376901 38376901 single base substitution C T synonymous_variant G2431G 7293G>A MELA-AU 19 38376901 38376901 single base substitution C T synonymous_variant G2470G 7410G>A MELA-AU 19 38376907 38376907 single base substitution G A synonymous_variant F2429F 7287C>T MELA-AU 19 38376907 38376907 single base substitution G A synonymous_variant F2468F 7404C>T MELA-AU 19 38376924 38376924 single base substitution C T missense_variant E2424K 7270G>A MELA-AU 19 38376924 38376924 single base substitution C T missense_variant E2463K 7387G>A MELA-AU 19 38376952 38376952 single base substitution G A synonymous_variant S2414S 7242C>T MELA-AU 19 38376952 38376952 single base substitution G A synonymous_variant S2453S 7359C>T MELA-AU 19 38376953 38376953 single base substitution G A missense_variant S2414F 7241C>T MELA-AU 19 38376953 38376953 single base substitution G A missense_variant S2453F 7358C>T MELA-AU 19 38377074 38377074 single base substitution G A missense_variant P2374S 7120C>T MELA-AU 19 38377074 38377074 single base substitution G A missense_variant P2413S 7237C>T MELA-AU 19 38377090 38377090 single base substitution G A synonymous_variant S2368S 7104C>T MELA-AU 19 38377090 38377090 single base substitution G A synonymous_variant S2407S 7221C>T MELA-AU 19 38377104 38377104 single base substitution C T missense_variant E2364K 7090G>A MELA-AU 19 38377104 38377104 single base substitution C T missense_variant E2403K 7207G>A MELA-AU 19 38377168 38377168 single base substitution C T synonymous_variant E2342E 7026G>A MELA-AU 19 38377168 38377168 single base substitution C T synonymous_variant E2381E 7143G>A MELA-AU 19 38377221 38377222 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant EE2324EK MELA-AU 19 38377221 38377222 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant EE2363EK MELA-AU 19 38377243 38377243 single base substitution C T synonymous_variant E2317E 6951G>A MELA-AU 19 38377243 38377243 single base substitution C T synonymous_variant E2356E 7068G>A MELA-AU 19 38377287 38377287 single base substitution C T missense_variant E2303K 6907G>A MELA-AU 19 38377287 38377287 single base substitution C T missense_variant E2342K 7024G>A MELA-AU 19 38377306 38377306 single base substitution C T synonymous_variant K2296K 6888G>A MELA-AU 19 38377306 38377306 single base substitution C T synonymous_variant K2335K 7005G>A MELA-AU 19 38377317 38377317 single base substitution C T missense_variant E2293K 6877G>A MELA-AU 19 38377317 38377317 single base substitution C T missense_variant E2332K 6994G>A MELA-AU 19 38377410 38377410 single base substitution C T missense_variant V2262I 6784G>A MELA-AU 19 38377410 38377410 single base substitution C T missense_variant V2301I 6901G>A MELA-AU 19 38377514 38377514 single base substitution G A missense_variant S2227F 6680C>T MELA-AU 19 38377514 38377514 single base substitution G A missense_variant S2266F 6797C>T MELA-AU 19 38377618 38377618 single base substitution G A synonymous_variant F2192F 6576C>T MELA-AU 19 38377618 38377618 single base substitution G A synonymous_variant F2231F 6693C>T MELA-AU 19 38377771 38377771 single base substitution C T synonymous_variant R2141R 6423G>A MELA-AU 19 38377771 38377771 single base substitution C T synonymous_variant R2180R 6540G>A MELA-AU 19 38377805 38377805 single base substitution G A missense_variant S2130L 6389C>T MELA-AU 19 38377805 38377805 single base substitution G A missense_variant S2169L 6506C>T MELA-AU 19 38377808 38377808 single base substitution C T missense_variant R2129Q 6386G>A MELA-AU 19 38377808 38377808 single base substitution C T missense_variant R2168Q 6503G>A MELA-AU 19 38377824 38377824 single base substitution C T missense_variant D2124N 6370G>A MELA-AU 19 38377824 38377824 single base substitution C T missense_variant D2163N 6487G>A MELA-AU 19 38377987 38377987 single base substitution T C synonymous_variant E2069E 6207A>G MELA-AU 19 38377987 38377987 single base substitution T C synonymous_variant E2108E 6324A>G MELA-AU 19 38378023 38378023 single base substitution C T synonymous_variant R2057R 6171G>A MELA-AU 19 38378023 38378023 single base substitution C T synonymous_variant R2096R 6288G>A MELA-AU 19 38378094 38378094 single base substitution C T missense_variant G2034R 6100G>A MELA-AU 19 38378094 38378094 single base substitution C T missense_variant G2073R 6217G>A MELA-AU 19 38378171 38378171 single base substitution C T missense_variant R2008K 6023G>A MELA-AU 19 38378171 38378171 single base substitution C T missense_variant R2047K 6140G>A MELA-AU 19 38378207 38378207 single base substitution C T missense_variant R1996K 5987G>A MELA-AU 19 38378207 38378207 single base substitution C T missense_variant R2035K 6104G>A MELA-AU 19 38378253 38378253 single base substitution T A stop_gained K1981* 5941A>T MELA-AU 19 38378253 38378253 single base substitution T A stop_gained K2020* 6058A>T MELA-AU 19 38378311 38378311 single base substitution C T synonymous_variant K1961K 5883G>A MELA-AU 19 38378311 38378311 single base substitution C T synonymous_variant K2000K 6000G>A MELA-AU 19 38378319 38378319 single base substitution C T missense_variant E1959K 5875G>A MELA-AU 19 38378319 38378319 single base substitution C T missense_variant E1998K 5992G>A MELA-AU 19 38378353 38378353 single base substitution C T synonymous_variant K1947K 5841G>A MELA-AU 19 38378353 38378353 single base substitution C T synonymous_variant K1986K 5958G>A MELA-AU 19 38378389 38378389 single base substitution C T missense_variant M1935I 5805G>A MELA-AU 19 38378389 38378389 single base substitution C T missense_variant M1974I 5922G>A MELA-AU 19 38378397 38378397 single base substitution C T missense_variant E1933K 5797G>A MELA-AU 19 38378397 38378397 single base substitution C T missense_variant E1972K 5914G>A MELA-AU 19 38378466 38378466 single base substitution C G missense_variant A1910P 5728G>C MELA-AU 19 38378466 38378466 single base substitution C G missense_variant A1949P 5845G>C MELA-AU 19 38378476 38378476 single base substitution C T synonymous_variant K1906K 5718G>A MELA-AU 19 38378476 38378476 single base substitution C T synonymous_variant K1945K 5835G>A MELA-AU 19 38378643 38378643 single base substitution C T missense_variant E1851K 5551G>A MELA-AU 19 38378643 38378643 single base substitution C T missense_variant E1890K 5668G>A MELA-AU 19 38378670 38378670 single base substitution C T missense_variant E1842K 5524G>A MELA-AU 19 38378670 38378670 single base substitution C T missense_variant E1881K 5641G>A MELA-AU 19 38378725 38378725 single base substitution C T missense_variant M1823I 5469G>A MELA-AU 19 38378725 38378725 single base substitution C T missense_variant M1862I 5586G>A MELA-AU 19 38378764 38378764 single base substitution C T missense_variant M1810I 5430G>A MELA-AU 19 38378764 38378764 single base substitution C T missense_variant M1849I 5547G>A MELA-AU 19 38378794 38378794 single base substitution C T synonymous_variant R1800R 5400G>A MELA-AU 19 38378794 38378794 single base substitution C T synonymous_variant R1839R 5517G>A MELA-AU 19 38378851 38378851 single base substitution C T synonymous_variant K1781K 5343G>A MELA-AU 19 38378851 38378851 single base substitution C T synonymous_variant K1820K 5460G>A MELA-AU 19 38378956 38378956 single base substitution C T synonymous_variant K1746K 5238G>A MELA-AU 19 38378956 38378956 single base substitution C T synonymous_variant K1785K 5355G>A MELA-AU 19 38378974 38378974 single base substitution C T synonymous_variant G1740G 5220G>A MELA-AU 19 38378974 38378974 single base substitution C T synonymous_variant G1779G 5337G>A MELA-AU 19 38379025 38379025 single base substitution C T stop_gained W1723* 5169G>A MELA-AU 19 38379025 38379025 single base substitution C T stop_gained W1762* 5286G>A MELA-AU 19 38379072 38379072 single base substitution C T missense_variant D1708N 5122G>A MELA-AU 19 38379072 38379072 single base substitution C T missense_variant D1747N 5239G>A MELA-AU 19 38379073 38379073 single base substitution C T synonymous_variant L1707L 5121G>A MELA-AU 19 38379073 38379073 single base substitution C T synonymous_variant L1746L 5238G>A MELA-AU 19 38379085 38379085 single base substitution C T synonymous_variant R1703R 5109G>A MELA-AU 19 38379085 38379085 single base substitution C T synonymous_variant R1742R 5226G>A MELA-AU 19 38379122 38379122 single base substitution T G missense_variant N1691T 5072A>C MELA-AU 19 38379122 38379122 single base substitution T G missense_variant N1730T 5189A>C MELA-AU 19 38379131 38379131 single base substitution T A missense_variant E1688V 5063A>T MELA-AU 19 38379131 38379131 single base substitution T A missense_variant E1727V 5180A>T MELA-AU 19 38379143 38379143 single base substitution C T missense_variant G1684E 5051G>A MELA-AU 19 38379143 38379143 single base substitution C T missense_variant G1723E 5168G>A MELA-AU 19 38379208 38379208 single base substitution C T synonymous_variant R1662R 4986G>A MELA-AU 19 38379208 38379208 single base substitution C T synonymous_variant R1701R 5103G>A MELA-AU 19 38379342 38379342 single base substitution G A stop_gained Q1618* 4852C>T MELA-AU 19 38379342 38379342 single base substitution G A stop_gained Q1657* 4969C>T MELA-AU 19 38379353 38379353 single base substitution C T missense_variant R1614K 4841G>A MELA-AU 19 38379353 38379353 single base substitution C T missense_variant R1653K 4958G>A MELA-AU 19 38379394 38379394 single base substitution C T synonymous_variant E1600E 4800G>A MELA-AU 19 38379394 38379394 single base substitution C T synonymous_variant E1639E 4917G>A MELA-AU 19 38379415 38379415 single base substitution C T synonymous_variant R1593R 4779G>A MELA-AU 19 38379415 38379415 single base substitution C T synonymous_variant R1632R 4896G>A MELA-AU 19 38379423 38379423 single base substitution C T missense_variant E1591K 4771G>A MELA-AU 19 38379423 38379423 single base substitution C T missense_variant E1630K 4888G>A MELA-AU 19 38379452 38379452 single base substitution C T missense_variant R1581Q 4742G>A MELA-AU 19 38379452 38379452 single base substitution C T missense_variant R1620Q 4859G>A MELA-AU 19 38379490 38379490 single base substitution G A synonymous_variant I1568I 4704C>T MELA-AU 19 38379490 38379490 single base substitution G A synonymous_variant I1607I 4821C>T MELA-AU 19 38379646 38379646 single base substitution C T synonymous_variant L1516L 4548G>A MELA-AU 19 38379646 38379646 single base substitution C T synonymous_variant L1555L 4665G>A MELA-AU 19 38379787 38379787 single base substitution C T synonymous_variant Q1469Q 4407G>A MELA-AU 19 38379787 38379787 single base substitution C T synonymous_variant Q1508Q 4524G>A MELA-AU 19 38379894 38379894 single base substitution T A missense_variant M1434L 4300A>T MELA-AU 19 38379894 38379894 single base substitution T A missense_variant M1473L 4417A>T MELA-AU 19 38379907 38379907 single base substitution C A missense_variant E1429D 4287G>T MELA-AU 19 38379907 38379907 single base substitution C A missense_variant E1468D 4404G>T MELA-AU 19 38379953 38379953 single base substitution C T missense_variant G1414E 4241G>A MELA-AU 19 38379953 38379953 single base substitution C T missense_variant G1453E 4358G>A MELA-AU 19 38379954 38379954 single base substitution C T missense_variant G1414R 4240G>A MELA-AU 19 38379954 38379954 single base substitution C T missense_variant G1453R 4357G>A MELA-AU 19 38379962 38379962 single base substitution C T missense_variant R1411K 4232G>A MELA-AU 19 38379962 38379962 single base substitution C T missense_variant R1450K 4349G>A MELA-AU 19 38379982 38379982 single base substitution C T synonymous_variant R1404R 4212G>A MELA-AU 19 38379982 38379982 single base substitution C T synonymous_variant R1443R 4329G>A MELA-AU 19 38379985 38379986 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant G1403E 4208GG>AA MELA-AU 19 38379985 38379986 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant G1442E 4325GG>AA MELA-AU 19 38380048 38380048 single base substitution G A synonymous_variant T1382T 4146C>T MELA-AU 19 38380048 38380048 single base substitution G A synonymous_variant T1421T 4263C>T MELA-AU 19 38380099 38380099 single base substitution C T synonymous_variant V1365V 4095G>A MELA-AU 19 38380099 38380099 single base substitution C T synonymous_variant V1404V 4212G>A MELA-AU 19 38380120 38380120 single base substitution C T synonymous_variant L1358L 4074G>A MELA-AU 19 38380120 38380120 single base substitution C T synonymous_variant L1397L 4191G>A MELA-AU 19 38380191 38380191 single base substitution C T missense_variant E1335K 4003G>A MELA-AU 19 38380191 38380191 single base substitution C T missense_variant E1374K 4120G>A MELA-AU 19 38380520 38380520 single base substitution C T missense_variant G1225E 3674G>A MELA-AU 19 38380520 38380520 single base substitution C T missense_variant G1264E 3791G>A MELA-AU 19 38380580 38380580 single base substitution T A missense_variant E1205V 3614A>T MELA-AU 19 38380580 38380580 single base substitution T A missense_variant E1244V 3731A>T MELA-AU 19 38380607 38380607 single base substitution C T missense_variant G1196E 3587G>A MELA-AU 19 38380607 38380607 single base substitution C T missense_variant G1235E 3704G>A MELA-AU 19 38380725 38380725 single base substitution C T missense_variant E1157K 3469G>A MELA-AU 19 38380725 38380725 single base substitution C T missense_variant E1196K 3586G>A MELA-AU 19 38380780 38380780 single base substitution G A synonymous_variant S1138S 3414C>T MELA-AU 19 38380780 38380780 single base substitution G A synonymous_variant S1177S 3531C>T MELA-AU 19 38380896 38380896 single base substitution G A missense_variant L1100F 3298C>T MELA-AU 19 38380896 38380896 single base substitution G A missense_variant L1139F 3415C>T MELA-AU 19 38380930 38380930 single base substitution C T intron_variant MELA-AU 19 38380957 38380957 single base substitution G A intron_variant MELA-AU 19 38380967 38380967 single base substitution G A intron_variant MELA-AU 19 38381053 38381053 single base substitution A C intron_variant MELA-AU 19 38381124 38381124 single base substitution C T intron_variant MELA-AU 19 38381446 38381446 single base substitution C T intron_variant MELA-AU 19 38381462 38381462 single base substitution C T intron_variant MELA-AU 19 38381729 38381729 single base substitution C T downstream_gene_variant MELA-AU 19 38381729 38381729 single base substitution C T intron_variant MELA-AU 19 38382124 38382124 single base substitution C T downstream_gene_variant MELA-AU 19 38382124 38382124 single base substitution C T intron_variant MELA-AU 19 38382244 38382244 single base substitution G A downstream_gene_variant MELA-AU 19 38382244 38382244 single base substitution G A synonymous_variant A1075A 3225C>T MELA-AU 19 38382244 38382244 single base substitution G A synonymous_variant A1114A 3342C>T MELA-AU 19 38382589 38382589 single base substitution G A downstream_gene_variant MELA-AU 19 38382589 38382589 single base substitution G A intron_variant MELA-AU 19 38382596 38382596 single base substitution A T downstream_gene_variant MELA-AU 19 38382596 38382596 single base substitution A T intron_variant MELA-AU 19 38382611 38382611 single base substitution G A downstream_gene_variant MELA-AU 19 38382611 38382611 single base substitution G A intron_variant MELA-AU 19 38382731 38382732 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 19 38382731 38382732 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 38382836 38382836 single base substitution C T downstream_gene_variant MELA-AU 19 38382836 38382836 single base substitution C T intron_variant MELA-AU 19 38382978 38382978 single base substitution C G downstream_gene_variant MELA-AU 19 38382978 38382978 single base substitution C G intron_variant MELA-AU 19 38382978 38382978 single base substitution C T downstream_gene_variant MELA-AU 19 38382978 38382978 single base substitution C T intron_variant MELA-AU 19 38383047 38383047 single base substitution G A downstream_gene_variant MELA-AU 19 38383047 38383047 single base substitution G A intron_variant MELA-AU 19 38383167 38383167 single base substitution G A downstream_gene_variant MELA-AU 19 38383167 38383167 single base substitution G A intron_variant MELA-AU 19 38383172 38383172 single base substitution G A downstream_gene_variant MELA-AU 19 38383172 38383172 single base substitution G A intron_variant MELA-AU 19 38383182 38383182 single base substitution G A downstream_gene_variant MELA-AU 19 38383182 38383182 single base substitution G A intron_variant MELA-AU 19 38383288 38383288 single base substitution C T downstream_gene_variant MELA-AU 19 38383288 38383288 single base substitution C T missense_variant E1019K 3055G>A MELA-AU 19 38383288 38383288 single base substitution C T missense_variant E980K 2938G>A MELA-AU 19 38383299 38383299 single base substitution C T downstream_gene_variant MELA-AU 19 38383299 38383299 single base substitution C T missense_variant S1015N 3044G>A MELA-AU 19 38383299 38383299 single base substitution C T missense_variant S976N 2927G>A MELA-AU 19 38383384 38383384 single base substitution G C downstream_gene_variant MELA-AU 19 38383384 38383384 single base substitution G C missense_variant L948V 2842C>G MELA-AU 19 38383384 38383384 single base substitution G C missense_variant L987V 2959C>G MELA-AU 19 38383783 38383783 single base substitution C T downstream_gene_variant MELA-AU 19 38383783 38383783 single base substitution C T missense_variant E815K 2443G>A MELA-AU 19 38383783 38383783 single base substitution C T missense_variant E854K 2560G>A MELA-AU 19 38383789 38383789 single base substitution C T downstream_gene_variant MELA-AU 19 38383789 38383789 single base substitution C T missense_variant E813K 2437G>A MELA-AU 19 38383789 38383789 single base substitution C T missense_variant E852K 2554G>A MELA-AU 19 38383845 38383845 single base substitution A G downstream_gene_variant MELA-AU 19 38383845 38383845 single base substitution A G missense_variant L794P 2381T>C MELA-AU 19 38383845 38383845 single base substitution A G missense_variant L833P 2498T>C MELA-AU 19 38383855 38383855 single base substitution G A downstream_gene_variant MELA-AU 19 38383855 38383855 single base substitution G A missense_variant R791C 2371C>T MELA-AU 19 38383855 38383855 single base substitution G A missense_variant R830C 2488C>T MELA-AU 19 38383991 38383991 single base substitution G A downstream_gene_variant MELA-AU 19 38383991 38383991 single base substitution G A synonymous_variant C745C 2235C>T MELA-AU 19 38383991 38383991 single base substitution G A synonymous_variant C784C 2352C>T MELA-AU 19 38383997 38383997 single base substitution G A downstream_gene_variant MELA-AU 19 38383997 38383997 single base substitution G A synonymous_variant Y743Y 2229C>T MELA-AU 19 38383997 38383997 single base substitution G A synonymous_variant Y782Y 2346C>T MELA-AU 19 38384075 38384075 single base substitution C T downstream_gene_variant MELA-AU 19 38384075 38384075 single base substitution C T synonymous_variant G717G 2151G>A MELA-AU 19 38384075 38384075 single base substitution C T synonymous_variant G756G 2268G>A MELA-AU 19 38384083 38384083 single base substitution C T downstream_gene_variant MELA-AU 19 38384083 38384083 single base substitution C T missense_variant E715K 2143G>A MELA-AU 19 38384083 38384083 single base substitution C T missense_variant E754K 2260G>A MELA-AU 19 38384113 38384113 single base substitution G A downstream_gene_variant MELA-AU 19 38384113 38384113 single base substitution G A missense_variant H705Y 2113C>T MELA-AU 19 38384113 38384113 single base substitution G A missense_variant H744Y 2230C>T MELA-AU 19 38384217 38384217 single base substitution G A downstream_gene_variant MELA-AU 19 38384217 38384217 single base substitution G A missense_variant S670F 2009C>T MELA-AU 19 38384217 38384217 single base substitution G A missense_variant S709F 2126C>T MELA-AU 19 38384290 38384290 single base substitution G A downstream_gene_variant MELA-AU 19 38384290 38384290 single base substitution G A missense_variant R646C 1936C>T MELA-AU 19 38384290 38384290 single base substitution G A missense_variant R685C 2053C>T MELA-AU 19 38384510 38384510 single base substitution G A downstream_gene_variant MELA-AU 19 38384510 38384510 single base substitution G A synonymous_variant S572S 1716C>T MELA-AU 19 38384510 38384510 single base substitution G A synonymous_variant S611S 1833C>T MELA-AU 19 38384798 38384798 single base substitution C T downstream_gene_variant MELA-AU 19 38384798 38384798 single base substitution C T synonymous_variant G476G 1428G>A MELA-AU 19 38384798 38384798 single base substitution C T synonymous_variant G515G 1545G>A MELA-AU 19 38384799 38384799 single base substitution C T downstream_gene_variant MELA-AU 19 38384799 38384799 single base substitution C T missense_variant G476E 1427G>A MELA-AU 19 38384799 38384799 single base substitution C T missense_variant G515E 1544G>A MELA-AU 19 38385303 38385303 single base substitution G A downstream_gene_variant MELA-AU 19 38385303 38385303 single base substitution G A missense_variant S308F 923C>T MELA-AU 19 38385303 38385303 single base substitution G A missense_variant S347F 1040C>T MELA-AU 19 38385419 38385419 single base substitution C T downstream_gene_variant MELA-AU 19 38385419 38385419 single base substitution C T synonymous_variant K269K 807G>A MELA-AU 19 38385419 38385419 single base substitution C T synonymous_variant K308K 924G>A MELA-AU 19 38385461 38385461 single base substitution C T downstream_gene_variant MELA-AU 19 38385461 38385461 single base substitution C T synonymous_variant E255E 765G>A MELA-AU 19 38385461 38385461 single base substitution C T synonymous_variant E294E 882G>A MELA-AU 19 38385553 38385554 multiple base substitution (>=2bp and <=200bp) CC GT downstream_gene_variant MELA-AU 19 38385553 38385554 multiple base substitution (>=2bp and <=200bp) CC GT missense_variant GE224GQ MELA-AU 19 38385553 38385554 multiple base substitution (>=2bp and <=200bp) CC GT missense_variant GE263GQ MELA-AU 19 38385740 38385740 single base substitution G A downstream_gene_variant MELA-AU 19 38385740 38385740 single base substitution G A synonymous_variant I162I 486C>T MELA-AU 19 38385740 38385740 single base substitution G A synonymous_variant I201I 603C>T MELA-AU 19 38385749 38385749 single base substitution G A downstream_gene_variant MELA-AU 19 38385749 38385749 single base substitution G A synonymous_variant V159V 477C>T MELA-AU 19 38385749 38385749 single base substitution G A synonymous_variant V198V 594C>T MELA-AU 19 38385798 38385798 single base substitution G C downstream_gene_variant MELA-AU 19 38385798 38385798 single base substitution G C missense_variant T143R 428C>G MELA-AU 19 38385798 38385798 single base substitution G C missense_variant T182R 545C>G MELA-AU 19 38385959 38385959 single base substitution C T downstream_gene_variant MELA-AU 19 38385959 38385959 single base substitution C T synonymous_variant L128L 384G>A MELA-AU 19 38385959 38385959 single base substitution C T synonymous_variant L89L 267G>A MELA-AU 19 38386129 38386129 single base substitution C T downstream_gene_variant MELA-AU 19 38386129 38386129 single base substitution C T intron_variant MELA-AU 19 38386143 38386143 single base substitution C T downstream_gene_variant MELA-AU 19 38386143 38386143 single base substitution C T intron_variant MELA-AU 19 38386394 38386394 single base substitution G A downstream_gene_variant MELA-AU 19 38386394 38386394 single base substitution G A intron_variant MELA-AU 19 38386561 38386561 single base substitution G A downstream_gene_variant MELA-AU 19 38386561 38386561 single base substitution G A intron_variant MELA-AU 19 38386573 38386573 single base substitution C T downstream_gene_variant MELA-AU 19 38386573 38386573 single base substitution C T intron_variant MELA-AU 19 38386579 38386579 single base substitution C T downstream_gene_variant MELA-AU 19 38386579 38386579 single base substitution C T intron_variant MELA-AU 19 38386602 38386602 single base substitution G A downstream_gene_variant MELA-AU 19 38386602 38386602 single base substitution G A intron_variant MELA-AU 19 38386628 38386628 single base substitution G A downstream_gene_variant MELA-AU 19 38386628 38386628 single base substitution G A intron_variant MELA-AU 19 38386786 38386786 single base substitution C T exon_variant MELA-AU 19 38386786 38386786 single base substitution C T intron_variant MELA-AU 19 38386786 38386786 single base substitution C T missense_variant E80K 238G>A MELA-AU 19 38386805 38386805 single base substitution C T exon_variant MELA-AU 19 38386805 38386805 single base substitution C T intron_variant MELA-AU 19 38386805 38386805 single base substitution C T stop_gained W73* 219G>A MELA-AU 19 38386898 38386898 single base substitution G A exon_variant MELA-AU 19 38386898 38386898 single base substitution G A synonymous_variant S42S 126C>T MELA-AU 19 38386977 38386977 single base substitution G A intron_variant MELA-AU 19 38387024 38387024 single base substitution G A intron_variant MELA-AU 19 38387150 38387150 single base substitution G A intron_variant MELA-AU 19 38387203 38387203 single base substitution G A intron_variant MELA-AU 19 38387236 38387236 single base substitution C T intron_variant MELA-AU 19 38387349 38387349 single base substitution C T intron_variant MELA-AU 19 38387848 38387848 single base substitution T A intron_variant MELA-AU 19 38387982 38387982 single base substitution G A intron_variant MELA-AU 19 38388040 38388040 single base substitution G A intron_variant MELA-AU 19 38388101 38388101 single base substitution C T intron_variant MELA-AU 19 38388436 38388436 single base substitution G A intron_variant MELA-AU 19 38388511 38388511 single base substitution G A intron_variant MELA-AU 19 38388630 38388630 single base substitution G A intron_variant MELA-AU 19 38388716 38388716 single base substitution G A intron_variant MELA-AU 19 38388871 38388871 single base substitution G A exon_variant MELA-AU 19 38388871 38388871 single base substitution G A synonymous_variant S3S 9C>T MELA-AU 19 38388892 38388892 single base substitution C T 5_prime_UTR_variant MELA-AU 19 38388892 38388892 single base substitution C T exon_variant MELA-AU 19 38388932 38388932 single base substitution G A splice_region_variant MELA-AU 19 38388980 38388980 single base substitution G A intron_variant MELA-AU 19 38388984 38388984 single base substitution C T intron_variant MELA-AU 19 38389141 38389141 single base substitution A G intron_variant MELA-AU 19 38389479 38389479 single base substitution A G intron_variant MELA-AU 19 38389986 38389986 single base substitution G A intron_variant MELA-AU 19 38390013 38390013 single base substitution T C intron_variant MELA-AU 19 38390077 38390077 single base substitution G A intron_variant MELA-AU 19 38390869 38390869 single base substitution G A intron_variant MELA-AU 19 38390872 38390872 single base substitution G A intron_variant MELA-AU 19 38390978 38390978 single base substitution G A intron_variant MELA-AU 19 38391374 38391374 single base substitution C T intron_variant MELA-AU 19 38391499 38391499 single base substitution G A intron_variant MELA-AU 19 38391833 38391833 single base substitution G A intron_variant MELA-AU 19 38392374 38392374 single base substitution G A intron_variant MELA-AU 19 38392704 38392704 single base substitution C T intron_variant MELA-AU 19 38392761 38392761 single base substitution C T intron_variant MELA-AU 19 38393078 38393078 single base substitution G A intron_variant MELA-AU 19 38393469 38393469 single base substitution A G intron_variant MELA-AU 19 38393572 38393572 single base substitution G A intron_variant MELA-AU 19 38393666 38393666 single base substitution C T intron_variant MELA-AU 19 38393830 38393831 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 38393920 38393920 single base substitution A G intron_variant MELA-AU 19 38393936 38393937 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 38393997 38393997 single base substitution G A intron_variant MELA-AU 19 38394124 38394124 single base substitution C T intron_variant MELA-AU 19 38394475 38394475 single base substitution T G intron_variant MELA-AU 19 38394618 38394618 single base substitution C T intron_variant MELA-AU 19 38394769 38394769 single base substitution C T intron_variant MELA-AU 19 38395363 38395363 single base substitution T C intron_variant MELA-AU 19 38396019 38396019 single base substitution C T intron_variant MELA-AU 19 38396346 38396346 single base substitution C T intron_variant MELA-AU 19 38396880 38396880 single base substitution A T intron_variant MELA-AU 19 38397074 38397074 single base substitution G A intron_variant MELA-AU 19 38398586 38398586 single base substitution G A upstream_gene_variant MELA-AU 19 38398807 38398807 single base substitution C T upstream_gene_variant MELA-AU 19 38399882 38399882 single base substitution C T upstream_gene_variant MELA-AU 19 38400074 38400074 single base substitution C T upstream_gene_variant MELA-AU 19 38400112 38400112 single base substitution G C upstream_gene_variant MELA-AU 19 38400517 38400517 single base substitution C T upstream_gene_variant MELA-AU 19 38400879 38400879 single base substitution C T upstream_gene_variant MELA-AU 19 38401277 38401277 single base substitution C T upstream_gene_variant MELA-AU 19 38402275 38402275 single base substitution C T upstream_gene_variant ORCA-IN 19 38376531 38376531 single base substitution C G missense_variant D2555H 7663G>C ORCA-IN 19 38376531 38376531 single base substitution C G missense_variant D2594H 7780G>C ORCA-IN 19 38378627 38378627 single base substitution C T missense_variant R1856K 5567G>A ORCA-IN 19 38378627 38378627 single base substitution C T missense_variant R1895K 5684G>A ORCA-IN 19 38380043 38380043 single base substitution C T missense_variant G1384E 4151G>A ORCA-IN 19 38380043 38380043 single base substitution C T missense_variant G1423E 4268G>A ORCA-IN 19 38384722 38384722 single base substitution G A downstream_gene_variant ORCA-IN 19 38384722 38384722 single base substitution G A missense_variant L502F 1504C>T ORCA-IN 19 38384722 38384722 single base substitution G A missense_variant L541F 1621C>T ORCA-IN 19 38385237 38385237 single base substitution C T downstream_gene_variant ORCA-IN 19 38385237 38385237 single base substitution C T missense_variant R330H 989G>A ORCA-IN 19 38385237 38385237 single base substitution C T missense_variant R369H 1106G>A ORCA-IN 19 38396108 38396108 single base substitution A G intron_variant ORCA-IN 19 38400285 38400285 single base substitution C T upstream_gene_variant OV-AU 19 38375792 38375792 single base substitution T A missense_variant E2801V 8402A>T OV-AU 19 38375792 38375792 single base substitution T A missense_variant E2840V 8519A>T OV-AU 19 38378609 38378609 single base substitution T C missense_variant Y1862C 5585A>G OV-AU 19 38378609 38378609 single base substitution T C missense_variant Y1901C 5702A>G OV-AU 19 38380839 38380839 single base substitution C T missense_variant E1119K 3355G>A OV-AU 19 38380839 38380839 single base substitution C T missense_variant E1158K 3472G>A OV-AU 19 38384161 38384161 single base substitution A C downstream_gene_variant OV-AU 19 38384161 38384161 single base substitution A C missense_variant L689V 2065T>G OV-AU 19 38384161 38384161 single base substitution A C missense_variant L728V 2182T>G OV-AU 19 38385934 38385934 single base substitution A T downstream_gene_variant OV-AU 19 38385934 38385934 single base substitution A T missense_variant F137I 409T>A OV-AU 19 38385934 38385934 single base substitution A T missense_variant F98I 292T>A OV-AU 19 38390734 38390734 single base substitution A C intron_variant OV-AU 19 38390806 38390806 single base substitution G C intron_variant PACA-AU 19 38372250 38372250 single base substitution C T downstream_gene_variant PACA-AU 19 38372416 38372416 single base substitution A G downstream_gene_variant PACA-AU 19 38373285 38373285 single base substitution C T downstream_gene_variant PACA-AU 19 38375693 38375693 single base substitution C T missense_variant R2834H 8501G>A PACA-AU 19 38375693 38375693 single base substitution C T missense_variant R2873H 8618G>A PACA-AU 19 38375790 38375790 single base substitution G A missense_variant R2802W 8404C>T PACA-AU 19 38375790 38375790 single base substitution G A missense_variant R2841W 8521C>T PACA-AU 19 38376584 38376584 single base substitution G A missense_variant A2537V 7610C>T PACA-AU 19 38376584 38376584 single base substitution G A missense_variant A2576V 7727C>T PACA-AU 19 38378818 38378818 single base substitution A G synonymous_variant P1792P 5376T>C PACA-AU 19 38378818 38378818 single base substitution A G synonymous_variant P1831P 5493T>C PACA-AU 19 38379287 38379287 single base substitution T G missense_variant K1636T 4907A>C PACA-AU 19 38379287 38379287 single base substitution T G missense_variant K1675T 5024A>C PACA-AU 19 38380593 38380593 single base substitution C T missense_variant V1201I 3601G>A PACA-AU 19 38380593 38380593 single base substitution C T missense_variant V1240I 3718G>A PACA-AU 19 38381642 38381642 single base substitution T C intron_variant PACA-AU 19 38386683 38386683 single base substitution C T exon_variant PACA-AU 19 38386683 38386683 single base substitution C T intron_variant PACA-AU 19 38389175 38389175 single base substitution C A intron_variant PACA-AU 19 38392705 38392705 deletion of <=200bp T - intron_variant PACA-AU 19 38396488 38396488 single base substitution C T intron_variant PACA-AU 19 38398491 38398494 deletion of <=200bp TTAG - upstream_gene_variant PACA-AU 19 38401619 38401619 deletion of <=200bp A - upstream_gene_variant PACA-CA 19 38371322 38371322 single base substitution T G downstream_gene_variant PACA-CA 19 38372172 38372172 single base substitution G C downstream_gene_variant PACA-CA 19 38372771 38372771 deletion of <=200bp T - downstream_gene_variant PACA-CA 19 38373720 38373720 single base substitution C G downstream_gene_variant PACA-CA 19 38374550 38374550 single base substitution T A downstream_gene_variant PACA-CA 19 38375137 38375137 single base substitution T A downstream_gene_variant PACA-CA 19 38375830 38375830 single base substitution G A synonymous_variant Y2788Y 8364C>T PACA-CA 19 38375830 38375830 single base substitution G A synonymous_variant Y2827Y 8481C>T PACA-CA 19 38377631 38377633 deletion of <=200bp TCT - disruptive_inframe_deletion EE2187E PACA-CA 19 38377631 38377633 deletion of <=200bp TCT - disruptive_inframe_deletion EE2226E PACA-CA 19 38378007 38378007 deletion of <=200bp T - frameshift_variant R2063 PACA-CA 19 38378007 38378007 deletion of <=200bp T - frameshift_variant R2102 PACA-CA 19 38379446 38379446 single base substitution C T missense_variant R1583Q 4748G>A PACA-CA 19 38379446 38379446 single base substitution C T missense_variant R1622Q 4865G>A PACA-CA 19 38379803 38379803 single base substitution C A missense_variant W1464L 4391G>T PACA-CA 19 38379803 38379803 single base substitution C A missense_variant W1503L 4508G>T PACA-CA 19 38380395 38380395 single base substitution C T missense_variant A1267T 3799G>A PACA-CA 19 38380395 38380395 single base substitution C T missense_variant A1306T 3916G>A PACA-CA 19 38380886 38380886 single base substitution G A missense_variant T1103M 3308C>T PACA-CA 19 38380886 38380886 single base substitution G A missense_variant T1142M 3425C>T PACA-CA 19 38381993 38381993 deletion of <=200bp G - downstream_gene_variant PACA-CA 19 38381993 38381993 deletion of <=200bp G - intron_variant PACA-CA 19 38382981 38382981 single base substitution G A downstream_gene_variant PACA-CA 19 38382981 38382981 single base substitution G A intron_variant PACA-CA 19 38383241 38383241 single base substitution T C downstream_gene_variant PACA-CA 19 38383241 38383241 single base substitution T C synonymous_variant K1034K 3102A>G PACA-CA 19 38383241 38383241 single base substitution T C synonymous_variant K995K 2985A>G PACA-CA 19 38384058 38384058 single base substitution C T downstream_gene_variant PACA-CA 19 38384058 38384058 single base substitution C T missense_variant R723H 2168G>A PACA-CA 19 38384058 38384058 single base substitution C T missense_variant R762H 2285G>A PACA-CA 19 38385358 38385358 single base substitution G A downstream_gene_variant PACA-CA 19 38385358 38385358 single base substitution G A missense_variant R290W 868C>T PACA-CA 19 38385358 38385358 single base substitution G A missense_variant R329W 985C>T PACA-CA 19 38387257 38387257 insertion of <=200bp - T intron_variant PACA-CA 19 38388041 38388041 single base substitution G T intron_variant PACA-CA 19 38388679 38388679 single base substitution G C intron_variant PACA-CA 19 38389237 38389237 single base substitution C A intron_variant PACA-CA 19 38394725 38394725 single base substitution A G intron_variant PACA-CA 19 38395488 38395488 single base substitution T C intron_variant PACA-CA 19 38396218 38396218 single base substitution A T intron_variant PACA-CA 19 38396994 38396994 single base substitution T A intron_variant PACA-CA 19 38397111 38397111 single base substitution A G intron_variant PACA-CA 19 38398437 38398437 single base substitution T C upstream_gene_variant PACA-CA 19 38402177 38402177 single base substitution C G upstream_gene_variant PACA-CA 19 38402276 38402276 single base substitution C T upstream_gene_variant PAEN-AU 19 38379121 38379121 single base substitution G A synonymous_variant N1691N 5073C>T PAEN-AU 19 38379121 38379121 single base substitution G A synonymous_variant N1730N 5190C>T PAEN-AU 19 38390394 38390394 single base substitution G T intron_variant PAEN-IT 19 38385624 38385624 single base substitution C T downstream_gene_variant PAEN-IT 19 38385624 38385624 single base substitution C T missense_variant S201N 602G>A PAEN-IT 19 38385624 38385624 single base substitution C T missense_variant S240N 719G>A PAEN-IT 19 38390534 38390534 single base substitution C A intron_variant PAEN-IT 19 38397308 38397308 single base substitution G A 5_prime_UTR_variant PAEN-IT 19 38397308 38397308 single base substitution G A upstream_gene_variant PBCA-DE 19 38370527 38370527 single base substitution T C downstream_gene_variant PBCA-DE 19 38372817 38372817 single base substitution G A downstream_gene_variant PBCA-DE 19 38376583 38376583 single base substitution C T synonymous_variant A2537A 7611G>A PBCA-DE 19 38376583 38376583 single base substitution C T synonymous_variant A2576A 7728G>A PBCA-DE 19 38378349 38378349 single base substitution G A missense_variant R1949W 5845C>T PBCA-DE 19 38378349 38378349 single base substitution G A missense_variant R1988W 5962C>T PBCA-DE 19 38380451 38380451 single base substitution C T missense_variant R1248H 3743G>A PBCA-DE 19 38380451 38380451 single base substitution C T missense_variant R1287H 3860G>A PBCA-DE 19 38381157 38381157 insertion of <=200bp - T intron_variant PBCA-DE 19 38387940 38387940 single base substitution T G intron_variant PBCA-DE 19 38388477 38388477 single base substitution G A intron_variant PBCA-DE 19 38396102 38396102 insertion of <=200bp - AAGT intron_variant PBCA-DE 19 38398583 38398583 single base substitution T A upstream_gene_variant PRAD-UK 19 38376690 38376690 single base substitution T A missense_variant T2502S 7504A>T PRAD-UK 19 38376690 38376690 single base substitution T A missense_variant T2541S 7621A>T PRAD-UK 19 38378093 38378093 single base substitution C G missense_variant G2034A 6101G>C PRAD-UK 19 38378093 38378093 single base substitution C G missense_variant G2073A 6218G>C PRAD-UK 19 38378145 38378145 single base substitution G A synonymous_variant L2017L 6049C>T PRAD-UK 19 38378145 38378145 single base substitution G A synonymous_variant L2056L 6166C>T PRAD-UK 19 38392232 38392232 single base substitution G A intron_variant PRAD-UK 19 38394545 38394545 single base substitution G T intron_variant READ-US 19 38375958 38375958 single base substitution C A missense_variant D2746Y 8236G>T READ-US 19 38375958 38375958 single base substitution C A missense_variant D2785Y 8353G>T READ-US 19 38375985 38375985 single base substitution G A missense_variant R2737W 8209C>T READ-US 19 38375985 38375985 single base substitution G A missense_variant R2776W 8326C>T READ-US 19 38376699 38376699 single base substitution T C missense_variant M2499V 7495A>G READ-US 19 38376699 38376699 single base substitution T C missense_variant M2538V 7612A>G READ-US 19 38377404 38377404 single base substitution C T missense_variant E2264K 6790G>A READ-US 19 38377404 38377404 single base substitution C T missense_variant E2303K 6907G>A READ-US 19 38377414 38377414 single base substitution C T synonymous_variant E2260E 6780G>A READ-US 19 38377414 38377414 single base substitution C T synonymous_variant E2299E 6897G>A READ-US 19 38378410 38378410 single base substitution C A missense_variant E1928D 5784G>T READ-US 19 38378410 38378410 single base substitution C A missense_variant E1967D 5901G>T READ-US 19 38378529 38378529 single base substitution C T missense_variant A1889T 5665G>A READ-US 19 38378529 38378529 single base substitution C T missense_variant A1928T 5782G>A READ-US 19 38379198 38379198 single base substitution C A missense_variant A1666S 4996G>T READ-US 19 38379198 38379198 single base substitution C A missense_variant A1705S 5113G>T READ-US 19 38379226 38379226 single base substitution C T synonymous_variant E1656E 4968G>A READ-US 19 38379226 38379226 single base substitution C T synonymous_variant E1695E 5085G>A READ-US 19 38380740 38380740 single base substitution C A missense_variant D1152Y 3454G>T READ-US 19 38380740 38380740 single base substitution C A missense_variant D1191Y 3571G>T READ-US 19 38386928 38386928 single base substitution C A exon_variant READ-US 19 38386928 38386928 single base substitution C A missense_variant K32N 96G>T RECA-EU 19 38372014 38372014 single base substitution A G downstream_gene_variant RECA-EU 19 38379024 38379024 single base substitution C A missense_variant D1724Y 5170G>T RECA-EU 19 38379024 38379024 single base substitution C A missense_variant D1763Y 5287G>T RECA-EU 19 38379578 38379578 single base substitution T C missense_variant K1539R 4616A>G RECA-EU 19 38379578 38379578 single base substitution T C missense_variant K1578R 4733A>G RECA-EU 19 38381822 38381822 single base substitution G T downstream_gene_variant RECA-EU 19 38381822 38381822 single base substitution G T intron_variant RECA-EU 19 38383593 38383593 single base substitution G A downstream_gene_variant RECA-EU 19 38383593 38383593 single base substitution G A missense_variant T878I 2633C>T RECA-EU 19 38383593 38383593 single base substitution G A missense_variant T917I 2750C>T RECA-EU 19 38383658 38383658 single base substitution T A downstream_gene_variant RECA-EU 19 38383658 38383658 single base substitution T A synonymous_variant V856V 2568A>T RECA-EU 19 38383658 38383658 single base substitution T A synonymous_variant V895V 2685A>T RECA-EU 19 38391108 38391108 single base substitution G A intron_variant RECA-EU 19 38393818 38393818 single base substitution G A intron_variant RECA-EU 19 38397155 38397155 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant RECA-EU 19 38397155 38397155 single base substitution G A exon_variant RECA-EU 19 38401595 38401595 single base substitution A T upstream_gene_variant SKCA-BR 19 38370525 38370525 single base substitution C T downstream_gene_variant SKCA-BR 19 38370626 38370626 single base substitution C T downstream_gene_variant SKCA-BR 19 38371655 38371656 deletion of <=200bp TA - downstream_gene_variant SKCA-BR 19 38371747 38371749 deletion of <=200bp ATT - downstream_gene_variant SKCA-BR 19 38371759 38371759 single base substitution T A downstream_gene_variant SKCA-BR 19 38371768 38371769 deletion of <=200bp TA - downstream_gene_variant SKCA-BR 19 38372014 38372014 insertion of <=200bp - AG downstream_gene_variant SKCA-BR 19 38373049 38373049 single base substitution T C downstream_gene_variant SKCA-BR 19 38373260 38373260 single base substitution C T downstream_gene_variant SKCA-BR 19 38374123 38374123 single base substitution G A downstream_gene_variant SKCA-BR 19 38374535 38374535 insertion of <=200bp - CAA downstream_gene_variant SKCA-BR 19 38374570 38374570 single base substitution C T downstream_gene_variant SKCA-BR 19 38375065 38375065 single base substitution C T downstream_gene_variant SKCA-BR 19 38375227 38375227 single base substitution C T downstream_gene_variant SKCA-BR 19 38375577 38375577 single base substitution G A missense_variant L2873F 8617C>T SKCA-BR 19 38375577 38375577 single base substitution G A missense_variant L2912F 8734C>T SKCA-BR 19 38376030 38376030 single base substitution C T missense_variant E2722K 8164G>A SKCA-BR 19 38376030 38376030 single base substitution C T missense_variant E2761K 8281G>A SKCA-BR 19 38377378 38377378 single base substitution C T synonymous_variant E2272E 6816G>A SKCA-BR 19 38377378 38377378 single base substitution C T synonymous_variant E2311E 6933G>A SKCA-BR 19 38378620 38378620 single base substitution C T synonymous_variant E1858E 5574G>A SKCA-BR 19 38378620 38378620 single base substitution C T synonymous_variant E1897E 5691G>A SKCA-BR 19 38378643 38378643 single base substitution C T missense_variant E1851K 5551G>A SKCA-BR 19 38378643 38378643 single base substitution C T missense_variant E1890K 5668G>A SKCA-BR 19 38379555 38379555 single base substitution C T missense_variant E1547K 4639G>A SKCA-BR 19 38379555 38379555 single base substitution C T missense_variant E1586K 4756G>A SKCA-BR 19 38381806 38381806 insertion of <=200bp - CT downstream_gene_variant SKCA-BR 19 38381806 38381806 insertion of <=200bp - CT intron_variant SKCA-BR 19 38381834 38381834 single base substitution C T downstream_gene_variant SKCA-BR 19 38381834 38381834 single base substitution C T intron_variant SKCA-BR 19 38381996 38381996 single base substitution G A downstream_gene_variant SKCA-BR 19 38381996 38381996 single base substitution G A intron_variant SKCA-BR 19 38383072 38383072 single base substitution T G downstream_gene_variant SKCA-BR 19 38383072 38383072 single base substitution T G intron_variant SKCA-BR 19 38383819 38383819 single base substitution G T downstream_gene_variant SKCA-BR 19 38383819 38383819 single base substitution G T missense_variant L803I 2407C>A SKCA-BR 19 38383819 38383819 single base substitution G T missense_variant L842I 2524C>A SKCA-BR 19 38385993 38385993 single base substitution G A downstream_gene_variant SKCA-BR 19 38385993 38385993 single base substitution G A missense_variant S117F 350C>T SKCA-BR 19 38385993 38385993 single base substitution G A missense_variant S78F 233C>T SKCA-BR 19 38386479 38386479 single base substitution C T downstream_gene_variant SKCA-BR 19 38386479 38386479 single base substitution C T intron_variant SKCA-BR 19 38388158 38388158 single base substitution C T intron_variant SKCA-BR 19 38388247 38388247 single base substitution G A intron_variant SKCA-BR 19 38388319 38388319 single base substitution T C intron_variant SKCA-BR 19 38390872 38390872 single base substitution G A intron_variant SKCA-BR 19 38392367 38392367 single base substitution T C intron_variant SKCA-BR 19 38392403 38392403 single base substitution G A intron_variant SKCA-BR 19 38392551 38392551 single base substitution C T intron_variant SKCA-BR 19 38392708 38392708 single base substitution C T intron_variant SKCA-BR 19 38392935 38392935 single base substitution A C intron_variant SKCA-BR 19 38394905 38394905 single base substitution G A intron_variant SKCA-BR 19 38396360 38396360 insertion of <=200bp - TA intron_variant SKCA-BR 19 38399256 38399257 deletion of <=200bp GT - upstream_gene_variant THCA-SA 19 38376103 38376103 single base substitution A G synonymous_variant F2697F 8091T>C THCA-SA 19 38376103 38376103 single base substitution A G synonymous_variant F2736F 8208T>C UCEC-US 19 38375841 38375841 single base substitution C A stop_gained E2785* 8353G>T UCEC-US 19 38375841 38375841 single base substitution C A stop_gained E2824* 8470G>T UCEC-US 19 38375886 38375886 single base substitution T G missense_variant K2770Q 8308A>C UCEC-US 19 38375886 38375886 single base substitution T G missense_variant K2809Q 8425A>C UCEC-US 19 38376205 38376205 single base substitution C T missense_variant M2663I 7989G>A UCEC-US 19 38376205 38376205 single base substitution C T missense_variant M2702I 8106G>A UCEC-US 19 38376210 38376210 single base substitution C T missense_variant E2662K 7984G>A UCEC-US 19 38376210 38376210 single base substitution C T missense_variant E2701K 8101G>A UCEC-US 19 38376398 38376398 single base substitution A G missense_variant L2599P 7796T>C UCEC-US 19 38376398 38376398 single base substitution A G missense_variant L2638P 7913T>C UCEC-US 19 38376888 38376888 single base substitution C A stop_gained E2436* 7306G>T UCEC-US 19 38376888 38376888 single base substitution C A stop_gained E2475* 7423G>T UCEC-US 19 38376913 38376913 single base substitution C A missense_variant R2427S 7281G>T UCEC-US 19 38376913 38376913 single base substitution C A missense_variant R2466S 7398G>T UCEC-US 19 38377061 38377061 single base substitution C T missense_variant G2378D 7133G>A UCEC-US 19 38377061 38377061 single base substitution C T missense_variant G2417D 7250G>A UCEC-US 19 38377118 38377118 single base substitution C A missense_variant S2359I 7076G>T UCEC-US 19 38377118 38377118 single base substitution C A missense_variant S2398I 7193G>T UCEC-US 19 38377170 38377170 single base substitution C A stop_gained E2342* 7024G>T UCEC-US 19 38377170 38377170 single base substitution C A stop_gained E2381* 7141G>T UCEC-US 19 38377669 38377669 single base substitution T C missense_variant I2175M 6525A>G UCEC-US 19 38377669 38377669 single base substitution T C missense_variant I2214M 6642A>G UCEC-US 19 38378002 38378002 single base substitution C A missense_variant E2064D 6192G>T UCEC-US 19 38378002 38378002 single base substitution C A missense_variant E2103D 6309G>T UCEC-US 19 38378045 38378045 single base substitution C A missense_variant R2050I 6149G>T UCEC-US 19 38378045 38378045 single base substitution C A missense_variant R2089I 6266G>T UCEC-US 19 38378398 38378398 single base substitution C T synonymous_variant Q1932Q 5796G>A UCEC-US 19 38378398 38378398 single base substitution C T synonymous_variant Q1971Q 5913G>A UCEC-US 19 38378473 38378473 single base substitution C A missense_variant E1907D 5721G>T UCEC-US 19 38378473 38378473 single base substitution C A missense_variant E1946D 5838G>T UCEC-US 19 38378528 38378528 single base substitution G T missense_variant A1889D 5666C>A UCEC-US 19 38378528 38378528 single base substitution G T missense_variant A1928D 5783C>A UCEC-US 19 38378710 38378710 single base substitution C A missense_variant K1828N 5484G>T UCEC-US 19 38378710 38378710 single base substitution C A missense_variant K1867N 5601G>T UCEC-US 19 38378871 38378871 single base substitution C A stop_gained E1775* 5323G>T UCEC-US 19 38378871 38378871 single base substitution C A stop_gained E1814* 5440G>T UCEC-US 19 38378956 38378956 single base substitution C A missense_variant K1746N 5238G>T UCEC-US 19 38378956 38378956 single base substitution C A missense_variant K1785N 5355G>T UCEC-US 19 38379015 38379015 single base substitution C A stop_gained E1727* 5179G>T UCEC-US 19 38379015 38379015 single base substitution C A stop_gained E1766* 5296G>T UCEC-US 19 38379099 38379099 single base substitution C A stop_gained E1699* 5095G>T UCEC-US 19 38379099 38379099 single base substitution C A stop_gained E1738* 5212G>T UCEC-US 19 38379163 38379163 single base substitution C A missense_variant E1677D 5031G>T UCEC-US 19 38379163 38379163 single base substitution C A missense_variant E1716D 5148G>T UCEC-US 19 38379193 38379193 single base substitution C A missense_variant K1667N 5001G>T UCEC-US 19 38379193 38379193 single base substitution C A missense_variant K1706N 5118G>T UCEC-US 19 38379226 38379226 single base substitution C A missense_variant E1656D 4968G>T UCEC-US 19 38379226 38379226 single base substitution C A missense_variant E1695D 5085G>T UCEC-US 19 38379271 38379271 single base substitution C A missense_variant E1641D 4923G>T UCEC-US 19 38379271 38379271 single base substitution C A missense_variant E1680D 5040G>T UCEC-US 19 38379386 38379386 single base substitution G A missense_variant A1603V 4808C>T UCEC-US 19 38379386 38379386 single base substitution G A missense_variant A1642V 4925C>T UCEC-US 19 38379394 38379394 single base substitution C A missense_variant E1600D 4800G>T UCEC-US 19 38379394 38379394 single base substitution C A missense_variant E1639D 4917G>T UCEC-US 19 38379402 38379402 single base substitution C T missense_variant E1598K 4792G>A UCEC-US 19 38379402 38379402 single base substitution C T missense_variant E1637K 4909G>A UCEC-US 19 38380081 38380081 single base substitution C A missense_variant K1371N 4113G>T UCEC-US 19 38380081 38380081 single base substitution C A missense_variant K1410N 4230G>T UCEC-US 19 38380255 38380255 single base substitution C A missense_variant E1313D 3939G>T UCEC-US 19 38380255 38380255 single base substitution C A missense_variant E1352D 4056G>T UCEC-US 19 38380768 38380768 single base substitution T G synonymous_variant S1142S 3426A>C UCEC-US 19 38380768 38380768 single base substitution T G synonymous_variant S1181S 3543A>C UCEC-US 19 38382414 38382414 single base substitution G A downstream_gene_variant UCEC-US 19 38382414 38382414 single base substitution G A missense_variant R1019W 3055C>T UCEC-US 19 38382414 38382414 single base substitution G A missense_variant R1058W 3172C>T UCEC-US 19 38383330 38383330 single base substitution T C downstream_gene_variant UCEC-US 19 38383330 38383330 single base substitution T C missense_variant K1005E 3013A>G UCEC-US 19 38383330 38383330 single base substitution T C missense_variant K966E 2896A>G UCEC-US 19 38383923 38383923 single base substitution C T downstream_gene_variant UCEC-US 19 38383923 38383923 single base substitution C T missense_variant R768Q 2303G>A UCEC-US 19 38383923 38383923 single base substitution C T missense_variant R807Q 2420G>A UCEC-US 19 38384165 38384165 single base substitution C A downstream_gene_variant UCEC-US 19 38384165 38384165 single base substitution C A missense_variant Q687H 2061G>T UCEC-US 19 38384165 38384165 single base substitution C A missense_variant Q726H 2178G>T UCEC-US 19 38384315 38384315 single base substitution T G downstream_gene_variant UCEC-US 19 38384315 38384315 single base substitution T G missense_variant K637N 1911A>C UCEC-US 19 38384315 38384315 single base substitution T G missense_variant K676N 2028A>C UCEC-US 19 38384338 38384338 single base substitution G A downstream_gene_variant UCEC-US 19 38384338 38384338 single base substitution G A missense_variant L630F 1888C>T UCEC-US 19 38384338 38384338 single base substitution G A missense_variant L669F 2005C>T UCEC-US 19 38384371 38384371 single base substitution G A downstream_gene_variant UCEC-US 19 38384371 38384371 single base substitution G A missense_variant R619W 1855C>T UCEC-US 19 38384371 38384371 single base substitution G A missense_variant R658W 1972C>T UCEC-US 19 38384713 38384713 single base substitution C T downstream_gene_variant UCEC-US 19 38384713 38384713 single base substitution C T missense_variant V505I 1513G>A UCEC-US 19 38384713 38384713 single base substitution C T missense_variant V544I 1630G>A UCEC-US 19 38384921 38384921 single base substitution C A downstream_gene_variant UCEC-US 19 38384921 38384921 single base substitution C A missense_variant E435D 1305G>T UCEC-US 19 38384921 38384921 single base substitution C A missense_variant E474D 1422G>T UCEC-US 19 38385088 38385088 single base substitution G T downstream_gene_variant UCEC-US 19 38385088 38385088 single base substitution G T missense_variant P380T 1138C>A UCEC-US 19 38385088 38385088 single base substitution G T missense_variant P419T 1255C>A UCEC-US 19 38385235 38385235 single base substitution G A downstream_gene_variant UCEC-US 19 38385235 38385235 single base substitution G A missense_variant R331W 991C>T UCEC-US 19 38385235 38385235 single base substitution G A missense_variant R370W 1108C>T UCEC-US 19 38385359 38385359 single base substitution G C downstream_gene_variant UCEC-US 19 38385359 38385359 single base substitution G C stop_gained Y289* 867C>G UCEC-US 19 38385359 38385359 single base substitution G C stop_gained Y328* 984C>G UCEC-US 19 38385624 38385624 single base substitution C T downstream_gene_variant UCEC-US 19 38385624 38385624 single base substitution C T missense_variant S201N 602G>A UCEC-US 19 38385624 38385624 single base substitution C T missense_variant S240N 719G>A UCEC-US 19 38385931 38385931 single base substitution G A downstream_gene_variant UCEC-US 19 38385931 38385931 single base substitution G A missense_variant R138W 412C>T UCEC-US 19 38385931 38385931 single base substitution G A missense_variant R99W 295C>T UCEC-US 19 38386786 38386786 single base substitution C A exon_variant UCEC-US 19 38386786 38386786 single base substitution C A intron_variant UCEC-US 19 38386786 38386786 single base substitution C A stop_gained E80* 238G>T UCEC-US 19 38386834 38386834 single base substitution C A exon_variant UCEC-US 19 38386834 38386834 single base substitution C A intron_variant UCEC-US 19 38386834 38386834 single base substitution C A missense_variant D64Y 190G>T UCEC-US 19 38386888 38386888 single base substitution A G exon_variant UCEC-US 19 38386888 38386888 single base substitution A G missense_variant F46L 136T>C UCEC-US 19 38386888 38386888 single base substitution A G splice_region_variant UCEC-US 19 38386928 38386928 single base substitution C A exon_variant UCEC-US 19 38386928 38386928 single base substitution C A missense_variant K32N 96G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand CSCC-29-T COSM4481770 c.2541C>T p.F847F Substitution - coding silent 19:37893045-37893045 - CHC1720T COSM4800538 c.1918C>T p.P640S Substitution - Missense 19:37893668-37893668 - TCGA-D8-A1XQ-01 COSM5225429 c.8542delT p.C2848fs*39 Deletion - Frameshift 19:37885129-37885129 - C086 COSM5541732 c.5350G>A p.E1784K Substitution - Missense 19:37888321-37888321 - TCGA-AA-3663-01 COSM1393301 c.2804C>T p.P935L Substitution - Missense 19:37892782-37892782 - YUJUBE COSM5389578 c.6264G>A p.R2088R Substitution - coding silent 19:37887290-37887290 - pfg043T COSM4753138 c.2522A>C p.K841T Substitution - Missense 19:37893064-37893064 - T24 COSM5343304 c.8135T>G p.I2712S Substitution - Missense 19:37885536-37885536 - PCSI_0162_Pa_P_526 COSM4964276 c.868C>T p.R290W Substitution - Missense 19:37894718-37894718 - ESCC-D1 COSM5045171 c.7672T>A p.S2558T Substitution - Missense 19:37885882-37885882 - L21 COSM5369422 c.1053delG p.C353fs*43 Deletion - Frameshift 19:37894650-37894650 - TCGA-DD-A3A9-01 COSM4920374 c.3350C>T p.P1117L Substitution - Missense 19:37891596-37891596 - RMS77_ COSM4988493 c.8327G>A p.R2776Q Substitution - Missense 19:37885344-37885344 - HCC93T COSM3707110 c.6326G>A p.R2109H Substitution - Missense 19:37887228-37887228 - PT13 COSM995876 c.1888C>T p.L630F Substitution - Missense 19:37893698-37893698 - TCGA-F4-6856-01 COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - CSCC-27-T COSM3749503 c.6790G>A p.E2264K Substitution - Missense 19:37886764-37886764 - ME049T COSM230381 c.923C>T p.S308F Substitution - Missense 19:37894663-37894663 - Au8 COSM5607215 c.5517G>A p.R1839R Substitution - coding silent 19:37888154-37888154 - TCGA-F5-6702-01 COSM3749506 c.6897G>A p.E2299E Substitution - coding silent 19:37886774-37886774 - pfg008T COSM4753143 c.2119T>G p.F707V Substitution - Missense 19:37893584-37893584 - YUWAPO COSM5389595 c.4789G>A p.E1597K Substitution - Missense 19:37888882-37888882 - SJHGG014_D COSM4970093 c.76-6C>A p.? Unknown 19:37896314-37896314 - PT50 COSM5937840 c.6572C>T p.P2191L Substitution - Missense 19:37886982-37886982 - TCGA-D1-A16Y-01 COSM995845 c.7133G>A p.G2378D Substitution - Missense 19:37886421-37886421 - HCA7 COSM4630459 c.8497G>A p.V2833M Substitution - Missense 19:37885057-37885057 - BCM695T COSM4802859 c.8107T>G p.F2703V Substitution - Missense 19:37885447-37885447 - S00825 COSM3201552 c.3694C>T p.R1232C Substitution - Missense 19:37889860-37889860 - TCGA-EI-6917-01 COSM3422755 c.8326C>T p.R2776W Substitution - Missense 19:37885345-37885345 - UM-SCC-11B COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - PTC-7C COSM4131763 c.7709A>T p.H2570L Substitution - Missense 19:37885845-37885845 - BCM723T COSM3201254 c.8500C>T p.R2834C Substitution - Missense 19:37885054-37885054 - PCSI_0135_Pa_X COSM3378713 c.2084T>A p.L695H Substitution - Missense 19:37893502-37893502 - TCGA-F5-6814-01 COSM3422765 c.3571G>T p.D1191Y Substitution - Missense 19:37890100-37890100 - BCM265T COSM4955159 c.6955G>T p.V2319L Substitution - Missense 19:37886716-37886716 - SC_9032 COSM5561529 c.3845C>A p.P1282H Substitution - Missense 19:37889709-37889709 - TCGA-CA-6717-01 COSM3201461 c.5148G>T p.E1716D Substitution - Missense 19:37888523-37888523 - TCGA-EA-A44S-01 COSM4822079 c.842G>A p.R281Q Substitution - Missense 19:37894744-37894744 - TCGA-EI-6917-01 COSM3422752 c.8236G>T p.D2746Y Substitution - Missense 19:37885318-37885318 - BICR_22 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - TCGA-F5-6864-01 COSM3422760 c.4996G>T p.A1666S Substitution - Missense 19:37888558-37888558 - PDA_025 COSM4999275 c.2285G>A p.R762H Substitution - Missense 19:37893418-37893418 - TCGA-CK-4952-01 COSM3749504 c.6907G>A p.E2303K Substitution - Missense 19:37886764-37886764 - TCGA-JW-A5VL-01 COSM4846472 c.3170C>G p.S1057C Substitution - Missense 19:37891659-37891659 - MO_1241 COSM5557758 c.5571A>G p.K1857K Substitution - coding silent 19:37887983-37887983 - PD6684a COSM5791529 c.1832C>G p.S611C Substitution - Missense 19:37893871-37893871 - 2521249 COSM5888449 c.3850G>A p.D1284N Substitution - Missense 19:37889821-37889821 - LP6005690-DNA_D01 COSM3201323 c.7343C>T p.P2448L Substitution - Missense 19:37886328-37886328 - CSCC-41-T COSM4539980 c.2767G>T p.A923S Substitution - Missense 19:37892819-37892819 - TCGA-AZ-4615-01 COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - ESCC_BICR_028T COSM5431754 c.3106G>T p.E1036* Substitution - Nonsense 19:37891723-37891723 - TCGA-CM-4743-01 COSM5155992 c.8496delA p.A2833fs*4 Deletion - Frameshift 19:37885175-37885175 - C089 COSM3201427 c.5551G>A p.E1851K Substitution - Missense 19:37888003-37888003 - RK165_C01 COSM1630896 c.8628T>G p.L2876L Substitution - coding silent 19:37885043-37885043 - S02279 COSM5683659 c.3647C>A p.T1216N Substitution - Missense 19:37889907-37889907 - Au4 COSM5605353 c.4074G>A p.L1358L Substitution - coding silent 19:37889480-37889480 - HCC128 COSM1612152 c.3961C>T p.P1321S Substitution - Missense 19:37889710-37889710 - TCGA-B5-A11E-01 COSM4870079 c.136T>C p.F46L Substitution - Missense 19:37896248-37896248 - ACA8 COSM4867322 c.5118G>T p.K1706N Substitution - Missense 19:37888553-37888553 - SW948 COSM3201394 c.6318C>T p.S2106S Substitution - coding silent 19:37887353-37887353 - AOCS-163-1-4 COSM4140588 c.3472G>A p.E1158K Substitution - Missense 19:37890199-37890199 - BHY COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - UM-SCC-2 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - 19M COSM3201530 c.4212G>A p.V1404V Substitution - coding silent 19:37889459-37889459 - 18195 COSM5346533 c.7711C>T p.L2571L Substitution - coding silent 19:37885960-37885960 - ESCC_BICR_013T COSM5439447 c.8137_8142delACACAG p.T2713_Q2714delTQ Deletion - In frame 19:37885412-37885417 - sysucc-1370T COSM5470997 c.6930G>T p.E2310D Substitution - Missense 19:37886741-37886741 - PTC-7C COSM3756726 c.8208T>C p.F2736F Substitution - coding silent 19:37885463-37885463 - SW948 COSM3201393 c.6201C>T p.S2067S Substitution - coding silent 19:37887353-37887353 - 9227_T COSM5040047 c.7339C>T p.P2447S Substitution - Missense 19:37886215-37886215 - 2492713 COSM5607212 c.6825G>A p.G2275G Substitution - coding silent 19:37886729-37886729 - CSCC-17-T COSM4526913 c.1545G>A p.G515G Substitution - coding silent 19:37894158-37894158 - 0070_CRUK_PC_0070_T1_DNA COSM4413790 c.6166C>T p.L2056L Substitution - coding silent 19:37887505-37887505 - 8068564 COSM3771036 c.3601G>A p.V1201I Substitution - Missense 19:37889953-37889953 - CSCC-20-T COSM4497968 c.509C>T p.S170F Substitution - Missense 19:37895077-37895077 - CSCC-27-T COSM4551289 c.5251G>A p.E1751K Substitution - Missense 19:37888303-37888303 - HCT116 COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - DLD1 COSM4623950 c.240T>A p.H80Q Substitution - Missense 19:37895346-37895346 - TCGA-E9-A243-01 COSM4815915 c.3496G>A p.A1166T Substitution - Missense 19:37890175-37890175 - LS411 COSM3201416 c.5822T>C p.V1941A Substitution - Missense 19:37887849-37887849 - RMS112_ COSM4987801 c.329G>A p.R110H Substitution - Missense 19:37895257-37895257 - C058 COSM4988492 c.8210G>A p.R2737Q Substitution - Missense 19:37885344-37885344 - TCGA-AM-5821-01 COSM3749506 c.6897G>A p.E2299E Substitution - coding silent 19:37886774-37886774 - STC291 COSM5056599 c.7811T>C p.L2604P Substitution - Missense 19:37885860-37885860 - CCK81 COSM3201634 c.2169A>G p.Q723Q Substitution - coding silent 19:37893534-37893534 - CSCC-7-T COSM3201534 c.4021G>A p.E1341K Substitution - Missense 19:37889533-37889533 - CSCC-47-T COSM4510216 c.8305C>T p.Q2769* Substitution - Nonsense 19:37885249-37885249 - TCGA-D8-A1XQ-01 COSM5225430 c.3058delG p.A1020fs*15 Deletion - Frameshift 19:37891771-37891771 - PT37 COSM4976255 c.3859C>T p.R1287C Substitution - Missense 19:37889812-37889812 - C086 COSM5541751 c.5199G>A p.E1733E Substitution - coding silent 19:37888355-37888355 - TCGA-AZ-4615-01 COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - 215 COSM4424517 c.3693C>G p.H1231Q Substitution - Missense 19:37889978-37889978 - TCGA-BS-A0UF-01 COSM4875471 c.412C>T p.R138W Substitution - Missense 19:37895291-37895291 - 8016470 COSM3388936 c.5493T>C p.P1831P Substitution - coding silent 19:37888178-37888178 - LUAD-5V8LT COSM401834 c.4490A>G p.H1497R Substitution - Missense 19:37889064-37889064 - 2492720 COSM5722931 c.4618G>A p.D1540N Substitution - Missense 19:37888936-37888936 - PT33 COSM5389581 c.5914G>A p.E1972K Substitution - Missense 19:37887757-37887757 - CSCC-30-T COSM4518190 c.5684_5685GG>AA p.R1895K Substitution - Missense 19:37887986-37887987 - TCGA-D5-6927-01 COSM4783260 c.873C>T p.S291S Substitution - coding silent 19:37894830-37894830 - TCGA-B5-A0JY-01 COSM995843 c.7306G>T p.E2436* Substitution - Nonsense 19:37886248-37886248 - D28 COSM5546122 c.2152A>T p.S718C Substitution - Missense 19:37893434-37893434 - CSCC-49-T COSM4547535 c.4371G>A p.R1457R Substitution - coding silent 19:37889300-37889300 - CHC892T COSM4794284 c.3273G>A p.K1091K Substitution - coding silent 19:37891556-37891556 - ESCC_79 COSM5635613 c.1168C>T p.R390C Substitution - Missense 19:37894535-37894535 - PCSI_0076_Pa_X COSM5419856 c.8364C>T p.Y2788Y Substitution - coding silent 19:37885190-37885190 - ATL045 COSM5707003 c.5030A>G p.E1677G Substitution - Missense 19:37888524-37888524 - 2492723 COSM394453 c.1715C>T p.S572F Substitution - Missense 19:37893871-37893871 - WSU-HN30 COSM4600982 c.8668T>G p.W2890G Substitution - Missense 19:37885003-37885003 - NOKSI COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - TCGA-AM-5821-01 COSM3749505 c.6780G>A p.E2260E Substitution - coding silent 19:37886774-37886774 - TCGA-CK-4952-01 COSM3756729 c.6777G>A p.E2259E Substitution - coding silent 19:37886777-37886777 - CSCC-60-T COSM4558417 c.7795G>A p.G2599R Substitution - Missense 19:37885876-37885876 - PCSI_0015_Pa_P_526 COSM4963273 c.4391G>T p.W1464L Substitution - Missense 19:37889163-37889163 - 2492721 COSM5722935 c.3514C>T p.L1172L Substitution - coding silent 19:37890040-37890040 - HCC93T COSM3707111 c.6443G>A p.R2148H Substitution - Missense 19:37887228-37887228 - TCGA-F5-6814-01 COSM3422756 c.7495A>G p.M2499V Substitution - Missense 19:37886059-37886059 - S0029 COSM5883106 c.8203G>A p.D2735N Substitution - Missense 19:37885468-37885468 - PDA_025 COSM4999274 c.2168G>A p.R723H Substitution - Missense 19:37893418-37893418 - TCGA-E9-A22G-01 COSM1480992 c.3714T>C p.D1238D Substitution - coding silent 19:37889840-37889840 - LP6005690-DNA_D01 COSM3201322 c.7226C>T p.P2409L Substitution - Missense 19:37886328-37886328 - TCGA-AO-A128-01 COSM3822925 c.2290T>C p.Y764H Substitution - Missense 19:37893296-37893296 - QC2-15-T2 COSM5652524 c.3794T>G p.L1265R Substitution - Missense 19:37889760-37889760 - sysucc-311T COSM5464552 c.6520G>T p.D2174Y Substitution - Missense 19:37887151-37887151 - sysucc-1397T COSM5474143 c.3054G>A p.M1018I Substitution - Missense 19:37891775-37891775 - HCC2998 COSM3201414 c.5901G>T p.E1967D Substitution - Missense 19:37887770-37887770 - TCGA-EA-A44S-01 COSM4822080 c.959G>A p.R320Q Substitution - Missense 19:37894744-37894744 - 2246942 COSM3712908 c.5684G>A p.R1895K Substitution - Missense 19:37887987-37887987 - HCC097T COSM5816434 c.6122G>A p.G2041E Substitution - Missense 19:37887432-37887432 - CSCC-44-T COSM4506153 c.829C>T p.H277Y Substitution - Missense 19:37894874-37894874 - TCGA-CA-6717-01 COSM4947992 c.8103A>C p.E2701D Substitution - Missense 19:37885568-37885568 - DLD1 COSM3201572 c.3293G>A p.R1098Q Substitution - Missense 19:37890261-37890261 - TCGA-AM-5820-01 COSM3756731 c.6421C>T p.R2141W Substitution - Missense 19:37887133-37887133 - 2293776 COSM4607705 c.8084G>T p.W2695L Substitution - Missense 19:37885470-37885470 - S00339 COSM5657337 c.2551C>T p.R851W Substitution - Missense 19:37893152-37893152 - sysucc-1370T COSM3201697 c.1106G>A p.R369H Substitution - Missense 19:37894597-37894597 - CSCC-20-T COSM4497969 c.626C>T p.S209F Substitution - Missense 19:37895077-37895077 - CHC892T COSM4960370 c.7607C>T p.P2536L Substitution - Missense 19:37886064-37886064 - TCGA-B0-5707-01 COSM474657 c.306A>C p.K102N Substitution - Missense 19:37895280-37895280 - RMS110_ COSM4987286 c.4835A>G p.K1612R Substitution - Missense 19:37888836-37888836 - PD4200a COSM4810100 c.2473C>G p.P825A Substitution - Missense 19:37893230-37893230 - 2492721 COSM5722933 c.4474G>A p.E1492K Substitution - Missense 19:37889080-37889080 - TCGA-AO-A128-01 COSM3822926 c.2407T>C p.Y803H Substitution - Missense 19:37893296-37893296 - TCGA-A6-6141-01 COSM3749505 c.6780G>A p.E2260E Substitution - coding silent 19:37886774-37886774 - 3885 COSM5043516 c.5386G>T p.E1796* Substitution - Nonsense 19:37888168-37888168 - Au3 COSM5602606 c.7207G>A p.E2403K Substitution - Missense 19:37886464-37886464 - YUOTHO COSM5389571 c.8467C>T p.Q2823* Substitution - Nonsense 19:37885204-37885204 - YURISA COSM5389586 c.5052G>A p.G1684G Substitution - coding silent 19:37888502-37888502 - WA12 COSM238438 c.8397C>T p.P2799P Substitution - coding silent 19:37885157-37885157 - 1N52-VS-1T52 COSM4976786 c.2917A>G p.N973D Substitution - Missense 19:37892786-37892786 - HCC002T COSM3201468 c.4942T>A p.L1648M Substitution - Missense 19:37888729-37888729 - TCGA-B5-A11E-01 COSM995885 c.129+7T>C p.? Unknown 19:37896248-37896248 - C086 COSM5541752 c.5316G>A p.E1772E Substitution - coding silent 19:37888355-37888355 - PT13 COSM3201458 c.5227G>A p.E1743K Substitution - Missense 19:37888444-37888444 - PT50 COSM5937841 c.6689C>T p.P2230L Substitution - Missense 19:37886982-37886982 - ESCC_109 COSM5638956 c.1383C>T p.F461F Substitution - coding silent 19:37894203-37894203 - YUKAT COSM3201521 c.4232G>A p.R1411K Substitution - Missense 19:37889322-37889322 - 585205 COSM324305 c.4411C>A p.H1471N Substitution - Missense 19:37889143-37889143 - WSU-HN13 COSM4601864 c.4763G>C p.R1588P Substitution - Missense 19:37888791-37888791 - B64-Tumor COSM3933021 c.6576G>C p.M2192I Substitution - Missense 19:37887095-37887095 - PT19_2 COSM4282420 c.4358G>A p.G1453E Substitution - Missense 19:37889313-37889313 - 227 COSM4425966 c.7423G>A p.V2475M Substitution - Missense 19:37886131-37886131 - STC291 COSM5056598 c.7694T>C p.L2565P Substitution - Missense 19:37885860-37885860 - sysucc-311T COSM5464554 c.6061G>T p.E2021* Substitution - Nonsense 19:37887610-37887610 - TCGA-MH-A561-01 COSM3989988 c.982C>A p.Q328K Substitution - Missense 19:37894604-37894604 - TCGA-AA-3510-01 COSM1393280 c.6631G>T p.E2211* Substitution - Nonsense 19:37886923-37886923 - TCGA-BS-A0UF-01 COSM995837 c.8353G>T p.E2785* Substitution - Nonsense 19:37885201-37885201 - HT115 COSM3201582 c.3208G>C p.E1070Q Substitution - Missense 19:37891621-37891621 - C0080T COSM4154197 c.2568A>T p.V856V Substitution - coding silent 19:37893018-37893018 - YUROG COSM5389619 c.355C>T p.H119Y Substitution - Missense 19:37895348-37895348 - PDA_075 COSM5002131 c.2327T>C p.M776T Substitution - Missense 19:37893376-37893376 - PT38 COSM5923336 c.5805G>A p.M1935I Substitution - Missense 19:37887749-37887749 - HCC58T COSM1612149 c.4017C>A p.H1339Q Substitution - Missense 19:37889537-37889537 - TCGA-BH-A2L8-01 COSM3822932 c.372C>A p.Y124* Substitution - Nonsense 19:37895331-37895331 - PT37 COSM4976254 c.3742C>T p.R1248C Substitution - Missense 19:37889812-37889812 - TCGA-GJ-A6C0-01 COSM4929991 c.457A>T p.M153L Substitution - Missense 19:37895129-37895129 - 93VU147T COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - S00035 COSM5656743 c.1156G>A p.D386N Substitution - Missense 19:37894547-37894547 - YURISA COSM5389587 c.5169G>A p.G1723G Substitution - coding silent 19:37888502-37888502 - TCGA-DD-A73A-01 COSM4916539 c.3887C>A p.S1296Y Substitution - Missense 19:37889784-37889784 - C086 COSM5541730 c.2126C>T p.S709F Substitution - Missense 19:37893577-37893577 - ESCC_143 COSM5649882 c.8538G>A p.L2846L Substitution - coding silent 19:37885133-37885133 - 0038_CRUK_PC_0038_T1_DNA COSM5422997 c.6101G>C p.G2034A Substitution - Missense 19:37887453-37887453 - HCC58T COSM1612150 c.4134C>A p.H1378Q Substitution - Missense 19:37889537-37889537 - 2492711 COSM5607215 c.5517G>A p.R1839R Substitution - coding silent 19:37888154-37888154 - TCGA-EI-6509-01 COSM3749506 c.6897G>A p.E2299E Substitution - coding silent 19:37886774-37886774 - UM-SCC-4 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - TCGA-D8-A1XQ-01 COSM5225431 c.3175delG p.A1059fs*15 Deletion - Frameshift 19:37891771-37891771 - RK184_C01 COSM1630897 c.8098A>G p.K2700E Substitution - Missense 19:37885456-37885456 - HCA7 COSM4630460 c.8614G>A p.V2872M Substitution - Missense 19:37885057-37885057 - PCSI_0098_Pa_P_526 COSM5031784 c.3102A>G p.K1034K Substitution - coding silent 19:37892601-37892601 - TCGA-AX-A0J0-01 COSM995875 c.1911A>C p.K637N Substitution - Missense 19:37893675-37893675 - 587298 COSM1232697 c.7710T>G p.H2570Q Substitution - Missense 19:37885844-37885844 - TCGA-AA-3510-01 COSM3201380 c.6748G>T p.E2250* Substitution - Nonsense 19:37886923-37886923 - 37M COSM5584257 c.2171C>T p.S724F Substitution - Missense 19:37893415-37893415 - CHC1720T COSM4800539 c.2035C>T p.P679S Substitution - Missense 19:37893668-37893668 - RK064_C01 COSM1630900 c.5170A>G p.K1724E Substitution - Missense 19:37888501-37888501 - YUNEKI COSM5389580 c.5797G>A p.E1933K Substitution - Missense 19:37887757-37887757 - HT115 COSM3201576 c.3255C>A p.G1085G Substitution - coding silent 19:37891574-37891574 - OSCC-GB_00410111 COSM3712910 c.4268G>A p.G1423E Substitution - Missense 19:37889403-37889403 - TCGA-D8-A1JA-01 COSM3822923 c.2491G>A p.A831T Substitution - Missense 19:37893095-37893095 - UM-SCC-4 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - C135 COSM3201546 c.3787G>T p.E1263* Substitution - Nonsense 19:37889767-37889767 - SC_9092 COSM5557899 c.8122A>G p.K2708E Substitution - Missense 19:37885432-37885432 - ESOSCC155T COSM1172623 c.6128G>A p.R2043K Substitution - Missense 19:37887426-37887426 - CSCC-35-T COSM4510484 c.8512C>T p.P2838S Substitution - Missense 19:37885159-37885159 - LIM2551 COSM4644202 c.3913C>A p.L1305I Substitution - Missense 19:37889641-37889641 - HCA7 COSM4630462 c.5443T>C p.L1815L Substitution - coding silent 19:37888228-37888228 - 38 COSM5733713 c.5042A>C p.K1681T Substitution - Missense 19:37888512-37888512 - OSCC-GB_00910111 COSM3201697 c.1106G>A p.R369H Substitution - Missense 19:37894597-37894597 - 8051715 COSM4406429 c.5190C>T p.N1730N Substitution - coding silent 19:37888481-37888481 - S02294 COSM5688777 c.2921C>A p.P974Q Substitution - Missense 19:37892782-37892782 - 587376 COSM1232693 c.5405G>T p.R1802M Substitution - Missense 19:37888149-37888149 - BD72T COSM3201395 c.6304delA p.R2102fs*11 Deletion - Frameshift 19:37887367-37887367 - 587376 COSM1232694 c.3733G>A p.D1245N Substitution - Missense 19:37889821-37889821 - TCGA-D8-A1JA-01 COSM3822930 c.1153G>A p.E385K Substitution - Missense 19:37894550-37894550 - 2492722 COSM5722934 c.4591G>A p.E1531K Substitution - Missense 19:37889080-37889080 - 2521249 COSM5888450 c.7515G>T p.Q2505H Substitution - Missense 19:37886039-37886039 - S01023 COSM5666527 c.4625T>C p.L1542P Substitution - Missense 19:37889046-37889046 - 6P2-2 COSM3734376 c.4877A>G p.K1626R Substitution - Missense 19:37888794-37888794 - PCSI_0162_Pa_P_526 COSM4964277 c.985C>T p.R329W Substitution - Missense 19:37894718-37894718 - TCGA-AY-6197-01 COSM1393304 c.2128G>A p.V710M Substitution - Missense 19:37893458-37893458 - UM-SCC-11B COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - C086 COSM5541736 c.5398G>A p.E1800K Substitution - Missense 19:37888273-37888273 - CSCC-10-T COSM4454389 c.4892A>C p.E1631A Substitution - Missense 19:37888779-37888779 - WSU-HN13 COSM4601865 c.4880G>C p.R1627P Substitution - Missense 19:37888791-37888791 - TCGA-CA-6717-01 COSM1393299 c.3270A>C p.K1090N Substitution - Missense 19:37891559-37891559 - HT115 COSM3201424 c.5751G>T p.K1917N Substitution - Missense 19:37887920-37887920 - CSCC-16-T COSM4548243 c.4542G>A p.R1514R Substitution - coding silent 19:37889129-37889129 - TCGA-BG-A0MQ-01 COSM4874447 c.1255C>A p.P419T Substitution - Missense 19:37894448-37894448 - ccRCC-29 COSM1665013 c.2083C>T p.L695F Substitution - Missense 19:37893503-37893503 - TCGA-B5-A0JY-01 COSM1590049 c.238G>T p.E80* Substitution - Nonsense 19:37896146-37896146 - TCGA-E9-A22G-01 COSM4814112 c.4782A>T p.E1594D Substitution - Missense 19:37888889-37888889 - CSCC-49-T COSM4481778 c.2542C>T p.L848L Substitution - coding silent 19:37893044-37893044 - 19M COSM5579986 c.7024G>A p.E2342K Substitution - Missense 19:37886647-37886647 - CSCC-35-T COSM4497993 c.5104C>T p.Q1702* Substitution - Nonsense 19:37888450-37888450 - TCGA-AM-5821-01 COSM3756725 c.8091T>C p.F2697F Substitution - coding silent 19:37885463-37885463 - CSCC-31-T COSM4549160 c.4777G>A p.G1593R Substitution - Missense 19:37888894-37888894 - TCGA-G4-6628-01 COSM1393278 c.6788G>T p.R2263M Substitution - Missense 19:37886766-37886766 - 587376 COSM995874 c.2061G>T p.Q687H Substitution - Missense 19:37893525-37893525 - TCGA-CK-4947-01 COSM4787098 c.3915C>T p.N1305N Substitution - coding silent 19:37889756-37889756 - RK207_C01 COSM3742933 c.6128A>T p.E2043V Substitution - Missense 19:37887543-37887543 - TCGA-BS-A0UV-01 COSM4864978 c.5085G>T p.E1695D Substitution - Missense 19:37888586-37888586 - 2492714 COSM5607213 c.6942G>A p.G2314G Substitution - coding silent 19:37886729-37886729 - CSCC-47-T COSM4558432 c.7804G>A p.E2602K Substitution - Missense 19:37885867-37885867 - TCGA-CK-5916-01 COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - LUAD-5V8LT COSM401833 c.8410T>C p.F2804L Substitution - Missense 19:37885144-37885144 - CSCC-10-T COSM4454388 c.4775A>C p.E1592A Substitution - Missense 19:37888779-37888779 - TCGA-AX-A0J0-01 COSM995870 c.3426A>C p.S1142S Substitution - coding silent 19:37890128-37890128 - CSCC-32-T COSM4560474 c.8575G>A p.E2859K Substitution - Missense 19:37885096-37885096 - CSCC-7-T COSM3201535 c.4138G>A p.E1380K Substitution - Missense 19:37889533-37889533 - RK165_C01 COSM1630895 c.8511T>G p.L2837L Substitution - coding silent 19:37885043-37885043 - 2492722 COSM5722935 c.3514C>T p.L1172L Substitution - coding silent 19:37890040-37890040 - S0029 COSM5883105 c.8086G>A p.D2696N Substitution - Missense 19:37885468-37885468 - 2492721 COSM394453 c.1715C>T p.S572F Substitution - Missense 19:37893871-37893871 - 35M COSM5583056 c.990C>T p.L330L Substitution - coding silent 19:37894713-37894713 - Detroit_562 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - HT115 COSM3201583 c.3325G>C p.E1109Q Substitution - Missense 19:37891621-37891621 - PT36 COSM5916786 c.76-8C>T p.? Unknown 19:37896316-37896316 - TCGA-D5-6927-01 COSM1393309 c.756C>T p.S252S Substitution - coding silent 19:37894830-37894830 - C547 COSM4282378 c.8161G>A p.E2721K Substitution - Missense 19:37885510-37885510 - PD24190a COSM5780838 c.7064A>T p.E2355V Substitution - Missense 19:37886607-37886607 - BCM695T COSM4802859 c.8107T>G p.F2703V Substitution - Missense 19:37885447-37885447 - TCGA-FU-A3HZ-01 COSM1393296 c.3798C>T p.N1266N Substitution - coding silent 19:37889756-37889756 - C135 COSM4611037 c.8275_8276delAA p.K2759fs*44 Deletion - Frameshift 19:37885395-37885396 - LS174T COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - TCGA-EP-A3JL-01 COSM4913865 c.1412G>A p.R471Q Substitution - Missense 19:37894291-37894291 - TCGA-F4-6460-01 COSM3749506 c.6897G>A p.E2299E Substitution - coding silent 19:37886774-37886774 - PT35 COSM5914225 c.125C>T p.S42F Substitution - Missense 19:37896259-37896259 - TCGA-CA-6717-01 COSM995859 c.5031G>T p.E1677D Substitution - Missense 19:37888523-37888523 - TCGA-AM-5820-01 COSM3756733 c.3141G>A p.P1047P Substitution - coding silent 19:37891688-37891688 - CSCC-16-T COSM4548242 c.4425G>A p.R1475R Substitution - coding silent 19:37889129-37889129 - SC_9057 COSM5548817 c.5081C>T p.A1694V Substitution - Missense 19:37888590-37888590 - EGC15 COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - UPCI:SCC090 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - TCGA-AZ-4315-01 COSM1393293 c.4482G>T p.E1494D Substitution - Missense 19:37889072-37889072 - TCGA-D8-A1J8-01 COSM3822909 c.6515C>G p.S2172* Substitution - Nonsense 19:37887039-37887039 - pfg008T COSM4747024 c.6678_6680delAGA p.E2227delE Deletion - In frame 19:37886991-37886993 - PT33 COSM5389580 c.5797G>A p.E1933K Substitution - Missense 19:37887757-37887757 - TCGA-AX-A0J0-01 COSM4867322 c.5118G>T p.K1706N Substitution - Missense 19:37888553-37888553 - TCGA-AM-5820-01 COSM3756734 c.3258G>A p.P1086P Substitution - coding silent 19:37891688-37891688 - HCC097T COSM5816435 c.6239G>A p.G2080E Substitution - Missense 19:37887432-37887432 - TCGA-CM-6162-01 COSM1393290 c.4762C>T p.R1588* Substitution - Nonsense 19:37888792-37888792 - 6P2-1 COSM3734375 c.4760A>G p.K1587R Substitution - Missense 19:37888794-37888794 - C0051T COSM4154192 c.5287G>T p.D1763Y Substitution - Missense 19:37888384-37888384 - YUJUBE COSM5389575 c.6768G>A p.V2256V Substitution - coding silent 19:37886903-37886903 - TCGA-CA-6717-01 COSM3201602 c.2717G>A p.R906Q Substitution - Missense 19:37892986-37892986 - TCGA-AN-A046-01 COSM3822912 c.6112A>C p.T2038P Substitution - Missense 19:37887559-37887559 - OSCC-GB_00410111 COSM3712908 c.5684G>A p.R1895K Substitution - Missense 19:37887987-37887987 - TCGA-B5-A11E-01 COSM4870246 c.1422G>T p.E474D Substitution - Missense 19:37894281-37894281 - TCGA-D1-A103-01 COSM4874548 c.2420G>A p.R807Q Substitution - Missense 19:37893283-37893283 - TCGA-AP-A0LM-01 COSM995850 c.6149G>T p.R2050I Substitution - Missense 19:37887405-37887405 - 93VU147T COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - BD180T COSM5495216 c.3991G>A p.G1331S Substitution - Missense 19:37889563-37889563 - HCC128 COSM1612151 c.3844C>T p.P1282S Substitution - Missense 19:37889710-37889710 - CSCC-15-T COSM4568559 c.1326T>G p.P442P Substitution - coding silent 19:37894377-37894377 - PDA_074 COSM5002086 c.4865G>A p.R1622Q Substitution - Missense 19:37888806-37888806 - ESCC_BICR_019T COSM5431633 c.7209_7210delAA p.R2404fs*53 Deletion - Frameshift 19:37886461-37886462 - PT37 COSM5921616 c.3992C>T p.P1331L Substitution - Missense 19:37889679-37889679 - Au8 COSM5607214 c.5400G>A p.R1800R Substitution - coding silent 19:37888154-37888154 - Au10 COSM5598951 c.5524G>A p.E1842K Substitution - Missense 19:37888030-37888030 - 2293776 COSM4607706 c.8201G>T p.W2734L Substitution - Missense 19:37885470-37885470 - CSCC-4-T COSM4502714 c.6200C>T p.S2067F Substitution - Missense 19:37887354-37887354 - C0080T COSM4154198 c.2685A>T p.V895V Substitution - coding silent 19:37893018-37893018 - TCGA-B5-A11E-01 COSM995872 c.2896A>G p.K966E Substitution - Missense 19:37892690-37892690 - TCGA-G4-6628-01 COSM1393305 c.2121G>A p.V707V Substitution - coding silent 19:37893465-37893465 - PCSI_0076_Pa_X COSM5419857 c.8481C>T p.Y2827Y Substitution - coding silent 19:37885190-37885190 - SNU-C4 COSM3201476 c.4878delA p.K1626fs*9 Deletion - Frameshift 19:37888793-37888793 - sysucc-1370T COSM3201696 c.989G>A p.R330H Substitution - Missense 19:37894597-37894597 - CSCC-10-T COSM4454233 c.4427A>G p.K1476R Substitution - Missense 19:37889127-37889127 - RK184_C01 COSM1630898 c.8215A>G p.K2739E Substitution - Missense 19:37885456-37885456 - RMS112_ COSM4987802 c.446G>A p.R149H Substitution - Missense 19:37895257-37895257 - ML_07_T_01 COSM5037552 c.4639G>A p.E1547K Substitution - Missense 19:37888915-37888915 - 1N52-VS-1T52 COSM4976785 c.2800A>G p.N934D Substitution - Missense 19:37892786-37892786 - HCC2998 COSM3201373 c.6866A>G p.E2289G Substitution - Missense 19:37886805-37886805 - PCSI_0015_Pa_P_526 COSM4963274 c.4508G>T p.W1503L Substitution - Missense 19:37889163-37889163 - 587376 COSM1232696 c.2600G>A p.R867Q Substitution - Missense 19:37892986-37892986 - Gp5D COSM3201299 c.7844G>A p.R2615H Substitution - Missense 19:37885827-37885827 - VACO4S COSM4657194 c.1339A>G p.I447V Substitution - Missense 19:37894247-37894247 - BCM265T COSM4955159 c.6955G>T p.V2319L Substitution - Missense 19:37886716-37886716 - YUTRAIN COSM5389607 c.3208G>A p.E1070K Substitution - Missense 19:37891738-37891738 - 587376 COSM1232692 c.5532G>T p.K1844N Substitution - Missense 19:37888022-37888022 - 41T COSM3712909 c.4151G>A p.G1384E Substitution - Missense 19:37889403-37889403 - TCGA-A6-6141-01 COSM3749503 c.6790G>A p.E2264K Substitution - Missense 19:37886764-37886764 - 2492712 COSM5607215 c.5517G>A p.R1839R Substitution - coding silent 19:37888154-37888154 - PCSI_0135_Pa_X COSM3378714 c.2201T>A p.L734H Substitution - Missense 19:37893502-37893502 - UD-SCC-2 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - TCGA-EI-6917-01 COSM995886 c.96G>T p.K32N Substitution - Missense 19:37896288-37896288 - C086 COSM5389577 c.6701G>A p.R2234Q Substitution - Missense 19:37886970-37886970 - YUFIT COSM5389602 c.3683G>A p.G1228E Substitution - Missense 19:37889871-37889871 - YUROG COSM5389618 c.238C>T p.H80Y Substitution - Missense 19:37895348-37895348 - HCC2998 COSM3201494 c.4712A>C p.K1571T Substitution - Missense 19:37888959-37888959 - TCGA-AK-3428-01 COSM3362833 c.3169A>T p.M1057L Substitution - Missense 19:37891777-37891777 - YUSIV COSM5389598 c.4156G>A p.E1386K Substitution - Missense 19:37889398-37889398 - SNU-C2B COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - 38 COSM5733714 c.5159A>C p.K1720T Substitution - Missense 19:37888512-37888512 - TCGA-AX-A0J0-01 COSM4867083 c.2028A>C p.K676N Substitution - Missense 19:37893675-37893675 - ESCC_79 COSM5635612 c.1051C>T p.R351C Substitution - Missense 19:37894535-37894535 - BCM723T COSM3201254 c.8500C>T p.R2834C Substitution - Missense 19:37885054-37885054 - CSCC-27-T COSM4541936 c.3098G>A p.R1033K Substitution - Missense 19:37891731-37891731 - pfg008T COSM4747023 c.6561_6563delAGA p.E2188delE Deletion - In frame 19:37886991-37886993 - TCGA-CA-6718-01 COSM4949073 c.3648C>G p.D1216E Substitution - Missense 19:37890023-37890023 - BD188T COSM5499601 c.5725C>G p.L1909V Substitution - Missense 19:37887829-37887829 - J90_T COSM3960005 c.5898A>G p.E1966E Substitution - coding silent 19:37887656-37887656 - TCGA-B5-A11N-01 COSM995858 c.5095G>T p.E1699* Substitution - Nonsense 19:37888459-37888459 - HCC102T COSM5806946 c.8441C>A p.T2814N Substitution - Missense 19:37885113-37885113 - 8048316 COSM3388934 c.8521C>T p.R2841W Substitution - Missense 19:37885150-37885150 - TCGA-BH-A2L8-01 COSM3822931 c.255C>A p.Y85* Substitution - Nonsense 19:37895331-37895331 - B64-Tumor COSM3933020 c.6459G>C p.M2153I Substitution - Missense 19:37887095-37887095 - LUAD-FH5PJ COSM394454 c.650T>C p.L217P Substitution - Missense 19:37894936-37894936 - ESCC-060T COSM3938068 c.2808G>C p.L936L Substitution - coding silent 19:37892778-37892778 - LIM2405 COSM4642301 c.1775G>A p.R592Q Substitution - Missense 19:37893811-37893811 - A9 COSM5350504 c.2666T>A p.I889N Substitution - Missense 19:37892920-37892920 - TCGA-CJ-5671-01 COSM474658 c.284G>A p.G95E Substitution - Missense 19:37895302-37895302 - 2492711 COSM5607214 c.5400G>A p.R1800R Substitution - coding silent 19:37888154-37888154 - LIM2405 COSM4642302 c.1892G>A p.R631Q Substitution - Missense 19:37893811-37893811 - TCGA-BS-A0UF-01 COSM995884 c.295C>T p.R99W Substitution - Missense 19:37895291-37895291 - TCGA-CK-4950-01 COSM3756730 c.6894G>A p.E2298E Substitution - coding silent 19:37886777-37886777 - 46M COSM5389588 c.4885G>A p.E1629K Substitution - Missense 19:37888669-37888669 - CSCC-31-T COSM4567695 c.8294_8295CC>TT p.S2765F Substitution - Missense 19:37885259-37885260 - 2492723 COSM5722931 c.4618G>A p.D1540N Substitution - Missense 19:37888936-37888936 - CSCC-35-T COSM4497994 c.5221C>T p.Q1741* Substitution - Nonsense 19:37888450-37888450 - CSCC-32-T COSM4504127 c.6694C>T p.L2232F Substitution - Missense 19:37886977-37886977 - TCGA-AM-5820-01 COSM3756723 c.8528G>A p.R2843Q Substitution - Missense 19:37885026-37885026 - PTC-28C COSM3756723 c.8528G>A p.R2843Q Substitution - Missense 19:37885026-37885026 - CSCC-60-T COSM4526905 c.1544G>A p.G515E Substitution - Missense 19:37894159-37894159 - BD242T COSM5495972 c.6119G>A p.R2040K Substitution - Missense 19:37887435-37887435 - YUDIVI COSM3201427 c.5551G>A p.E1851K Substitution - Missense 19:37888003-37888003 - CSCC-27-T COSM4551290 c.5368G>A p.E1790K Substitution - Missense 19:37888303-37888303 - CHC1209T COSM4804692 c.3527G>T p.R1176L Substitution - Missense 19:37890027-37890027 - PD9575a COSM5769677 c.2710G>A p.A904T Substitution - Missense 19:37892876-37892876 - TCGA-BS-A0TJ-01 COSM995868 c.3502A>G p.T1168A Substitution - Missense 19:37890052-37890052 - Au9 COSM5607671 c.3949G>A p.V1317I Substitution - Missense 19:37889722-37889722 - 215 COSM4424516 c.3576C>G p.H1192Q Substitution - Missense 19:37889978-37889978 - A6 COSM5350503 c.2856G>T p.Q952H Substitution - Missense 19:37892847-37892847 - MO_1094 COSM5547556 c.4894_4896delCAG p.Q1632delQ Deletion - In frame 19:37888658-37888660 - AOCS-090-1-0 COSM4140583 c.8402A>T p.E2801V Substitution - Missense 19:37885152-37885152 - PD4954a COSM5778267 c.2451T>A p.L817L Substitution - coding silent 19:37893252-37893252 - ESCC_BICR_058T COSM5430564 c.6079G>A p.E2027K Substitution - Missense 19:37887475-37887475 - TCGA-AA-3713-01 COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - TCGA-AX-A1C7-01 COSM4875376 c.1108C>T p.R370W Substitution - Missense 19:37894595-37894595 - TCGA-D8-A1JA-01 COSM3822929 c.1036G>A p.E346K Substitution - Missense 19:37894550-37894550 - BD114T COSM5504526 c.1096C>T p.P366S Substitution - Missense 19:37894490-37894490 - VACO4S COSM4657195 c.1456A>G p.I486V Substitution - Missense 19:37894247-37894247 - TCGA-CA-6717-01 COSM4947908 c.6000G>T p.K2000N Substitution - Missense 19:37887671-37887671 - 416 COSM4431481 c.5962delC p.R1988fs*15 Deletion - Frameshift 19:37887709-37887709 - CSCC-29-T COSM4481771 c.2658C>T p.F886F Substitution - coding silent 19:37893045-37893045 - S02274 COSM5682452 c.7206G>A p.E2402E Substitution - coding silent 19:37886348-37886348 - CSCC-30-T COSM4558840 c.7824G>A p.K2608K Substitution - coding silent 19:37885730-37885730 - CSCC-32-T COSM4504126 c.6577C>T p.L2193F Substitution - Missense 19:37886977-37886977 - 53M COSM5595563 c.7252A>G p.K2418E Substitution - Missense 19:37886302-37886302 - TCGA-D8-A1J8-01 COSM3822910 c.6632C>G p.S2211* Substitution - Nonsense 19:37887039-37887039 - GC8_T COSM148603 c.8500C>A p.R2834S Substitution - Missense 19:37885054-37885054 - PT15_1 COSM4526904 c.1427G>A p.G476E Substitution - Missense 19:37894159-37894159 - HCC71 COSM1612153 c.2844A>G p.L948L Substitution - coding silent 19:37892742-37892742 - HCC161T COSM3707112 c.1270G>A p.A424T Substitution - Missense 19:37894316-37894316 - 2334196 COSM324306 c.4949A>G p.K1650R Substitution - Missense 19:37888605-37888605 - TCGA-B8-4621-01 COSM474656 c.2858A>G p.H953R Substitution - Missense 19:37892728-37892728 - 8051715 COSM4406428 c.5073C>T p.N1691N Substitution - coding silent 19:37888481-37888481 - HCA7 COSM4630461 c.5326T>C p.L1776L Substitution - coding silent 19:37888228-37888228 - TCGA-CC-A123-01 COSM4915236 c.5691G>C p.Q1897H Substitution - Missense 19:37887863-37887863 - WT037 COSM3201408 c.5962C>T p.R1988W Substitution - Missense 19:37887709-37887709 - TCGA-AM-5821-01 COSM3756726 c.8208T>C p.F2736F Substitution - coding silent 19:37885463-37885463 - TCGA-BS-A0UV-01 COSM995852 c.5721G>T p.E1907D Substitution - Missense 19:37887833-37887833 - TCGA-AP-A0LM-01 COSM4873339 c.6266G>T p.R2089I Substitution - Missense 19:37887405-37887405 - SC_9092 COSM5557900 c.8239A>G p.K2747E Substitution - Missense 19:37885432-37885432 - PD13424a COSM5783556 c.2294A>C p.Q765P Substitution - Missense 19:37893292-37893292 - TCGA-G4-6628-01 COSM4782798 c.6905G>T p.R2302M Substitution - Missense 19:37886766-37886766 - PT35 COSM5389598 c.4156G>A p.E1386K Substitution - Missense 19:37889398-37889398 - C089 COSM3201428 c.5668G>A p.E1890K Substitution - Missense 19:37888003-37888003 - sysucc-1370T COSM4875471 c.412C>T p.R138W Substitution - Missense 19:37895291-37895291 - MO_1184 COSM5566903 c.2441G>A p.R814Q Substitution - Missense 19:37893262-37893262 - LIM2551 COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - TCGA-CA-6717-01 COSM1393287 c.5473G>T p.E1825* Substitution - Nonsense 19:37888081-37888081 - CSCC-49-T COSM4559495 c.8193G>A p.K2731K Substitution - coding silent 19:37885478-37885478 - YUQUEST COSM3201513 c.4337G>A p.G1446E Substitution - Missense 19:37889217-37889217 - 2492722 COSM5722933 c.4474G>A p.E1492K Substitution - Missense 19:37889080-37889080 - TCGA-B5-A11N-01 COSM995840 c.7984G>A p.E2662K Substitution - Missense 19:37885570-37885570 - 587222 COSM995866 c.4113G>T p.K1371N Substitution - Missense 19:37889441-37889441 - PT52 COSM1393274 c.8250G>A p.W2750* Substitution - Nonsense 19:37885304-37885304 - LS411 COSM3201415 c.5705T>C p.V1902A Substitution - Missense 19:37887849-37887849 - HCC58 COSM3707108 c.6817G>A p.E2273K Substitution - Missense 19:37886737-37886737 - CSCC-27-T COSM4541937 c.3215G>A p.R1072K Substitution - Missense 19:37891731-37891731 - TCGA-AP-A0LP-01 COSM4872170 c.7913T>C p.L2638P Substitution - Missense 19:37885758-37885758 - sysucc-311T COSM5464553 c.5944G>T p.E1982* Substitution - Nonsense 19:37887610-37887610 - 2492711 COSM5607213 c.6942G>A p.G2314G Substitution - coding silent 19:37886729-37886729 - S01563 COSM5701222 c.4177_4178insGA p.K1393fs*22 Insertion - Frameshift 19:37889376-37889377 - TCGA-CJ-5677-01 COSM3773867 c.6762A>G p.E2254E Substitution - coding silent 19:37886792-37886792 - TCGA-AP-A0LM-01 COSM4873232 c.8106G>A p.M2702I Substitution - Missense 19:37885565-37885565 - 6P2-1 COSM3734376 c.4877A>G p.K1626R Substitution - Missense 19:37888794-37888794 - TCGA-CC-A7IH-01 COSM4923942 c.6888G>A p.K2296K Substitution - coding silent 19:37886666-37886666 - TCGA-CK-4952-01 COSM3756730 c.6894G>A p.E2298E Substitution - coding silent 19:37886777-37886777 - SCC-25 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - WSU-HN30 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - CHC892T COSM4960369 c.7490C>T p.P2497L Substitution - Missense 19:37886064-37886064 - CSCC-30-T COSM4518189 c.5567_5568GG>AA p.R1856K Substitution - Missense 19:37887986-37887987 - SJBALL021507_D1 COSM4994149 c.6612C>A p.S2204R Substitution - Missense 19:37887059-37887059 - BD235T COSM5501677 c.623G>T p.G208V Substitution - Missense 19:37895080-37895080 - TCGA-AP-A0LF-01 COSM995871 c.3055C>T p.R1019W Substitution - Missense 19:37891774-37891774 - TCGA-AX-A1C7-01 COSM995881 c.991C>T p.R331W Substitution - Missense 19:37894595-37894595 - BD114T COSM5504527 c.1213C>T p.P405S Substitution - Missense 19:37894490-37894490 - HCC027T COSM5811789 c.417A>C p.A139A Substitution - coding silent 19:37895286-37895286 - 8049223 COSM3388931 c.8501G>A p.R2834H Substitution - Missense 19:37885053-37885053 - TCGA-EI-6917-01 COSM3422758 c.5665G>A p.A1889T Substitution - Missense 19:37887889-37887889 - TCGA-D1-A17Q-01 COSM1590048 c.190G>T p.D64Y Substitution - Missense 19:37896194-37896194 - C0078T COSM4154195 c.2633C>T p.T878I Substitution - Missense 19:37892953-37892953 - TCGA-AZ-4315-01 COSM4948440 c.4599G>T p.E1533D Substitution - Missense 19:37889072-37889072 - BD227T COSM5518031 c.6428A>T p.Q2143L Substitution - Missense 19:37887126-37887126 - SC_9032 COSM5561530 c.3962C>A p.P1321H Substitution - Missense 19:37889709-37889709 - TCGA-F4-6856-01 COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - RK064_C01 COSM1630899 c.5053A>G p.K1685E Substitution - Missense 19:37888501-37888501 - sysucc-783T COSM3388934 c.8521C>T p.R2841W Substitution - Missense 19:37885150-37885150 - SJBALL021507_D1 COSM4994148 c.6495C>A p.S2165R Substitution - Missense 19:37887059-37887059 - WSU-HN13 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - 2521249 COSM5888451 c.7632G>T p.Q2544H Substitution - Missense 19:37886039-37886039 - 0070_CRUK_PC_0070_T1_DNA COSM4413789 c.6049C>T p.L2017L Substitution - coding silent 19:37887505-37887505 - SC_9030 COSM5566925 c.2377C>T p.R793C Substitution - Missense 19:37893209-37893209 - TCGA-AY-6197-01 COSM4948372 c.2245G>A p.V749M Substitution - Missense 19:37893458-37893458 - S02237 COSM5676509 c.100T>C p.C34R Substitution - Missense 19:37896284-37896284 - CSCC-60-T COSM4549095 c.4759G>A p.E1587K Substitution - Missense 19:37888912-37888912 - TCGA-F4-6460-01 COSM3749503 c.6790G>A p.E2264K Substitution - Missense 19:37886764-37886764 - 37M COSM5584258 c.2288C>T p.S763F Substitution - Missense 19:37893415-37893415 - D28 COSM5546123 c.2269A>T p.S757C Substitution - Missense 19:37893434-37893434 - 2521243 COSM4526905 c.1544G>A p.G515E Substitution - Missense 19:37894159-37894159 - sysucc-1317T COSM5449262 c.6735T>C p.G2245G Substitution - coding silent 19:37886936-37886936 - TCGA-AA-3510-01 COSM1393300 c.2940G>T p.E980D Substitution - Missense 19:37892646-37892646 - LN229 COSM3201622 c.2390G>T p.W797L Substitution - Missense 19:37893313-37893313 - OSCC-GB_00910111 COSM3201696 c.989G>A p.R330H Substitution - Missense 19:37894597-37894597 - TCGA-C5-A1BF-01 COSM4836814 c.146C>A p.S49Y Substitution - Missense 19:37896238-37896238 - HCC058T COSM5805216 c.7382T>A p.V2461E Substitution - Missense 19:37886289-37886289 - PD23562a COSM5774110 c.7981C>G p.Q2661E Substitution - Missense 19:37885690-37885690 - TCGA-D1-A17Q-01 COSM995862 c.4923G>T p.E1641D Substitution - Missense 19:37888631-37888631 - ccRCC-49 COSM1665011 c.3527G>A p.R1176H Substitution - Missense 19:37890027-37890027 - HCC128T COSM1612152 c.3961C>T p.P1321S Substitution - Missense 19:37889710-37889710 - PD4127a COSM4809490 c.7964C>G p.P2655R Substitution - Missense 19:37885707-37885707 - YURAY COSM5389604 c.3182C>T p.S1061F Substitution - Missense 19:37891647-37891647 - TCGA-AA-3713-01 COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - YUOTHO COSM5389617 c.572_573CC>TT p.S191F Substitution - Missense 19:37895130-37895131 - TCGA-CC-A3MB-01 COSM4933609 c.2667G>C p.M889I Substitution - Missense 19:37893036-37893036 - 1047T COSM4868275 c.719G>A p.S240N Substitution - Missense 19:37894984-37894984 - CAL33 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - CSCC-31-T COSM4282377 c.8044G>A p.E2682K Substitution - Missense 19:37885510-37885510 - AOCS-163-1-4 COSM4140587 c.3355G>A p.E1119K Substitution - Missense 19:37890199-37890199 - CSCC-35-T COSM4510483 c.8395C>T p.P2799S Substitution - Missense 19:37885159-37885159 - D28 COSM5389573 c.7135G>A p.E2379K Substitution - Missense 19:37886536-37886536 - ESCC_BICR_042T COSM5443731 c.2944G>A p.E982K Substitution - Missense 19:37892759-37892759 - S02294 COSM5688776 c.2804C>A p.P935Q Substitution - Missense 19:37892782-37892782 - BD135T COSM5516839 c.3098A>C p.Q1033P Substitution - Missense 19:37892605-37892605 - 46M COSM5589358 c.5361A>T p.K1787N Substitution - Missense 19:37888310-37888310 - C086 COSM5541743 c.6921G>A p.E2307E Substitution - coding silent 19:37886633-37886633 - 2492722 COSM5722936 c.3631C>T p.L1211L Substitution - coding silent 19:37890040-37890040 - LUAD-S00488 COSM395086 c.2435G>T p.R812L Substitution - Missense 19:37893151-37893151 - TCGA-BS-A0UV-01 COSM4864366 c.8425A>C p.K2809Q Substitution - Missense 19:37885246-37885246 - TCGA-D1-A0ZO-01 COSM995883 c.602G>A p.S201N Substitution - Missense 19:37894984-37894984 - CCK81 COSM3201633 c.2052A>G p.Q684Q Substitution - coding silent 19:37893534-37893534 - S01020 COSM3749504 c.6907G>A p.E2303K Substitution - Missense 19:37886764-37886764 - 2492721 COSM5722934 c.4591G>A p.E1531K Substitution - Missense 19:37889080-37889080 - HT115 COSM3201320 c.7293G>A p.G2431G Substitution - coding silent 19:37886261-37886261 - ESCC_BICR_027T COSM5443232 c.5991G>C p.K1997N Substitution - Missense 19:37887680-37887680 - ESCC_BICR_013T COSM5439448 c.8254_8259delACACAG p.T2752_Q2753delTQ Deletion - In frame 19:37885412-37885417 - ICGC_MB35 COSM215768 c.5845C>T p.R1949W Substitution - Missense 19:37887709-37887709 - 2492720 COSM5722937 c.1832C>T p.S611F Substitution - Missense 19:37893871-37893871 - YUMOBER COSM5389613 c.1756G>A p.D586N Substitution - Missense 19:37893947-37893947 - ATL045 COSM5707004 c.5147A>G p.E1716G Substitution - Missense 19:37888524-37888524 - TCGA-DG-A2KM-01 COSM4851765 c.3581C>T p.S1194F Substitution - Missense 19:37890090-37890090 - TCGA-D5-6927-01 COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - LIM2551 COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - LPJ128 COSM1316926 c.2938G>A p.E980K Substitution - Missense 19:37892648-37892648 - CSCC-11-T COSM4558262 c.7718G>A p.R2573Q Substitution - Missense 19:37885953-37885953 - Au3 COSM5389576 c.6584G>A p.R2195Q Substitution - Missense 19:37886970-37886970 - KPOPBR-13-T COSM5963587 c.1838A>G p.D613G Substitution - Missense 19:37893865-37893865 - C135 COSM4611036 c.8158_8159delAA p.K2720fs*44 Deletion - Frameshift 19:37885395-37885396 - 3N48-VS-3T48 COSM3201304 c.7558G>A p.V2520I Substitution - Missense 19:37885996-37885996 - YURAY COSM4282420 c.4358G>A p.G1453E Substitution - Missense 19:37889313-37889313 - 2492714 COSM5607214 c.5400G>A p.R1800R Substitution - coding silent 19:37888154-37888154 - TCGA-B5-A11H-01 COSM995848 c.6525A>G p.I2175M Substitution - Missense 19:37887029-37887029 - CSCC-4-T COSM4502715 c.6317C>T p.S2106F Substitution - Missense 19:37887354-37887354 - YUJUBE COSM3201428 c.5668G>A p.E1890K Substitution - Missense 19:37888003-37888003 - C086 COSM5541738 c.5899G>A p.E1967K Substitution - Missense 19:37887772-37887772 - 2492712 COSM5607212 c.6825G>A p.G2275G Substitution - coding silent 19:37886729-37886729 - TCGA-B0-5707-01 COSM4857840 c.423A>C p.K141N Substitution - Missense 19:37895280-37895280 - 1N47-VS-1T47 COSM4976254 c.3742C>T p.R1248C Substitution - Missense 19:37889812-37889812 - sysucc-1370T COSM5470999 c.4322A>C p.Q1441P Substitution - Missense 19:37889349-37889349 - YUKSI COSM5389567 c.8570C>T p.P2857L Substitution - Missense 19:37885101-37885101 - TCGA-UB-A7MB-01 COSM4932022 c.1907T>C p.L636S Substitution - Missense 19:37893679-37893679 - LUAD-E01278 COSM394180 c.7320G>T p.M2440I Substitution - Missense 19:37886234-37886234 - 6T COSM3734375 c.4760A>G p.K1587R Substitution - Missense 19:37888794-37888794 - ESCC-060T COSM3938069 c.2925G>C p.L975L Substitution - coding silent 19:37892778-37892778 - ITNET_1047_T COSM995883 c.602G>A p.S201N Substitution - Missense 19:37894984-37894984 - TCGA-AN-A046-01 COSM3822921 c.2878G>A p.A960T Substitution - Missense 19:37892708-37892708 - LIM2405 COSM4613486 c.8467_8468insC p.Q2823fs*33 Insertion - Frameshift 19:37885203-37885204 - S02322 COSM5691318 c.5978C>G p.S1993C Substitution - Missense 19:37887576-37887576 - 2492722 COSM394453 c.1715C>T p.S572F Substitution - Missense 19:37893871-37893871 - S00339 COSM5657336 c.2434C>T p.R812W Substitution - Missense 19:37893152-37893152 - MO_1094 COSM5558631 c.4582C>A p.L1528I Substitution - Missense 19:37889089-37889089 - CSCC-31-T COSM4549159 c.4660G>A p.G1554R Substitution - Missense 19:37888894-37888894 - YUNEKI COSM5389581 c.5914G>A p.E1972K Substitution - Missense 19:37887757-37887757 - S02243 COSM5677755 c.7879G>T p.A2627S Substitution - Missense 19:37885675-37885675 - C547 COSM4282377 c.8044G>A p.E2682K Substitution - Missense 19:37885510-37885510 - TCGA-CC-5262-01 COSM4919296 c.5935G>T p.E1979* Substitution - Nonsense 19:37887619-37887619 - OSCC-GB_00070111 COSM3712906 c.7780G>C p.D2594H Substitution - Missense 19:37885891-37885891 - TCGA-A1-A0SH-01 COSM4814871 c.4588C>A p.Q1530K Substitution - Missense 19:37889083-37889083 - C086 COSM5541737 c.5782G>A p.E1928K Substitution - Missense 19:37887772-37887772 - TCGA-D1-A16Y-01 COSM3201461 c.5148G>T p.E1716D Substitution - Missense 19:37888523-37888523 - ESCC_BICR_028T COSM5431755 c.3223G>T p.E1075* Substitution - Nonsense 19:37891723-37891723 - TCGA-CK-5916-01 COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - ZZUFHECRKL-G032T COSM5432686 c.4859A>T p.Y1620F Substitution - Missense 19:37888695-37888695 - S02322 COSM5691319 c.6095C>G p.S2032C Substitution - Missense 19:37887576-37887576 - HCC001T COSM5808856 c.1287C>A p.G429G Substitution - coding silent 19:37894416-37894416 - TCGA-BS-A0UV-01 COSM995861 c.4968G>T p.E1656D Substitution - Missense 19:37888586-37888586 - 18195 COSM5346532 c.7594C>T p.L2532L Substitution - coding silent 19:37885960-37885960 - TCGA-BS-A0TC-01 COSM4871309 c.1630G>A p.V544I Substitution - Missense 19:37894073-37894073 - YUNIBO COSM5389610 c.2248C>T p.P750S Substitution - Missense 19:37893338-37893338 - BD110T COSM1393283 c.6187delA p.R2063fs*11 Deletion - Frameshift 19:37887367-37887367 - WSU-HN30 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - CSCC-15-T COSM4568558 c.1209T>G p.P403P Substitution - coding silent 19:37894377-37894377 - HCC2998 COSM3201493 c.4595A>C p.K1532T Substitution - Missense 19:37888959-37888959 - TCGA-AN-A046-01 COSM3822913 c.5237A>T p.K1746M Substitution - Missense 19:37888317-37888317 - RK207_C01 COSM3742932 c.6011A>T p.E2004V Substitution - Missense 19:37887543-37887543 - 2492713 COSM5607213 c.6942G>A p.G2314G Substitution - coding silent 19:37886729-37886729 - HCC058T COSM5805432 c.3285T>A p.P1095P Substitution - coding silent 19:37891661-37891661 - AOCS-158-1-6 COSM4140591 c.292T>A p.F98I Substitution - Missense 19:37895294-37895294 - PCSI_0098_Pa_P_526 COSM5031783 c.2985A>G p.K995K Substitution - coding silent 19:37892601-37892601 - CHC892T COSM4794285 c.3390G>A p.K1130K Substitution - coding silent 19:37891556-37891556 - 2492711 COSM5607212 c.6825G>A p.G2275G Substitution - coding silent 19:37886729-37886729 - 587222 COSM1232686 c.5739G>T p.E1913D Substitution - Missense 19:37887815-37887815 - TCGA-D1-A17Q-01 COSM995866 c.4113G>T p.K1371N Substitution - Missense 19:37889441-37889441 - TCGA-AG-3731-01 COSM3749504 c.6907G>A p.E2303K Substitution - Missense 19:37886764-37886764 - TCGA-A6-6141-01 COSM3756729 c.6777G>A p.E2259E Substitution - coding silent 19:37886777-37886777 - TCGA-UB-A7MB-01 COSM4930984 c.2408T>A p.L803Q Substitution - Missense 19:37893178-37893178 - YUDIVI COSM5389577 c.6701G>A p.R2234Q Substitution - Missense 19:37886970-37886970 - Au3 COSM5389577 c.6701G>A p.R2234Q Substitution - Missense 19:37886970-37886970 - C086 COSM5541753 c.5343G>A p.K1781K Substitution - coding silent 19:37888211-37888211 - 8068564 COSM3771037 c.3718G>A p.V1240I Substitution - Missense 19:37889953-37889953 - CSCC-41-T COSM4499652 c.5595C>G p.L1865L Substitution - coding silent 19:37888076-37888076 - PT37 COSM4549095 c.4759G>A p.E1587K Substitution - Missense 19:37888912-37888912 - HX31T COSM3746486 c.7728G>A p.A2576A Substitution - coding silent 19:37885943-37885943 - 2492721 COSM5722931 c.4618G>A p.D1540N Substitution - Missense 19:37888936-37888936 - TCGA-B5-A11N-01 COSM4864079 c.6309G>T p.E2103D Substitution - Missense 19:37887362-37887362 - TCGA-AA-3510-01 COSM1393279 c.6667G>T p.E2223* Substitution - Nonsense 19:37886887-37886887 - TCGA-AX-A0J0-01 COSM995886 c.96G>T p.K32N Substitution - Missense 19:37896288-37896288 - 35M COSM5583055 c.873C>T p.L291L Substitution - coding silent 19:37894713-37894713 - ATL048 COSM5706999 c.8546T>G p.L2849R Substitution - Missense 19:37885008-37885008 - TCGA-AP-A059-01 COSM995863 c.4808C>T p.A1603V Substitution - Missense 19:37888746-37888746 - 1990622 COSM1666755 c.4045C>G p.Q1349E Substitution - Missense 19:37889509-37889509 - CSCC-32-T COSM3201402 c.5987G>A p.R1996K Substitution - Missense 19:37887567-37887567 - TCGA-MH-A561-01 COSM3989989 c.1099C>A p.Q367K Substitution - Missense 19:37894604-37894604 - sysucc-311T COSM5464558 c.3390G>T p.K1130N Substitution - Missense 19:37891556-37891556 - SC_9057 COSM5548816 c.4964C>T p.A1655V Substitution - Missense 19:37888590-37888590 - Au4 COSM5605354 c.4191G>A p.L1397L Substitution - coding silent 19:37889480-37889480 - TCGA-AN-A046-01 COSM3822918 c.3650A>C p.K1217T Substitution - Missense 19:37890021-37890021 - Au3 COSM3712910 c.4268G>A p.G1423E Substitution - Missense 19:37889403-37889403 - CSCC-29-T COSM4510934 c.8644C>T p.R2882W Substitution - Missense 19:37885027-37885027 - BCM723T COSM3201255 c.8617C>T p.R2873C Substitution - Missense 19:37885054-37885054 - TCGA-DI-A0WH-01 COSM995842 c.7414A>G p.R2472G Substitution - Missense 19:37886140-37886140 - PT48 COSM4988493 c.8327G>A p.R2776Q Substitution - Missense 19:37885344-37885344 - sysucc-311T COSM5464551 c.6403G>T p.D2135Y Substitution - Missense 19:37887151-37887151 - KM12 COSM4612775 c.2123_2125delTCT p.F708delF Deletion - In frame 19:37893578-37893580 - RKO COSM3201642 c.2145G>A p.V715V Substitution - coding silent 19:37893558-37893558 - pfg043T COSM4753137 c.2768A>C p.E923A Substitution - Missense 19:37892935-37892935 - TCGA-AP-A0LM-01 COSM4873170 c.7141G>T p.E2381* Substitution - Nonsense 19:37886530-37886530 - YUQUEST COSM5389596 c.4247_4248insA p.R1418fs*12 Insertion - Frameshift 19:37889306-37889307 - OSCC-GB_01100111 COSM4888384 c.1504C>T p.L502F Substitution - Missense 19:37894082-37894082 - WSU-HN8 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - PT08_1 COSM5894055 c.1879G>A p.D627N Substitution - Missense 19:37893824-37893824 - 345973 COSM3726719 c.121C>T p.R41W Substitution - Missense 19:37896263-37896263 - LN229 COSM3201621 c.2273G>T p.W758L Substitution - Missense 19:37893313-37893313 - HCC2998 COSM3201399 c.6205G>A p.E2069K Substitution - Missense 19:37887466-37887466 - TCGA-F5-6814-01 COSM3422757 c.7612A>G p.M2538V Substitution - Missense 19:37886059-37886059 - 19685 COSM4923943 c.7005G>A p.K2335K Substitution - coding silent 19:37886666-37886666 - HCC002T COSM3201467 c.4825T>A p.L1609M Substitution - Missense 19:37888729-37888729 - 35M COSM5583050 c.7821C>T p.A2607A Substitution - coding silent 19:37885850-37885850 - Au3 COSM3712909 c.4151G>A p.G1384E Substitution - Missense 19:37889403-37889403 - ESCC_BICR_027T COSM5443231 c.5874G>C p.K1958N Substitution - Missense 19:37887680-37887680 - S00035 COSM5656740 c.4305C>A p.A1435A Substitution - coding silent 19:37889249-37889249 - TCGA-B5-A11N-01 COSM4864147 c.8101G>A p.E2701K Substitution - Missense 19:37885570-37885570 - CSCC-44-T COSM4502710 c.6200C>G p.S2067C Substitution - Missense 19:37887354-37887354 - HT115 COSM995859 c.5031G>T p.E1677D Substitution - Missense 19:37888523-37888523 - YUKAT COSM3201522 c.4349G>A p.R1450K Substitution - Missense 19:37889322-37889322 - TCGA-EI-6917-01 COSM3422754 c.8209C>T p.R2737W Substitution - Missense 19:37885345-37885345 - TCGA-AA-3510-01 COSM4948242 c.6784G>T p.E2262* Substitution - Nonsense 19:37886887-37886887 - HT115 COSM3201321 c.7410G>A p.G2470G Substitution - coding silent 19:37886261-37886261 - CHC892T COSM4960370 c.7607C>T p.P2536L Substitution - Missense 19:37886064-37886064 - PD22366a COSM5784342 c.4893C>G p.A1631A Substitution - coding silent 19:37888661-37888661 - TCGA-BS-A0UF-01 COSM4875762 c.8470G>T p.E2824* Substitution - Nonsense 19:37885201-37885201 - TCGA-AX-A0J0-01 COSM4867269 c.3543A>C p.S1181S Substitution - coding silent 19:37890128-37890128 - 3N07-VS-3T07 COSM4978906 c.1251C>T p.Y417Y Substitution - coding silent 19:37894452-37894452 - PT37 COSM5921618 c.7742C>T p.S2581F Substitution - Missense 19:37885929-37885929 - TCGA-AA-3492-01 COSM5096852 c.5895_5896insA p.Q1966fs*32 Insertion - Frameshift 19:37887775-37887776 - PD7530a COSM3769726 c.5241G>A p.K1747K Substitution - coding silent 19:37888313-37888313 - TCGA-AP-A0LM-01 COSM995847 c.7024G>T p.E2342* Substitution - Nonsense 19:37886530-37886530 - TCGA-DM-A1D6-01 COSM1393272 c.8581C>G p.L2861V Substitution - Missense 19:37884973-37884973 - CHC361TA COSM3668261 c.3261T>G p.A1087A Substitution - coding silent 19:37891685-37891685 - AOCS-141-8-0 COSM4140589 c.2065T>G p.L689V Substitution - Missense 19:37893521-37893521 - TCGA-BC-A10R-01 COSM4935979 c.7166C>A p.P2389H Substitution - Missense 19:37886388-37886388 - PDA_074 COSM5002085 c.4748G>A p.R1583Q Substitution - Missense 19:37888806-37888806 - YUKAT COSM5389584 c.5192A>T p.K1731I Substitution - Missense 19:37888362-37888362 - C086 COSM5541741 c.5863G>A p.D1955N Substitution - Missense 19:37887691-37887691 - 2492723 COSM5722932 c.4735G>A p.D1579N Substitution - Missense 19:37888936-37888936 - TCGA-A1-A0SH-01 COSM439380 c.4471C>A p.Q1491K Substitution - Missense 19:37889083-37889083 - MO_1012 COSM5554274 c.1633T>C p.F545L Substitution - Missense 19:37893953-37893953 - LUAD-5V8LT COSM401835 c.2360A>T p.N787I Substitution - Missense 19:37893226-37893226 - HT29 COSM3201450 c.5280G>C p.R1760S Substitution - Missense 19:37888274-37888274 - AOCS-141-3-2 COSM4140590 c.2182T>G p.L728V Substitution - Missense 19:37893521-37893521 - TCGA-B8-4621-01 COSM4857094 c.2975A>G p.H992R Substitution - Missense 19:37892728-37892728 - TCGA-AA-3510-01 COSM1393303 c.2718G>A p.G906G Substitution - coding silent 19:37892868-37892868 - CSCC-27-T COSM3749504 c.6907G>A p.E2303K Substitution - Missense 19:37886764-37886764 - C008 COSM5524187 c.4228G>A p.E1410K Substitution - Missense 19:37889326-37889326 - ESCC_109 COSM5638957 c.1500C>T p.F500F Substitution - coding silent 19:37894203-37894203 - 2492723 COSM5722935 c.3514C>T p.L1172L Substitution - coding silent 19:37890040-37890040 - YUQUEST COSM5389597 c.4364_4365insA p.R1457fs*12 Insertion - Frameshift 19:37889306-37889307 - 2000756 COSM1645125 c.2243T>C p.V748A Substitution - Missense 19:37893343-37893343 - HT55 COSM3201375 c.6850T>A p.S2284T Substitution - Missense 19:37886821-37886821 - RMS112_ COSM4987799 c.4672G>T p.E1558* Substitution - Nonsense 19:37888882-37888882 - CSCC-10-T COSM4454234 c.4544A>G p.K1515R Substitution - Missense 19:37889127-37889127 - TCGA-AP-A0LP-01 COSM995841 c.7796T>C p.L2599P Substitution - Missense 19:37885758-37885758 - 19M COSM5579985 c.6907G>A p.E2303K Substitution - Missense 19:37886647-37886647 - MO_1012 COSM5554275 c.1750T>C p.F584L Substitution - Missense 19:37893953-37893953 - WSU-HN30 COSM4600981 c.8551T>G p.W2851G Substitution - Missense 19:37885003-37885003 - PTC-28C COSM3756724 c.8645G>A p.R2882Q Substitution - Missense 19:37885026-37885026 - TCGA-EI-6917-01 COSM3422766 c.96G>T p.K32N Substitution - Missense 19:37896288-37896288 - HCC001T COSM5808845 c.590C>T p.T197M Substitution - Missense 19:37894996-37894996 - HCC137 COSM1612148 c.4749G>T p.V1583V Substitution - coding silent 19:37888922-37888922 - 1N45-VS-1T45 COSM4975827 c.3466C>G p.Q1156E Substitution - Missense 19:37890088-37890088 - YURAY COSM5389608 c.2357C>T p.P786L Substitution - Missense 19:37893229-37893229 - Au9 COSM5607670 c.3832G>A p.V1278I Substitution - Missense 19:37889722-37889722 - S00833 COSM5661106 c.2843T>A p.L948Q Substitution - Missense 19:37892743-37892743 - 35M COSM5583053 c.1377A>G p.E459E Substitution - coding silent 19:37894209-37894209 - ME044T COSM229335 c.8164G>A p.E2722K Substitution - Missense 19:37885390-37885390 - TCGA-CC-5264-01 COSM4915172 c.5258A>T p.E1753V Substitution - Missense 19:37888296-37888296 - CSCC-60-T COSM4558416 c.7678G>A p.G2560R Substitution - Missense 19:37885876-37885876 - C086 COSM5541746 c.1128C>T p.N376N Substitution - coding silent 19:37894575-37894575 - PT35 COSM5389599 c.4273G>A p.E1425K Substitution - Missense 19:37889398-37889398 - HCC58 COSM3707109 c.6934G>A p.E2312K Substitution - Missense 19:37886737-37886737 - 8031121 COSM3388937 c.4907A>C p.K1636T Substitution - Missense 19:37888647-37888647 - RKO COSM3201641 c.2028G>A p.V676V Substitution - coding silent 19:37893558-37893558 - 40M COSM995873 c.2303G>A p.R768Q Substitution - Missense 19:37893283-37893283 - TCGA-AN-A046-01 COSM3822911 c.5995A>C p.T1999P Substitution - Missense 19:37887559-37887559 - Au4 COSM5605351 c.4300A>T p.M1434L Substitution - Missense 19:37889254-37889254 - TCGA-EI-6509-01 COSM3749503 c.6790G>A p.E2264K Substitution - Missense 19:37886764-37886764 - S02325 COSM4387134 c.629C>T p.T210I Substitution - Missense 19:37894957-37894957 - YUFIT COSM5389603 c.3800G>A p.G1267E Substitution - Missense 19:37889871-37889871 - TCGA-AP-A059-01 COSM995853 c.5666C>A p.A1889D Substitution - Missense 19:37887888-37887888 - HCT8 COSM4634412 c.5154G>A p.L1718L Substitution - coding silent 19:37888400-37888400 - BD180T COSM5495217 c.4108G>A p.G1370S Substitution - Missense 19:37889563-37889563 - LS180 COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - HCC001T COSM5808846 c.707C>T p.T236M Substitution - Missense 19:37894996-37894996 - YUMOKI COSM5389592 c.4737G>A p.R1579R Substitution - coding silent 19:37888817-37888817 - LUAD-S01302 COSM395714 c.6763G>T p.E2255* Substitution - Nonsense 19:37886791-37886791 - WSU-HN6 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - CAL33 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - 2521243 COSM4526904 c.1427G>A p.G476E Substitution - Missense 19:37894159-37894159 - BD235T COSM5501676 c.506G>T p.G169V Substitution - Missense 19:37895080-37895080 - YUROG COSM3201398 c.6088G>A p.E2030K Substitution - Missense 19:37887466-37887466 - 9227_T COSM5042383 c.1394G>A p.G465E Substitution - Missense 19:37894309-37894309 - HCC058T COSM5805215 c.7265T>A p.V2422E Substitution - Missense 19:37886289-37886289 - 2172 COSM5013435 c.8650G>A p.G2884R Substitution - Missense 19:37885021-37885021 - TCGA-CK-4952-01 COSM3749503 c.6790G>A p.E2264K Substitution - Missense 19:37886764-37886764 - PD4955a COSM5785151 c.2284C>T p.R762C Substitution - Missense 19:37893419-37893419 - 2492723 COSM5722937 c.1832C>T p.S611F Substitution - Missense 19:37893871-37893871 - TCGA-D1-A16Y-01 COSM995859 c.5031G>T p.E1677D Substitution - Missense 19:37888523-37888523 - TCGA-BS-A0UF-01 COSM995865 c.4792G>A p.E1598K Substitution - Missense 19:37888762-37888762 - CSCC-44-T COSM4557434 c.7292G>A p.G2431E Substitution - Missense 19:37886262-37886262 - TCGA-Q1-A73O-01 COSM4835189 c.6496G>A p.E2166K Substitution - Missense 19:37887175-37887175 - 53M COSM5595564 c.7369A>G p.K2457E Substitution - Missense 19:37886302-37886302 - CHC1209T COSM4804693 c.3644G>T p.R1215L Substitution - Missense 19:37890027-37890027 - TCGA-AP-A0LM-01 COSM995839 c.7989G>A p.M2663I Substitution - Missense 19:37885565-37885565 - UM-SCC-17B COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - YUKSI COSM5389566 c.8453C>T p.P2818L Substitution - Missense 19:37885101-37885101 - 61 COSM5237298 c.5865G>T p.L1955F Substitution - Missense 19:37887806-37887806 - MO_1244 COSM5564353 c.3846G>T p.R1282S Substitution - Missense 19:37889825-37889825 - ME012T COSM224753 c.2047G>A p.G683R Substitution - Missense 19:37893539-37893539 - 49M COSM995873 c.2303G>A p.R768Q Substitution - Missense 19:37893283-37893283 - TCGA-AM-5820-01 COSM3756724 c.8645G>A p.R2882Q Substitution - Missense 19:37885026-37885026 - WSU-HN12 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - UM-SCC-47 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - C086 COSM5541735 c.5281G>A p.E1761K Substitution - Missense 19:37888273-37888273 - CN-AML-CR-62-Dx COSM5419857 c.8481C>T p.Y2827Y Substitution - coding silent 19:37885190-37885190 - YUROG COSM3201399 c.6205G>A p.E2069K Substitution - Missense 19:37887466-37887466 - PCSI_0135_Pa_X COSM3378712 c.4583T>G p.L1528R Substitution - Missense 19:37889088-37889088 - CHC361TA COSM3668260 c.3144T>G p.A1048A Substitution - coding silent 19:37891685-37891685 - TCGA-A6-6141-01 COSM3749504 c.6907G>A p.E2303K Substitution - Missense 19:37886764-37886764 - CSCC-29-T COSM4560035 c.827G>A p.G276E Substitution - Missense 19:37894759-37894759 - PCSI_0295_Pa_P_526 COSM4808732 c.3425C>T p.T1142M Substitution - Missense 19:37890246-37890246 - 9227_T COSM5040048 c.7456C>T p.P2486S Substitution - Missense 19:37886215-37886215 - EGC15 COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - LIM2551 COSM4644203 c.4030C>A p.L1344I Substitution - Missense 19:37889641-37889641 - pfg181T COSM4765713 c.4762_4763insA p.R1588fs*40 Insertion - Frameshift 19:37888791-37888792 - TCGA-D1-A17Q-01 COSM995874 c.2061G>T p.Q687H Substitution - Missense 19:37893525-37893525 - HCC71 COSM1612154 c.2961A>G p.L987L Substitution - coding silent 19:37892742-37892742 - PCSI_0295_Pa_P_526 COSM4808731 c.3308C>T p.T1103M Substitution - Missense 19:37890246-37890246 - MO_1244 COSM5564352 c.3729G>T p.R1243S Substitution - Missense 19:37889825-37889825 - 53M COSM5595561 c.7151G>A p.G2384E Substitution - Missense 19:37886403-37886403 - TCGA-B5-A0JY-01 COSM3201452 c.5355G>T p.K1785N Substitution - Missense 19:37888316-37888316 - HT115 COSM3201639 c.2029C>T p.P677S Substitution - Missense 19:37893557-37893557 - CSCC-27-T COSM4558862 c.7952G>A p.S2651N Substitution - Missense 19:37885719-37885719 - YURAY COSM4282419 c.4241G>A p.G1414E Substitution - Missense 19:37889313-37889313 - CSCC-27-T COSM4555864 c.6829G>A p.E2277K Substitution - Missense 19:37886842-37886842 - 35M COSM5583054 c.1494A>G p.E498E Substitution - coding silent 19:37894209-37894209 - TCGA-CK-4952-01 COSM3756727 c.6805A>G p.R2269G Substitution - Missense 19:37886749-37886749 - sysucc-1370T COSM5470996 c.6813G>T p.E2271D Substitution - Missense 19:37886741-37886741 - TCGA-AA-3492-01 COSM1393285 c.5778_5779insA p.Q1927fs*32 Insertion - Frameshift 19:37887775-37887776 - WT037 COSM215768 c.5845C>T p.R1949W Substitution - Missense 19:37887709-37887709 - S01563 COSM5701223 c.4294_4295insGA p.K1432fs*22 Insertion - Frameshift 19:37889376-37889377 - TCGA-CA-6717-01 COSM4785437 c.5590G>T p.E1864* Substitution - Nonsense 19:37888081-37888081 - RMS10_ COSM3201364 c.6808A>G p.K2270E Substitution - Missense 19:37886746-37886746 - CSCC-55-T COSM4553335 c.5995G>A p.E1999K Substitution - Missense 19:37887676-37887676 - SKCO-1 COSM4650156 c.4631C>T p.P1544L Substitution - Missense 19:37889040-37889040 - 35M COSM5583047 c.1474G>A p.D492N Substitution - Missense 19:37894112-37894112 - PT37 COSM5921615 c.3875C>T p.P1292L Substitution - Missense 19:37889679-37889679 - TCGA-AA-3510-01 COSM4948169 c.3057G>T p.E1019D Substitution - Missense 19:37892646-37892646 - CSCC-31-T COSM4554290 c.6287G>A p.R2096K Substitution - Missense 19:37887384-37887384 - TCGA-F5-6814-01 COSM3422763 c.5085G>A p.E1695E Substitution - coding silent 19:37888586-37888586 - 2492723 COSM5722933 c.4474G>A p.E1492K Substitution - Missense 19:37889080-37889080 - HCC58T COSM3707109 c.6934G>A p.E2312K Substitution - Missense 19:37886737-37886737 - CSCC-44-T COSM4557435 c.7409G>A p.G2470E Substitution - Missense 19:37886262-37886262 - SNU-C4 COSM1393292 c.4761delA p.K1587fs*9 Deletion - Frameshift 19:37888793-37888793 - Au8 COSM5607213 c.6942G>A p.G2314G Substitution - coding silent 19:37886729-37886729 - TCGA-E9-A22G-01 COSM4814118 c.3831T>C p.D1277D Substitution - coding silent 19:37889840-37889840 - 1N47-VS-1T47 COSM4976255 c.3859C>T p.R1287C Substitution - Missense 19:37889812-37889812 - TCGA-BH-A0DO-01 COSM3201531 c.4189C>T p.L1397L Substitution - coding silent 19:37889482-37889482 - YURAY COSM5389605 c.3299C>T p.S1100F Substitution - Missense 19:37891647-37891647 - CSCC-11-T COSM4552742 c.5691G>A p.Q1897Q Substitution - coding silent 19:37887863-37887863 - TCGA-CM-6162-01 COSM3201473 c.4879C>T p.R1627* Substitution - Nonsense 19:37888792-37888792 - 3N07-VS-3T07 COSM4978905 c.1134C>T p.Y378Y Substitution - coding silent 19:37894452-37894452 - SNUH_G76_S1 COSM3756724 c.8645G>A p.R2882Q Substitution - Missense 19:37885026-37885026 - S01020 COSM3749503 c.6790G>A p.E2264K Substitution - Missense 19:37886764-37886764 - UM-SCC-47 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - SCC-25 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - TCGA-B5-A0JY-01 COSM995856 c.5238G>T p.K1746N Substitution - Missense 19:37888316-37888316 - CSCC-16-T COSM4589720 c.8277_8278insA p.E2760fs*44 Insertion - Frameshift 19:37885393-37885394 - TCGA-UB-A7MB-01 COSM4932023 c.2024T>C p.L675S Substitution - Missense 19:37893679-37893679 - 53M COSM5595568 c.387C>T p.I129I Substitution - coding silent 19:37895316-37895316 - 78 COSM5013437 c.7547C>T p.A2516V Substitution - Missense 19:37886124-37886124 - TCGA-AA-3663-01 COSM4785910 c.6384A>T p.K2128N Substitution - Missense 19:37887287-37887287 - Gp2D COSM3201298 c.7727G>A p.R2576H Substitution - Missense 19:37885827-37885827 - 2492723 COSM5722936 c.3631C>T p.L1211L Substitution - coding silent 19:37890040-37890040 - LIM2405 COSM4613485 c.8350_8351insC p.Q2784fs*33 Insertion - Frameshift 19:37885203-37885204 - PD9575a COSM5769678 c.2827G>A p.A943T Substitution - Missense 19:37892876-37892876 - CSCC-6-T COSM4548919 c.4719G>A p.K1573K Substitution - coding silent 19:37888952-37888952 - Detroit_562 COSM4595281 c.6902T>A p.V2301E Substitution - Missense CN-AML-CR-62-Dx COSM5419856 c.8364C>T p.Y2788Y Substitution - coding silent 19:37885190-37885190 - Au3 COSM5602605 c.7090G>A p.E2364K Substitution - Missense 19:37886464-37886464 - TCGA-D1-A103-01 COSM995873 c.2303G>A p.R768Q Substitution - Missense 19:37893283-37893283 - TCGA-AD-6964-01 COSM1393306 c.1385T>C p.M462T Substitution - Missense 19:37894201-37894201 - sysucc-707T COSM5460076 c.6778G>T p.E2260* Substitution - Nonsense 19:37886893-37886893 - YUOTHO COSM5389589 c.5002G>A p.E1668K Substitution - Missense 19:37888669-37888669 - WSU-HN8 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - PD13424a COSM5783557 c.2411A>C p.Q804P Substitution - Missense 19:37893292-37893292 - TCGA-E9-A22G-01 COSM1480990 c.4665A>T p.E1555D Substitution - Missense 19:37888889-37888889 - N571T COSM236023 c.8471C>T p.A2824V Substitution - Missense 19:37885083-37885083 - HCC2998 COSM3201372 c.6749A>G p.E2250G Substitution - Missense 19:37886805-37886805 - TCGA-F5-6814-01 COSM3201414 c.5901G>T p.E1967D Substitution - Missense 19:37887770-37887770 - TCGA-CK-4947-01 COSM1393296 c.3798C>T p.N1266N Substitution - coding silent 19:37889756-37889756 - sysucc-1370T COSM995884 c.295C>T p.R99W Substitution - Missense 19:37895291-37895291 - TCGA-AN-A046-01 COSM3822914 c.5354A>T p.K1785M Substitution - Missense 19:37888317-37888317 - HCC137T COSM1612147 c.4632G>T p.V1544V Substitution - coding silent 19:37888922-37888922 - TCGA-AX-A0J0-01 COSM995860 c.5001G>T p.K1667N Substitution - Missense 19:37888553-37888553 - sysucc-311T COSM5464555 c.3292C>T p.R1098W Substitution - Missense 19:37890262-37890262 - CSCC-40-T COSM4558172 c.7697G>A p.W2566* Substitution - Nonsense 19:37885974-37885974 - DLD1 COSM4623951 c.357T>A p.H119Q Substitution - Missense 19:37895346-37895346 - pfg043T COSM4753141 c.2256A>C p.E752D Substitution - Missense 19:37893447-37893447 - TCGA-AP-A0LM-01 COSM4873538 c.5913G>A p.Q1971Q Substitution - coding silent 19:37887758-37887758 - YUFIT COSM5389569 c.8470G>A p.E2824K Substitution - Missense 19:37885201-37885201 - C086 COSM5541729 c.2009C>T p.S670F Substitution - Missense 19:37893577-37893577 - SC_9030 COSM5566926 c.2494C>T p.R832C Substitution - Missense 19:37893209-37893209 - PD18022a COSM5770799 c.2121C>A p.F707L Substitution - Missense 19:37893582-37893582 - J90_T COSM3960006 c.6015A>G p.E2005E Substitution - coding silent 19:37887656-37887656 - TCGA-D1-A16X-01 COSM4865801 c.2005C>T p.L669F Substitution - Missense 19:37893698-37893698 - CSCC-16-T COSM4589719 c.8160_8161insA p.E2721fs*44 Insertion - Frameshift 19:37885393-37885394 - 90203 COSM329605 c.921T>A p.F307L Substitution - Missense 19:37894665-37894665 - YUTRAIN COSM5389606 c.3091G>A p.E1031K Substitution - Missense 19:37891738-37891738 - CSCC-60-T COSM4549094 c.4642G>A p.E1548K Substitution - Missense 19:37888912-37888912 - HCC017T COSM5814855 c.6156A>T p.L2052F Substitution - Missense 19:37887398-37887398 - PT33 COSM5909793 c.7991C>T p.P2664L Substitution - Missense 19:37885680-37885680 - HCC58 COSM1612149 c.4017C>A p.H1339Q Substitution - Missense 19:37889537-37889537 - 8048316 COSM3388933 c.8404C>T p.R2802W Substitution - Missense 19:37885150-37885150 - TCGA-JW-A5VL-01 COSM4846473 c.3287C>G p.S1096C Substitution - Missense 19:37891659-37891659 - TCGA-JW-A5VL-01 COSM4847546 c.3345C>G p.I1115M Substitution - Missense 19:37891601-37891601 - 2492720 COSM5722935 c.3514C>T p.L1172L Substitution - coding silent 19:37890040-37890040 - TCGA-B0-4822-01 COSM3362835 c.3002G>C p.G1001A Substitution - Missense 19:37892701-37892701 - ACINAR01 COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - pfg008T COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - TCGA-AA-3663-01 COSM1393281 c.6267A>T p.K2089N Substitution - Missense 19:37887287-37887287 - ACA8 COSM5961451 c.5007G>T p.W1669C Substitution - Missense 19:37888547-37888547 - 2492714 COSM5607215 c.5517G>A p.R1839R Substitution - coding silent 19:37888154-37888154 - OSCC-GB_00410111 COSM3712907 c.5567G>A p.R1856K Substitution - Missense 19:37887987-37887987 - TCGA-BH-A0DO-01 COSM439381 c.4072C>T p.L1358L Substitution - coding silent 19:37889482-37889482 - YUKAT COSM5389582 c.5469G>A p.M1823I Substitution - Missense 19:37888085-37888085 - HCC71T COSM1612153 c.2844A>G p.L948L Substitution - coding silent 19:37892742-37892742 - TCGA-B5-A11E-01 COSM995879 c.1305G>T p.E435D Substitution - Missense 19:37894281-37894281 - 8031121 COSM3388938 c.5024A>C p.K1675T Substitution - Missense 19:37888647-37888647 - TCGA-AN-A046-01 COSM3822922 c.2995G>A p.A999T Substitution - Missense 19:37892708-37892708 - CSCC-32-T COSM4560473 c.8458G>A p.E2820K Substitution - Missense 19:37885096-37885096 - TCGA-BS-A0UV-01 COSM4864941 c.5838G>T p.E1946D Substitution - Missense 19:37887833-37887833 - A6 COSM5350502 c.2739G>T p.Q913H Substitution - Missense 19:37892847-37892847 - 2492720 COSM5722934 c.4591G>A p.E1531K Substitution - Missense 19:37889080-37889080 - PT08_2 COSM5894054 c.1762G>A p.D588N Substitution - Missense 19:37893824-37893824 - TCGA-EI-6917-01 COSM3422759 c.5782G>A p.A1928T Substitution - Missense 19:37887889-37887889 - TCGA-JW-A5VL-01 COSM4847545 c.3228C>G p.I1076M Substitution - Missense 19:37891601-37891601 - pfg181T COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - ZZUFHECRKL-G032T COSM5432687 c.4976A>T p.Y1659F Substitution - Missense 19:37888695-37888695 - WSU-HN30 COSM4600418 c.2459A>C p.Q820P Substitution - Missense 19:37893127-37893127 - HCC58 COSM1612150 c.4134C>A p.H1378Q Substitution - Missense 19:37889537-37889537 - HT115 COSM3201577 c.3372C>A p.G1124G Substitution - coding silent 19:37891574-37891574 - L21 COSM5369421 c.936delG p.C314fs*43 Deletion - Frameshift 19:37894650-37894650 - CHOL15 COSM1744747 c.6028G>A p.A2010T Substitution - Missense 19:37887643-37887643 - ESCC_BICR_019T COSM5431632 c.7092_7093delAA p.R2365fs*53 Deletion - Frameshift 19:37886461-37886462 - TCGA-B5-A11N-01 COSM995849 c.6192G>T p.E2064D Substitution - Missense 19:37887362-37887362 - pfg008T COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - YUDIVI COSM3201428 c.5668G>A p.E1890K Substitution - Missense 19:37888003-37888003 - 8031146 COSM1168873 c.7610C>T p.A2537V Substitution - Missense 19:37885944-37885944 - C135 COSM3201547 c.3904G>T p.E1302* Substitution - Nonsense 19:37889767-37889767 - S00035 COSM5656742 c.1039G>A p.D347N Substitution - Missense 19:37894547-37894547 - PT08_2 COSM5894055 c.1879G>A p.D627N Substitution - Missense 19:37893824-37893824 - TCGA-CK-4950-01 COSM3749505 c.6780G>A p.E2260E Substitution - coding silent 19:37886774-37886774 - 1N45-VS-1T45 COSM4975828 c.3583C>G p.Q1195E Substitution - Missense 19:37890088-37890088 - UM-SCC-17B COSM4599029 c.6539G>A p.R2180Q Substitution - Missense 19:37887132-37887132 - sysucc-1370T COSM5470998 c.4205A>C p.Q1402P Substitution - Missense 19:37889349-37889349 - ACA8 COSM5961452 c.5124G>T p.W1708C Substitution - Missense 19:37888547-37888547 - PT48 COSM4988492 c.8210G>A p.R2737Q Substitution - Missense 19:37885344-37885344 - ME049T COSM230380 c.5008G>A p.E1670K Substitution - Missense 19:37888546-37888546 - CSCC-11-T COSM4558261 c.7601G>A p.R2534Q Substitution - Missense 19:37885953-37885953 - TCGA-AM-5821-01 COSM3756729 c.6777G>A p.E2259E Substitution - coding silent 19:37886777-37886777 - 2492720 COSM5722932 c.4735G>A p.D1579N Substitution - Missense 19:37888936-37888936 - 2492712 COSM5607214 c.5400G>A p.R1800R Substitution - coding silent 19:37888154-37888154 - TCGA-D1-A15W-01 COSM474657 c.306A>C p.K102N Substitution - Missense 19:37895280-37895280 - 41T COSM3712910 c.4268G>A p.G1423E Substitution - Missense 19:37889403-37889403 - PD6422a COSM5772190 c.7586G>A p.R2529H Substitution - Missense 19:37885968-37885968 - C086 COSM5541733 c.5761G>A p.D1921N Substitution - Missense 19:37887793-37887793 - pfg043T COSM4753140 c.2139A>C p.E713D Substitution - Missense 19:37893447-37893447 - 587376 COSM1232691 c.6876G>T p.K2292N Substitution - Missense 19:37886678-37886678 - CSCC-31-T COSM4567696 c.8411_8412CC>TT p.S2804F Substitution - Missense 19:37885259-37885260 - MO_1094 COSM5558630 c.4465C>A p.L1489I Substitution - Missense 19:37889089-37889089 - 8016470 COSM3388935 c.5376T>C p.P1792P Substitution - coding silent 19:37888178-37888178 - HCC128T COSM1612151 c.3844C>T p.P1282S Substitution - Missense 19:37889710-37889710 - TCGA-CC-A7IH-01 COSM4923943 c.7005G>A p.K2335K Substitution - coding silent 19:37886666-37886666 - BCM695T COSM4802860 c.8224T>G p.F2742V Substitution - Missense 19:37885447-37885447 - sysucc-311T COSM5464549 c.6867G>T p.K2289N Substitution - Missense 19:37886687-37886687 - HCC102T COSM5806947 c.8558C>A p.T2853N Substitution - Missense 19:37885113-37885113 - ESCC_BICR_058T COSM5430565 c.6196G>A p.E2066K Substitution - Missense 19:37887475-37887475 - TCGA-AP-A0LM-01 COSM4873852 c.5440G>T p.E1814* Substitution - Nonsense 19:37888231-37888231 - sysucc-311T COSM5464550 c.6984G>T p.K2328N Substitution - Missense 19:37886687-37886687 - HCC2998 COSM3201312 c.7389G>T p.K2463N Substitution - Missense 19:37886165-37886165 - 9227_T COSM5042382 c.1277G>A p.G426E Substitution - Missense 19:37894309-37894309 - HCC137T COSM1612148 c.4749G>T p.V1583V Substitution - coding silent 19:37888922-37888922 - CHC361TA COSM3668261 c.3261T>G p.A1087A Substitution - coding silent 19:37891685-37891685 - CSCC-44-T COSM4506152 c.712C>T p.H238Y Substitution - Missense 19:37894874-37894874 - pfg181T COSM4765714 c.4879_4880insA p.R1627fs*40 Insertion - Frameshift 19:37888791-37888792 - ESCC_BICR_035T COSM5429443 c.2738A>T p.Q913L Substitution - Missense 19:37892848-37892848 - CSCC-11-T COSM4506737 c.7404C>T p.F2468F Substitution - coding silent 19:37886267-37886267 - PT42 COSM5926068 c.8623A>G p.I2875V Substitution - Missense 19:37885048-37885048 - TCGA-D8-A1XK-01 COSM3822934 c.104T>C p.L35P Substitution - Missense 19:37896280-37896280 - HT55 COSM3201374 c.6733T>A p.S2245T Substitution - Missense 19:37886821-37886821 - YUKAT COSM4282377 c.8044G>A p.E2682K Substitution - Missense 19:37885510-37885510 - BHY COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - CSCC-6-T COSM4548918 c.4602G>A p.K1534K Substitution - coding silent 19:37888952-37888952 - TCGA-AA-3663-01 COSM4785940 c.2921C>T p.P974L Substitution - Missense 19:37892782-37892782 - YUJUBE COSM5389574 c.6651G>A p.V2217V Substitution - coding silent 19:37886903-37886903 - TCGA-A7-A4SD-01 COSM3822927 c.1837G>T p.V613F Substitution - Missense 19:37893749-37893749 - HT115 COSM3201628 c.2254G>A p.E752K Substitution - Missense 19:37893449-37893449 - ORL-48 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - TCGA-AZ-4315-01 COSM4948496 c.4212G>T p.V1404V Substitution - coding silent 19:37889459-37889459 - GC_353T-GC_353N COSM4753143 c.2119T>G p.F707V Substitution - Missense 19:37893584-37893584 - CSCC-55-T COSM4454893 c.6171A>T p.L2057L Substitution - coding silent 19:37887500-37887500 - CSCC-60-T COSM4526904 c.1427G>A p.G476E Substitution - Missense 19:37894159-37894159 - PD22366a COSM5784343 c.5010C>G p.A1670A Substitution - coding silent 19:37888661-37888661 - TCGA-BP-4162-01 COSM4857100 c.4227C>T p.G1409G Substitution - coding silent 19:37889444-37889444 - TCGA-DM-A0XF-01 COSM4785614 c.2854C>A p.Q952K Substitution - Missense 19:37892849-37892849 - BCM695T COSM4802860 c.8224T>G p.F2742V Substitution - Missense 19:37885447-37885447 - 1990622 COSM1666756 c.4162C>G p.Q1388E Substitution - Missense 19:37889509-37889509 - TCGA-CC-A3MB-01 COSM4933608 c.2550G>C p.M850I Substitution - Missense 19:37893036-37893036 - 41T COSM3712908 c.5684G>A p.R1895K Substitution - Missense 19:37887987-37887987 - PT35 COSM5914226 c.125C>T p.S42F Substitution - Missense 19:37896259-37896259 - TCGA-AM-5821-01 COSM3749503 c.6790G>A p.E2264K Substitution - Missense 19:37886764-37886764 - SCC-15 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - TCGA-A6-6141-01 COSM3749506 c.6897G>A p.E2299E Substitution - coding silent 19:37886774-37886774 - CHC1720T COSM4800539 c.2035C>T p.P679S Substitution - Missense 19:37893668-37893668 - TCGA-D8-A1XK-01 COSM3822916 c.3972A>G p.E1324E Substitution - coding silent 19:37889699-37889699 - TCGA-B5-A11E-01 COSM4870513 c.3013A>G p.K1005E Substitution - Missense 19:37892690-37892690 - TCGA-AP-A0LM-01 COSM4873034 c.7193G>T p.S2398I Substitution - Missense 19:37886478-37886478 - YUKAT COSM5389585 c.5309A>T p.K1770I Substitution - Missense 19:37888362-37888362 - HCC027T COSM5811788 c.300A>C p.A100A Substitution - coding silent 19:37895286-37895286 - SKCO-1 COSM4650155 c.4514C>T p.P1505L Substitution - Missense 19:37889040-37889040 - YUOTHO COSM5389588 c.4885G>A p.E1629K Substitution - Missense 19:37888669-37888669 - YUPTER COSM5389615 c.754G>A p.D252N Substitution - Missense 19:37894949-37894949 - UM-SCC-2 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - SCC-15 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - 38 COSM5733716 c.4895G>T p.R1632M Substitution - Missense 19:37888776-37888776 - UM-SCC-17B COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - YUKAT COSM4282378 c.8161G>A p.E2721K Substitution - Missense 19:37885510-37885510 - TCGA-F5-6864-01 COSM3422761 c.5113G>T p.A1705S Substitution - Missense 19:37888558-37888558 - C086 COSM4558417 c.7795G>A p.G2599R Substitution - Missense 19:37885876-37885876 - 587298 COSM1232698 c.2537A>G p.H846R Substitution - Missense 19:37893049-37893049 - 61 COSM5237297 c.5748G>T p.L1916F Substitution - Missense 19:37887806-37887806 - 7T COSM3712905 c.7663G>C p.D2555H Substitution - Missense 19:37885891-37885891 - UM-SCC-17B COSM4599028 c.6422G>A p.R2141Q Substitution - Missense 19:37887132-37887132 - S02274 COSM5682453 c.7323G>A p.E2441E Substitution - coding silent 19:37886348-37886348 - ESCC_143 COSM5649881 c.8421G>A p.L2807L Substitution - coding silent 19:37885133-37885133 - TCGA-B5-A0JY-01 COSM4869690 c.7398G>T p.R2466S Substitution - Missense 19:37886273-37886273 - TCGA-D8-A1XK-01 COSM3822933 c.104T>C p.L35P Substitution - Missense 19:37896280-37896280 - YUPTER COSM5389614 c.637G>A p.D213N Substitution - Missense 19:37894949-37894949 - TCGA-BP-4162-01 COSM1136177 c.4110C>T p.G1370G Substitution - coding silent 19:37889444-37889444 - TCGA-CM-4743-01 COSM1393273 c.8379delA p.A2794fs*4 Deletion - Frameshift 19:37885175-37885175 - HCC71T COSM1612154 c.2961A>G p.L987L Substitution - coding silent 19:37892742-37892742 - HT115 COSM3201458 c.5227G>A p.E1743K Substitution - Missense 19:37888444-37888444 - U373 COSM5713341 c.727_729delTCC p.S243delS Deletion - In frame 19:37894974-37894976 - YUNIBO COSM5389611 c.2365C>T p.P789S Substitution - Missense 19:37893338-37893338 - C086 COSM5389576 c.6584G>A p.R2195Q Substitution - Missense 19:37886970-37886970 - TCGA-AG-3731-01 COSM3749503 c.6790G>A p.E2264K Substitution - Missense 19:37886764-37886764 - PT55 COSM4558416 c.7678G>A p.G2560R Substitution - Missense 19:37885876-37885876 - WSU-HN13 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - ORL-48 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - sysucc-311T COSM5464556 c.3409C>T p.R1137W Substitution - Missense 19:37890262-37890262 - C99 COSM4620381 c.6709C>T p.L2237L Substitution - coding silent 19:37886845-37886845 - YUQUEST COSM3201514 c.4454G>A p.G1485E Substitution - Missense 19:37889217-37889217 - BD227T COSM5518032 c.6545A>T p.Q2182L Substitution - Missense 19:37887126-37887126 - TCGA-F5-6814-01 COSM3422762 c.4968G>A p.E1656E Substitution - coding silent 19:37888586-37888586 - TCGA-EI-6509-01 COSM3749505 c.6780G>A p.E2260E Substitution - coding silent 19:37886774-37886774 - CSCC-47-T COSM4510217 c.8422C>T p.Q2808* Substitution - Nonsense 19:37885249-37885249 - YUKAT COSM5389573 c.7135G>A p.E2379K Substitution - Missense 19:37886536-37886536 - PT19_2 COSM4282419 c.4241G>A p.G1414E Substitution - Missense 19:37889313-37889313 - TCGA-CJ-5677-01 COSM3773868 c.6879A>G p.E2293E Substitution - coding silent 19:37886792-37886792 - 35M COSM5583048 c.1591G>A p.D531N Substitution - Missense 19:37894112-37894112 - TCGA-FU-A3HZ-01 COSM4840844 c.6885G>T p.K2295N Substitution - Missense 19:37886669-37886669 - HCC161 COSM3707112 c.1270G>A p.A424T Substitution - Missense 19:37894316-37894316 - TCGA-CC-5262-01 COSM4919297 c.6052G>T p.E2018* Substitution - Nonsense 19:37887619-37887619 - TCGA-D1-A17Q-01 COSM4865558 c.4917G>T p.E1639D Substitution - Missense 19:37888754-37888754 - TCGA-BS-A0UF-01 COSM4875636 c.4909G>A p.E1637K Substitution - Missense 19:37888762-37888762 - 35M COSM5583052 c.4218G>A p.L1406L Substitution - coding silent 19:37889453-37889453 - Au4 COSM5605352 c.4417A>T p.M1473L Substitution - Missense 19:37889254-37889254 - 38 COSM5733715 c.4778G>T p.R1593M Substitution - Missense 19:37888776-37888776 - OSCC-GB_00070111 COSM3712905 c.7663G>C p.D2555H Substitution - Missense 19:37885891-37885891 - PT36 COSM5916787 c.76-8C>T p.? Unknown 19:37896316-37896316 - TCGA-D8-A1JA-01 COSM3822924 c.2608G>A p.A870T Substitution - Missense 19:37893095-37893095 - 49M COSM4874548 c.2420G>A p.R807Q Substitution - Missense 19:37893283-37893283 - HCC161 COSM3707113 c.1387G>A p.A463T Substitution - Missense 19:37894316-37894316 - PCSI_0135_Pa_X COSM3378711 c.4466T>G p.L1489R Substitution - Missense 19:37889088-37889088 - 587376 COSM995886 c.96G>T p.K32N Substitution - Missense 19:37896288-37896288 - ATL048 COSM5707000 c.8663T>G p.L2888R Substitution - Missense 19:37885008-37885008 - CHC1209T COSM4804692 c.3527G>T p.R1176L Substitution - Missense 19:37890027-37890027 - S00938 COSM5663355 c.3342G>A p.E1114E Substitution - coding silent 19:37890212-37890212 - PD6684a COSM5791528 c.1715C>G p.S572C Substitution - Missense 19:37893871-37893871 - C086 COSM5541745 c.1011C>T p.N337N Substitution - coding silent 19:37894575-37894575 - TCGA-DM-A0XF-01 COSM1393302 c.2737C>A p.Q913K Substitution - Missense 19:37892849-37892849 - HCC058T COSM5805431 c.3168T>A p.P1056P Substitution - coding silent 19:37891661-37891661 - S00938 COSM5663356 c.3459G>A p.E1153E Substitution - coding silent 19:37890212-37890212 - ESCC_103 COSM5638192 c.6162G>T p.K2054N Substitution - Missense 19:37887509-37887509 - 19685 COSM4923942 c.6888G>A p.K2296K Substitution - coding silent 19:37886666-37886666 - 587342 COSM1232689 c.7666C>A p.L2556I Substitution - Missense 19:37885888-37885888 - TCGA-AZ-4315-01 COSM995859 c.5031G>T p.E1677D Substitution - Missense 19:37888523-37888523 - C008 COSM3201700 c.1040C>T p.S347F Substitution - Missense 19:37894663-37894663 - 7T COSM3712906 c.7780G>C p.D2594H Substitution - Missense 19:37885891-37885891 - TCGA-AM-5821-01 COSM3749504 c.6907G>A p.E2303K Substitution - Missense 19:37886764-37886764 - TCGA-CK-4950-01 COSM3756729 c.6777G>A p.E2259E Substitution - coding silent 19:37886777-37886777 - AOCS-090-1-0 COSM4140584 c.8519A>T p.E2840V Substitution - Missense 19:37885152-37885152 - HT115 COSM3201457 c.5110G>A p.E1704K Substitution - Missense 19:37888444-37888444 - TCGA-AP-A0LM-01 COSM995855 c.5323G>T p.E1775* Substitution - Nonsense 19:37888231-37888231 - CSCC-31-T COSM4554289 c.6170G>A p.R2057K Substitution - Missense 19:37887384-37887384 - RMS10_ COSM3201365 c.6925A>G p.K2309E Substitution - Missense 19:37886746-37886746 - HCC2998 COSM3201313 c.7506G>T p.K2502N Substitution - Missense 19:37886165-37886165 - TCGA-EI-6917-01 COSM3422753 c.8353G>T p.D2785Y Substitution - Missense 19:37885318-37885318 - ESCC_BICR_042T COSM5443730 c.2827G>A p.E943K Substitution - Missense 19:37892759-37892759 - BCM265T COSM4955158 c.6838G>T p.V2280L Substitution - Missense 19:37886716-37886716 - C113 COSM4441176 c.7688A>G p.E2563G Substitution - Missense 19:37885866-37885866 - HCC017T COSM5814856 c.6273A>T p.L2091F Substitution - Missense 19:37887398-37887398 - 40M COSM3712909 c.4151G>A p.G1384E Substitution - Missense 19:37889403-37889403 - sysucc-1317T COSM5449261 c.6618T>C p.G2206G Substitution - coding silent 19:37886936-37886936 - C113 COSM4441177 c.7805A>G p.E2602G Substitution - Missense 19:37885866-37885866 - YUKAT COSM5389600 c.4003G>A p.E1335K Substitution - Missense 19:37889551-37889551 - HCC93 COSM3707110 c.6326G>A p.R2109H Substitution - Missense 19:37887228-37887228 - Gp2D COSM3201299 c.7844G>A p.R2615H Substitution - Missense 19:37885827-37885827 - S00825 COSM3201553 c.3811C>T p.R1271C Substitution - Missense 19:37889860-37889860 - HCC58T COSM3707108 c.6817G>A p.E2273K Substitution - Missense 19:37886737-37886737 - CSCC-49-T COSM4560861 c.85G>A p.E29K Substitution - Missense 19:37896299-37896299 - TCGA-E2-A1IH-01 COSM4814095 c.3197C>G p.S1066C Substitution - Missense 19:37891749-37891749 - TCGA-AZ-4315-01 COSM3201461 c.5148G>T p.E1716D Substitution - Missense 19:37888523-37888523 - TCGA-D8-A1XQ-01 COSM3822920 c.3165G>T p.L1055L Substitution - coding silent 19:37891781-37891781 - PT52 COSM4948436 c.8367G>A p.W2789* Substitution - Nonsense 19:37885304-37885304 - 63 COSM5013438 c.6653A>G p.D2218G Substitution - Missense 19:37886901-37886901 - S01020 COSM3756727 c.6805A>G p.R2269G Substitution - Missense 19:37886749-37886749 - TCGA-CK-4950-01 COSM3749503 c.6790G>A p.E2264K Substitution - Missense 19:37886764-37886764 - UPCI:SCC090 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - TCGA-BG-A0MQ-01 COSM995880 c.1138C>A p.P380T Substitution - Missense 19:37894448-37894448 - TCGA-F5-6814-01 COSM3201413 c.5784G>T p.E1928D Substitution - Missense 19:37887770-37887770 - HCC2998 COSM3201413 c.5784G>T p.E1928D Substitution - Missense 19:37887770-37887770 - CSCC-55-T COSM4454892 c.6054A>T p.L2018L Substitution - coding silent 19:37887500-37887500 - YUKAT COSM5389601 c.4120G>A p.E1374K Substitution - Missense 19:37889551-37889551 - ESCC_BICR_035T COSM5429444 c.2855A>T p.Q952L Substitution - Missense 19:37892848-37892848 - U373 COSM5713340 c.610_612delTCC p.S204delS Deletion - In frame 19:37894974-37894976 - HT115 COSM3201519 c.4243A>C p.K1415Q Substitution - Missense 19:37889311-37889311 - Au8 COSM5607212 c.6825G>A p.G2275G Substitution - coding silent 19:37886729-37886729 - A9 COSM5350505 c.2783T>A p.I928N Substitution - Missense 19:37892920-37892920 - 2000756 COSM1645126 c.2360T>C p.V787A Substitution - Missense 19:37893343-37893343 - CHC361TA COSM3668260 c.3144T>G p.A1048A Substitution - coding silent 19:37891685-37891685 - TCGA-F4-6460-01 COSM3749504 c.6907G>A p.E2303K Substitution - Missense 19:37886764-37886764 - PD18022a COSM5770798 c.2004C>A p.F668L Substitution - Missense 19:37893582-37893582 - YUFIT COSM5389568 c.8353G>A p.E2785K Substitution - Missense 19:37885201-37885201 - PT33 COSM5909792 c.7874C>T p.P2625L Substitution - Missense 19:37885680-37885680 - TCGA-F4-6460-01 COSM3756730 c.6894G>A p.E2298E Substitution - coding silent 19:37886777-37886777 - MO_1241 COSM5557759 c.5688A>G p.K1896K Substitution - coding silent 19:37887983-37887983 - TCGA-EP-A3JL-01 COSM4913864 c.1295G>A p.R432Q Substitution - Missense 19:37894291-37894291 - TCGA-B5-A0JY-01 COSM4869695 c.7423G>T p.E2475* Substitution - Nonsense 19:37886248-37886248 - TCGA-D1-A16Y-01 COSM4871730 c.7250G>A p.G2417D Substitution - Missense 19:37886421-37886421 - TCGA-AB-2861-03 COSM1318313 c.2103T>A p.I701I Substitution - coding silent 19:37893483-37893483 - 0038_CRUK_PC_0038_T1_DNA COSM5422998 c.6218G>C p.G2073A Substitution - Missense 19:37887453-37887453 - CSCC-11-T COSM4552743 c.5808G>A p.Q1936Q Substitution - coding silent 19:37887863-37887863 - 53M COSM5595565 c.4863G>A p.V1621V Substitution - coding silent 19:37888691-37888691 - 2492721 COSM5722932 c.4735G>A p.D1579N Substitution - Missense 19:37888936-37888936 - CSCC-30-T COSM4485355 c.3039C>T p.T1013T Substitution - coding silent 19:37892664-37892664 - TCGA-CA-6718-01 COSM1393297 c.3531C>G p.D1177E Substitution - Missense 19:37890023-37890023 - TCGA-FU-A3HZ-01 COSM4840845 c.7002G>T p.K2334N Substitution - Missense 19:37886669-37886669 - TCGA-BC-A10R-01 COSM4935980 c.7283C>A p.P2428H Substitution - Missense 19:37886388-37886388 - RMS77_ COSM4988492 c.8210G>A p.R2737Q Substitution - Missense 19:37885344-37885344 - AOCS-141-8-0 COSM4140590 c.2182T>G p.L728V Substitution - Missense 19:37893521-37893521 - ME044T COSM229336 c.3889G>A p.E1297K Substitution - Missense 19:37889665-37889665 - PDA_075 COSM5002130 c.2210T>C p.M737T Substitution - Missense 19:37893376-37893376 - OSCC-GB_01100111 COSM4888385 c.1621C>T p.L541F Substitution - Missense 19:37894082-37894082 - YUSIV COSM5389599 c.4273G>A p.E1425K Substitution - Missense 19:37889398-37889398 - TCGA-DM-A1D6-01 COSM4784045 c.8698C>G p.L2900V Substitution - Missense 19:37884973-37884973 - CSCC-47-T COSM4558431 c.7687G>A p.E2563K Substitution - Missense 19:37885867-37885867 - 53M COSM5595566 c.4980G>A p.V1660V Substitution - coding silent 19:37888691-37888691 - Detroit_562 COSM4595280 c.6785T>A p.V2262E Substitution - Missense C086 COSM5541754 c.5460G>A p.K1820K Substitution - coding silent 19:37888211-37888211 - EGC8 COSM5056597 c.7858C>A p.L2620M Substitution - Missense 19:37885813-37885813 - BCM723T COSM3201255 c.8617C>T p.R2873C Substitution - Missense 19:37885054-37885054 - KYSE50 COSM4282406 c.6218G>A p.G2073E Substitution - Missense 19:37887453-37887453 - C086 COSM5541734 c.5878G>A p.D1960N Substitution - Missense 19:37887793-37887793 - 35M COSM5583051 c.4101G>A p.L1367L Substitution - coding silent 19:37889453-37889453 - TCGA-B2-4102-01 COSM1136176 c.6087C>T p.S2029S Substitution - coding silent 19:37887467-37887467 - 46M COSM5389589 c.5002G>A p.E1668K Substitution - Missense 19:37888669-37888669 - C086 COSM5541747 c.7677G>A p.K2559K Substitution - coding silent 19:37885877-37885877 - 587336 COSM1232688 c.7900C>A p.P2634T Substitution - Missense 19:37885654-37885654 - 35M COSM5583049 c.7704C>T p.A2568A Substitution - coding silent 19:37885850-37885850 - TCGA-F4-6460-01 COSM3756729 c.6777G>A p.E2259E Substitution - coding silent 19:37886777-37886777 - CHC1209T COSM4804693 c.3644G>T p.R1215L Substitution - Missense 19:37890027-37890027 - CSCC-41-T COSM4499651 c.5478C>G p.L1826L Substitution - coding silent 19:37888076-37888076 - PTC-7C COSM4131764 c.7826A>T p.H2609L Substitution - Missense 19:37885845-37885845 - YUDIVI COSM5389576 c.6584G>A p.R2195Q Substitution - Missense 19:37886970-37886970 - PD7530a COSM3769727 c.5358G>A p.K1786K Substitution - coding silent 19:37888313-37888313 - SNUH_G26_S1 COSM3756725 c.8091T>C p.F2697F Substitution - coding silent 19:37885463-37885463 - PT37 COSM5921617 c.7625C>T p.S2542F Substitution - Missense 19:37885929-37885929 - C058 COSM4988493 c.8327G>A p.R2776Q Substitution - Missense 19:37885344-37885344 - CHC892T COSM4794284 c.3273G>A p.K1091K Substitution - coding silent 19:37891556-37891556 - TCGA-GJ-A6C0-01 COSM4929992 c.574A>T p.M192L Substitution - Missense 19:37895129-37895129 - PD13771a COSM5780385 c.3523G>A p.V1175I Substitution - Missense 19:37890148-37890148 - TCGA-D1-A0ZO-01 COSM4868275 c.719G>A p.S240N Substitution - Missense 19:37894984-37894984 - TCGA-G4-6628-01 COSM4782778 c.2238G>A p.V746V Substitution - coding silent 19:37893465-37893465 - MO_1094 COSM5547557 c.5011_5013delCAG p.Q1671delQ Deletion - In frame 19:37888658-37888660 - 19M COSM3201529 c.4095G>A p.V1365V Substitution - coding silent 19:37889459-37889459 - TCGA-F5-6702-01 COSM3749505 c.6780G>A p.E2260E Substitution - coding silent 19:37886774-37886774 - 227 COSM4425967 c.7540G>A p.V2514M Substitution - Missense 19:37886131-37886131 - TCGA-AZ-6598-01 COSM4783234 c.3944T>C p.M1315T Substitution - Missense 19:37889727-37889727 - 2492723 COSM5722934 c.4591G>A p.E1531K Substitution - Missense 19:37889080-37889080 - C008 COSM5524188 c.4345G>A p.E1449K Substitution - Missense 19:37889326-37889326 - S00035 COSM5656741 c.4422C>A p.A1474A Substitution - coding silent 19:37889249-37889249 - TCGA-CC-A123-01 COSM4915237 c.5808G>C p.Q1936H Substitution - Missense 19:37887863-37887863 - TCGA-AZ-4315-01 COSM4948436 c.8367G>A p.W2789* Substitution - Nonsense 19:37885304-37885304 - ICGC_MB35 COSM3201408 c.5962C>T p.R1988W Substitution - Missense 19:37887709-37887709 - HX31T COSM3746485 c.7611G>A p.A2537A Substitution - coding silent 19:37885943-37885943 - BD110T COSM3201395 c.6304delA p.R2102fs*11 Deletion - Frameshift 19:37887367-37887367 - 345973 COSM3726720 c.121C>T p.R41W Substitution - Missense 19:37896263-37896263 - TCGA-CA-6717-01 COSM1393276 c.7986A>C p.E2662D Substitution - Missense 19:37885568-37885568 - AOCS-141-3-2 COSM4140589 c.2065T>G p.L689V Substitution - Missense 19:37893521-37893521 - EGC8 COSM5056596 c.7741C>A p.L2581M Substitution - Missense 19:37885813-37885813 - YUKAT COSM5389572 c.7018G>A p.E2340K Substitution - Missense 19:37886536-37886536 - Au10 COSM5598952 c.5641G>A p.E1881K Substitution - Missense 19:37888030-37888030 - 2492713 COSM5607214 c.5400G>A p.R1800R Substitution - coding silent 19:37888154-37888154 - HCC93 COSM3707111 c.6443G>A p.R2148H Substitution - Missense 19:37887228-37887228 - HT115 COSM3201520 c.4360A>C p.K1454Q Substitution - Missense 19:37889311-37889311 - PD3994a COSM4810036 c.2032C>T p.L678F Substitution - Missense 19:37893671-37893671 - 46M COSM5589357 c.5244A>T p.K1748N Substitution - Missense 19:37888310-37888310 - TCGA-D1-A17Q-01 COSM4865433 c.2178G>T p.Q726H Substitution - Missense 19:37893525-37893525 - TCGA-B5-A11H-01 COSM4868008 c.6642A>G p.I2214M Substitution - Missense 19:37887029-37887029 - TCGA-G4-6321-01 COSM4785017 c.7773G>T p.L2591L Substitution - coding silent 19:37885898-37885898 - KYSE50 COSM4282405 c.6101G>A p.G2034E Substitution - Missense 19:37887453-37887453 - WSU-HN30 COSM4600419 c.2576A>C p.Q859P Substitution - Missense 19:37893127-37893127 - TCGA-D1-A17Q-01 COSM4865393 c.4230G>T p.K1410N Substitution - Missense 19:37889441-37889441 - 2492712 COSM5607213 c.6942G>A p.G2314G Substitution - coding silent 19:37886729-37886729 - 6T COSM3734376 c.4877A>G p.K1626R Substitution - Missense 19:37888794-37888794 - PD4200a COSM165596 c.2356C>G p.P786A Substitution - Missense 19:37893230-37893230 - PT37 COSM5921613 c.3196C>T p.P1066S Substitution - Missense 19:37891633-37891633 - YUMOBER COSM5389612 c.1639G>A p.D547N Substitution - Missense 19:37893947-37893947 - pfg181T COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - 587222 COSM1168873 c.7610C>T p.A2537V Substitution - Missense 19:37885944-37885944 - PT36 COSM5389589 c.5002G>A p.E1668K Substitution - Missense 19:37888669-37888669 - CSCC-44-T COSM4502711 c.6317C>G p.S2106C Substitution - Missense 19:37887354-37887354 - TCGA-DD-A3A1-01 COSM4938245 c.5681A>C p.K1894T Substitution - Missense 19:37887873-37887873 - CAL27 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - CSCC-27-T COSM4558861 c.7835G>A p.S2612N Substitution - Missense 19:37885719-37885719 - C086 COSM5541750 c.4431G>A p.E1477E Substitution - coding silent 19:37889240-37889240 - TCGA-CK-4950-01 COSM3749506 c.6897G>A p.E2299E Substitution - coding silent 19:37886774-37886774 - HCT15 COSM3201573 c.3410G>A p.R1137Q Substitution - Missense 19:37890261-37890261 - sysucc-783T COSM3388933 c.8404C>T p.R2802W Substitution - Missense 19:37885150-37885150 - TCGA-B0-4822-01 COSM3362834 c.2885G>C p.G962A Substitution - Missense 19:37892701-37892701 - TCGA-F4-6460-01 COSM3749505 c.6780G>A p.E2260E Substitution - coding silent 19:37886774-37886774 - TCGA-CK-4952-01 COSM3749505 c.6780G>A p.E2260E Substitution - coding silent 19:37886774-37886774 - CSCC-49-T COSM4560862 c.85G>A p.E29K Substitution - Missense 19:37896299-37896299 - TCGA-AP-A059-01 COSM4866208 c.5783C>A p.A1928D Substitution - Missense 19:37887888-37887888 - YURAY COSM5389609 c.2474C>T p.P825L Substitution - Missense 19:37893229-37893229 - HCC126T COSM5818824 c.2725C>A p.L909M Substitution - Missense 19:37892978-37892978 - PD13771a COSM5780384 c.3406G>A p.V1136I Substitution - Missense 19:37890148-37890148 - TCGA-D1-A17R-01 COSM995877 c.1855C>T p.R619W Substitution - Missense 19:37893731-37893731 - TCGA-D1-A17Q-01 COSM4865567 c.5040G>T p.E1680D Substitution - Missense 19:37888631-37888631 - YUOTHO COSM5389570 c.8350C>T p.Q2784* Substitution - Nonsense 19:37885204-37885204 - LS174T COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - TCGA-D1-A17R-01 COSM3201647 c.1972C>T p.R658W Substitution - Missense 19:37893731-37893731 - RMS112_ COSM4987800 c.4789G>T p.E1597* Substitution - Nonsense 19:37888882-37888882 - AOCS-116-1-3 COSM4140586 c.5702A>G p.Y1901C Substitution - Missense 19:37887969-37887969 - pfg043T COSM4753136 c.2651A>C p.E884A Substitution - Missense 19:37892935-37892935 - TCGA-BS-A0UM-01 COSM995869 c.3440T>C p.I1147T Substitution - Missense 19:37890114-37890114 - CSCC-30-T COSM4558841 c.7941G>A p.K2647K Substitution - coding silent 19:37885730-37885730 - SJHGG014_D COSM4970094 c.76-6C>A p.? Unknown 19:37896314-37896314 - sysucc-707T COSM5460075 c.6661G>T p.E2221* Substitution - Nonsense 19:37886893-37886893 - CSCC-27-T COSM4555863 c.6712G>A p.E2238K Substitution - Missense 19:37886842-37886842 - PT08_1 COSM5894054 c.1762G>A p.D588N Substitution - Missense 19:37893824-37893824 - sysucc-1397T COSM5474144 c.3171G>A p.M1057I Substitution - Missense 19:37891775-37891775 - C058 COSM5389578 c.6264G>A p.R2088R Substitution - coding silent 19:37887290-37887290 - UD-SCC-2 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - BICR_22 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - S00833 COSM5661107 c.2960T>A p.L987Q Substitution - Missense 19:37892743-37892743 - TCGA-UB-A7MB-01 COSM4930985 c.2525T>A p.L842Q Substitution - Missense 19:37893178-37893178 - TCGA-CK-4952-01 COSM3749506 c.6897G>A p.E2299E Substitution - coding silent 19:37886774-37886774 - 587376 COSM995854 c.5484G>T p.K1828N Substitution - Missense 19:37888070-37888070 - TCGA-B0-5701-01 COSM474655 c.3818C>T p.A1273V Substitution - Missense 19:37889736-37889736 - 2492722 COSM5722937 c.1832C>T p.S611F Substitution - Missense 19:37893871-37893871 - 416 COSM4431480 c.5845delC p.R1949fs*15 Deletion - Frameshift 19:37887709-37887709 - TCGA-D1-A16X-01 COSM995876 c.1888C>T p.L630F Substitution - Missense 19:37893698-37893698 - U87 COSM3201694 c.1004G>C p.G335A Substitution - Missense 19:37894582-37894582 - TCGA-CK-4952-01 COSM3756728 c.6922A>G p.R2308G Substitution - Missense 19:37886749-37886749 - TCGA-BC-A10Y-01 COSM4936746 c.2687C>T p.T896I Substitution - Missense 19:37893016-37893016 - PCSI_0050_Pa_X COSM5002085 c.4748G>A p.R1583Q Substitution - Missense 19:37888806-37888806 - 2172 COSM5013434 c.8533G>A p.G2845R Substitution - Missense 19:37885021-37885021 - KPOPBR-13-T COSM5963586 c.1721A>G p.D574G Substitution - Missense 19:37893865-37893865 - PD4955a COSM5785150 c.2167C>T p.R723C Substitution - Missense 19:37893419-37893419 - PT37 COSM4549094 c.4642G>A p.E1548K Substitution - Missense 19:37888912-37888912 - TCGA-AP-A0LM-01 COSM995846 c.7076G>T p.S2359I Substitution - Missense 19:37886478-37886478 - TCGA-AP-A059-01 COSM4866125 c.4925C>T p.A1642V Substitution - Missense 19:37888746-37888746 - pfg008T COSM4753142 c.2002T>G p.F668V Substitution - Missense 19:37893584-37893584 - HCT15 COSM3201572 c.3293G>A p.R1098Q Substitution - Missense 19:37890261-37890261 - TCGA-FU-A3HZ-01 COSM4787098 c.3915C>T p.N1305N Substitution - coding silent 19:37889756-37889756 - PD3994a COSM165594 c.1915C>T p.L639F Substitution - Missense 19:37893671-37893671 - 1047T COSM995883 c.602G>A p.S201N Substitution - Missense 19:37894984-37894984 - TCGA-BS-A0UV-01 COSM4864488 c.5601G>T p.K1867N Substitution - Missense 19:37888070-37888070 - D28 COSM5389572 c.7018G>A p.E2340K Substitution - Missense 19:37886536-37886536 - CSCC-17-T COSM4526912 c.1428G>A p.G476G Substitution - coding silent 19:37894158-37894158 - TCGA-BS-A0UV-01 COSM995854 c.5484G>T p.K1828N Substitution - Missense 19:37888070-37888070 - ME018T COSM225406 c.176G>A p.R59K Substitution - Missense 19:37895410-37895410 - TCGA-AZ-4315-01 COSM1393274 c.8250G>A p.W2750* Substitution - Nonsense 19:37885304-37885304 - C99 COSM4620382 c.6826C>T p.L2276L Substitution - coding silent 19:37886845-37886845 - S00841 COSM5661892 c.7375G>A p.A2459T Substitution - Missense 19:37886179-37886179 - PT13 COSM4865801 c.2005C>T p.L669F Substitution - Missense 19:37893698-37893698 - ccRCC-49 COSM1665012 c.3644G>A p.R1215H Substitution - Missense 19:37890027-37890027 - HCC161T COSM3707113 c.1387G>A p.A463T Substitution - Missense 19:37894316-37894316 - CAL27 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - TCGA-D8-A1XQ-01 COSM5225428 c.8425delT p.C2809fs*39 Deletion - Frameshift 19:37885129-37885129 - C086 COSM5541739 c.4663G>A p.E1555K Substitution - Missense 19:37888891-37888891 - DLD1 COSM3201573 c.3410G>A p.R1137Q Substitution - Missense 19:37890261-37890261 - 381_T COSM3960003 c.7600C>A p.R2534R Substitution - coding silent 19:37885954-37885954 - MO_1184 COSM5566902 c.2324G>A p.R775Q Substitution - Missense 19:37893262-37893262 - TCGA-AM-5820-01 COSM3756732 c.6538C>T p.R2180W Substitution - Missense 19:37887133-37887133 - TCGA-CA-6717-01 COSM4947952 c.3387A>C p.K1129N Substitution - Missense 19:37891559-37891559 - ML_07_T_01 COSM5037553 c.4756G>A p.E1586K Substitution - Missense 19:37888915-37888915 - BD242T COSM5495973 c.6236G>A p.R2079K Substitution - Missense 19:37887435-37887435 - SC_9024 COSM3201323 c.7343C>T p.P2448L Substitution - Missense 19:37886328-37886328 - LUAD-FH5PJ COSM394453 c.1715C>T p.S572F Substitution - Missense 19:37893871-37893871 - ATL085 COSM5707002 c.6910G>T p.E2304* Substitution - Nonsense 19:37886761-37886761 - ESCC_BICR_027T COSM5443229 c.7673C>G p.S2558* Substitution - Nonsense 19:37885881-37885881 - YUOTHO COSM5389616 c.455_456CC>TT p.S152F Substitution - Missense 19:37895130-37895131 - WSU-HN12 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - SCC-9 COSM4590944 c.5655C>G p.N1885K Substitution - Missense 19:37887899-37887899 - 2492713 COSM5607215 c.5517G>A p.R1839R Substitution - coding silent 19:37888154-37888154 - TCGA-E9-A22G-01 COSM1480991 c.3858C>G p.L1286L Substitution - coding silent 19:37889696-37889696 - GC_353T-GC_353N COSM4753142 c.2002T>G p.F668V Substitution - Missense 19:37893584-37893584 - TCGA-A7-A4SD-01 COSM3822928 c.1954G>T p.V652F Substitution - Missense 19:37893749-37893749 - TCGA-BC-A10Y-01 COSM4936745 c.2570C>T p.T857I Substitution - Missense 19:37893016-37893016 - TCGA-B5-A0JV-01 COSM474657 c.306A>C p.K102N Substitution - Missense 19:37895280-37895280 - 40M COSM3712910 c.4268G>A p.G1423E Substitution - Missense 19:37889403-37889403 - HT29 COSM3201451 c.5397G>C p.R1799S Substitution - Missense 19:37888274-37888274 - TCGA-CC-5264-01 COSM4915173 c.5375A>T p.E1792V Substitution - Missense 19:37888296-37888296 - CSCC-32-T COSM3201403 c.6104G>A p.R2035K Substitution - Missense 19:37887567-37887567 - BD188T COSM5499602 c.5842C>G p.L1948V Substitution - Missense 19:37887829-37887829 - 2521249 COSM1232694 c.3733G>A p.D1245N Substitution - Missense 19:37889821-37889821 - TCGA-D8-A1XQ-01 COSM3822919 c.3048G>T p.L1016L Substitution - coding silent 19:37891781-37891781 - C0051T COSM4154191 c.5170G>T p.D1724Y Substitution - Missense 19:37888384-37888384 - PTC-14C COSM4131765 c.4407G>T p.Q1469H Substitution - Missense 19:37889147-37889147 - TCGA-BS-A0UV-01 COSM4864906 c.4056G>T p.E1352D Substitution - Missense 19:37889615-37889615 - YUMOKI COSM5389593 c.4854G>A p.R1618R Substitution - coding silent 19:37888817-37888817 - BD135T COSM5516838 c.2981A>C p.Q994P Substitution - Missense 19:37892605-37892605 - PD24190a COSM5780837 c.6947A>T p.E2316V Substitution - Missense 19:37886607-37886607 - TCGA-D1-A0ZQ-01 COSM4876110 c.984C>G p.Y328* Substitution - Nonsense 19:37894719-37894719 - TCGA-AM-5821-01 COSM3756730 c.6894G>A p.E2298E Substitution - coding silent 19:37886777-37886777 - 40M COSM4874548 c.2420G>A p.R807Q Substitution - Missense 19:37893283-37893283 - CSCC-29-T COSM4560036 c.944G>A p.G315E Substitution - Missense 19:37894759-37894759 - SNUH_G76_S1 COSM3756723 c.8528G>A p.R2843Q Substitution - Missense 19:37885026-37885026 - WSU-HN6 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - 2492720 COSM5722933 c.4474G>A p.E1492K Substitution - Missense 19:37889080-37889080 - TCGA-CA-6717-01 COSM1393284 c.5883G>T p.K1961N Substitution - Missense 19:37887671-37887671 - PT13 COSM3201457 c.5110G>A p.E1704K Substitution - Missense 19:37888444-37888444 - RK104_C01 COSM3701485 c.7513T>C p.F2505L Substitution - Missense 19:37886158-37886158 - BCM265T COSM4955158 c.6838G>T p.V2280L Substitution - Missense 19:37886716-37886716 - LUAD-S01356 COSM398080 c.2807T>A p.L936Q Substitution - Missense 19:37892779-37892779 - 587354 COSM1232687 c.2840G>A p.R947H Substitution - Missense 19:37892746-37892746 - TCGA-BS-A0UV-01 COSM4864417 c.5296G>T p.E1766* Substitution - Nonsense 19:37888375-37888375 - YUJUBE COSM3201427 c.5551G>A p.E1851K Substitution - Missense 19:37888003-37888003 - S02325 COSM4387135 c.746C>T p.T249I Substitution - Missense 19:37894957-37894957 - TCGA-AP-A0LF-01 COSM4875288 c.3172C>T p.R1058W Substitution - Missense 19:37891774-37891774 - SNU-C2B COSM1393275 c.8159delA p.K2720fs*57 Deletion - Frameshift 19:37885395-37885395 - TCGA-G4-6321-01 COSM1393277 c.7656G>T p.L2552L Substitution - coding silent 19:37885898-37885898 - SNUH_G26_S1 COSM3756726 c.8208T>C p.F2736F Substitution - coding silent 19:37885463-37885463 - 2492720 COSM394453 c.1715C>T p.S572F Substitution - Missense 19:37893871-37893871 - AOCS-116-1-3 COSM4140585 c.5585A>G p.Y1862C Substitution - Missense 19:37887969-37887969 - HCC001T COSM5808855 c.1170C>A p.G390G Substitution - coding silent 19:37894416-37894416 - CSCC-49-T COSM4547534 c.4254G>A p.R1418R Substitution - coding silent 19:37889300-37889300 - TCGA-AX-A0J0-01 COSM3422766 c.96G>T p.K32N Substitution - Missense 19:37896288-37896288 - C086 COSM5541748 c.7794G>A p.K2598K Substitution - coding silent 19:37885877-37885877 - U87 COSM3201695 c.1121G>C p.G374A Substitution - Missense 19:37894582-37894582 - RK104_C01 COSM3701484 c.7396T>C p.F2466L Substitution - Missense 19:37886158-37886158 - PT55 COSM4558417 c.7795G>A p.G2599R Substitution - Missense 19:37885876-37885876 - KM12 COSM3201247 c.8716C>T p.H2906Y Substitution - Missense 19:37884955-37884955 - TCGA-AK-3428-01 COSM3362832 c.3052A>T p.M1018L Substitution - Missense 19:37891777-37891777 - BD72T COSM1393283 c.6187delA p.R2063fs*11 Deletion - Frameshift 19:37887367-37887367 - HCT116 COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - ATL085 COSM5707001 c.6793G>T p.E2265* Substitution - Nonsense 19:37886761-37886761 - CSCC-41-T COSM4539981 c.2884G>T p.A962S Substitution - Missense 19:37892819-37892819 - YUJUBE COSM5389579 c.6381G>A p.R2127R Substitution - coding silent 19:37887290-37887290 - YUMOKI COSM5389591 c.4856A>T p.K1619I Substitution - Missense 19:37888815-37888815 - TCGA-DD-A3A1-01 COSM4938246 c.5798A>C p.K1933T Substitution - Missense 19:37887873-37887873 - 46M COSM3201457 c.5110G>A p.E1704K Substitution - Missense 19:37888444-37888444 - 78 COSM5013436 c.7430C>T p.A2477V Substitution - Missense 19:37886124-37886124 - TCGA-BS-A0UV-01 COSM995838 c.8308A>C p.K2770Q Substitution - Missense 19:37885246-37885246 - 63 COSM5013439 c.6770A>G p.D2257G Substitution - Missense 19:37886901-37886901 - Gp5D COSM3201298 c.7727G>A p.R2576H Substitution - Missense 19:37885827-37885827 - HCC126T COSM5818823 c.2608C>A p.L870M Substitution - Missense 19:37892978-37892978 - CHC892T COSM4960369 c.7490C>T p.P2497L Substitution - Missense 19:37886064-37886064 - TCGA-B5-A11N-01 COSM4864043 c.5212G>T p.E1738* Substitution - Nonsense 19:37888459-37888459 - TCGA-D1-A0ZQ-01 COSM995882 c.867C>G p.Y289* Substitution - Nonsense 19:37894719-37894719 - 3885 COSM5043517 c.5503G>T p.E1835* Substitution - Nonsense 19:37888168-37888168 - S02237 COSM5676508 c.100T>C p.C34R Substitution - Missense 19:37896284-37896284 - HT115 COSM3201461 c.5148G>T p.E1716D Substitution - Missense 19:37888523-37888523 - S02279 COSM5683660 c.3764C>A p.T1255N Substitution - Missense 19:37889907-37889907 - ACINAR01 COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - HCC137 COSM1612147 c.4632G>T p.V1544V Substitution - coding silent 19:37888922-37888922 - SCC-9 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - YUOTHO COSM4560474 c.8575G>A p.E2859K Substitution - Missense 19:37885096-37885096 - TCGA-D1-A17Q-01 COSM995864 c.4800G>T p.E1600D Substitution - Missense 19:37888754-37888754 - TCGA-B5-A0JY-01 COSM995844 c.7281G>T p.R2427S Substitution - Missense 19:37886273-37886273 - TCGA-E9-A22G-01 COSM4814117 c.3975C>G p.L1325L Substitution - coding silent 19:37889696-37889696 - CSCC-30-T COSM4485354 c.2922C>T p.T974T Substitution - coding silent 19:37892664-37892664 - pfg043T COSM4753139 c.2639A>C p.K880T Substitution - Missense 19:37893064-37893064 - TCGA-Q1-A73O-01 COSM4835188 c.6379G>A p.E2127K Substitution - Missense 19:37887175-37887175 - 8031146 COSM4781742 c.7727C>T p.A2576V Substitution - Missense 19:37885944-37885944 - TCGA-AZ-6598-01 COSM1393295 c.3827T>C p.M1276T Substitution - Missense 19:37889727-37889727 - KM12 COSM4612774 c.2006_2008delTCT p.F669delF Deletion - In frame 19:37893578-37893580 - PT42 COSM5926067 c.8506A>G p.I2836V Substitution - Missense 19:37885048-37885048 - YUWAPO COSM5389594 c.4672G>A p.E1558K Substitution - Missense 19:37888882-37888882 - 2492714 COSM5607212 c.6825G>A p.G2275G Substitution - coding silent 19:37886729-37886729 - 2492722 COSM5722931 c.4618G>A p.D1540N Substitution - Missense 19:37888936-37888936 - C086 COSM5541740 c.4780G>A p.E1594K Substitution - Missense 19:37888891-37888891 - HCT8 COSM4634413 c.5271G>A p.L1757L Substitution - coding silent 19:37888400-37888400 - KM12 COSM3201246 c.8599C>T p.H2867Y Substitution - Missense 19:37884955-37884955 - SC_9024 COSM3201322 c.7226C>T p.P2409L Substitution - Missense 19:37886328-37886328 - CHC1720T COSM4800538 c.1918C>T p.P640S Substitution - Missense 19:37893668-37893668 - C086 COSM5541749 c.4314G>A p.E1438E Substitution - coding silent 19:37889240-37889240 - TCGA-E9-A243-01 COSM1480993 c.3379G>A p.A1127T Substitution - Missense 19:37890175-37890175 - TCGA-AN-A046-01 COSM3822917 c.3533A>C p.K1178T Substitution - Missense 19:37890021-37890021 - ESCC_BICR_027T COSM5443230 c.7790C>G p.S2597* Substitution - Nonsense 19:37885881-37885881 - Detroit_562 COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - PD4127a COSM165595 c.7847C>G p.P2616R Substitution - Missense 19:37885707-37885707 - TCGA-D8-A1XK-01 COSM3822915 c.3855A>G p.E1285E Substitution - coding silent 19:37889699-37889699 - CSCC-31-T COSM4282378 c.8161G>A p.E2721K Substitution - Missense 19:37885510-37885510 - TCGA-F5-6814-01 COSM3422764 c.3454G>T p.D1152Y Substitution - Missense 19:37890100-37890100 - PCSI_0050_Pa_X COSM5002086 c.4865G>A p.R1622Q Substitution - Missense 19:37888806-37888806 - PT38 COSM5923337 c.5922G>A p.M1974I Substitution - Missense 19:37887749-37887749 - YUMOKI COSM5389590 c.4739A>T p.K1580I Substitution - Missense 19:37888815-37888815 - 587376 COSM1232690 c.8365G>A p.E2789K Substitution - Missense 19:37885189-37885189 - CSCC-40-T COSM4558171 c.7580G>A p.W2527* Substitution - Nonsense 19:37885974-37885974 - NOKSI COSM4590945 c.5772C>G p.N1924K Substitution - Missense 19:37887899-37887899 - TCGA-AP-A0LM-01 COSM995851 c.5796G>A p.Q1932Q Substitution - coding silent 19:37887758-37887758 - C086 COSM5541742 c.5980G>A p.D1994N Substitution - Missense 19:37887691-37887691 - N717T COSM236264 c.4655G>A p.R1552Q Substitution - Missense 19:37888899-37888899 - TCGA-BS-A0TC-01 COSM995878 c.1513G>A p.V505I Substitution - Missense 19:37894073-37894073 - ccRCC-29 COSM1665014 c.2200C>T p.L734F Substitution - Missense 19:37893503-37893503 - TCGA-EI-6509-01 COSM3749504 c.6907G>A p.E2303K Substitution - Missense 19:37886764-37886764 - CSCC-11-T COSM4506736 c.7287C>T p.F2429F Substitution - coding silent 19:37886267-37886267 - TCGA-DD-A73A-01 COSM4916538 c.3770C>A p.S1257Y Substitution - Missense 19:37889784-37889784 - S00841 COSM5661893 c.7492G>A p.A2498T Substitution - Missense 19:37886179-37886179 - RMS110_ COSM4987285 c.4718A>G p.K1573R Substitution - Missense 19:37888836-37888836 - TCGA-D1-A165-01 COSM474657 c.306A>C p.K102N Substitution - Missense 19:37895280-37895280 - PD6422a COSM5772191 c.7703G>A p.R2568H Substitution - Missense 19:37885968-37885968 - AOCS-158-1-6 COSM4140592 c.409T>A p.F137I Substitution - Missense 19:37895294-37895294 - TCGA-D5-6927-01 COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - TCGA-AZ-4315-01 COSM1393294 c.4095G>T p.V1365V Substitution - coding silent 19:37889459-37889459 - PTC-14C COSM4131766 c.4524G>T p.Q1508H Substitution - Missense 19:37889147-37889147 - ACA8 COSM995860 c.5001G>T p.K1667N Substitution - Missense 19:37888553-37888553 - 381_T COSM3960004 c.7717C>A p.R2573R Substitution - coding silent 19:37885954-37885954 - PD23562a COSM5774109 c.7864C>G p.Q2622E Substitution - Missense 19:37885690-37885690 - TCGA-E2-A1IH-01 COSM1480994 c.3080C>G p.S1027C Substitution - Missense 19:37891749-37891749 - 46M COSM3201458 c.5227G>A p.E1743K Substitution - Missense 19:37888444-37888444 - YUOTHO COSM4560473 c.8458G>A p.E2820K Substitution - Missense 19:37885096-37885096 - 587376 COSM1232695 c.3538G>T p.D1180Y Substitution - Missense 19:37890016-37890016 - ESCC_103 COSM5638191 c.6045G>T p.K2015N Substitution - Missense 19:37887509-37887509 - YUKAT COSM5389583 c.5586G>A p.M1862I Substitution - Missense 19:37888085-37888085 - PD4954a COSM5778266 c.2334T>A p.L778L Substitution - coding silent 19:37893252-37893252 - C008 COSM230381 c.923C>T p.S308F Substitution - Missense 19:37894663-37894663 - CSCC-49-T COSM4481779 c.2659C>T p.L887L Substitution - coding silent 19:37893044-37893044 - CSCC-55-T COSM4553334 c.5878G>A p.E1960K Substitution - Missense 19:37887676-37887676 - TCGA-CA-6717-01 COSM1232696 c.2600G>A p.R867Q Substitution - Missense 19:37892986-37892986 - TCGA-AD-6964-01 COSM4786427 c.1502T>C p.M501T Substitution - Missense 19:37894201-37894201 - HCC2998 COSM3201398 c.6088G>A p.E2030K Substitution - Missense 19:37887466-37887466 - S01023 COSM5666526 c.4508T>C p.L1503P Substitution - Missense 19:37889046-37889046 - LS180 COSM1734551 c.8276delA p.K2759fs*57 Deletion - Frameshift 19:37885395-37885395 - 53M COSM5595567 c.270C>T p.I90I Substitution - coding silent 19:37895316-37895316 - PTC-7C COSM3756725 c.8091T>C p.F2697F Substitution - coding silent 19:37885463-37885463 - TCGA-BS-A0UV-01 COSM995857 c.5179G>T p.E1727* Substitution - Nonsense 19:37888375-37888375 - 53M COSM5595562 c.7268G>A p.G2423E Substitution - Missense 19:37886403-37886403 - C0043T COSM4154194 c.4733A>G p.K1578R Substitution - Missense 19:37888938-37888938 - C0078T COSM4154196 c.2750C>T p.T917I Substitution - Missense 19:37892953-37892953 - C086 COSM5541744 c.7038G>A p.E2346E Substitution - coding silent 19:37886633-37886633 - 2492722 COSM5722932 c.4735G>A p.D1579N Substitution - Missense 19:37888936-37888936 - PT37 COSM5921614 c.3313C>T p.P1105S Substitution - Missense 19:37891633-37891633 - CHOL15 COSM1744746 c.5911G>A p.A1971T Substitution - Missense 19:37887643-37887643 - T24 COSM5343303 c.8018T>G p.I2673S Substitution - Missense 19:37885536-37885536 - PT36 COSM5389588 c.4885G>A p.E1629K Substitution - Missense 19:37888669-37888669 - 1862876 COSM1180612 c.5535T>A p.N1845K Substitution - Missense 19:37888019-37888019 - C058 COSM5389579 c.6381G>A p.R2127R Substitution - coding silent 19:37887290-37887290 - C086 COSM4558416 c.7678G>A p.G2560R Substitution - Missense 19:37885876-37885876 - 41T COSM3712907 c.5567G>A p.R1856K Substitution - Missense 19:37887987-37887987 - 2246942 COSM3712907 c.5567G>A p.R1856K Substitution - Missense 19:37887987-37887987 - S02243 COSM5677756 c.7996G>T p.A2666S Substitution - Missense 19:37885675-37885675 - PT15_1 COSM4526905 c.1544G>A p.G515E Substitution - Missense 19:37894159-37894159 - CSCC-49-T COSM4559494 c.8076G>A p.K2692K Substitution - coding silent 19:37885478-37885478 - 2492721 COSM5722936 c.3631C>T p.L1211L Substitution - coding silent 19:37890040-37890040 - TCGA-DD-A3A9-01 COSM4920373 c.3233C>T p.P1078L Substitution - Missense 19:37891596-37891596 - 6P2-2 COSM3734375 c.4760A>G p.K1587R Substitution - Missense 19:37888794-37888794 - QC2-15-T2 COSM5652525 c.3911T>G p.L1304R Substitution - Missense 19:37889760-37889760 - 3N48-VS-3T48 COSM3201305 c.7675G>A p.V2559I Substitution - Missense 19:37885996-37885996 - 8049223 COSM3388932 c.8618G>A p.R2873H Substitution - Missense 19:37885053-37885053 - TCGA-CK-4950-01 COSM3749504 c.6907G>A p.E2303K Substitution - Missense 19:37886764-37886764 - ESCC-D1 COSM5045172 c.7789T>A p.S2597T Substitution - Missense 19:37885882-37885882 - HT115 COSM3201627 c.2137G>A p.E713K Substitution - Missense 19:37893449-37893449 - TCGA-A6-6141-01 COSM3756730 c.6894G>A p.E2298E Substitution - coding silent 19:37886777-37886777 - CHC892T COSM4794285 c.3390G>A p.K1130K Substitution - coding silent 19:37891556-37891556 - TCGA-BS-A0UV-01 COSM995867 c.3939G>T p.E1313D Substitution - Missense 19:37889615-37889615 - 2492720 COSM5722936 c.3631C>T p.L1211L Substitution - coding silent 19:37890040-37890040 - 2492721 COSM5722937 c.1832C>T p.S611F Substitution - Missense 19:37893871-37893871 - HT115 COSM3201640 c.2146C>T p.P716S Substitution - Missense 19:37893557-37893557 - HT115 COSM3201423 c.5634G>T p.K1878N Substitution - Missense 19:37887920-37887920 - S01020 COSM3756728 c.6922A>G p.R2308G Substitution - Missense 19:37886749-37886749 - CSCC-29-T COSM4510933 c.8527C>T p.R2843W Substitution - Missense 19:37885027-37885027 - ITNET_1047_T COSM4868275 c.719G>A p.S240N Substitution - Missense 19:37894984-37894984 - OSCC-GB_00410111 COSM3712909 c.4151G>A p.G1384E Substitution - Missense 19:37889403-37889403 - TCGA-AA-3510-01 COSM4785797 c.2835G>A p.G945G Substitution - coding silent 19:37892868-37892868 - TCGA-DG-A2KM-01 COSM4851764 c.3464C>T p.S1155F Substitution - Missense 19:37890090-37890090 - C086 COSM5541731 c.5233G>A p.E1745K Substitution - Missense 19:37888321-37888321 - sysucc-311T COSM5464557 c.3273G>T p.K1091N Substitution - Missense 19:37891556-37891556 - LUAD-S01302 COSM395715 c.5296G>T p.E1766* Substitution - Nonsense 19:37888258-37888258 - C0043T COSM4154193 c.4616A>G p.K1539R Substitution - Missense 19:37888938-37888938 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.664181;Hs.664182;Hs.664183;Hs.664184;Hs.664186;Hs.664187;Hs.664188;Hs.664189;Hs.664190;Hs.664191;Hs.664193;Hs.664194 19q13.13

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.L2599P c.7796T>C 19 38376398 UCEC A G Synonymous p.D1238D c.3714T>C 19 38380480 BRCA A T Synonymous p.I701I c.2103T>A 19 38384123 AML C A Missense p.E1677D c.5031G>T 19 38379163 UCEC C A Missense p.L1916F c.5748G>T 19 38378446 LUAD C G Missense p.G962A c.2885G>C 19 38383341 RCCC C T Missense p.A1127T c.3379G>A 19 38380815 BRCA C T Missense p.G2378D c.7133G>A 19 38377061 UCEC C T Missense p.S201N c.602G>A 19 38385624 UCEC C T Missense p.V505I c.1513G>A 19 38384713 UCEC C T Synonymous p.A2537A c.7611G>A 19 38376583 MB G A Missense p.L639F c.1915C>T 19 38384311 BRCA G A Missense p.R1019W c.3055C>T 19 38382414 UCEC G A Missense p.R1949W c.5845C>T 19 38378349 MB G A Missense p.R331W c.991C>T 19 38385235 UCEC G A Missense p.R619W c.1855C>T 19 38384371 UCEC G A Nonsense p.Q1876* c.5626C>T 19 38378568 MM G A Nonsense p.R2534* c.7600C>T 19 38376594 MM G A Synonymous p.G1370G c.4110C>T 19 38380084 RCCC G A Synonymous p.L1358L c.4072C>T 19 38380122 BRCA G C Missense p.P2616R c.7847C>G 19 38376347 BRCA G C Missense p.P786A c.2356C>G 19 38383870 BRCA G C Missense p.S1027C c.3080C>G 19 38382389 BRCA G C Missense p.S933C c.2798C>G 19 38383428 MM G C Nonsense p.Y289* c.867C>G 19 38385359 UCEC G C Synonymous p.L1286L c.3858C>G 19 38380336 BRCA G T Missense p.H1471N c.4411C>A 19 38379783 SCLC G T Missense p.P380T c.1138C>A 19 38385088 UCEC G T Missense p.Q1491K c.4471C>A 19 38379723 BRCA G T Missense p.T389K c.1166C>A 19 38385060 LUAD T A Missense p.E1555D c.4665A>T 19 38379529 BRCA T A Missense p.M1018L c.3052A>T 19 38382417 RCCC T C Missense p.H953R c.2858A>G 19 38383368 RCCC T C Missense p.I2175M c.6525A>G 19 38377669 UCEC T C Missense p.K1650R c.4949A>G 19 38379245 SCLC T C Synonymous p.E2254E c.6762A>G 19 38377432 RCCC T G Missense p.K102N c.306A>C 19 38385920 RCCC