UBE2I
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
ACC1613643651364365+SilentSNPAAGTCGA-OR-A5LJ-01A-11D-A29I-10TCGA-OR-A5LJ-10A-01D-A29L-10g.chr16:1364365A>Gc.138A>Gc.(136-138)ccA>ccGp.P46P
BLCA1613747631374763+Missense_MutationSNPGGATCGA-DK-A3IU-01A-11D-A20D-08TCGA-DK-A3IU-10A-01D-A20D-08g.chr16:1374763G>Ac.446G>Ac.(445-447)cGa>cAap.R149Q
CESC1613702601370260+Missense_MutationSNPGGCTCGA-C5-A2LX-01A-11D-A18J-09TCGA-C5-A2LX-10A-01D-A18J-09g.chr16:1370260G>Cc.309G>Cc.(307-309)tgG>tgCp.W103C
CESC1613747641374764+SilentSNPAAGTCGA-FU-A3HZ-01A-11D-A20U-09TCGA-FU-A3HZ-10A-01D-A20U-09g.chr16:1374764A>Gc.447A>Gc.(445-447)cgA>cgGp.R149R
COAD1613640441364044+Missense_MutationSNPGGATCGA-AA-3672-01A-01W-0900-09TCGA-AA-3672-10A-01W-0900-09g.chr16:1364044G>Ac.13G>Ac.(13-15)Gcc>Accp.A5T
COAD1613643361364336+Missense_MutationSNPAAGTCGA-AA-3655-01A-02D-1719-10TCGA-AA-3655-11A-01D-1719-10g.chr16:1364336A>Gc.109A>Gc.(109-111)Aac>Gacp.N37D
COAD1613643371364337+Missense_MutationSNPAAGTCGA-D5-6541-01A-11D-1719-10TCGA-D5-6541-10A-01D-1719-10g.chr16:1364337A>Gc.110A>Gc.(109-111)aAc>aGcp.N37S
COAD1613643561364356+SilentSNPCCTTCGA-A6-5665-01A-01D-1650-10TCGA-A6-5665-10A-01D-1650-10g.chr16:1364356C>Tc.129C>Tc.(127-129)tgC>tgTp.C43C
COAD1613747491374749+SilentSNPCCTTCGA-AA-3663-01A-01D-1719-10TCGA-AA-3663-11A-01D-1719-10g.chr16:1374749C>Tc.432C>Tc.(430-432)taC>taTp.Y144Y
COADREAD1613640441364044+Missense_MutationSNPGGATCGA-AA-3672-01A-01W-0900-09TCGA-AA-3672-10A-01W-0900-09g.chr16:1364044G>Ac.13G>Ac.(13-15)Gcc>Accp.A5T
COADREAD1613643361364336+Missense_MutationSNPAAGTCGA-AA-3655-01A-02D-1719-10TCGA-AA-3655-11A-01D-1719-10g.chr16:1364336A>Gc.109A>Gc.(109-111)Aac>Gacp.N37D
COADREAD1613643371364337+Missense_MutationSNPAAGTCGA-D5-6541-01A-11D-1719-10TCGA-D5-6541-10A-01D-1719-10g.chr16:1364337A>Gc.110A>Gc.(109-111)aAc>aGcp.N37S
COADREAD1613643561364356+SilentSNPCCTTCGA-A6-5665-01A-01D-1650-10TCGA-A6-5665-10A-01D-1650-10g.chr16:1364356C>Tc.129C>Tc.(127-129)tgC>tgTp.C43C
COADREAD1613701981370198+Missense_MutationSNPCCATCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr16:1370198C>Ac.247C>Ac.(247-249)Cac>Aacp.H83N
COADREAD1613747491374749+SilentSNPCCTTCGA-AA-3663-01A-01D-1719-10TCGA-AA-3663-11A-01D-1719-10g.chr16:1374749C>Tc.432C>Tc.(430-432)taC>taTp.Y144Y
HNSC1613643141364314+SilentSNPAACTCGA-P3-A6T3-01A-11D-A34J-08TCGA-P3-A6T3-10A-01D-A34M-08g.chr16:1364314A>Cc.87A>Cc.(85-87)acA>acCp.T29T
HNSC1613747851374785+SilentSNPGGTTCGA-CN-5356-01A-01D-1434-08TCGA-CN-5356-10A-01D-1434-08g.chr16:1374785G>Tc.468G>Tc.(466-468)gcG>gcTp.A156A
KIPAN1613704531370453+Missense_MutationSNPAAGTCGA-P4-A5EA-01A-11D-A28G-10TCGA-P4-A5EA-11A-11D-A28G-10g.chr16:1370453A>Gc.348A>Gc.(346-348)atA>atGp.I116M
KIRP1613704531370453+Missense_MutationSNPAAGTCGA-P4-A5EA-01A-11D-A28G-10TCGA-P4-A5EA-11A-11D-A28G-10g.chr16:1370453A>Gc.348A>Gc.(346-348)atA>atGp.I116M
LUAD1613640381364038+Missense_MutationSNPGGTTCGA-86-A456-01A-11D-A24D-08TCGA-86-A456-10A-01D-A24F-08g.chr16:1364038G>Tc.7G>Tc.(7-9)Ggg>Tggp.G3W
LUAD1613747711374771+Missense_MutationSNPGGTTCGA-17-Z022-01A-01W-0746-08TCGA-17-Z022-11A-01W-0746-08g.chr16:1374771G>Tc.454G>Tc.(454-456)Gcc>Tccp.A152S
PRAD1613656721365672+SilentSNPCCTTCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr16:1365672C>Tc.168C>Tc.(166-168)ggC>ggTp.G56G
PRAD1613704731370473+Missense_MutationSNPCCTTCGA-EJ-7314-01A-31D-2114-08TCGA-EJ-7314-10A-01D-2114-08g.chr16:1370473C>Tc.368C>Tc.(367-369)cCa>cTap.P123L
READ1613701981370198+Missense_MutationSNPCCATCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr16:1370198C>Ac.247C>Ac.(247-249)Cac>Aacp.H83N
SARC1613643721364372+Missense_MutationSNPAAGTCGA-DX-AB2Z-01A-11D-A387-09TCGA-DX-AB2Z-10A-01D-A38A-09g.chr16:1364372A>Gc.145A>Gc.(145-147)Aaa>Gaap.K49E
SKCM1613643641364364+Missense_MutationSNPCCTTCGA-EE-A3AA-06A-11D-A196-08TCGA-EE-A3AA-10A-01D-A198-08g.chr16:1364364C>Tc.137C>Tc.(136-138)cCa>cTap.P46L
SKCM1613702121370212+SilentSNPCCTTCGA-DA-A1I8-06A-11D-A197-08TCGA-DA-A1I8-10A-01D-A199-08g.chr16:1370212C>Tc.261C>Tc.(259-261)taC>taTp.Y87Y
SKCM1613702121370212+SilentSNPCCTTCGA-EB-A5UN-06A-11D-A30X-08TCGA-EB-A5UN-10A-01D-A30X-08g.chr16:1370212C>Tc.261C>Tc.(259-261)taC>taTp.Y87Y
SKCM1613702131370213+Missense_MutationSNPCCTTCGA-DA-A1I8-06A-11D-A197-08TCGA-DA-A1I8-10A-01D-A199-08g.chr16:1370213C>Tc.262C>Tc.(262-264)Cct>Tctp.P88S
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-US1613747631374763single base substitutionGAdownstream_gene_variant
BLCA-US1613747631374763single base substitutionGAmissense_variantR149Q446G>A
BOCA-FR1613658021365802single base substitutionCTdownstream_gene_variant
BOCA-FR1613658021365802single base substitutionCTexon_variant
BOCA-FR1613658021365802single base substitutionCTintron_variant
BOCA-FR1613658021365802single base substitutionCTupstream_gene_variant
BRCA-EU1613505701350570insertion of <=200bp-Aupstream_gene_variant
BRCA-EU1613513481351348single base substitutionGCupstream_gene_variant
BRCA-EU1613519931351993single base substitutionAGupstream_gene_variant
BRCA-EU1613522031352203single base substitutionCTupstream_gene_variant
BRCA-EU1613525231352523single base substitutionCTupstream_gene_variant
BRCA-EU1613546351354635single base substitutionGCupstream_gene_variant
BRCA-EU1613546701354670single base substitutionCTupstream_gene_variant
BRCA-EU1613556591355659single base substitutionCTexon_variant
BRCA-EU1613556591355659single base substitutionCTupstream_gene_variant
BRCA-EU1613570561357056single base substitutionACexon_variant
BRCA-EU1613570561357056single base substitutionACupstream_gene_variant
BRCA-EU1613571811357181single base substitutionACexon_variant
BRCA-EU1613571811357181single base substitutionACupstream_gene_variant
BRCA-EU1613588691358869single base substitutionTGexon_variant
BRCA-EU1613588691358869single base substitutionTGupstream_gene_variant
BRCA-EU1613591571359157single base substitutionTA5_prime_UTR_variant
BRCA-EU1613591571359157single base substitutionTAexon_variant
BRCA-EU1613591571359157single base substitutionTAupstream_gene_variant
BRCA-EU1613598191359819single base substitutionGA5_prime_UTR_variant
BRCA-EU1613598191359819single base substitutionGAdownstream_gene_variant
BRCA-EU1613598191359819single base substitutionGAintron_variant
BRCA-EU1613598191359819single base substitutionGAupstream_gene_variant
BRCA-EU1613641161364116single base substitutionCTdownstream_gene_variant
BRCA-EU1613641161364116single base substitutionCTintron_variant
BRCA-EU1613641161364116single base substitutionCTupstream_gene_variant
BRCA-EU1613641321364132single base substitutionGAdownstream_gene_variant
BRCA-EU1613641321364132single base substitutionGAintron_variant
BRCA-EU1613641321364132single base substitutionGAupstream_gene_variant
BRCA-EU1613646571364657single base substitutionCAdownstream_gene_variant
BRCA-EU1613646571364657single base substitutionCAexon_variant
BRCA-EU1613646571364657single base substitutionCAintron_variant
BRCA-EU1613646571364657single base substitutionCAupstream_gene_variant
BRCA-EU1613669391366939single base substitutionGAdownstream_gene_variant
BRCA-EU1613669391366939single base substitutionGAexon_variant
BRCA-EU1613669391366939single base substitutionGAintron_variant
BRCA-EU1613669391366939single base substitutionGAupstream_gene_variant
BRCA-EU1613669601366960single base substitutionACdownstream_gene_variant
BRCA-EU1613669601366960single base substitutionACexon_variant
BRCA-EU1613669601366960single base substitutionACintron_variant
BRCA-EU1613669601366960single base substitutionACupstream_gene_variant
BRCA-EU1613690571369057single base substitutionAGdownstream_gene_variant
BRCA-EU1613690571369057single base substitutionAGintron_variant
BRCA-EU1613690571369057single base substitutionAGupstream_gene_variant
BRCA-EU1613696871369687single base substitutionCTdownstream_gene_variant
BRCA-EU1613696871369687single base substitutionCTintron_variant
BRCA-EU1613696871369687single base substitutionCTupstream_gene_variant
BRCA-EU1613697941369794single base substitutionTG3_prime_UTR_variant
BRCA-EU1613697941369794single base substitutionTGdownstream_gene_variant
BRCA-EU1613697941369794single base substitutionTGintron_variant
BRCA-EU1613697941369794single base substitutionTGupstream_gene_variant
BRCA-EU1613698481369848single base substitutionGA3_prime_UTR_variant
BRCA-EU1613698481369848single base substitutionGAdownstream_gene_variant
BRCA-EU1613698481369848single base substitutionGAintron_variant
BRCA-EU1613698481369848single base substitutionGAupstream_gene_variant
BRCA-EU1613710401371040single base substitutionGA3_prime_UTR_variant
BRCA-EU1613710401371040single base substitutionGAdownstream_gene_variant
BRCA-EU1613710401371040single base substitutionGAintron_variant
BRCA-EU1613721531372153single base substitutionGCdownstream_gene_variant
BRCA-EU1613721531372153single base substitutionGCintron_variant
BRCA-EU1613730851373085single base substitutionGCdownstream_gene_variant
BRCA-EU1613730851373085single base substitutionGCintron_variant
BRCA-EU1613734601373460single base substitutionCAdownstream_gene_variant
BRCA-EU1613734601373460single base substitutionCAintron_variant
BRCA-EU1613749771374977single base substitutionAG3_prime_UTR_variant
BRCA-EU1613749771374977single base substitutionAGdownstream_gene_variant
BRCA-EU1613750961375096single base substitutionGC3_prime_UTR_variant
BRCA-EU1613750961375096single base substitutionGCdownstream_gene_variant
BRCA-EU1613753741375374single base substitutionTC3_prime_UTR_variant
BRCA-EU1613753741375374single base substitutionTCdownstream_gene_variant
BRCA-EU1613754661375466single base substitutionCT3_prime_UTR_variant
BRCA-EU1613754661375466single base substitutionCTdownstream_gene_variant
BRCA-EU1613774391377439single base substitutionCTdownstream_gene_variant
BRCA-EU1613787001378700single base substitutionGAdownstream_gene_variant
BRCA-EU1613792211379221single base substitutionAGdownstream_gene_variant
BRCA-EU1613798881379888single base substitutionGAdownstream_gene_variant
BRCA-FR1613607021360702single base substitutionGAdownstream_gene_variant
BRCA-FR1613607021360702single base substitutionGAintron_variant
BRCA-FR1613607021360702single base substitutionGAupstream_gene_variant
BRCA-FR1613633461363346single base substitutionAGdownstream_gene_variant
BRCA-FR1613633461363346single base substitutionAGintron_variant
BRCA-FR1613633461363346single base substitutionAGupstream_gene_variant
BRCA-FR1613641321364132single base substitutionGAdownstream_gene_variant
BRCA-FR1613641321364132single base substitutionGAintron_variant
BRCA-FR1613641321364132single base substitutionGAupstream_gene_variant
BRCA-FR1613644651364465single base substitutionGAdownstream_gene_variant
BRCA-FR1613644651364465single base substitutionGAexon_variant
BRCA-FR1613644651364465single base substitutionGAintron_variant
BRCA-FR1613644651364465single base substitutionGAupstream_gene_variant
BRCA-FR1613665591366559single base substitutionGCdownstream_gene_variant
BRCA-FR1613665591366559single base substitutionGCexon_variant
BRCA-FR1613665591366559single base substitutionGCintron_variant
BRCA-FR1613665591366559single base substitutionGCupstream_gene_variant
BRCA-FR1613697941369794single base substitutionTG3_prime_UTR_variant
BRCA-FR1613697941369794single base substitutionTGdownstream_gene_variant
BRCA-FR1613697941369794single base substitutionTGintron_variant
BRCA-FR1613697941369794single base substitutionTGupstream_gene_variant
BRCA-FR1613748131374813single base substitutionCT3_prime_UTR_variant
BRCA-FR1613748131374813single base substitutionCTdownstream_gene_variant
BRCA-FR1613787001378700single base substitutionGAdownstream_gene_variant
BRCA-US1613705861370586single base substitutionCTdownstream_gene_variant
BRCA-US1613705861370586single base substitutionCTintron_variant
BRCA-US1613705861370586single base substitutionCTmissense_variantR161W481C>T
BTCA-JP1613655471365547single base substitutionCTdownstream_gene_variant
BTCA-JP1613655471365547single base substitutionCTexon_variant
BTCA-JP1613655471365547single base substitutionCTintron_variant
BTCA-JP1613655471365547single base substitutionCTupstream_gene_variant
BTCA-JP1613657731365773single base substitutionCTdownstream_gene_variant
BTCA-JP1613657731365773single base substitutionCTexon_variant
BTCA-JP1613657731365773single base substitutionCTintron_variant
BTCA-JP1613657731365773single base substitutionCTupstream_gene_variant
CESC-US1613586691358669single base substitutionGTexon_variant
CESC-US1613586691358669single base substitutionGTupstream_gene_variant
CESC-US1613588141358814single base substitutionGAexon_variant
CESC-US1613588141358814single base substitutionGAupstream_gene_variant
CESC-US1613701101370110single base substitutionGTdownstream_gene_variant
CESC-US1613701101370110single base substitutionGTexon_variant
CESC-US1613701101370110single base substitutionGTintron_variant
CESC-US1613702601370260single base substitutionGCdownstream_gene_variant
CESC-US1613702601370260single base substitutionGCexon_variant
CESC-US1613702601370260single base substitutionGCmissense_variantW103C309G>C
CESC-US1613747641374764single base substitutionAGdownstream_gene_variant
CESC-US1613747641374764single base substitutionAGsynonymous_variantR149R447A>G
CLLE-ES1613515451351545single base substitutionCTupstream_gene_variant
COAD-US1613643651364365single base substitutionAGdownstream_gene_variant
COAD-US1613643651364365single base substitutionAGexon_variant
COAD-US1613643651364365single base substitutionAGintron_variant
COAD-US1613643651364365single base substitutionAGsynonymous_variantP46P138A>G
COAD-US1613643651364365single base substitutionAGupstream_gene_variant
COAD-US1613747491374749single base substitutionCTdownstream_gene_variant
COAD-US1613747491374749single base substitutionCTexon_variant
COAD-US1613747491374749single base substitutionCTsynonymous_variantY144Y432C>T
COCA-CN1613579871357987single base substitutionGAintron_variant
COCA-CN1613579871357987single base substitutionGAupstream_gene_variant
COCA-CN1613581681358168single base substitutionGAintron_variant
COCA-CN1613581681358168single base substitutionGAupstream_gene_variant
COCA-CN1613586331358633single base substitutionGTexon_variant
COCA-CN1613586331358633single base substitutionGTupstream_gene_variant
COCA-CN1613587811358781single base substitutionGAexon_variant
COCA-CN1613587811358781single base substitutionGAupstream_gene_variant
COCA-CN1613641111364111single base substitutionCAdownstream_gene_variant
COCA-CN1613641111364111single base substitutionCAintron_variant
COCA-CN1613641111364111single base substitutionCAupstream_gene_variant
COCA-CN1613655841365584single base substitutionCTdownstream_gene_variant
COCA-CN1613655841365584single base substitutionCTexon_variant
COCA-CN1613655841365584single base substitutionCTintron_variant
COCA-CN1613655841365584single base substitutionCTupstream_gene_variant
COCA-CN1613656101365610single base substitutionGAdownstream_gene_variant
COCA-CN1613656101365610single base substitutionGAexon_variant
COCA-CN1613656101365610single base substitutionGAintron_variant
COCA-CN1613656101365610single base substitutionGAupstream_gene_variant
COCA-CN1613704301370430single base substitutionCTdownstream_gene_variant
COCA-CN1613704301370430single base substitutionCTintron_variant
COCA-CN1613748581374858single base substitutionTG3_prime_UTR_variant
COCA-CN1613748581374858single base substitutionTGdownstream_gene_variant
COCA-CN1613749381374938single base substitutionGA3_prime_UTR_variant
COCA-CN1613749381374938single base substitutionGAdownstream_gene_variant
EOPC-DE1613513171351317single base substitutionGAupstream_gene_variant
ESAD-UK1613521421352142single base substitutionACupstream_gene_variant
ESAD-UK1613539471353947single base substitutionGCupstream_gene_variant
ESAD-UK1613555491355549single base substitutionATexon_variant
ESAD-UK1613555491355549single base substitutionATupstream_gene_variant
ESAD-UK1613568521356852single base substitutionGAexon_variant
ESAD-UK1613568521356852single base substitutionGAupstream_gene_variant
ESAD-UK1613579871357987insertion of <=200bp-ATintron_variant
ESAD-UK1613579871357987insertion of <=200bp-ATupstream_gene_variant
ESAD-UK1613579881357988insertion of <=200bp-AAintron_variant
ESAD-UK1613579881357988insertion of <=200bp-AAupstream_gene_variant
ESAD-UK1613610801361080single base substitutionGCdownstream_gene_variant
ESAD-UK1613610801361080single base substitutionGCintron_variant
ESAD-UK1613610801361080single base substitutionGCupstream_gene_variant
ESAD-UK1613613091361309single base substitutionGAdownstream_gene_variant
ESAD-UK1613613091361309single base substitutionGAintron_variant
ESAD-UK1613613091361309single base substitutionGAupstream_gene_variant
ESAD-UK1613621181362118single base substitutionAC5_prime_UTR_variant
ESAD-UK1613621181362118single base substitutionACdownstream_gene_variant
ESAD-UK1613621181362118single base substitutionACintron_variant
ESAD-UK1613621181362118single base substitutionACupstream_gene_variant
ESAD-UK1613622011362201single base substitutionCG5_prime_UTR_variant
ESAD-UK1613622011362201single base substitutionCGdownstream_gene_variant
ESAD-UK1613622011362201single base substitutionCGexon_variant
ESAD-UK1613622011362201single base substitutionCGintron_variant
ESAD-UK1613622011362201single base substitutionCGupstream_gene_variant
ESAD-UK1613626821362682single base substitutionGAdownstream_gene_variant
ESAD-UK1613626821362682single base substitutionGAintron_variant
ESAD-UK1613626821362682single base substitutionGAupstream_gene_variant
ESAD-UK1613678371367837single base substitutionCTdownstream_gene_variant
ESAD-UK1613678371367837single base substitutionCTintron_variant
ESAD-UK1613678371367837single base substitutionCTupstream_gene_variant
ESAD-UK1613679061367906single base substitutionGAdownstream_gene_variant
ESAD-UK1613679061367906single base substitutionGAintron_variant
ESAD-UK1613679061367906single base substitutionGAupstream_gene_variant
ESAD-UK1613681271368127single base substitutionGTdownstream_gene_variant
ESAD-UK1613681271368127single base substitutionGTintron_variant
ESAD-UK1613681271368127single base substitutionGTupstream_gene_variant
ESAD-UK1613694871369487single base substitutionGTdownstream_gene_variant
ESAD-UK1613694871369487single base substitutionGTintron_variant
ESAD-UK1613694871369487single base substitutionGTupstream_gene_variant
ESAD-UK1613738041373804single base substitutionGAdownstream_gene_variant
ESAD-UK1613738041373804single base substitutionGAintron_variant
ESAD-UK1613743681374368single base substitutionGAdownstream_gene_variant
ESAD-UK1613743681374368single base substitutionGAintron_variant
ESAD-UK1613762811376281deletion of <=200bpC-3_prime_UTR_variant
ESAD-UK1613762811376281deletion of <=200bpC-downstream_gene_variant
ESAD-UK1613769721376972single base substitutionGT3_prime_UTR_variant
ESAD-UK1613769721376972single base substitutionGTdownstream_gene_variant
ESAD-UK1613770841377084single base substitutionGAdownstream_gene_variant
ESAD-UK1613796301379630single base substitutionCAdownstream_gene_variant
ESAD-UK1613803231380323single base substitutionGAdownstream_gene_variant
ESAD-UK1613804251380425single base substitutionCTdownstream_gene_variant
ESAD-UK1613806261380626single base substitutionCTdownstream_gene_variant
ESAD-UK1613812331381233single base substitutionGCdownstream_gene_variant
ESCA-CN1613585201358520single base substitutionGAexon_variant
ESCA-CN1613585201358520single base substitutionGAupstream_gene_variant
ESCA-CN1613585241358524single base substitutionGAexon_variant
ESCA-CN1613585241358524single base substitutionGAupstream_gene_variant
ESCA-CN1613585271358527single base substitutionATexon_variant
ESCA-CN1613585271358527single base substitutionATupstream_gene_variant
KIRP-US1613704531370453single base substitutionAGdownstream_gene_variant
KIRP-US1613704531370453single base substitutionAGexon_variant
KIRP-US1613704531370453single base substitutionAGmissense_variantI116M348A>G
LAML-KR1613640441364044single base substitutionGAdownstream_gene_variant
LAML-KR1613640441364044single base substitutionGAexon_variant
LAML-KR1613640441364044single base substitutionGAintron_variant
LAML-KR1613640441364044single base substitutionGAmissense_variantA5T13G>A
LAML-KR1613640441364044single base substitutionGAupstream_gene_variant
LAML-KR1613798391379839single base substitutionCTdownstream_gene_variant
LICA-FR1613578541357854single base substitutionAGintron_variant
LICA-FR1613578541357854single base substitutionAGupstream_gene_variant
LICA-FR1613579261357926single base substitutionTAintron_variant
LICA-FR1613579261357926single base substitutionTAupstream_gene_variant
LICA-FR1613795601379560single base substitutionGAdownstream_gene_variant
LINC-JP1613586461358646single base substitutionTGexon_variant
LINC-JP1613586461358646single base substitutionTGupstream_gene_variant
LINC-JP1613678871367887single base substitutionACdownstream_gene_variant
LINC-JP1613678871367887single base substitutionACintron_variant
LINC-JP1613678871367887single base substitutionACupstream_gene_variant
LINC-JP1613699461369946single base substitutionCGdownstream_gene_variant
LINC-JP1613699461369946single base substitutionCGexon_variant
LINC-JP1613699461369946single base substitutionCGintron_variant
LINC-JP1613746531374653single base substitutionCTdownstream_gene_variant
LINC-JP1613746531374653single base substitutionCTintron_variant
LIRI-JP1613521331352133single base substitutionGCupstream_gene_variant
LIRI-JP1613574531357453single base substitutionGTexon_variant
LIRI-JP1613574531357453single base substitutionGTupstream_gene_variant
LIRI-JP1613643931364393single base substitutionGAdownstream_gene_variant
LIRI-JP1613643931364393single base substitutionGAexon_variant
LIRI-JP1613643931364393single base substitutionGAintron_variant
LIRI-JP1613643931364393single base substitutionGAupstream_gene_variant
LIRI-JP1613646691364669single base substitutionGAdownstream_gene_variant
LIRI-JP1613646691364669single base substitutionGAexon_variant
LIRI-JP1613646691364669single base substitutionGAintron_variant
LIRI-JP1613646691364669single base substitutionGAupstream_gene_variant
LIRI-JP1613657871365787single base substitutionCTdownstream_gene_variant
LIRI-JP1613657871365787single base substitutionCTexon_variant
LIRI-JP1613657871365787single base substitutionCTintron_variant
LIRI-JP1613657871365787single base substitutionCTupstream_gene_variant
LIRI-JP1613662961366296single base substitutionGAdownstream_gene_variant
LIRI-JP1613662961366296single base substitutionGAexon_variant
LIRI-JP1613662961366296single base substitutionGAintron_variant
LIRI-JP1613662961366296single base substitutionGAupstream_gene_variant
LIRI-JP1613670041367004single base substitutionCTdownstream_gene_variant
LIRI-JP1613670041367004single base substitutionCTexon_variant
LIRI-JP1613670041367004single base substitutionCTintron_variant
LIRI-JP1613670041367004single base substitutionCTupstream_gene_variant
LIRI-JP1613673211367321single base substitutionGCdownstream_gene_variant
LIRI-JP1613673211367321single base substitutionGCintron_variant
LIRI-JP1613673211367321single base substitutionGCupstream_gene_variant
LIRI-JP1613677521367753deletion of <=200bpGA-downstream_gene_variant
LIRI-JP1613677521367753deletion of <=200bpGA-intron_variant
LIRI-JP1613677521367753deletion of <=200bpGA-upstream_gene_variant
LIRI-JP1613716461371646single base substitutionTC3_prime_UTR_variant
LIRI-JP1613716461371646single base substitutionTCdownstream_gene_variant
LIRI-JP1613716461371646single base substitutionTCintron_variant
LIRI-JP1613719421371942single base substitutionAGdownstream_gene_variant
LIRI-JP1613719421371942single base substitutionAGintron_variant
LIRI-JP1613747131374713single base substitutionCTdownstream_gene_variant
LIRI-JP1613747131374713single base substitutionCTintron_variant
LIRI-JP1613750841375084single base substitutionAG3_prime_UTR_variant
LIRI-JP1613750841375084single base substitutionAGdownstream_gene_variant
LIRI-JP1613753701375370single base substitutionAG3_prime_UTR_variant
LIRI-JP1613753701375370single base substitutionAGdownstream_gene_variant
LIRI-JP1613754091375409single base substitutionCA3_prime_UTR_variant
LIRI-JP1613754091375409single base substitutionCAdownstream_gene_variant
LIRI-JP1613773851377385single base substitutionGAdownstream_gene_variant
LIRI-JP1613792381379242deletion of <=200bpGAAAA-downstream_gene_variant
LIRI-JP1613816841381684single base substitutionGAdownstream_gene_variant
LUSC-KR1613514591351459single base substitutionCGupstream_gene_variant
LUSC-KR1613569191356919single base substitutionGTexon_variant
LUSC-KR1613569191356919single base substitutionGTupstream_gene_variant
LUSC-KR1613579531357953single base substitutionGAintron_variant
LUSC-KR1613579531357953single base substitutionGAupstream_gene_variant
LUSC-KR1613584641358464single base substitutionGAintron_variant
LUSC-KR1613584641358464single base substitutionGAupstream_gene_variant
LUSC-KR1613609531360953single base substitutionGTdownstream_gene_variant
LUSC-KR1613609531360953single base substitutionGTintron_variant
LUSC-KR1613609531360953single base substitutionGTupstream_gene_variant
LUSC-KR1613631041363104single base substitutionGTdownstream_gene_variant
LUSC-KR1613631041363104single base substitutionGTintron_variant
LUSC-KR1613631041363104single base substitutionGTupstream_gene_variant
LUSC-KR1613666431366643single base substitutionTAdownstream_gene_variant
LUSC-KR1613666431366643single base substitutionTAexon_variant
LUSC-KR1613666431366643single base substitutionTAintron_variant
LUSC-KR1613666431366643single base substitutionTAupstream_gene_variant
LUSC-KR1613705561370556single base substitutionCTdownstream_gene_variant
LUSC-KR1613705561370556single base substitutionCTintron_variant
LUSC-KR1613705561370556single base substitutionCTmissense_variantP151S451C>T
LUSC-KR1613741141374114single base substitutionACdownstream_gene_variant
LUSC-KR1613741141374114single base substitutionACintron_variant
LUSC-KR1613744191374419single base substitutionCTdownstream_gene_variant
LUSC-KR1613744191374419single base substitutionCTintron_variant
LUSC-KR1613749561374956single base substitutionCG3_prime_UTR_variant
LUSC-KR1613749561374956single base substitutionCGdownstream_gene_variant
LUSC-KR1613790201379020single base substitutionTAdownstream_gene_variant
LUSC-KR1613791171379117single base substitutionGAdownstream_gene_variant
LUSC-KR1613793681379368single base substitutionCGdownstream_gene_variant
LUSC-KR1613800151380015single base substitutionCAdownstream_gene_variant
LUSC-KR1613804301380430single base substitutionGCdownstream_gene_variant
MALY-DE1613712091371209single base substitutionGA3_prime_UTR_variant
MALY-DE1613712091371209single base substitutionGAdownstream_gene_variant
MALY-DE1613712091371209single base substitutionGAintron_variant
MALY-DE1613802411380247deletion of <=200bpCTGCCTG-downstream_gene_variant
MELA-AU1613506071350607single base substitutionGAupstream_gene_variant
MELA-AU1613510661351066single base substitutionGAupstream_gene_variant
MELA-AU1613510981351098single base substitutionGAupstream_gene_variant
MELA-AU1613517021351702single base substitutionGAupstream_gene_variant
MELA-AU1613518891351889single base substitutionTAupstream_gene_variant
MELA-AU1613519301351930single base substitutionAGupstream_gene_variant
MELA-AU1613521841352184single base substitutionGAupstream_gene_variant
MELA-AU1613529111352911single base substitutionGAupstream_gene_variant
MELA-AU1613529231352923single base substitutionGAupstream_gene_variant
MELA-AU1613529301352930single base substitutionCTupstream_gene_variant
MELA-AU1613531161353116single base substitutionGAupstream_gene_variant
MELA-AU1613531321353132single base substitutionCTupstream_gene_variant
MELA-AU1613536381353639multiple base substitution (>=2bp and <=200bp)GGAAupstream_gene_variant
MELA-AU1613537151353715single base substitutionGCupstream_gene_variant
MELA-AU1613538001353800single base substitutionCTupstream_gene_variant
MELA-AU1613538071353807single base substitutionCTupstream_gene_variant
MELA-AU1613538471353847single base substitutionGAupstream_gene_variant
MELA-AU1613544111354411single base substitutionGAupstream_gene_variant
MELA-AU1613545011354501single base substitutionGAupstream_gene_variant
MELA-AU1613546161354616single base substitutionCGupstream_gene_variant
MELA-AU1613546761354676single base substitutionCTupstream_gene_variant
MELA-AU1613549881354989multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
MELA-AU1613551391355139single base substitutionGAupstream_gene_variant
MELA-AU1613555221355522single base substitutionGAupstream_gene_variant
MELA-AU1613560061356006single base substitutionCTexon_variant
MELA-AU1613560061356006single base substitutionCTupstream_gene_variant
MELA-AU1613560091356009single base substitutionGAexon_variant
MELA-AU1613560091356009single base substitutionGAupstream_gene_variant
MELA-AU1613564381356438single base substitutionCTexon_variant
MELA-AU1613564381356438single base substitutionCTupstream_gene_variant
MELA-AU1613568061356806single base substitutionCTexon_variant
MELA-AU1613568061356806single base substitutionCTupstream_gene_variant
MELA-AU1613569521356952single base substitutionGAexon_variant
MELA-AU1613569521356952single base substitutionGAupstream_gene_variant
MELA-AU1613575131357513single base substitutionGAexon_variant
MELA-AU1613575131357513single base substitutionGAupstream_gene_variant
MELA-AU1613576361357636single base substitutionGAexon_variant
MELA-AU1613576361357636single base substitutionGAupstream_gene_variant
MELA-AU1613577771357777single base substitutionGTexon_variant
MELA-AU1613577771357777single base substitutionGTupstream_gene_variant
MELA-AU1613579451357945single base substitutionGAintron_variant
MELA-AU1613579451357945single base substitutionGAupstream_gene_variant
MELA-AU1613579651357965single base substitutionGAintron_variant
MELA-AU1613579651357965single base substitutionGAupstream_gene_variant
MELA-AU1613580251358025single base substitutionGAintron_variant
MELA-AU1613580251358025single base substitutionGAupstream_gene_variant
MELA-AU1613582111358211single base substitutionGAintron_variant
MELA-AU1613582111358211single base substitutionGAupstream_gene_variant
MELA-AU1613582471358247single base substitutionGAintron_variant
MELA-AU1613582471358247single base substitutionGAupstream_gene_variant
MELA-AU1613582881358288single base substitutionGAintron_variant
MELA-AU1613582881358288single base substitutionGAupstream_gene_variant
MELA-AU1613582921358292single base substitutionGAintron_variant
MELA-AU1613582921358292single base substitutionGAupstream_gene_variant
MELA-AU1613589081358908single base substitutionGA5_prime_UTR_variant
MELA-AU1613589081358908single base substitutionGAexon_variant
MELA-AU1613589081358908single base substitutionGAupstream_gene_variant
MELA-AU1613589091358909single base substitutionGA5_prime_UTR_variant
MELA-AU1613589091358909single base substitutionGAexon_variant
MELA-AU1613589091358909single base substitutionGAupstream_gene_variant
MELA-AU1613590971359097single base substitutionGA5_prime_UTR_variant
MELA-AU1613590971359097single base substitutionGAexon_variant
MELA-AU1613590971359097single base substitutionGAupstream_gene_variant
MELA-AU1613591081359108single base substitutionCT5_prime_UTR_variant
MELA-AU1613591081359108single base substitutionCTexon_variant
MELA-AU1613591081359108single base substitutionCTupstream_gene_variant
MELA-AU1613591181359118single base substitutionGA5_prime_UTR_variant
MELA-AU1613591181359118single base substitutionGAexon_variant
MELA-AU1613591181359118single base substitutionGAupstream_gene_variant
MELA-AU1613593221359322single base substitutionCT5_prime_UTR_variant
MELA-AU1613593221359322single base substitutionCTexon_variant
MELA-AU1613593221359322single base substitutionCTintron_variant
MELA-AU1613593221359322single base substitutionCTupstream_gene_variant
MELA-AU1613606471360647single base substitutionCTdownstream_gene_variant
MELA-AU1613606471360647single base substitutionCTintron_variant
MELA-AU1613606471360647single base substitutionCTupstream_gene_variant
MELA-AU1613606881360688single base substitutionCTdownstream_gene_variant
MELA-AU1613606881360688single base substitutionCTintron_variant
MELA-AU1613606881360688single base substitutionCTupstream_gene_variant
MELA-AU1613618241361824single base substitutionCTdownstream_gene_variant
MELA-AU1613618241361824single base substitutionCTintron_variant
MELA-AU1613618241361824single base substitutionCTupstream_gene_variant
MELA-AU1613621931362207deletion of <=200bpGGCCCGGTCTGGGGC-5_prime_UTR_variant
MELA-AU1613621931362207deletion of <=200bpGGCCCGGTCTGGGGC-downstream_gene_variant
MELA-AU1613621931362207deletion of <=200bpGGCCCGGTCTGGGGC-exon_variant
MELA-AU1613621931362207deletion of <=200bpGGCCCGGTCTGGGGC-intron_variant
MELA-AU1613621931362207deletion of <=200bpGGCCCGGTCTGGGGC-upstream_gene_variant
MELA-AU1613626811362681single base substitutionCTdownstream_gene_variant
MELA-AU1613626811362681single base substitutionCTintron_variant
MELA-AU1613626811362681single base substitutionCTupstream_gene_variant
MELA-AU1613635421363542single base substitutionCTdownstream_gene_variant
MELA-AU1613635421363542single base substitutionCTintron_variant
MELA-AU1613635421363542single base substitutionCTupstream_gene_variant
MELA-AU1613637641363764single base substitutionTC5_prime_UTR_variant
MELA-AU1613637641363764single base substitutionTCdownstream_gene_variant
MELA-AU1613637641363764single base substitutionTCintron_variant
MELA-AU1613637641363764single base substitutionTCupstream_gene_variant
MELA-AU1613638201363821multiple base substitution (>=2bp and <=200bp)CCTT5_prime_UTR_variant
MELA-AU1613638201363821multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU1613638201363821multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU1613638201363821multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
MELA-AU1613638971363897single base substitutionCT5_prime_UTR_variant
MELA-AU1613638971363897single base substitutionCTdownstream_gene_variant
MELA-AU1613638971363897single base substitutionCTintron_variant
MELA-AU1613638971363897single base substitutionCTupstream_gene_variant
MELA-AU1613643641364364single base substitutionCTdownstream_gene_variant
MELA-AU1613643641364364single base substitutionCTexon_variant
MELA-AU1613643641364364single base substitutionCTintron_variant
MELA-AU1613643641364364single base substitutionCTmissense_variantP46L137C>T
MELA-AU1613643641364364single base substitutionCTupstream_gene_variant
MELA-AU1613644591364459single base substitutionCTdownstream_gene_variant
MELA-AU1613644591364459single base substitutionCTexon_variant
MELA-AU1613644591364459single base substitutionCTintron_variant
MELA-AU1613644591364459single base substitutionCTupstream_gene_variant
MELA-AU1613649071364907single base substitutionCTdownstream_gene_variant
MELA-AU1613649071364907single base substitutionCTexon_variant
MELA-AU1613649071364907single base substitutionCTintron_variant
MELA-AU1613649071364907single base substitutionCTupstream_gene_variant
MELA-AU1613650481365048single base substitutionCTdownstream_gene_variant
MELA-AU1613650481365048single base substitutionCTexon_variant
MELA-AU1613650481365048single base substitutionCTintron_variant
MELA-AU1613650481365048single base substitutionCTupstream_gene_variant
MELA-AU1613650761365076single base substitutionCTdownstream_gene_variant
MELA-AU1613650761365076single base substitutionCTexon_variant
MELA-AU1613650761365076single base substitutionCTintron_variant
MELA-AU1613650761365076single base substitutionCTupstream_gene_variant
MELA-AU1613653481365348single base substitutionCTdownstream_gene_variant
MELA-AU1613653481365348single base substitutionCTexon_variant
MELA-AU1613653481365348single base substitutionCTintron_variant
MELA-AU1613653481365348single base substitutionCTupstream_gene_variant
MELA-AU1613657131365713single base substitutionCTdownstream_gene_variant
MELA-AU1613657131365713single base substitutionCTexon_variant
MELA-AU1613657131365713single base substitutionCTintron_variant
MELA-AU1613657131365713single base substitutionCTmissense_variantS70F209C>T
MELA-AU1613657131365713single base substitutionCTupstream_gene_variant
MELA-AU1613658591365859single base substitutionGAdownstream_gene_variant
MELA-AU1613658591365859single base substitutionGAexon_variant
MELA-AU1613658591365859single base substitutionGAintron_variant
MELA-AU1613658591365859single base substitutionGAupstream_gene_variant
MELA-AU1613668901366890single base substitutionCTdownstream_gene_variant
MELA-AU1613668901366890single base substitutionCTexon_variant
MELA-AU1613668901366890single base substitutionCTintron_variant
MELA-AU1613668901366890single base substitutionCTupstream_gene_variant
MELA-AU1613685031368503single base substitutionCTdownstream_gene_variant
MELA-AU1613685031368503single base substitutionCTintron_variant
MELA-AU1613685031368503single base substitutionCTupstream_gene_variant
MELA-AU1613693761369376single base substitutionCTdownstream_gene_variant
MELA-AU1613693761369376single base substitutionCTintron_variant
MELA-AU1613693761369376single base substitutionCTupstream_gene_variant
MELA-AU1613693861369387multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU1613693861369387multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU1613693861369387multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
MELA-AU1613698111369811single base substitutionTA3_prime_UTR_variant
MELA-AU1613698111369811single base substitutionTAdownstream_gene_variant
MELA-AU1613698111369811single base substitutionTAintron_variant
MELA-AU1613698111369811single base substitutionTAupstream_gene_variant
MELA-AU1613699431369943single base substitutionCTdownstream_gene_variant
MELA-AU1613699431369943single base substitutionCTexon_variant
MELA-AU1613699431369943single base substitutionCTintron_variant
MELA-AU1613703021370302single base substitutionCTdownstream_gene_variant
MELA-AU1613703021370302single base substitutionCTintron_variant
MELA-AU1613715351371535single base substitutionAC3_prime_UTR_variant
MELA-AU1613715351371535single base substitutionACdownstream_gene_variant
MELA-AU1613715351371535single base substitutionACintron_variant
MELA-AU1613715871371587single base substitutionGA3_prime_UTR_variant
MELA-AU1613715871371587single base substitutionGAdownstream_gene_variant
MELA-AU1613715871371587single base substitutionGAintron_variant
MELA-AU1613715991371599single base substitutionCT3_prime_UTR_variant
MELA-AU1613715991371599single base substitutionCTdownstream_gene_variant
MELA-AU1613715991371599single base substitutionCTintron_variant
MELA-AU1613728561372856single base substitutionCTdownstream_gene_variant
MELA-AU1613728561372856single base substitutionCTintron_variant
MELA-AU1613744441374444single base substitutionCTdownstream_gene_variant
MELA-AU1613744441374444single base substitutionCTintron_variant
MELA-AU1613746381374638single base substitutionCTdownstream_gene_variant
MELA-AU1613746381374638single base substitutionCTintron_variant
MELA-AU1613749071374907single base substitutionTC3_prime_UTR_variant
MELA-AU1613749071374907single base substitutionTCdownstream_gene_variant
MELA-AU1613749891374989single base substitutionCT3_prime_UTR_variant
MELA-AU1613749891374989single base substitutionCTdownstream_gene_variant
MELA-AU1613752881375288single base substitutionCT3_prime_UTR_variant
MELA-AU1613752881375288single base substitutionCTdownstream_gene_variant
MELA-AU1613754351375435single base substitutionCT3_prime_UTR_variant
MELA-AU1613754351375435single base substitutionCTdownstream_gene_variant
MELA-AU1613754611375461single base substitutionTA3_prime_UTR_variant
MELA-AU1613754611375461single base substitutionTAdownstream_gene_variant
MELA-AU1613757991375800multiple base substitution (>=2bp and <=200bp)CCTT3_prime_UTR_variant
MELA-AU1613757991375800multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU1613758801375880single base substitutionCT3_prime_UTR_variant
MELA-AU1613758801375880single base substitutionCTdownstream_gene_variant
MELA-AU1613762381376238single base substitutionCT3_prime_UTR_variant
MELA-AU1613762381376238single base substitutionCTdownstream_gene_variant
MELA-AU1613765721376572single base substitutionGA3_prime_UTR_variant
MELA-AU1613765721376572single base substitutionGAdownstream_gene_variant
MELA-AU1613769961376996single base substitutionCT3_prime_UTR_variant
MELA-AU1613769961376996single base substitutionCTdownstream_gene_variant
MELA-AU1613770401377040single base substitutionCTdownstream_gene_variant
MELA-AU1613770631377064multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU1613771801377180single base substitutionCTdownstream_gene_variant
MELA-AU1613771921377192single base substitutionCTdownstream_gene_variant
MELA-AU1613772551377255single base substitutionCTdownstream_gene_variant
MELA-AU1613773581377358single base substitutionTCdownstream_gene_variant
MELA-AU1613774111377411single base substitutionCTdownstream_gene_variant
MELA-AU1613786761378676single base substitutionCTdownstream_gene_variant
MELA-AU1613790061379006single base substitutionCTdownstream_gene_variant
MELA-AU1613791481379148single base substitutionCTdownstream_gene_variant
MELA-AU1613796251379625single base substitutionCTdownstream_gene_variant
MELA-AU1613799131379913single base substitutionGAdownstream_gene_variant
MELA-AU1613801411380141single base substitutionGAdownstream_gene_variant
MELA-AU1613803041380304single base substitutionGAdownstream_gene_variant
MELA-AU1613803211380321single base substitutionCTdownstream_gene_variant
MELA-AU1613804821380482single base substitutionGAdownstream_gene_variant
MELA-AU1613805441380544single base substitutionGAdownstream_gene_variant
MELA-AU1613806061380606single base substitutionGAdownstream_gene_variant
MELA-AU1613808441380844single base substitutionGAdownstream_gene_variant
MELA-AU1613808741380874single base substitutionCTdownstream_gene_variant
MELA-AU1613809381380938single base substitutionCTdownstream_gene_variant
MELA-AU1613810451381046multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU1613811091381109single base substitutionCTdownstream_gene_variant
ORCA-IN1613738731373873single base substitutionGCdownstream_gene_variant
ORCA-IN1613738731373873single base substitutionGCintron_variant
ORCA-IN1613806451380645single base substitutionGTdownstream_gene_variant
OV-AU1613517271351727single base substitutionGTupstream_gene_variant
OV-AU1613536741353674single base substitutionGAupstream_gene_variant
OV-AU1613590751359075single base substitutionCG5_prime_UTR_variant
OV-AU1613590751359075single base substitutionCGexon_variant
OV-AU1613590751359075single base substitutionCGupstream_gene_variant
OV-AU1613591471359147single base substitutionGA5_prime_UTR_variant
OV-AU1613591471359147single base substitutionGAexon_variant
OV-AU1613591471359147single base substitutionGAupstream_gene_variant
OV-AU1613606331360633single base substitutionATdownstream_gene_variant
OV-AU1613606331360633single base substitutionATintron_variant
OV-AU1613606331360633single base substitutionATupstream_gene_variant
OV-AU1613694661369466single base substitutionGTdownstream_gene_variant
OV-AU1613694661369466single base substitutionGTintron_variant
OV-AU1613694661369466single base substitutionGTupstream_gene_variant
OV-AU1613699101369910single base substitutionGAdownstream_gene_variant
OV-AU1613699101369910single base substitutionGAexon_variant
OV-AU1613699101369910single base substitutionGAintron_variant
OV-AU1613799741379974single base substitutionCTdownstream_gene_variant
PACA-AU1613521291352129single base substitutionCTupstream_gene_variant
PACA-AU1613554401355440single base substitutionGCupstream_gene_variant
PACA-AU1613571171357117single base substitutionGAexon_variant
PACA-AU1613571171357117single base substitutionGAupstream_gene_variant
PACA-AU1613607641360764single base substitutionGAdownstream_gene_variant
PACA-AU1613607641360764single base substitutionGAintron_variant
PACA-AU1613607641360764single base substitutionGAupstream_gene_variant
PACA-AU1613619281361928single base substitutionGT5_prime_UTR_variant
PACA-AU1613619281361928single base substitutionGTdownstream_gene_variant
PACA-AU1613619281361928single base substitutionGTintron_variant
PACA-AU1613619281361928single base substitutionGTupstream_gene_variant
PACA-AU1613651701365170single base substitutionCGdownstream_gene_variant
PACA-AU1613651701365170single base substitutionCGexon_variant
PACA-AU1613651701365170single base substitutionCGintron_variant
PACA-AU1613651701365170single base substitutionCGupstream_gene_variant
PACA-AU1613661191366119single base substitutionGAdownstream_gene_variant
PACA-AU1613661191366119single base substitutionGAexon_variant
PACA-AU1613661191366119single base substitutionGAintron_variant
PACA-AU1613661191366119single base substitutionGAupstream_gene_variant
PACA-AU1613669611366964deletion of <=200bpAAAC-downstream_gene_variant
PACA-AU1613669611366964deletion of <=200bpAAAC-exon_variant
PACA-AU1613669611366964deletion of <=200bpAAAC-intron_variant
PACA-AU1613669611366964deletion of <=200bpAAAC-upstream_gene_variant
PACA-AU1613685321368532single base substitutionCTdownstream_gene_variant
PACA-AU1613685321368532single base substitutionCTintron_variant
PACA-AU1613685321368532single base substitutionCTupstream_gene_variant
PACA-AU1613709331370933single base substitutionCA3_prime_UTR_variant
PACA-AU1613709331370933single base substitutionCAdownstream_gene_variant
PACA-AU1613709331370933single base substitutionCAintron_variant
PACA-AU1613730871373087single base substitutionGTdownstream_gene_variant
PACA-AU1613730871373087single base substitutionGTintron_variant
PACA-AU1613735411373541single base substitutionCTdownstream_gene_variant
PACA-AU1613735411373541single base substitutionCTintron_variant
PACA-AU1613765751376576deletion of <=200bpCT-3_prime_UTR_variant
PACA-AU1613765751376576deletion of <=200bpCT-downstream_gene_variant
PACA-CA1613569971356997insertion of <=200bp-Aexon_variant
PACA-CA1613569971356997insertion of <=200bp-Aupstream_gene_variant
PACA-CA1613626271362627single base substitutionGA5_prime_UTR_variant
PACA-CA1613626271362627single base substitutionGAdownstream_gene_variant
PACA-CA1613626271362627single base substitutionGAintron_variant
PACA-CA1613626271362627single base substitutionGAupstream_gene_variant
PACA-CA1613673601367360single base substitutionCGdownstream_gene_variant
PACA-CA1613673601367360single base substitutionCGintron_variant
PACA-CA1613673601367360single base substitutionCGupstream_gene_variant
PACA-CA1613706981370698single base substitutionGA3_prime_UTR_variant
PACA-CA1613706981370698single base substitutionGAdownstream_gene_variant
PACA-CA1613706981370698single base substitutionGAintron_variant
PACA-CA1613732871373287insertion of <=200bp-Adownstream_gene_variant
PACA-CA1613732871373287insertion of <=200bp-Aintron_variant
PACA-CA1613767911376791single base substitutionGA3_prime_UTR_variant
PACA-CA1613767911376791single base substitutionGAdownstream_gene_variant
PACA-CA1613772931377293single base substitutionGAdownstream_gene_variant
PACA-CA1613775701377570single base substitutionCTdownstream_gene_variant
PACA-CA1613798791379879single base substitutionCTdownstream_gene_variant
PAEN-IT1613655231365523single base substitutionCTdownstream_gene_variant
PAEN-IT1613655231365523single base substitutionCTexon_variant
PAEN-IT1613655231365523single base substitutionCTintron_variant
PAEN-IT1613655231365523single base substitutionCTupstream_gene_variant
PBCA-DE1613572461357246single base substitutionCTexon_variant
PBCA-DE1613572461357246single base substitutionCTupstream_gene_variant
PBCA-DE1613664721366472single base substitutionCTdownstream_gene_variant
PBCA-DE1613664721366472single base substitutionCTexon_variant
PBCA-DE1613664721366472single base substitutionCTintron_variant
PBCA-DE1613664721366472single base substitutionCTupstream_gene_variant
PBCA-DE1613765021376502single base substitutionAC3_prime_UTR_variant
PBCA-DE1613765021376502single base substitutionACdownstream_gene_variant
PBCA-DE1613796451379645deletion of <=200bpA-downstream_gene_variant
PRAD-CA1613580361358036single base substitutionTGintron_variant
PRAD-CA1613580361358036single base substitutionTGupstream_gene_variant
PRAD-CA1613595031359503single base substitutionGAdownstream_gene_variant
PRAD-CA1613595031359503single base substitutionGAintron_variant
PRAD-CA1613595031359503single base substitutionGAupstream_gene_variant
PRAD-UK1613531911353194deletion of <=200bpGTCT-upstream_gene_variant
PRAD-UK1613651511365151single base substitutionATdownstream_gene_variant
PRAD-UK1613651511365151single base substitutionATexon_variant
PRAD-UK1613651511365151single base substitutionATintron_variant
PRAD-UK1613651511365151single base substitutionATupstream_gene_variant
PRAD-UK1613762061376206single base substitutionCT3_prime_UTR_variant
PRAD-UK1613762061376206single base substitutionCTdownstream_gene_variant
PRAD-US1613704731370473single base substitutionCTdownstream_gene_variant
PRAD-US1613704731370473single base substitutionCTexon_variant
PRAD-US1613704731370473single base substitutionCTmissense_variantP123L368C>T
RECA-EU1613508971350897single base substitutionCTupstream_gene_variant
RECA-EU1613583681358368single base substitutionGTintron_variant
RECA-EU1613583681358368single base substitutionGTupstream_gene_variant
RECA-EU1613592431359243single base substitutionAC5_prime_UTR_variant
RECA-EU1613592431359243single base substitutionACexon_variant
RECA-EU1613592431359243single base substitutionACupstream_gene_variant
RECA-EU1613616671361667single base substitutionTAdownstream_gene_variant
RECA-EU1613616671361667single base substitutionTAintron_variant
RECA-EU1613616671361667single base substitutionTAupstream_gene_variant
RECA-EU1613782491378249single base substitutionAGdownstream_gene_variant
SKCA-BR1613514261351426single base substitutionCTupstream_gene_variant
SKCA-BR1613517321351732single base substitutionCTupstream_gene_variant
SKCA-BR1613521961352196single base substitutionGAupstream_gene_variant
SKCA-BR1613526611352663deletion of <=200bpCAA-upstream_gene_variant
SKCA-BR1613531441353144single base substitutionGAupstream_gene_variant
SKCA-BR1613544431354443single base substitutionTAupstream_gene_variant
SKCA-BR1613560861356086single base substitutionGAexon_variant
SKCA-BR1613560861356086single base substitutionGAupstream_gene_variant
SKCA-BR1613575961357596single base substitutionGAexon_variant
SKCA-BR1613575961357596single base substitutionGAupstream_gene_variant
SKCA-BR1613576561357656single base substitutionTGexon_variant
SKCA-BR1613576561357656single base substitutionTGupstream_gene_variant
SKCA-BR1613576721357672single base substitutionAGexon_variant
SKCA-BR1613576721357672single base substitutionAGupstream_gene_variant
SKCA-BR1613580031358003single base substitutionGAintron_variant
SKCA-BR1613580031358003single base substitutionGAupstream_gene_variant
SKCA-BR1613580091358009single base substitutionGAintron_variant
SKCA-BR1613580091358009single base substitutionGAupstream_gene_variant
SKCA-BR1613586331358633single base substitutionGTexon_variant
SKCA-BR1613586331358633single base substitutionGTupstream_gene_variant
SKCA-BR1613632891363289single base substitutionTGdownstream_gene_variant
SKCA-BR1613632891363289single base substitutionTGintron_variant
SKCA-BR1613632891363289single base substitutionTGupstream_gene_variant
SKCA-BR1613654151365415single base substitutionCTdownstream_gene_variant
SKCA-BR1613654151365415single base substitutionCTexon_variant
SKCA-BR1613654151365415single base substitutionCTintron_variant
SKCA-BR1613654151365415single base substitutionCTupstream_gene_variant
SKCA-BR1613657391365739single base substitutionCGdownstream_gene_variant
SKCA-BR1613657391365739single base substitutionCGexon_variant
SKCA-BR1613657391365739single base substitutionCGintron_variant
SKCA-BR1613657391365739single base substitutionCGsplice_region_variant
SKCA-BR1613657391365739single base substitutionCGupstream_gene_variant
SKCA-BR1613711231371123single base substitutionAG3_prime_UTR_variant
SKCA-BR1613711231371123single base substitutionAGdownstream_gene_variant
SKCA-BR1613711231371123single base substitutionAGintron_variant
SKCA-BR1613717461371746single base substitutionGA3_prime_UTR_variant
SKCA-BR1613717461371746single base substitutionGAdownstream_gene_variant
SKCA-BR1613717461371746single base substitutionGAintron_variant
SKCA-BR1613729871372988deletion of <=200bpCA-downstream_gene_variant
SKCA-BR1613729871372988deletion of <=200bpCA-intron_variant
SKCA-BR1613730241373024single base substitutionCGdownstream_gene_variant
SKCA-BR1613730241373024single base substitutionCGintron_variant
SKCA-BR1613751891375189single base substitutionCT3_prime_UTR_variant
SKCA-BR1613751891375189single base substitutionCTdownstream_gene_variant
SKCA-BR1613759771375977single base substitutionCT3_prime_UTR_variant
SKCA-BR1613759771375977single base substitutionCTdownstream_gene_variant
SKCA-BR1613779861377986single base substitutionACdownstream_gene_variant
SKCA-BR1613801631380163single base substitutionCTdownstream_gene_variant
SKCA-BR1613806821380682single base substitutionGAdownstream_gene_variant
SKCM-US1613643641364364single base substitutionCTdownstream_gene_variant
SKCM-US1613643641364364single base substitutionCTexon_variant
SKCM-US1613643641364364single base substitutionCTintron_variant
SKCM-US1613643641364364single base substitutionCTmissense_variantP46L137C>T
SKCM-US1613643641364364single base substitutionCTupstream_gene_variant
SKCM-US1613702121370212single base substitutionCTdownstream_gene_variant
SKCM-US1613702121370212single base substitutionCTexon_variant
SKCM-US1613702121370212single base substitutionCTsynonymous_variantY87Y261C>T
SKCM-US1613702131370213single base substitutionCTdownstream_gene_variant
SKCM-US1613702131370213single base substitutionCTexon_variant
SKCM-US1613702131370213single base substitutionCTmissense_variantP88S262C>T
STAD-US1613702171370217single base substitutionCTdownstream_gene_variant
STAD-US1613702171370217single base substitutionCTexon_variant
STAD-US1613702171370217single base substitutionCTmissense_variantS89L266C>T
STAD-US1613747491374749single base substitutionCTdownstream_gene_variant
STAD-US1613747491374749single base substitutionCTexon_variant
STAD-US1613747491374749single base substitutionCTsynonymous_variantY144Y432C>T
UCEC-US1613701821370182single base substitutionCT3_prime_UTR_variant
UCEC-US1613701821370182single base substitutionCTdownstream_gene_variant
UCEC-US1613701821370182single base substitutionCTexon_variant
UCEC-US1613701821370182single base substitutionCTsynonymous_variantF77F231C>T
UCEC-US1613705731370573single base substitutionCTdownstream_gene_variant
UCEC-US1613705731370573single base substitutionCTintron_variant
UCEC-US1613705731370573single base substitutionCTsynonymous_variantG156G468C>T
UCEC-US1613706361370636single base substitutionCAdownstream_gene_variant
UCEC-US1613706361370636single base substitutionCAintron_variant
UCEC-US1613706361370636single base substitutionCAsynonymous_variantL177L531C>A
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
SNUH_G16_S1COSM3678550c.332A>Cp.Q111PSubstitution - Missense16:1320282-1320282+
CCK81COSM2143500c.428A>Tp.E143VSubstitution - Missense16:1324744-1324744+
TCGA-ER-A194-01COSM3506062c.262C>Tp.P88SSubstitution - Missense16:1320212-1320212+
sysucc-311TCOSM5479033c.334-9C>Tp.?Unknown16:1320429-1320429+
TCGA-CG-4442-01COSM1375939c.432C>Tp.Y144YSubstitution - coding silent16:1324748-1324748+
PT24_1COSM5904437c.414-6C>Tp.?Unknown16:1324724-1324724+
YUDIALECOSM1708611c.239C>Tp.P80LSubstitution - Missense16:1320189-1320189+
HCC1395COSM32768c.334-1G>Cp.?Unknown16:1320437-1320437+
TCGA-BR-4292-01COSM4058386c.266C>Tp.S89LSubstitution - Missense16:1320216-1320216+
LUAD-F00089COSM339631c.311G>Tp.R104MSubstitution - Missense16:1320261-1320261+
MZ7-melCOSM27187c.111C>Tp.N37NSubstitution - coding silent16:1314337-1314337+
TCGA-AA-3672-01COSM267708c.13G>Ap.A5TSubstitution - Missense16:1314043-1314043+
TCGA-A6-5665-01COSM1375938c.129C>Tp.C43CSubstitution - coding silent16:1314355-1314355+
SNUH_G12_S1COSM3678550c.332A>Cp.Q111PSubstitution - Missense16:1320282-1320282+
CSCC-54-TCOSM4572184c.66T>Gp.F22LSubstitution - Missense16:1314096-1314096+
EGC3COSM5054650c.404C>Tp.T135MSubstitution - Missense16:1320508-1320508+
MZ7-melCOSM27187c.111C>Tp.N37NSubstitution - coding silent16:1314337-1314337+
PCSI_0295_Pa_P_526COSM3754656c.138A>Gp.P46PSubstitution - coding silent16:1314364-1314364+
TCGA-EJ-7314-01COSM1470858c.368C>Tp.P123LSubstitution - Missense16:1320472-1320472+
CH-103-T2COSM5650487c.230T>Gp.F77CSubstitution - Missense16:1320180-1320180+
TCGA-FU-A3HZ-01COSM4840544c.447A>Gp.R149RSubstitution - coding silent16:1324763-1324763+
TCGA-DK-A3IU-01COSM3794580c.446G>Ap.R149QSubstitution - Missense16:1324762-1324762+
YULOCUSCOSM5384237c.14C>Tp.A5VSubstitution - Missense16:1314044-1314044+
pfg103TCOSM2143502c.448G>Ap.A150TSubstitution - Missense16:1324764-1324764+
SNUH_G29_S1COSM3678550c.332A>Cp.Q111PSubstitution - Missense16:1320282-1320282+
TCGA-C5-A2LX-01COSM130036c.309G>Cp.W103CSubstitution - Missense16:1320259-1320259+
I2L-P31-Tumor-OrganoidCOSM5363604c.212C>Tp.S71LSubstitution - Missense16:1315715-1315715+
SNUH_G19_S1COSM3678550c.332A>Cp.Q111PSubstitution - Missense16:1320282-1320282+
TCGA-AG-A002-01COSM264517c.247C>Ap.H83NSubstitution - Missense16:1320197-1320197+
ESO-0129COSM1269619c.90A>Gp.K30KSubstitution - coding silent16:1314316-1314316+
T3340COSM4738677c.211T>Cp.S71PSubstitution - Missense16:1315714-1315714+
HN_62421COSM130036c.309G>Cp.W103CSubstitution - Missense16:1320259-1320259+
SNUH_G09_S1COSM3678551c.332A>Tp.Q111LSubstitution - Missense16:1320282-1320282+
YUNIBOCOSM3506062c.262C>Tp.P88SSubstitution - Missense16:1320212-1320212+
AML_14y_05_DXCOSM267708c.13G>Ap.A5TSubstitution - Missense16:1314043-1314043+
TCGA-EB-A5UN-06COSM3506061c.261C>Tp.Y87YSubstitution - coding silent16:1320211-1320211+
TCGA-AA-3663-01COSM1375939c.432C>Tp.Y144YSubstitution - coding silent16:1324748-1324748+
587264COSM1231542c.139G>Ap.G47RSubstitution - Missense16:1314365-1314365+
SNUH_G08_S1COSM3678550c.332A>Cp.Q111PSubstitution - Missense16:1320282-1320282+
SNUH_G31_S1COSM3678550c.332A>Cp.Q111PSubstitution - Missense16:1320282-1320282+
TCGA-AP-A0LM-01COSM967165c.231C>Tp.F77FSubstitution - coding silent16:1320181-1320181+
pfg143TCOSM4748496c.203A>Tp.Y68FSubstitution - Missense16:1315706-1315706+
TCGA-EE-A3AA-06COSM3506060c.137C>Tp.P46LSubstitution - Missense16:1314363-1314363+
C086COSM5363604c.212C>Tp.S71LSubstitution - Missense16:1315715-1315715+
TCGA-AM-5820-01COSM3754656c.138A>Gp.P46PSubstitution - coding silent16:1314364-1314364+
418COSM4431832c.247C>Tp.H83YSubstitution - Missense16:1320197-1320197+
MZ7-melCOSM27187c.111C>Tp.N37NSubstitution - coding silent16:1314337-1314337+
ATL034COSM5706009c.333+1G>Ap.?Unknown16:1320284-1320284+
TCGA-P4-A5EA-01COSM2143498c.348A>Gp.I116MSubstitution - Missense16:1320452-1320452+
6115115COSM5560705c.370A>Gp.N124DSubstitution - Missense16:1320474-1320474+
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.302845;Hs.302849;Hs.30290316p13.3601661
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AGSynonymousp.K30Kc.90A>G161364317ESCA
CAIntronicSNV.c.413+118C>A161370636UCEC
CCTTMissensep.P88Sc.261_262delinsTT161370212CM
CGIntronicSNV.c.223+75C>G161365802MB
CTIntronicSNV.c.151-92C>T161365563CM
CTMissensep.P123Lc.368C>T161370473PRAD
CTMissensep.P32Sc.94C>T161364321CM
CTMissensep.P46Lc.137C>T161364364CM
CTMissensep.P88Sc.262C>T161370213CM
CTMissensep.S89Lc.266C>T161370217STAD
GAIntronicSNV.c.150+292G>A161364669HC
GAIntronicSNV.c.223+144G>A161365871CM
GAMissensep.R149Qc.446G>A161374763BLCA
GCMissensep.W103Cc.309G>C161370260HNSC
GCSpliceAcceptorSNV.c.334-1G>C161370438BRCA
GTIntronicSNV.c.223+93G>T161365820ESCA
GTMissensep.A152Sc.454G>T161374771LUAD
GTSynonymousp.A156Ac.468G>T161374785HNSC