Primary Site >> Liver Cancer

Gene >> EXO1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000348581
Start 241881922:241881922(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2116G>A
AA Mutation p.Asp706Asn(p.D706N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000348581
Start 241867034:241867034(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1246A>G
AA Mutation p.Ile416Val(p.I416V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000348581
Start 241885388:241885388(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2286A>C
AA Mutation p.Arg762Ser(p.R762S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000348581
Start 241861477:241861477(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1016A>G
AA Mutation p.Asp339Gly(p.D339G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000348581
Start 241872166:241872166(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1402A>G
AA Mutation p.Thr468Ala(p.T468A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000348581
Start 241889542:241889542(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2483A>G
AA Mutation p.Glu828Gly(p.E828G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000348581
Start 241879124:241879124(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1890G>A
Mutation Classification Silent
Feature Type Transcript