Primary Site >> Stomach Cancer

Gene >> TOP2A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000423485
Start 40404206:40404206(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2229G>T
AA Mutation p.Lys743Asn(p.K743N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000423485
Start 40396423:40396423(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3580C>A
AA Mutation p.Pro1194Thr(p.P1194T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000423485
Start 40400882:40400882(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371274856
CDS Mutation c.2632C>T
AA Mutation p.Arg878Cys(p.R878C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000423485
Start 40390151:40390151(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4281C>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000423485
Start 40392637:40392637(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs190200755
CDS Mutation c.3912C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000423485
Start 40396390:40396390(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3613delA
AA Mutation p.Thr1205HisfsTer19(p.T1205Hfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000423485
Start 40390129:40390129(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs758129598
CDS Mutation c.4303delA
AA Mutation p.Arg1435GlyfsTer13(p.R1435Gfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000423485
Start 40406679:40406679(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1748delA
AA Mutation p.Asn583ThrfsTer49(p.N583Tfs*49)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000423485
Start 40392279:40392279(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4027delA
AA Mutation p.Thr1343LeufsTer27(p.T1343Lfs*27)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000423485
Start 40400343:40400344(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2865_2866insATTTTAGACACAATAGGTTGCTGATCAATTGTGAG
AA Mutation p.Asp956IlefsTer8(p.D956Ifs*8)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence splice_donor_variant
Transcription ID ENST00000423485
Start 40406383:40406383(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1953+1G>A
Mutation Classification Splice_Site
Feature Type Transcript