Primary Site >> Liver Cancer

Gene >> TOP2B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25612538:25612538(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3763A>G
AA Mutation p.Lys1255Glu(p.K1255E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264331
Start 25626784:25626784(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2097T>A
AA Mutation p.His699Gln(p.H699Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
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
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000264331
Start 25629041:25629041(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1794T>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000264331
Start 25626606:25626606(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2178C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000264331
Start 25628896:25628896(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1857delG
AA Mutation p.Trp619Ter(p.W619*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript