Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TOP2B

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25620799:25620799(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2745C>G
AA Mutation p.Asn915Lys(p.N915K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25627236:25627236(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757502615
CDS Mutation c.1967G>A
AA Mutation p.Arg656His(p.R656H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25630034:25630034(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1684G>A
AA Mutation p.Asp562Asn(p.D562N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25632575:25632575(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1137C>A
AA Mutation p.Asn379Lys(p.N379K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25612528:25612528(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3773T>C
AA Mutation p.Leu1258Pro(p.L1258P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25630060:25630060(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748179631
CDS Mutation c.1658G>A
AA Mutation p.Arg553His(p.R553H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25623658:25623658(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2584T>C
AA Mutation p.Tyr862His(p.Y862H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25626627:25626627(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2157C>A
AA Mutation p.Phe719Leu(p.F719L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25612582:25612582(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3719G>A
AA Mutation p.Arg1240Lys(p.R1240K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25645356:25645356(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.184G>A
AA Mutation p.Glu62Lys(p.E62K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25623586:25623586(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2656C>T
AA Mutation p.Pro886Ser(p.P886S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000264331
Start 25618802:25618802(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3111A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000264331
Start 25643737:25643737(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.288T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000264331
Start 25620787:25620787(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375021372
CDS Mutation c.2757G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000264331
Start 25606100:25606100(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4321delA
AA Mutation p.Ser1441ValfsTer41(p.S1441Vfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000264331
Start 25615469:25615469(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3469G>T
AA Mutation p.Glu1157Ter(p.E1157*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000264331
Start 25637238:25637238(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.616G>T
AA Mutation p.Glu206Ter(p.E206*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000264331
Start 25606099:25606100(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4321dupA
AA Mutation p.Ser1441LysfsTer20(p.S1441Kfs*20)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 19
Mutation Consequence frameshift_variant
Transcription ID ENST00000264331
Start 25604822:25604823(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.4426dupT
AA Mutation p.Ser1476PhefsTer11(p.S1476Ffs*11)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 20
Mutation Consequence frameshift_variant
Transcription ID ENST00000264331
Start 25645437:25645438(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.102dupA
AA Mutation p.Glu35ArgfsTer10(p.E35Rfs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 21
Mutation Consequence frameshift_variant
Transcription ID ENST00000264331
Start 25632451:25632452(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1260dupT
AA Mutation p.Lys421Ter(p.K421*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 22
Mutation Consequence splice_donor_variant
Transcription ID ENST00000264331
Start 25638163:25638163(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.541+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 23
Mutation Consequence inframe_deletion
Transcription ID ENST00000264331
Start 25638296:25638298(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.408_410delTAT
AA Mutation p.Ile137del(p.I137del)
Mutation Classification In_Frame_Del
Feature Type Transcript
Mutation ID 24
Mutation Consequence inframe_insertion
Transcription ID ENST00000264331
Start 25607305:25607306(version: GRCh38)
Mutation Type INS
dbSNP_RS rs746857248
CDS Mutation c.4161_4163dupTGA
AA Mutation p.Asp1388dup(p.D1388dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TOP2B

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25619901:25619901(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3024A>C
AA Mutation p.Lys1008Asn(p.K1008N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25598392:25598392(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs184041688
CDS Mutation c.4796G>A
AA Mutation p.Arg1599Gln(p.R1599Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25604841:25604841(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4408G>T
AA Mutation p.Asp1470Tyr(p.D1470Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25609578:25609578(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3921G>T
AA Mutation p.Lys1307Asn(p.K1307N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25629109:25629109(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1726A>C
AA Mutation p.Asn576His(p.N576H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25609300:25609300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3976G>A
AA Mutation p.Ala1326Thr(p.A1326T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264331
Start 25601143:25601143(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767046447
CDS Mutation c.4572G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000264331
Start 25643703:25643703(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.322G>T
AA Mutation p.Glu108Ter(p.E108*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript