Primary Site >> Liver Cancer

Gene >> APBA1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265381
Start 69516586:69516586(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.625G>A
AA Mutation p.Ala209Thr(p.A209T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265381
Start 69456351:69456351(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1684C>T
AA Mutation p.Arg562Trp(p.R562W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265381
Start 69516498:69516498(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.713A>G
AA Mutation p.Tyr238Cys(p.Y238C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000265381
Start 69516884:69516884(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.327G>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000265381
Start 69456343:69456343(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1692T>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000265381
Start 69516815:69516815(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.396G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000265381
Start 69449748:69449748(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2017G>T
AA Mutation p.Glu673Ter(p.E673*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript