DCUN1D2
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
ACC13114112384114112384+Missense_MutationSNPGGTTCGA-OR-A5JT-01A-11D-A29I-10TCGA-OR-A5JT-10A-01D-A29L-10g.chr13:114112384G>Tc.740C>Ac.(739-741)gCa>gAap.A247E
BLCA13114134912114134912+Missense_MutationSNPGGCTCGA-XF-A9ST-01A-11D-A42E-08TCGA-XF-A9ST-10A-01D-A42H-08g.chr13:114134912G>Cc.367C>Gc.(367-369)Cta>Gtap.L123V
BLCA13114134914114134914+Missense_MutationSNPAAGTCGA-UY-A8OB-01A-12D-A42E-08TCGA-UY-A8OB-11A-12D-A42H-08g.chr13:114134914A>Gc.365T>Cc.(364-366)tTt>tCtp.F122S
BLCA13114135050114135050+Missense_MutationSNPCCTTCGA-S5-A6DX-01A-11D-A31L-08TCGA-S5-A6DX-10A-01D-A31J-08g.chr13:114135050C>Tc.229G>Ac.(229-231)Gat>Aatp.D77N
BLCA13114138204114138204+SilentSNPCCTTCGA-XF-AAMF-01A-21D-A42E-08TCGA-XF-AAMF-10A-01D-A42H-08g.chr13:114138204C>Tc.171G>Ac.(169-171)cgG>cgAp.R57R
BLCA13114138263114138263+Missense_MutationSNPCCGTCGA-BT-A42E-01A-11D-A23U-08TCGA-BT-A42E-10A-01D-A23U-08g.chr13:114138263C>Gc.112G>Cc.(112-114)Gac>Cacp.D38H
BLCA13114138283114138283+Missense_MutationSNPGGATCGA-YC-A9TC-01A-22D-A391-08TCGA-YC-A9TC-10A-01D-A394-08g.chr13:114138283G>Ac.92C>Tc.(91-93)aCg>aTgp.T31M
BLCA13114138370114138370+Splice_SiteSNPTTCTCGA-GC-A3RD-01A-12D-A22Z-08TCGA-GC-A3RD-10B-01D-A22Z-08g.chr13:114138370T>Cc.5A>Gc.(4-6)cAt>cGtp.H2R
BRCA13114112365114112365+SilentSNPAACTCGA-A8-A0A6-01A-12W-A071-09TCGA-A8-A0A6-10A-01W-A071-09g.chr13:114112365A>Cc.759T>Gc.(757-759)ggT>ggGp.G253G
BRCA13114128499114128499+Missense_MutationSNPAAGTCGA-C8-A130-01A-31D-A10Y-09TCGA-C8-A130-10A-01D-A110-09g.chr13:114128499A>Gc.460T>Cc.(460-462)Ttt>Cttp.F154L
BRCA13114138226114138226+Missense_MutationSNPGGATCGA-B6-A0RO-01A-22D-A099-09TCGA-B6-A0RO-10A-01D-A099-09g.chr13:114138226G>Ac.149C>Tc.(148-150)tCg>tTgp.S50L
BRCA13114138363114138363+SilentSNPAAGTCGA-D8-A1XK-01A-21D-A14K-09TCGA-D8-A1XK-10A-01D-A14K-09g.chr13:114138363A>Gc.12T>Cc.(10-12)ctT>ctCp.L4L
COAD13114113636114113636+Missense_MutationSNPCCTTCGA-CM-6678-01A-11D-1835-10TCGA-CM-6678-10A-01D-1835-10g.chr13:114113636C>Tc.691G>Ac.(691-693)Gat>Aatp.D231N
COAD13114128489114128489+Missense_MutationSNPAACTCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr13:114128489A>Cc.470T>Gc.(469-471)tTt>tGtp.F157C
COADREAD13114113636114113636+Missense_MutationSNPCCTTCGA-CM-6678-01A-11D-1835-10TCGA-CM-6678-10A-01D-1835-10g.chr13:114113636C>Tc.691G>Ac.(691-693)Gat>Aatp.D231N
COADREAD13114128489114128489+Missense_MutationSNPAACTCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr13:114128489A>Cc.470T>Gc.(469-471)tTt>tGtp.F157C
GBMLGG13114135036114135036+SilentSNPAAGTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr13:114135036A>Gc.243T>Cc.(241-243)atT>atCp.I81I
HNSC13114112358114112358+Missense_MutationSNPGGATCGA-CV-5436-01A-01D-1512-08TCGA-CV-5436-10A-01D-1870-08g.chr13:114112358G>Ac.766C>Tc.(766-768)Cgc>Tgcp.R256C
LGG13114135036114135036+SilentSNPAAGTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr13:114135036A>Gc.243T>Cc.(241-243)atT>atCp.I81I
LIHC13114112422114112422+Splice_SiteSNPTTCTCGA-CC-A3MA-01A-11D-A20W-10TCGA-CC-A3MA-10A-01D-A20W-10g.chr13:114112422T>Cc.702A>Gc.(700-702)ggA>ggGp.G234G
LUAD13114128538114128538+SilentSNPGGATCGA-17-Z032-01A-01W-0746-08TCGA-17-Z032-11A-01W-0746-08g.chr13:114128538G>Ac.421C>Tc.(421-423)Ctg>Ttgp.L141L
LUAD13114134923114134923+Missense_MutationSNPCCTTCGA-55-8614-01A-11D-2393-08TCGA-55-8614-10A-01D-2393-08g.chr13:114134923C>Tc.356G>Ac.(355-357)aGa>aAap.R119K
LUAD13114138335114138335+Nonsense_MutationSNPGGATCGA-78-7167-01A-11D-2063-08TCGA-78-7167-11A-01D-2063-08g.chr13:114138335G>Ac.40C>Tc.(40-42)Cag>Tagp.Q14*
LUSC13114112392114112392+SilentSNPTTCTCGA-34-5927-01A-11D-1817-08TCGA-34-5927-10A-01D-1817-08g.chr13:114112392T>Cc.732A>Gc.(730-732)gtA>gtGp.V244V
LUSC13114138238114138238+Missense_MutationSNPTTCTCGA-18-3409-01A-01D-0983-08TCGA-18-3409-11A-01D-0983-08g.chr13:114138238T>Cc.137A>Gc.(136-138)cAa>cGap.Q46R
PRAD13114112358114112358+Missense_MutationSNPGGATCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr13:114112358G>Ac.766C>Tc.(766-768)Cgc>Tgcp.R256C
PRAD13114128477114128477+Missense_MutationSNPGGATCGA-YL-A9WX-01A-21D-A41K-08TCGA-YL-A9WX-10A-01D-A41N-08g.chr13:114128477G>Ac.482C>Tc.(481-483)aCc>aTcp.T161I
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-US13114138370114138370single base substitutionTC5_prime_UTR_variant
BLCA-US13114138370114138370single base substitutionTCintron_variant
BLCA-US13114138370114138370single base substitutionTCmissense_variantH2R5A>G
BLCA-US13114138370114138370single base substitutionTCsplice_region_variant
BLCA-US13114138370114138370single base substitutionTCupstream_gene_variant
BLCA-US13114150069114150069single base substitutionCTupstream_gene_variant
BRCA-EU13114105483114105483single base substitutionCGdownstream_gene_variant
BRCA-EU13114106687114106687single base substitutionCGdownstream_gene_variant
BRCA-EU13114107595114107595single base substitutionCTdownstream_gene_variant
BRCA-EU13114108169114108169single base substitutionCTdownstream_gene_variant
BRCA-EU13114108237114108237single base substitutionCAdownstream_gene_variant
BRCA-EU13114108925114108925single base substitutionCTdownstream_gene_variant
BRCA-EU13114111936114111936single base substitutionGA3_prime_UTR_variant
BRCA-EU13114111936114111936single base substitutionGAdownstream_gene_variant
BRCA-EU13114113526114113526single base substitutionCGdownstream_gene_variant
BRCA-EU13114113526114113526single base substitutionCGintron_variant
BRCA-EU13114117866114117866single base substitutionAGintron_variant
BRCA-EU13114117866114117866single base substitutionAGupstream_gene_variant
BRCA-EU13114118434114118434single base substitutionCGintron_variant
BRCA-EU13114118434114118434single base substitutionCGupstream_gene_variant
BRCA-EU13114121974114121974deletion of <=200bpA-intron_variant
BRCA-EU13114121974114121974deletion of <=200bpA-upstream_gene_variant
BRCA-EU13114123867114123867single base substitutionGCdownstream_gene_variant
BRCA-EU13114123867114123867single base substitutionGCintron_variant
BRCA-EU13114128462114128462single base substitutionTGdownstream_gene_variant
BRCA-EU13114128462114128462single base substitutionTGexon_variant
BRCA-EU13114128462114128462single base substitutionTGmissense_variantK166T497A>C
BRCA-EU13114128462114128462single base substitutionTGmissense_variantK33T98A>C
BRCA-EU13114129468114129468single base substitutionCTintron_variant
BRCA-EU13114129498114129498single base substitutionGAintron_variant
BRCA-EU13114133290114133290single base substitutionTGdownstream_gene_variant
BRCA-EU13114133290114133290single base substitutionTGintron_variant
BRCA-EU13114135325114135325single base substitutionCGdownstream_gene_variant
BRCA-EU13114135325114135325single base substitutionCGintron_variant
BRCA-EU13114135589114135589single base substitutionGCdownstream_gene_variant
BRCA-EU13114135589114135589single base substitutionGCintron_variant
BRCA-EU13114137731114137731single base substitutionCGdownstream_gene_variant
BRCA-EU13114137731114137731single base substitutionCGintron_variant
BRCA-EU13114138283114138283single base substitutionGCexon_variant
BRCA-EU13114138283114138283single base substitutionGCintron_variant
BRCA-EU13114138283114138283single base substitutionGCmissense_variantT16R47C>G
BRCA-EU13114138283114138283single base substitutionGCmissense_variantT31R92C>G
BRCA-EU13114139190114139190single base substitutionCGintron_variant
BRCA-EU13114139190114139190single base substitutionCGupstream_gene_variant
BRCA-EU13114139506114139506single base substitutionGAintron_variant
BRCA-EU13114139506114139506single base substitutionGAupstream_gene_variant
BRCA-EU13114140628114140628single base substitutionCTintron_variant
BRCA-EU13114140628114140628single base substitutionCTupstream_gene_variant
BRCA-EU13114141976114141976single base substitutionTCintron_variant
BRCA-EU13114141976114141976single base substitutionTCupstream_gene_variant
BRCA-EU13114142387114142387single base substitutionCTintron_variant
BRCA-EU13114142387114142387single base substitutionCTupstream_gene_variant
BRCA-EU13114142934114142934single base substitutionAGintron_variant
BRCA-EU13114142934114142934single base substitutionAGupstream_gene_variant
BRCA-EU13114144531114144531single base substitutionCGintron_variant
BRCA-EU13114144889114144889single base substitutionCAexon_variant
BRCA-EU13114144889114144889single base substitutionCAintron_variant
BRCA-EU13114144889114144889single base substitutionCAupstream_gene_variant
BRCA-EU13114145075114145075single base substitutionCT5_prime_UTR_variant
BRCA-EU13114145075114145075single base substitutionCTmissense_variantE18K52G>A
BRCA-EU13114145075114145075single base substitutionCTupstream_gene_variant
BRCA-EU13114147207114147207single base substitutionCGupstream_gene_variant
BRCA-EU13114150178114150178single base substitutionCTupstream_gene_variant
BRCA-FR13114113974114113974single base substitutionTAdownstream_gene_variant
BRCA-FR13114113974114113974single base substitutionTAintron_variant
BRCA-FR13114113974114113974single base substitutionTAupstream_gene_variant
BRCA-FR13114128462114128462single base substitutionTGdownstream_gene_variant
BRCA-FR13114128462114128462single base substitutionTGexon_variant
BRCA-FR13114128462114128462single base substitutionTGmissense_variantK166T497A>C
BRCA-FR13114128462114128462single base substitutionTGmissense_variantK33T98A>C
BRCA-FR13114135589114135589single base substitutionGCdownstream_gene_variant
BRCA-FR13114135589114135589single base substitutionGCintron_variant
BRCA-FR13114137731114137731single base substitutionCGdownstream_gene_variant
BRCA-FR13114137731114137731single base substitutionCGintron_variant
BRCA-FR13114138283114138283single base substitutionGCexon_variant
BRCA-FR13114138283114138283single base substitutionGCintron_variant
BRCA-FR13114138283114138283single base substitutionGCmissense_variantT16R47C>G
BRCA-FR13114138283114138283single base substitutionGCmissense_variantT31R92C>G
BRCA-FR13114144889114144889single base substitutionCAexon_variant
BRCA-FR13114144889114144889single base substitutionCAintron_variant
BRCA-FR13114144889114144889single base substitutionCAupstream_gene_variant
BRCA-FR13114145075114145075single base substitutionCT5_prime_UTR_variant
BRCA-FR13114145075114145075single base substitutionCTmissense_variantE18K52G>A
BRCA-FR13114145075114145075single base substitutionCTupstream_gene_variant
BRCA-FR13114147207114147207single base substitutionCGupstream_gene_variant
BRCA-FR13114150178114150178single base substitutionCTupstream_gene_variant
BRCA-UK13114105671114105671single base substitutionAGdownstream_gene_variant
BRCA-UK13114136509114136509single base substitutionCGdownstream_gene_variant
BRCA-UK13114136509114136509single base substitutionCGintron_variant
BRCA-US13114107723114107723single base substitutionCTdownstream_gene_variant
BRCA-US13114112365114112365single base substitutionAC3_prime_UTR_variant
BRCA-US13114112365114112365single base substitutionACdownstream_gene_variant
BRCA-US13114112365114112365single base substitutionACexon_variant
BRCA-US13114112365114112365single base substitutionACsynonymous_variantG120G360T>G
BRCA-US13114112365114112365single base substitutionACsynonymous_variantG253G759T>G
BRCA-US13114128499114128499single base substitutionAGdownstream_gene_variant
BRCA-US13114128499114128499single base substitutionAGexon_variant
BRCA-US13114128499114128499single base substitutionAGmissense_variantF154L460T>C
BRCA-US13114128499114128499single base substitutionAGmissense_variantF21L61T>C
BRCA-US13114138226114138226single base substitutionGAdownstream_gene_variant
BRCA-US13114138226114138226single base substitutionGAexon_variant
BRCA-US13114138226114138226single base substitutionGAintron_variant
BRCA-US13114138226114138226single base substitutionGAmissense_variantS35L104C>T
BRCA-US13114138226114138226single base substitutionGAmissense_variantS50L149C>T
BRCA-US13114138363114138363single base substitutionAG5_prime_UTR_variant
BRCA-US13114138363114138363single base substitutionAGexon_variant
BRCA-US13114138363114138363single base substitutionAGintron_variant
BRCA-US13114138363114138363single base substitutionAGsynonymous_variantL4L12T>C
BRCA-US13114138363114138363single base substitutionAGupstream_gene_variant
BRCA-US13114150035114150035single base substitutionCTupstream_gene_variant
BTCA-JP13114113606114113606single base substitutionCGdownstream_gene_variant
BTCA-JP13114113606114113606single base substitutionCGintron_variant
BTCA-JP13114115273114115273single base substitutionCGdownstream_gene_variant
BTCA-JP13114115273114115273single base substitutionCGintron_variant
BTCA-JP13114115273114115273single base substitutionCGupstream_gene_variant
BTCA-JP13114138155114138155single base substitutionCAdownstream_gene_variant
BTCA-JP13114138155114138155single base substitutionCAintron_variant
BTCA-JP13114138155114138155single base substitutionCAmissense_variantD59Y175G>T
BTCA-JP13114138155114138155single base substitutionCAmissense_variantD74Y220G>T
BTCA-JP13114138155114138155single base substitutionCAsplice_region_variant
CESC-US13114150193114150193single base substitutionCTupstream_gene_variant
CLLE-ES13114121470114121470single base substitutionACintron_variant
CLLE-ES13114121470114121470single base substitutionACupstream_gene_variant
CLLE-ES13114124699114124699single base substitutionCTdownstream_gene_variant
CLLE-ES13114124699114124699single base substitutionCTintron_variant
CLLE-ES13114138857114138857single base substitutionAGintron_variant
CLLE-ES13114138857114138857single base substitutionAGupstream_gene_variant
COAD-US13114107550114107550single base substitutionGAdownstream_gene_variant
COAD-US13114113636114113636single base substitutionCT3_prime_UTR_variant
COAD-US13114113636114113636single base substitutionCTdownstream_gene_variant
COAD-US13114113636114113636single base substitutionCTexon_variant
COAD-US13114113636114113636single base substitutionCTmissense_variantD231N691G>A
COAD-US13114113636114113636single base substitutionCTmissense_variantD98N292G>A
COAD-US13114150107114150107single base substitutionCTupstream_gene_variant
COCA-CN13114107701114107701single base substitutionCTdownstream_gene_variant
COCA-CN13114128312114128312single base substitutionCTdownstream_gene_variant
COCA-CN13114128312114128312single base substitutionCTintron_variant
COCA-CN13114144842114144842single base substitutionTCexon_variant
COCA-CN13114144842114144842single base substitutionTCintron_variant
COCA-CN13114144842114144842single base substitutionTCupstream_gene_variant
EOPC-DE13114124884114124884single base substitutionTCdownstream_gene_variant
EOPC-DE13114124884114124884single base substitutionTCintron_variant
EOPC-DE13114145772114145772single base substitutionACupstream_gene_variant
ESAD-UK13114106345114106345single base substitutionGAdownstream_gene_variant
ESAD-UK13114107769114107769single base substitutionTAdownstream_gene_variant
ESAD-UK13114108157114108157single base substitutionGAdownstream_gene_variant
ESAD-UK13114108595114108595single base substitutionGCdownstream_gene_variant
ESAD-UK13114109027114109027single base substitutionCTdownstream_gene_variant
ESAD-UK13114109749114109749single base substitutionCTdownstream_gene_variant
ESAD-UK13114109924114109924single base substitutionTGdownstream_gene_variant
ESAD-UK13114111490114111490single base substitutionCT3_prime_UTR_variant
ESAD-UK13114111490114111490single base substitutionCTdownstream_gene_variant
ESAD-UK13114112450114112450single base substitutionCAdownstream_gene_variant
ESAD-UK13114112450114112450single base substitutionCAintron_variant
ESAD-UK13114116270114116270deletion of <=200bpT-downstream_gene_variant
ESAD-UK13114116270114116270deletion of <=200bpT-intron_variant
ESAD-UK13114116270114116270deletion of <=200bpT-upstream_gene_variant
ESAD-UK13114116962114116962single base substitutionCTdownstream_gene_variant
ESAD-UK13114116962114116962single base substitutionCTintron_variant
ESAD-UK13114116962114116962single base substitutionCTupstream_gene_variant
ESAD-UK13114119398114119398single base substitutionGAintron_variant
ESAD-UK13114119398114119398single base substitutionGAupstream_gene_variant
ESAD-UK13114121369114121369single base substitutionCTintron_variant
ESAD-UK13114121369114121369single base substitutionCTupstream_gene_variant
ESAD-UK13114124406114124406single base substitutionCTdownstream_gene_variant
ESAD-UK13114124406114124406single base substitutionCTintron_variant
ESAD-UK13114124686114124686insertion of <=200bp-TGCCATdownstream_gene_variant
ESAD-UK13114124686114124686insertion of <=200bp-TGCCATintron_variant
ESAD-UK13114125494114125494single base substitutionACdownstream_gene_variant
ESAD-UK13114125494114125494single base substitutionACintron_variant
ESAD-UK13114127078114127078single base substitutionGAdownstream_gene_variant
ESAD-UK13114127078114127078single base substitutionGAintron_variant
ESAD-UK13114127117114127117single base substitutionGAdownstream_gene_variant
ESAD-UK13114127117114127117single base substitutionGAintron_variant
ESAD-UK13114128449114128449single base substitutionCGdownstream_gene_variant
ESAD-UK13114128449114128449single base substitutionCGexon_variant
ESAD-UK13114128449114128449single base substitutionCGmissense_variantQ170H510G>C
ESAD-UK13114128449114128449single base substitutionCGmissense_variantQ37H111G>C
ESAD-UK13114130009114130009single base substitutionCTdownstream_gene_variant
ESAD-UK13114130009114130009single base substitutionCTintron_variant
ESAD-UK13114136550114136550single base substitutionCTdownstream_gene_variant
ESAD-UK13114136550114136550single base substitutionCTintron_variant
ESAD-UK13114136953114136953single base substitutionGAdownstream_gene_variant
ESAD-UK13114136953114136953single base substitutionGAintron_variant
ESAD-UK13114137669114137669single base substitutionACdownstream_gene_variant
ESAD-UK13114137669114137669single base substitutionACintron_variant
ESAD-UK13114139415114139415insertion of <=200bp-TAAATAACintron_variant
ESAD-UK13114139415114139415insertion of <=200bp-TAAATAACupstream_gene_variant
ESAD-UK13114140626114140626single base substitutionGAintron_variant
ESAD-UK13114140626114140626single base substitutionGAupstream_gene_variant
ESAD-UK13114143067114143067single base substitutionTCintron_variant
ESAD-UK13114143067114143067single base substitutionTCupstream_gene_variant
ESAD-UK13114143235114143235single base substitutionACintron_variant
ESAD-UK13114143235114143235single base substitutionACupstream_gene_variant
ESAD-UK13114145317114145317single base substitutionGTupstream_gene_variant
ESAD-UK13114145345114145345single base substitutionGAupstream_gene_variant
ESAD-UK13114145517114145517single base substitutionCTupstream_gene_variant
ESAD-UK13114146605114146605single base substitutionCTupstream_gene_variant
ESAD-UK13114147389114147389single base substitutionTAupstream_gene_variant
ESAD-UK13114149272114149272single base substitutionCTupstream_gene_variant
ESAD-UK13114149324114149324single base substitutionCTupstream_gene_variant
GBM-US13114107590114107590single base substitutionCTdownstream_gene_variant
KIRC-US13114107552114107552single base substitutionCGdownstream_gene_variant
KIRC-US13114149923114149923single base substitutionCGupstream_gene_variant
KIRC-US13114149939114149939single base substitutionGAupstream_gene_variant
LAML-KR13114124884114124884single base substitutionTCdownstream_gene_variant
LAML-KR13114124884114124884single base substitutionTCintron_variant
LAML-KR13114125175114125175single base substitutionACdownstream_gene_variant
LAML-KR13114125175114125175single base substitutionACintron_variant
LAML-KR13114125402114125402single base substitutionGAdownstream_gene_variant
LAML-KR13114125402114125402single base substitutionGAintron_variant
LAML-KR13114125540114125540single base substitutionGAdownstream_gene_variant
LAML-KR13114125540114125540single base substitutionGAintron_variant
LAML-KR13114125676114125676single base substitutionGAdownstream_gene_variant
LAML-KR13114125676114125676single base substitutionGAintron_variant
LAML-KR13114138487114138487single base substitutionTC5_prime_UTR_variant
LAML-KR13114138487114138487single base substitutionTCintron_variant
LAML-KR13114138487114138487single base substitutionTCupstream_gene_variant
LAML-KR13114149891114149891single base substitutionTCupstream_gene_variant
LICA-FR13114117551114117551single base substitutionCAintron_variant
LICA-FR13114117551114117551single base substitutionCAupstream_gene_variant
LICA-FR13114142804114142804single base substitutionTCintron_variant
LICA-FR13114142804114142804single base substitutionTCupstream_gene_variant
LIHC-US13114107605114107632deletion of <=200bpGCGAGAGTACGAGGTGGTCCAGGCCCCC-downstream_gene_variant
LINC-JP13114106976114106976single base substitutionGCdownstream_gene_variant
LINC-JP13114111090114111090single base substitutionCT3_prime_UTR_variant
LINC-JP13114111090114111090single base substitutionCTdownstream_gene_variant
LINC-JP13114113747114113747single base substitutionACdownstream_gene_variant
LINC-JP13114113747114113747single base substitutionACexon_variant
LINC-JP13114113747114113747single base substitutionACintron_variant
LINC-JP13114115265114115265single base substitutionATdownstream_gene_variant
LINC-JP13114115265114115265single base substitutionATintron_variant
LINC-JP13114115265114115265single base substitutionATupstream_gene_variant
LINC-JP13114115495114115495single base substitutionTAdownstream_gene_variant
LINC-JP13114115495114115495single base substitutionTAintron_variant
LINC-JP13114115495114115495single base substitutionTAupstream_gene_variant
LINC-JP13114117098114117098single base substitutionTC3_prime_UTR_variant
LINC-JP13114117098114117098single base substitutionTCdownstream_gene_variant
LINC-JP13114117098114117098single base substitutionTCexon_variant
LINC-JP13114117098114117098single base substitutionTCintron_variant
LINC-JP13114117098114117098single base substitutionTCupstream_gene_variant
LINC-JP13114144904114144904single base substitutionAGexon_variant
LINC-JP13114144904114144904single base substitutionAGintron_variant
LINC-JP13114144904114144904single base substitutionAGupstream_gene_variant
LINC-JP13114145743114145743single base substitutionGCupstream_gene_variant
LINC-JP13114150174114150174single base substitutionTCupstream_gene_variant
LIRI-JP13114105996114105996single base substitutionACdownstream_gene_variant
LIRI-JP13114110495114110495single base substitutionAT3_prime_UTR_variant
LIRI-JP13114110495114110495single base substitutionATdownstream_gene_variant
LIRI-JP13114111855114111855single base substitutionTG3_prime_UTR_variant
LIRI-JP13114111855114111855single base substitutionTGdownstream_gene_variant
LIRI-JP13114113705114113705single base substitutionTC3_prime_UTR_variant
LIRI-JP13114113705114113705single base substitutionTCdownstream_gene_variant
LIRI-JP13114113705114113705single base substitutionTCexon_variant
LIRI-JP13114113705114113705single base substitutionTCmissense_variantI208V622A>G
LIRI-JP13114113705114113705single base substitutionTCmissense_variantI75V223A>G
LIRI-JP13114113911114113911single base substitutionTCdownstream_gene_variant
LIRI-JP13114113911114113911single base substitutionTCintron_variant
LIRI-JP13114113911114113911single base substitutionTCupstream_gene_variant
LIRI-JP13114114152114114152single base substitutionCTdownstream_gene_variant
LIRI-JP13114114152114114152single base substitutionCTintron_variant
LIRI-JP13114114152114114152single base substitutionCTupstream_gene_variant
LIRI-JP13114114962114114962single base substitutionGCdownstream_gene_variant
LIRI-JP13114114962114114962single base substitutionGCintron_variant
LIRI-JP13114114962114114962single base substitutionGCupstream_gene_variant
LIRI-JP13114115194114115194single base substitutionCTdownstream_gene_variant
LIRI-JP13114115194114115194single base substitutionCTintron_variant
LIRI-JP13114115194114115194single base substitutionCTupstream_gene_variant
LIRI-JP13114115417114115417single base substitutionCT3_prime_UTR_variant
LIRI-JP13114115417114115417single base substitutionCTdownstream_gene_variant
LIRI-JP13114115417114115417single base substitutionCTexon_variant
LIRI-JP13114115417114115417single base substitutionCTsynonymous_variantV185V555G>A
LIRI-JP13114115417114115417single base substitutionCTsynonymous_variantV52V156G>A
LIRI-JP13114115417114115417single base substitutionCTupstream_gene_variant
LIRI-JP13114116060114116060single base substitutionTCdownstream_gene_variant
LIRI-JP13114116060114116060single base substitutionTCintron_variant
LIRI-JP13114116060114116060single base substitutionTCupstream_gene_variant
LIRI-JP13114116240114116243deletion of <=200bpAGCA-downstream_gene_variant
LIRI-JP13114116240114116243deletion of <=200bpAGCA-intron_variant
LIRI-JP13114116240114116243deletion of <=200bpAGCA-upstream_gene_variant
LIRI-JP13114119408114119408single base substitutionCTintron_variant
LIRI-JP13114119408114119408single base substitutionCTupstream_gene_variant
LIRI-JP13114120537114120537single base substitutionTGintron_variant
LIRI-JP13114120537114120537single base substitutionTGupstream_gene_variant
LIRI-JP13114122493114122493single base substitutionGAintron_variant
LIRI-JP13114123020114123020insertion of <=200bp-Aintron_variant
LIRI-JP13114130922114130922single base substitutionTCdownstream_gene_variant
LIRI-JP13114130922114130922single base substitutionTCintron_variant
LIRI-JP13114135253114135253single base substitutionGCdownstream_gene_variant
LIRI-JP13114135253114135253single base substitutionGCintron_variant
LIRI-JP13114136157114136157single base substitutionCGdownstream_gene_variant
LIRI-JP13114136157114136157single base substitutionCGintron_variant
LIRI-JP13114139053114139053insertion of <=200bp-Aintron_variant
LIRI-JP13114139053114139053insertion of <=200bp-Aupstream_gene_variant
LIRI-JP13114142512114142512single base substitutionGTintron_variant
LIRI-JP13114142512114142512single base substitutionGTupstream_gene_variant
LIRI-JP13114148176114148176single base substitutionCAupstream_gene_variant
LIRI-JP13114148629114148629single base substitutionCTupstream_gene_variant
LIRI-JP13114149431114149431single base substitutionAGupstream_gene_variant
LIRI-JP13114149674114149674single base substitutionAGupstream_gene_variant
LUSC-KR13114105776114105776single base substitutionCGdownstream_gene_variant
LUSC-KR13114112287114112287single base substitutionCA3_prime_UTR_variant
LUSC-KR13114112287114112287single base substitutionCAdownstream_gene_variant
LUSC-KR13114112287114112287single base substitutionCAexon_variant
LUSC-KR13114112387114112387single base substitutionTG3_prime_UTR_variant
LUSC-KR13114112387114112387single base substitutionTGdownstream_gene_variant
LUSC-KR13114112387114112387single base substitutionTGexon_variant
LUSC-KR13114112387114112387single base substitutionTGmissense_variantY113S338A>C
LUSC-KR13114112387114112387single base substitutionTGmissense_variantY246S737A>C
LUSC-KR13114114420114114420single base substitutionCTdownstream_gene_variant
LUSC-KR13114114420114114420single base substitutionCTintron_variant
LUSC-KR13114114420114114420single base substitutionCTupstream_gene_variant
LUSC-KR13114119951114119951single base substitutionCGintron_variant
LUSC-KR13114119951114119951single base substitutionCGupstream_gene_variant
LUSC-KR13114123925114123925single base substitutionGAdownstream_gene_variant
LUSC-KR13114123925114123925single base substitutionGAintron_variant
LUSC-KR13114125185114125185single base substitutionAGdownstream_gene_variant
LUSC-KR13114125185114125185single base substitutionAGintron_variant
LUSC-KR13114125242114125242single base substitutionGAdownstream_gene_variant
LUSC-KR13114125242114125242single base substitutionGAintron_variant
LUSC-KR13114135015114135015single base substitutionCTdownstream_gene_variant
LUSC-KR13114135015114135015single base substitutionCTexon_variant
LUSC-KR13114135015114135015single base substitutionCTintron_variant
LUSC-KR13114135015114135015single base substitutionCTsynonymous_variantQ63Q189G>A
LUSC-KR13114135015114135015single base substitutionCTsynonymous_variantQ73Q219G>A
LUSC-KR13114135015114135015single base substitutionCTsynonymous_variantQ88Q264G>A
LUSC-KR13114142336114142336single base substitutionCGintron_variant
LUSC-KR13114142336114142336single base substitutionCGupstream_gene_variant
LUSC-KR13114142688114142688single base substitutionCTintron_variant
LUSC-KR13114142688114142688single base substitutionCTupstream_gene_variant
LUSC-KR13114147932114147932single base substitutionGCupstream_gene_variant
LUSC-US13114107615114107615single base substitutionGAdownstream_gene_variant
LUSC-US13114112392114112392single base substitutionTC3_prime_UTR_variant
LUSC-US13114112392114112392single base substitutionTCdownstream_gene_variant
LUSC-US13114112392114112392single base substitutionTCexon_variant
LUSC-US13114112392114112392single base substitutionTCsynonymous_variantV111V333A>G
LUSC-US13114112392114112392single base substitutionTCsynonymous_variantV244V732A>G
LUSC-US13114138238114138238single base substitutionTCdownstream_gene_variant
LUSC-US13114138238114138238single base substitutionTCexon_variant
LUSC-US13114138238114138238single base substitutionTCintron_variant
LUSC-US13114138238114138238single base substitutionTCmissense_variantQ31R92A>G
LUSC-US13114138238114138238single base substitutionTCmissense_variantQ46R137A>G
MALY-DE13114118211114118211single base substitutionGAintron_variant
MALY-DE13114118211114118211single base substitutionGAupstream_gene_variant
MALY-DE13114120197114120197single base substitutionGTintron_variant
MALY-DE13114120197114120197single base substitutionGTupstream_gene_variant
MALY-DE13114133796114133796single base substitutionCTdownstream_gene_variant
MALY-DE13114133796114133796single base substitutionCTintron_variant
MALY-DE13114139393114139393insertion of <=200bp-AATAAATAintron_variant
MALY-DE13114139393114139393insertion of <=200bp-AATAAATAupstream_gene_variant
MALY-DE13114139393114139393insertion of <=200bp-AATAintron_variant
MALY-DE13114139393114139393insertion of <=200bp-AATAupstream_gene_variant
MALY-DE13114148721114148721single base substitutionTGupstream_gene_variant
MELA-AU13114105189114105189single base substitutionGAdownstream_gene_variant
MELA-AU13114105258114105258single base substitutionGAdownstream_gene_variant
MELA-AU13114105361114105361single base substitutionTCdownstream_gene_variant
MELA-AU13114105363114105363single base substitutionCTdownstream_gene_variant
MELA-AU13114106681114106689deletion of <=200bpACAGAACTA-downstream_gene_variant
MELA-AU13114106813114106813single base substitutionGAdownstream_gene_variant
MELA-AU13114106919114106919single base substitutionGAdownstream_gene_variant
MELA-AU13114107026114107026single base substitutionGAdownstream_gene_variant
MELA-AU13114107194114107194single base substitutionCTdownstream_gene_variant
MELA-AU13114107380114107380single base substitutionGAdownstream_gene_variant
MELA-AU13114107464114107464single base substitutionGCdownstream_gene_variant
MELA-AU13114107749114107749single base substitutionCTdownstream_gene_variant
MELA-AU13114107989114107989single base substitutionGAdownstream_gene_variant
MELA-AU13114108635114108635single base substitutionGAdownstream_gene_variant
MELA-AU13114109034114109034single base substitutionGAdownstream_gene_variant
MELA-AU13114109361114109361single base substitutionGAdownstream_gene_variant
MELA-AU13114110276114110276single base substitutionCT3_prime_UTR_variant
MELA-AU13114110276114110276single base substitutionCTdownstream_gene_variant
MELA-AU13114111202114111202single base substitutionGT3_prime_UTR_variant
MELA-AU13114111202114111202single base substitutionGTdownstream_gene_variant
MELA-AU13114112430114112430single base substitutionGAdownstream_gene_variant
MELA-AU13114112430114112430single base substitutionGAintron_variant
MELA-AU13114112789114112789single base substitutionCTdownstream_gene_variant
MELA-AU13114112789114112789single base substitutionCTintron_variant
MELA-AU13114112813114112814multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU13114112813114112814multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU13114114413114114413single base substitutionGAdownstream_gene_variant
MELA-AU13114114413114114413single base substitutionGAintron_variant
MELA-AU13114114413114114413single base substitutionGAupstream_gene_variant
MELA-AU13114114644114114644single base substitutionGAdownstream_gene_variant
MELA-AU13114114644114114644single base substitutionGAintron_variant
MELA-AU13114114644114114644single base substitutionGAupstream_gene_variant
MELA-AU13114115155114115155single base substitutionGAdownstream_gene_variant
MELA-AU13114115155114115155single base substitutionGAintron_variant
MELA-AU13114115155114115155single base substitutionGAupstream_gene_variant
MELA-AU13114115250114115250single base substitutionGAdownstream_gene_variant
MELA-AU13114115250114115250single base substitutionGAintron_variant
MELA-AU13114115250114115250single base substitutionGAupstream_gene_variant
MELA-AU13114115637114115638multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU13114115637114115638multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU13114115637114115638multiple base substitution (>=2bp and <=200bp)GGAAupstream_gene_variant
MELA-AU13114115741114115741single base substitutionGAdownstream_gene_variant
MELA-AU13114115741114115741single base substitutionGAintron_variant
MELA-AU13114115741114115741single base substitutionGAupstream_gene_variant
MELA-AU13114115799114115799single base substitutionATdownstream_gene_variant
MELA-AU13114115799114115799single base substitutionATintron_variant
MELA-AU13114115799114115799single base substitutionATupstream_gene_variant
MELA-AU13114116077114116077single base substitutionGAdownstream_gene_variant
MELA-AU13114116077114116077single base substitutionGAintron_variant
MELA-AU13114116077114116077single base substitutionGAupstream_gene_variant
MELA-AU13114116216114116216single base substitutionGAdownstream_gene_variant
MELA-AU13114116216114116216single base substitutionGAintron_variant
MELA-AU13114116216114116216single base substitutionGAupstream_gene_variant
MELA-AU13114116543114116543single base substitutionGAdownstream_gene_variant
MELA-AU13114116543114116543single base substitutionGAintron_variant
MELA-AU13114116543114116543single base substitutionGAupstream_gene_variant
MELA-AU13114116849114116849single base substitutionATdownstream_gene_variant
MELA-AU13114116849114116849single base substitutionATintron_variant
MELA-AU13114116849114116849single base substitutionATupstream_gene_variant
MELA-AU13114116872114116872single base substitutionGAdownstream_gene_variant
MELA-AU13114116872114116872single base substitutionGAintron_variant
MELA-AU13114116872114116872single base substitutionGAupstream_gene_variant
MELA-AU13114116938114116938single base substitutionCAdownstream_gene_variant
MELA-AU13114116938114116938single base substitutionCAintron_variant
MELA-AU13114116938114116938single base substitutionCAupstream_gene_variant
MELA-AU13114117034114117034single base substitutionGAdownstream_gene_variant
MELA-AU13114117034114117034single base substitutionGAintron_variant
MELA-AU13114117034114117034single base substitutionGAupstream_gene_variant
MELA-AU13114118094114118094single base substitutionCGintron_variant
MELA-AU13114118094114118094single base substitutionCGupstream_gene_variant
MELA-AU13114119936114119936single base substitutionGAintron_variant
MELA-AU13114119936114119936single base substitutionGAupstream_gene_variant
MELA-AU13114120146114120146single base substitutionTAintron_variant
MELA-AU13114120146114120146single base substitutionTAupstream_gene_variant
MELA-AU13114120252114120252single base substitutionGAintron_variant
MELA-AU13114120252114120252single base substitutionGAupstream_gene_variant
MELA-AU13114120880114120881multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU13114120880114120881multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
MELA-AU13114120890114120890single base substitutionGAintron_variant
MELA-AU13114120890114120890single base substitutionGAupstream_gene_variant
MELA-AU13114120946114120946single base substitutionCTintron_variant
MELA-AU13114120946114120946single base substitutionCTupstream_gene_variant
MELA-AU13114121185114121185single base substitutionGAintron_variant
MELA-AU13114121185114121185single base substitutionGAupstream_gene_variant
MELA-AU13114121998114121998single base substitutionTAintron_variant
MELA-AU13114121998114121998single base substitutionTAupstream_gene_variant
MELA-AU13114122467114122467single base substitutionGAintron_variant
MELA-AU13114122480114122480single base substitutionGAintron_variant
MELA-AU13114122539114122539single base substitutionGAintron_variant
MELA-AU13114122867114122867single base substitutionGAintron_variant
MELA-AU13114123365114123365single base substitutionGAintron_variant
MELA-AU13114123514114123514single base substitutionGAdownstream_gene_variant
MELA-AU13114123514114123514single base substitutionGAintron_variant
MELA-AU13114123755114123755single base substitutionGAdownstream_gene_variant
MELA-AU13114123755114123755single base substitutionGAintron_variant
MELA-AU13114123837114123837single base substitutionATdownstream_gene_variant
MELA-AU13114123837114123837single base substitutionATintron_variant
MELA-AU13114124154114124154single base substitutionGAdownstream_gene_variant
MELA-AU13114124154114124154single base substitutionGAintron_variant
MELA-AU13114124363114124363single base substitutionATdownstream_gene_variant
MELA-AU13114124363114124363single base substitutionATintron_variant
MELA-AU13114125304114125304single base substitutionGAdownstream_gene_variant
MELA-AU13114125304114125304single base substitutionGAintron_variant
MELA-AU13114125708114125708single base substitutionACdownstream_gene_variant
MELA-AU13114125708114125708single base substitutionACintron_variant
MELA-AU13114126443114126443single base substitutionGAdownstream_gene_variant
MELA-AU13114126443114126443single base substitutionGAintron_variant
MELA-AU13114126678114126678single base substitutionGAdownstream_gene_variant
MELA-AU13114126678114126678single base substitutionGAintron_variant
MELA-AU13114126845114126845single base substitutionGAdownstream_gene_variant
MELA-AU13114126845114126845single base substitutionGAintron_variant
MELA-AU13114126921114126921single base substitutionGAdownstream_gene_variant
MELA-AU13114126921114126921single base substitutionGAintron_variant
MELA-AU13114127586114127586single base substitutionCTdownstream_gene_variant
MELA-AU13114127586114127586single base substitutionCTintron_variant
MELA-AU13114127592114127592single base substitutionGAdownstream_gene_variant
MELA-AU13114127592114127592single base substitutionGAintron_variant
MELA-AU13114127796114127796single base substitutionAGdownstream_gene_variant
MELA-AU13114127796114127796single base substitutionAGintron_variant
MELA-AU13114128228114128228single base substitutionGAdownstream_gene_variant
MELA-AU13114128228114128228single base substitutionGAintron_variant
MELA-AU13114128991114128991single base substitutionGAintron_variant
MELA-AU13114129658114129658single base substitutionCAintron_variant
MELA-AU13114129953114129953single base substitutionGAdownstream_gene_variant
MELA-AU13114129953114129953single base substitutionGAintron_variant
MELA-AU13114130897114130897single base substitutionAGdownstream_gene_variant
MELA-AU13114130897114130897single base substitutionAGintron_variant
MELA-AU13114131954114131954single base substitutionCAdownstream_gene_variant
MELA-AU13114131954114131954single base substitutionCAintron_variant
MELA-AU13114132044114132044single base substitutionACdownstream_gene_variant
MELA-AU13114132044114132044single base substitutionACintron_variant
MELA-AU13114132436114132436single base substitutionGAdownstream_gene_variant
MELA-AU13114132436114132436single base substitutionGAintron_variant
MELA-AU13114132888114132888single base substitutionCTdownstream_gene_variant
MELA-AU13114132888114132888single base substitutionCTintron_variant
MELA-AU13114133202114133202single base substitutionATdownstream_gene_variant
MELA-AU13114133202114133202single base substitutionATintron_variant
MELA-AU13114133243114133243single base substitutionGAdownstream_gene_variant
MELA-AU13114133243114133243single base substitutionGAintron_variant
MELA-AU13114133347114133348multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU13114133347114133348multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU13114133627114133627single base substitutionATdownstream_gene_variant
MELA-AU13114133627114133627single base substitutionATintron_variant
MELA-AU13114134265114134265single base substitutionGAdownstream_gene_variant
MELA-AU13114134265114134265single base substitutionGAintron_variant
MELA-AU13114134691114134691single base substitutionGAdownstream_gene_variant
MELA-AU13114134691114134691single base substitutionGAintron_variant
MELA-AU13114134730114134730single base substitutionCAdownstream_gene_variant
MELA-AU13114134730114134730single base substitutionCAintron_variant
MELA-AU13114134951114134951single base substitutionTAdownstream_gene_variant
MELA-AU13114134951114134951single base substitutionTAexon_variant
MELA-AU13114134951114134951single base substitutionTAintron_variant
MELA-AU13114134951114134951single base substitutionTAmissense_variantR110W328A>T
MELA-AU13114134951114134951single base substitutionTAmissense_variantR85W253A>T
MELA-AU13114134951114134951single base substitutionTAmissense_variantR95W283A>T
MELA-AU13114135190114135190single base substitutionGAdownstream_gene_variant
MELA-AU13114135190114135190single base substitutionGAintron_variant
MELA-AU13114135281114135281single base substitutionGAdownstream_gene_variant
MELA-AU13114135281114135281single base substitutionGAintron_variant
MELA-AU13114136261114136261single base substitutionGAdownstream_gene_variant
MELA-AU13114136261114136261single base substitutionGAintron_variant
MELA-AU13114136442114136442single base substitutionTGdownstream_gene_variant
MELA-AU13114136442114136442single base substitutionTGintron_variant
MELA-AU13114136445114136445single base substitutionTAdownstream_gene_variant
MELA-AU13114136445114136445single base substitutionTAintron_variant
MELA-AU13114136849114136849single base substitutionAGdownstream_gene_variant
MELA-AU13114136849114136849single base substitutionAGintron_variant
MELA-AU13114138783114138783single base substitutionGAintron_variant
MELA-AU13114138783114138783single base substitutionGAupstream_gene_variant
MELA-AU13114139347114139347single base substitutionCTintron_variant
MELA-AU13114139347114139347single base substitutionCTupstream_gene_variant
MELA-AU13114139419114139419single base substitutionTCintron_variant
MELA-AU13114139419114139419single base substitutionTCupstream_gene_variant
MELA-AU13114139658114139658single base substitutionAGintron_variant
MELA-AU13114139658114139658single base substitutionAGupstream_gene_variant
MELA-AU13114140119114140119single base substitutionCTintron_variant
MELA-AU13114140119114140119single base substitutionCTupstream_gene_variant
MELA-AU13114141545114141545single base substitutionGAintron_variant
MELA-AU13114141545114141545single base substitutionGAupstream_gene_variant
MELA-AU13114141903114141903single base substitutionGAintron_variant
MELA-AU13114141903114141903single base substitutionGAupstream_gene_variant
MELA-AU13114141935114141935single base substitutionGAintron_variant
MELA-AU13114141935114141935single base substitutionGAupstream_gene_variant
MELA-AU13114142575114142575single base substitutionCAintron_variant
MELA-AU13114142575114142575single base substitutionCAupstream_gene_variant
MELA-AU13114143647114143647single base substitutionCTintron_variant
MELA-AU13114145737114145737single base substitutionCTupstream_gene_variant
MELA-AU13114146014114146014single base substitutionCTupstream_gene_variant
MELA-AU13114147299114147299single base substitutionTCupstream_gene_variant
MELA-AU13114147423114147423single base substitutionCTupstream_gene_variant
MELA-AU13114147927114147927single base substitutionGTupstream_gene_variant
MELA-AU13114148014114148014single base substitutionCTupstream_gene_variant
MELA-AU13114148936114148936single base substitutionATupstream_gene_variant
MELA-AU13114149427114149427single base substitutionCTupstream_gene_variant
MELA-AU13114149553114149553deletion of <=200bpA-upstream_gene_variant
MELA-AU13114149937114149937single base substitutionCTupstream_gene_variant
MELA-AU13114150223114150223single base substitutionCTupstream_gene_variant
ORCA-IN13114137861114137861single base substitutionCTdownstream_gene_variant
ORCA-IN13114137861114137861single base substitutionCTintron_variant
OV-AU13114109449114109449single base substitutionCTdownstream_gene_variant
OV-AU13114113406114113406single base substitutionCTdownstream_gene_variant
OV-AU13114113406114113406single base substitutionCTintron_variant
OV-AU13114118022114118022single base substitutionGCintron_variant
OV-AU13114118022114118022single base substitutionGCupstream_gene_variant
OV-AU13114120016114120016single base substitutionCGintron_variant
OV-AU13114120016114120016single base substitutionCGupstream_gene_variant
OV-AU13114125256114125256single base substitutionACdownstream_gene_variant
OV-AU13114125256114125256single base substitutionACintron_variant
OV-AU13114127624114127624single base substitutionCAdownstream_gene_variant
OV-AU13114127624114127624single base substitutionCAintron_variant
OV-AU13114127625114127625single base substitutionAGdownstream_gene_variant
OV-AU13114127625114127625single base substitutionAGintron_variant
PACA-AU13114108537114108537single base substitutionTCdownstream_gene_variant
PACA-AU13114109278114109281deletion of <=200bpAAAC-downstream_gene_variant
PACA-AU13114110325114110325single base substitutionGC3_prime_UTR_variant
PACA-AU13114110325114110325single base substitutionGCdownstream_gene_variant
PACA-AU13114111202114111202single base substitutionGT3_prime_UTR_variant
PACA-AU13114111202114111202single base substitutionGTdownstream_gene_variant
PACA-AU13114114377114114377single base substitutionGAdownstream_gene_variant
PACA-AU13114114377114114377single base substitutionGAintron_variant
PACA-AU13114114377114114377single base substitutionGAupstream_gene_variant
PACA-AU13114117417114117417single base substitutionCGintron_variant
PACA-AU13114117417114117417single base substitutionCGupstream_gene_variant
PACA-AU13114125395114125395single base substitutionGAdownstream_gene_variant
PACA-AU13114125395114125395single base substitutionGAintron_variant
PACA-AU13114148881114148881single base substitutionTCupstream_gene_variant
PACA-CA13114108029114108029single base substitutionGAdownstream_gene_variant
PACA-CA13114108050114108050single base substitutionCGdownstream_gene_variant
PACA-CA13114112897114112897single base substitutionGAdownstream_gene_variant
PACA-CA13114112897114112897single base substitutionGAintron_variant
PACA-CA13114114387114114387single base substitutionTGdownstream_gene_variant
PACA-CA13114114387114114387single base substitutionTGintron_variant
PACA-CA13114114387114114387single base substitutionTGupstream_gene_variant
PACA-CA13114120197114120197single base substitutionGTintron_variant
PACA-CA13114120197114120197single base substitutionGTupstream_gene_variant
PACA-CA13114121415114121415single base substitutionGAintron_variant
PACA-CA13114121415114121415single base substitutionGAupstream_gene_variant
PACA-CA13114123366114123366single base substitutionGCintron_variant
PACA-CA13114125032114125032single base substitutionTGdownstream_gene_variant
PACA-CA13114125032114125032single base substitutionTGintron_variant
PACA-CA13114125175114125175single base substitutionACdownstream_gene_variant
PACA-CA13114125175114125175single base substitutionACintron_variant
PACA-CA13114125197114125197single base substitutionACdownstream_gene_variant
PACA-CA13114125197114125197single base substitutionACintron_variant
PACA-CA13114125402114125402single base substitutionGAdownstream_gene_variant
PACA-CA13114125402114125402single base substitutionGAintron_variant
PACA-CA13114125426114125426single base substitutionGCdownstream_gene_variant
PACA-CA13114125426114125426single base substitutionGCintron_variant
PACA-CA13114130632114130632single base substitutionCTdownstream_gene_variant
PACA-CA13114130632114130632single base substitutionCTintron_variant
PACA-CA13114134868114134868deletion of <=200bpA-downstream_gene_variant
PACA-CA13114134868114134868deletion of <=200bpA-exon_variant
PACA-CA13114134868114134868deletion of <=200bpA-intron_variant
PACA-CA13114136192114136192single base substitutionAGdownstream_gene_variant
PACA-CA13114136192114136192single base substitutionAGintron_variant
PACA-CA13114136302114136302insertion of <=200bp-Adownstream_gene_variant
PACA-CA13114136302114136302insertion of <=200bp-Aintron_variant
PACA-CA13114138106114138106single base substitutionCTdownstream_gene_variant
PACA-CA13114138106114138106single base substitutionCTintron_variant
PACA-CA13114139984114139984single base substitutionGTintron_variant
PACA-CA13114139984114139984single base substitutionGTupstream_gene_variant
PACA-CA13114140488114140488single base substitutionAGintron_variant
PACA-CA13114140488114140488single base substitutionAGupstream_gene_variant
PACA-CA13114140851114140851single base substitutionGAintron_variant
PACA-CA13114140851114140851single base substitutionGAupstream_gene_variant
PACA-CA13114141086114141086single base substitutionGAintron_variant
PACA-CA13114141086114141086single base substitutionGAupstream_gene_variant
PACA-CA13114143767114143767single base substitutionCGintron_variant
PACA-CA13114147329114147329single base substitutionTCupstream_gene_variant
PACA-CA13114149500114149500single base substitutionATupstream_gene_variant
PACA-CA13114149732114149733deletion of <=200bpCA-upstream_gene_variant
PACA-CA13114149983114149983single base substitutionGAupstream_gene_variant
PAEN-AU13114109805114109805single base substitutionCTdownstream_gene_variant
PAEN-AU13114135213114135213single base substitutionGTdownstream_gene_variant
PAEN-AU13114135213114135213single base substitutionGTintron_variant
PAEN-IT13114124879114124879single base substitutionGAdownstream_gene_variant
PAEN-IT13114124879114124879single base substitutionGAintron_variant
PBCA-DE13114115195114115195single base substitutionGAdownstream_gene_variant
PBCA-DE13114115195114115195single base substitutionGAintron_variant
PBCA-DE13114115195114115195single base substitutionGAupstream_gene_variant
PBCA-DE13114120197114120197single base substitutionGTintron_variant
PBCA-DE13114120197114120197single base substitutionGTupstream_gene_variant
PBCA-DE13114124977114124977single base substitutionGAdownstream_gene_variant
PBCA-DE13114124977114124977single base substitutionGAintron_variant
PBCA-DE13114125032114125032single base substitutionTGdownstream_gene_variant
PBCA-DE13114125032114125032single base substitutionTGintron_variant
PBCA-DE13114125185114125185single base substitutionAGdownstream_gene_variant
PBCA-DE13114125185114125185single base substitutionAGintron_variant
PBCA-DE13114125242114125242single base substitutionGAdownstream_gene_variant
PBCA-DE13114125242114125242single base substitutionGAintron_variant
PBCA-DE13114125297114125297single base substitutionTCdownstream_gene_variant
PBCA-DE13114125297114125297single base substitutionTCintron_variant
PBCA-DE13114125402114125402single base substitutionGAdownstream_gene_variant
PBCA-DE13114125402114125402single base substitutionGAintron_variant
PBCA-DE13114141390114141390insertion of <=200bp-GTAintron_variant
PBCA-DE13114141390114141390insertion of <=200bp-GTAupstream_gene_variant
PBCA-DE13114148971114148972deletion of <=200bpAT-upstream_gene_variant
PRAD-CA13114112787114112787single base substitutionCGdownstream_gene_variant
PRAD-CA13114112787114112787single base substitutionCGintron_variant
PRAD-CA13114122086114122086single base substitutionCTintron_variant
PRAD-CA13114122086114122086single base substitutionCTupstream_gene_variant
PRAD-CA13114125297114125297single base substitutionTCdownstream_gene_variant
PRAD-CA13114125297114125297single base substitutionTCintron_variant
PRAD-CA13114125568114125568single base substitutionTCdownstream_gene_variant
PRAD-CA13114125568114125568single base substitutionTCintron_variant
PRAD-CA13114125613114125613single base substitutionACdownstream_gene_variant
PRAD-CA13114125613114125613single base substitutionACintron_variant
PRAD-CA13114125656114125656single base substitutionTCdownstream_gene_variant
PRAD-CA13114125656114125656single base substitutionTCintron_variant
PRAD-CA13114138565114138565single base substitutionCAintron_variant
PRAD-CA13114138565114138565single base substitutionCAupstream_gene_variant
PRAD-UK13114119135114119135single base substitutionCTintron_variant
PRAD-UK13114119135114119135single base substitutionCTupstream_gene_variant
PRAD-UK13114120824114120824single base substitutionTCintron_variant
PRAD-UK13114120824114120824single base substitutionTCupstream_gene_variant
READ-US13114115432114115432single base substitutionCG3_prime_UTR_variant
READ-US13114115432114115432single base substitutionCGdownstream_gene_variant
READ-US13114115432114115432single base substitutionCGexon_variant
READ-US13114115432114115432single base substitutionCGsynonymous_variantA180A540G>C
READ-US13114115432114115432single base substitutionCGsynonymous_variantA47A141G>C
READ-US13114115432114115432single base substitutionCGupstream_gene_variant
READ-US13114138283114138283single base substitutionGAexon_variant
READ-US13114138283114138283single base substitutionGAintron_variant
READ-US13114138283114138283single base substitutionGAmissense_variantT16M47C>T
READ-US13114138283114138283single base substitutionGAmissense_variantT31M92C>T
RECA-EU13114110528114110528single base substitutionAT3_prime_UTR_variant
RECA-EU13114110528114110528single base substitutionATdownstream_gene_variant
RECA-EU13114123351114123351single base substitutionGAintron_variant
RECA-EU13114129395114129395single base substitutionATintron_variant
RECA-EU13114129396114129396single base substitutionAGintron_variant
RECA-EU13114141859114141859single base substitutionCTintron_variant
RECA-EU13114141859114141859single base substitutionCTupstream_gene_variant
SKCA-BR13114108122114108151deletion of <=200bpAGGCGTGCCTGTCACTGCCGCCCGCTGCGG-downstream_gene_variant
SKCA-BR13114109096114109096single base substitutionGAdownstream_gene_variant
SKCA-BR13114109193114109193single base substitutionTAdownstream_gene_variant
SKCA-BR13114109763114109763single base substitutionTGdownstream_gene_variant
SKCA-BR13114112430114112430single base substitutionGAdownstream_gene_variant
SKCA-BR13114112430114112430single base substitutionGAintron_variant
SKCA-BR13114114534114114534single base substitutionACdownstream_gene_variant
SKCA-BR13114114534114114534single base substitutionACintron_variant
SKCA-BR13114114534114114534single base substitutionACupstream_gene_variant
SKCA-BR13114115066114115066single base substitutionGAdownstream_gene_variant
SKCA-BR13114115066114115066single base substitutionGAintron_variant
SKCA-BR13114115066114115066single base substitutionGAupstream_gene_variant
SKCA-BR13114116393114116393single base substitutionCAdownstream_gene_variant
SKCA-BR13114116393114116393single base substitutionCAintron_variant
SKCA-BR13114116393114116393single base substitutionCAupstream_gene_variant
SKCA-BR13114116461114116461single base substitutionGAdownstream_gene_variant
SKCA-BR13114116461114116461single base substitutionGAintron_variant
SKCA-BR13114116461114116461single base substitutionGAupstream_gene_variant
SKCA-BR13114120521114120521single base substitutionGAintron_variant
SKCA-BR13114120521114120521single base substitutionGAupstream_gene_variant
SKCA-BR13114121896114121896single base substitutionGAintron_variant
SKCA-BR13114121896114121896single base substitutionGAupstream_gene_variant
SKCA-BR13114122511114122511single base substitutionGAintron_variant
SKCA-BR13114122691114122691single base substitutionGAintron_variant
SKCA-BR13114124977114124977single base substitutionGAdownstream_gene_variant
SKCA-BR13114124977114124977single base substitutionGAintron_variant
SKCA-BR13114125185114125185single base substitutionAGdownstream_gene_variant
SKCA-BR13114125185114125185single base substitutionAGintron_variant
SKCA-BR13114125191114125191single base substitutionGAdownstream_gene_variant
SKCA-BR13114125191114125191single base substitutionGAintron_variant
SKCA-BR13114125494114125494single base substitutionACdownstream_gene_variant
SKCA-BR13114125494114125494single base substitutionACintron_variant
SKCA-BR13114125540114125540single base substitutionGAdownstream_gene_variant
SKCA-BR13114125540114125540single base substitutionGAintron_variant
SKCA-BR13114125656114125656single base substitutionTCdownstream_gene_variant
SKCA-BR13114125656114125656single base substitutionTCintron_variant
SKCA-BR13114126886114126886single base substitutionGAdownstream_gene_variant
SKCA-BR13114126886114126886single base substitutionGAintron_variant
SKCA-BR13114128417114128417single base substitutionCTdownstream_gene_variant
SKCA-BR13114128417114128417single base substitutionCTintron_variant
SKCA-BR13114131704114131704single base substitutionGAdownstream_gene_variant
SKCA-BR13114131704114131704single base substitutionGAintron_variant
SKCA-BR13114131934114131934single base substitutionCAdownstream_gene_variant
SKCA-BR13114131934114131934single base substitutionCAintron_variant
SKCA-BR13114136196114136196single base substitutionGAdownstream_gene_variant
SKCA-BR13114136196114136196single base substitutionGAintron_variant
SKCA-BR13114139392114139392insertion of <=200bp-CAATAintron_variant
SKCA-BR13114139392114139392insertion of <=200bp-CAATAupstream_gene_variant
SKCA-BR13114139392114139396deletion of <=200bpCAATA-intron_variant
SKCA-BR13114139392114139396deletion of <=200bpCAATA-upstream_gene_variant
SKCA-BR13114139392114139404deletion of <=200bpCAATAAATAAATA-intron_variant
SKCA-BR13114139392114139404deletion of <=200bpCAATAAATAAATA-upstream_gene_variant
SKCA-BR13114145402114145402insertion of <=200bp-ACTCCCGGCupstream_gene_variant
SKCA-BR13114145908114145908single base substitutionTCupstream_gene_variant
SKCA-BR13114146337114146337single base substitutionTGupstream_gene_variant
SKCA-BR13114146385114146385single base substitutionTGupstream_gene_variant
SKCM-US13114107626114107626single base substitutionGAdownstream_gene_variant
SKCM-US13114107681114107681single base substitutionCTdownstream_gene_variant
SKCM-US13114150193114150193single base substitutionCTupstream_gene_variant
STAD-US13114107633114107633single base substitutionGTdownstream_gene_variant
STAD-US13114115385114115385single base substitutionCA3_prime_UTR_variant
STAD-US13114115385114115385single base substitutionCAdownstream_gene_variant
STAD-US13114115385114115385single base substitutionCAexon_variant
STAD-US13114115385114115385single base substitutionCAmissense_variantW196L587G>T
STAD-US13114115385114115385single base substitutionCAmissense_variantW63L188G>T
STAD-US13114115385114115385single base substitutionCAupstream_gene_variant
STAD-US13114150047114150047single base substitutionCTupstream_gene_variant
THCA-SA13114110362114110362single base substitutionGT3_prime_UTR_variant
THCA-SA13114110362114110362single base substitutionGTdownstream_gene_variant
THCA-SA13114115389114115389single base substitutionGC3_prime_UTR_variant
THCA-SA13114115389114115389single base substitutionGCdownstream_gene_variant
THCA-SA13114115389114115389single base substitutionGCexon_variant
THCA-SA13114115389114115389single base substitutionGCmissense_variantL195V583C>G
THCA-SA13114115389114115389single base substitutionGCmissense_variantL62V184C>G
THCA-SA13114115389114115389single base substitutionGCupstream_gene_variant
THCA-SA13114144994114144994single base substitutionGT5_prime_UTR_variant
THCA-SA13114144994114144994single base substitutionGTmissense_variantR45S133C>A
THCA-SA13114144994114144994single base substitutionGTupstream_gene_variant
UCEC-US13114107655114107655single base substitutionAGdownstream_gene_variant
UCEC-US13114107711114107711single base substitutionGAdownstream_gene_variant
UCEC-US13114128488114128488single base substitutionACdownstream_gene_variant
UCEC-US13114128488114128488single base substitutionACexon_variant
UCEC-US13114128488114128488single base substitutionACmissense_variantF157L471T>G
UCEC-US13114128488114128488single base substitutionACmissense_variantF24L72T>G
UCEC-US13114128506114128506single base substitutionTCdownstream_gene_variant
UCEC-US13114128506114128506single base substitutionTCexon_variant
UCEC-US13114128506114128506single base substitutionTCsynonymous_variantT151T453A>G
UCEC-US13114128506114128506single base substitutionTCsynonymous_variantT18T54A>G
UCEC-US13114128539114128539single base substitutionAGexon_variant
UCEC-US13114128539114128539single base substitutionAGsynonymous_variantL115L345T>C
UCEC-US13114128539114128539single base substitutionAGsynonymous_variantL125L375T>C
UCEC-US13114128539114128539single base substitutionAGsynonymous_variantL140L420T>C
UCEC-US13114128539114128539single base substitutionAGsynonymous_variantL7L21T>C
UCEC-US13114128570114128570single base substitutionCAsplice_acceptor_variant
UCEC-US13114134962114134962single base substitutionGAdownstream_gene_variant
UCEC-US13114134962114134962single base substitutionGAexon_variant
UCEC-US13114134962114134962single base substitutionGAintron_variant
UCEC-US13114134962114134962single base substitutionGAmissense_variantA106V317C>T
UCEC-US13114134962114134962single base substitutionGAmissense_variantA81V242C>T
UCEC-US13114134962114134962single base substitutionGAmissense_variantA91V272C>T
UCEC-US13114138211114138211single base substitutionGAdownstream_gene_variant
UCEC-US13114138211114138211single base substitutionGAexon_variant
UCEC-US13114138211114138211single base substitutionGAintron_variant
UCEC-US13114138211114138211single base substitutionGAmissense_variantS40F119C>T
UCEC-US13114138211114138211single base substitutionGAmissense_variantS55F164C>T
UCEC-US13114149930114149930single base substitutionCTupstream_gene_variant
UCEC-US13114149957114149957single base substitutionCTupstream_gene_variant
UCEC-US13114150081114150081single base substitutionGAupstream_gene_variant
UCEC-US13114150160114150160single base substitutionGTupstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
TCGA-BM-6198-01COSM3417393c.540G>Cp.A180ASubstitution - coding silent13:113461117-113461117-
CSCC-16-TCOSM4544427c.356G>Cp.R119TSubstitution - Missense13:113480608-113480608-
CHEWS002COSM3417394c.92C>Tp.T31MSubstitution - Missense13:113483968-113483968-
H1155COSM1195792c.539C>Tp.A180VSubstitution - Missense13:113461118-113461118-
TCGA-AX-A0J1-01COSM945608c.164C>Tp.S55FSubstitution - Missense13:113483896-113483896-
TCGA-B6-A0RO-01COSM432158c.149C>Tp.S50LSubstitution - Missense13:113483911-113483911-
TCGA-34-5927-01COSM695928c.732A>Gp.V244VSubstitution - coding silent13:113458077-113458077-
8COSM4166805c.122C>Tp.T41MSubstitution - Missense13:113483938-113483938-
J87_TCOSM3955418c.737A>Cp.Y246SSubstitution - Missense13:113458072-113458072-
TCGA-D1-A177-01COSM945604c.453A>Gp.T151TSubstitution - coding silent13:113474191-113474191-
TCGA-AP-A0LM-01COSM945605c.420T>Cp.L140LSubstitution - coding silent13:113474224-113474224-
LUAD-B00416COSM355378c.487A>Gp.T163ASubstitution - Missense13:113474157-113474157-
HCT15COSM1677817c.27G>Tp.K9NSubstitution - Missense13:113484033-113484033-
TCGA-GC-A3RD-01COSM3793151c.5A>Gp.H2RSubstitution - Missense13:113484055-113484055-
TCGA-AX-A0J1-01COSM945607c.317C>Tp.A106VSubstitution - Missense13:113480647-113480647-
PD13164aCOSM5793846c.92C>Gp.T31RSubstitution - Missense13:113483968-113483968-
TCGA-CD-A4MG-01COSM4046202c.587G>Tp.W196LSubstitution - Missense13:113461070-113461070-
SNU-175COSM2264377c.179T>Cp.V60ASubstitution - Missense13:113483881-113483881-
TCGA-CM-6678-01COSM1365604c.691G>Ap.D231NSubstitution - Missense13:113459321-113459321-
BD124TCOSM2264375c.220G>Tp.D74YSubstitution - Missense13:113483840-113483840-
HCT-15COSM1677817c.27G>Tp.K9NSubstitution - Missense13:113484033-113484033-
TCGA-AP-A051-01COSM945606c.390-1G>Tp.?Unknown13:113474255-113474255-
TCGA-D1-A16X-01COSM945603c.471T>Gp.F157LSubstitution - Missense13:113474173-113474173-
T3204COSM4676633c.258delTp.Q87fs*7Deletion - Frameshift13:113480706-113480706-
TCGA-18-3409-01COSM695927c.137A>Gp.Q46RSubstitution - Missense13:113483923-113483923-
RK201_C01COSM3744074c.555G>Ap.V185VSubstitution - coding silent13:113461102-113461102-
CSCC-10-TCOSM4533508c.198G>Ap.E66ESubstitution - coding silent13:113483862-113483862-
TCGA-AG-4021-01COSM3417394c.92C>Tp.T31MSubstitution - Missense13:113483968-113483968-
GC8_TCOSM147723c.735A>Gp.E245ESubstitution - coding silent13:113458074-113458074-
DN12105COSM5793846c.92C>Gp.T31RSubstitution - Missense13:113483968-113483968-
TCGA-C8-A130-01COSM432157c.460T>Cp.F154LSubstitution - Missense13:113474184-113474184-
RK059_C01COSM3744073c.622A>Gp.I208VSubstitution - Missense13:113459390-113459390-
LP6005334-DNA_E02COSM4413193c.510G>Cp.Q170HSubstitution - Missense13:113474134-113474134-
TCGA-D8-A1XK-01COSM3813477c.12T>Cp.L4LSubstitution - coding silent13:113484048-113484048-
J13_TCOSM3955419c.264G>Ap.Q88QSubstitution - coding silent13:113480700-113480700-
TCGA-A8-A0A6-01COSM3813476c.759T>Gp.G253GSubstitution - coding silent13:113458050-113458050-
226COSM3730203c.743G>Ap.R248QSubstitution - Missense13:113458066-113458066-
CSCC-55-TCOSM4502916c.626C>Tp.P209LSubstitution - Missense13:113459386-113459386-
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.74337113q34249091|dbSNP|BC056669|C/T|non-coding||1711|Validated
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AGMissensep.F154Lc.460T>C13114128499BRCA
GAMissensep.L195Fc.583C>T13114115389HNSC
GAMissensep.R256Cc.766C>T13114112358HNSC
GAMissensep.S50Lc.149C>T13114138226BRCA
GASynonymousp.L141Lc.421C>T13114128538LUAD
TCSynonymousp.T151Tc.453A>G13114128506UCEC
TCSynonymousp.V244Vc.732A>G13114112392LUSC
TG3-UTRSNV.c.777+492A>C13114111855HC