USP17L22
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
LAML-KR492643749264374single base substitutionACupstream_gene_variant
LAML-KR492643949264394single base substitutionTCupstream_gene_variant
LAML-KR492644219264421single base substitutionGCupstream_gene_variant
LAML-KR492650419265041single base substitutionATupstream_gene_variant
LAML-KR492666819266681single base substitutionAGupstream_gene_variant
LAML-KR492670379267037single base substitutionTCupstream_gene_variant
LAML-KR492676959267695single base substitutionTCupstream_gene_variant
LAML-KR492679589267958single base substitutionGCupstream_gene_variant
LAML-KR492680619268061single base substitutionTCupstream_gene_variant
LAML-KR492681209268120single base substitutionTGupstream_gene_variant
LAML-KR492681359268135single base substitutionGAupstream_gene_variant
LAML-KR492681379268137single base substitutionCGupstream_gene_variant
LAML-KR492686819268681single base substitutionGAupstream_gene_variant
LAML-KR492688599268859single base substitutionGAupstream_gene_variant
LAML-KR492689949268994single base substitutionCTupstream_gene_variant
LAML-KR492694199269419single base substitutionCAsynonymous_variantP25P75C>A
LAML-KR492695039269503single base substitutionTCsynonymous_variantD53D159T>C
LAML-KR492697889269788single base substitutionATsynonymous_variantA148A444A>T
LAML-KR492705209270520single base substitutionATmissense_variantR392S1176A>T
LAML-KR492705789270578single base substitutionCTmissense_variantH412Y1234C>T
LAML-KR492710289271028single base substitutionCTdownstream_gene_variant
LAML-KR492711009271100single base substitutionGAdownstream_gene_variant
LAML-KR492711779271177single base substitutionGTdownstream_gene_variant
LAML-KR492730139273013single base substitutionAGdownstream_gene_variant
LAML-KR492730379273037single base substitutionTCdownstream_gene_variant
LAML-KR492730499273049single base substitutionCGdownstream_gene_variant
LAML-KR492732499273249single base substitutionAGdownstream_gene_variant
LAML-KR492732939273293single base substitutionTCdownstream_gene_variant
LAML-KR492733079273307single base substitutionGCdownstream_gene_variant
LAML-KR492734899273489single base substitutionGAdownstream_gene_variant
LAML-KR492735559273555single base substitutionCTdownstream_gene_variant
LAML-KR492737139273713single base substitutionCTdownstream_gene_variant
LAML-KR492737399273739single base substitutionCTdownstream_gene_variant
LAML-KR492738119273811single base substitutionCGdownstream_gene_variant
LAML-KR492741649274164single base substitutionCAdownstream_gene_variant
LICA-FR492733579273357single base substitutionGCdownstream_gene_variant
LICA-FR492733609273360single base substitutionTAdownstream_gene_variant
LICA-FR492738389273838single base substitutionCAdownstream_gene_variant
LUSC-KR492643949264394single base substitutionTCupstream_gene_variant
LUSC-KR492644219264421single base substitutionGCupstream_gene_variant
LUSC-KR492647569264756single base substitutionTCupstream_gene_variant
LUSC-KR492650419265041single base substitutionATupstream_gene_variant
LUSC-KR492651459265145single base substitutionTCupstream_gene_variant
LUSC-KR492651529265152single base substitutionTGupstream_gene_variant
LUSC-KR492655429265542single base substitutionCTupstream_gene_variant
LUSC-KR492656769265676single base substitutionCTupstream_gene_variant
LUSC-KR492658879265887single base substitutionGCupstream_gene_variant
LUSC-KR492662819266281single base substitutionCTupstream_gene_variant
LUSC-KR492664509266450single base substitutionCGupstream_gene_variant
LUSC-KR492688509268850single base substitutionCAupstream_gene_variant
LUSC-KR492688599268859single base substitutionGAupstream_gene_variant
LUSC-KR492690939269093single base substitutionCAupstream_gene_variant
LUSC-KR492694119269411single base substitutionTGmissense_variantS23A67T>G
LUSC-KR492694199269419single base substitutionCAsynonymous_variantP25P75C>A
LUSC-KR492694589269458single base substitutionTCsynonymous_variantP38P114T>C
LUSC-KR492694789269478single base substitutionGCmissense_variantC45S134G>C
LUSC-KR492695039269503single base substitutionTCsynonymous_variantD53D159T>C
LUSC-KR492697889269788single base substitutionATsynonymous_variantA148A444A>T
LUSC-KR492698929269892single base substitutionTCmissense_variantV183A548T>C
LUSC-KR492701579270157single base substitutionCTsynonymous_variantT271T813C>T
LUSC-KR492732219273221single base substitutionGCdownstream_gene_variant
LUSC-KR492732229273222single base substitutionGAdownstream_gene_variant
LUSC-KR492733979273397single base substitutionCTdownstream_gene_variant
LUSC-KR492734019273401single base substitutionGTdownstream_gene_variant
LUSC-KR492734529273452single base substitutionCTdownstream_gene_variant
LUSC-KR492734559273455single base substitutionCAdownstream_gene_variant
LUSC-KR492734959273495single base substitutionCTdownstream_gene_variant
LUSC-KR492735169273516single base substitutionCGdownstream_gene_variant
LUSC-KR492735369273536single base substitutionGAdownstream_gene_variant
LUSC-KR492736049273604single base substitutionGAdownstream_gene_variant
LUSC-KR492737499273749single base substitutionAGdownstream_gene_variant
LUSC-KR492738119273811single base substitutionCGdownstream_gene_variant
LUSC-KR492738379273837single base substitutionGTdownstream_gene_variant
LUSC-KR492740209274020single base substitutionGTdownstream_gene_variant
LUSC-KR492740659274065single base substitutionCGdownstream_gene_variant
LUSC-KR492740779274077single base substitutionCTdownstream_gene_variant
LUSC-KR492741649274164single base substitutionCAdownstream_gene_variant
PAEN-AU492702049270204single base substitutionCTmissense_variantT287I860C>T
SKCA-BR492702899270289single base substitutionCTsynonymous_variantL315L945C>T
SKCA-BR492718959271895single base substitutionTGdownstream_gene_variant
SKCA-BR492734489273448single base substitutionGAdownstream_gene_variant
SKCA-BR492735209273520single base substitutionTCdownstream_gene_variant
SKCA-BR492736649273664single base substitutionCAdownstream_gene_variant
SKCA-BR492736789273678insertion of <=200bp-CAAdownstream_gene_variant
SKCA-BR492737449273744single base substitutionATdownstream_gene_variant